Tao Liua,
Chunlan Wang*a,
Gengliang Zoua,
Jiaying Jia and
Zao Yi*bc
aSchool of Science, Xi’an Polytechnic University, Xi’an 710048, China. E-mail: wangchunlan@whu.edu.cn
bSchool of Mathematics and Science, Southwest University of Science and Technology, Mianyang 621010, China. E-mail: yizaomy@swust.edu.cn
cSchool of Chemistry and Chemical Engineering, Jishou University, Jishou 416000, China
First published on 8th August 2025
Terahertz (THz) absorbers with ultra-broadband and ultra-narrowband absorption capabilities are crucial for integrated and efficient terahertz modulation. This study proposes a dual-mode tunable terahertz absorber based on the phase transition characteristics of vanadium dioxide (VO2), enabling dynamic switching between narrowband and broadband absorption through its insulating-to-metallic transition. In the insulating state, the excitation of quasi-bound states in the continuum (Q-BIC) resonance via geometric parameter modulation of silicon pillars is investigated, with its physical mechanism elucidated via impedance matching theory and multipole analysis. This mode demonstrates exceptional sensing performance at 8.017 THz: a refractive index sensitivity of 3.735 THz RIU−1, a quality factor (Q) of 4800.89, and a figure of merit (FOM) of 3822.93 RIU−1. When VO2 is transformed into the metallic state, the device achieves more than 90% ultra-broadband absorption in the range of 3.93 THz to 9.25 THz, and its broadband absorption properties originate from the electric dipole resonance. In addition, the performance of the device remains stable at different structural parameters. Compared to existing technologies, this design integrates dual functionalities in a single-layer hybrid structure, significantly reducing fabrication complexity.
New conceptsTerahertz metamaterials have played an important role in the development of terahertz technology, but most of today's metamaterials in the terahertz band exhibit poor performance and are mono-functional. This greatly limits the scalability and application potential of the devices. Therefore, we propose a terahertz-perfect absorber that utilizes vanadium dioxide (VO2) with phase transition properties to achieve active switching between ultra-wideband and high-Q ultra-narrowband regions. Prior to VO2 phase transition, the device achieves quasi-BIC resonance through geometric parameter optimization of silicon pillars. Through impedance matching theory and multipole analysis, we reveal its physical mechanism and demonstrate exceptional sensing performance at 8.017 THz: the refractive index sensitivity reaches 3.735 THz RIU−1, with a quality factor of 4800.89 and a figure of merit up to 3822.93 RIU−1. When VO2 transitions to the metallic state, the device achieves ultra-broadband absorption around 4.87 THz (absorption > 95%) or 5.32 THz (absorption > 90%). The physical mechanism of broadband absorption is elucidated through electromagnetic field distribution and multipole analysis. Furthermore, we systematically investigate the influences of the structural parameters and environmental refractive index on broadband absorption performance. Compared with existing technologies, this design integrates dual functionalities through a single-layer hybrid structure, significantly reducing process complexity. It provides new insights for developing terahertz sensors, environment-adaptive devices and integrated photonic chips. |
Landy et al. achieved 99% absorption efficiency at 11.65 GHz through rational structural design.11 In recent years, terahertz metamaterial absorbers have shown promising applications in stealth technology, sensing, and spectroscopy.12,13 Various perfect metamaterial absorbers have been successively reported, evolving from single-band to multi-band or broadband configurations.14–16 Although absorption characteristics can be adjusted by modifying unit structure dimensions and resonant patterns, current fabrication processes face challenges in multi-material integration and precision manufacturing, resulting in inefficient production and limited accuracy.17–19 Tunable metamaterial absorbers facilitate significant progress in both manufacturing and application by enabling performance modulation through external control without structural modifications.20–22 However, most existing tunable schemes can only adjust the intensity or frequency for either narrowband or broadband absorption individually or require complex multi-layer stacked structures to achieve functional switching. This severely limits the potential of devices in multi-scenario applications. Consequently, there is a pressing need to develop structurally simple, multifunctional terahertz devices capable of on-demand function switching.
