Distinct Reaction Characteristics of Electrolyte Additives for High-Voltage Lithium-Ion Batteries: Tris(trimethylsilyl) Phosphite, Borate, and Phosphate
- Authors
- Han, Young-Kyu; Yoo, Jaeik; Yim, Taeeun
- Issue Date
- Oct-2016
- Publisher
- PERGAMON-ELSEVIER SCIENCE LTD
- Keywords
- Battery electrolyte; additive reaction mechanism; high voltage; first-principles calculation
- Citation
- ELECTROCHIMICA ACTA, v.215, pp 455 - 465
- Pages
- 11
- Indexed
- SCI
SCIE
SCOPUS
- Journal Title
- ELECTROCHIMICA ACTA
- Volume
- 215
- Start Page
- 455
- End Page
- 465
- URI
- https://scholarworks.dongguk.edu/handle/sw.dongguk/23847
- DOI
- 10.1016/j.electacta.2016.08.131
- ISSN
- 0013-4686
1873-3859
- Abstract
- Tris(trimethylsilyl) phosphite, tris(trimethylsilyl) borate, and tris(trimethylsilyl) phosphate are well known as effective electrolyte additives that noticeably improve the electrochemical performance of the cathode material in high-voltage lithium-ion batteries. It is essential to understand the reaction characteristics of such additives for developing novel electrolyte additives for high-voltage batteries. This work reports the distinct reaction characteristics of the three popular additives via first-principles calculations of self-decomposition reactions and reactivity with HF and LiF that significantly degrade the cell performance. Spontaneous decomposition reactions of their neutral and cation species are all thermodynamically unfavorable, which indicates that the additives themselves have difficulty decomposing even in the cation state. The HF- and LiF-scavenging reactions of their neutral and cation species are all very favorable. Our results indicate that the strong reactivity of additives can efficiently remove the undesired molecules HF and LiF in the electrolyte and on the cathode surface, respectively. In particular, LiF-scavenging ability on the cathode surface is excellent. (C) 2016 Elsevier Ltd. All rights reserved.
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Collections - College of Engineering > Department of Energy and Materials Engineering > 1. Journal Articles

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