Superior supercapacitive performance of Cu2MnSnS4 asymmetric devices

Renewable energy sources are considered the cornerstone of achieving a sustainable future for today's modern world.


Introduction
Eco-friendly and efficient energy storage systems are emerging as an urgent need to meet the ever-increasing energy demands. Supercapacitors (SCs) in particular are attracting unparalleled attention because of their low weight, high power density, rapid charge discharge, extended cyclic ability, and robustness. 1,2 However, the current carbon-based SCs are affected by a low energy density when compared to batteries. It is therefore attractive to have a wide range of applications for supercapacitors that can deliver high energy density, which has evolved into an essential requirement. It is still believed today for these supercapacitors that, it would be possible to improve the energy density by increasing the cell potential, which can be achieved by electrode combinations. [3][4][5] Metal suldes have many redox reactions to form good quality SCs with battery-type electrode materials and they are considered as positive electrode materials. Depending on the device, they may exhibit an extended potential window and higher energy density than conventional supercapacitors. [6][7][8][9][10] Based on their electrochemical charge storage, generally pseudocapacitors (PCs) exhibit higher specic capacitance values than electric double layer capacitors (EDLCs). 11,12 The reason is that in EDLCs, the charges between the electrode and electrolyte interfaces are stored by processes such as the diffusion/charge accumulation process, whereas in pseudocapacitors, the charge is stored by redox reactions in the active substance (mass), such as the faradaic process. 13,14 Carbon-aerogel, carbon nanotubes, carbon cloth, graphene, and activated carbon are used in EDLCs, whereas metal oxides/hydroxides/suldes are extensively used as electrode materials in pseudocapacitors. 15,16 Metal oxides/ suldes, such as MnCo 2 O 4 , NiCo 2 O 4 , FeCo 2 O 4 , CoS, and Ni 3 S 2 , have attracted more research attention because they provide signicant benecial characteristics, such as a high energy and power density, and more specic capacitance thanks to their rapid and reversible rich redox reactions on the electrode/ electrolyte interface. Various transition metal sulde electroactive materials have been explored for electrochemical capacitors (ECs) due to their rich valence and desirable chemical stability. 17,18 Suldes are considered to be excellent pseudocapacitive materials, especially thanks to their multiple redox reactions, improved electrical conductivity, and low band gap, which lead to their superior performance, better oxidation state, and longer cycling capability when compared to metal oxides/ hydroxides. 19,20 In general, the pseudocapacitance capabilities of these suldes in alkaline solutions are exhibited in the faradaic reactions that are associated with the mutual transformation from ion diffusion into electrode materials with rich electroactive sites. Cu 2 XSnS 4 (X ¼ Mn, Fe, Co, Ni, Zn, and Cd) (CXTS) materials have excellent structural and optical properties, absorption coefficients, and catalytic efficacy in redox reactions due to their multiple oxidation states. 21,22 Among their most interesting benets in practice are the production of materials with a high surface area, good porosity, and production of comparatively labor-intensive planar and conformal nanostructured layers using a simple, low cost, quick, and measurable process. The metal chalcogenides have attracted great research interest due to their enhanced electrochemical properties. Molecular metal chalcogenide species can be broken down from the bulk chalcogenide complex and formed as a result of the basic nucleophilic reactions involving the chalcogenide anions. [23][24][25] The hydrothermal method is the best technique for designing a good quality micro/nano structure compared to all other methods. During the initial nucleation in the hydrothermal reaction, the acceleration of the endothermic reaction results in a disruption of the nuclei, which dissolves the urea ions, resulting in an insufficient activation surface energy and subsequent defects. 26,27 Acidic acid, citric acid, and oxalic acid are all well-known structure directing agents that can be clas-sied from dicarboxylic acid. They are also considered to be powerful reducing and chelating agent for metal cations. The acidic strength of oxalic acid is much greater than the other two, and therefore, it can lead to a better structure; thereby creating more ionic transport at the electrode/electrolyte interface, resulting in an improved electrochemical behavior. 28,29 In this study, a solvothermal process was pursued utilizing a ethanolmixed de-ionized water solution as the solvent. The structure directing agent's role in creating the Cu 2 MnSnS 4 nanostructure could be visualized from the FE-SEM analysis. Characterization of the materials was performed by several physicochemical, chemical, and electrochemical techniques. Here, superior supercapacitive performances of Cu 2 MnSnS 4 asymmetric devices could be reported. To the best of our knowledge, this was also the rst study to investigate and report the use of Cu 2 MnSnS 4 nanostructures fabricated based on the use of different directing agents for fabricating a positive electrode for supercapacitor applications.
