Efficient Separation Of Photogenerated Charges Research Articles

Insights into the function of metallic 1T phase tungsten disulfide as cocatalyst decorated zinc indium sulfide for enhanced photocatalytic hydrogen production activity

Improving the separation efficiency of carriers is an important part of enhancing photocatalytic activity. Herein, we successfully decorated metallic 1T phase tungsten disulfide (1T-WS2) on the surface of zinc indium sulfide (ZnIn2S4) and investigated the synergistic effect of 1T-WS2 on ZnIn2S4. The characterization results show that 1T-WS2 improves the light absorption capacity and utilization efficiency, increases the catalytic active site, improves the photogenerated charge separation efficiency, and optimizes the reduction potential of ZnIn2S4. Theoretical calculations show that compared with ZnIn2S4, 1T-WS2/ZnIn2S4 has a smaller adsorption Gibbs free energy of the intermediate state H*, which is conducive to the catalytic reaction. Under simulated solar irradiation, the hydrogen (H2) production rate of 1T-WS2/ZnIn2S4 with a loading of 12 wt% reaches 30.90 mmol h−1 g−1, which is 3.38 times higher than that of single ZnIn2S4 (9.13 mmol h−1 g−1). In addition, the apparent quantum efficiency of 1T-WS2/ZnIn2S4 with a loading of 12 wt% reaches 21.14 % under monochromatic light at a wavelength of λ = 370 nm. This work analyzes the light absorption and carrier separation to the catalytic site, and elucidates the mechanism for the enhancement of the photocatalytic hydrogen production performance.

Efficient Proton Transfer and Charge Separation within Covalent Organic Frameworks via Hydrogen-Bonding Network to Boost H2O2 Photosynthesis.

Photocatalytic synthesis based on the oxygen reduction reaction (ORR) has shown great promise for H2O2 production. However, the low activity and selectivity of 2e- ORR result in a fairly low efficiency of H2O2 production. Herein, we propose a strategy to enhance the proton-coupled electron transfer (PCET) process in covalent organic frameworks (COFs), thereby significantly boosting H2O2 photosynthesis. We demonstrated that the construction of a hydrogen-bonding network, achieved by anchoring the H3PO4 molecular network on COF nanochannels, can greatly improve both proton conductivity and photogenerated charge separation efficiency of COFs. Thus, COF@H3PO4 exhibited superior photocatalytic performance in generating H2O2 without sacrificial agents, with a solar-to-chemical conversion efficiency as high as 0.69%. Results indicated that a much more localized spatial distribution of energy band charge density on COF@H3PO4 led to efficient charge separation, and the small energy barrier of the rate-limiting step from *OOH to H2O2 endowed COF@H3PO4 with higher 2e- ORR selectivity.

Enhanced Light Absorption and Photo-Generated Charge Separation Efficiency for Boosting Photocatalytic H2 Evolution through TiO2 Quantum Dots with N-Doping and Concomitant Oxygen Vacancy.

Low-range light absorption and rapid recombination of photo-generated charge carriers have prevented the occurrence of effective and applicable photocatalysis for decades. Quantum dots (QDs) offer a solution due to their size-controlled photon properties and charge separation capabilities. Herein, well-dispersed interstitial nitrogen-doped TiO2 QDs with stable oxygen vacancies (N-TiO2-x-VO) are fabricated by using a low-temperature, annealing-assisted hydrothermal method. Remarkably, electrostatic repulsion prevented aggregation arising from negative charges accumulated in situ on the surface of N-TiO2-x-VO, enabling complete solar spectrum utilization (200-800 nm) with a 2.5 eV bandgap. Enhanced UV-vis photocatalytic H2 evolution rate (HER) reached2757µmol g-1 h-1, 41.6 times higher than commercial TiO2 (66µmol g-1 h-1). Strikingly, under visible light, HER rate was 189µmol g-1 h-1. Experimental and simulated studies of mechanisms reveal that VO can serve as an electron reservoir of photo-generated charge carriers on N-doped active sites, and consequently, enhance the separation rate of exciton pairs. Moreover, the negative free energy (-0.35 V) indicates more favorable thermodynamics for HER as compared with bulk TiO2 (0.66 V). This research work paves a new way of developing efficient photocatalytic strategies of HER that are applicable in the sustainable carbon-zero energy supply.

