Advances in harvesting water and energy from ubiquitous atmospheric moisture

Atmospheric moisture contains huge amounts of water and energy potential, which, bene ﬁ ting from the advances of nanomaterials, hold great promise in delivering circular economies for the prevalent interwoven water and energy crises. Atmospheric water harvesting (AWH) and moisture-enabled energy generation (MEEG), emerging technologies capable of extracting water and energy from moisture are rapidly developing and advancing toward distributed and decentralized systems. In this review, sorbent-assisted AWH and moisture-enabled energy generation are reviewed in parallel, revealing the correlation between these two technologies. Sorbent-assisted AWH and MEEG are found to be inextricably linked in view of the similarities between both technologies with respect to the moisture/material interactions and basic material prerequisites. Mechanisms, innovative material and structural designs, as well as recent progress in developing devices, are critically discussed. Besides, AWH infrastructures integrated with renewable solar energy for water harvesting and other forms of energy conversion are covered, featuring sought-after energy e ﬃ ciency and multifunctionality. Furthermore, future directions for water and energy harvesting from moisture are outlined, encompassing scienti ﬁ c research and practical applications


Introduction
Many major cities across the globe are at risk of water and energy crises as the demand and consumption of water and energy are soaring due to population explosion, industrialization, urbanization, environmental pollution, and climate change. [1][2][3][4] To address these crises, many efforts have been devoted to exploring alternative water and energy solutions, like seawater desalination, wastewater treatment, photovoltaics, hydroelectricity, wind power, tidal energy, as well as geothermal energy. Nevertheless, these techniques seem unsustainable due to their inherent limitations in terms of geography, climate, energy uctuation, and complex and costly installation. [5][6][7][8][9][10][11] Atmospheric water or moisture is ubiquitously present in the air regardless of geographical and hydrologic conditions, and it plays a key role in the global hydrologic cycle since it holds tremendous amounts of water and energy within it. 12,13 The developments of new materials, particularly, nanostructured materials have seen advanced technologies that can extract water and energy out of this long-neglected resource, suggesting a promising and sustainable approach to address the water and energy crises. These technologies include atmospheric water harvesting (AWH) which refers to the direct generation of water from moisture, and moisture-enabled electricity generators, actuators, and heat batteries to yield electrical, mechanical, and thermal energy via the interaction between moisture and a variety of materials. Water and energy extraction from moisture has become a hotbed of research with a surge in the number of publications reviewing advances in atmospheric water and energy generation technologies. [14][15][16][17][18][19][20][21][22][23][24][25][26] However, most of these review papers either discuss the water and energy strategies separately or one type of energy conversion, without establishing an association between these strategies.
Water and energy are inextricably linked and intertwined. As such, energy is required for water production while water is oen consumed for energy generation. Increasing energy efficiency can lessen the pressure on water resources, and vice versa. 27 This concept of the water-energy nexus has drawn great attention as both water and energy scarcity is becoming increasingly severe. 6,[28][29][30] Thus, in this review, water and energy generation advances will be discussed in the same context with a focus on materials and structural innovation in developing sorbents and devices for moisture-enabled water and energy generation. By having alongside discussion on moistureenabled water and energy generation technologies, the correlation between these two technologies from the perspective of materials design and engineering can be grasped. As summarised in Fig. 1, the technologies of harvesting water and energy from moisture are found to be rooted in the interactions between moisture and materials. These moisture/materials interactions are essentially determined by materials' water affinity, porosity, specic surface area, and thermal/electrical conductivity. Some of the emerging materials such as hydrogels and composites are well-suited for these two technologies. Such a correlation will enable good headway in these technologies as achievement in one technology will promote the progress of the other, considering the interdependency of energy and water commodities.
The structure of this review is organized as follows. First, the development of AWH technologies, especially sorbentassisted AWH is discussed, including mechanisms behind the moisture/sorbent interaction, advanced sorbents emerging in recent years, strategies of engineering materials to boost the water generation performance and energy efficiency, and also recent water generation systems. Next, the technologies developed to harvest moisture-enabled energies, such as heat batteries, actuators, and electricity generators, are introduced, delving into the mechanisms and materials' engineering behind these technologies. Thereaer, the intrinsic connection and key principles in material design for water and energy generation from moisture are summarized. Finally, the future challenges and direction for wide and largescale applications of these moisture-enabled water and energy generations are presented.

Water harvesting from moisture
Atmospheric water harvesting (AWH), as one of the decentralized strategies for freshwater generation, has the potential to provide exible, distributed, community-managed, off-grid access to safe potable water, especially in areas where water scarcity is geographically or economically presented. 12 There are three common ways for AWH, including (1) fog collection by using large nets to capture water droplets suspended in air, (2) cooling air below its dew point to condense and collect water, and (3) sorbent-assisted harvesting where a sorbent or desiccant is employed for AWH. Compared with fog collection and air cooling, sorbent-assisted harvesting demonstrates superiority in terms of applicability to a wide variety of climates and geographies, water production, and energy efficiency. 15,19 2.1 Overview of sorbent-assisted atmospheric water harvesting Sorbent-assisted AWH primarily includes two stages: sorption and desorption. At the sorption stage, the sorbent captures moisture or water vapor and separates it from air. During the Ghim Wei Ho received her PhD in semiconductor nanostructures at the Nanoscience Centre, University of Cambridge in 2006. She is a professor at the Department of Electrical and Computer Engineering at the National University of Singapore (NUS). She leads the sustainable smart solar system research group working on fundamental and applied research on nano-systems with emerging low dimensional nanomaterials, interfacial interactions, and hybridized functionalities for energy, environment, electronics, and healthcare. desorption stage, the sorbent is heated to release the vapor into an enclosed area to create local conditions with high humidity levels. This in turn reduces the sensible cooling requirement and the corresponding specic energy consumption for vapor condensation, especially under arid conditions. 31 The theoretical water production of the sorbent-assisted AWH is the difference between the sorption capacity under the sorption condition and the remaining water in the sorbents under the desorption condition. The energy requirement for sorbents to release water and to be regenerated during the desorption process determines the energy efficiency of the devices, and also denes the possibility to utilize renewable energy, such as solar light for AWH. Choosing a suitable sorbent is crucial to improve the AWH performance in terms of e.g., sorption capacity, regeneration temperature, as well as the adsorption/desorption rate. The primary merits expected of a model sorbent include (1) large water sorption capability at a dened temperature and relative humidity (RH), (2) low regeneration temperature, ideally less than 100°C to utilize solar energy or low-grade waste heat, and (3) a rapid sorption/desorption rate. 32 Other characteristics such as thermal and mechanical stability, non-toxicity, accessibility, and cost, should also be considered when choosing AWH sorbents. Together with the appropriate choice of sorbents, structural design innovation at a device level would enhance the utilization of renewable energy, synergistically bolstering water production and energy efficiency.
This section will focus on strategies of material and structural design for improving sorbents toward water-productive and energy-saving AWH. First, mechanisms underlying the interaction between moisture and the sorbents are examined, followed by the discussion of materials' properties desirable for AWH, aiming to provide a fundamental understanding of AWH sorbents. Then, advances in developing AWH are elaborated with focus on emerging sorbents that have effectively addressed long-standing challenges faced by traditional sorbents (e.g., limited sorption capacity, applicable humidity range, and high energy consumption). Also, innovations to boost the efficiencies of water production and energy consumption, including the integration of photothermal materials and structures as well as stimuli-responsiveness into AWH are summarised. Finally, various sorbent-assisted AWH systems spurred by these material and structural innovations are reviewed, such as desiccant-AWH, solar-driven AWH, and autonomous AWH.

