过电位
材料科学
析氧
催化作用
异质结
纳米技术
合理设计
曲面重建
化学物理
电子结构
纳米针
纳米颗粒
密度泛函理论
吸收(声学)
氧气
本地字段
领域(数学)
原位
工作(物理)
曲面(拓扑)
电子效应
化学工程
电场
场电子发射
电流密度
光电子学
电极
作者
Peifang Guo,Haiwei Yang,Da Liu,Jie Zhou,Xinqiang Wang,Wen‐Gang Cui,Christian Durante,Lin Jiang,Hongge Pan,Renbing Wu
出处
期刊:ACS Nano
[American Chemical Society]
日期:2026-06-12
标识
DOI:10.1021/acsnano.6c00615
摘要
The rational regulation of the surface reconstruction in transition-metal-based electrocatalysts to optimize the catalytic performance for the oxygen evolution reaction (OER) is increasingly important yet remains challenging. Herein, we develop a strategy of the electronic interaction and tip-enhanced local field to synergistically tune the surface reconstruction. As a demonstration, a heterostructure catalyst comprising an FeCo 2 S 4 hollow nanoneedle decorated with MoO 3 nanoparticles (MoO 3 @FeCo 2 S 4 ) at the tip is constructed. The combined theoretical and in situ X-ray absorption investigations indicate that the abundant Co–O–Mo motifs at the interface improve the electron transfer, facilitating the surface reconstruction into Co(Fe)OOH-MoO 3 . Meanwhile, the sharp tip of the hollow nanoneedles enhances the local electric field and increases the pH near the tip to promote the formation of active CoOOH. Accordingly, the as-constructed MoO 3 @FeCo 2 S 4 shows a low overpotential of 277 mV at a current density of 100 mA cm –2 during the alkaline OER and maintains stable operation at 200 mA cm –2 for 100 h. This work not only provides insights for the rational regulation of surface reconstruction but also highlights the important integration of the electronic interaction with a local environment to design advanced transition-metal-based catalysts.
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