Vanadium dioxide (VO2), a classic transition metal oxide, exhibits an insulator-to-metal phase transition near room temperature (≈340 K), with its property changes originating from crystal structural transformations.23,24 Other phase-change materials such as Ge2Sb2Te5 (GST) face limitations in terahertz applications requiring rapid switching due to their slower response speeds and higher phase transition temperatures.25 Hence, VO2 emerges as the preferred phase-change material for realizing high-performance dynamic terahertz devices.26–29 In 2022, Zheng et al. designed a VO2–SiO2–gold hybrid terahertz absorber that achieved switchable broadband perfect absorption and total reflection over a wide frequency range.27 In 2024, Niu's team developed a six-layer multifunctional terahertz absorber with mode-switching capability, realizing switching between quad-narrowband and 3.62 THz-range perfect absorption.28 In 2025, Shakiba et al. leveraged VO2's IMT characteristics and graphene's electrical tunability to create a multifunctional absorber capable of broadband-narrowband switching, demonstrating over 80% absorption across the range of 4.28–7.55 THz.29 Beyond utilizing VO2's phase transition properties, altering incident wave direction has also emerged as an effective approach for achieving absorption bandwidth switching.30,31 Generally, these studies demonstrate that effective switching between broadband and narrowband absorption modes typically relies on complex stacked multilayered structures or combinations of multiple active materials. However, it is worth noting that while achieving the expected functions, this complex design brings about huge manufacturing challenges and high processing costs, thereby hindering the process of equipment miniaturization and integration. In addition, existing solutions still have room for improvement regarding the Q-factor in narrowband modes or the coverage range in broadband modes.
This study designs a terahertz absorber exploiting VO2 insulator-to-metal transition (IMT) to achieve switchable narrowband and broadband absorption. Initially, before VO2 phase transition, the device exhibits ultra-narrowband absorption. Adjusting the asymmetry of silicon pillars (via length L2) excites a quasi-bound state in the continuum (Q-BIC) within the terahertz spectrum. The mechanism underpinning narrowband perfect absorption is comprehensively elucidated through impedance matching theory and Cartesian multipole decomposition. The Q-BIC resonance demonstrates an ultrahigh Q-factor and narrow linewidth, enabling high-sensitivity sensing. Analysis reveals that at 8.0175 THz, the narrowband mode achieves a refractive index sensitivity S of 3.735 THz RIU−1, a full width at half maximum (FWHM) of 0.00167 THz, a figure of merit (FOM) of 3822.93 RIU−1, and a Q-factor of 4800.89—performance metrics significantly surpassing existing studies. Following VO2 phase transition, the device operates in an ultra-broadband absorption mode with a >90% absorption bandwidth around 4.87 THz. Impedance matching theory, multipole analysis, and electromagnetic field distributions collectively demonstrate that broadband absorption primarily originates from electric dipole resonance induced in the VO2 layer. Furthermore, the influence of structural parameters and varying air refractive indices on broadband absorption is systematically investigated. This dual-mode absorber design exhibits promising applications in terahertz sensing and switching devices.
