Tunable Luminescence Properties Research Articles

Synthesis and tunable luminescence properties of SrY₂O₄:Dy³⁺ phosphors

In this study, SrY₂O₄:Dy³⁺ phosphors were synthesized using the solid-state reaction method and evaluated after heat treatment at 1300 °C for 5 h. XRD analysis confirmed the orthorhombic structure of SrY₂O₄ with residual Y₂O₃ present. The addition of Dy³⁺ ions caused lattice expansion, impacting grain size and crystallinity. SEM images showed that the phosphor particles had irregular shapes with minimal size variation, although they tended to agglomerate due to high-temperature heat treatment. Optical analysis revealed significant absorption and emission peaks, with a strong excitation band in the 200–306 nm range and prominent sharp peaks in the 306–480 nm range, particularly at a 0.5 mol% doping concentration. Emission spectra indicated the highest intensity at 0.5 mol% Dy³⁺ concentration, with intensity decreasing due to concentration quenching at higher levels. Thermal stability tests showed peak emission intensity at 70 °C, with stability maintained up to 190 °C before notable thermal quenching. Chromaticity coordinates remained within the warm white region at both temperatures. This study provides detailed insights into the effects of Dy³⁺ doping on the structural, optical, and thermal properties of SrY₂O₄ phosphors. Compared to previous studies on rare-earth-doped SrY₂O₄ phosphors, this work is the first to systematically explore the substitution of Y³⁺ ions with Dy³⁺ ions until full replacement. The study not only confirmed that the highest emission intensity occurs at 0.5 mol% Dy³⁺ concentration, but also demonstrated that Dy³⁺-doped SrY₂O₄ phosphors exhibit excellent thermal stability, with emission stability maintained below 150 °C. These findings expand the potential applications of Dy³⁺-doped SrY₂O₄ phosphors, particularly in high-temperature environments and solid-state lighting.

Tunable Luminescent Properties and Multifunctional Imaging Applications of (Gd1-xRx)2O2S:Tb3+ (R = Y, La) Phosphor and Screen.

Gd2O2S:Tb3+ phosphor screens are widely used in image intensifiers, computed tomography, and neutron imaging. To improve the luminescent properties and thermal stability, (Gd1-xRx)2O2S:yTb3+ (R = Y, La) (x = 0, 0.05, 0.15, 0.25, and 0.35; y = 0.02, 0.04, 0.06, 0.08, and 0.10) phosphors were successfully prepared by the carbothermal reduction method. The luminescent spectra showed that the optimum concentrations of Tb3+ ions were 6 and 4 mol % when excited by 292 nm UV light and cathode ray, respectively. The emission wavelengths mainly peaked at 489 and 544 nm. It was found that the introduction of Y3+ ions could improve the luminescent intensity, and the luminescent intensity of (Gd1-xYx)2O2S:0.06Tb3+ was the highest at x = 0.25, while La3+ ions played the opposite role. Then, the thermal stability also improved, and the emission intensities of Gd2O2S:0.06Tb3+, (Gd0.75Y0.25)2O2S:0.06Tb3+, and (Gd0.75La0.25)2O2S:0.06Tb3+ phosphors at 423 K decreased to 66.22%, 68.23%, and 76.10% of the emission intensities at 303 K, respectively. Finally, the (Gd0.75Y0.25)2O2S:0.06Tb3+ phosphor screen was successfully prepared by the gravity deposition method and could be well imaged under UV light and cathode ray excitation with a CMOS camera. In summary, this study demonstrates that (Gd1-xRx)2O2S:Tb3+ (R = Y, La) is a phosphor with excellent luminescent and thermal stability properties and has great potential for application in the field of low-level-light night vision, nondestructive testing, and medical imaging.

Maximizing Upconversion Luminescence of Co-Doped CaF₂:Yb, Er Nanoparticles at Low Laser Power for Efficient Cellular Imaging.

