Heterojunction Composites Research Articles

Enhanced charge transfer kinetics across the graphdiyne-metal sulfide ohmic interface for boosting photocatalytic hydrogen evolution

The design and construction of photocatalysts are the crucial step for solar-driven hydrogen evolution. Herein, a new type of graphdiyne (CnH2n-2)-based photocatalyst, which was prepared by one pot method, was used to promote hydrogen evolution reaction by constructing GDY/VS2 ohmic junction with S sites anchoring on the surface. Actually, the unique two-dimensional conjugated carbon network of GDY can maintain the structural stability. The uneven surface facilitates the flow of electrons, which makes GDY a good electron donor. In addition, the expanded interlayer spacing of VS2 exposes more hydrogen evolution active sites. The increase in surface electronegativity of composite catalysts enhances their redox ability and charge transfer kinetics. The band edge of the graphdiyne-metal sulfide Ohmic contact interface is bent, allowing electrons to flow into the co catalyst without resistance. These synergistic effects lead to the robust hydrogen production of GDY/VS2, which was increased by nearly 10.3 times compared with that of pure GDY. Finally, charge migration at the interface of graphdiyne-metal sulfide heterojunction was proposed and further verified combining in situ XPS and theory calculation. This research marks a significant stride for enhance the efficiency of photocatalytic hydrogen evolution by designing and constructing composite heterojunction materials.

A novel BiVO4/vermiculite Z-scheme heterojunction with enhanced removal rate of dyes through adsorption photodegradation synergistic mechanism

Water pollution, exacerbated by industrialization, poses severe threats to aquatic ecosystems and human health, particularly due to persistent organic pollutants like dyes. To mitigate this issue, the development of effective and sustainable water treatment technologies is essential. This study presents the synthesis of a novel bismuth vanadate (BVO)/vermiculite (Vt) adsorption-photocatalytic self-cycling composite using a simple hydrothermal method. The composite's Z-scheme heterojunction structure, along with the introduction of surface oxygen vacancies, significantly reduces electron-hole recombination and enhances charge separation. These modifications lead to a 1.64-fold increase in adsorption capacity compared to Vt and a 6.4-fold improvement in photocatalytic efficiency over BVO. The material maintained a 76 % removal efficiency after five usage cycles and demonstrated high efficacy in methylene blue (MB) solutions, even at concentrations up to 300 mg/L. Moreover, the composite displayed stable performance under repeated use and in high-pollutant environments, highlighting its durability and practicality. These characteristics underscore its strong potential for widespread application in environmental remediation and sustainable water resource management, offering an innovative solution to the global challenge of water pollution.

Dual-Driven Ion/Electron Migration and Sodium Storage by In Situ Introduction of Copper Ions and a Carbon-Conductive Framework in a Tin-Based Sulfide Anode.

Tin sulfide (SnS) has emerged as a promising anode material for sodium ion batteries (SIBs) due to its high theoretical capacity and large interlayer spacing. However, several challenges, such as severe insufficient electrochemical reactivity, rapid capacity degradation, and poor rate performance, still hinder its application in SIBs. In this study, in situ introduction of copper ions and a carbon conductive framework to form SnS nanocrystals embedded in a Cu2SnS3 lamellar structure heterojunction composite (SnS/Cu2SnS3/RGO) with graphene as the supporting material is proposed to achieve dual-driven sodium ion/electron migration during the continuous electrochemical process. The designed structure facilitates the preferential electrochemical reduction of copper ions into copper nanocrystals during the discharge process and functions as a catalytically active center to promote multivalence tin sodiation reaction. Furthermore, during the charging process, the presence of copper nanocrystals also facilitates efficient desodiation of NaxSn and further activates to form higher valence state sulfides. As a result, the SnS/Cu2SnS3/RGO composite demonstrates high cycling stability with a high reversible capacity of 395 mAh g-1 at 5A g-1 after 500 cycles with a capacity retention of 85.6%. In addition, the assembled Na3V2(PO4)3∥SnS/Cu2SnS3/RGO sodium ion full cell achieves 93.7% capacity retention after 80 cycles at 0.5 A g-1.

