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Metal-organic frameworks derived N,S,O-doped carbon sheets coated CoP/Co3S4 hybrids for enhanced electrocatalytic hydrogen evolution reaction
被引:14
|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.
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页码:28894 / 28903
页数:10
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