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Electron transfer kinetics in CdS/Pt heterojunction photocatalyst during water splitting

Electron transfer kinetics in CdS/Pt heterojunction photocatalyst during water splitting

作     者:Jianjun Zhang Gaoyuan Yang Bowen He Bei Cheng Youji Li Guijie Liang Linxi Wang 张建军;杨高元;何博文;程蓓;李佑稷;梁桂杰;王临曦

作者机构:Laboratory of Solar FuelFaculty of Materials Science and ChemistryChina University of GeosciencesWuhan 430074HubeiChina Hubei Key Laboratory of Low Dimensional Optoelectronic Materials and DevicesHubei University of Arts and ScienceXiangyang 441053HubeiChina State Key Laboratory of Advanced Technology for Materials Synthesis and ProcessingWuhan University of TechnologyWuhan 430070HubeiChina College of chemistry and Chemical engineeringJishou UniversityJishou 416000HunanChina 

基  金:国家重点研发计划(2018YFB1502001) 国家自然科学基金(51961135303,51932007,U1905215,21871217,52073223) 中国博士后科学基金(2021TQ0310,2021TQ0311,2021M702990) 

出 版 物:《Chinese Journal of Catalysis》 (催化学报(英文))

年 卷 期:2022年第43卷第10期

页      码:2530-2538页

摘      要:Noble metal cocatalysts have shown great potential in boosting the performance of CdS in photocatalytic water ***,the mechanism and kinetics of electron transfer in noble-metal-decorated CdS during practical hydrogen evolution is not clearly ***,Pt-nanoparticle-decorated CdS nanorods(CdS/Pt)are utilized as the model system to analyze the electron transfer kinetics in CdS/Pt *** femtosecond transient absorption spectroscopy,three dominating exciton quenching pathways are observed and assigned to the trapping of photogenerated electrons at shallow states,recombination of free electrons and trapped holes,and radiative recombination of locally photogenerated electron-hole *** introduction of Pt cocatalyst can release the electrons trapped at the shallow states and construct an ultrafast electron transfer tunnel at the CdS/Pt *** CdS/Pt is dispersed in acetonitrile,the lifetime and rate for interfacial electron transfer are respectively calculated to be~5.5 ps and~3.5×10^(10) s^(−1).The CdS/Pt is again dispersed in water to simulate photocatalytic water *** lifetime of the interfacial electron transfer decreases to~5.1 ps and the electron transfer rate increases to~4.9×10^(10) s^(−1),confirming that Pt nanoparticles serve as the main active sites of hydrogen *** work reveals the role of Pt cocatalysts in enhancing the photocatalytic performance of CdS from the perspective of electron transfer kinetics.

主 题 词:Femtosecond transient absorption spectroscopy Photocatalytic water splitting CdS Electron transfer kinetics Trap state 

学科分类:081702[081702] 081704[081704] 081705[081705] 07[理学] 0806[工学-电气类] 08[工学] 0817[工学-轻工类] 070304[070304] 0827[工学-食品科学与工程类] 0805[工学-能源动力学] 0703[理学-化学类] 0702[理学-物理学类] 

核心收录:

D O I:10.1016/S1872-2067(22)64108-1

馆 藏 号:203115085...

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