Atomically dispersed Ru oxide catalyst with lattice oxygen participation for efficient acidic water oxidation

被引:120
作者
Yao, Na [1 ]
Jia, Hongnan [1 ]
Zhu, Juan [1 ]
Shi, Zhaoping [2 ]
Cong, Hengjiang [1 ]
Ge, Junjie [2 ]
Luo, Wei [1 ]
机构
[1] Wuhan Univ, Coll Chem & Mol Sci, Wuhan 430072, Hubei, Peoples R China
[2] Chinese Acad Sci, Changchun Inst Appl Chem, State Key Lab Electroanalyt Chem, Changchun 130022, Jilin, Peoples R China
来源
CHEM | 2023年 / 9卷 / 07期
基金
中国国家自然科学基金;
关键词
METAL-ORGANIC-FRAMEWORK; EVOLUTION REACTION; ELECTROCATALYSTS; IDENTIFICATION; CHALLENGES; STABILITY; REDOX; RAMAN;
D O I
10.1016/j.chempr.2023.03.005
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The development of highly efficient and stable electrocatalysts toward the acidic oxygen evolution reaction (OER) is essential for the practical application of proton-exchange membrane water electrolyzers. Although Ru oxides possess remarkable initial activity toward the acidic OER due to the kinetically favorable lattice oxygen oxidation mechanism pathway, the soluble high-valence oxygen -vacancy intermediate (*Vo-RuO42-) may accelerate the dissolution of Ru species, leading to dramatically decreased activity and unsatisfied long-term stability. Here, we developed a robust metal-organic framework anchored strategy by stabilizing atomically isolated Ru oxide on UiO-67-bpydc with strong coordinating pyridine ligands. Theory calculations and experimental results including in situ Raman, X-ray absorption spectroscopy, and 18O-labeled differential electrochemical mass spectrometry reveal that the Ru-N bonds between Ru oxide and UiO-67-bpydc could not only accelerate the participation of lattice oxygen during the OER process but also stabilize the soluble *Vo-RuO42- intermediate, which contribute to the enhanced OER performance and long-term stability of up to 115 h.
引用
收藏
页码:1882 / 1896
页数:16
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