Accelerating water dissociation at carbon supported nanoscale Ni/NiO heterojunction electrocatalysts for high-efficiency alkaline hydrogen evolution

被引:19
|
作者
Li, Cong [1 ,2 ]
Xue, Jiang-Yan [1 ]
Zhang, Wei [1 ]
Li, Fei-Long [3 ]
Gu, Hongwei [1 ]
Braunstein, Pierre [4 ]
Lang, Jian-Ping [1 ,2 ]
机构
[1] Soochow Univ, Coll Chem Chem Engn & Mat Sci, Suzhou 215123, Peoples R China
[2] Chinese Acad Sci, Shanghai Inst Organ Chem, State Key Lab Organometall Chem, Shanghai 200032, Peoples R China
[3] Changshu Inst Technol, Sch Chem & Mat Engn, ,, Changshu 215500, Peoples R China
[4] Univ Strasbourg, Inst Chim, CNRS, UMR 7177, 4 Rue Blaise Pascal,CS 90032, F-67081 Strasbourg, France
基金
中国国家自然科学基金;
关键词
water dissociation; Ni; NiO heterojunction; metal-organic frameworks (MOFs) derivatives; hydrogen evolution reaction; reduction pyrolysis; METAL-ORGANIC FRAMEWORKS; BIFUNCTIONAL ELECTROCATALYSTS; DOPED GRAPHENE; POROUS CARBON; NANOPARTICLES; REDUCTION; COMPOSITE; CATALYSTS; ACID;
D O I
10.1007/s12274-022-5194-5
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 synergistic catalysis of heterojunction electrocatalysts for the multi-step process in hydrogen evolution reaction (HER) is a promising approach to enhance the kinetics of alkaline HER. Herein, we proposed a strategy to form nanoscale Ni/NiO heterojunction porous graphitic carbon composites (Ni/NiO-PGC) by reduction-pyrolysis of the preformed Ni-metal-organic framework (MOF) under H-2/N-2 atmosphere. Benefiting from low electron transfer resistance, increased number of active sites, and unique hierarchical micro-mesoporous structure, the optimized Ni/NiO-PGC(10-1-400) exhibited excellent electrocatalytic performance and robust stability for alkaline HER (eta(10) = 30 mV, 65 h). Density functional theory (DFT) studies revealed that the redistribution of electrons at the Ni/NiO interface enables the NiO phase to easily initiate the dissociation of alkaline H2O, and shifts down the d-band center of Ni and optimizes the H* adsorption-desorption process of Ni, thereby leading to extremely high HER activity. This work contributes to a further understanding of the synergistic promotion of the multi-step HER processes by heterojunction electrocatalysts.
引用
收藏
页码:4742 / 4750
页数:9
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