Te2− modulated heterogeneous remodeling of S atoms in ultrathin ZnIn2S4 nanosheets containing S vacancies synergistically enhances CO2 photoreduction

Reconfiguration of in situ heterojunction composites without interfacial resistance by substitution of homologous anions for the formation of gradient work function differences inducing the formation of built-in electric field is an effective strategy to enhance the charge separation efficiency. Herein, Te2−/ZnIn2S4-VS (Te2−/ZIS-VS) in situ heterojunction was synthesized by substitution of Te2− ions for S2− in ultrathin ZIS containing S vacancies, which can significantly promote photogenerated charge separation, surface electron enrichment, and CO2 adsorption/activation. The presence of S vacancies and adjacent Te2−/S2− double anions, the double active sites constructed by defect engineering promote the desorption of *CO molecules while inhibiting the protonation toward *CHO, which was more favorable for selective CO2 photoreduction to CO. The experimental results showed that the CO yield of Te2−/ZIS-VS was significantly increased to 672.1 μmol g−1 h−1 compared with pristine ZIS (54.3 μmol g−1 h−1) and the CO selectivity was close to 83 %. Notably, the life cycle assessment (LCA) of Te2−/Znln2S4 nanosheets with S-vacancy was performed. The evaluation results showed that most of the 17 impact categories showed low overall impact values and were environmentally friendly. Based on the results of this LCA, suggestions were put forward to further optimize the product to reduce carbon emissions.

Trivacant Keggin-type polyoxometalate/TiO2 composite for enhanced sonocatalytic degradation of AR88 from aqueous solutions

Polyoxometalates (POMs) have been limited in their widespread use in catalysis in previous studies due to their strong carrier complexation and limited solubility. To overcome this limitation, in this study, Z-type heterojunction composites constructed with trivacant Keggin-type POMs K9SbW9O33·19.5H2O and TiO2 were synthesized by the sol–gel method and used for the sonocatalytic removal of the organic pollutant AR88. The results showed that, compared with pure K9SbW9O33·19.5H2O, the optimum K9SbW9O33·19.5H2O/TiO2 showed a significantly higher sonocatalytic degradation efficiency of 87.2 % for AR88, and the mineralization rate reached 51.8 %. Parameters such as dye pH and sonication power were optimized to determine the best conditions for sonocatalysis. In addition, the K9SbW9O33·19.5H2O/TiO2 Z-type heterojunction composites showed good stability and reusability. The excellent catalytic performance is attributed to the effective separation of charges and holes by the Z-type heterojunction, which enables them to produce active substances for AR88 decomposition. This study demonstrates the high potential of POMs for the application of sonocatalysis in the treatment of organic pollutants.

VS2/ Blue Phosphorus composites for high speed lithium ions storage

Based on first-principles calculations, the potential of the H-VS2/Blue P heterojunction composite as a lithium-ion battery anode is systematically investigated. This heterojunction composite enhances the stability of the VS2 structure and increases its overall mechanical strength.The Young's modulus of the composite is 144.69 N/m, markedly exceeding that of the single layer. Furthermore, it modifies the electronic properties of the Blue P monolayer, converting it from an insulating to a metallic state.The H-VS2/Blue P heterojunction composite exhibits a high lithium adsorption energy of 4.34 eV and a low diffusion barrier of 0.15-0.19 eV, facilitating rapid lithium-ion migration during charge/discharge cycles. And the theoretical capacity of the heterojunction composite is up to 1211 mAh/g. The combination of elevated adsorption energy, low diffusion barrier, and high theoretical capacity indicates that the H-VS2/Blue P heterojunction composite is a highly promising anode material for lithium-ion batteries.

Engineering Ag3PO4/SnS2 heterojunction composite: A promising electrocatalyst for hydrogen evolution reaction in acidic medium

A Ag3PO4/SnS2 heterojunction composite electrocatalyst was fabricated using combined facile liquid exfoliation and hydrothermal technique by varying the concentration of SnS2 in Ag3PO4. Tin disulfide (SnS2) is a transition metal dichalcogenide that is a promising non-precious catalyst for hydrogen evolution reaction (HER) application. However, the practical application of this material is limited due to its poor electrical conductivity, to overcome this limitation it is made as a composite with Ag3PO4 as a n-type semiconductor which function by absorbing visible light with its suitable bandgap. The HER is evaluated through the three-electrode electrochemical set-up, where the catalyst coated on carbon cloth serves as a working electrode along with Ag/AgCl and platinum wire as reference and counter electrode respectively. The electrocatalyst is considered as best when it has certain criteria including lesser value of overpotential implying low current requirement to produce hydrogen. The catalyst should obey the following criteria like low resistance, high conductive nature, smaller exchange current density and has large surface area to actively participate in the electrochemical reaction. Apparently Ag3PO4/5 wt% of SnS2 is found to be the best performing composite as evidenced from the experimental data. This work may be useful for heterojunction composite catalyst for the practical application in electrochemical water splitting.

