钴
X射线吸收光谱法
金属
拉曼光谱
活动站点
分解水
硫黄
硫化钴
硫化物
吸收光谱法
克劳斯过程
光化学
化学
硫化氢
结晶学
无机化学
物理化学
催化作用
有机化学
光催化
电化学
物理
光学
量子力学
电极
作者
Yonggui Zhao,Wenchao Wan,Rolf Erni,Long Pan,Greta R. Patzke
标识
DOI:10.1002/anie.202400048
摘要
Metal-based chalcogenides exhibit great promise for overall water splitting, yet their intrinsic catalytic reaction mechanisms remain to be fully understood. In this work, we employed operando X-ray absorption (XAS) and in situ Raman spectroscopy to elucidate the structure-activity relationships of low-crystalline cobalt sulfide (L-CoS) catalysts toward overall water splitting. The operando results for L-CoS catalyzing the alkaline hydrogen evolution reaction (HER) demonstrate that the cobalt centers in the bulk are predominantly coordinated by sulfur atoms, which undergo a kinetic structural rearrangement to generate metallic cobalt in S-Co-Co-S moieties as the true catalytically active species. In comparison, during the acidic HER, L-CoS undergoes local structural optimization of Co centers, and H
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