Common-cation based Z-scheme ZnS@ZnO core-shell nanostructure for efficient solar-fuel production

被引:56
作者
Li, Pan [1 ,2 ]
He, Tao [1 ,2 ]
机构
[1] Natl Ctr Nanosci & Technol, CAS Ctr Excellence Nanosci, CAS Key Lab Nanosyst & Hierarch Fabricat, Beijing 100190, Peoples R China
[2] Univ Chinese Acad Sci, Beijing 100049, Peoples R China
关键词
ZnS@ZnO; Core-shell nanostructure; Z-scheme mechanism; Photocatalysis; Solar fuel; VISIBLE-LIGHT IRRADIATION; STATE Z-SCHEME; CO2; REDUCTION; PHOTOCATALYTIC PERFORMANCE; ARTIFICIAL PHOTOSYNTHESIS; 2-STEP PHOTOEXCITATION; HYDROGEN EVOLUTION; ELECTRON MEDIATOR; CHARGE-TRANSFER; REDOX MEDIATOR;
D O I
10.1016/j.apcatb.2018.07.057
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Inspired by the nature photosynthesis, fabrication of Z-scheme system is an effective strategy to enhance the photocatalytic activity, via which photogenerated electrons and holes that take part in the redox reactions can be separated spatially and temporally, while their strong redox capability can still be preserved. It is of great importance to construct good Z-scheme demo systems, and yet a considerable challenge to verify the charge transfer direction, which is vital for designing and fabricating the photocatalytic systems with high efficiency. Here ZnS@ZnO core-shell nanostructures were fabricated via simply annealing ZnS(en)(0.5) precursor, which exhibited superior activity for solar fuel production to ZnS. The Z-scheme mechanism was proposed based on the experimental results of charge transfer study. Direct intimate contact is formed at interface due to in-situ growth with common Zn cation. Specifically, ZnSXO1-X( and/or defects may be formed at the interface, which behave like a mediator in a Z-scheme system. All these account for the observed efficient separation of charge carriers and enhanced activity of photocatalytic reduction.
引用
收藏
页码:518 / 524
页数:7
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