The working electrode was formulated by mixing Cu 2 MnSnS 4 (prepared with AA, CA, or OA) as an active cathode material, activated carbon as the anode material, and polyvinylidene uoride (PVDF) as a binder in a 75 : 20 : 5, weight ratio. Then, all three materials were ground for at least 30 min. Thereaer, the mixed electrode material was dispersed in the solvent Nmethyl-2-pyrrolidone (NMP) and ground for 1 h to prepare the electrode slurry. Well-cleaned nickel foam was employed as a substrate (1 Â 2 cm 2 ). A 1 Â 1 cm 2 section of nickel foam was coated with the prepared slurry using a mercury premium art small size brush. The coated nickel foam was dried in a hot air oven at 80 C for 12 h and the loading material was adjusted to 2 mg cm À2 on the electrode surface. These Cu 2 MnSnS 4 (AA, CA, OA) electrodes, platinum (Pt) wire, and Ag/AgCl were utilized as the working, counter, and reference electrodes. Electrochemical measurements in 2 M KOH electrolyte were performed using a BioLogic potentiostat. CVs at different scan rates ranging from 10 to 100 mV s À1 were recorded at a 0.6 V constant potential, and 0.5 to 5A g À1 current densities at 0.5 V potential were utilized for the galvanostatic charge discharge (GCD) readings. The electrochemical impedance spectroscopy (EIS) study results were analyzed by Nyquist plots and tted by Z t analysis. Eqn (1) was employed to estimate the specic capacitance from the GCD prole, and similarly the two-electrode (full-cell) system was set up with the two equal loadings mass balanced using the and then coated on to the positive and negative electrodes. The full-cell device parameters such as energy (E) and power (P) density, were measured using eqn (2) and (3). Eqn (4) was used to calculate the coulombic efficiency of the materials from the GCD curves.
where, t d and t c are the discharging and charging time, respectively. 30,31

Trasatti method analysis
The Trasatti method was rst used to identify the EDLC behavior and PC behavior by the eminent scientist S. Trasatti in 1990 using the formula where q T is the total voltammetric charge, q i is the charge stored at the inner surface, q o is the charge stored at the outer surface, and C T is the total capacity, which is the sum of the pseudocapacity and the electric double layer capacity. In general, in the outer surface V / N; therefore it just allows the surface process to happen. Hence, the more accessible area is in the electrode electrolyte interface. In the same way, at the inner surface, V / 0; therefore it gives sufficient time for the diffusion and for more ions to react. Hence, it has less accessible area.
Step 2. Calculate the specic capacity (C g À1 ) at each scan rate using the following formula, where C q denotes the specic capacity (C g À1 ), S is the area enclosed by the CV curve, n is the scan rate (mV s À1 ), and m is the active mass in the electrode surface.
Step 3. Estimation of the total capacity (C T ). Let us assume semi-innite linear ion diffusion (i.e., ions randomly diffuse from the bulk electrolyte to the electrode/ electrolyte interface, when V / 0, q / q T ). Based on the Cottrell equation, a linear correlation between the reciprocal of the calculated specic capacity (1/C q ) and the square root of scan rates (n 1/2 ) gives the maximum total capacity by extrapolation to the Y intercept.
Multiply both sides by dU: Step 4. Estimation of the charge stored at the outer surface (C o ).
