Nickel nanoparticle-activated MoS2 for efficient visible light photocatalytic hydrogen evolution

被引:13
|
作者
Shi, Xinying [1 ,2 ]
Zhang, Meng [3 ]
Wang, Xiao [3 ]
Kistanov, Andrey A. [1 ]
Li, Taohai [1 ,4 ]
Cao, Wei [1 ]
Huttula, Marko [1 ]
机构
[1] Univ Oulu, Nano & Mol Syst Res Unit, POB 3000, FI-90014 Oulu, Finland
[2] Jiangsu Normal Univ, Sch Phys & Elect Engn, Xuzhou 221116, Jiangsu, Peoples R China
[3] East China Univ Sci & Technol, Dept Phys, Shanghai 200237, Peoples R China
[4] Xiangtan Univ, Minist Educ, Key Lab Environm Friendly Chem & Applicat, Coll Chem, Xiangtan 411105, Peoples R China
基金
中国国家自然科学基金; 欧洲研究理事会; 芬兰科学院;
关键词
CATALYTIC-ACTIVITY; MONOLAYER MOS2; BASAL-PLANE; WATER; SOLAR; DENSITY; DISPERSION; NANOSHEETS; SITES;
D O I
10.1039/d2nr01489k
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Direct sunlight-induced water splitting for photocatalytic hydrogen evolution is the dream for an ultimate clean energy source. So far, typical photocatalysts require complicated synthetic processes and barely work without additives or electrolytes. Here, we report the realization of a hydrogen evolution strategy with a novel Ni-Ag-MoS2 ternary nanocatalyst under visible/sun light. Synthesized through an ultrasound-assisted wet method, the composite exhibits stable catalytic activity for long-term hydrogen production from both pure and natural water. A high efficiency of 73 mu mol g(-1) W-1 h(-1) is achieved with only a visible light source and the (MoS2)(84)Ag10Ni6 catalyst, matching the values of present additive-enriched photocatalysts. Verified by experimental characterizations and first-principles calculations, the enhanced photocatalytic ability is attributed to effective charge migration through the dangling bonds at the Ni-Ag-MoS2 alloy interface and the activation of the MoS2 basal planes.
引用
收藏
页码:8601 / 8610
页数:11
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