Surface Plasmon Resonance Effect Research Articles

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.

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.

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.

High-performance SERS substrate based on gold nanoparticles-decorated micro/nano-hybrid hierarchical structure

Owing to its excellent localized surface plasmon resonance (LSPR) effect, noble metal nanoparticles (NPs) find extensive application in the preparation of surface-enhanced Raman scattering (SERS) substrates. However, due to process limitations, the practicality and testing effectiveness of SERS substrates still leaves much to be desired. Here, a wafer-scale gold (Au) NPs silicon (Si) micro/nano-hybrid structured substrate is prepared. This is achieved through two-step etching, followed by decorating Au-NPs onto the structure via self-assembly process induced by de-wetting. Finite-difference time-domain (FDTD) simulations reveal that the significant enhancement of local electric field in the voids between Au-NPs and Si is crucial for enhancing SERS. Using Rhodamine 6G (R6G) as the probe molecule, performance of the fabricated SERS substrate is investigated. It demonstrates a minimum detection limit of 10−11 M, with a calculated enhancement factor of 4.40 × 108, indicating its high sensitivity. The minimum relative standard deviation for the substrate is 5.254 %. After 20 days of placement, the SERS performance show tiny variation. Even after four cycles of cleaning experiments, it still maintains outstanding SERS performance. This demonstrates its excellent stability, uniformity and reusability. Our research provides guidance for the efficient and low-cost fabrication of high-performance SERS substrates.

Optical Fiber Biosensors Based on Surface Plasmon Resonance Effect: A Review

Optical Fiber Biosensors Based on Surface Plasmon Resonance Effect: A Review

Incorporation of Gold Nanoparticle into ZnO Electron Transport Layer to Improve Performance of Hybrid Bulk Heterojunction Solar Cell

Abstract We have investigated the effect of localized surface plasmon resonance (LSPR) from gold nanoparticles incorporated into the electron transport layer (ETL) of zinc oxide (ZnO) on charge carrier transport in order to improve the performance of inverted hybrid bulk-heterojunction solar cells. Synthesis of gold nanoparticles capped by 3-mercaptopropionic acid (AuMPA) and oleylamine (AuOA) was carried out by use of the reduction method and the fabrication of solar cell device with the configuration of ITO/ZnO:AuNPs/P3HT:PCBM/PEDOT:PSS/Ag was done by spin coating and thermal evaporation techniques. The absorbance spectra show a plasmonic peak of AuMPA in solution at 521 nm, while AuOA has a plasmonic peak at 531 nm, with both solutions showing a red-wine color. In our investigation, the incorporation of AuMPA about 2.65wt% or AuOA about 3.5 wt% in the ZnAc solution is quite stable. With the addition of 1.77 wt% AuMPA, the fabricated devices show a significant improvement at short circuit condition (JSC) from 46.67 mA/cm2 to 83.11 mA/cm2, resulting in an increase in power conversion efficiency (PCE) from 5.64% to 9.00% under the illumination of 100 mW/cm2 simulated solar irradiation. While the AuOA addition of 2.65 wt%, the JSC increased from 22.67 mA/cm2 to 44.12 mA/cm2 along with an improvement of PCE from 2.71% to 5.32%. The experiment results suggest that the electron mobility or charge carrier transport to the indium tin oxide (ITO) cathode is improved by the local electric field enhancement around the zinc oxide (ZnO) electron transport layer due to the effect of gold nanoparticles (AuNPs).

Highly sensitive, reproducible, and stable core–shell MoN SERS substrate synthesized via sacrificial template method

Molybdenum nitride is a promising candidate for surface-enhanced Raman scattering (SERS) substrates due to its high conductivity, surface plasmon resonance, and chemical stability. Core-shell structures possess unique physical and chemical properties, such as high-volume ratio, low density, short diffusion length, and high load-bearing capacity, making them favorable for SERS applications. In this research, core–shell MoO3 is first synthesized as a precursor oxide using a sacrificial template method, and core–shell MoN microspheres are successfully prepared via subsequent nitriding. As a representative transition metal nitride, the obtained core–shell MoN nanospheres show strong localized surface plasmon resonance and SERS effects. Using these MoN microspheres as Raman substrates allows a range of highly targeted compounds to be accurately detected, and the detection limits for this non-precious-metal substrate morphology are exceptionally high, reaching 10−10 M. In addition, MoN nanospheres exhibit excellent resistance to acid–base corrosion, oxidation, and radiation, thus rendering them suitable for use as substrates in harsh environments.

