2D/2D Heterostructured CdS/WS2 with Efficient Charge Separation Improving H2 Evolution under Visible Light Irradiation

被引:136
|
作者
Zhang, Ke [1 ,2 ]
Fujitsuka, Mamoru [1 ]
Du, Yukou [2 ]
Majima, Tetsuro [1 ]
机构
[1] Osaka Univ, Inst Sci & Ind Res SANKEN, Mihogaoka 8-1, Osaka, Ibaraki 5670047, Japan
[2] Soochow Univ, Coll Chem Chem Engn & Mat Sci, Suzhou 215123, Peoples R China
基金
中国国家自然科学基金;
关键词
CdS; WS2; two dimerisional hetemstructure; photocatalytic H-2 evolution; charge separation; PHOTOCATALYTIC HYDROGEN EVOLUTION; REDUCED GRAPHENE OXIDE; CDS NANORODS; DRIVEN PHOTOCATALYST; METHANOL OXIDATION; WS2; NANOSHEETS; QUANTUM DOTS; ONE-POT; HYBRID; MOS2;
D O I
10.1021/acsami.8b04080
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
Efficient Efiicient water splitting for H-2 evolution sender visible light irradiation has attracted more attention for solving the global environmental and energy issues, but it is still a major, challenge to develop an earth-abundant and effluent photocatalyst. Herein, we report two-dimensional (2D))/2D heterostructured CdS/WS2, (CdS/WS2), composed of nano sheet CdS (CdS) and nanosheet WS2 (WS2), as an efficient photocatalyst for H-2 evolution. As a noble metal-free visible light-driven catalyst for H-2, evolution, CdS/WS2 with 10 wt % WS2 exhibited the largest H-2 evolution rate of 14.1 mmol g(-1) h(-1) under visible light,irradiation to be 8 times larger than that if pure Cds. The lifetime and dynamics of photogenerated electrons were evaluated by femtosecond time-resolved diffuse reflectance spectroscopy, indicating that WS2 works as an electron-trapping site and a cocatalyst to cause H-2 evolution under visible light irradiation. This work suggests that Cds/Ws(2) has great potential as a low-cost and highly efficient photocatalyst for water splitting.
引用
收藏
页码:20458 / 20466
页数:9
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