Mechanisms underlying moisture/sorbent interactions
Sorbents, discussed in this paper, can be broadly categorized into two groups, namely adsorbents and absorbents. Adsorbents do not change chemically or physically in the presence of water vapor, whereas absorbents undergo chemical or physical change when they absorb water. 12 Correspondingly, the process of capturing moisture by the sorbents can be classied into adsorption and absorption. Generally, solid sorbents are adsorbents and adsorption tends to be a surface phenomenon, while liquid sorbents are absorbents and absorption is a bulk phenomenon. The moisture capture by the liquid sorbents such as high-concentration solutions of inorganic salts (e.g., CaCl 2 , 33,34 LiCl, 35,36 and LiBr 37,38 ) and ionic liquids, [39][40][41] is an absorption process where the water vapor diffuses into the liquid sorbents driven by the difference in the vapor partial pressure between the air and the surface of liquid sorbents. Solid sorbents such as silica gels, zeolites, activated alumina, and conventional composites capture moisture molecules in the air through physical adsorption (or physisorption), chemical adsorption (or chemisorption), or composite sorption (Fig. 2). 42 2.2.1 Physisorption. Physisorption occurs when moisture is bonded to the sorbent surface by weak van der Waals forces, and is an exothermic and reversible process (Fig. 2a). Thus, physical sorbents commonly feature low adsorption enthalpy, low activation energy, high adsorption/desorption rate, excellent reversibility, and stable cycle performance. The sorption capacity of the physical sorbents largely depends on the surface area, and commonly used physical sorbents include conventional porous sorbents with high specic surface areas, such as silica gels, activated carbon, zeolites, and aluminophosphates.
The sorption/desorption capacity of the porous sorbents can be evaluated from their sorption isotherms which present the equilibrium moisture uptake or loss at different water vapor pressures (or RH) and temperatures. 43 Fig. 2b shows six types of isotherms according to the classication of the International Union of Pure and Applied Chemistry (IUPAC). Type I isotherms are normally observed in hydrophilic microporous structures, like activated carbons, and zeolites. In a Type I isotherm, steep water uptake is presented at very low p/p 0 (or RH) as a result of monolayer sorption or micropore (<2 nm) lling induced by the strong gas-solid interaction between water vapor molecules and the porous materials. The water uptake approaches a limiting value as RH increases because it is determined by the accessible micropore volume rather than the surface area. Type II and III isotherms are depicted by the physisorption of most gases on nonporous or microporous (50-100 nm) sorbents. For Type II, the strong gas-solid interaction allows monolayer adsorption at low RH, and unrestricted monolayer-multilayer adsorption occurs as RH increases further. As for Type III, the water uptake is very low at low RH due to the weak gas-solid interaction or strong hydrophobicity. As RH increases the adsorbed molecules start to cluster around the most favorable sites on the porous structures, leading to an increase of water uptake at high RH. As the favorable sites are nite for Type III sorbents, the water uptake remains nite even at the saturation pressure (e.g., p/p 0 = 1), and they differ from Type II sorbents where the water uptake seems to increase without limit. Type IV isotherms are observed in hydrophilic mesoporous (2-50 nm) sorbents in which the sorption processes involve monolayer coverage induced by the strong gas-solid interaction, multilayer adsorption, and mesopore lling due to capillary condensation that occurs when the pore size is above a critical diameter, D c . Capillary condensation refers to the phenomenon where vapor condensation occurs in a pore at a pressure less than the saturation pressure of the bulk liquid. The pore's critical diameter D c can be estimated by using 44 where s = 0.28 nm is roughly the size of the water molecule, T is the temperature, and T c = 674 K is the bulk critical temperature for water. At room temperature (T = 298 K), the D c is estimated to be 2 nm. This indicates that when the pore size is below 2 nm, a reversible and continuous pore lling due to monolayer or cluster adsorption will occur. However, when the pore size is above 2 nm, the pore lling occurs due to capillary condensation. As this pore lling is irreversible, a hysteresis loop will appear on the isotherm curve. 45,46 Type V isotherms are seen for hydrophobic microporous and mesoporous sorbents. Type VI isotherms are representative of layer-by-layer adsorption on highly uniform nonporous surfaces.
According to the sorption isotherms, Type III sorbents are not good candidates for AWH sorbents because their water uptake starts at high RH and the sorption capacity is quite limited even at saturated vapor pressure. Though sorbents showing isotherms with Type I, II, and IV characteristics can work for moisture adsorption at low RH, they require lots of energy or high temperature to release the captured moisture. Type V sorbents, on the other hand, are regarded as ideal sorbents for AWH because of their S-shaped or step-shaped isotherms that allude to large water uptake and release through relatively small temperature or pressure gradients and warrant large sorption capacity with low energy consumption. 15,31,32 2.2.2 Chemisorption. Chemisorption is caused by the formation of strong chemical bonding (e.g., hydrogen bonding, 47,48 coordination effect, 49,50 and electrostatic interaction 51 ) between moisture and the sorbent surface (Fig. 2c), and is slow, irreversible, and oen requires high activation energy. But compared to physical sorbents, chemical sorbents are superior in their sorption capacity, for example, the water uptake of typical chemical sorbents such as hygroscopic salts (e.g., LiCl, LiBr, CaCl 2 , Ca(NO 3 ) 2 , and MgSO 4 ), can be more than 1 g g −1 . 52,53 The moisture capture process of most hygroscopic salts is essentially a hydration reaction between the salt ions and water vapor. At the molecular level, both water and salts are polar, and when moisture interacts with salts, cations will be attracted to the negatively charged end (oxygen atom side) of water molecules, while anions will be pulled to the positively charged end (hydrogen atom side). As a result, chemical bonding, specically the electrostatic interaction is established, which then seizes the water molecules. Polymers, such as poly(acrylic acid) sodium salt (PAAS), 54,55 poly(diallyl dimethylammonium chloride) (PDDA), 56,57 and chloride-doped polypyrrole (PPy-Cl) 58 also have high sorption capacity because these polymers usually have many hydrophilic functional groups like -OH, -COOH, and -NH 2 that would form hydrogen bonding with water molecules. The coordination effect is oen observed in the interaction between water molecules and many transition metal-containing coordination complexes. 59,60 Similar to physical sorbents, the sorption capacity of chemical sorbents strongly depends on the surface area, where a larger surface area means more active sites to take up moisture. As the water molecules diffuse into the chemical sorbents, some sorbents may undergo signicant volume expansion and agglomeration, which would impede mass/heat transfer and degrade sorption/desorption. Another major concern about the use of hygroscopic salts for AWH is deliquescence. Most hygroscopic salts have a low deliquescence relative humidity (DRH), for example, LiCl and CaCl 2 have a DRH of 11% and 29% at 30°C, respectively. 32 Above DRH, deliquescence will occur which suggests the potential risks of liquid leakage and reactor corrosion when using hygroscopic salts for AWH.

