Abstract
Precise manipulation of Bragg reflection in cholesteric liquid crystals (CLCs) is essential for advancing reconfigurable optics. However, existing photo-responsive material-doped CLC technologies that rely on single-wavelength photoisomerization encounter several challenges, including slow response times, limited tunability, inadequate spatial control, and instability caused by pitch variations due to diffusion. Here, we present a robust dual-wavelength photoisomerization method to simultaneously achieve trans-to-cis and cis-to-trans photoisomerization of chiral azobenzene-doped CLCs, which enables broadband, reversible, and spatially addressable control over the Bragg reflection spectrum. By employing counterpropagating laser beams at 405 nm and 532 nm, we precisely control the trans–cis isomerization dynamics of azobenzene chiral dopants, achieving spectral shifts exceeding 100 nm primarily through reversible modulation of the helical pitch of the CLCs. Furthermore, manipulating the intensity ratio and geometry of the excitation beams allows for tailored pitch gradients, reflection bandwidths, and central wavelengths with remarkable fidelity. Our approach enhances pitch boundaries and reduces molecular diffusion, facilitating the micrometer-scale patterning of optical textures, which surpasses traditional single-wavelength methods. Additionally, we present an innovative narrowband spectral filtering technique by sequentially transmitting light through pitch-selective CLC regions under circular polarization control. This reconfigurable manipulation strategy paves the way for developing programmable photonic systems, including adaptive optics, diffractive optics, and tunable displays.
1 Introduction
Nature showcases extraordinary structural coloration, particularly through the complex nanoscale architectures in butterfly wings [1] and beetle exoskeletons [2]. These biologically inspired structures facilitate dynamic color changes essential for functions such as camouflage [3], [4] and visual display [5]. Consequently, researchers have sought to harness responsive soft materials to develop self-assembled photonic structures. Cholesteric liquid crystals (CLCs) are particularly noteworthy for their ability to form helical superstructures [6], [7], [8], [9] that produce a photonic bandgap (PBG), selectively reflecting circularly polarized light in accordance with Bragg’s law [10]. The unique optical properties of CLCs have led to diverse applications, including display technologies [11], diffraction gratings [12], imaging systems [13], and smart window applications [7], [14], [15]. However, achieving precise and reversible control over the helical superstructures and their optical characteristics in response to external stimuli remains a challenging endeavor in materials engineering.
A promising strategy to address these challenges involves integrating chiral photo-switches, which enable the dynamic manipulation of molecular arrangements and optical properties in response to light stimuli [2]. Over the past decade, various chiral molecules have been developed as dopants within CLC systems. Among these, chiral photo-switches such as azobenzenes [16], [17], [18], molecular motors [19], [20], [21], and diarylethenes [22], [23] have garnered significant attention due to their ability to reversibly alter the molecular organization of LCs in response to light stimuli. This responsiveness facilitates tunable Bragg reflections, thereby supporting the development of reconfigurable photonic devices. Traditional methodologies have primarily focused on blending chiral dopants with photo-switchable molecules; however, challenges persist in achieving uniform and thermally stable tuning of the helical structure. Notably, diarylethenes, which consist of two thiophene units connected by an ethene bridge, are particularly esteemed for their impressive fatigue resistance, reversibility, and thermal stability [24], [25], [26]. Incorporating chiral side groups, such as binaphthyl moieties, onto achiral diarylethenes can produce robust and thermally stable chiral dopants [27]. Nevertheless, the minimal conformational changes occurring during the photocyclization process often fail to effectively influence the pendant chiral side groups within CLCs, resulting in limited helicity variations and complications in achieving helical inversion. Furthermore, these extrinsic chiral modifications frequently yield low asymmetric induction during photocyclization, producing diastereomers with opposing stereogenic centers [24]. Consequently, this phenomenon can lead to the emergence of multiple helical domains, contributing to orientation disorder within the LC matrix and ultimately diminishing optical efficiency.
Azobenzene-based chiral dopants have gained attention for their ability to undergo reversible trans–cis photoisomerization, facilitating light-driven modulation of helical twisting power (HTP) [24], [28], [29]. However, much of the current research emphasizes single-wavelength or broadband exposure without selective control, which restricts precise spectral tunability and may lead to challenges such as uncontrolled isomerization and uneven pitch distributions, resulting in limited spectral selectivity and inefficient suppression of off-band transmission due to insufficient modulation depth and static structural configurations. These constraints pose significant challenges for practical applications in narrowband light filtering, where precise control over wavelength and polarization is crucial. To overcome these challenges, previous studies have examined using azobenzene-doped CLCs for photonic applications, highlighting the advantages of dual-wavelength exposure. For instance, Chen et al. developed a quantum dot-embedded CLC laser incorporating a chiral azobenzene moiety, enabling reversible PBG tuning and lasing wavelength tuning through alternating dual-wavelength (UV and blue light) exposure [30]. Although this method demonstrated optical stability and tunability, the tuning range remained limited to ∼60 nm for the PBG and 40 nm for the lasing wavelength. Moreover, it did not provide precise spatial control over pitch gradients and bandwidth, which is critical for advanced photonic devices. Similarly, Fuh et al. introduced an optical filter employing two phototunable CLC cells in a reflection mode, facilitating adjustment of the central wavelength from 510 nm to 628 nm, with bandwidths varying from 13 nm to 79 nm through dual-beam exposure [31]. However, this configuration primarily addressed wavelength and bandwidth tunability while neglecting spatial pitch modulation and dynamic reconfigurability of the reflection band, thereby constraining its applicability in designs necessitating meticulous spectral control. Additionally, White et al. demonstrated photo-induced broadening of CLC reflectors through UV exposure, significantly enhancing the reflection bandwidth from approximately 100 nm to as much as 1700 nm [32]. Despite this considerable enhancement, the method relied on passive exposure and did not incorporate reversible or spatially controlled modulation. Furthermore, Wu et al. reported on photoisomerization-driven molecular migration in azobenzene polymer systems, highlighting the formation of UV-assisted surface relief gratings through light-induced mass transport [33]. However, this technique is constrained by its reliance on single-wavelength photoisomerization, which limits bidirectional, reversible control over helical pitch and Bragg reflection spectra. Such limitations hinder the dynamic and reconfigurable manipulation of photonic properties, which are essential for advancing adaptive optical devices.
