NiCo2S4 nanocores in-situ encapsulated in graphene sheets as anode materials for lithium-ion batteries

被引:83
作者
Chen, Haijun [1 ]
Ma, Xudong [1 ]
Shen, Pei Kang [1 ]
机构
[1] Guangxi Univ, Guangxi Key Lab Electrochem Energy Mat, Collaborat Innovat Ctr Sustainable Energy Mat, Nanning 530004, Guangxi, Peoples R China
基金
中国国家自然科学基金;
关键词
Lithium-ion battery; NiCo2S4; Graphene sheet; Cation adsorption; Hydrothermal-annealing; Full battery; HIGH-PERFORMANCE ANODE; ENHANCED ELECTROCHEMICAL PERFORMANCE; 3-DIMENSIONAL NETWORK; SODIUM; FOAM; COMPOSITES; STORAGE; NANOPARTICLES; ELECTRODES; FRAMEWORK;
D O I
10.1016/j.cej.2019.01.119
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Bimetallic sulfides were extensively studied as an advanced electrode material for lithium-ion batteries because of their high conductivity and superior capacity compared to metal oxides. We herein have successfully fabricated ultrafine NiCo2S4 nanocores in-situ encapsulated in graphene sheets (NiCo2S4@GS) with three-dimensional porous network structures through a cation adsorption process and subsequent hydrothermal-annealing reaction. In the NiCo2S4@graphene sheets nanohybrids, graphene sheets with abundant mesoporous network structure can be served as a conductive matrix and also be a protective buffer layer to suppress the volume expansion of NiCo2S4 nanoparticles. The NiCo2S4@GS-1 electrodes deliver a high reversible capacity of 813 mAh g(-1) upon 200 cycles at 0.2 A g(-1), ultralong cycling life of 535 mAh g(-1) upon 1000 cycles at 2 A g(-1), and excellent rate capability. Additionally, the advanced button-type full batteries were assembled via coupling NiCo2S4@GS-1 anodes with commercial LiFePO4 cathodes showing superior cycle stability and practicability. This work points out an innovative and scalable strategy for preparing composite electrode materials for lithium-ion batteries.
引用
收藏
页码:167 / 176
页数:10
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