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Science China Materials 2023年第10期66卷 4133-4134页

作者： linxi wang Jiaguo Yu Laboratory of Solar Fuel Faculty of Materials Science and ChemistryChina University of GeosciencesWuhan 430078China

Hydrogenation refers to the addition of hydrogen(H)atoms to unsaturated bonds.It is one of the most important transformation reactions in the organic synthesis of chemicals and pharmaceuticals[1].Based on different hy... 详细信息

关键词： hydrogenation transfer bonds

Photodeposition of CoOx and MoS2 on CdS as dual cocatalysts for photocatalytic H2 production

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Journal of Materials Science & Technology 2022年第29期124卷 209-216页

作者： Tingmin Di Quanrong Deng Geming wang Shenggao wang linxi wang Yuhua Ma Hubei Key Laboratory of Plasma Chemistry and Advanced Materials School of Materials Science and EngineeringWuhan Institute of TechnologyWuhan 430205China Laboratory of Solar Fuel Faculty of Materials Science and ChemistryChina University of GeosciencesWuhan 430074China College of Chemistry and Chemical Engineering Xinjiang Normal UniversityUrumqi 830054China

Photocatalytic Hproduction from water splitting has a promising prospect for alleviating energy and environmental issues.However,the fast recombination of photogenerated charge carriers limits the photocatalytic efficiency and its practical application.Cocatalyst engineering is an effective strategy to spatially separate photogenerated charge carriers.In this work,noble-metal-free MoSand CoOcocatalysts are loaded on CdS nanorods by a two-step photodeposition method.The MoSfunctions as the reduction cocatalyst to trap electrons and Co Oas the oxidation cocatalyst to trap holes.Transmission electron microscopy(TEM),inductively coupled plasma(ICP),X-ray photoelectron spectroscopy(XPS)and MottSchottky results demonstrate the effectiveness of photodeposition for loading MoSand CoOdual cocatalysts on CdS and their impact on the photochemical properties.The optimized CdS-MoS-CoOcomposite exhibits a high photocatalytic H-production rate of 7.4 mmol g^(-1)h^(-1)and an apparent quantum efficiency(QE)of 7.6%at 420 nm.Further analysis on time-resolved photoluminescence(TRPL)indicates that the introduction of dual cocatalysts greatly prolongs the lifetime of photogenerated charge carriers and deceases the charge recombination rates,consequently leading to superior photocatalytic H-production performance.This work provides a facile and effective strategy for the construction of highly efficient dual-cocatalyst-modified CdS photocatalyst for high-performance photocatalytic Hproduction.

关键词： Photocatalytic H2 production CdS Dual cocatalysts MoS2 CoOx Photodeposition

Review on g-C_(3)N_(4)-based S-scheme heterojunction photocatalysts

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Journal of Materials Science & Technology 2022年第30期125卷 128-144页

作者： Yunfeng Li Zhiling Xia Qing Yang linxi wang Yan Xing Xi’an Key Laboratory of Textile Chemical Engineering Auxiliaries College of Environmental and Chemical EngineeringXi’an Polytechnic UniversityXi’an 710000China Laboratory of Solar Fuel Faculty of Materials Science and ChemistryChina University of GeosciencesWuhan 430074China Jilin Provincial Key Laboratory of Advanced Energy Materials Department of ChemistryNortheast Normal UniversityChangchun 130024China

With the rapid development of economy and modern industry,serious environmental pollution and energy shortage have become major urgent challenges to the human society.Photocatalysis is a promising technology to provide green energy.As a typical metal-free polymer photocatalyst,g-C_(3)N_(4) has attracted more and more attention due to its excellent performance.Unfortunately,the fast recombination of photo-induced charges,limited light response range as well as weak oxidation ability are still the key drawback that restrict the photocatalytic performance of g-C_(3)N_(4).These problems can be effectively addressed by constructing g-C_(3)N_(4)-based heterojunctions with two or more semiconductor materials,during which the respective advantages can be integrated.Up to now,the various oxidation semiconductor photocatalysts have been tried to construct the novel S-scheme heterojunction photocatalysts with g-C_(3)N_(4).Thus,this review provides a comprehensive introduction of g-C_(3)N_(4)-based S-scheme heterojunctions,including the main characteristics of the S-scheme heterojunction,photocatalytic mechanisms,design rules and preparation methods of g-C_(3)N_(4)-based S-scheme heterojunction photocatalysts.Moreover,this review summarizes recently reported works on the potential applications of g-C_(3)N_(4)-based S-scheme photocatalysts in various important photocatalytic reactions,including photocatalytic hydrogen production,photocatalytic degradation of contaminants,photo-reduction of CO_(2) into fuels,and photocatalytic sterilization.Finally,based on the current research progress,we propose some shortages in the preparation methods and applications of g-C_(3)N_(4)-based S-scheme heterojunctions,which are to be further investigated and resolved in this promising and creative research field.

