Metal-organic frameworks derived N,S,O-doped carbon sheets coated CoP/Co3S4 hybrids for enhanced electrocatalytic hydrogen evolution reaction

被引:15
作者
Jiang, Wei [1 ,2 ]
Jiang, Yu [1 ]
Wang, Jia [1 ]
Wu, Yuanyuan [1 ]
Zhou, Shi [1 ]
Liu, Bo [1 ]
Li, Hongji [1 ,3 ]
Zhou, Tianyu [1 ,3 ]
Liu, Chunbo [1 ,2 ]
Che, Guangbo [1 ,3 ]
机构
[1] Jilin Normal Univ, Key Lab Preparat & Applicat Environm Friendly Mat, Minist Educ, Changchun 130103, Peoples R China
[2] Jilin Normal Univ, Coll Environm Sci & Engn, Siping 136000, Peoples R China
[3] Baicheng Normal Univ, Baicheng 137000, Peoples R China
关键词
Metal-organic framework; Hydrogen evolution reaction; Electrocatalyst; PERFORMANCE;
D O I
10.1016/j.ijhydene.2022.06.217
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
Evidence shows that embedding metal-based hybrid into carbon matrix is an up-and-coming method to improve the efficiency and decrease the cost of electrocatalysts. Here-in, by using a metal-organic framework (MOF) with 4,4-bipyridine and 2,5-thiophenedicarboxylic acid as a precursor, a CoP/Co3S4 hybrid embedded into N, S, O -doped carbon sheets (CoP/Co3S4@NSOC) was constructed through pyrolysis and phosphorization processes. The lamellar morphology, hetero-atom doping, and graphite carbon were favorable for fast electron and mass transfer. Moreover, the strong intrinsic activities of CoP and Co3S4 promoted electrocatalytic performance. In the electrochemical experiments, CoP/Co3S4@NSOC showed the lowest overpotential of 132 mV@10 mA cm(-2) for hydrogen evolution reaction (HER) among all the precursors. In addition, the electro-catalytic activity and structure of CoP/Co3S4@NSOC exhibited long-term stability over 60 h. The present work provides a feasible strategy for the construction of robust MOF-derived electrocatalysts. (c) 2022 Hydrogen Energy Publications LLC. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:28894 / 28903
页数:10
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