Lattice-Matched CoP/CoS2 Heterostructure Cocatalyst to Boost Photocatalytic H2 Generation

被引:56
|
作者
Hong, Xiaoyang [1 ]
Yu, Xiaohui [1 ]
Wang, Lele [1 ]
Liu, Qinqin [1 ]
Sun, Jingfang [2 ]
Tang, Hua [1 ]
机构
[1] Jiangsu Univ, Sch Mat Sci & Engn, Zhenjiang 212013, Jiangsu, Peoples R China
[2] Nanjing Univ, Jiangsu Prov Key Lab Vehicle Exhaust Pollut Contr, Nanjing 210000, Jiangsu, Peoples R China
基金
中国国家自然科学基金;
关键词
COBALT PHOSPHIDE; EFFICIENT; HETEROJUNCTION; NANOPARTICLES; G-C3N4; COP; NANOSTRUCTURES; CONSTRUCTION;
D O I
10.1021/acs.inorgchem.1c01716
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
Transition-metal phosphides and sulfides are considered as promising cocatalysts for the photocatalytic hydrogen evolution reaction (HER), and the cocatalytic effect can be improved by directed heterostructure engineering. In this study, a novel lattice-matched CoP/CoS2 heterostructure having a nano- sheet morphology was developed as an HER cocatalyst and integrated in situ onto graphitic carbon nitride (g-C3N4) nanosheets via a successive phosphorization and vulcanization route. First-principles density functional theory calculations evidenced that the construction of the lattice-matched CoP/CoS2 heterostructure resulted in the redistribution of interface electrons, enhanced metallic characteristics, and improved H* adsorption. As a result of these effects, the CoP/CoS2 heterostructure cocatalyst formed a 2D/2D Schottky junction with the g-C3N4 nanosheets, thus promoting photoelectron transfer to CoP/CoS2 and realizing fast charge-carrier separation and good HER activity. As expected, the CoP/CoS2 heterostructure exhibited excellent cocatalytic activity, and the optimal loading of the cocatalyst on g-C3N4 enhanced its HER activity to 3.78 mmol g(-1) h(-1). This work furnishes a new perspective for the development of highly active noble-metal-free cocatalysts via heterostructure engineering for water splitting applications.
引用
收藏
页码:12506 / 12516
页数:11
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