• 文献标题:   Graphene oxide wrapped Na3V2(PO4)(3)/C nanocomposite as superior cathode material for sodium-ion batteries
  • 文献类型:   Article
  • 作  者:   CHU ZL, YUE CB
  • 作者关键词:   energy storage, rechargeable sodiumion batterie, na3v2 po4 3 /c, conducting graphene, electrochemical performance
  • 出版物名称:   CERAMICS INTERNATIONAL
  • ISSN:   0272-8842 EI 1873-3956
  • 通讯作者地址:   Anhui Univ Technol
  • 被引频次:   25
  • DOI:   10.1016/j.ceramint.2015.09.003
  • 出版年:   2016

▎ 摘  要

Na3V2(PO4)(3) is one of the most promising cathode materials for rechargeable sodium-ion batteries, which can deliver two Na+ ions extraction/insertion from/into the crystal structure. To further improve the electrochemical performance of the carbon-coated Na3V2(PO4)(3) electrode, the conducting graphene has been adopted. In this paper, graphene-wrapped Na3V2(PO4)(3)/C nanocomposite has been successfully synthesized through a hydrothermal-assisted sol gel method. X-ray diffraction (XRD) results demonstrate that the obtained nanocomposite is well crystallized with NASICON-type structure. The scanning electron microscopy (SEM) and transmission electron microscopy (TEM) images reveal that the modification of Na3V2(PO4)(3)/C with graphene could construct an effective conducting network, which significantly enhances the electronic conductivity of Na3V2(PO4)(3)/C based sample. Thus, the graphene-wrapped Na3V2(PO4)(3)/C exhibits superior high-rate capacity and excellent cycling stability. It shows an initial charge capacity of 113 mA h g(-1) and a discharge capacity of 106.5 mA h g(-1) at 0.1 C, and retains stable discharge capacities of 104.3, 101.1, 96.4 and 93 mA h g(-1) at current rates of 0.2 C, 0.5 C, 1 C and 2 C, respectively. Even at higher rate of 5 C, it can still deliver a discharge capacity of 88.7 mA h g(-1) with remarkable capacity retention of 92.5% after 200 cycles. This synthetic strategy should be helpful for the design of other conducting network structured electrodes with high-performances. (C) 2015 Elsevier Ltd and Techna Group S.r.l. All rights reserved.