Localized Surface Plasmon Resonance Research Articles

Tuneability and optimum functionality of plasmonic transparent conducting oxide-Ag core-shell nanostructures

Tunning localized surface plasmon resonance (LSPR) in transparent conducting oxides (TCO) has a great impact on various LSPR-based technologies. In addition to the commonly reported mechanisms used for tunning LSPR in TCOs (e.g., size, shape, carrier density modifications via intrinsic and extrinsic doping), integrating them in core-shell structures provides an additional degree of freedom to expand its tunability, enhance its functionality, and widen its versatility through application-oriented core-shell geometrical optimization. In this work, we explore the tuneability and functionality of two TCO nanostructures; indium doped tin oxide (ITO) and gallium doped zinc oxide (GZO) encapsulated with silver shell within the extended theoretical Mie theory formalism. The effect of core and shell sizes on LSPR peak position and line width as well as absorption and scattering coefficients is numerically investigated. Simulations showed that LSPRs of ITO-Ag and GZO-Ag core-shell nanostructures have great tunning capabilities, spanning from VIS to IR spectral range including therapeutic window of human tissue and essential solar energy spectrum. Potential functionality as refractive index sensor (RIS) and solar energy absorber (SEA) are examined using appropriate figure of merits (FoM). Simulations indicate that a geometrically optimized core-shell architecture with exceptional FoMs for RIS and SEA can be realized. Contrary to carrier density manipulation, integrating TCO cores to metallic shells proves to be an effective approach to enhance tunability and optimize functionality for high performance TCO-based plasmonic devices, with minimum impact on the inherited physical and chemical properties of the used TCO-core materials.

Plasmon and N-vacancy synergistically enhanced tubular carbon nitride-based S-scheme heterojunction photocatalyst with one stone five birds function: Pathways, DFT calculation and mechanism insight

From the perspectives of innovation and broad-spectrum, tubular carbon nitride-based photocatalyst, viz., Ag/AgI/g-C3N4 S-scheme heterojunction photocatalyst, with enhancement of nitrogen vacancy and localized surface plasmon resonance (LSPR) effect is reasonably devised and manufactured via combining hydrothermal, calcination and photo-reduction techniques. The optimal specimen displays high photocatalytic activity in removal of dyes (such as crystalline violet, 100.00 %/60 min), antibiotics (such as levofloxacin, 88.72 %/50 min) and Cr6+ (100.00 %, 30 min), photocatalytic hydrogen evolution (1023.3 μmol h−1 g−1) and H2O2 generation (866.2 μmol h−1 g−1), achieving broad-spectrum natures, viz., realizing the function of “one stone five birds”. The broad-spectrum natures are attributed to the synergisms of nitrogen vacancy, LSPR effect of Ag, hollow tube structure and S-scheme heterojunction, which facilitate the separation and migration of photo-generated carriers and inject “hot electrons” generated by Ag into the conduction band of Ag/AgI/g-C3N4, increase the specific surface area and broaden the spectral response range. Further, the degraded intermediates of crystalline violet and levofloxacin and possible degradation pathways are rationally advanced by the aid of LCMS spectra, and synergistically enhanced photocatalytic mechanism of Ag/AgI/g-C3N4 hollow tube S-scheme heterojunction is confirmed based upon a series of sound experiments, fs-TA spectra, in-situ XPS and DFT calculation, etc.

Zr-MOF/MXene composite for enhanced photothermal catalytic CO2 reduction in atmospheric and industrial flue gas streams

