电解质
催化作用
化学
动力学
无定形固体
析氧
无机化学
氧化还原
活化能
化学工程
物理化学
电化学
电极
有机化学
工程类
物理
量子力学
作者
Yan Duan,Nicolas Dubouis,Jiaqiang Huang,Daniel Alves Dalla Corte,Vanessa Pimenta,Zhichuan J. Xu,Alexis Grimaud
标识
DOI:10.1021/acscatal.0c00490
摘要
Recent studies have revealed the critical role played by the electrolyte composition on the oxygen evolution reaction (OER) kinetics on the surface of highly active catalysts. While numerous works were devoted to understand the effect of the electrolyte composition on the physical properties of the catalysts' surface, very little is known yet about its exact impact on the OER kinetics parameters. In this work, we reveal that the origin for the electrolyte-dependent OER activity for Co-based catalysts originates from two different effects. Increasing the alkaline electrolyte concentration for La1–xSrxCoO3−δ perovskites with x > 0 and for amorphous CoOOH increases the pre-exponential factor, which can be explained either by an increase of the concentration of active sites or by a change in the entropy of activation. However, changing the alkali cation results in a decrease of the apparent activation enthalpy for Fe-containing amorphous films, traducing a change in intermediates' binding energies.
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