析氧
分解水
氧化还原
非阻塞I/O
氧气
材料科学
化学
催化作用
光化学
电化学
化学工程
化学物理
纳米技术
光催化
无机化学
电极
物理化学
工程类
有机化学
生物化学
出处
期刊:Energy & environmental materials
日期:2023-01-09
卷期号:6 (2)
被引量:7
摘要
Developing highly active and robust oxygen evolution reaction (OER) electrocatalysts is still a critical challenge for water electrolyzers and metal–air batteries. Realizing the dynamic evolution of the intermediate and charge transfer during OER and developing a clear OER mechanism is crucial to design high‐performance OER catalysts. Recently in Nature, Xue and colleagues revealed a new OER mechanism, coupled oxygen evolution mechanism (COM), which involves a switchable metal and oxygen redox under light irradiation in nickel oxyhydroxide‐based materials. This newly developed mechanism requires a reversible geometric conversion between octahedron (NiO 6 ) and square planar (NiO 4 ) to achieve electronic states with both “metal redox” and “oxygen redox” during OER. The asymmetric structure endows NR‐NiOOH with a nonoverlapping region between the dz 2 orbitals and a 1g * bands, which facilitate the geometric conversion and enact the COM pathway. As a result, NR‐NiOOH exhibited better OER activity and stability than the traditional NiOOH.
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