Plasmon Resonance Effect Research Articles

Plasmonic S-type Bi/TiO2@C Heterojunction Composites for Efficient Visible-Light Photocatalytic Removal of Multi-Antibiotics and Dyes

In this work, two series of plasmonic S-type heterojunction photocatalysts containing Bi, TiO2, and biochar (Bi/TiO2@C) have been developed through a biomass-assisted hydrothermal-calcination strategy, utilizing grapefruit peel as a reducing agent and C resource. The calcination temperature and the mass ratio of biomass were optimized to obtain the optimal nanocomposite, which shows excellent adsorptive and visible-light photocatalytic performance in the removal of diverse antibiotic and dye pollutants, including tetracycline, oxytetracycline, ciprofloxacin, sulfamethoxazole, sulfisoxazole, malachite green, and rhodamine B. The remarkable performance can be attributed to the enhanced absorption of light absorption resulting from the localized surface plasmon resonance effect of the semimetal Bi, and the formation of heterogeneous interface between Bi and TiO2, which accelerates the transfer of photogenerated charge. Furthermore, trapping tests and electron spin resonance (ESR) analysis reveal that ∙O2- and h+ are the primary active species involved in the removal of tetracycline. A plausible charge transfer mechanism has been proposed.

Novel rod-like bifunctional nanocomposites: Enhanced NIR-IIb luminescence and microwave heat conversion property by local surface plasmon resonance effect and space-dielectric confinement effect

A novel halloysite nanotubes(HNT)@WO3-x@GdF3:Yb3+,Er3+ rod-like bi-functional nanocomposites with strong NIR-IIb (near-infrared second window 1500–1700 nm) luminescent and microwave heat conversion property was obtained by introducing the local surface plasmon resonance effects (LSPR) and the space-dielectric confinement effect. The novel nanocomposites were characterized in terms of the structure, morphology and property. The result of XRD, SEM and TEM analysis showed that WO3-x and GdF3:Yb3+,Er3+ nanocrystals were successfully deposited on the surface of HNT. In comparison to GdF3:Yb3+,Er3+, the NIR-IIb emission intensity of HNT@WO3-x@GdF3:Yb3+,Er3+ rod-like nanocomposites is significantly enhanced (8.4 times) and improved fluorescence lifetime (0.1591us to 0.1725 us) at 808 nm excitation. This results suggested that LSPR of WO3-x can regulate the NIR-IIb luminescent properties of HNT@WO3-x@GdF3:Yb3+,Er3+ nanocomposites. And HNT@WO3-x@GdF3:Yb3+,Er3+ rod-like nanocomposites had stronger microwave thermal conversion property based on space confinement effect and dielectric confinement effect. The HNT@WO3-x@GdF3:Yb3+,Er3+ rod-like nanocomposites successfully combined NIR-IIb luminescent and microwave heat conversion property to one, in addition, halloysite nanotubes be endowed to NIR-IIb luminescent properties and microwave heat conversion property. This study provides a new idea and method for the preparation of new bi-functional nanocomposites.

Shining light on broad-spectrum responded NaYF4:Yb,Er,Tm@Bi@BiOI: Understanding the enhanced photodegradation performance of bisphenol A and mechanisms

This work reported a novel ternary heterogeneous photocatalyst NaYF4:Yb,Er,Tm@Bi@BiOI (NBEG-6h). NBEG-6h exhibits broad-spectrum absorption from ultraviolet to near-infrared. The elimination efficiency of BPA by NBEG-6h under simulated sunlight and near-infrared light irradiation was 88% (24 min) and 93.9% (160 min), respectively. It also has the universality of degrading various pollutants, good reusability and stability. The exceptional photocatalytic activity can be attributed to the absorption of near-infrared light by NaYF4:Yb,Er,Tm, which improves the total efficiency of sunlight utilization. The localized surface plasmon resonance effect of Bi nanoparticles enhances the light absorption performance of the heterostructure. Furthermore, combining Bi and BiOI accelerates carrier migration and improves the separation efficiency of photogenerated electron-hole pairs. h+, ·O2− and 1O2 play the pivotal roles during the photocatalytic process. This research offers new insights into the design, development, and mechanism understanding of full-spectrum-driven heterostructure photocatalysts. It provides an environmentally sustainable approach to the treatment of harmful organic pollutants.

