期刊文献+

锂/氟化碳电池电解液的研究进展

Research progress on electrolyte for Li/CF_(x) battery
在线阅读 下载PDF
导出
摘要 锂/氟化碳(Li/CF_(x))电池作为一种具有最高理论比容量(860 mAh/g)和能量密度(2180 Wh/kg)的一次电池,具有高安全性能、低自放电率、平稳的放电电压和环境友好等优点,广泛应用于医疗、军事、电子科技和航空航天等领域。电解液作为Li/CF_(x)电池必不可缺的一部分,在正负极之间起到传递离子的作用,具有重要的研究意义。本文从Li/CF_(x)电池的低温性能、倍率性能以及放电平台等方面综述了Li/CF_(x)电池电解液的研究进展;重点阐述了电解液理化性质、界面浸润与相容、锂离子溶剂化结构、C—F键活化和LiF形成与溶解等因素对Li/CF_(x)电池放电性能的影响;最后,对Li/CF_(x)电池新型电解液的研究提出了思考与展望。 Li/CF_(x) battery,a primary battery with the highest theoretical specific capacity and energy density,has the advantages of high safety performance,low self-discharge rate,stable discharge voltage,and eco-friendliness and is widely used in the medical,military,electronic technology,aerospace,and other fields.Electrolyte,an indispensable component of Li/CF_(x) battery,plays a pivotal role in transferring ions between the anode and cathode;it has important research significance.In this review,we summarize the research progress on electrolytes for Li/CF_(x) batteries,especially emphasizing the relationships between electrolyte factors,such as the physicochemical properties of electrolytes,interface wettability and compatibility,lithium-ion solvation structure,C—F bond activation,LiF formation,and dissolution,and the electrochemical performance of Li/CF_(x) batteries,such as low-temperature performance,high-rate performance,and discharge voltage platform.Finally,future research directions for Li/CF_(x) battery electrolytes are discussed.
作者 卢俊杰 彭丹 倪文静 杨媛 汪靖伦 LU Junjie;PENG Dan;NI Wenjing;YANG Yuan;WANG Jinglun(School of Chemistry and Chemical Engineering,Key Laboratory of Theoretical Organic Chemistry and Functional Molecule,Ministry of Education,Hunan University of Science and Technology,Xiangtan 411201,Hunan,China)
出处 《储能科学与技术》 CAS CSCD 北大核心 2024年第5期1487-1495,共9页 Energy Storage Science and Technology
基金 湖南省普通高校青年骨干教师培养项目(H22105) 湖南省自然科学基金项目(2024JJ80) 岳麓山工业创新中心项目(2023YCII0108)。
关键词 电化学 锂/氟化碳电池 电解液 低温性能 倍率性能 electrochemistry Li/CF_(x)battery electrolytes low temperature performance high rate performance
  • 相关文献

参考文献8

二级参考文献28

共引文献86

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部