A bifunctional catalyst for hydrogen evolution reaction: The interactive influences between CdS and MoS2 on photoelectrochemical activity

被引:25
作者
Ji, Jing [1 ]
Guo, Liangliang [1 ]
Li, Qian [1 ]
Wang, Feng [1 ]
Li, Zhilin [1 ]
Liu, Jingjun [1 ]
Jia, Yi [1 ]
机构
[1] Beijing Univ Chem Technol, Beijing Key Lab Electrochem Proc & Technol Mat, State Key Lab Chem Resource Engn, Beijing 100029, Peoples R China
关键词
CdS/MoS2; hybrid; Photocatalytic property; Electrocatalytic property; p-n heteroj unction; HER; Tafel slope; PHOTOCATALYTIC H-2 EVOLUTION; HIGH QUANTUM EFFICIENCY; VISIBLE-LIGHT; CADMIUM-SULFIDE; PT-PDS/CDS; WATER; NANOPARTICLES; COCATALYST; GRAPHENE; NANOCRYSTALS;
D O I
10.1016/j.ijhydene.2015.01.075
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
Bifunctional leaf-like CdS/MoS2 hybrids were successfully prepared by electrodeposition. The interactive influences between MoS2 and CdS on the photoelectrocatalytic activity for catalyst of CdS/MoS2 were characterized by analyzing the current density (J)-potential (V) curves of cathodic and anodic polarization. On the one hand, the CdS/MoS2 hybrid showed the improved photoelectrochemical performance which was attributed to the visible light absorption enhanced by MoS2 and the formation of p-n junction between CdS and MoS2. On the other hand, the CdS/MoS2 hybrid exhibited superior electrocatalytic activity in the hydrogen evolution reaction (HER) relative to the MoS2 catalyst. A Tafel slope of -42 mV/decade was measured for CdS/MoS2 hybrid in the HER, which exceeded by far the activity of previous MoS2 catalysts and resulted from the abundance of catalytic edge sites on the MoS2 nanoparticles. The Tafel slope of similar to 42 mV/decade suggested the Volmer_Heyrovsky mechanism for the CdS/MoS2-catalyzed HER, with electrochemical desorption of hydrogen as the rate-limiting step. Copyright (C) 2015, Hydrogen Energy Publications, LLC. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:3813 / 3821
页数:9
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