Upconversion nanoparticles (UCNPs) are well-reported for bioimaging. However, their applications are limited by low luminescence intensity. To enhance the intensity, often the UCNPs are coated with macromolecules or excited with high laser power, which is detrimental to their long-term biological applications. Herein, we report a novel approach to prepare co-doped CaF2:Yb3+ (20%), Er3+ with varying concentrations of Er (2%, 2.5%, 3%, and 5%) at ambient temperature with minimal surfactant and high-pressure homogenization. Strong luminescence and effective red emission of the UCNPs were seen even at low power and without functionalization. X-ray diffraction (XRD) of UCNPs revealed the formation of highly crystalline, single-phase cubic fluorite-type nanostructures, and transmission electron microscopy (TEM) showed co-doped UCNPs are of ~12 nm. The successful doping of Yb and Er was evident from TEM-energy dispersive X-ray analysis (TEM-EDAX) and X-ray photoelectron spectroscopy (XPS) studies. Photoluminescence studies of UCNPs revealed the effect of phonon coupling between host lattice (CaF2), sensitizer (Yb3+), and activator (Er3+). They exhibited tunable upconversion luminescence (UCL) under irradiation of near-infrared (NIR) light (980 nm) at low laser powers (0.28-0.7 W). The UCL properties increased until 3% doping of Er3+ ions, after which quenching of UCL was observed with higher Er3+ ion concentration, probably due to non-radiative energy transfer and cross-relaxation between Yb3+-Er3+ and Er3+-Er3+ ions. The decay studies aligned with the above observation and showed the dependence of UCL on Er3+ concentration. Further, the UCNPs exhibited strong red emission under irradiation of 980 nm light and retained their red luminescence upon internalization into cancer cell lines, as evident from confocal microscopic imaging. The present study demonstrated an effective approach to designing UCNPs with tunable luminescence properties and their capability for cellular imaging under low laser power.

Preparation and application of wormlike micelles generated from a rosin-based aggregation-induced emission surfactant through coordinating aggregation

Fluorescent nanomaterials have drawn considerable attentions due to their high fluorescence sensitivity, excellent signal stability and tunable luminescent properties. A bio-based aggregation-induced emission (AIE) surfactant (Sodium 4-(tetraphenylstyrene)maleate, MPA-TPE-Na) was prepared from rosin, which showed typical AIE characteristic, obvious solvatochromism and a large Stokes shift (>100 nm). AIE viscoelastic solutions were further prepared by complexing MPA-TPE-Na and cetyltrimethylammonium bromide (CTAB) through coordinating aggregation and their microstructure, fluorescence properties and viscoelasticities were investigated. The aggregates in the viscoelastic solutions were wormlike micelles. As the concentration of MPA-TPE-Na increased, the fluorescence intensity of the viscoelastic solutions increased, and their viscosity increased at first and then decreased. The fluorescence emission intensity of the viscoelastic solutions was barely affected by the change in pH. But reducing the pH could increase its viscosity. This system can specifically recognize Fe3+ without any organic solvent and has anti-interference ability. The present work provided a bio-based fluorescent nanomaterial and verified the feasibility of preparing aqueous AIE nanomaterials by modifying AIE groups with rosin skeleton.

Tunable bandgap and luminescence properties by engineering exciton coupling in Ag NP embedded Er3+ bismuth tellurite glass system

Tunable bandgap and luminescence properties by engineering exciton coupling in Ag NP embedded Er3+ bismuth tellurite glass system

Stepwise Charge/Energy Transfer in MR-TADF Molecule-Doped Exciplex for Ultralong Persistent Luminescence Activated with Visible Light.

Organic long-persistent luminescence (OLPL), which relies on energy storage for delayed light emission by the charge separation state, has attracted intense attention in various optical applications. However, charge separation (CS) is efficient only under ultraviolet excitation in most OLPL systems because it requires a driving force from the large energy difference between the local excited (LE) and charge transfer (CT) states. In this study, a multiresonance thermally activated delayed fluorescence (MR-TADF) molecule is incorporated into an exciplex system to achieve efficient OLPL in a composite material activated by visible light via a stepwise charge/energy transfer process. The enhanced absorption of the composite material facilitated a tenfold increase in the duration of the OLPL, which can last for several hours under visible light excitation. The excited state of the MR-TADF molecule tends to charge transfer to the acceptor, followed by energy transfer to the exciplex, which benefits from the small difference between the LE and CT states owing to the inherent CS characteristics of the opposing resonance effect. Afterglow displays of these composite materials are fabricated to demonstrate their considerable potential in encryption patterns and emergency lights, which take advantage of their excellent processability, visible light activation, and tunable luminescence properties.