Plasmon-Enhanced Photoelectrochemistry of Photosystem II on a Hierarchical Tin Oxide Electrode for Ultrasensitive Detection of 17β-Estradiol.

Despite its excellent efficiency in natural photosynthesis, the utilization of photosystem II (PSII)-based artificial photoelectrochemical (PEC) systems for analytical purposes is hindered due to the low enzyme loading density and ineffective electron transfer (ET) processes. Here, we present a straightforward and effective approach to prepare a PSII-based biohybrid photoanode with remarkable photoresponse, enabled by the use of a hierarchically structured inverse-opal tin oxide (IO-SnO2) electrode combined with gold nanoparticles (Au NPs). The porous, carbon-containing IO-SnO2 structure allows for a high density and photoactivity loading of PSII complexes, while also providing strong electrical coupling between the protein film and the electrode. A new electron transfer pathway mediated by Au NPs was identified at the protein-electrode interface, which efficiently shuttles the photogenerated electrons from the enzyme to the IO-SnO2 electrode. Furthermore, the PEC response of the electrode was significantly enhanced by the surface plasmon resonance (SPR) effect of Au NPs. Upon light irradiation, this PSII-based photoanode exhibited an impressively high and stable photocurrent output, which was utilized to fabricate an aptasensor for 17β-Estradiol (E2) detection. Under optimal conditions, a detection limit of 0.33 pM was obtained, along with a broad detection range from 15 pM to 30 nM. The applicability of the aptasensor was assessed by measuring E2 in water and urine samples, demonstrating its feasibility in environmental monitoring and clinical tests.

Ag–Pt Alloy Nanoparticles Modified Zn‐Based Nanosheets for Highly Selective CO2 Photoreduction to CH4

AbstractMulti‐electron involved photoreduction of CO2 to hydrocarbon fuels is a long‐standing challenge, particularly in manipulating the selectivity of the target products. Here, a novel Ag–Pt bimetallic alloy on Zn‐based supports by photo‐deposition is designed for photocatalytic CO2 reduction to CH4 without any additives. This photocatalyst exhibits ≈ 98.9% selectivity for CH4. Experimental and theoretical calculations demonstrated that the excellent performance of the photocatalyst can be attributed to the localized surface plasmon resonance effect of metals, as well as the synergistic effects of the bimetallic sites. These factors are found to be beneficial not only for capturing solar radiation and facilitating electron migration but also for promoting the adsorption and activation of CO2 and the protonation of *CO. As a result, the photocatalyst achieved high selectivity and activity of photoreduction of CO2 to CH4. This work provides insights into the design of photocatalysts with highly selective target products for CO2 reduction.

Plasmon‐Promoted Interatomic Hot Carriers Regulation Enhanced Electrocatalytic Nitrogen Reduction Reaction

AbstractUtilizing hot carriers for efficient plasmon‐mediated chemical reactions (PMCRs) to convert solar energy into secondary energy is one of the most feasible solutions to the global environmental and energy crisis. Finding a plasmonic heterogeneous nanostructure with a more efficient and reasonable hot carrier transport path without affecting the intrinsic plasmonic properties is still a major challenge that urgently needs to be solved in this field. Herein, the mechanism by which plasmon‐promoted interatomic hot electron redistribution on the surface of Au3Cu alloy nanoparticles promotes the electrocatalytic nitrogen reduction reaction (ENRR) is successfully clarified. The localized surface plasmon resonance (LSPR) effect can boost the transfer of plasmon hot electrons from Au atoms to Cu atoms, trigger the interatomic electron regulation of Au3Cu alloy nanoparticles, enhance the desorption of ammonia molecules, and increase the ammonia yield by approximately 93.9 %. This work provides an important reference for rationally designing and utilizing the LSPR effect to efficiently regulate the distribution and mechanism of plasmon hot carriers on the surface of heterogeneous alloy nanostructures.