0D/2D dual Fenton α-Fe2O3/Fe-doped g-C3N4 photocatalyst and the synergistic photo-Fenton catalytic mechanism insight

A novel dual Photo-Fenton photocatalyst Fe2O3–Fe–CN with excellent Fe(III)/Fe(II) conversion efficiency and trace metal ion leaching rate has been fabricated by in-situ deposition of α-Fe2O3 quantum dots on ultrathin porous Fe-doped carbon nitride (Fe–CN) nanosheets. The iron species in Fe–CN and α-Fe2O3 QDs constitute a mutually reinforcing dual Photo-Fenton effect. The 4% Fe2O3–Fe–CN showed superior performance with kobs values 8.60 and 4.80 folders greater than pure CN and Fe–CN, respectively. The synergistic effect between α-Fe2O3 QDs and the ultrathin porous structure of Fe–CN is the primary reason for the outstanding catalytic performance exhibited by α-Fe2O3/Fe–CN. On one hand, the ultrathin porous structure of Fe–CN promotes the rapid transfer of photogenerated electrons. On the other hand, the efficient photogenerated charge separation at the α-Fe2O3/Fe–CN interface enables more photogenerated electrons to participate in the Fe3+/Fe2+ conversion and H2O2 activation. The trapping experiments demonstrate that •OH and •O2− are the primary active species in TC degradation. This work presents novel insights into the design of efficient heterogeneous Fenton catalysts for practical applications.

Ternary heterojunction of cross-linked benzene Polymer/Bi2MoO6-Graphene oxide catalysts promote efficient adsorption and photocatalytic removal of oxytetracycline

Antibiotics are refractory degradable organic pollutants that present a significant hazard to water environments. In this work, a ternary composite (KB/BMO-GO) comprising of graphene oxide (GO), Bi2MoO6 (BMO), and a cross-linked benzene polymer (KB) was synthesized and applied to promote the synergistic adsorption-photocatalytic degradation of the refractory pollutant, oxytetracycline (OTC). The inclusion of GO and KB in the composite enhanced the OTC adsorption performance of the catalysts, and the construction of Z-scheme heterojunction promoted the photogenerated charge separation efficiency and broadened the range of light absorption, thereby enhancing the photocatalytic performance. Moreover, we compared the performance of catalysts loaded with different mass ratios of KB (x% KB/BMO-GO). Among them, the 15 % KB/BMO-GO catalyst sample had the best OTC degradation performance. Specifically, 15 % KB/BMO-GO could adsorb 69.7 % of OTC in 30 min, reaching an OTC degradation rate of 93.3 % under visible light irradiation. h+ and 1O2 are the main active substances in the photocatalytic process. In addition, the catalysts are acid-alkali and salt-resistant, as well as good reusability. This study provides a valuable reference for the preparation of highly efficient photocatalysts for synergistic adsorption-photodegradation processes.

S-scheme heterojunction Cu-porphyrin/TiO2 nanosheets with highly efficient photocatalytic reduction of CO2 in ambient air

Directly capturing CO2 in ambient air and converting it into value-added fuels using photocatalysis is a potentially valuable technology. In this study, Cu-porphyrin (tetrakis-carboxyphenyl porphyrin copper, CuTCPP) was innovatively anchored on the surface of TiO2 (titanium dioxide) nanosheets to form an S-scheme heterojunction. Based on this, a photocatalytic reaction system for stably converting CO2 in ambient air into value-added fuels at the gas–solid interface was constructed without addition of sacrificial agents and alkaline liquids. Under the illumination of visible light and sunlight, the evolution rate of CO is 56 μmol·g−1·h−1 and 73 μmol·g−1·h−1, respectively, with a potential CO2 conversion rate of 35.8 % and 50.4 %. The enhanced of photocatalytic performance is attributed to the introduction of CuTCPP, which provides additional active sites, significantly improves capture capacity of CO2 and the utilization of electrons. Additionally, the formation of S-scheme heterojunction expands the redox range and improves the separation efficiency of photo-generated charges.