To tackle these challenges, we propose a spectrally reconfigurable chiral azobenzene-doped negative CLC (azo-nCLC) device, which enables dynamic and reversible control of the PBG via dual-wavelength photoisomerization using UV (405 nm) and green (532 nm) light. This innovative device enables the simultaneous trans–cis and cis–trans isomerization of chiral azobenzene dopants under specific optical stimuli (Figure 1). Unlike conventional single-wavelength techniques, our device employs counterpropagating laser beams at UV and green wavelengths to achieve precise control over the isomeric state of chiral azobenzene-based dopants. This dual mode activation exploits distinct π–π* transitions induced by UV light and n–π* transitions stimulated by visible light, thereby promoting efficient and reversible photoisomerization. The resulting transformation alters molecular geometry and dipole moment, thereby adjusting the HTP of the chiral dopants and dynamically modulating the supramolecular pitch of the CLC. Consequently, the CLC cell exhibits a broadband and tunable reflection from the visible to the near-infrared spectrum. When encapsulated within a planar-aligned cell, the CLC forms a helical superstructure that selectively reflects circularly polarized light according to Bragg’s law. Moreover, we showcase spatially selective photopatterning within the CLC device. By employing a photomask patterned in the shape of the letter “E” in the path of the 405 nm UV laser. This approach enables localized trans–cis photoisomerization of azobenzene dopants. This method generates spatial variations in helical pitch, resulting in a patterned modulation of the photonic bandgap across the film. We achieve pitch gradients and spectral shifts with submicron spatial resolution by incorporating left- and right-handed chiral azobenzene dopants within a nematic matrix. Notably, including bulky tail groups mitigates excessive diffusion, allowing for sharper pitch gradients and enhanced surface anchoring, both crucial for obtaining spatially resolved spectral features [34], [35], [36]. This approach facilitates precise, reversible manipulation of the reflection band’s position and bandwidth, while offering greater adaptability for diverse photonic applications. By effectively overcoming previous limitations, such as poor reversibility, restricted modulation depth, and uncontrolled diffusion, our methodology paves the way for advancements in adaptive optics, tunable filters, wavelength-selective mirrors, and high-resolution reflective displays in next-generation photonic technologies.

A schematic illustration of the dual-wavelength exposure on the azo-nCLC cell and its promising applications in spectral sculpting.
2 Results and discussion
2.1 Tunable reflection in azo-nCLCs through dual-wavelength azobenzene photoisomerization
To elucidate the spectral tunability of photo-switchable azo-nCLC cells, we examined the effects of counterpropagating 405 nm and 532 nm laser beams (Figure 2(a)). The pristine CLC cell exhibited a right-handed helical structure, displaying a near-infrared Bragg reflection centered at 811 nm (bandwidth: 73 nm), as determined by the interplay between the left-handed azobenzene chiral dopant (ChAD-2-S) and the right-handed dopant (Table S1, Figure S1). Upon exposure to 405 nm light, trans–cis photoisomerization of the azobenzene units through π–π* excitation results in a 180° rotation around the N=N bond. The resulting bent conformation of the cis-isomer leads to a reduced HTP, causing a contraction of the cholesteric pitch and a subsequent blue shift of the reflection band to 665 nm (bandwidth: 60 nm), as shown in Figure S1. Subsequent exposure to 532 nm light promotes cis–trans back-isomerization via n–π* excitation and nonradiative decay, restoring the original higher HTP and causing a red shift in the reflection band. The orientation kinetics of the azobenzene dopants reveal rapid molecular reorientation during both trans–cis and cis–trans isomerizations. The bent cis-isomers disrupt local director alignment, leading to a decrease in effective HTP, while back-isomerization reinstates molecular order. This reversible molecular reorientation is crucial for the observed dynamic and stable spectral tuning. This bidirectional spectral tuning primarily derives from the photo-controlled variations in helical pitch induced by the trans–cis isomerization of azobenzene molecules, while the average refractive index remains effectively unchanged. This reversible isomerization process facilitates dynamic and tunable spectral modulation. The observed spectral modulation characteristics align with theoretical predictions derived using the transformed-matrix method for anisotropic helical structures [37]. This method provides an exact formulation for the reflection spectra of CLCs, dependent on pitch and birefringence parameters, thereby enhancing the quantitative analysis of experimentally obtained dual-wavelength reflection-tuning results. Furthermore, no significant surface degradation, delamination, or photobleaching was observed during irradiation. The optical properties of the azo-nCLC samples remained stable across multiple cycles of dual-wavelength photoisomerization, demonstrating the exceptional photostability of this material system under the prescribed illumination conditions.

Spectral modulation of the Azo-nCLC cell under dual-wavelength exposure. (a) Schematic illustration of the azo-nCLC cell under simultaneous dual-wavelength counterpropagating beam exposure. (b) Transmission spectra obtained from continuous dual-beam exposure with a fixed 532 nm laser at 5 mW/cm2 and varying intensities of a 405 nm laser. (c) Transmission spectra recorded with a fixed 532 nm laser at 20 mW/cm2, varying the intensity of the 405 nm laser. (d) Simultaneous transmission spectra of the cell exposed to varying intensities of 405 nm and 532 nm lasers, maintaining proportional intensity relationships. During the spectra measurements shown in (b)–(d), the azo-nCLC cell was continuously applied an AC voltage of 100 V pp with a frequency of 1 kHz.
To further elucidate the optical properties of the photo-responsive LC superstructure, we implemented a dual-wavelength counterpropagating beam configuration, applying an AC field of 100 V pp at 1 kHz across the azo-nCLC cell (Figure 2(b)). This external electric stimulus was crucial for establishing uniform planar alignment and minimizing scattering effects caused by azobenzene diffusion. Under the dual-wavelength exposure setup (Figure S2), a constant green light intensity of 5.0 mW/cm2 combined with varying UV intensities (0.5–5.0 mW/cm2) resulted in a progressive blue shift of the reflection peak from 785 to 698 nm, alongside a narrowing of the bandwidth from 81 to 73 nm (Table S2). This shift is attributed to the increased concentration of cis-isomers near the UV-illuminated surface, which induces a spatial pitch gradient along the helical axis. Regions adjacent to the green interface maintain a longer pitch owing to trans-isomer predominance, while the resultant pitch gradient enhances spectral broadening. To further analyze the effects of optical intensity, we fixed the green light intensity at 20 mW/cm2 while varying the UV intensity (Figure 2(c)). At a UV intensity of 2.5 mW/cm2, the reflection bandwidth expanded to 101 nm, centered at 778 nm. Increasing the UV intensity to 5.0 mW/cm2 shifted the center to 754 nm and broadened the band to 109 nm. When both wavelengths were set to equal intensities of 20 mW/cm2, the center wavelength shifted to 694 nm with a narrowed bandwidth of 83 nm (Table S3). These results confirm that enhanced optical excitation intensifies the pitch gradient by elevating cis-isomers’ population near the UV-exposed surface, while the region illuminated by green light predominantly remains in the trans state. A comparative analysis of Tables (S2-S3) reveals that the bandwidth decreases at the spectral extremes (λ e ≈ 840 nm and λ o ≈ 690 nm) but reaches a maximum around intermediate wavelengths (∼750 nm). This behavior can be attributed to the relative distributions of cis and trans isomers: at spectral extremes, the dominance of a single isomer results in a weak pitch gradient and narrower bandwidth. Conversely, near 750 nm, the coexistence of both isomers produces the steepest gradient, yielding the broadest reflection band.
