• 文献标题:   P2-Na2/3Ni1/3Mn5/9Al1/9O2 Microparticles as Superior Cathode Material for Sodium-Ion Batteries: Enhanced Properties and Mechanisam via Graphene Connection
  • 文献类型:   Article
  • 作  者:   ZHANG XH, PANG WL, WAN F, GUO JZ, LU HY, LI JY, XING YM, ZHANG JP, WU XL
  • 作者关键词:   sodium ion batterie, cathode, layered transition metal oxide, diffusion coefficient, reduced graphene oxide
  • 出版物名称:   ACS APPLIED MATERIALS INTERFACES
  • ISSN:   1944-8244 EI 1944-8252
  • 通讯作者地址:   Northeast Normal Univ
  • 被引频次:   73
  • DOI:   10.1021/acsami.6b03944
  • 出版年:   2016

▎ 摘  要

As a promising alternative for lithium ion batteries, room-temperature sodium ion batteries (SIBs) have become one significant research frontier of energy storage devices although there are still many difficulties, to be overcome. For the moment, the studies still concentrate on the preparation of new electrode materials for SIBs to meet the applicability. Herein, one new P2 Na2/3Ni1/3Mn5/9Al1/9O2 (NMA) cathode material is successfully prepared via a simple and facile liquid-state method. The prepared NMA is layered transition metal oxide, which can keep stable crystal structure during sodiation/desodiation as demonstrated by the ex situ X-ray diffraction, and its electrochemical properties can be further enhanced by connecting the cake-like NMA microparticles with reduced graphene oxide (RGO) using a ball milling method. Electrochemical tests show that the formed RGO-connected NMA (NMA/RGO) can deliver a higher reversible capacity of up to 138 mAh g(-1) at 0.1 C and also exhibit a superior high-rate capabilities and cycling stability in comparison to pure NMA. The much improved properties should be attributed to the reduced particle size and improvement of electrical conductivity and apparent Na+ diffusion due to RGO incorporation, which is comprehensively verified by the electrochemical technologies of galvanostatic intermittent titration technique, electrochemical impedance spectroscopy and cyclic voltammetry at various scan rate as well as ex-situ X-ray diffraction studies.