In situ grown Co3O4 nanocubes on N-doped graphene as a synergistic hybrid for applications in nickel metal hydride batteries

被引:25
|
作者
Li, M. M.
Wang, Y.
Yang, C. C. [1 ]
Jiang, Q. [1 ]
机构
[1] Jilin Univ, Key Lab Automobile Mat, Minist Educ, Changchun 130022, Jilin, Peoples R China
基金
中国国家自然科学基金;
关键词
N-doped graphene; Synergistic effect; Hydrogen storage alloy; High-rate dischargeability; Nickel metal hydride battery; HYDROGEN-STORAGE ALLOYS; LITHIUM-ION BATTERIES; HIGH-RATE PERFORMANCE; ANODE MATERIALS; ELECTROCHEMICAL PROPERTIES; ELECTRODE MATERIALS; SURFACE-TREATMENT; ENERGY-STORAGE; NI/MH BATTERY; OXIDE;
D O I
10.1016/j.ijhydene.2018.08.054
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
The development of high-power batteries for applications in electric vehicles, power tools, military devices, etc. has attracted great attentions in recent years. Here the synergistic effect between Co3O4 nanocubes and N-doped graphene has been considered to focus on the major obstacle of the sluggish kinetics of carrier transport and electrochemical reaction during charging/discharging. As an example, we have fabricated the Co3O4 nanocubes/Ndoped graphene hybrid material and combined it with hydrogen storage alloys. The asfabricated composite exhibits superior rate performance for applications in nickel metal hydride battery. An ultra-high capacity of 223.1 mAh g(-1) is achieved at a specific current of 3000 mA g(-1), which is 3.2 times that of the commercial alloy electrode (68.7 mAh g(-1)). Such remarkable high-rate dischargeability originates from the unique three-dimensional integrated porous structure of Co3O4/N-doped graphene, which provides: (1) small internal resistances due to the conductive substrate of N-doped graphene; (2) high electrocatalytic activity of Co3O4 nanocubes; (3) a suppression of re-stacking of N-doped graphene nanosheets; and (4) efficient ion and electron pathways and also short transport distances. (C) 2018 Hydrogen Energy Publications LLC. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:18421 / 18435
页数:15
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