• 文献标题:   Bi@C Nanospheres with the Unique Petaloid Core-Shell Structure Anchored on Porous Graphene Nanosheets as an Anode for Stable Sodium- and Potassium-Ion Batteries
  • 文献类型:   Article
  • 作  者:   ZHANG F, LIU XJ, WANG BB, WANG G, WANG H
  • 作者关键词:   bismuth, petaloid coreshell structure, graphene nanosheet, sodiumion batterie, potassiumion batterie
  • 出版物名称:   ACS APPLIED MATERIALS INTERFACES
  • ISSN:   1944-8244 EI 1944-8252
  • 通讯作者地址:  
  • 被引频次:   13
  • DOI:   10.1021/acsami.1c16946 EA DEC 2021
  • 出版年:   2021

▎ 摘  要

Bismuth (Bi) has emerged as a prospective candidate as Na-ion and potassium-ion battery anodes because of its unique advantages of low cost, high theoretical gravimetric capacity (386 mAh g(-1)), and superior volumetric capacity (3800 mAh cm(-3)). However, the low electronic conductivity and the huge volume expansion of Bi during the alloying/dealloying reactions are extremely detrimental to cycling stability, which seriously hinder its practical application. To overcome these issues, we propose a rational design: Bi@C nanospheres with the unique petaloid core-shell structure are synthesized in one step for the first time and then combined with different contents of graphene (GR) nanosheets to form the composites Bi@C@GR. The Bi@C nanospheres with a core-shell structure are beneficial to shortening the transmission path of electrons/ions and reducing the risk from structural rupture of the particles during cycling. In addition, the combination of BipC nanospheres and porous GR could greatly improve the conductivity and prevent the aggregation of particles, which is conducive to better cycling stability and rate performance. Consequently, Bi@C@GR-2 presents a superior reversible capacity for sodium storage (300 mAh g(-1) over 80 cycles) and potassium storage (200 mAh g(-1) over 70 cycles) at 0.1 A g(-1). Furthermore, in situ electrochemical impedance spectroscopy and ex situ transmission electron microscopy are carried out to analyze and reflect the kinetic reaction mechanism and the phase change of the Bi@C@GR-2 electrode during the charge/ discharge processes.