The middle layer employs silicon dioxide (SiO2) with a refractive index of 1.46. In the terahertz band, SiO2 behaves as a nearly lossless medium, allowing destructive interference through multiple reflections and transmissions at its top and bottom interfaces, thereby enabling perfect absorption. The top VO2 synthetic pattern consists of four ellipses of the same size, intersecting a square in the middle, as shown in Fig. 1(c). The silicon component, with a dielectric constant of εSi = 11.6 + 0.00002i, adopts an asymmetric trapezoidal geometry along the x-axis. The design deliberately breaks the structural symmetry so that a BIC with a zero radiation loss and a near-zero linewidth can be transformed into a Q-BIC mode with an ultra-high Q and a sub-wavelength linewidth.34,35
To analyze the absorber's performance, we employed the wave optics module in COMSOL Multiphysics to simulate absorption spectra and electromagnetic field distributions. Periodic boundary conditions were applied along the x- and y-axes, while a perfectly matched layer boundary condition was set along the z-axis.36,37 Incident waves were configured to propagate perpendicular to the device's top surface along the z-direction. The device fabrication process involves low-pressure chemical vapor deposition and magnetron sputtering. First, a 2-μm-thick Au layer is deposited via magnetron sputtering onto the substrate, followed by the growth of a 7.5 μm SiO2 layer through thermal oxidation. For the top-layer structure, arrays of patterned VO2 can be generated by direct sputtering of the metal mask plate first, due to the good process tolerance of the multifunctional terahertz absorber that we have designed. The silicon layer is initially deposited using either atmospheric pressure chemical vapor deposition (APCVD) or plasma-enhanced chemical vapor deposition (PECVD), as both methods operate at relatively low temperatures, enabling the production of a low-stress material with enhanced fracture toughness. This is followed by spin-coating a photoresist layer and defining a periodic array pattern via electron beam lithography. Finally, the silicon layer is subjected to etching via inductively coupled plasma processing.38,39
The behavior of IMT produced by temperature-induced VO2 in the terahertz band range can be described by the Drude model, where eqn (1) expresses the relative permittivity of VO2,40
![]() | (1) |
![]() | (2) |
In the above equation, σ0 = 3 × 105 S m−1 and ωp(σ) = 1.4 × 1015 rad s−1. The phase transition mechanism in VO2 originates from its crystal structure transformation: at room temperature, it exhibits a monoclinic crystal structure, which transitions to a tetragonal rutile structure as temperature increases beyond the phase transition point.
Accompanying this structural reorganization, dramatic alterations occur in the electronic density of states, leading to abrupt several orders-of-magnitude changes in electrical conductivity within an ultrashort timeframe.42 Notably, this phase transition process is fully reversible. As shown in Fig. 1(d), the functional relationship between VO2 conductivity and temperature was derived theoretically. Below 313 K, the material maintains low conductivity under 200 S m−1, corresponding to the insulating state of VO2. Near the critical phase transition temperature of 341 K, conductivity undergoes an abrupt three-order-of-magnitude surge. When temperature further rises above 345 K, the peak conductivity reaches 2 × 105 S m−1. Crucially, this dramatic five-order-of-magnitude transition fundamentally governs the evolution of the device's absorption characteristics.43 While VO2 can be transformed by manipulating the ambient temperature or by heating the device with laser pulses to realize the transition of the phase state, for example, Sun et al. used a circular ceramic heating element as a heater to heat the ambient environment around the device to achieve a non-contact, constant-temperature ambient heating to achieve conductivity switching of VO2.44 However, these conventional approaches face significant challenges in achieving precise conductivity regulation, posing substantial obstacles for practical device implementation and manufacturing. Therefore, this study therefore focuses on vanadium dioxide's two distinct states: the insulating state below 313 K, where the device operates in narrowband absorption mode, and the metallic state above 345 K, during which the device switches to broadband absorption mode. Critically, the multifunctional terahertz absorber maintains stable performance even when temperatures slightly deviate below 313 K or exceed 345 K, where minor conductivity fluctuations (either reduction or enhancement) exhibit a negligible impact on device characteristics. This temperature tolerance significantly reduces control complexity and associated costs.45