Composite sorption.
Composite sorption applies to the sorbents that are formulated with chemical sorbents dispersed within a porous matrix. The incorporation of chemical sorbents signicantly enhances the sorption capacity, while the physical porous sorbents boost the sorption rate and effectively prevent the volume expansion, agglomeration, and even liquid leakage of the chemical sorbents. 61 The moisture sorption process of composites can be broken down into a series of processes: rst, moisture is captured by the porous matrix due to the hydrophilic pore surface or pore structure; second, the hydration reaction occurs due to the interaction between chemical sorbents and the water molecule; third, with the increase in time or RH, deliquescence of some chemical sorbents like hygroscopic salts occurs to form a liquid sorbent that continues moisture adsorption until an equilibrium of water vapor pressure is reached in a diluted salt solution (Fig. 2d). Desorption is a reverse process involving solution evaporation, salt crystallization, salt dehydration, and vapor escape. This composite sorption process may concurrently or sequentially involve physisorption, chemisorption, and bulk absorption, which reveals the way how most sorbents work for AWH i.e., sorption mechanisms can evolve or transform 62 and couple. This is also disclosed in the recent AWH sorbent innovations (more details will be discussed later). Classic composite sorbents include diverse combinations of porous sorbents and hygroscopic salts, such as LiBr@silica gel, 63 LiCl@silica gel, 64 LiBr/LiCl@silica gel, 65 CaCl 2 @silica gels, 66 MgCl 2 @activated carbon, 67 and CaCl 2 @activated carbon. 68 The sorption capacity and sorption rate have been found to depend on the type and amount of the loaded hygroscopic salts, the water affinity, size, distribution, and the volume of the pores within the porous sorbents, as well as the manufacturing methods. [69][70][71][72] 2.2.4 Materials' properties for sorption. Based on the moisture/sorbent interaction mechanisms discussed above, the material properties to be considered when selecting or designing sorbents for AWH can be summarised as follows: (1) material affinity towards water vapor, which affects the sorption capacity and is also strongly related to the lowest relative humidity where sorbents can work; (2) specic surface area, which signies the number of sorption sites available on sorbents; (3) pore features including pore size, distribution, and volume, which dictate the types of sorption/desorption isotherms, speed of mass exchange, and also the sorption capacity; and (4) thermal conductivity which facilitates heat exchange and the corresponding sorption/desorption. Thus, at the materials' level, approaches that could adjust these properties would be effective strategies to endow sorbents with desirable features for AWH applications.
Surface functionalization is one of the effective methods to enhance the materials' affinity towards water vapor, where materials' surfaces can be modied to possess favourable functional groups to adsorb moisture. For example, functionalizing inorganic mesoporous carbon with amino-containing molecules such as poly(N-izopropylacryl amide) has resulted in a moisture adsorption capacity that is 7.2 times greater than that of the commercial silica gels. 73 The presence of oxygen-containing functional groups such as -COOH contributes to the water affinity of many carbon materials, which can be increased by oxidation treatment. Aside, an enhanced oxidation process has been shown to increase the O/C ratio of graphene oxide by 33%, which has led to a sorption capacity increase from 0.51 g g −1 to 0.61 g g −1 . 74 Similarly, the oxidation of activated carbon has been found to create copious functional groups on its surface, hence resulting in a moisture sorption capacity larger than that of commercial silica gel. Besides the creation of functional groups, the enhancement of the moisture uptake has also been attributed to specic surface area and pore volume augmentation. 75 By optimizing the preparation conditions such as the activation temperature and time, and ZnCl 2 impregnation ratio, the specic surface area of activated carbons can reach 1893.6 m 2 g −1 , which, together with the microporous structures created, has resulted in a Type V isotherm and moisture sorption of 0.56 g g −1 . Designing the pore structure of sorbents is another effective strategy to control the sorption/desorption behavior. A hierarchical porous aluminosilicate has been found to outperform commercial zeolite 3A and silica gel at both low and high RHs. This has been attributed to the chemically modied sorption sites, and also the hierarchical porous structures where both mesopores and micropores exist in a highly ordered hexagonal structure. This ordered structure endows the aluminosilicate with good stability, while the hierarchical meso-and micro-pores afford abundant sorption sites, and more importantly, they facilitate water vapor diffusion in the sorbents. 76 Furthermore, metal or activated carbon with high thermal conductivities has been mixed into the sorbents to improve the heat transfer properties of sorbents. For example, by employing activated carbon as the porous matrix to host silica gel and LiCl, the thermal conductivity of the composite can reach 0.253 W m −1 K −1 , almost 1.6 times that of silica gel. 77 Besides that, increasing the packing density, for example, by compressing loose particle sorbents can enhance the thermal conductivity by 3 times. 78 In addition to consideration of materials' properties, it is also benecial to instil innovations that could help lower energy consumption or engage renewable energy both at the materials and device levels. In the next section, recent advances in sorbent-assisted AWH will be introduced, where strategies adopted to improve the performance of the sorbents and energy efficiency will be discussed.
2.3 Advances in sorbent-assisted AWH 2.3.1 Emerging sorbents for AWH. Fig. 3 summarises the emerging sorbents used for AWH in recent years, which include metal-organic frameworks (MOFs), covalent organic frameworks (COFs), hydrogels, and advanced composites. These advanced sorbents possess numerous attributes such as large surface areas, structural and compositional tunability, accessible pores, physicochemical stability, etc.
2.3.1.1 MOFs. Metal-organic frameworks (MOFs) are porous coordination networks constructed by linking inorganic clusters with organic linkers. 79,80 The wide variety of inorganic clusters, organic linkers, and network topologies used in constructing MOFs, confers MOFs with a high degree of chemical and structural tunability for diverse applications, such as gas storage and separation, catalysis, biomedical applications, electronic and ionic conduction, and sensors. [81][82][83] Together with other remarkable features such as high specic surface areas and high pore volumes, MOFs have been widely accepted as promising AWH sorbents. 31,44,[84][85][86] As mentioned, evolving and coupling sorption/desorption mechanisms govern the recent developments of AWH sorbents. MOFs capture water molecules through multiple mechanisms including (1) chemisorption, whereby water molecules are adsorbed on the metallic clusters, (2) monolayer-multilayer or cluster adsorption, and (3) irreversible pore lling due to capillary condensation. 44 MOF-74 has a Type I isotherm with a preferred moisture uptake at a low relative pressure (e.g., 10% RH), and its moisture adsorption stems from the strong water interaction with open metal ions, e.g. Ni 2+ , Mg 2+ , Co 2+ , and Zn 2+ . 87 Similar phenomena are also observed in HKUST-1 where the high water affinity of the open metal sites, Cu 2+ , contributes to its moisture uptake at around 25% RH. 88 The chemisorption and cluster adsorption function together for the moisture adsorption of UiO-66. 89 The pore size of MIL-101(Cr), ranging from 2.9 to 3.4 nm, is larger than that of MOF-74 and UiO-66 (∼1 nm) and greater than the critical pore diameter (D C = 2 nm) for capillary condensation, or irreversible pore lling. The pore size of MIL-101(Cr), in addition to the chemisorption related to open metal sites, contributes to the Sshaped (or step-shaped, Type V) isotherm and sorption capacity up to 1.4 g g −1 . 90 It is crucial to develop sorbents that can facilitate atmospheric water harvesting in arid and desert climates since other freshwater generation techniques (e.g., fog capture and dewing) and conventional sorbents such as silica gels, zeolites, and hygroscopic salts tend to be energy intensive and impractical. In recent years, Yaghi and colleagues have devoted to creating efficacious devices that can capture moisture in extremely dry air and simultaneously exploit the abundant solar energy in arid areas to minimize the energy cost for freshwater generation.
The key component of these devices are MOF-based sorbents (Fig. 3a)  harvest water up to 0.25-0.84 g g −1 at relatively low RH (0.1 < p/ p 0 < 0.4). Moreover, these MOF-based sorbents can be dehydrated and regenerated at a low temperature (∼65°C) that can be attained by solar irradiation. The thermal insulating nature of MOFs limits the sorption/desorption kinetics, which consequently restricts the sorption/desorption cycling number and hence, the water productivity. In 2022, Zhu's group reported a MOF-derived nanoporous carbon with a density of binding sites up to 40% and a pore size of ∼1 nm. By virtue of the minimized diffusion resistance, efficient solar-thermal heating, and high thermal conductivity, the sorption/desorption kinetics are accelerated. As such, the water productivity of the MOFderived nanoporous carbon can reach 0.18 L kg −1 h −1 at 30% RH under one-sun illumination. 97 When it comes to the practical application of MOFs for AWH, hydrolytic stability is the rst consideration. Some MOFs may undergo hydrolysis or linker displacement which can weaken or even break the metal-ligand bond, 98 losing their hydrolytic stability for AWH. To enhance water stability, selecting appropriate linkers and metal ions is an effective strategy. 99 Linkers such as pyrazolate and imidazolate are favorable in forming water-stable MOFs. 100,101 Modifying the linker with different functional groups is also helpful in improving water stability. For example, non-polar functional groups could provide the steric shielding effect to effectively limit water diffusion to the metal nodes and thus improve stability. 102 Polar functional groups could also work as they are capable of drawing water away from the metal nodes. 103 Highly charged metal ions such as Zr 4+ , Ti 4+ , and U 6+ tend to enhance hydrolytic stability as they are oen highly coordinated to exert a steric shielding effect to protect MOFs from water attack. Also, the kinetic inertness of the metal ions plays a critical role in improving MOFs' water stability. For example, the water stability of the isostructural MIL-53 is found to be consistent with the inertness of the central metals. 104 In addition to improving MOFs' water stability, selecting appropriate linkers and metals is widely sought to enhance their water harvesting performances. As mentioned, the uncoordinated or open metal sites are favourable for water binding, underpinning the sorption capacity of MOFs like HKUST-1 and MOF-74 (ref. 87 and 88) at a low relative humidity. Functionalizing metal clusters or the organic ligands of MOFs with various functional groups also helps to tune MOFs' moisture sorption behaviours. For example, decorating the Zr cluster in Zr(IV)-MOFs with functional groups having high water affinity can lead to a lower operating RH and higher water uptake. 105 The water uptake of CAU-10-X is found to be proportional to the size of the functional group, X, attached to the organic ligands. 106 Essentially, MOFs are porous solids, of which the moisture sorption behaviour can be determined by the porous structures. The pore size is found to play a more important role than the hydrophilicity in determining the sorption behaviour of MOFs. Owing to its ideal micropore size, the water uptake of MOF-801, despite not having any hydroxyl group, is much higher than that of its counterparts having hydroxyl groups (MOF-804 and MOF-805). 91 Modifying MOFs with hydrophilic functional groups can bring about an improvement in water uptake, but in some cases, the modication may also cause an increase in the pore size and the occurrence of capillary condensation. Capillary condensation will lead to a hysteresis sorption/desorption loop, which means that lower RHs or more energies are required for complete moisture desorption.
2.3.1.2 COFs. Covalent organic frameworks (COFs) are porous and crystalline polymers produced by covalently linked organic molecular building units with pre-designed geometry. Owing to their unique features such as low densities, high crystallinity, highly porous structures, large internal surface areas, regular pore structures, and exibly tailored functionalities, COFs have been recognized for wide applications in the elds of adsorption, gas storage, and separation, catalysis, and optoelectronics. [107][108][109][110][111] Similar to MOFs, the water uptake behavior of COFs can be tuned by systematically adjusting chemical functionality and pore size. 112,113 A thorough study details the water uptake behavior of a series of chemically stable Schiff-based COFs (the le panel of Fig. 3b), which reveals the effect of functionality, surface area, and hydrophilicityhydrophobicity on their moisture harvesting performance. Among these Schiff-based COFs, TpPa-1 without any functional groups decorating each COF pore shows excellent performance for water adsorption. It possesses an S-shaped sorption isotherm with a sorption capacity of 0.3 g g −1 and 0.45 g g −1 at 30% RH and 90% RH, respectively. 114 In 2020, Yaghi reported a new, 2D-linked framework, termed COF-432 [(ETTA) 3

