In situ growth of Co3O4 on nitrogen-doped hollow carbon nanospheres as air electrode for lithium-air batteries

被引:29
作者
Wang, Junbo [1 ]
Fan, Meiling [1 ]
Tu, Wenmao [1 ]
Chen, Kai [2 ]
Shen, Yafei [2 ]
Zhang, Haining [1 ]
机构
[1] Wuhan Univ Technol, State Key Lab Adv Technol Mat Synth & Proc, Wuhan 430070, Hubei, Peoples R China
[2] Wuhan Jingce Elect Technol Co, Wuhan 430070, Hubei, Peoples R China
关键词
Li-O-2; battery; Bifunctional catalysts; Nitrogen-doped hollow carbon nanospheres; Transition metal oxide; Air electrode; HIGH-PERFORMANCE ANODE; OXYGEN REDUCTION; RAMAN-SPECTROSCOPY; FACILE SYNTHESIS; GRAPHENE; NANOPARTICLES; CATHODE; ELECTROCATALYST; CATALYSTS; COBALT;
D O I
10.1016/j.jallcom.2018.11.062
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
Design and synthesis of efficient bifunctional electrocatalysts for both oxygen reduction reaction and oxygen evolution reactions are of great significant for metal-air batteries. In this work, bifunctional catalysts consisting of Co3O4 nanocrystals and nitrogen-doped hollow carbon nanospheres are synthesized through in situ growth of Co3O4 nanocrystals on the surface of nitrogen-doped hollow carbon nanospheres. The observed Co-N bond formation is an indication of the nucleation of Co3O4 nanocrystals starting from N-sites in nitrogen-doped hollow carbon nanospheres. The resulted hybrids exhibit improved activity towards oxygen reduction reaction compared to pristine nitrogen-doped hollow carbon nanospheres in terms of the 42 mV positive shift of half-wave potential and comparable activity towards oxygen evolution reactions with commercial RuO2 and IrO2 catalysts. The thus-assembled Li-O-2 battery delivers an initial discharge capacity of 3325 mAhg(-1) at 100 mAg(-1) using mixed gas of O-2 and Ar (20% of O-2 in volume). The battery fails after 27 discharge/charge cycles due to the accumulation of discharge products on electrode. (C) 2018 Elsevier B.V. All rights reserved.
引用
收藏
页码:944 / 953
页数:10
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