关键词： Photocatalysis Semiconductor g-C_(3)N_(4) Heterojunction S-scheme

3D ordered macroporous sulfur-doped g-C_(3)N_(4)/TiO_(2)S-scheme photocatalysts for efficient H_(2)O_(2)production in pure water

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Journal of Materials Science & Technology 2023年第31期162卷 1-10页

作者： Zicong Jiang Qing Long Bei Cheng Rongan He linxi wang State Key Laboratory of Advanced Technology for Materials Synthesis and Processing Wuhan University of TechnologyWuhan 430070China Hunan Key Laboratory of Applied Environmental Photocatalysis Changsha UniversityChangsha 410022China Laboratory of Solar Fuel Faculty of Materials Science and ChemistryChina University of GeosciencesWuhan 430074China

Photocatalytic hydrogen peroxide(H_(2)O_(2))production offers a clean and cost-efficient alternative to the traditional anthraquinone oxidation approach.Herein,a step-scheme(S-scheme)heterojunction photocat-alyst is fabricated by coupling TiO_(2)with three dimensionally ordered macroporous sulfur-doped graphitic carbon nitride(3DOM SCN/T)by electrostatic self-assembly.The optimized photocatalyst achieved a high photocatalytic H_(2)O_(2)production activity with a yield of 2128μmol h^(−1)g^(−1)without the addition of hole scavengers.The remarkable performance was attributed to the synergy between the 3DOM framework and the S-scheme heterojunction.The former enhances light harvesting and provides abundant active sites for surface reactions,while the latter promotes the spatial separation of photogenerated carriers and enhances the redox power.Finally,the mechanism of photocatalytic H_(2)O_(2)production over the 3DOM SCN/T S-scheme composite is proposed.This work provides novel insights into the development of effi-cient photocatalysts for H_(2)O_(2)production from water and O_(2).

关键词： Photocatalysis Step-scheme heterojunction Three dimensionally ordered macroporous Hydrogen peroxide O_(2)reduction reaction

TiO_(2)/In_(2)S_(3)S-scheme photocatalyst with enhanced H_(2)O_(2)-production activity

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Nano Research 2023年第4期16卷 4506-4514页

作者： Yi Yang Bei Cheng Jiaguo Yu linxi wang Wingkei Ho State Key Laboratory of Advanced Technology for Materials Synthesis and Processing Wuhan University of TechnologyWuhan 430070China Laboratory of Solar Fuel Faculty of Materials Science and ChemistryChina University of Geosciences388 Lumo RoadWuhan 430074China Department of Science and Environmental Studies The Education University of Hong KongTai PoHong Kong 999077China

Photocatalytic production of hydrogen peroxide(H_(2)O_(2))is an ideal pathway for obtaining solar fuels.Herein,an S-scheme heterojunction is constructed in hybrid TiO_(2)/In_(2)S_(3)photocatalyst,which greatly promotes the separation of photogenerated carriers to foster efficient H_(2)O_(2)evolution.These composite photocatalysts show a high H_(2)O_(2)yield of 376μmol/(L·h).The mechanism of charge transfer and separation within the S-scheme heterojunction is well studied by computational methods and experiments.Density functional theory and in-situ irradiated X-ray photoelectron spectroscopy results reveal distinct features of the S-scheme heterojunction in the TiO_(2)/In_(2)S_(3)hybrids and demonstrate charge transfer mechanisms.The density functional theory calculation and electron paramagnetic resonance results suggest that O_(2)reduction to H_(2)O_(2)follows stepwise one-electron processes.In_(2)S_(3)shows a much stronger interaction with O_(2)than TiO_(2)as well as a higher reduction ability,serving as the active sites for H_(2)O_(2)generation.The work provides a novel design of S-scheme photocatalyst with high H_(2)O_(2)evolution efficiency and mechanistically demonstrates the improved separation of charge carriers.