In this study, a novel composite was engineered by integrating Zr-MOF (NH2-UIO-66) with MXene layers through electrostatic self-assembly. Under simulated sunlight and at 80 °C, this composite material achieved nearly complete conversion of low-concentration atmospheric CO2 to CO and CH4 without additional sacrificial agents or alkaline absorption liquids, marking one of the few reports demonstrating near-complete reduction of low-concentration CO2 directly from the air. For high-concentration CO2 in industrial flue gas, the composite utilized residual heat at 80 °C without additional energy input, exhibiting excellent CO2 reduction efficiency with CO and CH4 production rates of 127 μmol·g-1·h-1 and 330 μmol·g-1·h-1, respectively, resulting in a total production rate 4.76 times higher than that in the air. Compared to most reports on thermocatalytic CO2 reduction (>300 °C), this material shows significant advantages below 100 °C. The performance improvement is attributed to the introduction of Zr-MOF, which provides additional active sites and reduces activation energy. Additionally, the localized surface plasmon resonance (LSPR) effect of MXene facilitates the migration of thermal charge carriers to Zr4+ sites within the MOF. Density Functional Theory (DFT) calculations validate these findings. Overall, Zr-MOF/MXene composite holds potential for reducing CO2 in air and industrial settings, advancing energy conversion and environmental management.

Anisotropic Fluorescence Surface Quenching of Quantum Dot-in-Rods on Silver Nanopatterned Film

Semiconductor quantum dot-in-rods (QDIRs) have served in the broad applications such as luminescent applications, sensor technology, quantum information processing, due to their polarized emission and polarized absorption characteristics. The localized surface plasmon resonance (LSPR) characteristics of the noble metal nanostructures can regulate the fluorescence intensity by controlling the radiation and non-radiation channels of fluorescent substances. However, the reports on the fluorescence surface quenching of QDIRs by plasmonic nanoparticles (NPs) are very rare. Herein, we propose a new method to realize QDIRs orientation, as well as the fluorescence intensity can be regulated. The effect of Ag nanopatterned film on the fluorescence surface quenching of QDIRs is discussed from both theoretical and experimental perspectives. Generally, the direct combination of Ag nanopatterned film and QDIRs results in 75% fluorescence surface quenching. Through FDTD simulation, we further analyzed the modulation of fluorescence intensity of the dipole source by the Ag nanopatterned film. This work will be useful for the development of QDIRs in the future.

Localized surface plasmon resonance effect-mediated in-situ photochemical–formation of H2O2 for high epoxidation performance over LaSrCoNiO6 nanoparticles

Selective aerobic epoxidation of allylic alcohols and olefins presents a promising solution to the modern chemical industry. However, the development of non-noble metal catalysts with superior catalytic performance for this reaction remains a significant challenge. This study introduces a plasmonic photothermal-catalytic system centered around nano LaSrCoNiO6 (LSCNi-N) catalyst, enabling the epoxidation of cinnamyl alcohol and styrene mediated by LSPR effect under visible light illumination (>420 nm). This catalyst exhibits superior epoxidation catalytic performance, with selectivities of up to 72.3 % in a 93.4 % conversion of cinnamyl alcohol and 91.8 % selectivity of styrene oxide at almost 100 % conversion of styrene. Mechanistic studies reveal that the high selectivity derives from the in-situ photochemical formation of H2O2 mediated by the localized surface plasmon resonance effect of LSCNi-N and hole scavenger effect of cinnamyl alcohol. These findings highlight the potential of designing plasmonic transition-metal oxidic catalysts to overcome challenges in selectively synthesizing fine chemicals through visible light catalysis.

Titanium Nitride-Gold Nanoislands: Harnessing Electrical and Optical Properties for Enhanced Localized Surface Plasmon Resonance Sensing

Titanium nitride-gold nanoislands (TANIs) are experimentally investigated to explore their electrical and optical properties induced by the incorporation of Au into TiN. A film is first fabricated on a glass substrate using the radio frequency (RF) magnetron sputtering technique at 300 K, with a thickness of approximately 20 nm (± 2.5 nm) and an Au:TiN ratio of 0 to 0.47. Subsequent thermal annealing provides a nanoisland structure of TiN-Au. Characterization techniques such as X-ray diffraction and X-ray photoelectron spectroscopy confirmed the presence of TiN and Au in the fabricated TiN-Au nanoislands. Spectroscopic ellipsometry measurements show that the TANIs posses excellent optical properties. Furthermore, numerical evaluations of energy dissipation are conducted to assess carrier transport deterioration due to the inelastic scattering effects in the TANIs and the inclusion of Au in the nanostructure significantly have reduced the dielectric loss tangent at energies greater than 4.5 eV, compensating for high losses and enhancing optical performance. The biosensing capability of TANIs is also demonstrated with the sensing of biotin, such that a strong biotin-phase response relationship is formed with a limit of detection of 0.842 ng/ml. This study contributes valuable insights into the electrical, optical and biosensing properties of TANIs, providing direction for sensing applications, where the optimization of the TANIs structure could bring about advancements in optical performance and pave the way for the potential design of novel plasmonic sensors.

