MOF-derived Co/Co3O4/C hollow structural composite as an efficient electrocatalyst for hydrogen evolution reaction

被引:26
|
作者
Do, Ha Huu [1 ]
Tekalgne, Mahider Asmare [1 ]
Tran, Vy Anh [1 ,2 ]
Van Le, Quyet [3 ]
Cho, Jin Hyuk [3 ]
Ahn, Sang Hyun [1 ]
Kim, Soo Young [3 ]
机构
[1] Chung Ang Univ, Sch Chem Engn & Mat Sci, 84 Heukseok Ro, Seoul 06974, South Korea
[2] Gachon Univ, Dept Chem & Biol Engn, 1342 Seongnamdaero, Seongnam Si 13120, South Korea
[3] Korea Univ, Inst Green Mfg Technol, Dept Mat Sci & Engn, 145 Anam Ro, Seoul 02841, South Korea
基金
新加坡国家研究基金会;
关键词
Metal-organic frameworks; Cobalt; Cobalt oxide; Electrocatalyst; Hydrogen evolution reaction; BIFUNCTIONAL ELECTROCATALYSTS; ACTIVE ELECTROCATALYST; OXYGEN; CATALYSTS; ENERGY; WATER; HETEROSTRUCTURES; OXIDATION; NANOSTRUCTURES; MICROSPHERES;
D O I
10.1016/j.fuel.2022.125468
中图分类号
TE [石油、天然气工业]; TK [能源与动力工程];
学科分类号
0807 ; 0820 ;
摘要
Stable, efficient catalysts are crucial for electrochemical water splitting. Metal-organic frameworks (MOFs) can be used to create electrocatalysts meeting these criteria; however, the lack of high-quality electrode materials for the hydrogen evolution reaction impedes their adoption. In this study, a hollow-structured Co/Co3O4/C composite was prepared using a Co-based MOF precursor through a two-step pyrolysis-oxidation process. This composite outperformed nonhollow Co/Co3O4/C structures as well as hollow Co/C and Co3O4/C composites as a catalyst for hydrogen production in alkaline media. It had a low overvoltage of 169 mV at a current density of 10 mA cm(-2) and a moderate Tafel slope of 60.7 mV dec-(1). Moreover, it exhibited remarkable durability with 2000 cycles and 12 h of testing. This can be attributed to the synergistic effect of Co, Co3O4, and the hollow morphological architecture, which promote the dissociation of HO-H bonds, recombination of hydrogen intermediates, and efficient electron transfer. The results of this study are highly promising for the fabrication of cost-effective electrode materials for water splitting.
引用
收藏
页数:8
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