关键词： step-scheme heterojunction photocatalytic H_(2)O_(2)production TiO_(2)/In_(2)S_(3)nanofibres

Light-enhanced metal-support interaction for synergetic photo/thermal catalytic formaldehyde oxidation

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Journal of Materials Science & Technology 2023年第36期167卷 74-81页

作者： Jiawei Ye linxi wang Bicheng Zhu Bei Cheng Rongan He Laboratory of Solar Fuel Faculty of Materials Science and ChemistryChina University of GeosciencesWuhan 430078China State Key Laboratory of Advanced Technology for Materials Synthesis and Processing Wuhan University of TechnologyWuhan 430070China Hunan Key Laboratory of Applied Environmental Photocatalysis Changsha UniversityChangsha 410022China

The strong metal-support interaction(SMSI)plays a pivotal role in regulating electronic properties and activating surface oxygen species.In this work,we report light-irradiation-modulated SMSI for enhanced formaldehyde(HCHO)oxidation.Specifically,the SMSI between Pt nanoparticles(NPs)and Bi_(2)MoO_(6)cre-ated surface-active oxygen at Pt-Bi_(2)MoO_(6)interfaces to activate HCHO to dioxymethylene(DOM).Notably,light irradiation boosted the SMSI and catalytic activity.Moreover,photogenerated holes in Bi_(2)MoO 6 im-proved HCHO adsorption and activation,while photogenerated electrons migrated from Bi_(2)MoO_(6)to Pt NPs to promote O_(2)adsorption and activation,accelerating the oxidation of DOM to CO_(2)and H_(2)O.The light-modulated SMSI and the synergy between photocatalysis and thermocatalysis lead to enhanced cat-alytic oxidation activity,providing a practical strategy for indoor volatile organic compound(VOC)de-composition under ambient conditions.

关键词： Formaldehyde oxidation Strong metal-support interaction Photocatalysis Photo-thermal synergy Electron transfer

Electron transfer dynamics in Schottky junction photocatalyst during electron donor-assisted hydrogen production

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Journal of Materials Science & Technology 2023年第28期159卷 1-9页

作者： Jianjun Zhang Jingjing Liu Zheng Meng Sanjib Jana linxi wang Bicheng Zhu Laboratory of Solar Fuel Faculty of Materials Science and ChemistryChina University of Geosciences68 Jincheng StreetWuhan 430078China School of Chemistry Chemical Engineering and BiotechnologyNanyang Technological University21 Nanyang LinkSingapore 637371Singapore Jiangxi Key Laboratory of Surface Engineering Jiangxi Science and Technology Normal UniversityNanchang 330038China

Electron donors(EDs)are widely used to improve the H 2 production performance of Schottky junction photocatalysts,but the functions of EDs are still unknown from the perspective of electron transfer dy-namics.Herein,Pt nanocluster-decorated CdS nanorod is successfully prepared to construct a typical CdS/Pt Schottky junction.Pt nanoclusters with a diameter of∼2 nm are deposited on the surface of CdS nanorods by in situ photoreduction at sub-zero temperature.The CdS/Pt photocatalyst using lactic acid shows a higher H_(2)production rate of 4762μmol g^(-1)h^(-1)compared to that using methanol,tri-ethanolamine,and glycerol.To understand the cause,the dynamics of photogenerated carriers in CdS/Pt photocatalysts during ED-assisted H_(2)production are revealed by femtosecond transient absorption spec-troscopy.Among the four organic EDs,lactic acid enables the fastest electron transfer rate of 1.8×10^(9)s^(-1)and the highest electron transfer efficiency of 76%at the CdS/Pt interface due to the most efficient hole consumption.This work sheds light on the importance of efficient interfacial electron transfer for im-proving the photocatalytic performance of Schottky junction photocatalysts.

关键词： Transient absorption spectroscopy Interfacial electron transfer Electron transfer rate Electron transfer efficiency Hole consumption

BiOBr/COF S-scheme photocatalyst for H_(2)O_(2) production via concerted two-electron pathway

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Journal of Materials Science & Technology 2023年第35期166卷 241-249页

作者： Haozhen Zhang Jingjing Liu Yong Zhang Bei Cheng Bicheng Zhu linxi wang Laboratory of Solar Fuel Faculty of Materials Science and ChemistryChina University of Geosciences68 Jincheng StreetWuhan 430078China State Key Laboratory of Advanced Technology for Materials Synthesis and Processing Wuhan University of TechnologyWuhan 430070China

