Engineering of the d-Band Center of Perovskite Cobaltite for Enhanced Electrocatalytic Oxygen Evolution

被引:50
|
作者
Sun, Yiqiang [1 ]
Zhao, Zihan [1 ]
Wu, Si [1 ]
Li, Wenjuan [1 ]
Wu, Bo [3 ]
Liu, Guangning [1 ]
Chen, Guozhu [1 ]
Xu, Bo [1 ]
Kang, Baotao [1 ]
Li, Yue [2 ]
Li, Cuncheng [1 ]
机构
[1] Univ Jinan, Sch Chem & Chem Engn, Jinan 250022, Shandong, Peoples R China
[2] Chinese Acad Sci, Inst Solid State Phys, Anhui Key Lab Nanomat & Nanotechnol, Key Lab Mat Phys, Hefei 230031, Anhui, Peoples R China
[3] Southwest Univ Sci & Technol, State Key Lab Environm Friendly Energy Mat, Mianyang 621010, Sichuan, Peoples R China
基金
中国国家自然科学基金;
关键词
adsorption; electrocatalysis; oxygen evolution; perovskites; doping; METAL; VACANCIES; LACOO3; OXIDES; STATE;
D O I
10.1002/cssc.201903470
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Great efforts have been made to understand and upgrade the kinetically sluggish oxygen evolution reaction (OER). In this study, a series of V-doped LaCoO3 (V-LCO) OER electrocatalysts with optimized d-band centers are fabricated. When utilized as an electrode for the OER, as-formed LaCo0.8V0.2O3 (V-LCO-II) requires an overpotential of only 306 mV to drive a geometrical catalytic current density of 10 mA cm(-2). Furthermore, at a given overpotential of 350 mV, the OER current density of V-LCO-II is about 22 times that of pure LaCoO3 (LCO) nanoparticles. Tailoring of the d-band center by V doping facilitates the adsorption of OER intermediates and promotes the formation of amorphous active species on the surface of LCO through the exchange interaction between high-spin V4+ and low-spin Co2+. This work may create new opportunities for developing other highly active OER catalysts through d-band center engineering.
引用
收藏
页码:2671 / 2676
页数:6
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