Enhanced photocatalytic ammonia oxidation over WO3@TiO2 heterostructures by constructing an interfacial electric field

WO3 nanorods and xWO3@TiO2 (WO3/TiO2 mass ratio (x) = 1−5) photocatalysts were synthesized using the hydrothermal and sol-gel methods, respectively. The photocatalytic activities of xWO3@TiO2 for NH3 oxidation first increased and then decreased with a rise in TiO2 content. Among them, the heterostructured 3WO3@TiO2 photocatalyst showed the highest NH3 conversion (58 %) under the simulated sunlight irradiation, which was about two times higher than those of WO3 and TiO2. Furthermore, the smallest amounts of by-products (i.e., NO and NO2) were produced over 3WO3@TiO2. The enhancement in photocatalytic performance (i.e., NH3 conversion and N2 selectivity) of 3WO3@TiO2 was mainly attributed to the formed interfacial electric field between WO3 and TiO2, which promoted efficient separation and transfer of photogenerated charge carriers. Based on the results of reactive species trapping and active radical detection, photocatalytic oxidation of NH3 over 3WO3@TiO2 was governed by the photogenerated holes and superoxide radicals. This work combines two strategies of morphological regulation and interfacial electric field construction to simultaneously improve light utilization and photogenerated charge separation efficiency, which promotes the development of full-spectrum photocatalysts for the removal of ammonia.

Amine-Rich Hydrogels for Molecular Nanoarchitectonics of Photosystem II and Inverse Opal TiO2 toward Solar Water Oxidation.

Solar water oxidation is a crucial process in light-driven reductive synthesis, providing electrons and protons for various chemical reductions. Despite advances in light-harvesting materials and cocatalysts, achieving high efficiency and stability remains challenging. In this study, we present a simple yet effective strategy for immobilizing natural photosystems (PS) made of abundant and inexpensive elements, using amine-rich polyethylenimine (PEI) hydrogels, to fabricate organic/inorganic hybrid photoanodes. Natural PS II extracted from spinach was successfully immobilized on inverse opal TiO2 photoanodes in the presence of PEI hydrogels, leading to greatly enhanced solar water oxidation activity. Photoelectrochemical (PEC) analyses reveal that PS II can be immobilized in specific orientations through electrostatic interactions between the positively charged amine groups of PEI and the negatively charged stromal side of PS II. This specific orientation ensures efficient photogenerated charge separation and suppresses undesired side reactions such as the production of reactive oxygen species. Our study provides an effective immobilization platform and sheds light on the potential utilization of PS II in PEC water oxidation.

Amino Acid Modified Hyper‐Cross‐Linked Polymer Enabling High‐efficient Photocatalytic Amines Oxidation Coupled with H2O2 Production

AbstractThe simultaneous production of imine and hydrogen peroxide (H2O2) via photocatalytic aerobic amine oxidation is a bright way to obtain value added products, however, rapid recombination of photogenerated charge leads to low conversion efficiency and selectivity. Herein, a metal‐free amino acid modified hyper‐cross‐linked polymer (H3LP‐HCPs) photocatalyst was synthesized for photocatalytic amines oxidation by regulating the ratio of L‐phenylalanine (L‐Phe) and hexaphenylbenzene (Hex). The results showed that the H3LP‐HCPs photocatalyst with 1 : 3 molar ratio of L‐Phe and Hex achieves close to 100 % conversion efficiency and 100 % selectivity toward benzylamine oxidation under 455 nm blue LED lamp irradiation. Furthermore, a high yield of H2O2 (9.2 mmol ⋅ gcat−1 ⋅ h−1) was synchronously obtained in benzylamine oxidation. Experiments and time‐dependent density functional theory calculation results revealed that the N‐functional groups in H3LP‐HCPs photocatalyst not only remarkably broadens light‐response range, but also facilitates electrons transfer from L‐Phe to the Hex, thus accelerating photogenerated charge separation efficiency and the formation of reactive oxygen species (ROS).