Investigating SERS performance of controllable fabricated Ag periodic nanostructures with morphologies of nanoclaws and nanocones in detecting SARS-CoV-2 S protein

Surface-enhanced Raman scattering (SERS) spectroscopy plays an important role in enabling high-precision detection and non-invasive diagnostics. Periodic metallic nanostructures with strong electromagnetic fields and tunable localized surface plasmon resonance can achieve high SERS sensitivity, but fabricating such nanostructures remains a challenge. In this work, the anodic aluminum oxide (AAO) nanocavity template-assisted process of fabricating periodic nanostructures with modulating morphologies from Ag nanoclaws (AgNCWs) to Ag nanocones (AgNCEs) is proposed. The morphologies-related SERS performances of nanostructures are analyzed by using rhodamine 6 g (R6G) as a probe molecule and the optimized AgNCEs possess a limit of detection (LOD) of 1 × 10−9 M. A sandwich strategy is applied to detect SARS-CoV-2 S protein in phosphate-buffered saline (PBS) and pharyngeal swab solution (PSS). The ACE2-modified AgNCEs (ACE2/AgNCEs) structure is applied to bind to the SARS-CoV-2 S protein. The 4-MBA and SARS-CoV-2 S antibody functionalized Au nanoparticles (AuNPs) are used as nanotags. By forming the ACE2/AgNCEs-SARS-CoV-2 S protein-nanotags sandwich structure, characteristic peak intensities of 1580 cm−1 are used as the report signal, and the LOD for SARS-CoV-2 S protein in PBS and PSS solution are 10 fg/mL.

Graphene/black phosphorus-based infrared metasurface absorbers with van der Waals Schottky junctions

Black phosphorus (BP) is a promising candidate for fabricating infrared (IR) photodetectors because its bandgap in the IR region can be controlled by varying the number of layers. BP-based metasurfaces have attracted considerable attention for applications in wavelength-selective and/or polarization-selective IR absorbers. Graphene and BP (Gr/BP) van der Waals (vdW) heterostructures are expected to enhance the performance of BP-based IR photodetectors. However, the Gr/BP vdW heterostructure forms a Schottky junction; thus, the electron transfer between Gr and BP should be investigated to determine the precise optical properties of Gr/BP vdW heterostructure-based metasurfaces. In this study, the electron transfer in the Gr/BP vdW heterostructure is investigated theoretically. The metasurface absorber structure proposed based on the results comprises periodic Gr/BP vdW heterostructure strips on top, a middle dielectric layer, and a bottom reflector. Numerical calculations indicated that the Gr/BP vdW heterostructure has strong wavelength- and polarization-selective near-unity IR absorption. The absorbance is increased and absorption wavelength is shortened compared with those of the monolayer-BP-based metasurface. The absorption wavelength can be controlled by changing the width of the Gr/BP strips owing to the hybrid localized surface plasmons of Gr/BP. This is attributed to the electron transfer through the Schottky junction between Gr and BP with enhanced localized surface plasmon resonance. The results suggest that the Gr/BP vdW heterostructure is a promising platform for realizing wavelength-selective and/or polarization-selective IR photodetectors and IR absorbers/emitters. The resulting photodetectors exhibit high responsivity and low noise because the BP bandgap corresponds to the IR wavelength region.