Metal-Based Oxygen Reduction Electrocatalysts for Efficient Hydrogen Peroxide Production.

Hydrogen peroxide (H2O2) is a high-value chemical widely used in electronics, textiles, paper bleaching, medical disinfection, and wastewater treatment. Traditional production methods, such as the anthraquinone oxidation process and direct synthesis, require high energy consumption, and involve risks from toxic substances and explosions. Researchers are now exploring photochemical, electrochemical, and photoelectrochemical synthesis methods to reduce energy use and pollution. This review focuses on the 2-electron oxygen reduction reaction (2e- ORR) for the electrochemical synthesis of H2O2, and discusses how catalyst active sites influence O2 adsorption. Strategies to enhance H2O2 selectivity by regulating these sites are presented. Catalysts require strong O2 adsorption to initiate reactions and weak *OOH adsorption to promote H2O2 formation. The review also covers advances in single-atom catalysts (SACs), multi-metal-based catalysts, and highlights non-noble metal oxides, especially perovskite oxides, for their versatile structures and potential in 2e- ORR. The potential of localized surface plasmon resonance (LSPR) effects to enhance catalyst performance is also discussed. In conclusion, emphasis is placed on optimizing catalyst structures through theoretical and experimental methods to achieve efficient and selective H2O2 production, aiming for sustainable and commercial applications.

Highly sensitive multiplexed colorimetric lateral flow immunoassay by plasmon-controlled metal-silica isoform nanocomposites: PINs.

Lateral flow assay (LFA) systems use metal nanoparticles for rapid and convenient target detection and are extensively studied for the diagnostics of various diseases. Gold nanoparticles (AuNPs) are often used as probes in LFAs, displaying a single red color. However, there is a high demand for colorimetric LFAs to detect multiple biomarkers, requiring the use of multicolored NPs. Here, we present a highly sensitive multiplexed colorimetric lateral flow immunoassay by multicolored Plasmon-controlled metal-silica Isoform Nanocomposites (PINs). We utilized the localized surface plasmon resonance effect to create multi-colored PINs by precisely adjusting the distance between the NPs on the surface of PINs through the controlled addition of reduced gold and silver precursors. Through simulations, we also confirmed that the distance between nanoparticles on the surface of PINs significantly affects the color and colorimetric signal intensity of the PINs. We achieved multicolored PINs that exhibit stronger colorimetric signals, offering a new solution for LFA detection with high sensitivity and a 33 times reduced limit of detection (LOD) while maintaining consistent size deviations within 5%. We expect that our PINs-based colorimetric LFA will facilitate the sensitive and simultaneous detection of multiple biomarkers in point-of-care testing.

Free Electron Density Gradients Enhanced Biosensor for Ultrasensitive and Accurate Affinity Assessment of the Immunotherapy Drugs.

Accurate affinity assessments play an important role in drug discovery, screening, and efficacy evaluation. Label-free affinity biosensors are recognized as a dependable and standard technology for addressing this challenge. This study constructs a free electron density gradient-enhanced meta-surface plasmon resonance (FED-MSPR) biosensor through a finite-difference time-domain simulation model, the biosensor demonstrates superior detection performance in accurately determining affinity and kinetic rate constants. By controlling the dielectric properties of the metal on the surface of the nanocup arrays, the plasmon resonance effects are easily tuned without changing the nanostructure design. Compared with the single-layer gold chip, the triple-layer FED-MSPR chip demonstrated a four-fold improvement in resolution at the optimal resonance peak. Additionally, the sensitivity and figure of merit (FOM) of the multi-layer chip increased by 3.5 and 7.99 times, respectively. Following modification with high- and low-staggered carboxylation, the noise-signal ratio and baseline stability of the real-time kinetic curves based on these chips are significantly enhanced. The developed carboxylation FED-MSPR platform is successfully used to perform affinity assays for Adalimumab and TNF-α protein, resulting in favorable dynamic curves. These findings validate the proposed FED-MSPR biosensor platform as cost-effective, rapid, sensitive, and label-free, facilitating real-time quality control in drug development.

