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Fabrication of SiOx-G/PAA-PANi/Graphene Composite With Special Cross-Doped Conductive Hydrogels as Anode Materials for Lithium Ion Batteries.
Liao, Yuanhong; Liang, Kang; Ren, Yurong; Huang, Xiaobing.
  • Liao Y; School of Materials Science and Engineering, Jiangsu Collaborative Innovation Center of Photovoltaic Science and Engineering, Changzhou University, Changzhou, China.
  • Liang K; School of Materials Science and Engineering, Jiangsu Collaborative Innovation Center of Photovoltaic Science and Engineering, Changzhou University, Changzhou, China.
  • Ren Y; School of Materials Science and Engineering, Jiangsu Collaborative Innovation Center of Photovoltaic Science and Engineering, Changzhou University, Changzhou, China.
  • Huang X; Hunan Province Cooperative Innovation Center for the Construction & Development of Dongting Lake Ecological Economic Zone, College of Chemistry and Materials Engineering, Hunan University of Arts and Science, Changde, China.
Front Chem ; 8: 96, 2020.
Article en En | MEDLINE | ID: mdl-32154216
ABSTRACT
Silicon oxides (SiOx) have been considered to be the likeliest material to substitute graphite anode for lithium-ion batteries (LIBs) due to its high theoretical capacity, appropriate working potential plus rich abundance. Nevertheless, the two inherent disadvantages of volume expansion and low electrical conductivity of SiOx have been a main obstacle to its application. Here, SiOx-G/PAA-PANi/graphene composite has been successfully synthesized by in-situ polymerization, in which SiOx-G particles linked together by a graphene-doped polyacrylic acid-polyaniline conductive flexible hydrogel and SiOx-G is encapsulated inside the conductive hydrogel. We demonstrate that SiOx-G/PAA-PANi/graphene composite possesses a discharge-specific capacity of 842.3 mA h g-1 at a current density of 500 mA g-1 after a cycle life of 100 cycles, and a good initial coulombic efficiency (ICE) of 74.77%. The superior performance probably due to the lithium ion transmission rate and the electric conductivity enhanced by the three-dimensional (3D) structured conductive polymer hydrogel.
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