Construction and photothermal properties of Ag nanoparticles modified multilevel porous CuO film with ultra-wide infrared spectrum absorption

Based on lattice vibration and energy band theory, narrow bandgap inorganic semiconductor materials have become a new type of photothermal material, but it is difficult to achieve absorption for long wavelength infrared radiation to meet the application requirements of ultra-wide spectrum (2.5–20 μm) infrared detectors. From the perspective of structural optics, this paper constructed a multilevel porous CuO film with both coral-like micro-porous and flower-like nano-porous structures based on chemical bath deposition technique, and the Ag nanoparticles were uniformly embedded in the "petal" gaps of flower-like nano-porous CuO by optimizing the dosages of PVP. Benefiting from the synergistic effect of multilevel porous structure and loaded Ag nanoparticles, the Ag nanoparticles modified multilevel porous CuO (CuO@Ag-PVP 0.05) film had an average absorption of 94.17 % over the wavelength range of 2.5–20 μm. The photothermal conversion efficiency of CuO@Ag-PVP 0.05 film can reach up to 81.12 % and 86.96 % over near-infrared and far-infrared light ranges, respectively. The various material characterizations and simulations analysis showed that the multilevel porous structure containing coral-like and flower-like multi-scale pores can form two guiding modes for light, and based on the synergistic effect of the two guiding modes, the CuO film can form a strong trapping effect for light over ultra-wide spectral range, broaden its absorption range, and enhance its absorption characteristics. The loaded Ag nanoparticles contain a large number of free electrons, which can capture light energy and convert it into heat energy through local surface plasmon resonance (LSPR) effect, further enhancing the light absorption and photothermal conversion efficiency.

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.

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.

Exploring the thermal and optical characteristics of Ti3C2 MXene for enhanced photothermal conversion

Ti3C2 MXene, a member of the two-dimensional (2D) transition metal carbides family, has garnered significant attention for its exceptional photothermal properties. To understand the mechanistic underpinnings of this feature, we conducted a comprehensive first-principles density functional theory analysis. This study was aimed at investigating the electronic band structure and vibrational characteristics of Ti3C2 MXene to unravel its microscopic process of photothermal conversion. After obtaining its optical and thermal properties, the process by which the material moves from light absorption to heat release is elucidated. The presence of localized surface plasmon resonance (LSPR) effects in Ti3C2 is proved by Finite-difference time-domain (FDTD) simulations. The synergy between the high thermal conductivity network in the Ti layers and the LSPR phenomenon is believed to be responsible for the superior photothermal conversion capabilities. This investigation enhances the understanding of the intrinsic properties of Ti3C2 MXene, confirming its status as an ultrahigh photothermal conversion material.

Unveiling the potential: Gallium-doped zinc oxide/silver-nanoparticles/glass structure for superior anode performance in polymer light-emitting diodes

This study examines the effectiveness of gallium-doped zinc oxide (GZO) combined with silver nanoparticles (Ag-NPs) on glass substrates as anodes for polymer light-emitting diodes (PLEDs). The proposed GZO/Ag-NPs/glass structure achieved superior electrical and optical properties, with a peak luminance of 5834 cd/m2 and an average current efficiency of 1.91 cd/A, significantly outperforming the conventional GZO/Ag-NPs/GZO/glass anode. The GZO/Ag-NPs/glass anode enhanced electroluminescence intensity by 379 % compared to the GZO/glass anode, while the GZO/Ag-NPs/GZO/glass anode showed a 196 % enhancement. This highlights the potential for improved PLED performance through enhanced anode conductivity and localized surface plasmon resonance effects.

