催化作用
金属
化学
结晶学
无机化学
材料科学
有机化学
生物化学
作者
Conghui Li,Cheng‐Zong Yuan,Chenliang Zhou,Xuan Yang,Ruilong Xu,Fuling Wu,Xin Lei,Lingxian Wang,Xiaomeng Zhang,Kwun Nam Hui,Shufeng Ye,Yunfa Chen
出处
期刊:ACS Catalysis
[American Chemical Society]
日期:2025-04-21
卷期号:15 (9): 7403-7413
被引量:15
标识
DOI:10.1021/acscatal.5c01190
摘要
Exploring highly efficient and stable single-atom electrocatalysts for the oxygen evolution reaction (OER) is urgent for cost-effective hydrogen production by a proton exchange membrane water electrolyzer, but their stability is limited owing to the harsh corrosive and oxidative environments. Herein, we propose the synthesis of stable Ru single atoms (SAs) on the La-doped Co3O4 surface (Ru@La/Co3O4-20) via a strong metal–support interaction (SMSI), which exhibits a low overpotential at 10 mA cm–2 (η10: 244 mV) and a stability of 30 h (decay rate: 3.7 mV h–1) at 10 mA cm–2, outperforming Ru SAs on the Co3O4 surface (Ru@Co3O4) (η10: 295 mV; decay rate: 12.7 mV h–1) and benchmark RuO2. Experiments and density functional theory calculations demonstrate that electron transfer occurs from Ru SAs to asymmetric La/Co3O4 supports through bridge O atoms, strengthening the SMSI. Compared to Ru@Co3O4, the stronger SMSI between Ru SAs and asymmetric La/Co3O4 supports could help to adjust the Ru 4d and 2p band center’s location, which optimizes the adsorption of O intermediates and weakens Ru–O covalency, thus boosting the acidic OER activity and stability of Ru@La/Co3O4-20.
科研通智能强力驱动
Strongly Powered by AbleSci AI