析氧
过电位
氧化物
化学
催化作用
镧系元素
密度泛函理论
氧气
石墨烯
机制(生物学)
组合化学
协同催化
反应机理
纳米技术
工作(物理)
兴奋剂
化学工程
无机化学
作者
Weiwei Yang,Liangyong Jia,Jing Cao,Yuqing Miao,Bingbao Mei,Ruizhuo Ouyang,Jianbin Luo,Xiaoyi Dou,Tianli Wu,Yuhai Dou,Chao Wu,Jinchen Fan,Ming Zhao
出处
期刊:Nano Letters
[American Chemical Society]
日期:2026-02-26
卷期号:26 (11): 3873-3881
标识
DOI:10.1021/acs.nanolett.6c00082
摘要
Regulating the reaction pathway of the oxygen evolution reaction (OER) is pivotal in enhancing the activity and stability of RuO2-based catalysts. However, it remains challenging to achieve the desired oxide pathway mechanism (OPM) for RuO2-based catalysts. Herein, we use density functional theory calculations to predict that Sm doping can tune the OER pathway of RuO2 toward the OPM. We successfully synthesize various lanthanide-doped RuO2 catalysts and demonstrate an overpotential as low as 184 mV at 10 mA cm-2 for Sm-doped RuO2 supported on reduced graphene oxide (Sm-RuO2/rGO). Sm-RuO2/rGO exhibits a stable operation for over 200 h at 500 mA cm-2. In situ characterizations confirm the functionality of incorporated Sm atoms in triggering an OPM pathway for RuO2. Our work demonstrates an effective strategy to regulate the OER pathway of RuO2-based catalysts, enabling highly efficient and durable OER under acidic conditions and showing great promise for industrial applications.
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