(TFB) 4 ]
imine. This COF-432 exhibits attractive water sorption properties, including long-term stability upon water uptake/release cycling,a hysteresis-free S-shaped water sorption isotherm, and low heat of adsorption that allows for regeneration at low temperature or by using low-grade energy sources (Fig. 3b). 115 Distinct from MOFs where metal ions, especially heavy metal ions such as Ni 2+ , Co 2+ , and Cr 3+ , are resting in the center of MOFs, COFs are composed of light elements (e.g., B, C, N, O, and Si) linked together by strong covalent bonds. This metalfree nature of COFs can eliminate the concerns of the potential contamination of metal ion seepage into the freshwater collected. COFs are essentially porous solids formed by covalently linked organic clusters. Thus, functionalizing the organic units with various functional groups to control their hydrophilicity or pore structures is effective to improve the water harvesting performance of COFs.
2.3.1.3 Hydrogels. Hydrogels are networks of hydrophilic polymer chains that are physically or chemically crosslinked, characterized by numerous sites that interact with water molecules, e.g., the hydrophilic/hydrophobic functional groups, the spaces between the network chains, micro-or macro-pores, and voids. 116 This allows for high hygroscopicity and hydration of the hydrogels. Together with their solid states, scalability, and compatibility with practical sorbent-assisted AWH device features, hydrogels, or hygroscopic porous polymers have recently become the focus of next-generation sorbents for AWH. 117 Fig. 3c shows one such hydrogel network with high hygroscopicity and hydration, which is formed by crosslinking quaternary ammonium monomers. Followed by an ionexchange process, the anions in the hydrogel network can be varied to exhibit different moisture sorption behaviors. 118 Similar to MOFs, water sorption of hydrogels supports multiple mechanisms, including chemisorption owing to the hydrogen bonding between hydrophilic functional groups and water molecules, physisorption by mono-/multi-layer adsorption, and capillary condensation due to the presence of nanopores. First principle density functional theory (DFT) calculations have been performed to estimate the energy required to bond water molecules to a hydrogel made from nonstoichiometric zinc oxide. The bonding energy is initially 1.04 eV when a few water molecules are introduced into the hydrogel structures, and then it decreases to 0.7 eV as the number of water molecules increases. The initial high and the decreased bonding energies correspond to hydroxylation (one form of chemisorption) at the early phase of sorption, and the water cluster or layer formation due to physisorption. 119,120 It is noted that the kinetics of hydrogel sorption is distinct from that of other solid sorbents like silica gels and MOFs because vapor transport and liquid transport are coupled with the sorption of hydrogel-based sorbents. When exposed to a humid environment, water vapor rst enters the hydrogel through the interconnected gaseous micropores. Next, due to the presence of a vapor pressure difference, the vapor will diffuse from the center to the walls of micropores, leading to sorption on the liquid-gas interface of the micropores. At the same time, the liquid diffuses through the nanopores of the hydrogel network as a result of the water chemical potential difference between the wet and dry regions of the hydrogel network, which will result in the expansion of the hydrogel network and the shrinkage of the micropores. Through model calculation and experimental verication, the vapor transport is found to be signicant at the initial state when the water content is low and the gaseous micropores occupy a large volume ratio of the hydrogel, while the sorption kinetics tends to be dominated by the liquid transport as the sorption and the liquid transport proceed. This study also demonstrates that for faster kinetics, a thinner hydrogel with a higher shear modulus (to enhance the liquid transport) and appropriate porosity (to balance the vapor and liquid transport) are preferred. 123 For hydrogels in their pure form without any added hygroscopic additives (e.g., inorganic salt or organic additives), the sorption capacity mainly relies on surcial hydrophilic functional groups and porous structure, and is oen less than 1 g g −1 even at high RH. 118 However, the hydrogel network is an exceptional platform for diverse material modication and functionalization, 124,125 which allows for the addition of various hygroscopic salts and photothermal materials to the hydrogel, imparting high sorption capacity and energy efficiency to the composites. Details about the functionalization of hydrogels and the development of composite sorbents will be discussed in the next section on advanced composites.
2.3.1.4 Advanced composites. Conventional composite sorbents are typically prepared by distributing hygroscopic salts (e.g., CaCl 2 and LiCl) in porous matrices like silica gels and activated carbon, with aims to increase the water sorption capacity, sorption/desorption kinetics, and meanwhile, avoid salt leakage. 61 As many innovative sorbents like MOFs and hydrogels have emerged in recent years, the development of composite sorbents also gives rise to new combinations of sorbents, striving to boost AWH performance.
Owing to their large pore volume, huge specic surface area, robust pore structures, and tunable chemical features, MOFs are new and promising porous matrix materials to load large amounts of salt to achieve high sorption capacity. Hygroscopic salts such as CaCl 2 and LiCl have been conned in various MOF matrices and without exception, the sorption capacities of these salt@MOF composites have improved. 121,[126][127][128] For example, the sorption capacity of LiCl@UiO-66 with a salt loading of 35 wt% is six times that of UiO-66 at 60% RH at 25°C. 126 Likewise, conning LiCl in MIL-101(Cr) (le panel of Fig. 3d) changes the sorption isotherm and increases the sorption at 30% RH to 0.3 g g −1 . In contrast, a pure MIL-101(Cr) has a sorption isotherm where the inection of water uptake appears at 40 to 50% RH, which indicates its negligible water uptake at low RH (e.g., #30% RH). 121 The amount of salts loaded in the rigid porous matrices is mainly determined by the total pore volume, and noting that excessive salt loading will lead to the overow of salt solutions, also known as salt leakage. This means that even for MOF materials with huge pore volumes, the salt loading amount and hence the improvement in the sorption capacity is limited, especially when working at high RH. Different from the rigid porous matrices, hydrogels possess crosslinked and exible networks of polymer chains that can host a large amount of water and salt solution, suggesting the feasibility of holding a signicant salt content within hydrogels. The CaCl 2 mass loading has been reported to be as high as 4.0 g per gram of the polyacrylamide (PAM) matrix, exhibiting a sorption capacity of 1.2 g g −1 at 60% RH. 129 CaCl 2 and binary salts (LiCl and CaCl 2 ) have been incorporated inside the biopolymeric alginate network with a loading percentage of 78 wt% and 86 wt%, respectively. These salts@alginate composites exhibit excellent sorption performance over a wide range of humidities: the sorption capacity can be 1.0 g g −1 and 5.6 g g −1 at 26% RH and 90% RH, respectively. 130,131 Zwitterionic polymers possess oppositely charged cationic and anionic functional groups alongside their polymer chains. This characteristic endows a unique salt-responsive anti-polyelectrolyte effect, more specically, the introduction of salt species into the polymer network screens the self-association effect between oppositely charged functional groups and allows the polymer chains to stay stretched even in a high concentrated salt solution (middle and right panels of Fig. 3d). This distinctive anti-polyelectrolyte effect not only helps to coordinate more salt species, but by creating stretched conformations of polymer chains, it also improves the liquid transport (e.g., water solubility and swelling) in hydrogels. The liquid transport is the key to boosting the sorption/desorption kinetics in hydrogel-based materials. Such composite sorbents of a salt@zwitterionic hydrogel exhibit a water sorption capacity of up to 0.62 g g −1 at 30% RH within 2 hours and 1.3 g g −1 at 60% RH. 122,132 Besides the commonly used inorganic salts, organic hygroscopic salts are also incorporated into the hydrogel network to enhance their sorption capacity. For example, introducing polypyrrole chloride (PPy-Cl) into the hydrogel network of poly(N-isopropyl acrylamide) (PNIPAAM) has boosted the sorption capacity from 0.2 (ref. 133) to 6.7 g g −1 . 58 In addition to MOFs and hydrogels, other nanosized porous materials such as activated carbon bers, [134][135][136] and nanosized carbon hollow spheres, 137 are also employed as the matrix for hygroscopic salts. The water sorption capacities of these salt@nanosized porous structures are higher by virtue of nanosized porous structures with large surface areas to host copious well-distributed salts and reduced barriers for mass/ heat exchange during the sorption and desorption process. Moreover, many of these nanosized porous materials such as carbon-based materials have high thermal conductivity, which will benet the sorption/desorption kinetics. 19,77 2.3.2 Engineered sorbents for energy efficient AWH. The materials-by-design paradigm highlights the rational material design strategies to develop materials with desirable properties and functions. Specically, for the development of AWH sorbents, engineering sorbents with photothermal and responsive materials can endow sorbents with explicit features such as light-heat conversion and responsivity to external stimuli. These features will effectively boost AWH's energy efficiency.
2.3.2.1 Nanostructured photothermal materials. Incorporating nanostructured photothermal materials into the sorbents is an effective strategy to improve the energy efficiency of AWH, not only because of the engagement of renewable solar energy for sorbent regeneration (and water release) but also the utilization of solar energy with high energy conversion efficiency. 8,138 By doing so, the localization of thermal energy conversion at the air/liquid interface is ensured to reduce thermal losses and improve the energy conversion efficiency of sorbent regeneration. In 2018, Wang's group reported a bilayered AWH device, where the bottom layer is a salt-loaded brous membrane to capture moisture from air while the top layer is a photothermal layer of CNTs to convert solar energy to heat and release the captured moisture upon sunlight illumination. This bilayered device can work in an arid climate with the humidity down to 15% RH and release water under regular or even weakened sunlight (e.g., 0.7 kW m −2 ). 139 Fig. 4a shows a composite sorbent consisting of active carbon ber felts as a photothermal matrix to host LiCl. This composite sorbent has achieved an ultra-high sorption capacity of 2.83 g g −1 at 70% RH, and the absorbed moisture can be released under one sun illumination. Nanostructured photothermal materials like CNTs are also infused into the hydrogel network to form a hybrid hydrogel network to exploit solar energy for AWH. 129,131,140 Fig. 4b shows one of the typical examples to illustrate the release of the collected water under solar irradiation from a CNT-infused hybrid hydrogel. It is worth noting that in such a hybrid hydrogel functionalized by photothermal materials, the energy efficiency improvement would be more signicant because of the presence of a large proportion of intermediate water within the hydrogel network that effectively reduces the overall energy demand of vapor generation during the desorption process. 9,141 In addition to CNTs, many other nanostructured photothermal materials are found to play a role in solar-driven AWH, including novel nanoparticles, 142,143 graphene, 144  Nanostructured interfacial photothermal materials have also found innovative use in liquid sorbent-based AWH. Vast energy consumption is a well-known issue of AWH based on liquid sorbents, and pertinently, the progress in interfacial solar evaporation is promising to overcome this bottleneck. In 2019, Zhu's group demonstrated an AWH based on a highconcentrated liquid sorbent, of which the desorption process is expected to be energy-consuming. However, by placing a saltresistant GO-based aerogel at the liquid-gas interface as a solar interfacial heater, desorption of the high-concentrated liquid sorbent can be achieved with a solar energy efficiency as high as 66.9%, and the device can produce freshwater of 2.89 kg m −2 $per day at about 70% RH. 34 In this device, the surface of the liquid sorbent is fully covered by photothermal materials, and freshwater is generated based on sequential absorptiondesorption processes. By simply changing the photothermal materials (e.g., the carbon ber membrane) from full coverage to partial coverage over the liquid sorbent surface, as schematically shown in Fig. 4c, this AWH can change the working mode from sequential to simultaneous adsorption-desorption to continuously harvest water from atmospheric air. 40 2.3.2.2 Stimuli-responsive polymers. The terms, stimuliresponsive, smart, or intelligent materials refer to materials that undergo a reversible phase transition accompanied by notable changes in shapes, volumes, transport of ions and molecules, wettability, and adhesion of different species in response to external physical, chemical, and/or biological stimuli. [152][153][154] Owing to their adaptivity and sensitivity to changes in the environment, smart polymers are playing an increasingly important role in manifold elds such as drug delivery, biology, medicine, biosensors, oil-gas industries, coatings, and textiles. [152][153][154][155][156][157][158][159] One of the most widely employed smart polymers is thermal responsive polymers which, in response to temperature, will swily change their physical and/ or chemical properties. There are two types of thermal responsive polymers as shown by the phase diagram in Fig. 5a. If a homogeneous polymer solution starts to separate into heterogeneous phases above a critical temperature (dened as the lower critical solution temperature, LCST), this polymer is an LCST-type polymer. In contrast, if the phase separation happens below a critical temperature (referred to as the upper critical solution temperature, UCST), it is a UCST-type polymer. 153 The most well-known and extensively investigated thermal responsive polymer is poly(N-isopropyl acrylamide), abbreviated as PNIPAAM. PNIPAAM is an LCST-type polymer, which undergoes a reversible phase transition from a hydrophilic coil state to a hydrophobic globule state when the temperature is elevated above its LCST at around 30-35°C. 160 This means that when the temperature is lower than the LCST, PNIPAM is hydrophilic and it can adsorb and store water. Conversely, when the temperature is higher than the LCST, it becomes hydrophobic and starts to repel water out of its polymer network. This unique feature of PNIPAAM is reminiscent of ideal sorbents for atmospheric water harvesting. As reported, an ideal sorbent should preferably be temperature-sensitive; specically, at a designated temperature, the water sorption capacity increases linearly with relative humidity (RH) in the sorption process, and drops steeply with increased temperature in the desorption process. 15 Fig. 5b shows the moisture sorption isotherms of a PNIPAAM interpenetrating polymer network (IPN) gel (the inset of Fig. 5b) at various temperatures. 133 It can be found that the moisture adsorption capacity grows rapidly with RH at low temperatures (<30°C), and it drops signicantly at temperatures above 35°C. This remarkable change in the moisture adsorption capacity with temperature is attributed to the change of the PNIPAAM chains from hydrophilic to hydrophobic, which perfectly illustrates that it has great potential to function as a temperature-sensitive sorbent for atmospheric water harvesting.
Besides conferring temperature sensitivity, the innovative application of PNIPAAM in moisture sorbents can also revolutionize the freshwater collection method in AWH. Gaseous water is adsorbed by freeze-dried PNIPAAM gels and retained as liquid water in the water-swollen PNIPAAM hydrogels. The stored liquid water is oozed out of the hydrogels due to a temperature-triggered (>32°C) change in the hydrophilicity/ hydrophobicity of the PNIPAM chains. This direct water oozing has successfully avoided the cumbersome water collection method used by a conventional sorbent-assisted AWH where the freshwater is collected by a multi-step process involving water vaporization (by heating the saturated sorbent) and the ensuing moisture condensation. 133 By incorporating hygroscopic materials such as MOFs and salts into PNIPAAM, the water sorption capacity can be signicantly increased without an adverse inuence on its water oozing behavior at its LCST. 58,133,142,145,161 In a PNIPAAM-MOF-hybridized matrix (Fig. 5c), the sorption capacity can hit 6 g g −1 at 90% RH, and strikingly, freshwater generation in this hybrid is autonomous and continuous. The captured moisture will spontaneously seep from the hybrid matrix to offer a freshwater supply. Importantly, it can sustain its sorption performance, without having to halt the sorption to proceed with desorption to collect water and regenerate the sorbents. 142 Apart from the gel form, PNIPAAM also paves a way for AWH through diverse forms such as polymer brushes, 162,163 bers, 164,165 and thin lms or membranes. [166][167][168] Many polymers have an LCST close to that of PNIPAAM, around the human physiological temperature, such as poly(N,Ndimethyl acrylamide) (PDEAAM), 169 poly(N-vinyl caprolactam) (PVCL), [170][171][172] poly(methyl vinyl ether) (PMVE), 173 and poly(2isopropyl-2-oxazoline) (PIZO). 174 Other polymers having different ranges of LCST include PEG (polyethylene glycolbased) copolymers (20-85°C), derivatives of 2-oxazoline (PO X ) (23-75°C), and some natural polymers such as methyl cellulose (MC, 40°C), hydroxypropyl cellulose (HPC, 45°C), and hydroxypropylmethyl cellulose (HPMC, 69°C). 160 It should be noted that the LCST can be further tuned by varying the length of the polymer chain, 175,176 the tacticity of polymers, 177 the end group, 178,179 and the type and ratio of the incorporated co-polymer, 180,181 or by adjusting a synthesis condition like pressure. 182 This LCST tunability as well as the discovery of natural LCSTtype polymers offers the feasibility of AWH devices working at different temperatures and eliminates toxicity concerns. Some smart polymers not only respond to one specic external stimulus but can respond to dual-/multi-stimuli. The stimuliresponsive behavior of smart polymers stems from different functional groups within the polymer chain that respond to different stimuli. Combining several functional moieties within one polymer has been proven effective to create dual-/multistimuli-responsive smart polymers. [183][184][185] Currently, although few investigations have conducted on employing dual-/multistimuli-responsive smart polymers in AWH, we can anticipate their promising applications. For example, incorporating lightsensitive functional moieties into a PNIPAAM gel will mobilize a light switch in addition to the temperature switch for this smart sorbent, which would boost its AWH performance, especially in cold seasons or regions.