Synergistic Coordination and Surface Plasmon Resonance of Quantum Dots in Enhancing Photocatalytic Hydrogen Evolution.

Recent studies have revealed that the integration of metal nanoparticles (NPs) with photocatalysts allows the metal NPs to serve as cocatalysts, significantly enhancing reactant efficiency near nanostructures through the surface plasmon resonance (SPR) effect. On this basis, we synthesized highly reactive FePt quantum dots (FePt QDs) with tailored configurations, manipulating the Pt coordination environment and combining FePt QDs with ultrathin two-dimensional nickel metal-organic layer (Ni-MOL) nanosheets. X-ray absorption fine spectroscopy (XAFS) confirmed the distinctive Pt-Fe configuration after photoactivation. The optimized loading amount of FePt QDs led to a hydrogen evolution reaction (HER) yield of 113 mmol·g-1·h-1 after activation, with the catalyst remaining stable over five cycles. The improved reaction efficiency stemmed from Pt coordination adjustments and a localized SPR effect, supported by ultraviolet-visible (UV-vis), infrared (IR), Raman, and XAFS characterizations. A comparative analysis was conducted with Ni-MOL deposited with platinum NPs, further underscoring the distinct advantages of FePt QDs and corroborating by density functional theory (DFT) calculations, which revealed favorable d-band center properties. These findings offer a promising avenue for the development of highly efficient and stable nanoalloy photocatalysts.

Chemically bonded nonmetallic LSPR S-scheme hollow heterostructure for boosting photocatalytic performance

The light absorption, mass transfer, and charges separation are essential to the efficiency of photocatalytic reaction, but constructing photocatalyst with the three excellent properties is still challenging. Herein, the interfacial Mo-S bonds and oxygen vacancy synchronously decorated MoO3-x/Zn3In2S6 (MoO3-x/ZIS) heterostructure was rationally designed and synthesized. The oxygen-defective MoO3-x nanotubes showed hollow structure and local surface plasmonic resonance (LSPR) effect, which improved mass transfer and solar light absorption. Besides, the built-in electric field and interfacial Mo-S bond provided endogenetic impetus and channels for rapid photoexcited charge carriers transfer and separation. The photocatalytic hydrogen (H2) evolution and hydrogen peroxide (H2O2) production on optimal MoO3-x/ZIS composite were 17.34 and 4.47 mmol g−1 h−1, respectively. The apparent quantum efficiency of MoO3-x/ZIS for H2 evolution at 400 nm was about 13.92 %, which was 8.09 times higher than that of ZIS. Moreover, the MoO3-x/ZIS also displayed excellent activities on the selective 5-hydroxymethylfurfural dehydrogenation. The in-situ X-ray photoelectron spectroscopy, electron paramagnetic resonance, in-situ selective photodeposition, and density functional theory calculation confirmed the S-scheme charge transfer pathway between MoO3-x and ZIS. This study provides an effective avenue for designing multifunctional photocatalysts based on the synergistic effects of chemically bonded S-scheme heterostructure and nonmetallic LSPR effect.

Suppressed recombination of a flexible TiO2 nanowires photoanode by coupling of plasmonic Ag nanoparticles in the photoelectrochemical ultraviolet photodetector

The noble metal nanoparticles can improve the efficiency of photoelectric conversion via enhancement of light harvesting for the localized surface plasmon resonance (LSPR) effect. Here, TiO2 nanowires were constructed on carbon fiber cloth as a flexible photoanode for photoelectrochemical (PEC) ultraviolet (UV) photodetector. By decorated noble metal Ag nanoparticles on TiO2 nanowires, the photocurrent was improved from 35.9 μA cm−2 to 268.4 μA cm−2, and the rise and decay time were increased by 0.14 s and 0.12 s, respectively. Moreover, the recombination of photon-generated electrons and holes was also decreased in photoanode due to the Schottky barrier between Ag and TiO2. This work provided an approach to promote the performances of the PEC UV photodetector.