Tunable luminescent properties and structure of Sn2+-doped boroaluminate glasses

A series of novel Sn2+ doped boroaluminate glasses were prepared by the traditional melt quenching method in this work. Their glass network structure, luminescent properties, and mechanisms were studied in detail. The main framework of the glass network was dependent on the glass network former (B2O3) and intermediate (Al2O3), and was characterized by the 11B and 27Al NMR spectra. Broadband tunable blue-violet emissions ranging from 320 to 550 nm were realized by regulating the glass network structure through optical basicity. The quantitative relationship between optical basicity and emission/excitation peak positions and intensities, FWHM, and Stokes-Shift of this Sn2+-doped glass were revealed, according to which the luminescent properties of Sn2+ could be modulated and even predicted in the future. This work will enrich our understanding of the luminescent properties of Sn2+ ions and the variations of glass network structure, guiding the design of efficient and tunable luminescent boroaluminate glass.

Eu3+-Directed Supramolecular Metallogels with Reversible Quadruple-Stimuli Response Behaviors.

Smart luminescent materials that have the ability to reversibly adapt to external environmental stimuli and possess a wide range of responses are continually emerging, which place higher demands on the means of regulation and response sites. Here, europium ions (Eu3+)-directed supramolecular metallogels are constructed by orthogonal self-assembly of Eu3+ based coordination interactions and hydrogen bonding. A new organic ligand (L) is synthesized, consisting of crown ethers and two flexible amide bonds-linked 1,10-phenanthroline moieties to coordinate with Eu3+. Synergistic intermolecular hydrogen bonding in L and Eu3+-L coordination bonding enable Eu3+ and L to self-assemble into shape-persistent 3D coordination metallogels in MeOH solution. The key to success is the utilization of crown ethers, playing dual roles of acting both as building blocks to build L with C2-symmetrical structure, and as the ideal monomer for increasing the energy transfer from L to Eu3+'s excited state, thus maintaining the excellent luminescence of metallogels. Interestingly, such assemblies show K+, pH, F-, and mechano-induced reversible gel-sol transitions and tunable luminescence properties. Above findings are useful in the studies of molecular switches, dynamic assemblies, and smart luminescent materials.

Stimuli‐responsive fluorescent hydrogels: Strategies and applications

AbstractStimuli‐responsive fluorescent hydrogels are three‐dimensional networked polymeric materials with tunable luminescence and dynamic properties, which play an important role as a water‐rich soft material in the fields of information encryption, bionic actuation, bioimaging, environmental monitoring, and luminescent materials. Compared with conventional hydrogels, their unique luminescent properties allow the visualization of microscopic dynamics within the polymer network. By rational inclusion of dynamic motifs, such as photoswitches, AIEgens, lanthanide complexes, and host–guest complexes, these materials are endowed with tunability of emission, shape, and phase in time and space in response to environmental effectors. In this review, we summarize the fabrication strategies that are mainly used by recently reported stimuli‐responsive fluorescent hydrogels and the applications of these materials.

Assessment of the correlation between optical properties and CQD preparation approaches

Various production procedures, for carbon quantum dots (CQDs), are still being extensively researched to understand the nature of CQD luminescence. This study compares and examines the impact of chemical as well as green methods on the structural and optical properties of CQDs. We present a straightforward, cost-effective bottom-up method for producing fluorescent CQDs from lemon peels (L-CQDs), orange juice (O-CQDs), and citric acid (C-CQDs) without having to deal with time-consuming or ineffective post-processing processes. The proposed green synthesis has no toxic by-products, and the residual resources utilized promote the large-scale production of CQDs. X-ray diffraction, high-resolution transmission electron microscopy, FTIR, Raman, DLS, and UV–Vis spectroscopy are utilized to investigate the structure and optical characteristics of the prepared CQDs. The as-prepared CQDS possess small particle sizes of 5.6 nm, 6.2 nm, and 1.1 nm for L-CQDs, O-CQDs, and C-CQDs samples, respectively. FTIR results reveal the coexistence of carboxylic and hydroxyl groups on the surface of the CQDs, as also supported by zeta-potential values. Maximal fluorescence intensity was reached at excitation wavelengths of 365, 250, and 280 nm with an emission color of blue, indigo, and light blue for L-CQDs, O-CQDs, and C-CQDs, respectively. The presented approaches show a high quantum yield of 88% for O-CQDs, 49% for L-CQDs, and 37% for C-CQDs. Due to their minuscule particle size, perfect water solubility, high stability, and tunable luminescence properties, the prepared CQDs are preferred for potential applications in multicolor imaging, metal ion sensing, and wastewater technologies.