Sorbent-assisted AWH systems
Beneting from advances in sorbent engineering and development, many sorbent-assisted AWH systems have recently been developed. In accordance with the energy required for the desorption process, these systems can be classied into three modes, that is, desiccant AWH, solar-driven AWH, and autonomous AWH. Among them, desiccant AWH and solar-driven AWH conform to a similar moisture sorption and desorption cycle to extract atmospheric water. The major difference between them lies in the energy input to release the moisture and regenerate sorbents whereby external heaters are required for desiccant AWH, while solar energy is exploited via photothermal materials for solar-driven AWH. Distinct from desiccant and solar-driven AWH, autonomous AWH does not necessarily follow the water sorption/desorption cycle. Instead, autonomous AWH exploits responsive and adaptable materials as sorbents to enable autonomous water release and achieve uninterrupted regeneration of hydro-active sites for continuous sorption.
A typical desiccant AWH is presented in Fig. 6a, in which a combination of heating strips and fans is implemented for forced convective heating during the desorption process. 95 During convective heating, the sorbent bed can be heated to 80-120°C to trigger the release of water vapor and sorbent dehydration for use in the next sorption cycle. The sorption/ desorption cycle can be programmed as desired. With the use of MOF-303, a sorption/desorption cycle can transpire within minutes, which effectively takes advantage of the initial fastest stage of the sorption process and maximizes the number of cycles within a day to boost water productivity. Consequently, the device can deliver water of 1.3 L kg −1 day −1 in an arid environment (32% RH), and at extremely low RH (10% RH), the produced water can be 0.7 L kg −1 day −1 . Besides the heating strips, other electrical heating materials can also be employed, for example, carbon scaffolds, 186 carbon bers, 187 and metal foam. 188 Commonly, these electrical heating materials also work as a backbone to support sorbents, imparting an intimate contact and hence localized electrical heating at the heater/ sorbent interface. Compared with traditional heating methods, the use of localized electrical heating can realize rapid and uniform heating, leading to complete and fast water desorption. At 28-32% RH, a water productivity of 1.95 L kg −1 day −1 can be reached. 186 At 60-88% RH, the water harvesting cycles can be performed eight times over 24 hours and generate water of 2.2 L kg −1 day −1 . 188 Solar-driven AWH has been extensively developed because it can absorb light energy for the desorption process without requiring additional heat or electricity. Many solar-driven AWH systems with diverse structures have been developed, including the single basin, 190,191 the multi-shelves, 192 and the tubular solar still. 193,194 By virtue of its simple conguration, the single basin has been widely applied in solar-driven AWH. 85,92,93,134,195 In these solar-driven AWH systems, moisture sorption happens during nighttime to take advantage of natural cooling. During daytime, the basin is closed and the sun rays are allowed to pass through the basin cover to heat the sorbents, causing the adsorbed moisture to be released and then condensed on the basin walls that are attached to an active or passive cooler. Most solar-driven AWH works in one sorption/night-and-desorption/ day cycle. Using only natural cooling and ambient sunlight as the energy source, 0.1-0.25 L kg −1 day −1 of water can be produced by these solar-driven AWH systems in an arid environment (10-40% RH). 85,92 If an active condenser is added, the water vapor condensation process can be greatly enhanced, leading to daily water productivity of 2.8 L kg −1 day −1 . 93 A recent innovative solar-driven AWH has demonstrated, without an active condenser, manifesting enhanced water productivity by a heat loss reduction tactic. Fig. 6b shows a dual-stage device with the capability to recycle the latent heat of condensation to improve water productivity. Specically, during the solar-driven desorption process, the water vapor released from the rst stage (close to the solar absorber) is condensed at the passive condenser surface, accompanying the condensation heat release. The released condensation heat is collected and exploited by the second stage for desorption. The daily water productivity reaches 0.77 L kg −1 day −1 , which is twice that of a single-stage device. 189 Fig . 6c shows an autonomous AWH system comprising a responsive polymer-MOF-Au-mixed matrix with a cone array geometry, in which directional migration of water droplets can be realized by the gravitation effect to accelerate water removal and refresh the sorbent active sites. 142 An all-day water harvesting process can be realized in such an autonomous AWH system. As shown in the right panel of Fig. 6c, 3.74 g g −1 water has been extracted from the ambient air (90% RH) during the rst 12 hours of moisture exposure, of which 90 wt% is directly released from AWH without activating any heat or solar-driven desorption. The remaining 10 wt% can be fully released via solar light. All in all, this autonomous AWH system can yield 6.39 g g −1 of water in a daily cycle. Note that in addition to solar light, waste heat in the environment can also be used to dehydrate the matrix, suggesting its independence from sunlight and its self-sufficiency in delivering freshwater.