Novel MoS2-based heterojunction as an efficient and magnetically retrievable piezo-photocatalyst for diclofenac sodium degradation

It is a challenging and meaningful task to design a piezo-photocatalyst with excellent performance under mild mechanical stirring conditions rather than ultrasonic irradiation. Herein, a hydraulic-driven piezo-photocatalytic process was proposed, using MoS2-based heterojunction as catalysts for diclofenac sodium (DCF) degradation. A magnetically retrievable MoS2/TiO2/Fe3O4 composite was designed and successfully prepared by a facile one-step solvothermal process. Among various heterojunction composites and pure MoS2, the ternary composite MoS2/TiO2/Fe3O4 exhibited the strongest piezo-photocatalysis capability, with a DCF degradation efficiency of 99.6% and a pseudo-first-order rate constant of 0.733 min−1. Additionally, the degradation efficiency of DCF was still up to 85.2% in 6 min after 5 cycles by MoS2/TiO2/Fe3O4. The ternary composite can be easily collected and separated using a magnet. There was an optimum hydraulic gradient value (0.45 s–1) for DCF degradation. •OH played a major role in DCF degradation during the hydraulic-driven piezo-photocatalytic process. A satisfactory DCF degradation was found in the actual water media. The results verify the existence of a synergetic effect between piezo and photocatalytic processes. Thereupon, the hydraulic-driven piezo-photocatalysis can be an efficient, sustainable, and energy-saving process for water treatment.

Visible-light-assisted peroxymonosulfate activation using MIL-88A(Fe)/BiOI heterojunction composite to drive charge transport for eliminating acid red 18

A novel rod-shaped MIL-88A(Fe)/BiOI heterojunction composite is fabricated by an in-suit chemical deposition method for visible-light-assisted peroxymonosulfate activation to eliminate AR18 (acid red 18). A series of x%MIL-88A(Fe)/BiOI are obtained according to the mass ratio of MIL-88A(Fe) to BiOI. Among them, 30 %MIL-88A(Fe)/BiOI could remove 97.79 % AR18 within 40 minutes. The reaction parameters on this process are investigated, such as PMS concentration, catalyst dosage, initial pH and dye concentration. The optimal conditions are determined to be [catalyst]= 1 g·L−1, [PMS]=1 mM, pH=7.02. The scavenging experiments and EPR analysis manifest that 1O2 is the main active species for AR18 degradation. In accordance with the band structure, active species, XPS, PL, EIS and photocurrent response, the Z-scheme electron transfer path of the composite catalyst is proved under 500 W (λ > 420 nm) Xenon lamp irradiation. In the end, the stability and universality of the composite catalyst in practical application are evaluated by three cyclic tests and inorganic anion experiments. This work provides valuable guidance for synthesizing efficient and stable MOF based heterojunction photocatalysts.

Construction of SnO2/Cu2O heterojunctions for enhanced photocatalytic degradation of moxifloxacin

Herein, SnO2/Cu2O heterojunction composites were prepared using a hydrothermal method for moxifloxacin removal from water. Cu2O and SnO2 were detected in the composite samples, which exhibited between the two semiconductors. The introduction of SnO2 into pure Cu2O, forming a heterojunction structure, can enhance device charge conversion, improve photocurrent intensity and photogenerated electron-hole separation efficiency, and greatly improve photocatalytic performance. Moxifloxacin degradation by SnO2/Cu2O composites reached 86.4 %. The proposed catalytic mechanism was based on radical scavenging, with • O2‐ identified as the main active species. In addition, the moxifloxacin degradation intermediates were analyzed, with possible degradation pathways suggested.