Construction of Ag-modified ZnO/g-C3N4 heterostructure for enhanced photocatalysis performance.

ZnO/g-C3N4 heterojunction modified with Ag nanoparticles (ZnO/CN/Ag) was synthesized by depositing ZnO nanorods/Ag nanoparticles onto g-C3N4 nanosheets. Under xenon lamp irradiation, 99% of Rhodamine B (RhB) was degraded by ZnO/CN/Ag-5% composite within 30min, which was much higher than the degradation efficiency of ZnO and ZnO/CN. The synergistic effect of g-C3N4 and ZnO, along with the localized surface plasmon resonance effect of Ag NPs, contributes to the improvement of photocatalytic performance. Ag nanoparticle provides another charge transfer path from g-C3N4 to ZnO, which speeds up the separation of electron-hole pairs. Meanwhile, the catalyst had good stability and recyclability. Finite-difference time-domain method and the density functional theory were used to obtain the charge transfer process. The photodegradation process has been studied in depth.

Localized surface plasmon resonance induced nonlinear absorption and optical limiting activity of gold decorated graphene/MoS2 hybrid

The synergistic supremacy of a hybrid nanocomposite made of reduced graphene oxide (rGO), molybdenum disulfide (MoS2) and gold nanoparticles (Au) for Q-switching and optical limiting applications is investigated. Hydrothermally synthesized Au-rGO-MoS2 hybrid with varying concentrations of Au (2.5, 5, 7.5 and 10 wt%) was subjected to interact with Q-switched Nd:YAG nanosecond green laser pulses. The intensity dependent nonlinear absorption studies revealed a switch over in the nonlinear behaviour from saturable absorption (SA) to reverse saturable absorption (RSA) behaviour. SA occurs due to ground state bleaching at comparatively lower laser irradiances serving the need for Q-switching and optical communications. The RSA trait at higher laser irradiance is attributed to sequential two-photon absorption which serves as the platform for optical limiting behaviour prompting laser safety and effective photothermal therapy applications. The strong mid-visible and UV absorption promotes the availability of multiple energy bands for energy transitions of excited state absorption (ESA). Enhanced local fields due to localized surface plasmon resonance effect, structural defects, hierarchical morphology, increased absorption cross-section and plasmon induced energy transfer promotes robust ESA process. These tunable nonlinear optical properties make Au-rGO-MoS2 hybrid promising futuristic candidates for applications in nonlinear photonic devices, ultrafast optical switches and all-optical signal processing systems.

Functional design of PGMA-co-PDFHM/Ti3C2Tx MXene composite materials for anti-icing in simulated outdoor environment

To improve anti-icing traits of outdoor coatings, a synergy between photothermal and hydrophobic anti-icings was utilized to fabricate copolymer/Ti3C2Tx MXene composite coatings with good transparency and adhesion. MXene contributes to photothermal trait from local surface plasmon resonance effect. Copolymer enables hydrophobicity from perfluoroalkyls-induced low surface energy and high surface roughness. An increase in MXene dose results in an increased surface roughness. With 140.0 ± 2.2° of water contact angle and 70% of light transmittance, the optimal film bears 2 wt% of MXene. High MXene dose results in large temperature-increase of film under sunlight. After 15 min of sunlight exposure, the temperature of optimal film surface in icing simulation increases from − 18 ℃ to 7.2 ℃. After 48 h of acid immersion, the temperature-increase of optimal film surface based on 300 s of sunlight irradiation reaches 28.7 ± 1.2 ℃. After 48 h of ultraviolet irradiation, the temperature-increase of optimal film surface is 30.7 ± 0.8 ℃. This surface has a water contact angle of 132.7 ± 1.1° after 48 h of acid immersion. This study gives impetus to a preparation of various composite coatings for outdoor anti-icing/deicing.