Energy harvesting from moisture
More than 70% of the Earth's surface is covered by water. When the Sun's irradiation hits the Earth's surface, water becomes the largest carrier of energy on the Earth. 13 Atmospheric water or moisture is formed through water evaporation, which contains large-scale and inexhaustible energy because the liquid-to-gas phase transition has absorbed a large amount of heat from the sun and ground radiation. In light of the development of nanomaterials and nanotechnology, many technologies to harvest energy from water have materialized in recent years, with the emerging hydrovoltaic technology being one striking example. 26 Hydrovoltaic technology refers to electricity generation through the interaction between nanostructured materials with water in its diverse forms, including owing liquids, moving droplets, uctuating waves, as well as oating moisture. Moisture is abundant and ubiquitous in air and the interaction with materials (e.g., moisture sorption) can be regulated and heightened, as illustrated in Section 2. This suggests that energy harvesting from moisture possesses the characteristics of AWH like exible, distributed, and off-grid accessibility, and promises to supply decentralized, uninterruptable, clean, and green energy. 6,26,196,197 Here, technologies developed in recent years to harvest energy from moisture or gaseous water are reviewed, where moisture takes on multiple roles as an energy contributor or as a mediator in various energy conversions. Specically, these technologies include moisture-enabled electricity generation (direct moisture-electricity generation and evaporationdriven electricity generation), moisture-responsive actuation, and moisture-mediated heat battery.

Moisture-enabled electricity generation
Nanomaterials usually have a high exposure of their atoms on the surfaces, allowing for substantial interactions with water molecules. The generation of electricity through signicant interactions with moisture has been observed in a variety of nanomaterials, which can be explained primarily by two suggested mechanisms, namely the ionic gradient and stream potential. According to the underlying mechanisms, moistureenabled electricity generation can be categorized into direct moisture-electricity generation (MEG) and evaporation-driven electricity generation (EEG), respectively.
3.1.1 Ionic gradient. Fig. 7a schematically shows the mechanism of the ionic gradient to explain direct moistureelectricity generation. The ionic gradient mechanism oen occurs in nanomaterials with a prebuilt gradient of functional groups, e.g., the hydrophilic oxygen-containing groups of -COOH. These functional groups oen have high water affinity to absorb moisture. The interactions with moisture will weaken or break the polar chemical bonds within functional groups, dissociating the functional groups to release mobile ions, like the protons (H + ) released through the dissociation of -COOH. Thus, when nanomaterials with a prebuilt gradient of functional groups are exposed to moisture, a gradient of the ionic concentration will be established. Driven by this ionic gradient, the mobile ions released during the hydration process will move from the high-concentration region to the low-concentration region, resulting in electricity generation.
The mechanism of ionic gradient underlies many of the socalled direct moisture-electricity generation (MEG) systems where electricity is generated by the interactions of ubiquitous moisture and nanomaterials with ionized groups. 24 Qu's group has pioneered studies on MEG systems. The le panel of Fig. 7b shows a typical moisture-electricity generator consisting of a pair of electrodes and reduced graphene oxide (rGO) with a chemical-gradient structure, e.g., the gradient of oxygen- containing functional groups. 198 Once exposed to air, the functional groups of the MEG active materials start to release free H + due to the ionization of water molecules. Due to the prebuilt gradient of functional groups, the concentration of free H + will be higher at the bottom, driving H + to move towards the top, thus producing voltage and current. Furthermore, this chemical gradient-based MEG can be modied by adding an extra layer of graphene oxide (GO) to feed more mobile ions for electricity generation. Besides, employing asymmetrical electrodes with well-aligned work functions makes the electrons ow in the external circuit consistent with the proton migration within the MEG materials (the middle panel of Fig. 7b). Such a modication can result in a high-voltage MEG with the output approaching 1.5 V. 198 The key to such a MEG system is to create an ionic gradient, e.g., by prebuilding a gradient of functional groups. This chemical gradient can be prebuilt within materials by diverse methods, including electrochemical treatment, 200 air plasma treatment, 201 laser treatment, 198,[202][203][204][205] and concentrationcontrolled electrodeposition. 206,207 Many materials are found to be MEG active, such as graphene quantum dots, 204 graphene oxides, 198,[202][203][204][208][209][210] porous carbon lms, 201 and polymers. [205][206][207]211,212 Besides, instituting a water gradient within materials is a simple but effective method to generate an ionic gradient for MEG. For example, sealing the bottom of the device from moisture and exposing the top to moisture will cause a water gradient and hence an ionic gradient increasing from the bottom to the top, consequently yielding an electrical output. 213 An asymmetrically moisturizing MEG system can be readily achieved by employing two electrodes with different air permeabilities. 214,215 Depending on the nature of the MEG active materials and the structural geometry, the electrical output of MEGs can be either instantaneous pulses in response to humidity variations, or a continuous sustained power output. 21 Restricted by the low concentration of free ions (due to the low coverage of ionized groups in thin-lmed MEG materials) and the fast charge transfer (prompted by the porous structures of MEG materials), the generated voltage or current of typical MEGs tends to occur as electrical pulses that would collapse within tens of seconds (the right panel of Fig. 7b). By increasing the lm thickness of the graphene oxides to hundreds of micrometers, or adopting materials having a large volume of functional groups, the pulses can be changed into a continuous electrical output. 208,215-217 One example is a MEG device that is made from two asymmetrical electrodes and a porous thin lm of protein nanowires. In humid air, a self-maintained water gradient is presented along the thickness of the protein nanowire network, which, combined with ample functional groups bonded to the protein nanowires and the electrode asymmetry, contributes a power supply that is continuous and can last for more than two months. In most cases, the ions responsible for MEG share the same polarity. Recently, inspired by the transmembrane potential across the lipid bilayer of many cells, MEG devices featuring an oppositely charged heterojunction have emerged to deliver continuous power, where ions with opposite electrical polarities are engaged for moisture-induced electricity generation (Fig. 7c). 199,218-220 3.1.2 Streaming potential. When a liquid makes contact with a solid, an electric double layer (EDL) is formed at the liquid-solid interface. 221,222 This EDL, as shown in Fig. 8a (le  panel), is composed of a surface layer rmly adsorbed on the solid (known as the Stern layer) and a diffusion layer that is rich in counter-ions. The boundary between the Stern layer and the diffusion layer is the shear plane, and the distance between the shear plane and the nearest bulk liquid region is the Debye length, in which the concentration of counter-ions is decreasing from the shear plane to the bulk liquid. The liquid ow in a solid channel will transport the counter-ions along with the liquid and form an electrical potential and current which is dened as stream potential or stream current (the right panel of Fig. 8a). 26 For channels with a nanoscale size close to the Debye length of the liquid (typically ranging from 1 to 100 nm (ref. 223)), the EDL will overlap and have more counter-ions in the narrow channel, resulting in a heightened stream potential or current. This phenomenon has been reported for porous materials like stacked carbon nanoparticles, 224-226 silicon nanowire arrays, 227 natural wood, 228 or transition metal oxide nanowires. 229,230 The electrical output of the moisture-enabled electricity generator based on the streaming potential depends on the hydrodynamics within the device. The voltage (or current) of such devices can be continuous without any interruption once the liquid ow in the nanochannels is sustained.
Inspired by the transpiration process of plants, evaporationdriven electricity generation is developed, where the water evaporation process is leveraged to offer uninterrupted liquid ow for streaming potential. Fig. 8b and c show the evaporation-driven electricity generator made from aluminium oxides and its electrical output. 231 A large volume of nanopores presented in these stacked aluminium oxide nanoparticles are ideal nanochannels for streaming potential and also help to drive water through the capillary pressure. 231,232 Similar evaporation-driven electricity generation has been observed on carbon nanoparticles, 224,225 biomaterials, 233 and zinc oxide lms. 234 Besides water evaporation, engineering porous materials with heterogeneous hygroscopicity, for example, by depositing hygroscopic inorganic salts at one end of the device, has proven to be effective in facilitating the liquid ow from the salt-deposited end to the salt-free end, hence resulting in electricity generation. 149,235,236