Novel 2D/2D/2D heterojunction of ZnIn2S4/g-C3N4/MoS2 for enhanced photocatalytic hydrogen evolution reaction

Photocatalysts for hydrogen evolution reaction (HER) have widely been explored but fine-tuning and engineering multiphase photocatalyst components are still challenging. Among catalysts, ZnIn2S4 has shown promise but maximizing the use of ZnIn2S4-photogenerated carriers and enhancing quantum yield still require further investigation. One way to achieve this is by enhancing the photon utilization and reducing the recombination of shallow carriers in ZnIn2S4. Accordingly, novel ZnIn2S4/g-C3N4/MoS2 type-II heterojunction composites with 2D/2D/2D structures (abbreviated ZIS/CN/MS) were synthesized in the present work by simple thermal condensation-solvothermal method. The optimized ZIS/CN/MS exhibited a photocatalytic hydrogen evolution rate of 13.6 mmol g−1 h−1 under visible light (λ ≥ 420 nm) irradiation, a value much higher than those of pure-phases ZIS and CN, as well as the binary composite of ZIS/CN. The apparent quantum efficiency of the optimized ZIS/CN/MS at a wavelength of 420 nm reached 27.0 % coupled with excellent cycling stability. The significantly improved photocatalytic performance and the excellent stability can mainly be attributed to the unique 2D/2D/2D arrangement of the ternary components of ZIS, CN, and MS in ZIS/CN/MS photocatalyst, providing a large number of close interfacial contacts between the components for shortened migration distance of photogenerated charges and more pathways for electron separation and transport in type-II heterostructures. Overall, the proposed methodology and ZIS/CN/MS composites with type-II heterojunction and 2D/2D/2D structures have great potential for use in solar-to-hydrogen energy conversion and can be extended to the preparation of other photocatalysts.

Facile boosting catalytic thermal decomposition of ammonium perchlorate from 3D porous nano Co3O4@ZnO composites

The design of efficient catalysts for the pyrolysis of ammonium perchlorate (AP) is important for the performance of composite solid propellants. Co3O4@ZnO heterojunction composites were fabricated by hydrothermal and calcination treatments and used to promote the thermal decomposition of AP. The influences of the Co/Zn molar ratio on the catalytic performance and the content of decomposition products of AP were investigated by various techniques such as TEM, XPS, BET, EIS, and TG-IR. The results revealed that the Co/Zn = 3 sample exhibited excellent performance with the high-temperature decomposition (HTD) temperature of AP reduced from 410°C to 295 °C and the apparent activation energy decreased to 98.7 kJ/mol in the case of 2 wt% addition, attributed to the construction of a heterojunction with abundant active sites enhancing the charge transfer capability between the Co3O4 and ZnO. The decomposition pathway of AP is influenced by the catalyst components, and the Co/Zn = 3 nanostructures demonstrated outstanding catalytic performance by accelerating the decomposition of HClO4 and the conversion of NH3, and promoting the production of N2O, NO, and NO2. This work provides a feasible strategy for the development of Co3O4@ZnO catalysts with excellent catalytic activity towards AP.

Anchoring MnWO4 Nanorods on LaTiO2N Nanoplates for Boosted Visible Light-Driven Overall CO2 Reduction.

The photocatalytic conversion of CO2 into hydrocarbon fuel holds immense potential for achieving a carbon closed loop and carbon neutrality. Developing efficient photocatalysts plays a pivotal role in enabling the widespread application of photocatalytic CO2 reduction on a large scale. Herein, a novel S-scheme MnWO4/LaTiO2N heterojunction composite is successfully synthesized by a hydrothermal method. This composite catalyst demonstrates excellent photocatalytic activity in the reduction of CO2 to CO and CH4 using water molecules as electron donors under visible light irradiation, and the optimized 30% MnWO4/LaTiO2N composite displays significantly enhanced CO and CH4 yields of 3.94 and 0.81 μmol g-1 h-1, respectively, and the corresponding utilized photoelectron number reaches 14.7 μmol g-1 h-1, which is approximately 7.7 and 12.9 times that of LaTiO2N and MnWO4. The enhancement in photocatalytic activity of the composites can be ascribed to the construction of an S-scheme heterojunction, which exhibits improved charge transfer dynamics, retains the strongest redox capacity, and effectively suppresses back reactions. In situ Fourier-transform infrared imaging provides evidence, to a certain extent, for the existence of a temporal gradient order in the generation of multiple products during the photocatalytic reduction of CO2.

Construction of S/g-C3N4@β-Bi2O3 heterojunction and its photocatalytic degradation of toluene in the gas phase.