Facile synthesis of self-nitrogen-doped carbon spheres for high-efficient photocatalytic CO2 reduction to CO

In this work, self-nitrogen-doped carbon microsphere photocatalysts were prepared by hydrothermal and carbonation pyrolysis with first application in photocatalytic CO2 reduction. Coupled with relevant characterization, nitrogen-doped carbon microspheres were successfully prepared and the introduction of nitrogen significantly improved the photogenerated charge separation efficiency and CO2 photoreduction to CO activity, leading to the highest photocatalytic reduction activity with a CO yield of 185.71 μmol g−1 (9 h) under simulated sunlight irradiation. More importantly, its performance remains at about 98 % after ten consecutive cycle tests, indicating the excellent active stability of self-nitrogen-doped carbon spheres. Possible mechanisms for photocatalytic reduction and the role of nitrogen in photocatalytic adsorption and reduction processes are analyzed and proposed. The research provides novel strategies for the design of bifunctional catalysts that offer robust adsorption and efficient reduction, enabling the sustainable conversion of CO2.

Enhanced Charge Transfer Process and Photocatalytic Activity over a Phosphonate-based MOF via Amorphization Strategy.

Recently, amorphous materials have gained great attention as an emerging kind of functional material, and their characteristics such as isotropy, absence of grain boundaries, and abundant defects are very likely to outrun the disadvantages of crystalline counterparts, such as low conductivity, and ultimately lead to improved charge transfer efficiency. Herein, we investigated the effect of amorphization on the charge transfer process and photocatalytic performance with a phosphonate-based metal-organic framework (FePPA) as the research object. Comprehensive experimental results suggest that compared to crystalline FePPA, amorphous FePPA has more distorted metal nodes, which affects the electron distribution and consequently improves the photogenerated charge separation efficiency. Meanwhile, the distorted metal nodes in amorphous FePPA also greatly promote the adsorption and activation of O2. Hence, amorphous FePPA exhibits a better performance of photocatalytic C(sp3)-H bond activation for selective oxidation of toluene to benzaldehyde. This work illustrates the advantages of amorphous MOFs in the charge transfer process, which is conducive to the further development of high performance MOFs-based photocatalysts.

Enhanced Charge Transfer Process and Photocatalytic Activity over a Phosphonate‐based MOF via Amorphization Strategy

AbstractRecently, amorphous materials have gained great attention as an emerging kind of functional material, and their characteristics such as isotropy, absence of grain boundaries, and abundant defects are very likely to outrun the disadvantages of crystalline counterparts, such as low conductivity, and ultimately lead to improved charge transfer efficiency. Herein, we investigated the effect of amorphization on the charge transfer process and photocatalytic performance with a phosphonate‐based metal–organic framework (FePPA) as the research object. Comprehensive experimental results suggest that compared to crystalline FePPA, amorphous FePPA has more distorted metal nodes, which affects the electron distribution and consequently improves the photogenerated charge separation efficiency. Meanwhile, the distorted metal nodes in amorphous FePPA also greatly promote the adsorption and activation of O2. Hence, amorphous FePPA exhibits a better performance of photocatalytic C(sp3)−H bond activation for selective oxidation of toluene to benzaldehyde. This work illustrates the advantages of amorphous MOFs in the charge transfer process, which is conducive to the further development of high performance MOFs‐based photocatalysts.