Perspectives of Fluctuation-Enhanced Gas Sensing by Two-Dimensional Materials

We present the results of gas sensing using the fluctuation-enhanced sensing method in selected two-dimensional materials (2DMs). We claim that gas sensing selectivity can be improved further by considering semiconducting two-dimensional materials doped by noble metal nanoparticles. The 2DMs’ structures exhibit some imperfections defined by their structure, occurring repeatedly there. These imperfections are adsorption–desorption centers responsible for gas-sensing properties and generating flicker noise of various intensities. We consider how these imperfections can be modulated and utilized for fluctuations-enhanced gas sensing. We propose the decoration of 2DMs by noble metal nanoparticles that impact flicker noise. Additionally, we consider utilizing localized surface plasmonic resonance induced by irradiation at selected wavelengths.

Highly Active MXene Quantum Dots/CuSe n-p Plasmonic Heterostructures for Ultrafast Photocatalytic Removal of Cr(VI) under Full Solar Spectrum.

Identifying effective plasmonic photocatalysts exhibiting robust activities across the entire solar spectrum poses a significant challenge. CuSe, with its local surface plasmon resonance (LSPR) effect, has garnered attention as a prospective plasmonic photocatalyst. However, severe charge recombination and insufficient light absorption limit its photocatalytic performance. To enhance the performance, constructing CuSe-based n-p plasmonic semiconductor heterostructures is a potential strategy. MXene quantum dots (MQDs), a kind of n-type plasmonic semiconductor with metallic conductivity and a high LSPR effect, are a promising candidate to couple with p-type CuSe. According to the complementary principle, we designed a 0D/2D MQDs/CuSe n-p plasmonic semiconductor, achieved by wrapping CuSe nanosheets with MQDs. This n-p plasmonic heterostructure exhibits a synergistic effect on an enhanced electronic field, facilitating charge transfer and separation, thereby enhancing charge excitation, carrier migration, and photothermal effect. Furthermore, optimizing the MQD loading content leads to an ultrafast photocatalytic reaction rate, achieving 100% Cr(VI) reduction efficiency within just 60 min with a reaction kinetics of 0.069 min-1, surpassing the performance of bare CuSe. Our work presents a promising approach for developing advanced n-p plasmonic heterostructures based on MQDs for wastewater treatment and other photocatalytic applications.

Gold Nanoparticles: Multifunctional Properties, Synthesis, and Future Prospects

Gold nanoparticles (NPs) are among the most commonly employed metal NPs in biological applications, with distinctive physicochemical features. Their extraordinary optical properties, stemming from strong localized surface plasmon resonance (LSPR), contribute to the development of novel approaches in the areas of bioimaging, biosensing, and cancer research, especially for photothermal and photodynamic therapy. The ease of functionalization with various ligands provides a novel approach to the precise delivery of these molecules to targeted areas. Gold NPs’ ability to transfer heat and electricity positions them as valuable materials for advancing thermal management and electronic systems. Moreover, their inherent characteristics, such as inertness, give rise to the synthesis of novel antibacterial and antioxidant agents as they provide a biocompatible and low-toxicity approach. Chemical and physical synthesis methods are utilized to produce gold NPs. The pursuit of more ecologically sustainable and economically viable large-scale technologies, such as environmentally benign biological processes referred to as green/biological synthesis, has garnered increasing interest among global researchers. Green synthesis methods are more favorable than other synthesis techniques as they minimize the necessity for hazardous chemicals in the reduction process due to their simplicity, cost-effectiveness, energy efficiency, and biocompatibility. This article discusses the importance of gold NPs, their optical, conductivity, antibacterial, antioxidant, and anticancer properties, synthesis methods, contemporary uses, and biosafety, emphasizing the need to understand toxicology principles and green commercialization strategies.