Other forms of moisture-enabled energy conversion
In addition to moisture-enabled electricity generation, immense efforts have been made to harness moisture in air to play a crucial role in a variety of energy conversions, harvesting mechanical and thermal energies.
3.2.1 Moisture-responsive actuation. In nature, there are many examples illustrating shape deformation in response to humidity in the environment. For example, the opening/closing of pinecones, and the expansion/shrinking of spider silk, 237 bacillus spores, 238 wood, 239 and paper 240 take place as a result of humidity changes. With the wisdom borrowed from nature, many efforts have been devoted to developing water-responsive materials that promise high energy actuation, 241-243 through the expansion/contraction of these water-responsive materials in response to changes in humidity or a water/humidity gradient. Fig. 9a shows a moisture-responsive actuator made from a PEE-PPy polymer composite. This polymer composite can exchange water molecules with the environment to induce lm expansion and contraction, leading to rapid and continuous locomotion powered by the humidity gradient. Besides the moistureresponsive ips, this polymer composite enables the attached piezoelectric elements to convert the moisture-induced mechanical energy into electricity. 242,244 Moisture-induced mechanical energy generation (or moisture-responsive actuation) has also been observed in the networks or bers of polymers, 80,243,[245][246][247][248] bers of graphene oxide and carbon nanotubes, 249-252 membranes of graphene oxide, 253 and composites of graphene/polymer, bacterial spores/polymer, 254 and MXene/cellulose. 255,256 3.2.2 Moisture-mediated heat battery. The moisture adsorption and desorption process essentially involves heat exchange between materials and environments. Thus, the interaction between moisture and sorbents is oen used for thermal storage and heat management. As shown in Fig. 9b (le), when moisture is driven away from the sorbents, the sorbents can be charged with the thermal energy from the environment. Conversely, when moisture is attracted to the sorbents, the charged thermal energy will be discharged back to the environment by a moisture sorption process. 258,259 This heat exchange can be performed in a controllable fashion and can be used for environmental heating and cooling. The moisture sorption of hollow SiO 2 spheres/LiCl composite sorbents can achieve a temperature li of 20°C. A heat battery system based on the SiO 2 spheres/LiCl composite sorbents, when combined with seawater desalination, could be used for household thermal management, as shown in Fig. 9b. 257 In hot weather, the solar thermal energy is charged into the sorbent via a solardriven desorption process, and in turn, during the moisture adsorption process, the energy is discharged to power seawater evaporation to cool the indoor environment. In cold weather, moisture adsorption is directly used for heating. Other means of tapping waste heat exchange include integrating This journal is © The Royal Society of Chemistry 2023 thermoelectric [260][261][262] or pyroelectric elements 6 into the moisturemediated heat battery system to achieve electricity generation. Undeniably, these combinatory efforts of utilizing freely available moisture and waste heat to generate electricity can revolutionize the production of renewable energy.
3.3 Two-in-one water and energy harvesting from moisture As discussed above, owing to the developments of new materials such as advanced porous materials, smart polymers, hydrogels, nanostructured carbon, and photothermal materials, many strategies have been shown to extract freshwater and energy from atmospheric air where the tremendous amount of water and energy has previously been neglected. However, most of the techniques, so far, are designed for a single function-either for solitary water or energy harvesting.
Some recent studies have demonstrated the possibility of a two-in-one system where both water and energy can be harvested from the atmosphere. For example, the GO/PAAS composite comprises the fundamental components of both water and energy generators. 55,216 The moisture-enabled electricity generator based on an HCl/PVA gel can generate a voltage of up to 0.348 V due to moisture sorption; meanwhile, the moisture sorption of this gel can reach around 1.06 g g −1 . 235 A hygroscopic salt-modied corn stalk can harvest atmospheric water with a sorption capacity of 1.84 g g −1 , and upon coating a layer of carbon ink, it can produce an electrical voltage output of 0.6 V. 149 In most previously reported MEGs, the electricity generation was attributed to the ionic gradient built in a single moisture sorption process. In 2022, Qu's group discovered that in addition to the ionic gradient, the ion-hydration energy difference can also account for the driving force of ion movements from the less-hydrated to the more-hydrated regions, consequently generating electricity during a moisture desorption process. 263 This study has demonstrated that power generation can be integrated into a closed moisture sorption and desorption loop, which suggests concurrent atmospheric water and energy harvesting.
It is acknowledged that the hydration capacity of materials, as well as the dependence of the electrical output on materials' hydration level, is of concern when developing such a two-inone system because it can strongly affect the water and electricity generation performance. The hydration capacity of conventional MEG materials is limited, suggesting that these materials, especially at high RH, would rapidly become watersaturated with limited water uptake and tend to produce a short-term output. Recently, Ho et al. reported a moistureenabled water and electricity generator comprising an anioncation heterostructured hydrogel (Fig. 9c). 220 Such a hydrogel heterojunction inherits a high hydration capacity and exhibits exceptional hygroscopicity for AWH. Moreover, the ionic double layer (IDL) and the built-in electric eld of this heterojunction ensure a self-regulating ionic gradient for MEG, making it possible to continuously output power over a wide RH range and a stretched period. The electricity generation strongly depends on the ionic concentration in hydrogels, which can be increased by either ionization during moisture sorption or the solution concentration during the desorption process. All these features synchronize the MEG with AWH to simultaneously generate water and energy.