Promoting the carrier mobility of Nb2SiTe4 through cation coordination engineering

Ternary two-dimensional (2D) monoclinic Nb2SiTe4 has garnered significant attention for its potential applications in anisotropic photoelectronics. Yet, its intrinsic indirect bandgap nature and low hole mobility, attributed to the short Nb–Nb dimer configurations, hinder the efficient photogenerated carrier separation and transport. In this Letter, using density functional theory calculations, we demonstrate the interlayer intercalation of Si results in the formation of a metastable orthorhombic Nb2SiTe4 structure devoid of detrimental short Nb–Nb dimers. Notably, this Si intercalation leads to a remarkable reduction of hole effective masses of orthorhombic Nb2SiX4 (X = S, Se, and Te), a crucial factor for achieving high carrier mobility. Taking the orthorhombic Nb2SiTe4 monolayer as an example, the calculated hole mobility (>100 cm2 V−1 s−1) is comparable in magnitude to the respectable hole mobility observed in multiple layers of the monoclinic Nb2SiTe4. To simultaneously enhance electron and hole mobility, we establish a van der Waals junction between the monoclinic and orthorhombic Nb2SiTe4 structures, achieving high and comparable carrier mobilities. The Nb2SiTe4 junction exhibits a nearly direct bandgap of 0.35 eV, rendering it suitable for infrared light harvesting. Furthermore, carriers within the Nb2SiTe4 junction become spatially separated across different layers, resulting in an intrinsic built-in electric field, which is superior for efficient photo-generated charge separation and decreases the potential nonradiative carrier recombination. Our findings highlight the impact of cation coordination engineering on the electronic and optical properties of 2D Nb2SiTe4 and provide a feasible solution to achieve better carrier transport in low-dimensional photovoltaic functionalities.

Self-Powered and Broadband Photodetectors Based on High-performance Mixed Dimensional Sb2O3/PdTe2/Si Heterojunction for Multiplex Environmental Monitoring.

Solar-blind ultraviolet (SBUV) to near-infrared (NIR) broadband photodetectors (BB-PD) have important applications in environmental monitoring and other applications. However, it is challenging to prepare SBUV-IR photosensitive materials via simple steps and to construct SBUV-IR broadband devices for multiplex detection with high sensitivity at different wavelengths. Here, self-powered and broadband photodetectors using a high-performance mixed dimensional Sb2O3 nanorod 1-dimension (1D)/monodisperse microdiamond-like PdTe2 3-dimension (3D)/Si (3D) heterojunction for multiplex detection of environmental pollutants with high sensitivity at broadband wavelength are developed. The 1D/3D mixed dimensional Sb2O3/PdTe2/Si structure combines the advantages of strong light absorption, high carrier transport efficiency of 1D Sb2O3 nanorods, and expansion of interface barrier caused by 3D microdiamond-like PdTe2 interlayer to improve the photocurrent density and self-powered ability. The efficient photogenerated charge separation enables anon/off ratio of more than 5×106. The device exhibits excellent photoelectric properties from 255 to 980nm with the responsivity from 4.56×10-2 to 6.55×10-1AW-1, the detectivity from 2.36×1012 to 3.39×1013Jones, and the sensitivity from 3.90×107 to 1.10×1010cm2W-1 without external bias. Finally, the proposed device is applied for the multiplex monitoring of environmental pollution gases NO2 with the detection limit of 200ppb and PM2.5 particles at mild pollution at broadband wavelength. The proposed BB-PD has great potential for multiplex detection of environmental pollutants and other analytes at broadband wavelength.