2.1.1 Central wavelength and bandwidth control in dual-wavelength photoisomerization
In the realm of photonic applications, the ability to manipulate the central wavelength and bandwidth of the PBG through dual-wavelength photoisomerization offers a substantial advancement for dynamic photonic devices. The prepared azo-nCLC cell demonstrates independent bandwidth control without altering the central reflection wavelength by maintaining a fixed intensity ratio of UV to green light while adjusting the absolute power (Figure 2(d)). With a ratio of 1:4 (4.0/16.0 mW/cm2), the reflection was centered at 755 nm, featuring a bandwidth of 101 nm (Table 1). Reducing both intensities proportionately results in 75 nm and 62 nm bandwidths at central wavelengths of 753 nm and 751 nm, respectively. This indicates increased intensity leads to bandwidth broadening via enhanced pitch gradients, provided the intensity ratio remains constant. Moreover, varying the intensity ratios (20:1 and 1:1) produces interesting effects, as shown in Figure S3. At an intensity ratio of 20:1 (0.25/5.0 and 1.0/20.0 mW/cm2), the central wavelength (∼797 nm) remains stable while the bandwidth expands from 78 nm to 87 nm. Conversely, at an intensity ratio of 1:1 (5.0/5.0 and 20.0/20.0 mW/cm2), a minor shift in peak occurs from 698 nm to 694 nm, accompanied by an increase in bandwidth from 73 nm to 82 nm (Table S4). These findings demonstrate that enhancing overall intensity broadens bandwidth and preserves a stable intensity ratio, thereby strengthening control over the central wavelength. Furthermore, a comparative analysis of counterpropagating and copropagating beam geometries (Figures S4-S7) uncovers a noteworthy shift in reflection, with the trans-dominant configuration yielding 815 nm and a bandwidth of 78 nm, while the cis-dominant configuration reveals 666 nm and a bandwidth of 63 nm (Table S1-S3). Copropagating beams exhibit mutual attenuation, which confines isomerization gradients to the near-surface region, thus limiting spectral modulation. In contrast, counterpropagating beams facilitate a broader photo-induced cis–trans isomer distribution and enhanced pitch gradients, enabling more effective tuning of the optical response. Notably, even in the copropagating configuration (Figure S7, Table S3), an increase in intensity results in spectral broadening, albeit with reduced efficiency. The reflection shift demonstrates a nearly linear correlation with optical power at low intensities, transitioning to saturation at higher powers as photostationary equilibrium is established between the trans and cis isomers [38], [39]. A similar dependence of azobenzene orientation on light power has been observed in polymer-based azobenzene systems [40], where molecular reorientation correlates with excitation intensity. In contrast, our dual-wavelength azo-nCLC methodology facilitates concurrent control of both trans–cis and cis–trans isomerization, broadening the response to reversible helical pitch modulation and enhancing broadband spectral tunability. This research provides a solid foundation for advancing next-generation light-responsive photonic components, including dynamic optical filters, tunable mirrors, and adaptive light modulators.
Center wavelengths (
| Light intensity (mW/cm2) 405 nm / 532 nm |
|
Δλ (nm) |
|---|---|---|
| 0.25 / 1.0 | 751 | 62 |
| 1.0 / 4.0 | 753 | 75 |
| 4.0 / 16.0 | 756 | 101 |
2.2 Enhanced boundary sharpness in CLCs through single and dual-wavelength exposure
The meticulous manipulation of LC configurations is essential for advancing high-performance photonic devices. We examined the fabrication of binary CLC cells through two photonic exposure methods: single-wavelength patterned UV exposure and dual-wavelength exposure, which employs patterned UV light in conjunction with uniform green light from the reverse side of the sample. To evaluate the impact of these optical conditions on interfacial boundary sharpness, we utilized 15 μm-thick homogeneously aligned LC cells filled with the specified binary CLC formulation. A photomask depicting the letter “E” defined the spatial characteristics of the UV exposure. Structures were analyzed using polarized optical microscopy (POM), revealing distinct colorimetric responses based on the exposure wavelength. Under short-wavelength illumination, regions treated with azobenzene-based chiral dopants exhibited a yellow-orange hue [41], [42]. In crossed polarizers with a 20° offset, unexposed long-pitch regions appeared orange, while UV-exposed short-pitch domains exhibited a deep red hue. The interface between exposed and unexposed regions demonstrated a high-contrast transition, indicating pitch diffusion across the boundary. Figure 3a(i-ii) demonstrates the gradual enhancement of the gradient observed during 5- and 10-minute UV exposures at 405 nm (0.80 mW/cm2). In contrast, Figure 3a(iii-iv) shows the results of simultaneously dual-wavelength exposure using a 532 nm green laser (0.60 mW/cm2) applied from behind the sample. Notably, single-wavelength exposure produced broader transition zones characterized by gradual pitch variability ranging from approximately 464 to 532 nm. Conversely, dual-wavelength exposure resulted in sharply defined interfaces. This enhancement is attributed to the spatially modulated isomerization equilibrium of the azobenzene dopants. Under UV-only conditions, trans–cis isomerization induces a concentration gradient that promotes molecular diffusion. Conversely, applying a green light facilitates the efficient back-isomerization of cis-azobenzene to its trans form in unexposed regions, effectively minimizing dopant diffusion and preserving spatial fidelity. Furthermore, interfacial boundaries can be sharpened by increasing exposure durations, employing lower-viscosity host materials, or utilizing higher light intensities. These modifications not only expedite diffusion kinetics but also amplify the photochemical back-conversion effects. Our findings underscore the effectiveness of dual-wavelength exposure as a powerful technique for reducing azobenzene diffusion while enhancing the spatial resolution of pitch-modulated chiral nematic LC structures. This paves the way for novel, high-performance photonic applications.

Optical response and switching dynamics of the Azo-nCLC cell under single- and dual-wavelength exposure. (a) POM images of binary CLCs fabricated under (i) single-wavelength 405 nm light exposure at 0.80 mW/cm2 for 5 min, (ii) 10 min, and (iii) dual-wavelength exposure combining 405 nm (0.80 mW/cm2) and 532 nm (0.60 mW/cm2) light for 5 min and (iv) 10 min. (b) Transmission spectra of binary CLCs produced via single-wavelength exposure to 405 nm, single-wavelength exposure to 532 nm, and dual-wavelength exposure, measured with an applied AC voltage of 100 V pp at 1 kHz. (c) (i) POM image of a dual-wavelength exposed 2D periodic binary CLC; (ii) microscopic image of the photomask viewed under POM, with the polarizer (P) and analyzer (A) oriented at 20°, and L indicating the direction of homogeneous alignment.
2.2.1 Precision control in dual-wavelength photo-patterning of azo-nCLCs using a 2D photomask
In our pursuit of enhancing spatially periodic photonic structures, we employ a two-dimensional square-patterned photomask with a grid size of 1 mm2. This approach enabled precise control over the UV intensity distribution, supplemented by uniform green light exposure from an opposing direction. The experimental setup (Figure S8). Figure 3(b) presents the transmission spectroscopy of the azo-nCLC cell applied with an AC voltage of 100 V pp at 1 kHz, highlighting the distinct spectral responses elicited by various light exposure regimes: UV light, green light, and their combination. The POM images in Figure 3(c-i) illustrate the binary CLCs under dual-wavelength exposure, corresponding to the spectral data in Figure 3(b). Additionally, Figure 3(c-ii) displays the photomask under POM, confirming the periodic grid pattern employed to spatially control UV exposure across the LC cell. The opaque regions of the mask, represented by the orange areas, exhibit reflection spectra ranging from 756 to 821 nm, with a pitch of approximately 506 nm. In contrast, the transparent regions (green areas) yield reflection spectra of about 674–727 nm, corresponding to a pitch near 450 nm. Notably, dual-wavelength exposure resulted in asymmetric reflectance characteristics; the shorter pitch regions (674–727 nm, pitch ∼450 nm) displayed an increasing reflectance trend with wavelength, while the longer pitch regions (756–821 nm, pitch ∼506 nm) exhibited a decreasing reflectance pattern. This spectral asymmetry results from the diffusion of photoresponse azobenzene, where concentration gradients between irradiated and unirradiated areas lead to pitch redistribution from 450 to 506 nm, thus resulting in intermediate reflection bands. To mitigate spectral broadening linked to diffusion, we propose two strategic solutions. The first strategy involves increasing the photomask grid size to restrict lateral diffusion, though this may compromise spatial resolution. The second strategy advocates the implementation of pixelated LC domains that incorporate physical or chemical barriers to confine diffusion to designated regions. This latter approach shows considerable promise for enhancing high-resolution, wavelength-selective optical components.