Cu surface plasmon resonance promoted charge transfer in S-scheme system enhanced visible light photocatalytic hydrogen evolution

Reasonably constructing nanocomposite photocatalysts with fast charge transfer and broad solar response capabilities is significant for efficiently converting solar energy into chemical energy. Cu modifies P25/CeO2 heterojunctions prepared by photodeposition (P25 is commercial TiO2). The local surface plasmon resonance (LSPR) effect caused by Cu nanoparticles broadens the spectral response range and generates significant photothermal effects. After 90 s of irradiation, the temperature of 9.5 %Cu-P25/CeO2 increases to 148.1 °C. The photocatalytic hydrogen evolution rate (HER) of 9.5 %Cu-P25/CeO2 under visible light (λ = 400 nm) reaches 1538.2 μmol h−1 g−1, which is 158.6 times, 17.7 times, and 2.5 times higher than that of Cerium dioxide (CeO2), P25, and P25/CeO2, respectively. This catalyst has stronger light absorption, easier carrier transfer, and separation. This study guides the construction of efficient hydrogen evolution photocatalysts.

Controlled synthesis of 3D pseudocubic Fe2O3/BiFeO3 heterojunction photocatalyst for effective ciprofloxacin-HCl and methyl orange degradation

Nano-particle-based Iron (III) oxide (Fe2O3) and nanosheet-based bismuth ferrite (BiFeO3) photocatalysts were successfully prepared through a solid-state thermal decomposition approach. Especially, loading BiFeO3 over Fe2O3 demonstrated a 3D pseudocubic-based hierarchical architecture of Fe2O3/BiFeO3 (FeBiOx), which exhibits enhanced photodegradation efficiency of about 98.3 % for antibiotic ciprofloxacin-HCl (C-HCl) and 97.8 % for pollutant methyl orange (MO) under ultraviolet (UV) light irradiation within 180 and 150 min, respectively, compared to pure BiFeO3 and Fe2O3. The improved photocatalytic performance of FeBiOx was ascribed to the increased surface area, Type-II charge transfer scheme, effective charge migration efficiency induced by the surface plasmon resonance (SPR) effect of metal-Bi, and reduced bandgap energy.

Photochemical Synthesis of Sericin-Coated Gold Nanorods and Their Antibacterial Activity under Low-Level Near-Infrared Light.

Gold nanorods (GNRs) are unique nanoparticles with easily functionalized surfaces, multiple synthesis methods, photothermal conversion, and surface plasmon resonance effects. These properties make GNRs suitable for various biological applications. However, a rapid synthesis of GNRs using less toxic chemicals is needed. The photochemical method is a viable option that can synthesize GNRs quickly while using fewer chemicals. A photochemical method is reported for the synthesis of GNRs using Irgacure-2959 as a reducing agent. This method could be used to synthesize GNRs with a rod-like shape within 30 min. Additionally, GNRs were coated with sericin (GNRs-SC) to further reduce their toxicity in human dermal fibroblast adult cells. Low-level near-infrared (NIR) light was applied to enhance the photothermal therapy of both GNRs and GNRs-SC. The results showed that GNRs and GNRs-SC under low-level NIR light have enhanced antibacterial activity against Staphylococcus aureus and Escherichia coli, as well as antibiofilm activity against S. aureus. Furthermore, GNRs-SC showed good biocompatibility with antibacterial and antibiofilm activities. These results indicate that GNRs-SC are good candidates for various biological applications.