To elucidate the physical mechanisms behind these dual-mode perfect absorption characteristics, we employ impedance matching theory. The absorption rate and relative impedance of this multifunctional terahertz device can be expressed as follows:49,50
![]() | (3) |
![]() | (4) |
To further investigate the physical mechanism of perfect absorption in narrowband mode, we calculated the electric and magnetic field distributions at frequency f1. Fig. 3(a) shows the z-component of the electric field on the xy-plane, revealing strong field localization at the edges of the Si structures. And almost no electric field is excited at VO2, which is due to the fact that VO2 in the insulating state is similar to a dielectric material and does not undergo electromagnetic resonance with incident electromagnetic waves from outside.51,52 This confirms that the narrowband absorption originates from high-refractive-index Si excitation. Notably, positive and negative charges concentrate at the upper and lower edges of each Si pillar, forming paired electric dipoles. This indicates activated electric dipole resonance in individual Si pillars. The antiparallel alignment of dipoles in adjacent pillars transforms them into an electric quadrupole resonance, enabling strong electromagnetic coupling that suppresses reflection and facilitates near-perfect absorption.53 Further analysis of the normalized magnetic field distribution in the xz plane of Fig. 3(b) reveals that the magnetic field energy of the device is mainly concentrated in the two Si pillars and the air gap between them. In addition, the direction of displacement current is marked with arrows, and the ring current with opposite rotation directions is excited at each of the two Si columns, thus exciting two magnetic dipoles with opposite directions along the Y axis and finally forming a magnetic dipole resonance.54
Multipole analysis can provide insight into the physical mechanisms of electromagnetic resonance and scattering. Based on this, we further explore the principle of narrow-band absorption in devices and calculate the specific multipole components directly from the displacement current density j on metamaterials.55,56
Electric dipole (ED):
![]() | (5) |
Magnetic dipole (MD):
![]() | (6) |
Toroidal dipole (TD):
![]() | (7) |
Electric quadrupole (EQ):
![]() | (8) |
Magnetic quadrupole (MQ):
![]() | (9) |
For the ultra-narrowband absorption mode, the BIC must be converted into a Q-BIC with a high Q-factor to enable practical applications. By modifying the width of the Si pillar l2, the BIC state is broken and transformed into a Q-BIC. As shown in Fig. 4(a), when the L2 is 3 μm, the absorption curve shows a smooth curve at this point. This also proves that it is in the BIC state at this time, and since the BIC mode is not coupled to free space, no resonance phenomenon can be observed in the absorption spectrum.59 To investigate the characteristics of Q-BIC resonances in the absorption spectrum, we convert the BIC mode into a leaky mode by varying the l2. When the l2 deviates from this critical value of 3 μm, the BIC is transformed into a Q-BIC with a finite yet high Q-factor. As the l2 gradually shifts away from the critical value, the resonance frequency redshifts, and the linewidth broadens. This signifies an evolution of the device from a non-radiative BIC configuration toward a radiative Q-BIC regime with a high Q-factor. As shown in Fig. 4(b), as the l2 approaches 3 μm, the Q-factor progressively increases, the FWHM decreases, and the BIC evolves into a Q-BIC with a finite but high Q-factor. This process leads to enhanced energy radiation outward.60
In addition, we investigated the effect of Si geometrical parameters on the absorption properties of the proposed narrow band. As shown in Fig. 4(c) and (d), while maintaining the dimensions of Si pillars l1 = 3 μm and l2 = 1.5 μm, the resonance frequency of the absorption peak redshifts as the length L of the Si pillars increases. Similarly, increasing the thickness H of the Si pillars also induces a redshift in the resonance wavelength. This phenomenon may arise because the enhanced thickness of the Si material causes the magnetic dipole in Fig. 3(b) to extend further along the Z-axis, altering the device's response to incident electromagnetic waves and thereby triggering the redshift. Furthermore, modifying only L or H does not achieve the conversion from BIC to Q-BIC but allows tuning of the resonance wavelength position. This enables the resonance wavelength to be tailored to specific target bands by adjusting geometric parameters, offering a novel approach for the design and application of sensors.
