Eliminating over-oxidation of ruthenium oxides by niobium for highly stable electrocatalytic oxygen evolution in acidic media

被引:130
|
作者
Liu, Hai [1 ]
Zhang, Zhuang [1 ]
Fang, Jinjie [2 ]
Li, Mengxuan [1 ]
Sendeku, Marshet Getaye [3 ]
Wang, Xian [4 ]
Wu, Haoyang [1 ]
Li, Yaping [1 ]
Ge, Junjie [5 ]
Zhuang, Zhongbin [2 ]
Zhou, Daojin [1 ]
Kuang, Yun [1 ,3 ]
Sun, Xiaoming [1 ]
机构
[1] Beijing Univ Chem Technol, State Key Lab Chem Resource Engn, Beijing 100029, Peoples R China
[2] Beijing Univ Chem Technol, Beijing Adv Innovat Ctr Soft Matter Sci & Engn, State Key Lab Organ Inorgan Composites, Beijing 100029, Peoples R China
[3] Tsinghua Univ Shenzhen, Ocean Hydrogen Energy R&D Ctr, Res Inst, Shenzhen, Peoples R China
[4] Chinese Acad Sci, Changchun Inst Appl Chem, State Key Lab Electroanalyt Chem, Changchun 130022, Jilin, Peoples R China
[5] Univ Sci & Technol China, Sch Appl Chem & Engn, Hefei 230026, Peoples R China
基金
美国国家科学基金会;
关键词
WATER; PERFORMANCE; STABILITY; CATALYSTS; CORROSION; INSIGHTS; SITES;
D O I
10.1016/j.joule.2023.02.012
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Proton exchange membrane (PEM) water electrolysis shows advan-tages including high current density, high efficiency, and compact configuration but suffers from the scarcity and high price of iridium (Ir)-based anodic catalysts. Herein, insoluble niobium (Nb)-incorpo-rated RuO2 with a high valence state was designed as an Ir-free cata-lyst for active and stable acidic oxygen evolution reaction (OER). Nb0.1Ru0.9O2 exhibited a low overpotential (204 mV) and superb stability with an ultralow degradation rate (25 mV/h) over a 360-h durability test at 200 mA cm -2, which is only 1/100th of the decay rates of other Ru-based catalysts measured at 10 mA cm -2. The PEM electrolyzer with Nb0.1Ru0.9O2 as an anode survived from a 1 00-h operation at 300 mA cm -2. The strengthened adsorption of oxygen intermediates to active Ru sites reduced the OER energy barrier, while the enhanced electron transfer to Ru by Nb doping and formation of Nb5+ during the OER process extended catalyst's durability.
引用
收藏
页码:558 / 573
页数:17
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