双金属片
双金属
析氧
催化作用
金属有机骨架
钴
过电位
电化学
材料科学
化学工程
无机化学
金属
化学
电极
物理化学
冶金
有机化学
吸附
工程类
作者
Weiren Cheng,Zhi‐Peng Wu,Deyan Luan,Shuang‐Quan Zang,Xiong Wen Lou
标识
DOI:10.1002/ange.202112775
摘要
Abstract The development of efficient oxygen electrocatalysts and understanding their underlying catalytic mechanism are of significant importance for the high‐performance energy conversion and storage technologies. Herein, we report novel CoCu‐based bimetallic metal–organic framework nanoboxes (CoCu‐MOF NBs) as promising catalysts toward efficient electrochemical oxygen evolution reaction (OER), fabricated via a successive cation and ligand exchange strategy. With the highly exposed bimetal centers and the well‐designed architecture, the CoCu‐MOF NBs show excellent OER activity and stability, with a small overpotential of 271 mV at 10 mA cm −2 and a high turnover frequency value of 0.326 s −1 at an overpotential of 300 mV. In combination of quasi in situ X‐ray absorption fine structure spectroscopy and density‐functional theory calculations, the post‐formed CoCu‐based oxyhydroxide analogue during OER is believed to account for the high OER activity of CoCu‐MOF NBs, where the electronic synergy between Co and neighbouring Cu atoms promotes the O−O bond coupling toward fast OER kinetics.
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