A high-performance ultra-compact plasmonic metamaterial structure for optical THz absorption

This study presents the design and analysis of a high-performance metamaterial absorber for the optical terahertz (THz) regime. The proposed absorber utilizes a unique nested flower-shaped structure composed of nickel (Ni) and silicon dioxide (SiO2), achieving an average absorption exceeding 97.91% with a broad bandwidth of 1320 THz (180 THz − 1500 THz). A unit cell size of 66 nm × 66 nm × 24 nm makes this design highly attractive for miniaturized devices. Strong absorption originates from localized surface plasmon resonance (LSPR), where light interacts with the electrons on the Ni surface. Notably, the design maintains excellent absorption performance even at oblique incident angles up to 60° with polarization insensitivity. These results highlight the Ultra-Compact Plasmonic Metamaterial (UCPM) absorber’s potential for diverse applications due to its broad spectral response, high absorption efficiency, and minimal footprint, making it valuable for energy harvesting, infrared imaging, and electromagnetic stealth technologies.

Solid phase extraction-surface enhanced Raman spectroscopy (SPE-SERS) test of antibiotic residues in Milk based on au@ MIL-101 NPs

A SPE-SERS method was developed for the detection of several antibiotic residues in dairy products. Gold nanoparticles (Au NPs) encapsulated with an ultrathin Cr-MIL-101 shell (Au@Cr-MIL-101 NPs) have been synthesized, and the thickness of Cr-MIL-101 shell can be precisely controlled to 3 nm. As a superior solid phase extraction (SPE) adsorbent, Cr-MIL-101 acts as a shell layer to effectively enrich antibiotics within the localized surface plasmon resonance (LSPR) field of Au NPs, which enhances the SERS signal and eliminates background interference. The method can achieve highly sensitive and high-throughput detection for tetracycline hydrochloride, sulfapyridine and benzylpenicillin sodium in dairy products, and the detection limits (LOD) are as low as 2.237, 2.644 and 4.662 ppb respectively. The recoveries of antibiotic residues in spiked dairy products ranged from 72.31 % to 146.7 % with matrix effects (ME) of −15.13 % to 28.68 %. Thus, this method holds significant promise for rapid detection of antibiotics in milk.

Core–Shell–Satellite Au@CeO2–Pd Plasmonical Photocatalysts for Suzuki–Miyaura Coupling Reaction

ABSTRACTIntegration of localized surface plasmon resonance (LSPR) metallic nanocrystals into photocatalysis is an intriguing approach for light‐driven organic transformations. However, uncertain direction of hot carriers is a grand challenge, which fails to take full advantage of the LSPR excitation. In this work, core–shell gold@ceria nanosphere–supported segregated palladium species (Au@CeO2–Pd) have developed to steer the light absorption capability and charge carrier migration. Under simulated solar light irradiation, the core–shell–satellite Au@CeO2–Pd exhibited efficient light harvesting and colossal activity in the Suzuki coupling reaction. The plasmon‐induced hot electrons overpassed the Schottky barrier at the Au@CeO2 interfaces and migrated from Au core to CeO2 shell accordingly. Subsequently, the photogenerated electrons and hot electrons migrated from Au@CeO2 core–shells to Pd, which acted as an electron acceptor. Detailed photocatalytic mechanism studies revealed that both photoexcited electrons and holes were the main active species involved in the photocatalytic Suzuki coupling reaction process. In particular, the diphenyl yield over Au@CeO2–Pd catalyst was ~1.7 times higher than that of core–shell–satellite Au@SiO2–Pd, where a 19‐nm‐thick SiO2 shell was introduced to prevent the migration of hot electrons. This distinctly certified that the hot electrons transfer in the core–shell–satellite Au@CeO2–Pd under illumination played an important role to drive Suzuki reaction. Overall, this design of core–shell–satellite Au@CeO2–Pd plasmonic photocatalyst has the potential in the field of photo‐driven organic transformations.