In the same way, assuming semi-innite linear ion diffusion (i.e., ions randomly diffuse from the bulk electrolyte to the electrode/electrolyte interface, when V / N, q / q 0 ), based on the Cottrell equation, a linear correlation between specic capacity (C q ) and the reciprocal of square root of scan rates (n À1/ 2 ) gives the charge stored at outer surface (C o ) by extrapolation of the intercept to the Y axis.
Divide both sides by dU Step 5. Estimation of the inner surface (C i ). Based on the Cottrell equation, the maximum capacity (C T ) and charge stored at the outer surface (C o ) could be calculated. The maximum capacity (C T ) is the sum of the inner (C i ) and outer surface (C o ), i.e., C T ¼ C i + C o , where C T is the total capacitance, C i is responsible for the maximum pseudocapacitance (C i ), and C 0 corresponds to the maximum electric double layer capacitance. Subtracting C o from C T gives the maximum pseudocapacitance (C i ).
Step 6. Estimation of the percentage capacitive contribution.

Results and discussion
The obtained material crystal structure was characterized using X-ray diffraction analysis ( Fig. 1(a) Table 1.
The growth mechanism of the Cu 2 MnSnS 4 product in the presence of the chloride precursor in the solvothermal reaction mixture in the well-closed Teon tube produced Cu 2+ , Mn 2+ , Sn 4+ , and S 2À . Most importantly, when the compounds were combined with thiourea, sulfur ions were released in the autoclave during the reaction mixture. Here, the S 2À ions reacted with the metal ions Cu, Mn, and Sn during the nucleation formation of Cu 2 MnSnS 4 , as suggested by the following equations. 32 (18) The small crystalline size and poor crystallinity of the material were explored for improving the electrochemical performance. This is because of the fact that poor crystalline materials create more ion transport channels than crystalline materials, which is an important factor in electrochemical supercapacitors. Photoluminescence was utilized as an eminent tool to investigate the emission behavior of the synthesized Cu 2 MnSnS 4 (AA, CA, OA). In Fig. 1 .34), and 542 nm (2.28 eV). Here, a higher intensity suggests a faster recombination rate. Seven photoluminescence peaks could be detected and with almost the same PL emission bands, expect for the intensity. The strong and broad blue emission band located at 485 nm was in good agreement with the Cu-S hierarchical structures, which absorb more photons to produce electron-hole pairs, which may start from the excitonic band edge or free-charge carrier transition at 2.55 eV. Weak green emission bands were observed at 529 and 542 nm. The blue emission band at 420 nm had a slightly broad band, which represented defects present in the prepared samples. The emission peaks assigned at 446 and 460 nm indicated different defects, which largely depended on the high density of sulfur and tin vacancies. 34,35 The lattice vibrations of a material can be measured using Raman spectroscopy and so was used here, as shown in Fig. 1(c). The characteristic Raman band occurred at 282 cm À1 , which was attributed to the Sn-S phases in Cu 2 MnSnS 4 . The Cu-S stretching mode vibration was detected at 449 cm À1 . The small peak located at 720 cm À1 revealed a second-order Raman scattering mode of the prepared samples. In the synthesized product, the main broad peak existed in the Vis-NIR region at 1090 cm À1 . C-C stretching vibrations were observed for the remaining bands present at 1736 and 2432 cm À1 . 36 FTIR spectrometry is a well-known technique used to characterize the molecular ngerprint region of synthesized products, and so was used here (Fig. 1(d)). Initially, a small quantity of the sample was mixed with potassium bromide (KBr) and nely grounded and then pressed well into a hydraulic press to be converted into a pellet shape. The acquired spectrum was within the range of 4000 to 400 cm À1 . The characteristic spectrum 3448 cm À1 corresponded to the OH stretching vibration of water molecules observed on the sample. The vibrations at 1639 and 1820 cm À1 were because of the bending vibrations of OH water molecules. The absorption bands located at 2853 and 2929 cm À1 were due to the CH stretching vibration mode. The  Fig. 2 shows the morphological images of the