2.3 Spectral filtering using photo-responsive azo-nCLCs for narrowband light source generation
To establish tunable narrowband light sources for advanced photonic applications, we investigated a spectral filtering approach that utilizes photo-responsive azo-nCLC cells. This innovative approach diverges from traditional cholesteric lasers [43] and materials engineering techniques [44], [45], [46], offering an efficient, flexible solution for the selective transmission of specific wavelengths from broadband light sources. Our results unveil a mechanism for precise wavelength control through the intrinsic properties of CLCs, which reflect circularly polarized light within a defined PBG determined by their helical pitch. Upon exposure to UV light at a power density of 5 mW/cm2 for 5 min, azobenzene molecules in the CLC undergo trans-to-cis isomerization, resulting in significant modulation of the helical pitch. This creates two distinct regions within the LC cell: one with a shorter pitch (irradiated area) and another with a longer pitch (nonirradiated area). This localized alteration enables tunable spectral filtering, leveraging multiple light passes through the CLC cell to enhance selectivity, as illustrated in the experimental setup shown in Figure S9. During the filtering process, right-handed circularly polarized light (|R>) is predominantly reflected during its first traversal through the long-pitch region, while left-handed light (|L>) is transmitted. A first mirror (Mirror 1) redirects the transmitted light to invert its handedness, facilitating a second interaction with the CLC. A second mirror (Mirror 2) further directs the light through the short-pitch region, refining the spectral output (Figure 4(a)).

Spectral filtering of reconfigurable narrowband unpolarized light sources. (a) Schematic of spectrum filtering using CLC. (b) Transmission spectrum of the CLC after passing through the long-pitch region of the cell. (c) The transmission spectrum follows traversal through the short-pitch region of the CLC cell. (d) Combined transmission spectrum when light passes through both long- and short-pitch regions of the CLC cell. (e) Comparative analysis of original light (unpolarized) intensity versus intensity after traversing both pitch regions of the CLC cell once and twice.
We systematically varied the positioning of the CLC cell within the optical path to evaluate its spectral transmission characteristics under different filtering conditions. Figure 4(b) displays the transmission spectra from light passage through the long-pitch region, both once and twice, and offers a comparison with the short-pitch region (Figure 4(c)). Figure 4(d) shows the spectra observed following sequential light passage through both regions, underscoring the impact of multiple traversals. Specifically, a single pass through the CLC attenuates approximately 50 % of reflected spectral components, while two passes nearly eliminate these components. Spectral elements outside the reflection band exhibited minimal intensity loss, attributable to cumulative reflections and scattering at material interfaces. In Figure 4(e), we compare the initial broadband intensity with the outputs after one and two filtering cycles, demonstrating effective suppression within the targeted band while preserving broadband characteristics beyond 850 nm. Notably, the light filtered outside the reflection band remains unpolarized, indicating negligible distortion during the filtering process. This unpolarized filtering effect is achieved through sequential interactions of light with regions of short and long pitch situated between two mirrors, paralleling the principles of Fabry–Perot unpolarized filtering mechanisms [47]. Our dual-wavelength patterned CLC architecture presents a passive, tunable, and spatially programmable solution, eliminating the need for additional polarization management. Future optimization may involve fine-tuning the position and width of the reflection band through variations in dopant concentration or the application of dual-wavelength photoirradiation (UV and green), thereby enhancing dynamic modulation of adjacent Bragg bands. Overall, this technique constitutes a reconfigurable, passive mechanism for generating narrowband unpolarized light, highlighting its significant potential for integration into compact, wavelength-selective photonic devices and sensors.
3 Conclusions
In summary, we present a pioneering dual-wavelength photoisomerization method that allows for precise manipulation of the spectral sculpting properties of photonic materials using azo-nCLCs. The prepared device enables reversible trans–cis isomerization of chiral dopants, thereby enabling dynamic adjustment of the helical pitch, an essential parameter for spectral tuning through concurrent excitation at 405 nm and 532 nm. We have achieved impressive bidirectional shifts in the reflection band, exceeding 140 nm in spectral range and 100 nm in tunable bandwidth. By optimizing beam intensity ratios and adjusting propagation geometries, we can tailor customized pitch domains to significantly alter the reflection bandwidth and central wavelength, achieving remarkable spectral and spatial control. Our counterpropagating beam configurations offer smooth pitch gradients, enabling continuous tuning that surpasses traditional copropagating methods. Additionally, employing photomasking with dual-beam irradiation enables the creation of sharply defined pitch domains with minimal molecular diffusion, which is essential for high-resolution binary and pixelated CLC architectures. This passive operation requires no electrical bias and supports reconfigurable optical filtering and spectral shaping. The inherent circular polarization selectivity of our CLCs promotes narrowband reflection and dynamic light routing, establishing a versatile framework for light-programmable systems. Notably, our multipass optical architecture improves spectral discrimination through polarization-selective reflection, effectively filtering undesired spectral components with high fidelity. Overall, this groundbreaking approach to isomerization-driven photonic bandgap engineering enables spatially programmable, multiband reflections with sub-nanometer precision, opening new avenues for energy-efficient optics and integrated optical communication systems.
4 Experimental section/methods
4.1 Preparation of the azo-nCLCs cell
CLC mixtures were prepared by adding a right-handed chiral dopant (R1011, HTP ≈ +32 μm−1) along with a photo-responsive azobenzene-based chiral dopant (ChAD-2-S, BEAM Co.) into a nematic host that exhibits negative dielectric anisotropy (HNG30400-200, FUSOL MATERIAL CO., LTD). The CLC mixture was carefully formulated with a weight ratio of 88.8:7.3:3.9 for the nematic host, chiral azobenzene, and chiral host, respectively. The unique azobenzene dopant undergoes wavelength-dependent isomerization between its trans state (HTP ≈ −12.4 μm−1) and cis state (HTP ≈ 0 μm−1 due to the doped chiral dopant, R1011), allowing for dynamic modulation of CLC properties. The mixture was confined between two glass substrates, each treated with an indium tin oxide coating and a unidirectionally rubbed polyvinyl alcohol alignment layer to ensure uniform planar alignment. To construct the cell, the glass substrates were arranged with 30 μm-thick spacers and filled with the CLC mixture using a capillary action technique. This carefully engineered platform enables tunable modulation of the helical pitch via photoinduced trans–cis isomerization of ChAD-2-S, achieved through selective laser exposure at 405 nm and 532 nm. This innovative capability facilitates dynamic and reversible control over the spectral characteristics of the Bragg reflection band within the CLC, representing a significant advancement toward the development of reconfigurable photonic applications.