AuNPs enhanced electrochemical and optical dual-mode fiber optic sensor for trace Hg2+ detection

Efficient and low-concentration detection of heavy metal ions is crucial for healthcare and environmental monitoring. Traditional fiber optic surface plasmon resonance (SPR) sensors face challenges in detecting trace heavy metal ions due to limited sensitivity and the need for complex specific modifications. To overcome these challenges, an innovative electrochemical and optical dual-mode fiber optic sensor for in situ, real-time detection of trace mercury ions is proposed in this paper. The sensor utilizes a reflection-type fiber optic probe coated with thin gold (Au)/indium tin oxide (ITO) film and gold nanoparticles (AuNPs), enabling simultaneous electrochemical and optical interrogation. The coupling effect between the SPR of thin film and the localized surface plasmon resonance (LSPR) of AuNPs significantly improves optical sensitivity, with AuNPs also offering additional active sites for the redox reaction of Hg2+. The ITO film not only facilitates the stripping of Hg2+, leading to sharper stripping peaks but also enhances the ability of the sensor to rapidly respond to anomalous potential changes. Experimental results show that the sensor has a wide dynamic detection range from 10−10 M to 10−5 M, with a limit of detection reaching the pM level. The dual-mode functionality allows the simultaneous collection of voltage, current, and optical information, enabling cross-validation of the detection results and improving the accuracy and reliability of detection.

Helicoid Grating-Coupled Surface Plasmon Resonance Sensor.

Ultrasensitive, rapid, and reliable biomolecular sensing is essential for biomedical diagnostics, requiring real-time monitoring and detection of trace samples. Optical sensing, particularly plasmonic biosensing, meets these demands through noninvasive, high-sensitivity detection based on the interaction between light and molecules. Here, we present novel plasmonic metamaterial-based sensing strategy, utilizing the circular dichroism (CD) response of grating-coupled surface plasmon resonance (SPR) from chiral nanoparticle grating structure (i.e., 2D helicoid crystal) on gold substrate. Strong chiroptic response of helicoids has been effectively expanded to produce a remarkable CD/greflection response in the SPR mode, achieved by spectral coupling of SPR with localized surface plasmon resonance (LSPR) in helicoids. This CD response, derived from the differential of left and right circularly polarized light, corrects optical fluctuations, enhancing sensitivity and reliability. Our SPR-CD-based approach achieves a sensitivity of 379.2 nm/RIU and detection limit of a few mM for d-glucose, offering a new paradigm for high-performance optical biosensors.

In situ formation of oxygen-deficient WO3-x nanosheets for enhanced photocatalytic activity in water splitting and plastic reforming

Photocatalytic pathways are essential for the sustainable production of chemicals and fuels, pivotal for achieving a pollution-free planet. Electron-hole recombination is a critical problem that has, so far, limited the efficiency of the photocatalytic materials. Here, oxygen-deficient WO3-x nanosheets were in situ grown in a polymeric carbon nitride (PCN) support during the thermal polycondensation of melamine. The introduction of defect in WO3-x, accompanied by spin polarization and the formed WO3-x/PCN heterostructure, greatly accelerated the charge separation and transfer. The synthesized WO3-x/PCN composite exhibited a tenfold increase in hydrogen generation activity than pure PCN under visible-light (420 ≤ λ ≤ 780 nm). The WO3-x/PCN also demonstrated consecutive 24 h and stable photocatalytic H2 production in the aqueous plastic-containing [poly(vinyl alcohol) (PVA), poly(ethylene terephthalate) (PET) and the PET bottle] solutions under visible light. The hydrogen production rates were determined to be 111.2, 50.5, and 7.8 μmol·h−1·g−1 in PVA, PET and PET bottle, respectively. In addition, the oxygen vacancies WO3 with their localized surface plasmon resonance effect, facilitated efficient utilization of NIR photon and the hydrogen evolution rate over WO3-x/PCN reached to 120 μmol h−1·g−1 under NIR light (700 ≤ λ ≤ 780 nm). This research not only advances the potential applications of WO3-x/PCN in sustainable energy production but also provides insights into environmental remediation through the conversion of plastic wastes.

