Interfacing electrolytes with electrodes in Li ion batteries

被引:367
作者
Xu, Kang [1 ]
von Cresce, Arthur [1 ]
机构
[1] USA, Res Lab, Sensor & Electron Devices Directorate, Electrochem Branch,Power & Energy Div, Adelphi, MD 20783 USA
关键词
RAY PHOTOELECTRON-SPECTROSCOPY; ORIENTED PYROLYTIC-GRAPHITE; SULFONE-BASED ELECTROLYTES; THIN-FILM ELECTRODES; NATURAL GRAPHITE; ELECTROCHEMICAL PERFORMANCE; SOLID-ELECTROLYTE; SPINEL CATHODE; GRAPHITE/ELECTROLYTE INTERFACE; SURFACE MODIFICATION;
D O I
10.1039/c0jm04309e
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070305 [高分子化学与物理];
摘要
-A poetic definition of a binary liquid/solid interface by Luis de Camoes (1572). Since its birth in early 1990s, Li ion battery technology has been powering the rapid digitization of our daily life and finally made its debut in 2010 into the large format application for electrified vehicles such as the Nissan Leaf and GM Chevrolet Volt; however, much of the chemistry and processes underneath this amazing energy storage device still remain to be understood, among which is the interphase between electrolyte and electrodes. Interphases are formed in situ on electrode surfaces from sacrificial decomposition of electrolytes. Their ad hoc chemistry supports the reversible Li+-intercalation in both anode and cathode materials at extreme potentials, while preventing parasitic reductions/oxidations on the reactive surfaces of those electrodes; but their existence places restrictions on energy and power densities of the device by impeding Li+-transport and setting operating voltage limits, respectively. It has been the dream of battery engineers to maximize the former and minimize the latter. This review summarizes the most recent knowledge about the chemistry and formation mechanism of this elusive battery component on both anode and cathode surfaces. The attempts to tailor a desired interphasial chemistry via diversified means were also discussed.
引用
收藏
页码:9849 / 9864
页数:16
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