For the ultra-narrowband absorption mode prior to phase transition, its narrow linewidth and high Q-factor make it highly promising for refractive index sensing applications. We simulated the absorption spectra of the device under ambient air with refractive indices ranging from 1 to 1.04. As shown in Fig. 5(a), the absorption peak exhibits a significant redshift as the environmental refractive index increases. Here, we introduce two critical performance metrics for evaluating refractive index: sensitivity S and FOM,61
![]() | (10) |
![]() | (11) |
The sensitivity of the device in the narrowband absorption mode can be derived from the slope of the fitted linear curve in Fig. 5(b), with an average sensitivity S of 3.735 THz RIU−1. In addition, Fig. 5(c) and (d) also show the curves of the FWHM and FOM as a function of the ambient refractive index, with a gradual decrease in the FWHM as the ambient refractive index increases and a gradual increase in the FOM, with the maxima being 3822.93 RIU−1 And 3822.93 RIU−1, respectively. This indicates that the designed hypersurface sensor has high sensitivity and a very narrow linewidth, which has great potential for application in refractive index sensors.
For the broadband absorption mode, Fig. 6(a) and (b) demonstrate the normalized real components of the z-direction electric field distribution at two resonance frequencies. Distinctly opposite charges are observed accumulating predominantly on the Si columns and opposite sides of the elliptical VO2 structure, forming multiple dipole resonances that enable exceptional absorption performance. At frequency f3, while maintaining opposite-polarity charges on the elliptical VO2 surfaces, the electric field primarily concentrates within the interior cavities of the dual Si columns. This phenomenon principally arises from dipole resonances induced by coupling effects between complex geometric patterns. Specifically, the combined optical response is generated by periodically arranged exterior cavities and interior cavities of the structural elements.62 Furthermore, the electric field intensity at f3 significantly exceeds that at f2, explaining why 99.41% absorption is achieved at f3 compared to 98.97% at f2. In addition, as shown in Fig. 6(c), we also utilize the multipole analysis theory to analyze it in detail. The data results show that the ED dominates the radiation, and the intensity of ED radiation is significantly higher at the high-frequency position than at the middle and low frequencies, which matches the results in Fig. 6(a) and (b), suggesting that the ultra-broadband absorption is a wide range of high absorption dominated by the electric dipole resonance. In addition, we have quantified the collective multipole contributions in the broadband range of 3.93–9.25 THz and revealed that the ED accounts for 67.25% of the total response, while the TD accounts for 15.58%, and all remaining multipoles only account for 17.17% of the total response. Therefore, it is proved that the ED mainly controls broadband absorption by combining electromagnetic field distribution analysis with multipole decomposition.63
The current structure, while simple, must still account for potential errors in actual manufacturing processes. We therefore conducted further analysis on how structural parameters affect absorption and discussed the impact of possible errors. Notably, the structural parameters of Si pillars primarily influence ultra-narrowband absorption while having no impact on ultra-wideband absorption. Fig. 7(a) demonstrates that as the major axis (a) of elliptical VO2 increases, both the absorption intensity and bandwidth gradually expand, maintaining an absorption rate of over 90% across a bandwidth exceeding 5 THz. In Fig. 7(b), the absorption bandwidth gradually increases as the short axis (b) of the ellipse increases. When b = 4 μm, the absorption bandwidth and absorption rate are slightly lower, which is due to the fact that the slit between the four notched ellipses becomes larger at this point, resulting in the weakening of the dipole resonance.64 Similarly, in Fig. 7(c), when b = 6.5 μm, the four notched ellipses will be connected together, and the slit is not present, which makes the local electric field decrease and the absorption bandwidth decrease. And when the slits are present (b ≥ 7 μm), the overall absorption bandwidth and absorption rate of the device remain essentially unchanged. Fig. 7(d) illustrates the absorption spectra under varying h values. The absorber shows a minimal variation in the 4–9 THz range with slightly reduced absorption rates, while the 3–4 THz region exhibits gradual bandwidth expansion and absorption enhancement as thickness h increases. These phenomena can be explained by interference theory: partial incident waves are directly reflected by surface Si and VO2 layers, while others penetrate the dielectric layer. Multiple reflections within the dielectric layer, functioning as a Fabry–Pérot resonant cavity, create constructive/destructive interference that modulates the absorption spectrum.65
In addition to the geometrical parameter modulation, the effects of the ambient refractive index and the refractive index of the SiO2 medium on the absorption spectra are shown in Fig. 8(a) and (b). When the ambient refractive index is increased from 1 to 1.08, a good ambient generalization is demonstrated. The broadband absorption pattern maintains the perfect absorption of the device's ultra-broadband under refractive index perturbation, confirming the stable working ability of this multifunctional device in different environments.66–68 In addition, Fig. 8(b) demonstrates the effect of different refractive indices of SiO2 in the dielectric layer on the absorption spectra. The simulated data show that the absorption in the range of 9–10 THz decreases with the increase of the refractive index of the dielectric layer, but the overall absorption remains stable in the range of 4–9 THz. This multifunctional device can therefore be adapted to a wider range of electromagnetic environments and is also suitable for practical applications.
