金属间化合物
再分配(选举)
材料科学
化学物理
催化作用
析氧
溶解
电子结构
电子转移
电荷(物理)
氧气
化学工程
原子轨道
基本电荷
纳米技术
工作(物理)
活化能
电子
氧化还原
过渡金属
降级(电信)
密度泛函理论
电解质
物理化学
化学稳定性
氧还原反应
电催化剂
结构稳定性
作者
Junjie Hu,Zhitong Li,Lei Xia,Yanyi Wang,Wenbo Peng,Shuyu Cui,Kelin Chen,G Liu,Tian Lang,Peide Zhu,Xiaolong Zhou,Sarayut Tunmee,Jintara Padchasri,Suttipong Wannapaiboon,Xingzhu Wang,Lei Yan,Xiongwei Zhong,Baomin Xu
出处
期刊:ACS Nano
[American Chemical Society]
日期:2026-02-04
卷期号:20 (11): 9147-9158
被引量:1
标识
DOI:10.1021/acsnano.5c18246
摘要
Transitional metals (TMs)-based high-entropy alloys (HEAs) have demonstrated exceptional oxygen evolution reaction (OER) activity due to tunable electronic configurations and multimetallic synergy. However, their stability is hindered by oxidation and structural degradation resulting from intermetallic electron interactions during operation. Herein, we propose a cerium-mediated charge redistribution strategy in FeCoNiMnCe HEA, facilitating charge transfer from electron-rich Ce to neighboring TMs. This Ce-introduced HEA features increased dissolving activation energy of Fe/Mn and optimized electronic orbitals of Co/Ni, which inhibits the deactivation of active sites induced by high oxidized states during OER. Benefiting from charge accumulation on TMs, FeCoNiMnCe HEA achieves outstanding durability with negligible decay over 1000 h for OER at 10 mA cm–2 and enables stable zinc-air batteries operation for 4600 h at 2 mA cm–2. This work provides a robust strategy for designing stable HEA electrocatalysts through targeted electronic modulation.
科研通智能强力驱动
Strongly Powered by AbleSci AI