• 文献标题:   Efficient Laser-Induced Construction of Oxygen-Vacancy Abundant Nano-ZnCo2O4/Porous Reduced Graphene Oxide Hybrids toward Exceptional Capacitive Lithium Storage
  • 文献类型:   Article
  • 作  者:   LI L, XIE ZJ, JIANG GX, WANG YJ, CAO BQ, YUAN CZ
  • 作者关键词:   laserinduced synthesi, lithiumion batterie, nanoscale znco2o4, oxygen vacancy, porous reduced graphene oxide
  • 出版物名称:   SMALL
  • ISSN:   1613-6810 EI 1613-6829
  • 通讯作者地址:   Univ Jinan
  • 被引频次:   1
  • DOI:   10.1002/smll.202001526 EA JUN 2020
  • 出版年:   2020

▎ 摘  要

Recently, binary ZnCo(2)O(4)has drawn enormous attention for lithium-ion batteries (LIBs) as attractive anode owing to its large theoretical capacity and good environmental benignity. However, the modest electrical conductivity and serious volumetric effect/particle agglomeration over cycling hinder its extensive applications. To address the concerns, herein, a rapid laser-irradiation methodology is firstly devised toward efficient synthesis of oxygen-vacancy abundant nano-ZnCo2O4/porous reduced graphene oxide (rGO) hybrids as anodes for LIBs. The synergistic contributions from nano-dimensional ZnCo(2)O(4)with rich oxygen vacancies and flexible rGO guarantee abundant active sites, fast electron/ion transport, and robust structural stability, and inhibit the agglomeration of nanoscale ZnCo2O4, favoring for superb electrochemical lithium-storage performance. More encouragingly, the optimal L-ZCO@rGO-30 anode exhibits a large reversible capacity of approximate to 1053 mAh g(-1)at 0.05 A g(-1), excellent cycling stability (approximate to 746 mAh g(-1)at 1.0 A g(-1)after 250 cycles), and preeminent rate capability (approximate to 686 mAh g(-1)at 3.2 A g(-1)). Further kinetic analysis corroborates that the capacitive-controlled process dominates the involved electrochemical reactions of hybrid anodes. More significantly, this rational design holds the promise of being extended for smart fabrication of other oxygen-vacancy abundant metal oxide/porous rGO hybrids toward advanced LIBs and beyond.