In Situ Growth of CoP Nanoparticles Anchored on Black Phosphorus Nanosheets for Enhanced Photocatalytic Hydrogen Production

被引:68
作者
Liang, Qingshuang [1 ]
Shi, Fangbing [2 ]
Xiao, Xiufeng [1 ]
Wu, Xiaofeng [2 ]
Huang, Keke [2 ]
Feng, Shouhua [2 ]
机构
[1] Fujian Normal Univ, Coll Chem & Mat Sci, Fuzhou 350007, Fujian, Peoples R China
[2] Jilin Univ, Coll Chem, State Key Lab Inorgan Synth & Preparat Chem, Changchun 130012, Jilin, Peoples R China
基金
中国国家自然科学基金;
关键词
heterostructures; hydrogen; nanoparticles; phosphorus; photocatalysis; HIGHLY EFFICIENT; NICKEL PHOSPHIDE; EVOLUTION; WATER; CATALYST; ANODE; ELECTROCATALYSTS; PERFORMANCE; H-2;
D O I
10.1002/cctc.201701907
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
A novel zero-dimensional/two-dimensional CoP/black phosphorus heterostructure was successfully constructed by insitu growth of CoP nanoparticles on the surface of black phosphorus (BP) nanosheets through a facile solvothermal method. The as-prepared CoP/BP heterostructure exhibited excellent photocatalytic H-2 production activity under visible- and near-infrared-light irradiation. The hydrogen evolution rate of the CoP/BP heterostructure was 694 mu mol h(-1) g(-1), which is about two times higher than that of the Pt/BP heterostructure. The insitu growth of CoP nanoparticles in black phosphorus nanosheets gives rise to excellent interfacial contact between the light-harvesting material and the co-catalysts, promotes fast charge transfer, and reduces charge recombination. Because the CoP nanoparticles are anchored on the surface of the BP nanosheets, agglomeration of the CoP nanoparticles is suppressed, and thus, the high surface area and large number of active sites are effectively maintained.
引用
收藏
页码:2179 / 2183
页数:5
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