4.2 Measurement setup
To examine the azo-nCLCs Cell, we employed a 405 nm and 532 nm Nd: YAG laser (Unice E-O Services Inc.). A DET36A photodetector (Thorlabs) and a DS4034 digital oscilloscope (RIGOL Technologies) were used to facilitate detection and analysis. A standard tungsten halogen lamp (HL-2000, Ocean Optics, Inc.) served as the light source, with intensity controlled by an attenuator to keep levels within the saturation limits of the spectrometer. To prevent the short-wavelength component of the probe light from affecting the azobenzene material in the LC mixture, a 650 nm high-pass filter was installed prior to the probe light entering the azo-nCLCs Cell.
Funding source: National Science and Technology Council
Award Identifier / Grant number: 113-2221-E-008-045-MY3
-
Research funding: National Science and Technology Council, Taiwan (113-2221-E-008-045-MY3).
-
Author contribution: PS contributed to the writing – review & editing, writing – original draft, validation, investigation, formal analysis. M-HY was involed in visualization, validation, methodology, investigation, formal analysis, data curation. C-KL was responsible for validation, methodology, investigation, formal analysis, data curation. K-TC handled the writing – review & editing, writing – original draft, validation, supervision, resources, project administration, methodology, investigation, funding acquisition, formal analysis, conceptualization. All authors have accepted responsibility for the entire content of this manuscript and consented to its submission to the journal, reviewed all the results, and approved the final version of the manuscript.
-
Conflict of interest: Authors state no conflicts of interest.
-
Informed consent: Informed consent was obtained from all individuals included in this study.
-
Ethical statement: Our research was conducted following ethical guidelines. All experiments involving cholesteric liquid crystal (CLC) technologies were executed with integrity and transparency, yielding accurate and reproducible findings. Throughout the research process, we consistently uphold academic integrity and transparency. All requisite approvals for the study were duly obtained.
-
Data availability: The data used in this work are not publicly available. However, the authors will disclose them upon reasonable request.
References
[1] V. J. Lloyd et al.., “The actin cytoskeleton plays multiple roles in structural colour formation in butterfly wing scales,” Nat. Commun., vol. 15, no. 1, p. 4073, 2024, https://doi.org/10.1038/s41467-024-48060-3.Search in Google Scholar PubMed PubMed Central
[2] H. K. Bisoyi and Q. Li, “Light‐directed dynamic chirality inversion in functional self‐organized helical superstructures,” Angew. Chem. Int. Ed., vol. 55, no. 9, pp. 2994–3010, 2016, https://doi.org/10.1002/anie.201505520.Search in Google Scholar PubMed
[3] S. H. Choi et al.., “Bioinspired dynamic colour change,” Nat. Rev. Bioeng., vol. 3, no. 7, pp. 1–17, 2025. https://doi.org/10.1038/s44222-025-00298-2.Search in Google Scholar
[4] C. Finet, “Light as matter: Natural structural colour in art,” Humanit. Soc. Sci. Commun., vol. 10, no. 1, pp. 1–14, 2023, https://doi.org/10.1057/s41599-023-01854-0.Search in Google Scholar
[5] Z. Zhang, Z. Chen, L. Shang, and Y. Zhao, “Structural color materials from natural polymers,” Adv. Mater. Technol., vol. 6, no. 11, p. 2100296, 2021, https://doi.org/10.1002/admt.202100296.Search in Google Scholar
[6] M. Wang, H. Yang, X. Li, X. Zhang, and H. Yang, “Self‐assembled 3D blue phase liquid crystals for intelligent photonic crystals and functional devices,” Adv. Opt. Mater., vol. 13, no. 6, p. 2402581, 2025, https://doi.org/10.1002/adom.202402581.Search in Google Scholar
[7] P. Selvaraj et al.., “Self‐assembled multistable scattering mode for versatile energy‐saving smart windows,” Laser Photonics Rev., vol. 18, no. 5, p. 2301001, 2023. https://doi.org/10.1002/lpor.202301001.Search in Google Scholar
[8] J. Lv, X. Gao, B. Han, Y. Zhu, K. Hou, and Z. Tang, “Self-assembled inorganic chiral superstructures,” Nat. Rev. Chem., vol. 6, no. 2, pp. 125–145, 2022, https://doi.org/10.1038/s41570-021-00350-w.Search in Google Scholar PubMed
[9] P. Selvaraj, F.-T. Lin, C.-T. Huang, P.-H. Tuan, and K.-T. Cheng, “Stimuli-driven control of self-assembled radial-lying hierarchical superstructures of chiral nematics by using acoustic waves,” Opt. Express, vol. 33, no. 4, pp. 8640–8649, 2025, https://doi.org/10.1364/oe.543168.Search in Google Scholar PubMed
[10] D. Broer, J. Lub, and G. Mol, “Wide-band reflective polarizers from cholesteric polymer networks with a pitch gradient,” Nature, vol. 378, no. 6556, pp. 467–469, 1995, https://doi.org/10.1038/378467a0.Search in Google Scholar
[11] T. Liu et al.., “Electrically‐triggered oblique helicoidal cholesterics with a single‐layer architecture for next‐generation full‐color reflective displays,” Adv. Funct. Mater., vol. 34, no. 48, p. 2408855, 2024, https://doi.org/10.1002/adfm.202408855.Search in Google Scholar
[12] R. S. Zola, H. K. Bisoyi, H. Wang, A. M. Urbas, T. J. Bunning, and Q. Li, “Dynamic control of light direction enabled by stimuli‐responsive liquid crystal gratings,” Adv. Mater., vol. 31, no. 7, p. 1806172, 2019, https://doi.org/10.1002/adma.201806172.Search in Google Scholar PubMed
[13] L.-L. Ma et al.., “Self-assembled liquid crystal architectures for soft matter photonics,” Light Sci. Appl., vol. 11, no. 1, p. 270, 2022, https://doi.org/10.1038/s41377-022-00930-5.Search in Google Scholar PubMed PubMed Central
[14] W. Shen and G. Li, “Recent progress in liquid crystal‐based smart windows: Materials, structures, and design,” Laser Photonics Rev., vol. 17, no. 1, p. 2200207, 2023, https://doi.org/10.1002/lpor.202200207.Search in Google Scholar
[15] C. T. Wu, P. Selvaraj, Y. C. Tsai, C. T. Huang, C. C. Sun, and K. T. Cheng, “Stimuli‐responsive smart glass with switchable unidirectional light source for enhanced privacy/indoor illumination,” Adv. Opt. Mater., vol. 13, no. 8, p. 2403088, 2025, https://doi.org/10.1002/adom.202403088.Search in Google Scholar
[16] H. Wang, H. K. Bisoyi, A. M. Urbas, T. J. Bunning, and Q. Li, “Reversible circularly polarized reflection in a self-organized helical superstructure enabled by a visible-light-driven axially chiral molecular switch,” J. Am. Chem. Soc., vol. 141, no. 20, pp. 8078–8082, 2019, https://doi.org/10.1021/jacs.9b03231.Search in Google Scholar PubMed
[17] H. Wang, H. K. Bisoyi, X. Zhang, F. Hassan, and Q. Li, “Visible light‐driven molecular switches and motors: Recent developments and applications,” Chem.–A Eur. J., vol. 28, no. 18, p. e202103906, 2022, https://doi.org/10.1002/chem.202103906.Search in Google Scholar PubMed