Constructing step-scheme(S-scheme)heterojunctions has become a popular strategy for efficient pho-tocatalytic H_(2)O_(2) generation.Herein,we in situ grew BiOBr nanosheets(NSs)on a Schiff-base covalent organic framework(COF)with largeπ-conjugated structures to prepare S-scheme BiOBr/COF photocat-alysts for H_(2)O_(2) synthesis.The highest photocatalytic H_(2)O_(2) production performance of the composite sample constituting the S-scheme heterojunction is 3749μmol g−1 h−1,which was 1.85 and 27 times the rates of COF and BiOBr,respectively.The construction of S-scheme heterojunction contributed to ef-ficient carrier transfer and separation in space and enhanced redox power.Moreover,the lying-down O_(2)-adsorption configuration on the COF surface favors the concerted two-electron O_(2) reduction process,which greatly reduced the reduction potential requirement for O_(2)-to-H_(2)O_(2) conversion.The synergy be-tween the S-scheme heterojunction and the unique O_(2)-COF interaction boosted photocatalytic H_(2)O_(2) pro-duction activity.

关键词： S-scheme heterojunction Photocatalytic H_(2)O_(2)production Covalent organic frameworks Concerted two-electron O_(2)reduction O_(2)-adsorption configuration

Molecular-level Engineering of S-scheme Heterojunction:the Site-specific Role for Directional Charge Transfer

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Chinese Journal of Structural Chemistry 2022年第6期41卷 3-5页

作者： Jianjun Zhang linxi wang Mitra Mousavi Jahan B.Ghasemi Jiaguo Yu Laboratory of Solar Fuel Faculty of Materials Science and ChemistryChina University of GeosciencesWuhan 430074China School of Chemistry College of ScienceUniversity of TehranP.O.Box 14155-6455TehranIran

The promising S-scheme heterojunction photocatalysts are considered as a novel frontier due to their superiority in various solar-driven energy-related applications.Recently,a novel atom-specific tailoring strategy has been introduced on the construction of S-scheme het-erojunction for promoting the electronic transferability.The S-scheme heterojunction is regulated by integrating high-crystalline carbon nitride with Co-doped CeO_(2).Specifically,this atom-specific regulation of S-scheme heterojunction boosts directional electron-driving effect towards functionalized Co sites,benefit-ing for effective photogenerated charge carrier transferability.Moreover,a series of tracking characterizations show that Co-embedded modification promotes CO_(2)photoreduction into hydrogenation steps,resulting in high performance towards CO_(2)-to-CH_(4)photoreduction,which provides new opportunities for the development of multifunctional cooperation in heterogeneous photocatalysis.

关键词： S-scheme heterojunction functionalized Co-doped regulation directional electron-driving effect CO_(2)photoreduction

S-scheme ZnO/WO3 heterojunction photocatalyst for efficient H2O2 production

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Journal of Materials Science & Technology 2022年第29期124卷 193-201页

作者： Zicong Jiang Bei Cheng Yong Zhang S.Wageh Ahmed A.Al-Ghamdi Jiaguo Yu linxi wang State Key Laboratory of Advanced Technology for Materials Synthesis and Processing Wuhan University of TechnologyWuhan 430070China Laboratory of Solar Fuel Faculty of Materials Science and ChemistryChina University of GeosciencesWuhan 430074China Department of Physics Faculty of ScienceKing Abdulaziz UniversityJeddah 21589Saudi Arabia

Designing highly efficient photocatalyst for hydrogen peroxide(HO)production is an ideal strategy to avoid the shortcomings of traditional HOproduction and to realize the conversion of solar energy to chemical energy.In this work,a step-scheme(S-scheme)heterojunction photocatalyst composed of Zn O and WOis carefully prepared by hydrothermal and calcination method for efficient photocatalytic HOproduction.The ZW30 composite photocatalysts exhibit enhanced activity with the highest HO-production rate of 6788μmol Lh.The results show that the photocatalytic HOproduction process is dominated by a direct two-electron Oreduction pathway.The enhanced photocatalytic HO-production activity is attributed to the formation of interfacial internal electric field(IEF)in the S-scheme heterojunction,which boosts the spatial separation of charge carriers and enables electrons with the strongest reduction power to participate in HOproduction.This work provides an in-depth insight of the great advantages of S-scheme heterojunction in photocatalytic HOproduction.

关键词： Photocatalysis Hydrogen peroxide Step-scheme heterojunction O2 reduction Zinc oxide