![]() | ||
Fig. 8 Absorption spectra in broadband absorption mode for (a) different ambient refractive indices and (b) different refractive index dielectric layers. |
Table 1 summarizes the performance of recent terahertz devices in narrowband absorption, broadband absorption, and broadband-narrowband switching. Compared with conventional single-function terahertz narrowband absorbers, our proposed devices exhibit excellent sensing performance when operating in ultra-narrowband absorption mode, exhibiting ultra-high sensitivity and a significantly enhanced Q-factor. This performance enhancement stems from the excitation of Q-BIC by EQ and MD resonances, which is achieved by intentionally destroying the silicon-based structure under the symmetry-protecting conditions. This synergistic effect leads to absorption enhancement and Q amplification, with 99.3% perfect absorption in the ultra-narrow band achieved at 8.0175 THz. In addition, our multifunctional device exhibits a superior absorption bandwidth when in broadband absorption mode compared to a single terahertz broadband absorber, and the device has excellent process tolerance. Compared with other broadband-narrowband switchable absorbers, our proposed single-layer hybrid structure achieves bifunctional integration through structural innovation and significantly reduces fabrication complexity without affecting performance. Notably, we have also made great progress in our research methodology, firstly, by introducing Q-BIC with a field enhancement effect to improve the Q value and enhance the absorption and secondly, by introducing the multipole analysis theory to analyze in detail the mechanism arising from the perfect absorption in both narrowband and broadband regions.
Principal material | Function type | S (THz RIU−1) | Q-factor | Tunable bandwidth | FB (%) | Number of layers | Year | Ref. |
---|---|---|---|---|---|---|---|---|
A: Narrowband perfect absorber. B: Wideband perfect absorber. C: The perfect absorber that is actively switchable between wideband and narrowband regions. | ||||||||
Au and VO2 | A | 0.398 | 49.00 | — | — | 3 | 2024 | 69 |
MXene and graphene | A | 0.400 | 102.9 | — | — | 4 | 2025 | 70 |
Bulk Dirac semimetals and VO2 | A | 0.555 | 44.49 | — | — | 3 | 2025 | 71 |
Graphene | B | — | — | 3.28–5.24 | 46.00 | 3 | 2024 | 72 |
Potassium chloride and VO2 | B | — | — | 3.6–7.3 | 67.89 | 4 | 2024 | 73 |
Potassium chloride and graphene | B | — | — | 7.676–9.172 | 17.76 | 5 | 2025 | 74 |
Graphene | C | 0.5 | 13.23 | 2.16–1.27 | 51.89 | 3 | 2023 | 75 |
Copper and VO2 | C | — | — | 3.36–6.98 | 70.02 | 6 | 2024 | 28 |
Graphene and VO2 | C | 0.875 | 900 | 4.8–17.6 | 114.28 | 5 | 2025 | 76 |
Graphene and VO2 | C | 1.326 | 347.45 | 6.45–11.53 | 56.51 | 5 | 2025 | 77 |
Si and VO2 | C | 3.735 | 4800.89 | 3.93–9.25 | 80.72 | 3 | 2025 | Pro. |
This journal is © The Royal Society of Chemistry 2025 |