prepared Cu 2 MnSnS 4 with using different structure directing agents, i.e., acidic acid (AA), citric acid (OA), and oxalic acid (OA), as studied using FE-SEM analysis. Irregular shapes with non-uniform size morphologies were found in the AA and CA samples, whereas well-formed ower shapes were found with the addition of oxalic acid, which exhibited a strong role in the ower-shape formation. The thickness of a few micrometer of the 2D thick plate-like petals was loosely covered with rose-like thrones. The structure of the ower shape facilitates high ionic transport and increases the accessible specic surface area. However, the petals in the ower were tightly stacked and appeared as thin pieces. 39 It was clearly evidenced that when using the structure directing agents AA and CA in constant hydrothermal reactions, the particles agglomerated to form irregular akes ( Fig. 2(a-d)), while OA exhibited a ne ower-shaped morphology, as shown in Fig. 2(e and f). When compared to the AA and CA samples, the OA samples in the ethanol and distilled water mixture in the solvothermal route co-ordinate metal ions to urea and so are stronger combined. However, the petals in the owers are stacked tightly, resembling thin slices. Initially, nanocrystals of Cu 2 MnSnS 4 are formed as the seeds for microcrystal formation. The aggregated nanocrystals become larger and they coalesce to grow into akes due to the CA addition in the hydrothermal reactions. The hydrogen bond interacted with urea to form selfassembled ower-like microstructures by the addition of oxalic acid at a constant temperature. By the proper selection of structure directing agents, the sheet-like structures selfassembled and coalesce into a ower-shaped morphology. During this formation, the surface energy decreased. 40 Elemental analysis or chemical characterization of an area can be studied using EDS analysis. Fig. 2(g-k) shows the EDS SEM mapping images of the Cu 2 MnSnS 4 -OA sample. The  higher peak in a spectrum revealed a higher concentration in the elemental composition. Fig. 2(l) shows the EDAX spectrum of the Cu 2 MnSnS 4 -OA electrode, which was composed of Cu, Mn, Sn, and S elements with good atomic and weight percentages as shown in the inset of Fig. 2(l). The elemental purity of the samples was conrmed by the absence of impurity peaks. 41 Fig. 3 presents the TEM images of the synthesized Cu 2 MnSnS 4 nanostructure with the addition of oxalic acid. Non-uniform ower-like structures were located in many places with sizes in the 1-3 mm range. The well-resolved lattice fringe distances were approximately 0.31 nm, which well matched with the (112) crystal plane for the Cu 2 MnSnS 4 -OA electrode, as shown in Fig. 3(c). The selected area electron diffraction (SAED) pattern of the Cu 2 MnSnS 4 -OA electrodes showed the good crystallinity of the sample (Fig. 3(c)), which correlated with the X-ray results. The elemental constituents present in the product Cu 2 -MnSnS 4 were studied using XPS (Fig. 4). Fig. 4(a) presents the survey spectrum of the as-obtained Cu 2 MnSnS 4 compound. The Cu binding energy species are shown by major peaks at 931.62 eV (Cu2p 3/2 ) and 951.61 eV (Cu2p 1/2 ) and the corresponding satellite peaks at 941.67 eV (Cu2p 3/2 , Sat) and 961.42 eV (Cu2p 1/2 , Sat) ( Fig. 4(b)). Here, the peak splitting of 19.99 eV represents the Cu(I) congurations. Two 2p peaks appeared at 648.28 eV for Mn2p 1/2 and at 640.43 eV for Mn2p 3/2 (Fig. 4(c)). The peak splitting of 7.85 eV indicated the Mn(II) conguration. The binding energies located at 485.51 and 493.83 eV were due to Sn3d 5/2 and Sn3d 1/2 , respectively ( Fig. 4(d)). The peak splitting of 8.52 eV indicates the Sn(IV) conguration. The binding energies from 160 to 164 eV were related to the sulde phases (Fig. 4(e)). S2p 3/2 and S2p 1/2 showed peaks at 161.08 and 160.01 eV, respectively, with the peak splitting of 1.07 eV. 42 The surface area (m 2 g À1 ) and pore-size (cm 3 g À1 ) distribution of the synthesized Cu 2 MnSnS 4 electrodes were measured using Brunauer-Emmett-Teller (BET) analysis, as displayed in Fig. 5(a). All the fabricated electrodes exhibited type IV isotherms, which are a general distinctive isotherm of mesoporous specimens ( Table 2). The Cu 2 MnSnS 4 -OA electrodes provide high electrolyte contact