过电位
电解质
铂金
镍
离解(化学)
催化作用
碱金属
无机化学
化学
氢
金属
星团(航天器)
电化学
电极
物理化学
有机化学
程序设计语言
计算机科学
作者
Song Xue,Richard W. Haid,Regina M. Kluge,Xing Ding,Batyr Garlyyev,Johannes Fichtner,Sebastian Watzele,Shujin Hou,Aliaksandr S. Bandarenka
标识
DOI:10.1002/anie.202000383
摘要
Abstract Herein, we demonstrate an easy way to improve the hydrogen evolution reaction (HER) activity of Pt electrodes in alkaline media by introducing Ni–Fe clusters. As a result, the overpotential needed to achieve a current density of 10 mA cm −2 in H 2 ‐saturated 0.1 m KOH is reduced for the model single‐crystal electrodes down to about 70 mV. To our knowledge, these modified electrodes outperform any other reported electrocatalysts tested under similar conditions. Moreover, the influence of 1) Ni to Fe ratio, 2) cluster coverage, and 3) the nature of the alkali‐metal cations present in the electrolyte on the HER activity has been investigated. The observed catalytic performance likely originates from both the improved water dissociation at the Ni–Fe clusters and the subsequent optimal hydrogen adsorption and recombination at Pt atoms present at the Ni–Fe/Pt boundary.
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