The Spin Modulation Stimulated Efficient Electrocatalytic Oxygen Evolution Reaction over LaCoO3 Perovskite

被引:9
|
作者
Zhou, Fangping [1 ]
Zhao, Zhao [1 ]
Xu, Ming [1 ]
Wang, Ting [1 ]
Yang, Huiru [1 ]
Wang, Rong [1 ]
Wang, Jiahui [1 ]
Li, Haibo [1 ]
Feng, Ming [1 ]
机构
[1] Jilin Normal Univ, Minist Educ, Key Lab Funct Mat Phys & Chem, Changchun 130103, Peoples R China
基金
中国国家自然科学基金;
关键词
electrocatalysis; magnetic fields; oxygen evolution reaction; perovskite; spin sate; Z-SCHEME LACOO3/G-C3N4; CO; DESIGN; HYBRID; NICKEL; STATES;
D O I
10.1002/chem.202104157
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Perovskite is a promising non-noble catalyst and has been widely investigated for the electrochemical oxygen evolution reaction (OER). However, there is still serious lack of valid approaches to further enhance their catalytic performance. Herein, we propose a spin state modulation strategy to improve the OER electrocatalytic activity of typical perovskite material of LaCoO3. Specifically, the electronic configuration transition was realized by a simple high temperature thermal reduction process. M-H hysteresis loop results reveal that the reduction treatment can produce more unpaired electrons in 3d orbit by promoting the electron transitions of Co from low spin state to high spin state, and thus lead to the increase of the spin polarization. Electrochemical measurements show that the catalytic performance of LaCoO3 is strongly dependent on its electronic configuration. With the optimized reduction treatment, the overpotential for the OER process in 0.5 M KOH electrolyte solution at 10 mA cm(-2) current density was 396 mV, significantly lower than that of the original state. Furthermore, it can mediate efficient OER with an overpotential of 383 mV under an external magnetic field, which is attributed to the appropriate electron filling. Our results show that electron spin state regulation is a new way to boost the OER electrocatalytic activity.
引用
收藏
页数:6
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