Synergistic Effect Between 0D CQDs and 2D MXene to Enhance the Photothermal Conversion of Hydrogel Evaporators for Efficient Solar Water Evaporation, Photothermal Sensing and Electricity Generation.

Solar-powered interfacial water evaporation is a promising technique for alleviating freshwater stress. However, the evaporation performance of solar evaporators is still constrained by low photothermal conversion efficiency and high water evaporation enthalpy. Herein, 0D carbon quantum dots (CQDs) are combined with 2D MXene to serve as a hybrid photothermal material to enhance the light absorption and photothermal conversion ability, meanwhile sodium carboxymethyl cellulose (CMC)/polyacrylamide (PAM) hydrogels are used as a substrate material for water transport to reduce the enthalpy of water evaporation. The synergistic effect in 0D CQDs/2D MXene hybrid photothermal materials accelerate the carrier transfer, inducing efficient localized surface plasmon resonance (LSPR) effect. This results in the enhanced photothermal conversion efficiency. The integrated hydrogel evaporators demonstrate a high evaporation rate (1.93 and 2.86kgm-2h-1 under 1 and 2 sunlights, respectively) and low evaporation enthalpy (1485Jg-1). In addition, the hydrogel evaporators are applied for photothermal sensing and temperature difference power generation (TEG). The TEG device presents an efficient output power density (230.7mWm-2) under 1 sunlight. This work provides a feasible approach for regulating and controlling the evaporation performances of hydrogel evaporators, and gives a proof-of-concept for the design of multipurpose solar evaporation systems.

Fabrication of Three-Dimensional Dendritic Ag Nanostructures: A SERS Substrate for Non-Invasive Detection.

This paper discusses the fabrication of three-dimensional dendritic Ag nanostructures, showcasing pronounced Localized Surface Plasmon Resonance (LSPR) effects. These nanostructures, employed in surface-enhanced Raman scattering (SERS), function as sensors for lactic acid in artificial sweat. The dendritic structures of the silver nanoparticles (AgNPs) create an effective SERS substrate, with additional hotspots at branch junctures enhancing LSPR. We achieve differential LSPR effects by varying the distribution and spacing of branches and the overall morphology. Adjustments to electrodeposition parameters, such as current and plating solution protective agents on an anodized aluminum oxide (AAO) base, allow for precise control over LSPR intensities. By pre-depositing AgNPs, the electron transmission paths during electrodeposition are modified, which leads to optimized dendritic morphology and enhanced LSPR effects. Parameter optimization produces elongated rods with main and secondary branches, covered with uniformly sized, densely packed, non-overlapping spherical AgNPs. This configuration enhances the LSPR effect by generating additional hotspots beyond the branch tips. Fine-tuning the electrodeposition parameters improved the AgNPs' morphology, achieving uniform particle distribution and optimal spacing. Compared to non-SERS substrates, our structure amplified the Raman signal for lactic acid detection by five orders of magnitude. This method can effectively tailor SERS substrates for specific analytes and laser-based detection.

Multi-species defect engineering synergistic localized surface plasmon resonance boosting photocatalytic CO2 reduction

Inadequate charge carrier kinetics and a scarcity of active sites still challenge photocatalytic CO2 reduction reaction (CO2RR). We exploit the synergy between multi-species defect engineering and the localized surface plasmon resonance (LSPR) effect in Bi/BiV1-mO4-m to address these limitations. Theoretical calculations show that V and O defects collectively modulate the work function of BiVO4, which induces hot electrons to transfer from Bi nanoparticles to BiV1-mO4-m. These electrons are then captured by O defects, confirmed by femtosecond transient absorption spectroscopy. Electron density is significantly increased at the O defects, enhancing CO2 adsorption and establishing it as a new reaction site. Bi/BiV1-mO4-m achieves photocatalytic CO2RR in pure water; Bi/BiV1-mO4-m achieves direct solar-driven photocatalytic CO2RR with a CO yield of 501 μmol/g/h under concentrated sunlight.