非阻塞I/O
材料科学
异质结
化学工程
离解(化学)
介孔材料
催化作用
分解水
氢
密度泛函理论
纳米技术
无机化学
化学
光催化
物理化学
计算化学
工程类
有机化学
生物化学
光电子学
作者
Cong Li,Jiangyan Xue,Wei Zhang,Feilong Li,Hongwei Gu,Pierre Braunstein,Jian‐Ping Lang
出处
期刊:Nano Research
[Springer Science+Business Media]
日期:2022-12-15
卷期号:16 (4): 4742-4750
被引量:48
标识
DOI:10.1007/s12274-022-5194-5
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 H2/N2 atmosphere. Benefiting from low electron transfer resistance, increased number of active sites, and unique hierarchical micro-mesoporous structure, the optimized Ni/NiO-PGC10−1−400 exhibited excellent electrocatalytic performance and robust stability for alkaline HER (η10 = 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.
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