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Cited by 1,059

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Superconcentrated electrolytes for a high-voltage lithium-ion battery

Open access
Wang, Jianhui, Yamada, Yuki, Sodeyama, Keitaro, Chiang, Ching Hua, Tateyama, Yoshitaka, Yamada, Atsuo·2016·Nature Communications

Abstract

Finding a viable electrolyte for next-generation 5 V-class lithium-ion batteries is of primary importance. A long-standing obstacle has been metal-ion dissolution at high voltages. The LiPF 6 salt in conventional electrolytes is chemically unstable, which accelerates transition metal dissolution of the electrode material, yet beneficially suppresses oxidative dissolution of the aluminium current collector; replacing LiPF 6 with more stable lithium salts may diminish transition metal dissolution but unfortunately encounters severe aluminium oxidation. Here we report an electrolyte design that can solve this dilemma. By mixing a stable lithium salt LiN(SO 2 F)2 with dimethyl carbonate solvent at extremely high concentrations, we obtain an unusual liquid showing a three-dimensional network of anions and solvent molecules that coordinate strongly to Li+ ions. This simple formulation of superconcentrated LiN(SO 2 F)2/dimethyl carbonate electrolyte inhibits the dissolution of both aluminium and transition metal at around 5 V, and realizes a high-voltage LiNi 0.5 Mn 1.5 O 4/graphite battery that exhibits excellent cycling durability, high rate capability and enhanced safety.

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Metadata

Authors
Wang, J., Yamada, Y., Sodeyama, K., Chiang, C. H., Tateyama, Y., & Yamada, A.
Venue
Nature Communications
Published
2016-06-29
Volume
7
Issue
1
Pages
12032-12032
ISSN
2041-1723 (ISSN-L)
OpenAlex
W2469089667
Cited by
1,059
References
1
FWCI
34.00
Type
journal article
Language
en
Open access
gold

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CoChat. (2026). Citation check: Superconcentrated electrolytes for a high-voltage lithium-ion battery. https://app.cochat.ai/papers/10.1038/ncomms12032
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Wang, J., Yamada, Y., Sodeyama, K., Chiang, C. H., Tateyama, Y., & Yamada, A. (2016). Superconcentrated electrolytes for a high-voltage lithium-ion battery. Nature Communications. https://doi.org/10.1038/ncomms12032

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