Highly efficient photocatalytic H2 evolution using the Ni2P-Zn0.5Cd0.5S photocatalyst under visible light irradiation

被引:78
|
作者
Shao, Zhuwang [1 ]
He, Yinna [1 ]
Zeng, Tiantian [1 ]
Yang, Yanan [1 ]
Pu, Xipeng [1 ]
Ge, Bo [1 ]
Dou, Jianmin [1 ]
机构
[1] Liaocheng Univ, Sch Mat Sci & Engn, Shandong Prov Key Lab Chem Energy Storage & Novel, Liaocheng 252000, Shandong, Peoples R China
关键词
Hydrogen evolution; Photocatalysis; Zn0.5Cd0.5S; Ni2P; REDUCED GRAPHENE OXIDE; HYDROGEN EVOLUTION; COMBUSTION SYNTHESIS; AQUEOUS-SOLUTIONS; H-2-PRODUCTION ACTIVITY; FACILE FABRICATION; COCATALYST; WATER; NI2P; COMPOSITE;
D O I
10.1016/j.jallcom.2018.08.064
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
The development of a highly-efficient co-catalyst using earth-abundant elements is important to improve photocatalytic H-2 evolution. Herein, we prepared Ni2P-Zn0.5Cd0.5S (NPZCS) porous composites suitable for photocatalytic H-2 evolution under visible light irradiation. The in-situ synthesis and loading of Ni2P nanoparticles onto the porous structure of ZCS was achieved in one-step by a hydrothermal method without the addition of any surfactants or templates. It was revealed that porous ZCS exhibited advanced photocatalytic performance. Furthermore, the optimized NPZCS showed remarkably enhanced photocatalytic activity for H-2 evolution under visible light irradiation. An optimal H-2 evolution rate of 912.57 mu mol.h(-1) was observed over NPZCS loaded with 0.125% Ni2P, with a calculated apparent quantum efficiency of 37.5% at 420 nm. Loading of the Ni2P co-catalyst provided active reaction sites, boosted the efficiency of photoinduced electron-hole pair separation and extended the lifetime of photoinduced charge, resulting in enhanced photocatalytic H-2 evolution efficiency under visible light irradiation. (C) 2018 Elsevier B.V. All rights reserved.
引用
收藏
页码:889 / 897
页数:9
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