Developments in Localized Surface Plasmon Resonance

AbstractLocalized surface plasmon resonance (LSPR) is a nanoscale phenomenon associated with noble metal nanostructures that has long been studied and has gained considerable interest in recent years. These resonances produce sharp spectral absorption and scattering peaks, along with strong electromagnetic near-field enhancements. Over the past decade, advancements in the fabrication of noble metal nanostructures have propelled significant developments in various scientific and technological aspects of LSPR. One notable application is the detection of molecular interactions near the nanoparticle surface, observable through shifts in the LSPR spectral peak. This document provides an overview of this sensing strategy. Given the broad and expanding scope of this topic, it is impossible to cover every aspect comprehensively in this review. However, we aim to outline major research efforts within the field and review a diverse array of relevant literature. We will provide a detailed summary of the physical principles underlying LSPR sensing and address some existing inconsistencies in the nomenclature used. Our discussion will primarily focus on LSPR sensors that employ metal nanoparticles, rather than on those utilizing extended, fabricated structures. We will concentrate on sensors where LSPR acts as the primary mode of signal transduction, excluding hybrid strategies like those combining LSPR with fluorescence. Additionally, our examination of biological LSPR sensors will largely pertain to label-free detection methods, rather than those that use metal nanoparticles as labels or as means to enhance the efficacy of a label. In the subsequent section of this review, we delve into the analytical theory underpinning LSPR, exploring its physical origins and its dependency on the material properties of noble metals and the surrounding refractive index. We will discuss the behavior of both spherical and spheroidal particles and elaborate on how the LSPR response varies with particle aspect ratio. Further, we detail the fundamentals of nanoparticle-based LSPR sensing. This includes an exploration of single-particle and ensemble measurements and a comparative analysis of scattering, absorption, and extinction phenomena. The discussion will extend to how these principles are applied in practical sensing scenarios, highlighting the key experimental approaches and measurement techniques.

Active Photonic Glass for Hydrogen Generation.

Chirality is vital in many living species since it is responsible for structural iridescent coloration and plays a key role in light harvesting during natural photosynthesis. Developing photoactive materials with such chiral structures is a challenging but promising strategy for energy applications. Here, we describe a straightforward method to establish an active photonic glass obtained through the co-condensation oftetramethyl orthosilicate (TMOS) and titanium diisopropoxide bis(acetylacetonate) (TAA) dissolved in a liquid crystal formed from cellulose nanocrystalline (CNC). The inorganic glass maintains a long range of chiral nematic ordering, displaying iridescent colors characterized by a Bragg peak reflection. The reflected wavelengths are tuned all over the UV-visible range, demonstrating that the replica of the chiral nematic structure generates photonic properties. Incorporation of gold nanoparticles (Au NPs) into the films is further performed by impregnation/chemical reduction. We show that the charge carrier density and photocatalytic H2 generation were amplified when the photonic band gap edges matched the absorbance of the TiO2 and localized surface plasmon resonance (LSPR) of AuNPs. This photocatalytic glass with chiral nematic ordering and a tunable photonic bandgap paves the way for the development of metamaterials with new applications, such as asymmetric photocatalysis.

Hybrid Functional ITO/Silver Nanowire Transparent Conductive Electrodes for Enhanced Output Efficiency of Ultraviolet GaN-Based Light-Emitting Diodes.

We investigated hybrid functional transparent conductive electrodes (HFTCEs) composed of indium-tin-oxide (ITO) and silver nanowires (AgNWs) for the enhancement of output efficiency in GaN-based ultraviolet light-emitting diodes (UVLEDs). The HFTCEs demonstrated an optical transmittance of 69.5% at a wavelength of 380 nm and a sheet resistance of 16.4 Ω/sq, while the reference ITO TCE exhibited a transmittance of 76.4% and a sheet resistance of 18.7 Ω/sq. Despite the 8.9% lower optical transmittance, the UVLEDs fabricated with HFTCEs achieved a 25% increase in output efficiency compared to reference UVLEDs. This improvement is attributed to the HFTCE's twofold longer current spreading length under operating forward voltages, and more significantly, the enhanced out-coupling of localized surface plasmon (LSP) resonance with the trapped wave-guided light modes.