Pushing the Theoretical Limit of Li-CFx Batteries: A Tale of Bifunctional Electrolyte

被引:80
|
作者
Rangasamy, Ezhiylmurugan [1 ]
Li, Juchuan [2 ]
Sahu, Gayatri [1 ]
Dudney, Nancy [2 ]
Liang, Chengdu [1 ]
机构
[1] Oak Ridge Natl Lab, Ctr Nanophase Mat Sci, Oak Ridge, TN 37831 USA
[2] Oak Ridge Natl Lab, Div Mat Sci & Technol, Oak Ridge, TN 37831 USA
关键词
IONIC-CONDUCTIVITY; LITHIUM; MECHANISM; LI/CFX; XPS;
D O I
10.1021/ja5026358
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
In a typical battery, the inert electrolyte functions solely as the ionic conductor without contribution to the cell capacity. Here we demonstrate that the most energy-dense Li-CFx battery delivers a capacity exceeding the theoretical maximum of CFx with a solid electrolyte of Li3PS4 (LPS) that has dual functions: as the inert electrolyte at the anode and the active component at the cathode. Such a bifunctional electrolyte reconciles both inert and active characteristics through a synergistic discharge mechanism of CFx and LPS. The synergy at the cathode is through LiF, the discharge product of CFx which activates the electrochemical discharge of LPS at a close electrochemical potential of CFx. Therefore, the solid-state Li-CFx batteries output 126.6% energy beyond their theoretic limits without compromising the stability of the cell voltage. The additional energy comes from the electrochemical discharge of LPS, the inert electrolyte. This bifunctional electrolyte revolutionizes the concept of conventional batteries and opens a new avenue for the design of batteries with unprecedented energy density.
引用
收藏
页码:6874 / 6877
页数:4
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