at the electrode and electrolyte interface because of its large surface area. This leads to better ionic transport for faradaic reactions than the other two electrodes. The pore-size distribution was observed employing the Barrett-Joyner-Halenda (BJH) approach, which suggested that the entire prepared electrode had pore sizes in the 3 to 50 nm range, which clearly signied that the three samples were in the mesoporous range (Fig. 5(b)). Furthermore, the high specic surface area and mesoporous nature of the Cu 2 MnSnS 4 -OA electrode allows more specic parts of the electrolyte to diffuse effectively at the electrode with minimum internal resistance. 43 Electrochemical studies, such as CV, GCD, and EIS, were used to investigate the charge-storage performances of Cu 2 -MnSnS 4 (AA, CA, OA) in three-electrode setups. Fig. 6(a-c) show typical CV plots from 10 to 100 mV s À1 . The pair of redox reactions that are invisible in electrical double layer capacitors are evident in the CV curves and conrmed its battery-type behavior, which is the key characteristic of the pseudocapacitive mechanism. 44 The good redox peaks indicated charge storage derived from the Faraday process in battery-type electrodes. The apparent changes at high scan rates showed the improved rate performances of the electrode. 45 A pair of oxidation and reduction reactions of the anodic and cathodic voltage peaks at 10 mV s À1 scan rate was observed at E a ¼ 0.50, 0.45, 0.41 V and E c ¼ 0.38, 0.33, 0.28 V for AA, CA, and OA, respectively. When the scan rate was increased from 10 to 100 mV s À1 , the redox peaks moved toward higher and lower energies and the corresponding peak current (i p ) also increased.
At low scan rates, the electrolyte ions and active species have sufficient time to interact with each other. This increases the probability of redox reactions occurring; nevertheless, at high  scan rates, the interaction of ions is not perfect due to their short residence time, which limits the different reactions between them. Cyclic voltammetric curves are affected by diffusion-controlled and kinetic-controlled processes. If a redox process is only affected by diffusion, the peak potential should generally be independent of the scan rate. Nevertheless, in contrast, if the electrode kinetics is dominant, the peak potential is affected by the voltammetric changes due to the increasing scan rates. Furthermore, the nature of the redox process can be easily identied by the cathodic and anodic shis. In view of the fact that this electrode material exhibited a battery-like behavior, there should be an apparent change in the peak shi. 44 Furthermore, this reduces the reaction kinetics because of the material polarization and ohmic resistance during the redox process, resulting in the formation of reversible peaks. The anodic peak current increased when the scan rate increased, which also led to an increase in the CV curves area directly proportional to the specic capacity. In all three samples, the lower scan rate (10 mV s À1 ) exhibited a higher capacity, which  gives sufficient time for the ions to diffuse and react in the electrode/electrolyte interface. As a result, there is less accessible area occupied at the lower surface of the electrode for the electrochemical reaction process to occur. 46 The calculated specic capacity values are summarized in Table 3. The OA electrode displayed the highest specic capacity, which may be due to the well-arranged structure of the samples as proven in the FE-SEM analysis. This is because of the obtained nanostructures, which enhance the electrode specic surface area and rational pore-size distribution and greatly enhances the specic capacity, as clearly evidenced from the BET surface analysis. The specic capacity, stability, and time reversibility of the Cu 2 MnSnS 4 electrode material were studied by GCD characterization study. Fig. 6(d-f) display the GCD curves comparison of the prepared as-fabricated Cu 2 MnSnS 4 electrode materials. The highest reversible time was observed for the OA sample than AA and CA. The calculated specic capacitance values for OA, CA, and AA were 649, 453, and 442 F g À1 at 0.5 A g À1 . The cone diagram displays the specic capacitance values at different current density ranges. The long-term cyclic stability up to 5000 cycles was assessed and capacitive retentions of 83%, 87%, and 89% were achieved for the AA, CA, and OA electrodes, respectively (Fig. 6g-i). Due to the electrode properties, such as internal resistance, polarization, and electrolytic ions insertion, and removal due to mechanical stress, its specic capacitance Fig. 7 (a and d), (b and e), and (c and f) linear fits of C vs. n À1/2 and C À1 vs. n 1/2 for AA, CA, and OA, (g) capacitive (EDLC) and diffusive (PC) charging derived from Trasatti's method, (h) specific capacitance from GCD, and (i) Nyquist plot. value decreases due to a high current density. 