高熵合金
过电位
析氧
材料科学
无定形固体
价(化学)
氧气
化学工程
化学物理
电极
冶金
电化学
物理化学
化学
微观结构
结晶学
有机化学
工程类
作者
Tao Zhang,Hui-Feng Zhao,Keyan Wang,Zhen-Jie Chen,Li Li,Jing Peng,Peng Xu,Yongjiang Huang,Hai‐Bin Yu
出处
期刊:Materials futures
[IOP Publishing]
日期:2023-08-10
卷期号:2 (4): 045101-045101
被引量:14
标识
DOI:10.1088/2752-5724/aceef3
摘要
Abstract Even in their bulk forms, complex alloys like high-entropy alloys (HEAs) exhibit favorable activity and stability as electrocatalysts for the oxygen evolution reaction (OER). However, the underlying reasons are not yet fully understood. In a family of Mo-doped CrFeCoNi-based HEAs, we have identified three crucial factors that govern their performance: (i) homogeneous solid solution phase of HEAs helps to maintain high-valence states of metals; (ii) surface reconstruction results in a hybrid material comprising amorphous domains and percolated crystalline structures; (iii) diversity of active intermediate species (M–O, M–OOH, and, notably, the abundance of superoxide μ –OO), which display stronger adsorption capacity on the reconstructed surface. These results are revealing due to their resemblance to findings in other families of electrocatalysts for OER, as well as their unique features specific to HEAs. In line with these factors, a CrFeCoNiMo 0.2 bulk integrated electrode displays a low overpotential of 215 mV, rapid kinetics, and long-term stability of over 90 d. Bulk HEAs hold great potential for industrial applications.
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