过电位
电化学
材料科学
催化作用
氢
电流密度
电极
可逆氢电极
化学工程
密度泛函理论
分解水
吸附
交换电流密度
无机化学
纳米技术
物理化学
化学
参比电极
计算化学
塔菲尔方程
有机化学
工程类
物理
光催化
量子力学
作者
Kaixi Sun,Tong Zhang,Liming Tan,Dexia Zhou,Yuqin Qian,Xiaoxia Gao,Fahui Song,Hongtao Bian,Zhou Lu,Jingshuang Dang,Hong Gao,Jeremy Shaw,Shutang Chen,Gugang Chen,Yi Rao
标识
DOI:10.1021/acsami.0c06644.s001
摘要
The
development of active, durable, and nonprecious electrocatalysts for
hydrogen electrochemistry is highly desirable but challenging. In
this work, we design and fabricate a novel interface catalyst of Ni
and Co2N (Ni/Co2N) for hydrogen evolution reaction
(HER) and hydrogen oxidation reaction (HOR). The Ni/Co2N interfacial catalysts not only achieve a current density of −10.0
mA cm–2 with an overpotential of 16.2 mV for HER
but also provide a HOR current density of 2.35 mA cm–2 at 0.1 V vs reversible hydrogen electrode (RHE). Furthermore, the
electrode couple made of the Ni/Co2N interfacial catalysts
requires only a cell voltage of 1.57 V to gain a current density of
10 mA cm–2 for overall water splitting. Hybridizations
in the three elements of Ni-3d, N-2p, and Co-3d result in charge transfer
in the interfacial junction of the Ni and Co2N materials.
Our density functional theory calculations show that both the interfacial
N and Co sites of Ni/Co2N prefer to hydrogen adsorption
in the hydrogen catalytic activities. This study provides a new approach
for the construction of multifunctional catalysts for hydrogen electrochemistry.
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