Stabilizing electron-rich Ni single-atoms on black phosphorus nanosheets boosts photocatalytic carbon dioxide reduction

The development of unique single-atom catalysts with electron-rich feature is essential to promoting the photocatalytic CO2 reduction, yet remains a big challenge. Here, a conceptionally new single-atom catalyst constructed from atomically dispersed Ni–P3 species on black phosphorus (BP) nanosheets (BP-Ni) is synthesized for realizing highly efficient visible-light-driven CO2 reduction when trapping photogenerated electrons from homogeneous light absorbers in the presence of triethanolamine as the sacrificial agent. Both the experimental and theoretical calculation data reveal that the Ni–P3 species on BP nanosheets own the electron-rich feature that can improve the photogenerated charge separation efficiency and lower the activation barrier of CO2 conversion. This unique feature makes BP-Ni exhibit the much higher activity as cocatalyst in the photocatalytic CO2 reduction than BP nanosheets. The BP-Ni can also be applied as a cocatalyst for enhanced photocatalytic CO2 reduction after combining with CdSe/S colloidal crystal photocatalyst. The present study offers valuable inspirations for the design and construction of effective catalytic sites toward photocatalytic CO2 reduction reactions.

Boosted visible-light photocatalysis via p-n heterojunction synergy in 3D tin Sulfide-Graphitic carbon nitride nanohybrids

Creating superior nanohybrids with a narrow band gap to harness a larger portion of the solar spectrum is a contemporary necessity. In this study, we utilized a streamlined solvothermal approach to develop a three-dimensional, flower-like tin sulfide (3DF-SnS2) which was integrated atop graphitic nitride layers (g-C3N4). Using a suite of standardized characterization techniques, we delved deep into understanding the design intricacies, structural aspects, photophysical properties, chemical interplay, and surface dynamics of the produced nanohybrids. A noteworthy enhancement in the photocatalytic activity was observed in the p-n heterojunction (3DF-SnS2/g-C3N4) when tested under visible light using the benchmark organic pollutant, Rhodamine B (RhB). When pitted against other nanohybrids from this study, the optimized 3DF-SnS2/g-C3N4 structure displayed a remarkable aptitude for RhB degradation. This was largely due to its adept ability to segregate photo-generated charges efficiently and the harmonious synergy between the 3D and 2D structures, streamlining the charge transfer processes. This commendable photocatalytic efficacy can be attributed to several factors. First, band gap narrowing, the hybrid structure successfully reduces its band gap, allowing for a broader spectrum of solar energy absorption. Second, harmonized charge separation, the interplay between the 3D flower and the 2D sheet structures ensures an effective and efficient separation of photo-generated charges, optimizing their availability for catalytic reactions. 3D/2D Interface Dynamics: The interaction between the 3D floral configuration and the 2D sheet enhances charge mobility, further boosting efficiency. Third, enhanced surface area, the 3D flower-like design of SnS2, in conjunction with the planar nature of g-C3N4, offers abundant active sites for photocatalytic reactions.

Development of a novel ternary FeWO4/CoP/Mn0.5Cd0.5S composite photocatalyst for photocatalytic hydrogen evolution in watersplitting

The construction of a non-homogeneous photocatalyst system with the advantages of both efficient photogenerated charge separation efficiency and abundant number of active sites remains a major challenge in the field of photocatalysis. A new ternary MnCdS-based photocatalyst combined with FeWO4 and CoP modifications was successfully prepared by chemical precipitation and thermal reduction methods. The ternary FeWO4/CoP/Mn0.5Cd0.5S photocatalyst exhibited a maximum hydrogen evolution activity of 30.45 mmol⋅g−1⋅h−1, which was 6.86 times higher than that of pureMn0.5Cd0.5S. The enhancement of the hydrogen production performance of the FeWO4/CoP/Mn0.5Cd0.5Sphotocatalyst was attributed to the p-n heterojunction constructed at the interface of FeWO4 and Mn0.5Cd0.5S, which strengthened the charge separation ability of the system. On the other hand, the decoration of CoP remarkably diminishes the hydrogen evolution potential of the system and supplies richer active sites for the catalytic reaction.

