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Li+-Desolvation Dictating Lithium-Ion Battery’s Low-Temperature Performances
Author(s) -
Qiuyan Li,
Dongping Lu,
Jianming Zheng,
Shuhong Jiao,
Langli Luo,
Chongmin Wang,
Kang Xu,
JiGuang Zhang,
Wu Xu
Publication year - 2017
Publication title -
acs applied materials and interfaces
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.535
H-Index - 228
eISSN - 1944-8252
pISSN - 1944-8244
DOI - 10.1021/acsami.7b13887
Subject(s) - battery (electricity) , electrochemistry , materials science , lithium (medication) , electrolyte , ion , electronics , kinetic energy , lithium ion battery , energy storage , graphite , nanotechnology , work (physics) , molecule , chemical physics , chemical engineering , electrode , chemistry , thermodynamics , organic chemistry , physics , medicine , power (physics) , quantum mechanics , composite material , endocrinology , engineering
Lithium (Li) ion battery has penetrated almost every aspect of human life, from portable electronics, vehicles, to grids, and its operation stability in extreme environments is becoming increasingly important. Among these, subzero temperature presents a kinetic challenge to the electrochemical reactions required to deliver the stored energy. In this work, we attempted to identify the rate-determining process for Li + migration under such low temperatures, so that an optimum electrolyte formulation could be designed to maximize the energy output. Substantial increase in the available capacities from graphite∥LiNi 0.80 Co 0.15 Al 0.05 O 2 chemistry down to -40 °C is achieved by reducing the solvent molecule that more tightly binds to Li + and thus constitutes a high desolvation energy barrier. The fundamental understanding is applicable universally to a wide spectrum of electrochemical devices that have to operate in similar environments.

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