Cascade enzyme-mimicking with spatially separated gold-ceria for dual-mode detection of superoxide anions

Metal-semiconductor nanozyme of dumbbell Au-CeO2 with spatially separated heterostructure has cascade superoxide dismutase (SOD)-like and peroxidase (POD)-like activities for superoxide anions detection. It was synthesized by selective growth of CeO2 at the ends of Au nanorod (Au NR). Taking advantage of the excellent local surface plasmon resonance (LSPR) effect of Au NR, the spatially separated Au-CeO2 has a higher photothermal effect than the continuously growing core-shell structure of Au@CeO2. Meanwhile, the hot electrons of Au NR could transfer to CeO2 under 808 nm laser irradiation, changing the ratio of Ce3+/Ce4+ redox couples over CeO2 and facilitating H2O2 decomposition thus enhancing POD-like activity. Based on the SOD-like activity of Au-CeO2, superoxide anion (O2·−) can be transformed into hydrogen peroxide (H2O2). Dual-mode including absorbance and temperature sensing detection of O2·−, with the detection range from nM to μM i.e., 0.1–150 μM and LOD of 0.033 μM (S/N = 3) was achieved through the cascade catalysis and photothermal effect. The as-proposed method was applicable to both cancer and normal cell samples with satisfactory accuracy and recovery.

Synthesis of Ag/Cu decorated 3D self-assembled nanowire TiO2 photocatalyst for hydrogen production: a promising pathway towards sustainable energy generation.

Here, synthesis and characterization of TiO2 with different morphologies along with the cost-effective bimetallic decoration on optimized 3D self-assembled nanowire TiO2 (NWT) photocatalyst (Ag/Cu-NWT) with overwhelming hydrogen production rate is reported. All the photocatalysts were well characterized by different characterization techniques. Initially, the effect of morphology change obtained by changing the NaOH concentration has been studied for TiO2. Morphology obtained at 10M NaOH solution, i.e., NWT (678μmol/g), showed better hydrogen production than morphology obtained at 5M (410μmol/g), 15M (210μmol/g), and 20M (160μmol/g) NaOH solutions. Further, with the aim to achieve comparable or better activity low-cost photocatalyst as compared to Pt-TiO2 system, NWT was decorated with various Cu percentages and then with a minimal percentage of Ag on an optimized Cu-NWT photocatalyst. The observed trend for photocatalytic hydrogen production has been found to be P25 TiO2 < NWT < 1.0Cu-NWT < 0.5Pt-NWT ≤ 0.1Ag/1.0Cu-NWT. The marked increase by a factor of 103 in hydrogen production for the optimized bimetallic 0.1Ag/1.0Cu-NWT (10,184μmol/g) photocatalyst compared to P25 TiO2 (99μmol/g), nearly threefold increment in hydrogen production than an optimized 1.0 Cu-NWT (3907μmol/g) photocatalyst and comparable hydrogen production as compared to 0.5Pt-NWT (10,050μmol/g) may be attributed to the successful synthesis of a highly porous NWT morphology, which offers large surface area, increased light absorption combined with the synergistic effects of surface plasmon resonance (SPR), and the Schottky barrier for H+ reduction to H2 gas. The optimization of TiO2 morphology and an inexpensive bimetallic decoration strategy opens up promising opportunities for the development of cost-effective photocatalysts in the realm of energy and environment.

Fabrication and photocatalysis of novel Z-scheme Cu2O/Cu-Ag/AgCl heterojunction possessed broad-spectrum antibacterial performance and degradation capabilities