[18] Q. Li, Y. Li, J. Ma, D. K. Yang, T. J. White, and T. J. Bunning, “Directing dynamic control of red, green, and blue reflection enabled by a light‐driven self‐organized helical superstructure,” Adv. Mater., vol. 23, no. 43, pp. 5069–5073, 2011, https://doi.org/10.1002/adma.201103362.Search in Google Scholar PubMed
[19] A. Ryabchun, F. Lancia, J. Chen, D. Morozov, B. L. Feringa, and N. Katsonis, “Helix inversion controlled by molecular motors in multistate liquid crystals,” Adv. Mater., vol. 32, no. 47, p. 2004420, 2020, https://doi.org/10.1002/adma.202004420.Search in Google Scholar PubMed
[20] R. Eelkema et al.., “Nanomotor rotates microscale objects,” Nature, vol. 440, no. 7081, p. 163, 2006, https://doi.org/10.1038/440163a.Search in Google Scholar PubMed
[21] T. van Leeuwen, A. S. Lubbe, P. Štacko, S. J. Wezenberg, and B. L. Feringa, “Dynamic control of function by light-driven molecular motors,” Nat. Rev. Chem., vol. 1, no. 12, p. 0096, 2017, https://doi.org/10.1038/s41570-017-0096.Search in Google Scholar
[22] Z. Zheng et al.., “Digital photoprogramming of liquid-crystal superstructures featuring intrinsic chiral photoswitches,” Nat. Photonics, vol. 16, no. 3, pp. 226–234, 2022, https://doi.org/10.1038/s41566-022-00957-5.Search in Google Scholar
[23] S. Lin, Y. Tang, W. Kang, H. K. Bisoyi, J. Guo, and Q. Li, “Photo-triggered full-color circularly polarized luminescence based on photonic capsules for multilevel information encryption,” Nat. Commun., vol. 14, no. 1, p. 3005, 2023, https://doi.org/10.1038/s41467-023-38801-1.Search in Google Scholar PubMed PubMed Central
[24] M. Irie, T. Fukaminato, K. Matsuda, and S. Kobatake, “Photochromism of diarylethene molecules and crystals: Memories, switches, and actuators,” Chem. Rev., vol. 114, no. 24, pp. 12174–12277, 2014, https://doi.org/10.1021/cr500249p.Search in Google Scholar PubMed
[25] S.-Z. Pu, Q. Sun, C.-B. Fan, R.-J. Wang, and G. Liu, “Recent advances in diarylethene-based multi-responsive molecular switches,” J. Mater. Chem. C, vol. 4, no. 15, pp. 3075–3093, 2016, https://doi.org/10.1039/c6tc00110f.Search in Google Scholar
[26] H. Tian and S. Yang, “Recent progresses on diarylethene based photochromic switches,” Chem. Soc. Rev., vol. 33, no. 2, pp. 85–97, 2004, https://doi.org/10.1039/b302356g.Search in Google Scholar PubMed
[27] Y. Li, M. Wang, H. Wang, A. Urbas, and Q. Li, “Rationally designed axially chiral diarylethene switches with high helical twisting power,” Chem.–A Eur. J., vol. 20, no. 49, pp. 16286–16292, 2014, https://doi.org/10.1002/chem.201403705.Search in Google Scholar PubMed
[28] D. Zhao et al.., “Precisely tuning helical twisting power via photoisomerization kinetics of dopants in chiral nematic liquid crystals,” Langmuir, vol. 34, no. 2, pp. 700–708, 2018, https://doi.org/10.1021/acs.langmuir.7b03786.Search in Google Scholar PubMed
[29] H. K. Bisoyi and Q. Li, “Liquid crystals: Versatile self-organized smart soft materials,” Chem. Rev., vol. 122, no. 5, pp. 4887–4926, 2021, https://doi.org/10.1021/acs.chemrev.1c00761.Search in Google Scholar PubMed
[30] L.-J. Chen, J.-D. Lin, and C.-R. Lee, “An optically stable and tunable quantum dot nanocrystal-embedded cholesteric liquid crystal composite laser,” J. Mater. Chem. C, vol. 2, no. 22, pp. 4388–4394, 2014, https://doi.org/10.1039/c4tc00128a.Search in Google Scholar
[31] A. Y.-G. Fuh, S.-J. Ho, S.-T. Wu, and M.-S. Li, “Optical filter with tunable wavelength and bandwidth based on phototunable cholesteric liquid crystals,” Appl. Opt., vol. 53, no. 8, pp. 1658–1662, 2014, https://doi.org/10.1364/ao.53.001658.Search in Google Scholar PubMed
[32] T. J. White, A. S. Freer, N. V. Tabiryan, and T. J. Bunning, “Photoinduced broadening of cholesteric liquid crystal reflectors,” J. Appl. Phys., vol. 107, no. 7, p. 073110, 2010, https://doi.org/10.1063/1.3369437.Search in Google Scholar
[33] X. Wu, T. T. N. Nguyen, I. Ledoux-Rak, C. T. Nguyen, and N. D. Lai, “UV beam-assisted efficient formation of surface relief grating on azobenzene polymers,” Appl. Phys. B, vol. 107, no. 3, pp. 819–822, 2012, https://doi.org/10.1007/s00340-012-4987-8.Search in Google Scholar
[34] F. de Lera-Garrido et al.., “Effect of bulky side groups on photophysical properties and electroluminescent performance of oligo (styryl) benzenes,” Dyes Pigm., vol. 213, p. 111179, 2023.10.1016/j.dyepig.2023.111179Search in Google Scholar
[35] T. B. Koch and H. Briesen, “Water–triglyceride interfaces limit permeability and diffusion of aroma molecules in butter,” Eur. J. Lipid Sci. Technol., vol. 126, no. 12, p. 2300248, 2024, https://doi.org/10.1002/ejlt.202300248.Search in Google Scholar
[36] Y. Kanakubo et al.., “Cell-sized confinements alter molecular diffusion in concentrated polymer solutions due to length-dependent wetting of polymers,” ACS Materials Au, vol. 3, no. 5, pp. 442–449, 2023, https://doi.org/10.1021/acsmaterialsau.3c00018.Search in Google Scholar PubMed PubMed Central
[37] I. Abdulhalim, “Effect of the number of sublayers on axial optics of anisotropic helical structures,” Appl. Opt., vol. 47, no. 16, pp. 3002–3008, 2008, https://doi.org/10.1364/ao.47.003002.Search in Google Scholar PubMed
[38] M. Dudek et al.., “Linear and nonlinear optical properties of azobenzene derivatives modified with an (amino) naphthalene moiety,” J. Phys. Chem. B, vol. 126, no. 32, pp. 6063–6073, 2022, https://doi.org/10.1021/acs.jpcb.2c03078.Search in Google Scholar PubMed PubMed Central
[39] A. Sharma, M. Bekir, N. Lomadze, and S. Santer, “Photo-isomerization kinetics of azobenzene containing surfactant conjugated with polyelectrolyte,” Molecules, vol. 26, no. 1, p. 19, 2020, https://doi.org/10.3390/molecules26010019.Search in Google Scholar PubMed PubMed Central
[40] A. R. M. Timóteo, J. H. Ribeiro, P. A. Ribeiro, and M. Raposo, “Dynamics of creation photoinduced birefringence on (PAH/PAZO) n layer-by-layer films: Analysis of consecutive cycles,” Opt. Mater., vol. 51, pp. 18–23, 2016, https://doi.org/10.1016/j.optmat.2015.11.005.Search in Google Scholar
[41] C.-K. Liu, C.-Y. Chiu, S. M. Morris, M.-C. Tsai, C.-C. Chen, and K.-T. Cheng, “Optically controllable linear-polarization rotator using chiral-azobenzene-doped liquid crystals,” Materials, vol. 10, no. 11, p. 1299, 2017, https://doi.org/10.3390/ma10111299.Search in Google Scholar PubMed PubMed Central
[42] C.-K. Liu, M.-C. Tsai, S. M. Morris, C.-Y. Chiu, C.-C. Chen, and K.-T. Cheng, “Dynamics of pitch change in chiral azobenzene-doped liquid crystals,” J. Mol. Liq., vol. 263, pp. 406–412, 2018, https://doi.org/10.1016/j.molliq.2018.04.104.Search in Google Scholar