In this paper, a modification of g-C3N4 was carried out by combining non-metal doping with the construction of heterojunctions, and a type II heterojunction composite, S/g-C3N4@β-Bi2O3, was prepared. The phase structure, morphology, elemental composition, valence band structure, and light absorption performance of the photocatalyst were analyzed using characterization techniques such as X-ray diffraction (XRD), scanning electron microscopy (SEM), X-ray photoelectron spectroscopy (XPS), and UV-vis diffuse reflectance spectroscopy (UV-vis DRS). The performance of the composite photocatalyst in the photocatalytic degradation of gaseous toluene, one of the typical volatile organic compounds (VOCs), under simulated solar light was studied. The effects of preparation conditions, toluene concentration, and recycling on the photocatalytic performance of the composite photocatalyst were investigated. The results show that under the optimal preparation conditions, S/g-C3N4@β-Bi2O3 achieved a degradation efficiency of 74.0% for 5ppm toluene after 5h of light irradiation. Although the degradation efficiency decreased to 61.2% after five cycles, it maintained 83% of its initial activity, indicating good stability of the composite photocatalyst. Free radical quenching experiments demonstrated that h+ was the main active species in the photocatalytic degradation of toluene, followed by ·O2-. Based on all experimental results, the migration law of photo-generated charges was analyzed, and a possible photocatalytic mechanism was proposed. In this study, a new material was obtained for the photocatalytic removal of VOCs by improving the photocatalytic properties of g-C3N4.

Efficient CQDs/Cu2S @Ti-TPA-MOF heterojunction incorporation: A visible-light-photocatalytic composite with extended separated charges lifetime

A sustainable strategy to tackle water pollution involves using innovative composites based on MOFs for photodecomposing antibiotic contaminants. A core-shell structure was synthesized using a solvothermal method, combining Cu2S, carbon quantum dots (CQDs), and Ti-TPA-MOF, resulting in a material with excellent visible-light capture capabilities. Spectroscopic (XRD, XPS, BET, DRS, DLS, ESR, and PL), electrochemical (photocurrent), and microscopic (TEM) analyses were performed to characterize the photocatalyst. Adding 20 mg of Cu2S and CQDs greatly improved gentamicin photodegradation compared to other prepared photocatalysts. This was due to enhanced electron conductivity, increased photocurrent density, a narrower energy gap, and a longer charge separation lifetime. The heterojunction composites at 150 mg/l showed a 2–6 times increase in efficiency after 90 min, surpassing the pure materials. The outcomes showed evidence of pseudo-first-order kinetics, photocatalytic activity, and excitation by visible light in the photodegradation. The stability of the photocatalytic process is evident after five cycles.

Fabricating built-in electric field in fully enclosed carbon nitride/Fe-based MIL heterojunction for efficient CO2 photoreduction

Designing structures such as heterojunctions to establish built-in electric fields, introduces inherent driving forces for charge separation and migration. The partial surface contact in the current g-C3N4/MIL-88B(Fe) heterojunction composites limits the migration capability of interfacial charges and the formation of a built-in electric field. In this study, we fabricated a built-in electric field in the fully enclosed g-C3N4/MIL-88B(Fe) (CNNS/M-NS) heterojunction using electrostatic self-assembly. The electric field facilitated the migration of photo-excited electrons from the M-NS conduction band to the CNNS valence band, while corresponding band bending prevented the electron backflow from the CNNS conduction band to the M-NS conduction band. The fully contacted CNNS/M-NS heterojunction demonstrated a CO yield of 13.09 μmol g−1 h−1, which was 5.62 times of pristine CNNS. This significant improvement was primarily due to the complete encapsulation of M-NS by CNNS, which improved charge separation efficiency and reduced the charge transfer resistance. DRIFTS tests confirmed that CNNS/M-NS effectively converted to CO through the sequential transformation of CO2*, COOH*, and CO* intermediates. DFT calculations revealed that M-NS had a higher work function than CNNS, leading to the charge transfer at the interface and the formation of a built-in electric field from CNNS to M-NS. This work proposes a novel design of fully enclosed g-C3N4/MIL-88B(Fe) heterojunctions using electrostatic self-assembly to improve CO2 photoreduction efficiency.