Metal halide perovskite polymer composites for indirect X-ray detection.

Metal halide perovskites (MHPs) have emerged as a promising class of materials for radiation detection due to their high atomic numbers and thus high radiation absorption, tunable and efficient luminescent properties and simple solution processability. Traditional MHP scintillators, however, suffer from environmental degradation, spurring interest in perovskite-polymer composites. This paper reviews recent developments in these composites tailored for scintillator applications. It discusses various synthesis methods, including solution-based and mechanochemical techniques, that enable the formation of composites with enhanced performance metrics such as light yield, detection limit, and environmental stability. The review also covers the remaining challenges and opportunities in fabrication techniques and performance metric evaluations of this class of materials. By offering a comprehensive overview of current research and future perspectives, this paper underscores the potential of perovskite-polymer composites to revolutionize the field of radiation detection.

Assembly of two new self-interpenetrating metal-organic frameworks with tunable luminescent properties

Two newly isostructural Zn-MOFs, namely [Zn2(DMTDC)2(H2O)(TPT)]·4H2O (JOU-8) and [Zn2(DMTDC)2(H2O)(TPY)]·4H2O (JOU-9), have been solvothermally synthesized and characterized (H2DMTDC = 3,4-DiMethylthieno(2,3-b)thiophene-2,5-dicarboxylic acid, TPT = 2,4,6-tri(pyridin-4-yl)-1,3,5-triazine, TPY = 2,4,6-tri(pyridin-4-yl)pyridine). Single-crystal X-ray diffraction revealed that JOU-8 and JOU-9 displayed three-dimensional self-interpenetrating structure with a new type of (6,6)-connected topology. Further studies revealed that strong π-π interactions between conjugated ligand DMTDC and TPT/TPY leaded to the formation of ligand-to-ligand charge transfer, which not only extended the absorption band edge of MOFs but also induced new emission peaks. The emission peaks at 401 nm for JOU-8 and 402 nm for JOU-9 were derived from the ligands, while the emission peaks at 489 nm for JOU-8 and 499 nm for JOU-9 may be derived from the π-π interactions between DMTDC and TPT/TPY. Moreover, the emission peak intensity of JOU-8 and JOU-9 are tunable depending upon the excitation wavelength. Thus, both JOU-8 and JOU-9 were potential dual-emission materials. This work provides new clues for the preparation of entangled MOFs with tunable luminescent properties.

Wide-Range Color-Tunable Organic Scintillators for X-Ray Imaging Through Host-Guest Doping.

With the increasing demands of X-ray detection and medical diagnosis, organic scintillators with intense and tunable X-ray excited emission have been becoming important. To guarantee the X-ray absorption, heavy atoms were widely added in reported organic scintillators, which led to emission quenching. In this work, we propose a new strategy to realize organic scintillators through the host-guest doping strategy. Then the X-ray absorption centers (host) and emission centers (guest) are separated. Under X-ray excitation, these materials displayed intense and readily tunable emissions ranging from green (520 nm) to near infrared (NIR) regions (682 nm). Besides, the relationship between the X-ray absorption and spatial arrangement of the heavy atoms in the host matrix was also revealed. The potential application of these wide-range color tunable organic host-guest scintillators in X-ray imaging were demonstrated. This work provides a new feasible strategy for constructing high-performance organic scintillators with tunable luminescence properties.

Wide‐Range Color‐Tunable Organic Scintillators for X‐Ray Imaging Through Host‐Guest Doping

AbstractWith the increasing demands of X‐ray detection and medical diagnosis, organic scintillators with intense and tunable X‐ray excited emission have been becoming important. To guarantee the X‐ray absorption, heavy atoms were widely added in reported organic scintillators, which led to emission quenching. In this work, we propose a new strategy to realize organic scintillators through the host‐guest doping strategy. Then the X‐ray absorption centers (host) and emission centers (guest) are separated. Under X‐ray excitation, these materials displayed intense and readily tunable emissions ranging from green (520 nm) to near infrared (NIR) regions (682 nm). Besides, the relationship between the X‐ray absorption and spatial arrangement of the heavy atoms in the host matrix was also revealed. The potential application of these wide‐range color tunable organic host‐guest scintillators in X‐ray imaging were demonstrated. This work provides a new feasible strategy for constructing high‐performance organic scintillators with tunable luminescence properties.