47 According to the CV and GCD studies, the Cu 2 MnSnS 4 -OA electrode may be preferred as a suitable electrode material. The CV studies further indicated that the redox reaction is a diffusion-controlled process, which may be the main cause of the pesudocapactive behavior with the increasing scan rates. The two differentiation methods, namely (i) Trasatti method and (ii) Dunn method, were then used to analyze the diffusioncontrolled faradaic and non-diffusion-controlled battery-type processes of the synthesized electrodes. 48 In the Dunn method, the peak current (i p ) vs., the scan rate gives the power law i p ¼ av b . The linear t slope values give the 'b' value. A value of b ¼ 0.5 means diffusion-controlled faradaic process, while b ¼ 1 means a non-diffusion-controlled process due to surface redox reactions. Among the two studied methods, the Trasatti method is the simplest one to describe the mechanism of the electrode. Fig. 7(a, d, b, e, c and f) show the linear t of C vs. n À1/ 2 and C À1 vs. n 1/2 for the AA, CA, and OA samples, respectively.
The non-linear behavior of the graphs explored was due to the ohmic drop of the intrinsic resistance. 49 The specic capacities of the AA, CA, and OA samples with their EDLC (capacitive) and pseudocapacitive (diffusive) behavior are shown in Fig. 7(g). The AA sample exhibited 16% and 84% capacity derived from the EDLC and PC contributions, while CA offered 44% and 56% capacity derived from the EDLC and PC contributions, and OA delivered 64% and 36% capacity for the EDLC and PC.
The interfacial structure and its kinetic response due to electrical variation were studied by electrochemical impedance spectroscopy. The opposition force to an electrical current is known as impedance and it is denoted by the unit of resistance (U). There are three factors that determine the concepts of resistance used in an AC circuit: (i) the alternating current (AC) and voltage in phase, (ii) frequency independent, and (iii) all current and voltages. Nevertheless, the majority of these failed because the phase angle was not zero and almost in all cases capacitive and/or inductive effects were present at almost all the frequencies. Hence, it becomes an issue of frequency dependence. In these cases, the concept of impedance was used to denote the electrical current opposition in AC circuits. 50 Here, EIS spectra were plotted by the real vs. the imaginary part of the impedance, which determines the inter phase resistance between the working electrode and the electrolyte. Fig. 7(i) shows Nyquist plots of the OA, CA, and AA samples with the consequent equal circuit model. The overall impedance contribution was simplied to transform the EIS spectrum into  its corresponding equivalent circuit and the physical process involved in the samples was determined using equivalent circuit parameters. The following tted equivalent circuit (R 1 + Q 2 /R 2 + Q 3 ) was used to assess the different components of the cell resistance, where R 1 corresponds to the ohmic drop in the electrolyte, R 2 refers to the charge ion displacement through the electrode mass interface, and Q 2 and Q 3 represent the constant phase components. 51 All the electrical components values are summarized in Table 4 and clearly show that the value of resistance decreases while the capacitance increases gradually, which signicantly improve the bias potential. This behavior enhances the electron-transfer dynamics and causes signicant changes, leading to improvements in the charge-transfer process. Also, from Table 4, the OA sample exhibited lower R ct values than the other two, which further supported the CV and GCD results.

