Sulfur-modified Co3O4 as a bifunctional oxygen catalyst for zinc-air batteries

被引:0
|
作者
Ma, Shuwen [1 ]
Zhu, Binji [1 ]
Gan, Ruihui [1 ]
Wang, Yue [1 ]
Zhou, Bangguo [1 ]
Shi, Jingli [1 ]
Song, Yan [2 ]
Shao, Xiaodong [3 ]
Ma, Chang [1 ]
机构
[1] Tiangong Univ, Tianjin Municipal Key Lab Adv Fiber & Energy Stora, Tianjin 300387, Peoples R China
[2] Chinese Acad Sci, Inst Coal Chem, CAS Key Lab Carbon Mat, Taiyuan 030001, Peoples R China
[3] Sungkyunkwan Univ, Dept Chem, Suwon 16419, South Korea
关键词
REDUCTION REACTION; CARBON; EFFICIENT; VACANCIES;
D O I
10.1007/s10853-024-10484-z
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
The development of highly active non-precious metal bifunctional oxygen catalysts is of great significance in improving the efficiency of zinc-air batteries (ZABs). In this work, Co3O4 is modified by a simple sulfur-doping strategy, which achieves a sulfur-doped Co3O4 (S-Co3O4) with significantly-enhanced oxygen catalytic activity. The doping of sulfur promotes the exposure of cobalt active sites and brings abundant oxygen vacancies, which provide additional active sites and enhance the conductivity of Co3O4. Consequently, S-Co3O4 exhibits a low overpotential of 318 mV in the oxygen evolution reaction (OER) and an improved half-wave potential (0.788 V) for oxygen reduction reaction (ORR). In addition, the sulfur doping increases the ORR kinetic current density of pristine Co3O4 by a factor of 49. The assembled ZABs based on S-Co3O4 cathodes show a higher peak power density (98.90 mW cm-2) than the commercial Pt/C + RuO2-based ZABs. This work reveals that the intrinsic oxygen catalytic activity of Co3O4 can be significantly strengthened by sulfur doping, which can modify its structural characteristics and introduce structural defects.
引用
收藏
页码:355 / 366
页数:12
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