• 文献标题:   Facile renewable synthesis of nitrogen/oxygen co-doped graphene-like carbon nanocages as general lithium-ion and potassium-ion battery anodes
  • 文献类型:   Article
  • 作  者:   SUN YH, ZHU DM, LIANG ZF, ZHAO YX, TIAN WF, REN XC, WANG J, LI XY, GAO Y, WEN W, HUANG YB, LI XL, TAI RZ
  • 作者关键词:  
  • 出版物名称:   CARBON
  • ISSN:   0008-6223 EI 1873-3891
  • 通讯作者地址:   Chinese Acad Sci
  • 被引频次:   1
  • DOI:   10.1016/j.carbon.2020.06.046
  • 出版年:   2020

▎ 摘  要

Environmentally-friendly carbon-based materials possess the potential applications as general anode for alkali-ion batteries. However, the existing carbon-based materials cannot satisfy the increasing demand for high energy density and need further active exploration. Herein, nitrogen/oxygen co-doped graphene-like carbon nanocages (NOGCN) is synthesized from biomass cytidine on hydro-soluble sodium chloride nanocrystals by a one-step method as a general lithium and potassium-ion batteries anode. All reactants are completely renewable and readily available. The nitrogen/oxygen-doping, large interlayer spacing and robust self-supporting nanocage architecture greatly favour electrolyte penetration and improve the kinetics for ion and electron transport, resulting in extraordinary electrochemical performance. The synthesized NOGCN electrodes exhibit a high lithiation storage capacity of 620 mA h g(-1) over 500 cycles at 500 mA g(-1), with continuously magnifying capacity. Moreover, the impressive reversible potassiation capacity (355 mA h g(-1) at 200 mA g(-1)) and rate capability (114 mA h g(-1) at 1000 mA g(-1)) were achieved despite the large-sized potassium ions. Kinetic analysis and density functional theory calculations elaborately illustrate the Li/K-absorption properties of the N/O-doped graphene-like structure, further demonstrating the chemical affinity and superiority in Li/K storage. This study provides a facile and completely renewable method to prepare promising general anode material for alkali-ion batteries. (C) 2020 Elsevier Ltd. All rights reserved.