用户名: 密码: 验证码:
Understanding the accumulated cycle capacity fade caused by the secondary particle fracture of LiNi1-x-yCoxMnyO2 cathode for lithium ion batteries
详细信息    查看全文
  • 作者:Guangyin Li ; Zhanjun Zhang ; Zhenlei Huang
  • 关键词:Secondary particle ; Fracture ; Capacity fade ; Cathode
  • 刊名:Journal of Solid State Electrochemistry
  • 出版年:2017
  • 出版时间:March 2017
  • 年:2017
  • 卷:21
  • 期:3
  • 页码:673-682
  • 全文大小:
  • 刊物类别:Chemistry and Materials Science
  • 刊物主题:Physical Chemistry; Electrochemistry; Energy Storage; Characterization and Evaluation of Materials; Analytical Chemistry; Condensed Matter Physics;
  • 出版者:Springer Berlin Heidelberg
  • ISSN:1433-0768
  • 卷排序:21
文摘
Effect of secondary particle fracture on the accumulated cycle capacity fade of LiNi1-x-yCoxMnyO2 cathode is difficult to evaluate since performance degradation of electrode material is always caused by several factors simultaneously. Herein, LiNi0.5Co0.2Mn0.3O2 single particles (Sin-P) are prepared and introduced as a reference to understand the accumulated cycle capacity fade caused by the secondary particle fracture of LiNi0.5Co0.2Mn0.3O2 secondary particles (Sec-P). Sec-P exhibited accumulated cycle capacity fade compared to Sin-P when cycled at high rate, high voltage, and high temperature. The accumulated cycle capacity fade was mainly caused by the secondary particle fracture of Sec-P, which was confirmed by the X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), and scanning electron microscope (SEM) analysis. Further, XPS and electrochemical impedance spectroscopy (EIS) analysis indicated that the surface property changes and resistance rise were responsible for the accumulated cycle capacity fade. The study provides a novel way to analyze the accumulated cycle capacity fade caused by the secondary particle fracture and is helpful for understanding the performance degradation mechanism of electrode material.

© 2004-2018 中国地质图书馆版权所有 京ICP备05064691号 京公网安备11010802017129号

地址:北京市海淀区学院路29号 邮编:100083

电话:办公室:(+86 10)66554848;文献借阅、咨询服务、科技查新:66554700