He Yan, Yu Tao, Wen Hui, Guo Rui
School of Materials Science and Engineering, Northeastern University, Shenyang 110819, China.
Dalton Trans. 2021 Jul 21;50(28):9746-9753. doi: 10.1039/d1dt01469b.
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.
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。