Enriched electrophilic oxygen species facilitate acidic oxygen evolution on Ru-Mo binary oxide catalysts

被引:0
|
作者
Yaya Wang
Yunzhou Wen
Yumeng Cheng
Xinhong Chen
Mengjiao Zhuansun
Tongbao Wang
Jun Li
Debora Meira
Huarui Sun
Jun Wei
Jia Zhou
Yuhang Wang
Sisi He
机构
[1] Harbin Institute of Technology (Shenzhen),Shenzhen Key Laboratory of Flexible Printed Electronics Technology
[2] Harbin Institute of Technology (Shenzhen),School of Science
[3] Soochow University,Institute of Functional Nano & Soft Materials (FUNSOM), Jiangsu Key Laboratory of Advanced Negative Carbon Technologies
[4] Shanghai Jiao Tong University,Frontiers Science Center for Transformative Molecules
[5] Canadian Light Source,Science Division
[6] Argonne National Laboratory,Photon Science Division
[7] Harbin Institute of Technology,School of Materials Science and Engineering
[8] (Shenzhen),undefined
来源
Nano Research | 2024年 / 17卷
关键词
electrocatalysis; oxygen evolution reaction (OER); ruthenium (Ru)-based oxide; molybdenum; electrophilic oxygen;
D O I
暂无
中图分类号
学科分类号
摘要
The polymer electrolyte membrane (PEM) electrolyzers are burdened with costly iridium (Ir)-based catalysts and high operation overpotentials for the oxygen evolution reaction (OER). The development of earth-abundant, highly active, and durable electrocatalysts to replace Ir is a critical step in reducing the cost of green hydrogen production. Here we develop a Ru5Mo4Ox binary oxide catalyst that exhibits high activity and stability in acidic OER. The electron-withdrawing property of Mo enriches the electrophilic surface oxygen species, which promotes acidic OER to proceed via the adsorbate evolution pathway. As a result, we achieve a 189 mV overpotential at 10 mA·cm−2 and a Tafel slope of 48.8 mV·dec−1. Our catalyst demonstrates a substantial 18-fold increase in intrinsic activity, as evaluated by turnover frequency, compared to commercially available RuO2 and IrO2 catalysts. Moreover, we report a stable OER operation at 10 mA·cm−2 for 100 h with a low degradation rate of 2.05 mV·h−1.
引用
收藏
页码:1165 / 1172
页数:7
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