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通过Cr改性提高FeOOH/Ni(OH)的电荷转移以实现优异的析氧反应

Boosting the charge transfer of FeOOH/Ni(OH) for excellent oxygen evolution reaction Cr modification.

作者信息

He Yan, Yu Tao, Wen Hui, Guo Rui

机构信息

School of Materials Science and Engineering, Northeastern University, Shenyang 110819, China.

出版信息

Dalton Trans. 2021 Jul 21;50(28):9746-9753. doi: 10.1039/d1dt01469b.

Abstract

For the electrocatalytic oxygen evolution reaction (OER) in alkaline media, there is an urgent need to optimize the adsorption strength of OH*. Here, a flower-like hybrid of Cr-doped FeOOH/Ni(OH)2 was used as an OER catalyst with a low overpotential of 291 mV at 50 mA cm-2. The results showed that faster charge transfer was achieved at the electrode/solution interface during the OER process after the FeOOH/Ni(OH)2 was modified by Cr, which facilitates the rate-determining step of the Volmer reaction. Furthermore, the results of faradaic efficiency and X-ray photoelectron spectroscopy (XPS) measurements confirmed that the synergistic effect between the ternary metal and oxygen vacancies led to excellent OER performance. This work provides a new strategy for the preparation of high-efficiency and low-cost oxygen evolution electrocatalysts.

摘要

对于碱性介质中的电催化析氧反应(OER),迫切需要优化OH*的吸附强度。在此,采用Cr掺杂的FeOOH/Ni(OH)₂ 花状杂化物作为OER催化剂,在50 mA cm⁻² 时过电位低至291 mV。结果表明,FeOOH/Ni(OH)₂ 经Cr修饰后,在OER过程中电极/溶液界面实现了更快的电荷转移,这促进了Volmer反应的速率决定步骤。此外,法拉第效率和X射线光电子能谱(XPS)测量结果证实,三元金属与氧空位之间的协同效应导致了优异的OER性能。这项工作为制备高效低成本析氧电催化剂提供了一种新策略。

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