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Synthesis and Properties of Acyclic Ammonium-based Ionic Liquids with Allyl Substituents as Electrolytes

Several new acyclic ammonium-TFSI ionic liquids with an allyl substituent(s) were synthesized and their physicochemical and electrochemical properties were characterized. [AAMM]Am-TFSI (3) with two allyl groups showed the widest electrochemical stability window (5.9 V) among the ammonium-based ILs r...

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Autores principales: Yim, Taeeun, Choi, Chang Young, Mun, Junyoung, Oh, Seung M., Kim, Young Gyu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Molecular Diversity Preservation International 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6254279/
https://www.ncbi.nlm.nih.gov/pubmed/19471204
http://dx.doi.org/10.3390/molecules14051840
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author Yim, Taeeun
Choi, Chang Young
Mun, Junyoung
Oh, Seung M.
Kim, Young Gyu
author_facet Yim, Taeeun
Choi, Chang Young
Mun, Junyoung
Oh, Seung M.
Kim, Young Gyu
author_sort Yim, Taeeun
collection PubMed
description Several new acyclic ammonium-TFSI ionic liquids with an allyl substituent(s) were synthesized and their physicochemical and electrochemical properties were characterized. [AAMM]Am-TFSI (3) with two allyl groups showed the widest electrochemical stability window (5.9 V) among the ammonium-based ILs reported to date because of the increment of both the anodic and cathodic limits. The charge-discharge performance of a LiCoO(2)-based half-cell containing [AAMM]Am-TFSI as an electrolyte was better in cycleability (the capacity retention ratio: 99% after 20 cycles) than that of the cell with the corresponding partially saturated analogue, [AMMP]Am-TFSI (2) (the capacity retention ratio: 92% after 20 cycles).
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spelling pubmed-62542792018-11-30 Synthesis and Properties of Acyclic Ammonium-based Ionic Liquids with Allyl Substituents as Electrolytes Yim, Taeeun Choi, Chang Young Mun, Junyoung Oh, Seung M. Kim, Young Gyu Molecules Article Several new acyclic ammonium-TFSI ionic liquids with an allyl substituent(s) were synthesized and their physicochemical and electrochemical properties were characterized. [AAMM]Am-TFSI (3) with two allyl groups showed the widest electrochemical stability window (5.9 V) among the ammonium-based ILs reported to date because of the increment of both the anodic and cathodic limits. The charge-discharge performance of a LiCoO(2)-based half-cell containing [AAMM]Am-TFSI as an electrolyte was better in cycleability (the capacity retention ratio: 99% after 20 cycles) than that of the cell with the corresponding partially saturated analogue, [AMMP]Am-TFSI (2) (the capacity retention ratio: 92% after 20 cycles). Molecular Diversity Preservation International 2009-05-15 /pmc/articles/PMC6254279/ /pubmed/19471204 http://dx.doi.org/10.3390/molecules14051840 Text en © 2009 by the authors; licensee Molecular Diversity Preservation International, Basel, Switzerland. This article is an open-access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/3.0/).
spellingShingle Article
Yim, Taeeun
Choi, Chang Young
Mun, Junyoung
Oh, Seung M.
Kim, Young Gyu
Synthesis and Properties of Acyclic Ammonium-based Ionic Liquids with Allyl Substituents as Electrolytes
title Synthesis and Properties of Acyclic Ammonium-based Ionic Liquids with Allyl Substituents as Electrolytes
title_full Synthesis and Properties of Acyclic Ammonium-based Ionic Liquids with Allyl Substituents as Electrolytes
title_fullStr Synthesis and Properties of Acyclic Ammonium-based Ionic Liquids with Allyl Substituents as Electrolytes
title_full_unstemmed Synthesis and Properties of Acyclic Ammonium-based Ionic Liquids with Allyl Substituents as Electrolytes
title_short Synthesis and Properties of Acyclic Ammonium-based Ionic Liquids with Allyl Substituents as Electrolytes
title_sort synthesis and properties of acyclic ammonium-based ionic liquids with allyl substituents as electrolytes
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6254279/
https://www.ncbi.nlm.nih.gov/pubmed/19471204
http://dx.doi.org/10.3390/molecules14051840
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