MnCO3-RGO composite anode materials: In-situ solvothermal synthesis and electrochemical performances

被引:32
|
作者
Zhao, Yan [1 ,2 ]
Mu, Yanlin [2 ]
Wang, Li [2 ]
Liu, Mengjiao [2 ]
Lai, Xin [2 ]
Bi, Jian [2 ]
Gao, Daojiang [2 ]
Chen, Yuanfu [1 ]
机构
[1] Univ Elect Sci & Technol China, State Key Lab Elect Thin Films & Integrated Devic, Chengdu 610054, Sichuan, Peoples R China
[2] Sichuan Normal Univ, Coll Chem & Mat Sci, Chengdu 610068, Sichuan, Peoples R China
关键词
MnCO3-RGO composite; In-situ solvothermal synthesis; Electrochemical performance; Cyclic stability; MORPHOLOGY-CONTROLLED SYNTHESIS; LITHIUM-ION BATTERIES; STORAGE CAPABILITY; FACILE SYNTHESIS; GRAPHENE; ELECTRODE; MICROSPHERES; EFFICIENT; OXIDES; FOAM;
D O I
10.1016/j.electacta.2019.06.001
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
The MnCO3-RGO composite, constructed by MnCO3 microcrystals in-situ nucleated and grown on reduced graphene oxide (RGO) sheets, are synthesized via a facile one-pot solvothermal process. When the MnCO3-RGO composite is used as anode material, it delivers outstanding electrochemical performance: it exhibits a large capacity of 873 mAh g(-1) even after 400 cycles at a current rate of 1 C, which is over 55.6% higher than that of bare MnCO3 (561 mAh g(-1)); most importantly, the MnCO3-RGO composite demonstrates a superior high-rate performance and long-term stability with a very large capacity of 546 mAh g(-1) even after 1000 cycles at a very large current rate of 5 C. This terrific electrochemical performance of MnCO3-RGO composite is mainly ascribed to its unique architecture: the excellent mechanical flexibility of RGO sheets can stabilize the microstructure of MnCO3 and guarantee the long-term stability during charge/discharge even at large current rate; the high conductivity of RGO sheets can effectively accelerate the transfer of electrons. This work presents a facile and cost-effective synthesis strategy, which gives a guidance for the synthesis of the other transition metal oxides-RGO composite. (c) 2019 Elsevier Ltd. All rights reserved.
引用
收藏
页码:786 / 794
页数:9
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