Summary of mechanisms and materials' properties underpinning moisture-enabled energy generation
According to the above discussions about moisture-enabled energy generation (MEEG) technologies, it can be summarized that these technologies, including the moisture-enabled electricity generator, moisture-responsive actuator, and moisturemediated heat battery, are based on the interactions between moisture and materials. These moisture/material interactions essentially convert the chemical potential energy difference of water molecules between a high-energy gaseous state and a lowenergy absorbed state into various forms of energy, like electricity, mechanical deformation, and heat. 24,259,264 Specically, for the moisture-electricity generator (MEG), gaseous moisture comes into contact with the MEG active materials, anchors to the functional groups of the active materials, and remains in the absorbed state, charging ions with the chemical potential energy. With an asymmetric structure, based on either the predetermined functional group concentrations or the electrodes with different water permeabilities, the chemical potential energy of free ions is transformed into electricity through ionic diffusion. As for the moisture-responsive actuator, the released chemical potential energy is converted into mechanical energy via hydro-expansion of the active materials. To obtain a large deformation, an asymmetric structure is preferred for a moisture-responsive actuator, which typically assumes a bi-layered structure consisting of layers with different responses to moisture, 265,266 or a homogeneous lm structure that is exposed to an environment with moisture gradients. 253,267 The moisturemediated battery mainly exploits the heat exchange with the environment, which is accompanied by moisture sorption/ desorption of the active materials. It should be noted that power generation from the evaporation-driven electricity generator stems from the energy harvested from the environment to sustain water evaporation, where moisture or steam generated by water evaporation acts as a mediator for energy generation rather than a main contributor.
As the fundamental aspect of moisture-enabled energy generation (MEEG), the moisture/material interactions can be tuned to control the performance of these energy generators. Therefore, the strategies employed to enhance the moisture/ material interactions and hence, AWH are expected to also be applicable for the improvement of MEEG performance. These strategies are summarised as (1) the water affinity, (2) specic surface area, (3) porous structure, and (4) thermal/electrical conductivity. Almost all MEG materials, such as graphene oxides, 198,[202][203][204][208][209][210] polymers, [205][206][207]211,212 cellulose bers, 215 etc., have high affinities toward water due to abundant hydrophilic surface functional groups. Hygroscopic materials, such as graphene oxides, 253 polyvinyl alcohol (PVA), 265 Nylon, 268 and moisture sorbents 259 are pivotal to the moisture-responsive actuators and the moisture-mediated heat batteries. These ndings demonstrate the critical role of materials' water affinity in boosting the MEEG performance. For example, introducing hygroscopic sodium polyacrylate (PAAS) into the graphene oxide (GO) framework has been proven efficacious to increase the moisture uptake of the GO/PAAS composite, which has delivered an electrical output that can last for more than 120 hours by augmenting ionic dissociation and transport. 216 Electrochemical treatment 200 and air plasma treatment 201 can be employed to create excess hydrophilic functional groups on MEG materials to elevate their water affinity efficacy and hence, their MEEG performance. As discussed, large specic surface areas signify that more atoms, functional groups, or active sites are exposed to have full interactions with moisture, while porous structures will facilitate the diffusion of water molecules within active materials to promote moisture/material interactions. This explains why most MEEG devices are made from assemblies of various nanomaterials, from quantum dots 204 to nanowires 206,256,269 to nanosheets, 5,270 where abundant active sites and hierarchical pores are synergized to provide high moisture capacity and sensitivity for energy harvesting. The efficient channels for moisture circulation endowed by the porous structure allow for a fast moisture sorption/desorption, laying the groundwork for actuators with fast response. 244,256 Also, the sorption/desorption kinetics can be accelerated by tuning the materials' thermal conductivity. MXenes (Ti 3 C 2 T x ) a type of 2D material with high thermal conductivity, have been incorporated as llers into a polymer matrix to increase the thermal conductivity of the composite. 271 Introducing MXenes for moisture-triggered actuators can lead to a much faster response than those based on polymers. 256,265 The materials' electrical conductivity is one other key factor to be concerned with when optimizing the output power density, especially for moisture-enabled electricity generation. A certain level of electrical conductivity is required to transport charges but being too conductive will facilitate charge transfer and screen the surface change quickly, which can signicantly compromise the output potential. On the other hand, high internal resistance will consume a large portion of energy and lower the output power density. 208,210 Therefore, a good trade-off between the electrical conductivity and the thickness should be considered when designing materials for MEEG.

Perspectives
In this review, we focus on materials and structural innovations for developing sorbents for AWH and devices for moistureenabled energy generation. For sorbent-assisted AWH, mechanisms underlying the moisture sorption of various sorbents are discussed, followed by reviews on recent advances in designing sorbents with excellent water harvesting performance and high energy efficiency. The emerging sorbents, namely MOFs, COFs, hydrogels, and composites, as well as the smart stimuliresponsive and photothermal material incorporated sorbents, demonstrate sorbent-assisted AWH that exhibits high sorption capacity even at extremely low RH (∼10-40%) with high energy efficiency. For moisture-enabled energy generation, we have discussed a variety of moisture-enabled energy conversions including electricity generation, mechanical deformation, and thermal energy storage and management. Besides, craing a two-in-one system for concurrent water and energy generation from moisture has been demonstrated.
Consolidated discussion on water and energy generation technologies can be rendered since both technologies are mutually based on the interaction between moisture and materials. Accordingly, enhancing the moisture/material interaction will greatly boost the performance of the moistureenabled water and energy generators, which, from the perspective of materials design and engineering, can be achieved by improving materials' water affinity, specic surface area, porosity, and thermal/electrical conductivity. This also unravels the intrinsic link between water and energy, where advancement made on water can promote progress in energy pursuit and vice versa. When it comes to moisture-enabled water and energy generation, the learned lessons and wisdom can be shared between the technologies. The same material systems like GO frameworks, hydrogels, and composites have been commonly implemented for both water and energy technologies. Besides, moisture-enabled water and energy generation can be integrated into one system, for example, the two-in-one water and electricity generator, and the moisture-engaged heat batteries. These features, together with the abundance and ubiquity of moisture in air, as well as recent advances in moisture-enabled water and energy generations, illustrate that these technologies hold much promise for addressing challenges of the water-energy nexus, by offering sustainable, uninterruptable, decentralized, and off-grid access to potable water and green energy commodities.
Despite remarkable progress in recent years, it is acknowledged that studies on moisture-enabled water and energy harvesting are still in their infancy. Much of the research is still in the early stage and restrictive in scaling up. The mechanisms are not yet well-established to comprehensively explain, especially at an atomistic level, the moisture/materials interactions, the mass/energy exchange between materials and environments, as well as the water and energy generation courses. Some of these challenges and perspectives are summarized as follows.

Boosting the water and energy generation performance
High water productivity and output power density are the ultimate goals for generators, but currently, these numbers of most reported water and energy generators are still too small for practical applications, necessitating more efforts to boost their performances. Water productivity is not only dependent on the water sorption capacity of sorbents but also largely related to the moisture sorption/desorption kinetics as it will determine the number of sorption/desorption cycles and the water production within a certain time accordingly. Most of the current research tends to focus on increasing sorbents' sorption capacities or evaluating the water production on a single sorption/desorption cycle basis, with little attention paid to the sorption/desorption kinetics and the water production based on a multi-cycling mode. Therefore, the sorption/desorption kinetics of sorbents as well as the cycling performance are expected to be augmented when developing sorbents for AWH. As demonstrated by recent advances in AWH sorbents, employing nanostructured materials with high specic surface area and exploring approaches to engineer and functionalize materials' surfaces will enhance the moisture/material interaction, which in turn, will improve the energy generation enabled by moisture. Thus, the progress achieved in the development of AWH sorbents, e.g., the emerging materials can work as a reference and guide for increasing the output power density.

Increasing energy conversion efficiency
For AWH, energy consumption is always of concern. Although notable progress has been made in recent years by combining smart stimuli-responsive materials and photothermal materials in sorbents, there is still a lot of room for further exploration. For example, the use of temperature-responsive polymers makes it possible to release the captured moisture and dehydrate the sorbents at a temperature as low as around 30°C, largely reducing the consumed energy. However, most of the studies on AWH sorbents have been centered around temperature-responsive polymers, particularly PNIPAAM. Given their impressive efficacy in increasing energy efficiency, studies on a wider variety of temperature-responsive and stimuliresponsive materials are expected in the future. Currently, most photothermal materials are composited with ready-made sorbents (e.g., MOFs or hydrogels), merely acting as a lightinduced heater. It is known that the thermal conductivity of carbon-based photothermal materials like CNTs and graphene oxides, are superior to that of most MOFs and hydrogels, which is desirable for high sorption/desorption kinetics. Moreover, it is possible to readily fabricate porous matrices of these carbon materials so as to engineer the properties of these materials. 55,201,[272][273][274] Hence, this spurs the porous carbon-based photothermal materials to be directly used in a solar-driven AWH. Formulating a hybrid energy harvesting system not only achieves various moisture-enabled energy conversions, but also harnesses multiple types of low-grade energy from the environment when combined with other functional materials or structures, e.g., thermoelectric, piezoelectric, and photothermal materials. Such a synergistic design of a hybrid system will enhance the energy conversion efficiency of a moisture-enabled energy generator.

Fundamental studies
Despite the overall mechanisms available to explain moistureenabled water and energy generation, fundamental details that can unravel the moisture/material interaction at the atomic level are not precisely grasped. For example, metal ions centered in the porous MOF structures are considered to be dominant sites for moisture capture, but recent X-ray diffraction studies on MOF-303 show that the polar organic linkers have more to do with moisture sorption. 96 The streaming potential is believed to govern the moisture-enabled electricity generation of porous carbon materials, but it is not clear how the ionic gradient mechanism plays a role in delivering power, given the fact that numerous functional groups are present on the surfaces of these carbon materials. Moreover, the electrical double layers (EDLs) are the basis of streaming potential generation, but their structures and chemical components are theoretically predicted without sound experimental evidence. The selection and conguration of electrodes are crucial for moisture-enabled electricity generation because different electrodes may contribute differently to and even dominate electricity production, but to date, research on the effects of electrodes is scarce to further understand these fundamental issues. Hence, more fundamental studies are expected to reveal the underlying principle to guide future developments in water and energy generators.

Device-level optimization
Although this review focuses on strategies for boosting water and energy generation at the material level, future progress in device-level optimization is expected as it is required for wide and large-scale applications. Optimizing the device layout to ensure the best vapor/heat exchange between the generator and environment would promote the thermodynamics and kinetics of moisture sorption/desorption and vapor condensation, leading to enhanced water and energy productivity per volume/ area. Successful integration of water and energy generation into one system would further optimize the utilization of moisture. Moreover, by effectively combining a moisture-enabled water and energy generator with other techniques like the heat battery, thermo-/pyroelectric modules, as well as seawater desalination systems, waste heat can be fully capitalized and transformed into useful energies.

Conflicts of interest
There are no conicts to declare.