催化作用
中心(范畴论)
分解水
对偶(语法数字)
钌
金属
材料科学
化学
结晶学
光催化
冶金
有机化学
文学类
艺术
作者
Yinqiang Zhang,Ming Liu,Hanyu Wang,Xinghao Zhang,Zhigang Li,Wei Li,Na Li,Xian‐He Bu
出处
期刊:ACS Catalysis
[American Chemical Society]
日期:2025-06-12
卷期号:15 (13): 11082-11092
被引量:24
标识
DOI:10.1021/acscatal.5c02366
摘要
Regulating the d-band center (εd) is an effective strategy to enhance the electrocatalytic performance by optimizing the adsorption and desorption of reaction intermediates. However, the targeted control of εd for different reactions remains challenging. Here, we strategically engineer εd to optimize the intermediate adsorption on a dual-metal site catalyst (Ru@NiBDC/NF) via Ni–O–Ru bridges. The synergistic effect of atomically Ru–Ni dual-metal sites in Ru@NiBDC/NF enhances catalytic activity for both the hydrogen evolution reaction (HER) and oxygen evolution reaction (OER), achieving overpotentials of 18 and 230 mV at 10 mA cm–2, respectively. Operando Raman spectra and X-ray absorption spectroscopy reveal that Ru@NiBDC/NF reconstructs into Ru@Ni(OH)2/Ru@NiOOH with abundant Ni–O–Ru bridges during HER/OER. Theoretical calculations indicate that Ni–O–Ru bridge formation facilitates electron redistribution, downshifting εd of Ni sites in Ru@Ni(OH)2 and upshifting it in Ru@NiOOH, respectively. This modulation optimizes the adsorption energies of intermediates, thereby enhancing reaction kinetics and catalytic efficiency.
科研通智能强力驱动
Strongly Powered by AbleSci AI