Tunable luminescence properties of the Ca3-xLuxSc2-xMgxSi3O12:Ce3+ phosphor based LD lighting

In white-light laser diodes (LD) illumination, the full width at half maximum (FWHM) of the emission spectrum of blue LD is too narrow, leading to the cyan light deficiency, while the emitting color of the material limits the red component of the device. Therefore, in this paper, Ca3-xLuxSc2-xMgxSi3O12:Ce3+ (CLSMS:Ce3+, x = 0, 0.5, 1, 1.5, 2) phosphor samples were successfully prepared based on Ca3Sc2Si3O12 (CSS) cyan-green fluorescent materials with different concentrations of Lu–Mg ions introduced in the matrix instead of Ca–Sc ions. And their luminescence properties were systematically investigated. The peak of the sample was shifted from 508 nm to 590 nm as the concentration of Lu–Mg increased. The thermal stability of the series phosphors gradually deteriorated with increasing Lu–Mg concentration. At 423 K, the emission intensity of the samples was 98.11 %, 94.13 %, 92.18 %, 81.96 % and 77.60 % of that at 298 K, respectively. And the thermal quenching activation energy also gradually decreases. The CLSMS:Ce3+ fluorescent materials were prepared into LD devices and tested. It was found that the series of samples showed a gradual decrease in cyan-green light and a gradual increase in red light with increasing Lu–Mg concentration. The CSS compounded with CaLu2Mg2Si3O12 (CLMS) obtained a white LD device with color coordinates of (0.3440, 0.3455), and the cyan and red components of the samples were compensated. In summary, this study demonstrates that CLSMS:Ce3+ is a very promising fluorescent material to extend the color gamut coverage of fluorescent materials. And it has a potential reference value for the field of white-light LD lighting.

Heteroatom-engineered multicolor lignin carbon dots enabling bimodal fluorescent off-on detection of metal-ions and glutathione

Carbon dots (CDs) have emerged as a promising subclass of optical nanomaterials with versatile functions in multimodal biosensing. Howbeit the rapid, reliable and reproducible fabrication of multicolor CDs from renewable lignin with unique groups (e.g., –OCH3, –OH and –COOH) and alterable moieties (e.g., β-O-4, phenylpropanoid structure) remains challenging due to difficult-to-control molecular behavior. Herein we proposed a scalable acid-reagent strategy to engineer a family of heteroatom-doped multicolor lignin carbon dots (LCDs) that are functioned as the bimodal fluorescent off-on sensing of metal-ions and glutathione (GSH). Benefiting from the modifiable photophysical structure via heteroatom-doping (N, S, W, P and B), the multicolor LCDs (blue, green and yellow) with a controllable size distribution of 2.06–2.22 nm deliver the sensing competences to fluorometric probing the distinctive metal-ion systems (Fe3+, Al3+ and Cu2+) under a broad response interval (0–500 μM) with excellent sensitivity and limit of detection (LOD, 0.45–3.90 μM). Meanwhile, we found that the addition of GSH can efficiently restore the fluorescence of LCDs by forming a stable Fe3+-GSH complex with a LOD of 0.97 μM. This work not only sheds light on evolving lignin macromolecular interactions with tunable luminescent properties, but also provides a facile approach to synthesize multicolor CDs with advanced functionalities.

Multicolor Mechanoluminescence in Sr2Ga2GeO7: Pr3+ for Stress Sensing and Anticounterfeiting

AbstractMechanical luminescence (ML) is the conversion of mechanical energy into light energy when a material is subjected to a force. It is challenging to develop ML materials with tunable luminescent properties by single ion doping, which have broad application prospects in the fields of stress sensing and dynamic signature anticounterfeiting. In this study, a Pr3+ doped Sr2Ga2GeO7 tunable ML material is reported. Due to the traps resulting from unequal substitution of Pr3+–Sr2+ in [SrO6] heptahedra, the deep/shallow traps redistribution occurs towards a multicolor ML from red to green. In addition, even after continuous friction sliding force (15 N), the ML intensities can be recovered after ultraviolet pre‐irradiation, indicating that Sr2Ga2GeO7: Pr3+ has excellent ML emission stability. Based on thermoluminescence analysis, potential PersL and ML mechanisms are further elaborated by a lattice engineering (trap regulation) strategy. In all, the development of single‐ion doped multicolor ML materials may have crucial research value and show a variety of potential applications in the fields of anticounterfeiting and information encryption.

