详细信息
Bimetallic MMoS4 (M = Ni, Co, Cu) cocatalysts architected CdS nanoflowers for synergistically boosting visible-light-driven photocatalytic H2 evolution from water and benzyl alcohol ( SCI-EXPANDED收录 EI收录) 被引量:7
文献类型:期刊文献
英文题名:Bimetallic MMoS4 (M = Ni, Co, Cu) cocatalysts architected CdS nanoflowers for synergistically boosting visible-light-driven photocatalytic H2 evolution from water and benzyl alcohol
作者:Li, Chunhe[1,2];Du, Shiwen[3];Lu, Congrong[1,2];Ren, Kuankuan[1,2];Wang, Qi[1,2];Shan, Shunyi[1,2];Li, Qiang[1,2];Fang, Zebo[1,2];Li, Xiudong[1,2];Dou, Weidong[1,2]
机构:[1]Shaoxing Univ, Lab Low Dimens Carbon Mat, Shaoxing 312000, Peoples R China;[2]Shaoxing Univ, Sch Math Informat, Dept Phys, Shaoxing 312000, Peoples R China;[3]Chinese Acad Sci, Dalian Inst Chem Phys, Dalian Natl Lab Clean Energy, Dalian 116023, Peoples R China
年份:2022
卷号:924
外文期刊名:JOURNAL OF ALLOYS AND COMPOUNDS
收录:SCI-EXPANDED(收录号:WOS:000879067100001)、、EI(收录号:20220104686)、Scopus(收录号:2-s2.0-85135715806)、WOS
基金:This work is supported by the Natural Science Foundation of Zhejiang Province, China (Grant No. LQ21B030005, LQ22A040001 and LY19F040005) , Postdoctoral Science Foundation, China (No. 2021M692459) , and the National Natural Science Foundation of China (Grant No. 51872186) .
语种:英文
外文关键词:Photocatalytic H 2 evolution; Transition bimetal sulfides cocatalysts; DFT calculations
外文摘要:Exploring efficient photocatalysts to facilitate water splitting into green hydrogen (H2) energy is of great significance nowadays. In this work, we successfully synthesized CdS nanoflowers coated by zero -dimen-sional MMoS4 (M = Ni, Co, Cu) cocatalysts using a mild two-pot solvothermal method. Notably, 2.5%-NiMoS4/CdS catalyst exhibits optimal photocatalytic H2 evolution from benzyl alcohol aqueous solution under visible-light irradiation, and its photocatalytic H2 activity (7269.5 mu molGreek ano teleiah-1Greek ano teleiag-1) is 10.1 times higher than that of pure CdS (716.6 mu molGreek ano teleiah-1Greek ano teleiag-1). Simultaneously, benzyl alcohol can be synergistically converted into benzaldehyde after dehydrogenation. Such excellent photocatalytic performance mainly benefits from the existence of an internal electric field (IEF), which is demonstrated by experimental analysis and density functional theory calculations. And the IEF greatly accelerates the separation of electron-hole pairs during the photocatalytic H2 evolution process. (c) 2022 Elsevier B.V. All rights reserved.
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