Two-electrode fabrication of an ASC device
The electrochemical performance of Cu 2 MnSnS 4 //AC was evaluated under a two-electrode conguration via a specically assembled asymmetric supercapacitor (ASC), with Cu 2 MnSnS 4 as the working positive electrode and activated carbon (AC) as the negative electrode in 2 M KOH as the electrolyte. The operation voltage of the full cell was set to 0-1.5 V for all the studies. The loading mass of an electrode was estimated employing the formula: m + /m À ¼ c À Â 1V À /c + Â 1V + . Fig. 8(a) displays a comparative graph of the positive and negative electrodes. In order to analyze a proper voltage window for the ASC device, the potential windows were varied in the CV study, as shown in Fig. 8(b), which revealed both the battery-type and electric double layer effects. 52 Very quick charge-transfer performance was exhibited by Cu 2 MnSnS 4 //AC ASC when the current density was increased from 10 to 60 mV s À1 and there was no distortion of the CV shape found. Fig. 8(c) presents GCD curves of Cu 2 MnSnS 4 //AC ASC, from which the electrochemical performance, such as energy and power density, was calculated (Table 5). For the highest current density of 20 A g À1 , 2.5 W h kg À1 and 15 000 W kg À1 energy and power density were obtained, respectively. Here in order to remove the stability barriers, we used a switch lock-type device to test the stability behavior. Initially the stability decreased due to the fast reaction kinetics of the electrode/electrolyte interactions. Then aer a few cycles more (1000 cycles), constant stability was reached, which may be due to the stabilized reaction kinetics. The best cyclic stability test was carried out for 21 000 cycles and 80.35% capacity as well as 97.54% coulombic efficiency were retained, thus indicating the quality of the chosen electrode, as shown in Fig. 8(d). Fig. 8(e) displays a Ragone plot of the energy vs. the power density with other comparative literature values, and these are summarized in Table 6. Further, for the practical demonstration of real-time application, two Cu 2 MnSnS 4 //AC ASCs were cascaded and were able to light up a blue LED and run a small-sized motor (Fig. 8(f)). Hence, Cu 2 MnSnS 4 //AC ASC devices may be suitable for electrochemical storage applications.
In this study, a Cu 2 MnSnS 4 electrode with a high working potential for aqueous asymmetric supercapacitors was proposed. The structure directing agent's role in fabrication of the Cu 2 MnSnS 4 nanostructure was investigated. Here, OA electrodes showed the highest capacity and best cyclic stability. Moreover, the fabricated device exhibited a high energy density and power density.

Conclusions
In summary, Cu 2 MnSnS 4 electrode materials fabricated with the use of varying structure directing agents (AA, CA, OA) in a three-electrode conguration were successfully developed. Two electrode devices and their electrochemical measurements were tested to determine the best electrode. The calculated specic capacitance values for electrodes fabricates with the use of OA, CA, and AA were 649, 453, and 442 F g À1 at 0.5 A g À1 . The electrodes demonstrated 83%, 87%, and 89% capacity retention and cycling stability aer 5000 cycles for the AA, CA, and OA electrodes. An asymmetric device was designed and exhibited 27 W h kg À1 energy and 759 W kg À1 power density at 1 A g À1 . Moreover, the device provided 80.35% capacity retention and 97.54% Coulombic efficiency aer 21 000 cycles. Thus excellent electrochemical effects were obtained for the Cu 2 MnSnS 4 -OA// AC electrode.

Conflicts of interest
We hereby declare that there are no conicts of interest.