[43] D. Statman and I. Janossy, “Study of photoisomerization of azo dyes in liquid crystals,” J. Chem. Phys., vol. 118, no. 7, pp. 3222–3232, 2003, https://doi.org/10.1063/1.1538598.Search in Google Scholar
[44] Y. Li, D. Luo, and Z. H. Peng, “Full-color reflective display based on narrow bandwidth templated cholesteric liquid crystal film,” Opt. Mater. Express, vol. 7, no. 1, pp. 16–24, 2016, https://doi.org/10.1364/ome.7.000016.Search in Google Scholar
[45] Y. Huang and S. Zhang, “Optical filter with tunable wavelength and bandwidth based on cholesteric liquid crystals,” Opt. Lett., vol. 36, no. 23, pp. 4563–4565, 2011, https://doi.org/10.1364/ol.36.004563.Search in Google Scholar
[46] V. I. Kopp, B. Fan, H. Vithana, and A. Z. Genack, “Low-threshold lasing at the edge of a photonic stop band in cholesteric liquid crystals,” Opt. Lett., vol. 23, no. 21, pp. 1707–1709, 1998, https://doi.org/10.1364/ol.23.001707.Search in Google Scholar PubMed
[47] I. Abdulhalim, “Unique optical properties of anisotropic helical structures in a Fabry-Perot cavity,” Opt. Lett., vol. 31, no. 20, pp. 3019–3021, 2006, https://doi.org/10.1364/ol.31.003019.Search in Google Scholar PubMed
Supplementary Material
This article contains supplementary material (https://doi.org/10.1515/nanoph-2025-0455).
© 2025 the author(s), published by De Gruyter, Berlin/Boston
This work is licensed under the Creative Commons Attribution 4.0 International License.
Articles in the same Issue
- Frontmatter
- Reviews
- Light-driven micro/nanobots
- Tunable BIC metamaterials with Dirac semimetals
- Large-scale silicon photonics switches for AI/ML interconnections based on a 300-mm CMOS pilot line
- Perspective
- Density-functional tight binding meets Maxwell: unraveling the mysteries of (strong) light–matter coupling efficiently
- Letters
- Broadband on-chip spectral sensing via directly integrated narrowband plasmonic filters for computational multispectral imaging
- Sub-100 nm manipulation of blue light over a large field of view using Si nanolens array
- Tunable bound states in the continuum through hybridization of 1D and 2D metasurfaces
- Integrated array of coupled exciton–polariton condensates
- Disentangling the absorption lineshape of methylene blue for nanocavity strong coupling
- Research Articles
- Demonstration of multiple-wavelength-band photonic integrated circuits using a silicon and silicon nitride 2.5D integration method
- Inverse-designed gyrotropic scatterers for non-reciprocal analog computing
- Highly sensitive broadband photodetector based on PtSe2 photothermal effect and fiber harmonic Vernier effect
- Online training and pruning of multi-wavelength photonic neural networks
- Robust transport of high-speed data in a topological valley Hall insulator
- Engineering super- and sub-radiant hybrid plasmons in a tunable graphene frame-heptamer metasurface
- Near-unity fueling light into a single plasmonic nanocavity
- Polarization-dependent gain characterization in x-cut LNOI erbium-doped waveguide amplifiers
- Intramodal stimulated Brillouin scattering in suspended AlN waveguides
- Single-shot Stokes polarimetry of plasmon-coupled single-molecule fluorescence
- Metastructure-enabled scalable multiple mode-order converters: conceptual design and demonstration in direct-access add/drop multiplexing systems
- High-sensitivity U-shaped biosensor for rabbit IgG detection based on PDA/AuNPs/PDA sandwich structure
- Deep-learning-based polarization-dependent switching metasurface in dual-band for optical communication
- A nonlocal metasurface for optical edge detection in the far-field
- Coexistence of weak and strong coupling in a photonic molecule through dissipative coupling to a quantum dot
- Mitigate the variation of energy band gap with electric field induced by quantum confinement Stark effect via a gradient quantum system for frequency-stable laser diodes
- Orthogonal canalized polaritons via coupling graphene plasmon and phonon polaritons of hBN metasurface
- Dual-polarization electromagnetic window simultaneously with extreme in-band angle-stability and out-of-band RCS reduction empowered by flip-coding metasurface
- Record-level, exceptionally broadband borophene-based absorber with near-perfect absorption: design and comparison with a graphene-based counterpart
- Generalized non-Hermitian Hamiltonian for guided resonances in photonic crystal slabs
- A 10× continuously zoomable metalens system with super-wide field of view and near-diffraction–limited resolution
- Continuously tunable broadband adiabatic coupler for programmable photonic processors
- Diffraction order-engineered polarization-dependent silicon nano-antennas metagrating for compact subtissue Mueller microscopy
- Lithography-free subwavelength metacoatings for high thermal radiation background camouflage empowered by deep neural network
- Multicolor nanoring arrays with uniform and decoupled scattering for augmented reality displays
- Permittivity-asymmetric qBIC metasurfaces for refractive index sensing
- Theory of dynamical superradiance in organic materials
- Second-harmonic generation in NbOI2-integrated silicon nitride microdisk resonators
- A comprehensive study of plasmonic mode hybridization in gold nanoparticle-over-mirror (NPoM) arrays
- Foundry-enabled wafer-scale characterization and modeling of silicon photonic DWDM links
- Rough Fabry–Perot cavity: a vastly multi-scale numerical problem
- Classification of quantum-spin-hall topological phase in 2D photonic continuous media using electromagnetic parameters
- Light-guided spectral sculpting in chiral azobenzene-doped cholesteric liquid crystals for reconfigurable narrowband unpolarized light sources
- Modelling Purcell enhancement of metasurfaces supporting quasi-bound states in the continuum
- Ultranarrow polaritonic cavities formed by one-dimensional junctions of two-dimensional in-plane heterostructures
- Bridging the scalability gap in van der Waals light guiding with high refractive index MoTe2
- Ultrafast optical modulation of vibrational strong coupling in ReCl(CO)3(2,2-bipyridine)
- Chirality-driven all-optical image differentiation
- Wafer-scale CMOS foundry silicon-on-insulator devices for integrated temporal pulse compression
- Monolithic temperature-insensitive high-Q Ta2O5 microdisk resonator
- Nanogap-enhanced terahertz suppression of superconductivity
- Large-gap cascaded Moiré metasurfaces enabling switchable bright-field and phase-contrast imaging compatible with coherent and incoherent light
- Synergistic enhancement of magneto-optical response in cobalt-based metasurfaces via plasmonic, lattice, and cavity modes
- Scalable unitary computing using time-parallelized photonic lattices
- Diffusion model-based inverse design of photonic crystals for customized refraction
