Interface Engineering a High Content of Co3+ Sites on Co3O4 Nanoparticles to Boost Acidic Oxygen Evolution

被引:4
|
作者
Liu, Ziyi [1 ]
Ji, Qianqian [1 ]
Li, Na [1 ]
Tang, Bing [1 ]
Lv, Liyang [1 ]
Liu, Yuying [1 ]
Wang, Huijuan [2 ]
Hu, Fengchun [1 ]
Cai, Liang [3 ]
Yan, Wensheng [1 ]
机构
[1] Univ Sci & Technol China, Natl Synchrotron Radiat Lab, Hefei 230029, Peoples R China
[2] Univ Sci & Technol China, Expt Ctr Engn & Mat Sci, Hefei 230026, Peoples R China
[3] Tokyo Inst Technol, MDX Res Ctr Element Strategy, Int Res Frontiers Initiat, Yokohama 2268503, Japan
基金
中国国家自然科学基金;
关键词
OXIDATION; COBALT; WATER; CATALYST;
D O I
10.1021/acs.langmuir.3c02171
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Non-noble metal oxides have emerged as potential candidate electrocatalysts for acidic oxygen evolution reactions (OERs) due to their earth abundance; however, improving their catalytic activity and stability simultaneously in strong acidic electrolytes is still a major challenge. In this work, we report Co3O4@carbon core-shell nanoparticles on 2D graphite sheets (Co3O4@C-GS) as mixed-dimensional hybrid electrocatalysts for acidic OER. The obtained Co3O4@C-GS catalyst exhibits a low overpotential of 350 mV and maintains stability for 20 h at a current density of 10 mA cm(-2) in H2SO4 (pH = 1) electrolyte. X-ray photoelectron and X-ray absorption spectroscopies illustrate that the higher content of Co3+ sites boosts acidic OER. Operando Raman spectroscopy reveals that the catalytic stability of Co3O4@C nanoparticles during the acidic OER is enhanced by the introduction of graphite sheets. This interface engineering of non-noble metal sites with high valence states provides an efficient approach to boost the catalytic activity and enhance the stability of noble-metal-free electrocatalysts for acidic OER.
引用
收藏
页码:16415 / 16421
页数:7
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