The construction of nanostructured Z-heterostructures is a potent strategy for achieving efficient photocatalyst synthesis. Herein, a novel Cu2O/Cu-Ag/AgCl (CCAA) Z-scheme heterostructure was created via photoreduction precipitation and utilized for pollutant decomposition and microorganism inactivation. Subject to visible light (λ > 420 nm) illumination, specimen CCAA-2 demonstrated superior photodegradation competence for Congo Red (CR), achieving a degradation rate of 92.6 % within 60 min. The superior removal performance is attributed to the Z-scheme heterostructure, featuring precise interfacial contact, and the combined effect of adsorption and photocatalytic activity. Meanwhile, the optimal sample, CCAA-2, was able to achieve 100 % inactivation of Escherichia coli (E. coli) and Staphylococcus aureus (S. aureus) within 15 min under visible light. The photocatalytic performance of CCAA nanocomposites is primarily attributed to the surface plasmon resonance (SPR) effect of the noble metal Ag and the fabrication of Z-Scheme heterostructures to improve the utilization efficiency of electrons (e-) and holes (h+). Particularly, the photocatalytic mechanism was scrutinized via active substance capture experiments and electron spin resonance (ESR) analysis, uncovering that •O2ˉ and h+ served as key active constituents. Hence, this research presents a feasible approach for designing and constructing Z-Scheme heterojunctions for efficacious removal of contaminants from water.

Single layered Ag/NiO plasmonic nanocoatings: A new green synthesis method for selective solar absorber

This study presents the synthesis of environmentally benign, single-layered spectrally selective Ag/NiO nanocoating absorbers using a green synthesis method. Various characterization techniques, including Rutherford backscattering spectroscopy (RBS), X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), and atomic force microscopy (AFM), were used to examine the effects of plasmonic Ag concentration on the structural, chemical composition, and surface morphology of the nanocomposites. The optical properties of the deposited nanocoatings were investigated using a UV–Vis-NIR spectrophotometer in the solar spectrum region (300–2500 nm) and an FT-IR spectrophotometer in the infrared wavelength region (3000–20,000 nm). XRD results confirmed the coexistence of a face-centered cubic phase of Ag and NiO in the Ag/NiO nanocermet thin films. SEM and TEM topography revealed uniformly distributed nanosphere NiO thin films and cubic Ag metal with better dispersibility and crystallization. The RBS spectrum of the samples showed a homogeneous distribution of Ni, Ag, and O atoms throughout the coatings. Ag/NiO nanocoatings deposited with 8 wt% Ag content exhibited excellent solar absorptance (α) = 0.95 and thermal emittance of (ɛ) of 0.08. This enhancement is primarily attributed to the localized surface plasmon resonance (LSPR) effect associated with the embedded Ag nanoparticles, which facilitates more effective utilization of light.

SPR Effect Enables Flexible Electronic Environment and Activity of Cd0.7In2.2S4-30 for High-Performance Pyro-PEC Catalytic Capability.

Plasma-semiconductor systems hold significant promise in the field of photoelectrocatalysis. In this study, the pyroelectric material cadmium indium sulfide (Cd0.7In2.2S4-30) and Pt were used as catalysts, and a temperature gradient was introduced to investigate the influence of surface plasmon resonance (SPR) effect on the pyroelectric and photocatalytic performance. Interestingly, under the influence of the SPR effect, Cd0.7In2.2S4-30 demonstrates a 1.6-fold and 1.4-fold increase in current density under photocatalytic and pyro-photoelectrocatalytic conditions at 1.23 V vs RHE, respectively. Furthermore, under the protection of surface metal Pt, a notable enhancement in the charge separation efficiency and stability of the photoelectrode material is observed. The combination of outstanding performance reveals that Pt noble metal ions, influenced by the SPR effect, generate a localized electric field at the adjacent semiconductor interface, enhancing the charge transfer capability between metal nanoparticles and the semiconductor, thereby promoting electron-hole separation and improving semiconductor photocatalytic activity. Additionally, the SPR effect increases the yield of high-energy pyro-electrons on plasma metal and facilitates their effective transfer to the semiconductor, thereby promoting the generation of thermally induced electrons. This study reveals the multifaceted of SPR effects on the behaviors of semiconductors and provides an opportunity to rationally design metal-semiconductor photocatalytic materials for efficient solar energy conversion.