- Wafer-scale integration of photonic integrated circuits and atomic vapor cells
- Optical see-through augmented reality via inverse-designed waveguide couplers
- One-dimensional dielectric grating structure for plasmonic coupling and routing
- MCP-enabled LLM for meta-optics inverse design: leveraging differentiable solver without LLM expertise
- Broadband variable beamsplitter made of a subwavelength-thick metamaterial
- Scaling-dependent tunability of spin-driven photocurrents in magnetic metamaterials
- AI-based analysis algorithm incorporating nanoscale structural variations and measurement-angle misalignment in spectroscopic ellipsometry
Articles in the same Issue
- Frontmatter
- Reviews
- Light-driven micro/nanobots
- Tunable BIC metamaterials with Dirac semimetals
- Large-scale silicon photonics switches for AI/ML interconnections based on a 300-mm CMOS pilot line
- Perspective
- Density-functional tight binding meets Maxwell: unraveling the mysteries of (strong) light–matter coupling efficiently
- Letters
- Broadband on-chip spectral sensing via directly integrated narrowband plasmonic filters for computational multispectral imaging
- Sub-100 nm manipulation of blue light over a large field of view using Si nanolens array
- Tunable bound states in the continuum through hybridization of 1D and 2D metasurfaces
- Integrated array of coupled exciton–polariton condensates
- Disentangling the absorption lineshape of methylene blue for nanocavity strong coupling
- Research Articles
- Demonstration of multiple-wavelength-band photonic integrated circuits using a silicon and silicon nitride 2.5D integration method
- Inverse-designed gyrotropic scatterers for non-reciprocal analog computing
- Highly sensitive broadband photodetector based on PtSe2 photothermal effect and fiber harmonic Vernier effect
- Online training and pruning of multi-wavelength photonic neural networks
- Robust transport of high-speed data in a topological valley Hall insulator
- Engineering super- and sub-radiant hybrid plasmons in a tunable graphene frame-heptamer metasurface
- Near-unity fueling light into a single plasmonic nanocavity
- Polarization-dependent gain characterization in x-cut LNOI erbium-doped waveguide amplifiers
- Intramodal stimulated Brillouin scattering in suspended AlN waveguides
- Single-shot Stokes polarimetry of plasmon-coupled single-molecule fluorescence
- Metastructure-enabled scalable multiple mode-order converters: conceptual design and demonstration in direct-access add/drop multiplexing systems
- High-sensitivity U-shaped biosensor for rabbit IgG detection based on PDA/AuNPs/PDA sandwich structure
- Deep-learning-based polarization-dependent switching metasurface in dual-band for optical communication
- A nonlocal metasurface for optical edge detection in the far-field
- Coexistence of weak and strong coupling in a photonic molecule through dissipative coupling to a quantum dot
- Mitigate the variation of energy band gap with electric field induced by quantum confinement Stark effect via a gradient quantum system for frequency-stable laser diodes
- Orthogonal canalized polaritons via coupling graphene plasmon and phonon polaritons of hBN metasurface
- Dual-polarization electromagnetic window simultaneously with extreme in-band angle-stability and out-of-band RCS reduction empowered by flip-coding metasurface
- Record-level, exceptionally broadband borophene-based absorber with near-perfect absorption: design and comparison with a graphene-based counterpart
- Generalized non-Hermitian Hamiltonian for guided resonances in photonic crystal slabs
- A 10× continuously zoomable metalens system with super-wide field of view and near-diffraction–limited resolution
- Continuously tunable broadband adiabatic coupler for programmable photonic processors
- Diffraction order-engineered polarization-dependent silicon nano-antennas metagrating for compact subtissue Mueller microscopy
- Lithography-free subwavelength metacoatings for high thermal radiation background camouflage empowered by deep neural network
- Multicolor nanoring arrays with uniform and decoupled scattering for augmented reality displays
- Permittivity-asymmetric qBIC metasurfaces for refractive index sensing
- Theory of dynamical superradiance in organic materials
- Second-harmonic generation in NbOI2-integrated silicon nitride microdisk resonators
- A comprehensive study of plasmonic mode hybridization in gold nanoparticle-over-mirror (NPoM) arrays
- Foundry-enabled wafer-scale characterization and modeling of silicon photonic DWDM links
- Rough Fabry–Perot cavity: a vastly multi-scale numerical problem
- Classification of quantum-spin-hall topological phase in 2D photonic continuous media using electromagnetic parameters
- Light-guided spectral sculpting in chiral azobenzene-doped cholesteric liquid crystals for reconfigurable narrowband unpolarized light sources
- Modelling Purcell enhancement of metasurfaces supporting quasi-bound states in the continuum
- Ultranarrow polaritonic cavities formed by one-dimensional junctions of two-dimensional in-plane heterostructures
- Bridging the scalability gap in van der Waals light guiding with high refractive index MoTe2
- Ultrafast optical modulation of vibrational strong coupling in ReCl(CO)3(2,2-bipyridine)
- Chirality-driven all-optical image differentiation
- Wafer-scale CMOS foundry silicon-on-insulator devices for integrated temporal pulse compression
- Monolithic temperature-insensitive high-Q Ta2O5 microdisk resonator
- Nanogap-enhanced terahertz suppression of superconductivity
- Large-gap cascaded Moiré metasurfaces enabling switchable bright-field and phase-contrast imaging compatible with coherent and incoherent light
- Synergistic enhancement of magneto-optical response in cobalt-based metasurfaces via plasmonic, lattice, and cavity modes
- Scalable unitary computing using time-parallelized photonic lattices
- Diffusion model-based inverse design of photonic crystals for customized refraction
- Wafer-scale integration of photonic integrated circuits and atomic vapor cells
- Optical see-through augmented reality via inverse-designed waveguide couplers
- One-dimensional dielectric grating structure for plasmonic coupling and routing
- MCP-enabled LLM for meta-optics inverse design: leveraging differentiable solver without LLM expertise
- Broadband variable beamsplitter made of a subwavelength-thick metamaterial
- Scaling-dependent tunability of spin-driven photocurrents in magnetic metamaterials
- AI-based analysis algorithm incorporating nanoscale structural variations and measurement-angle misalignment in spectroscopic ellipsometry