Luminescent materials with dual-mode excitation and tunable emission color for anti-counterfeiting applications

GdVO4-based dual-mode phosphors were successfully synthesized via a hydrothermal approach. The X-ray diffraction analysis determined the tetragonal structure as well as I41/amd space group of products by comparing with a reference pattern no. ICDD #01-072-0277. The morphology of yielded phosphors was confirmed by transmission electron microscopy and scanning electron microscopy. Detailed spectroscopy analysis revealed tunable luminescence properties with an increasing Yb3+ content in series of GdVO4: x% Yb3+, y% Tm3+, 5% Eu3+ (x = 5, 10, 15, 20; y = 0.1, 0.5, 1) phosphors. For Yb3+, Tm3+, and Eu3+- codoped phosphors we observed bands related to the 1G4 → 3H6 and 1G4 → 3F4 transitions of Tm3+ ions, occurred through the cooperative up-conversion mechanism, where two nearby Yb3+ ions were involved in near-infrared absorption. Moreover, the GdVO4: 20% Yb3+, 0.5% Tm3+, 5% Eu3+ showed the most outstanding color tunability from red color (x = 0.6338, y = 0.3172) under UV to blue color (x = 0.2640, y = 0.1988) under NIR excitation, which can be applied in anti-counterfeiting activity.

Arene-Perfluoroarene Force Driven Sublimation-Removable Chiral Coassemblies.

Multiple constituent coassembly is an emerging strategy to manipulate supramolecular chirality and chiroptical properties such as circularly polarized luminescence (CPL). However, the second or third constituent could not be removed from pristine self-assembly. Here we developed a constitute-removable chiral coassembly using sublimation that could realize coassembly with tunable supramolecular chirality, luminescence and CPL properties. Octafluoronapthalene (OFN) with small sublimation enthalpy formed coassemblies with perylene-conjugated peptoids via arene-perfluoroarene (AP) interaction that induced the emergence of macroscopic chirality and hypochromic luminescence from yellow to green. Coassembly with OFN accelerated one-dimensional growth and induced the emergence of macroscopic chirality and CPL. Despite the stability at ambient conditions, vacuum-treatment triggered fast sublimation of OFN, which behaved as a sacrificial template. Physical removal of OFN retained the helical nanoarchitectures as well as the basic features of Cotton effects and CPL activities. X-ray diffraction suggested the back-fill consolidation occurred on the molecular voids by OFN removal that slightly varied the templated molecular arrangements. Sublimation of perfluorinated building units is green and efficient and non-destructive, which is potentially applicable in constructing template-directed chiroptical materials and devices.

Arene‐Perfluoroarene Force Driven Sublimation‐Removable Chiral Coassemblies

AbstractMultiple constituent coassembly is an emerging strategy to manipulate supramolecular chirality and chiroptical properties such as circularly polarized luminescence (CPL). However, the second or third constituent could not be removed from pristine self‐assembly. Here we developed a constitute‐removable chiral coassembly using sublimation that could realize coassembly with tunable supramolecular chirality, luminescence and CPL properties. Octafluoronapthalene (OFN) with small sublimation enthalpy formed coassemblies with perylene‐conjugated peptoids via arene‐perfluoroarene (AP) interaction that induced the emergence of macroscopic chirality and hypsochromic luminescence from yellow to green. Coassembly with OFN accelerated one‐dimensional growth and induced the emergence of macroscopic chirality and CPL. Despite the stability at ambient conditions, vacuum‐treatment triggered fast sublimation of OFN, which behaved as a sacrificial template. Physical removal of OFN retained the helical nanoarchitectures as well as the basic features of Cotton effects and CPL activities. X‐ray diffraction suggested the back‐fill consolidation occurred on the molecular voids by OFN removal that slightly varied the templated molecular arrangements. Sublimation of perfluorinated building units is green and efficient and non‐destructive, which is potentially applicable in constructing template‐directed chiroptical materials and devices.