Position-selected cocatalyst modification on a Z-scheme Cd_(0.5)Zn_(0.5)S/NiTiO_(3) photocatalyst for boosted H_(2) evolution  

作　　者：Bifang Li Wenyu Guo Xue Feng Lu Yidong Hou Zhengxin Ding Sibo Wang 

机构地区：[1]State Key Laboratory of Photocatalysis on Energy and Environment,College of Chemistry,Fuzhou University,Fuzhou,Fujian,350116,PR China

出　　处：《Materials Reports(Energy)》2023年第4期52-59,共8页材料导报（能源）（英文）

基　　金：supported by the National Key R&D Program of China(2021YFA1502100 and 2022YFE0114800);the National Natural Science Foundation of China(22372035,22302039 and 22311540011).

摘　　要：Photocatalytic water splitting by semiconductors is a promising technology to produce clean H_(2) fuel,but the efficiency is restrained seriously by the high overpotential of the H_(2)-evolution reaction together with the high recombination rate of photoinduced charges.To enhance H_(2) production,it is highly desirable yet challenging to explore an efficient reductive cocatalyst and place it precisely on the right sites of the photocatalyst surface to work the proton reduction reaction exclusively.Herein,the metalloid NixP cocatalyst is exactly positioned on the Z-scheme Cd_(0.5)Zn_(0.5)S/NiTiO_(3)(CZS/NTO)heterostructure through a facile photodeposition strategy,which renders the cocatalyst form solely at the electron-collecting locations.It is revealed that the directional transfer of photoexcited electrons from Cd_(0.5)Zn_(0.5)S to Ni_(x)P suppresses the quenching of charge carriers.Under visible light,the CZS/NTO hybrid loaded with the Ni_(x)P cocatalyst exhibits an optimal H_(2) yield rate of 1103μmol h^(-1)(i.e.,27.57 mmol h^(-1)g^(-1)),which is about twofold of pristine CZS/NTO and comparable to the counterpart deposited with the Pt cocatalyst.Besides,the high apparent quantum yield(AQY)of 56%is reached at 400 nm.Further,the mechanisms of the cocatalyst formation and the H2 generation reaction are discussed in detail.

关 键 词：Photocatalysis Ni_(x)P COCATALYSTS Z-scheme H_(2)evolution 

分 类 号：O643.36[理学—物理化学] O644.1[理学—化学]