A quadruple-strategy of modification on carbon nitride boosts oxygen reduction for high performance photocatalytic hydrogen peroxide production

This paper reports a quadruple-strategy for material design, simultaneously applying morphology control, group modification, defect engineering and alkali metal doping to the design of catalysts, and successfully constructing irregular clusters of carbon nitride (pMNK-CN) with excellent photogenerated carrier separation performance and structural stability. The pMNK-CN is an irregular flower cluster-like morphology with a nanosheet structure on the surface, and the repolymerization process of the prepolymer in the microvoid of the metal salt gives it an open pore structure. With the help of essential characterization, it was confirmed that the heptazine unit in the backbone underwent partial decomposition due to the etching of metal salts at high temperatures, reducing the overall polymerization and introducing cyano and nitrogen vacancies. Meanwhile, the potassium ion embedded in the lattice can induce the growth of ordered structures and thus improve the short-range order. The pMNK-CN possesses a hydrogen peroxide production efficiency of 240.0 μmol·g−1·h−1 in pure water, which is 31 times higher than that of bulk carbon nitride. And the apparent quantum efficiencies of pMNK-CN in the 380 and 420 nm bands are 17.5 % and 14.8 % in the presence of isopropanol. The effects of each modification strategies on the electronic structure of carbon nitride were investigated using First-Principles, and it was demonstrated that the multiple modification strategies synergistically enhanced the optical absorption, photogenerated charge separation efficiency, and lowered the reaction energy barrier, thus greatly contributing to the oxygen reduction to hydrogen peroxide performance.

Preparation of rose-like Bi2O2CO3 photocatalyst with enhanced performance for photocatalytic degradation of mineral flotation wastewater

Eight kinds of bismuth oxycarbonate (Bi2O2CO3, BOC) with different microscopic morphology were prepared to study the influence of microscopic morphology on its photocatalytic performance. The crystal structure and microscopic morphology of Bi2O2CO3 were regulated by different synthetic recipes and routes. The SEM and TEM show the samples can be classified into two-dimensional (2D) and three-dimensional (3D) Bi2O2CO3 materials. The BOC-8 possesses a rose-like structure and a specific surface area (SBET) of 44.93 m2/g. In the experiments of degrading mineral flotation agent sodium isobutyl xanthate (SIBX). The photocatalytic performance of 3D samples is generally superior to that of 2D samples, and BOC-8 exhibits the best photocatalytic performance. After 90 min of simulated sunlight irradiation, the degradation ratio of SIBX over BOC-8 is 92.41 %. The transient photocurrent-time curves, electrochemical impedance spectroscopy (EIS) and photoluminescence (PL) spectra show that BOC-8 has excellent photogenerated electron and hole separation efficiency. The degradation pathway of SIBX was explored. And the hydroxyl radicals (OH) is the main active oxygen species for SIBX degrading. The enhanced photocatalytic degradation performance of BOC-8 samples originated from the increase of SBET, improved light utilization and more efficient photogenerated charge separation caused by the formation of 3D structure.

Investigation on the Structural and Photocatalytic Performance of Oxygen-Vacancy-Enriched SnO2-CeO2 Heterostructures.

In this study, pure CeO2 and oxygen-vacancy-enriched SnO2-CeO2 composite materials were prepared using the sol-gel method, and their microstructures and photocatalytic properties were investigated. The results indicate that SnO2 coupling promotes the separation and transfer of photogenerated electrons and holes and suppresses their recombination. The 50% SnO2-CeO2 composite material exhibited a decreased specific surface area compared to pure CeO2 but significantly increased oxygen vacancy content, demonstrating the highest photogenerated charge separation efficiency and the best photocatalytic performance. After 120 min of illumination, the degradation degree of MB by the 50% SnO2-CeO2 composite material increased from 28.8% for pure CeO2 to 90.8%, and the first-order reaction rate constant increased from 0.002 min-1 to 0.019 min-1.