兴奋剂
无定形固体
析氧
电解水
催化作用
价(化学)
材料科学
过渡金属
阳极
掺杂剂
化学工程
氧化物
化学
纳米技术
无机化学
电极
电解
物理化学
冶金
光电子学
电化学
结晶学
生物化学
工程类
有机化学
电解质
作者
Sicheng Li,Tong Liu,Wei Zhang,Mingzhen Wang,Huijuan Zhang,Chunlan Qin,Lingling Zhang,Yudan Chen,Shuaiwei Jiang,Dong Liu,Xiaokang Liu,Huijuan Wang,Qiquan Luo,Tao Ding,Tao Yao
标识
DOI:10.1038/s41467-024-47736-0
摘要
Abstract In-depth comprehension and modulation of the electronic structure of the active metal sites is crucial to enhance their intrinsic activity of electrocatalytic oxygen evolution reaction (OER) toward anion exchange membrane water electrolyzers (AEMWEs). Here, we elaborate a series of amorphous metal oxide catalysts (FeCrO x , CoCrO x and NiCrO x ) with high performance AEMWEs by high-valent chromium dopant. We discover that the positive effect of the transition from low to high valence of the Co site on the adsorption energy of the intermediate and the lower oxidation barrier is the key factor for its increased activity by synchrotron radiation in-situ techniques. Particularly, the CoCrO x anode catalyst achieves the high current density of 1.5 A cm −2 at 2.1 V and maintains for over 120 h with attenuation less than 4.9 mV h −1 in AEMWE testing. Such exceptional performance demonstrates a promising prospect for industrial application and providing general guidelines for the design of high-efficiency AEMWEs systems.
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