化学
催化作用
锰
拉曼光谱
析氧
电化学
无机化学
原位
氧化物
同位素标记
光化学
分解水
氧化还原
反应中间体
电极
光催化
物理化学
有机化学
物理
光学
作者
Kang Hee Cho,Sunghak Park,Hongmin Seo,Seungwoo Choi,Moo Young Lee,Changwan Ko,Ki Tae Nam
标识
DOI:10.1002/ange.202014551
摘要
Abstract Electrochemical water splitting is a promising means to produce eco‐friendly hydrogen fuels. Inspired by the Mn 4 CaO 5 cluster in nature, substantial works have been performed to develop efficient manganese (Mn)‐based heterogeneous catalysts. Despite improvements in catalytic activity, the underlying mechanism of the oxygen evolution reaction (OER) is not completely elucidated owing to the lack of direct spectroscopic evidence for the active Mn‐oxo moieties. We identify water oxidation intermediates on the surface of Mn 3 O 4 nanoparticles (NPs) in the OER at neutral pH by in situ Raman spectroscopy. A potential‐dependent Raman peak was detected at 760 cm −1 and assigned to the active Mn IV =O species generated during water oxidation. Isotope‐labeling experiments combined with scavenger experiments confirmed the generation of surface terminal Mn IV =O intermediates in the Mn‐oxide NPs. This study provides an insight into the design of systems for the observation of reaction intermediates.
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