A novel synthesis of Nb2O5@rGO nanocomposite as anode material for superior sodium storage

被引:23
|
作者
Zhang, Yu [1 ]
Fang, Li [1 ]
Sun, Wang [1 ]
Shi, Bin [2 ]
Chen, Xiaotao [2 ]
Gu, Yujie [3 ]
Ding, Kunpeng [3 ]
Wang, Zhenhua [1 ]
Sun, Kening [1 ]
机构
[1] Beijing Inst Technol, Beijing Key Lab Chem Power Source & Green Catalys, Sch Chem & Chem Engn, BIT QUB Joint Ctr Novel Energy & Mat Res, Beijing 100081, Peoples R China
[2] Guizhou Meiling Power Sources Co Ltd, State Key Lab Adv Chem Power Sources, Zunyi 563003, Guizhou, Peoples R China
[3] Yinlong Energy Co Ltd, Zhuhai 519000, Peoples R China
基金
中国国家自然科学基金;
关键词
Nb2O5@rGO nanocomposite; Microemulsion; Anode material; Sodium-ion battery; ENHANCED ELECTROCHEMICAL PERFORMANCE; FACILE SYNTHESIS; HYBRID ANODE; ION BATTERY; LITHIUM; COMPOSITE; CARBON; OXIDE; PSEUDOCAPACITANCE; INTERCALATION;
D O I
10.1016/j.cclet.2020.09.006
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The development of novel anode materials, with superior rate capability, is of utmost significance for the successful realization of sodium-ion batteries (SIBs). Herein, we present a nanocomposite of Nb2O5 and reduced graphene oxide (rGO) by using hydrothermal-assisted microemulsion route. The water-in-oil microemulsion formed nanoreactors, which restrained the particle size of Nb2O5 and shortened the diffusion length of ions. Moreover, the rGO network prevented agglomeration of Nb2O5 nanoparticles and improved electronic conductivity. Consequently, Nb2O5@rGO nanocomposite is employed as anode material in SIBs, delivering a capacity of 195 mAh/g after 200 charge/discharge cycles at 0.2 A/g. Moreover, owing to conductive rGO network, the Nb2O5@rGO electrode rendered a specific capacity of 76 mAh/g at high current density of 10 A/g and maintained 98 mAh/g after 1000 charge/discharge cycles at 2 A/g. The Nb2O5@rGO electrode material prepared by microemulsion method shows promising possibilities for application of SIBs. (C) 2020 Chinese Chemical Society and Institute of Materia Medica, Chinese Academy of Medical Sciences. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:1144 / 1148
页数:5
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