Multiple strategies enhance visible-light photocatalytic degradation levofloxacin of Fe-doped MOF/AgCl Z-scheme heterojunction composites based on pyrazole carboxylic ligand

The construction of visible-light catalysts to degrade water pollutants is significant in environmental governance and solar energy conversion. In this work, a novel Zn-MOF with unsaturated coordination sites was constructed using 1-(Carboxymethyl)-pyrazole-4-carboxylic acid as the organic ligand. Its crystal structure was studied through single crystal X-ray diffraction. To enhance visible light catalytic performance, ZnFe-MOF/AgCl-x Z-scheme heterojunction composites were constructed. The optimized ZnFe-MOF/AgCl-50 material exhibits excellent photocatalytic performance, which can degrade 90.33 % of levofloxacin in 21 min. The results indicate that Fe doping and the construction of the ZnFe-MOF/AgCl-x Z-scheme heterojunction not only broaden the responsive range to visible light, but also effectively promote the internal and interfacial charges transfer efficiency, leading to a superior catalytic performance. In addition, the Ag nanoparticles (NPs) generated during the photocatalytic process can serve as a bridge, achieving rapid charge transfer in Z-scheme heterojunction. This work can offer an innovative perspective for the development of novel and efficient MOF-based Z-scheme heterojunction photocatalysts for wastewater treatment applications.

Synthesis of SnO2-ZnO heterojunction composites for effective degradation of methylene blue and chromium (VI) under solar light irradiation

Synthesis of SnO2-ZnO heterojunction composites for effective degradation of methylene blue and chromium (VI) under solar light irradiation

Construction of S-scheme heterojunction via Cu2ZnSnS4 coupled with g-C3N4 for enhancing HER performance

It is shown that replacing non-noble metals with noble metals in photocatalytic water splitting is pivotal for increased and sustained hydrogen production. However, the challenge persists in designing and developing a cost-effective, highly active catalyst with effective carrier separation and providing sufficient H+ reduction sites to enhance photocatalytic H2 evolution efficiency. Herein, a series of S-scheme Cu2ZnSnS4/g-C3N4 (CZTS/CN) heterojunction composites were prepared via the hydrothermal method, followed by comprehensive characterizations for in-depth investigation. The TEM image exhibits a clear interface, showing the heterojunction formation between CZTS and CN nanosheets. The results show that incorporating CZTS cocatalyst significantly improves CN photocatalytic hydrogen evolution reaction (HER) and its performance is notably influenced by CZTS to CN mass ratio. Among CZTS/CN heterojunction composites, the 5% CZTS/CN heterojunction composite exhibited a significantly improved HER of 243.64 μmol g−1h−1, which is 29.4 and 7.08 folds superior as compared to CN (8.29 μmol g−1h−1) and CZTS (34.42 μmol g−1h−1), respectively. The mechanism study revealed that the excellent superior H2 evolution performance resulted from the established internal electric field (IEF) in p-n heterojunction, which expedites the efficient separation and migration of photoinduced carriers coupled with the distinctive flower-like configuration of CZTS offering a substantial surface area and enough active reduction sites for photocatalysis process. This work presents a rational design and an inexpensive and efficient heterojunction photocatalysis system suitable for diverse applications.

Construction of Ag3PO4/g-C3N4 Z-Scheme Heterojunction Composites with Visible Light Response for Enhanced Photocatalytic Degradation.

Ag3PO4/g-C3N4 photocatalytic composites were synthesized via calcination and hydrothermal synthesis for the degradation of rhodamine B (RhB) in wastewater, and characterized using X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), X-ray photoelectron spectroscopy (XPS), and diffuse reflectance spectroscopy (DRS). The degradation of RhB by Ag3PO4/g-C3N4 composites was investigated to evaluate their photocatalytic performance and cyclic degradation stability. The experimental results showed that the composites demonstrated notable photocatalytic activity and stability during degradation. Their high degradation efficiency is attributed to the Z-scheme transfer mechanism, in which the electrons in the Ag3PO4 conduction band and the holes in the g-C3N4 valence band are annihilated by heterojunction recombination, which greatly limits the recombination of photogenerated electrons and holes in the catalyst and enhances the activity of the composite photocatalyst. In addition, measurements of photocurrent (PC) and electrochemical impedance spectroscopy (EIS) confirmed that the efficient charge separation of photo-generated charges stemmed from strong interactions at the close contact interface. Finally, the mechanism for catalytic enhancement in the composite photocatalysts was proposed based on hole and radical trapping experiments, electron paramagnetic resonance (EPR) analysis, and work function evaluation.