Monolayer to Bilayer Structural Transition in Confined Pyrrolidinium-Based Ionic Liquids

Ionic liquids can be intricately nanostructured in the bulk and at interfaces resulting from a delicate interplay between interionic and surface forces. Here we report the structuring of a series of dialkylpyrrolidinium-based ionic liquids induced by confinement. The ionic liquids containing cations...

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主要な著者: Smith, A, Lovelock, K, Gosvami, N, Licence, P, Dolan, A, Welton, T, Perkin, S
フォーマット: Journal article
言語:English
出版事項: 2013
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author Smith, A
Lovelock, K
Gosvami, N
Licence, P
Dolan, A
Welton, T
Perkin, S
author_facet Smith, A
Lovelock, K
Gosvami, N
Licence, P
Dolan, A
Welton, T
Perkin, S
author_sort Smith, A
collection OXFORD
description Ionic liquids can be intricately nanostructured in the bulk and at interfaces resulting from a delicate interplay between interionic and surface forces. Here we report the structuring of a series of dialkylpyrrolidinium-based ionic liquids induced by confinement. The ionic liquids containing cations with shorter alkyl chain substituents form alternating cation-anion monolayer structures on confinement to a thin film, whereas a cation with a longer alkyl chain substituent leads to bilayer formation. The crossover from monolayer to bilayer structure occurs between chain lengths of n = 8 and 10 for these pyrrolidinium-based ionic liquids. The bilayer structure for n = 10 involves full interdigitation of the alkyl chains; this is in contrast with previous observations for imidazolium-based ionic liquids. The results are pertinent to these liquids' application as electrolytes, where the electrolyte is confined inside the pores of a nanoporous electrode, for example, in devices such as supercapacitors or batteries. © 2013 American Chemical Society.
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spelling oxford-uuid:8d653b43-7ce2-4739-8246-4eb4aeddecc52022-03-26T22:50:59ZMonolayer to Bilayer Structural Transition in Confined Pyrrolidinium-Based Ionic LiquidsJournal articlehttp://purl.org/coar/resource_type/c_dcae04bcuuid:8d653b43-7ce2-4739-8246-4eb4aeddecc5EnglishSymplectic Elements at Oxford2013Smith, ALovelock, KGosvami, NLicence, PDolan, AWelton, TPerkin, SIonic liquids can be intricately nanostructured in the bulk and at interfaces resulting from a delicate interplay between interionic and surface forces. Here we report the structuring of a series of dialkylpyrrolidinium-based ionic liquids induced by confinement. The ionic liquids containing cations with shorter alkyl chain substituents form alternating cation-anion monolayer structures on confinement to a thin film, whereas a cation with a longer alkyl chain substituent leads to bilayer formation. The crossover from monolayer to bilayer structure occurs between chain lengths of n = 8 and 10 for these pyrrolidinium-based ionic liquids. The bilayer structure for n = 10 involves full interdigitation of the alkyl chains; this is in contrast with previous observations for imidazolium-based ionic liquids. The results are pertinent to these liquids' application as electrolytes, where the electrolyte is confined inside the pores of a nanoporous electrode, for example, in devices such as supercapacitors or batteries. © 2013 American Chemical Society.
spellingShingle Smith, A
Lovelock, K
Gosvami, N
Licence, P
Dolan, A
Welton, T
Perkin, S
Monolayer to Bilayer Structural Transition in Confined Pyrrolidinium-Based Ionic Liquids
title Monolayer to Bilayer Structural Transition in Confined Pyrrolidinium-Based Ionic Liquids
title_full Monolayer to Bilayer Structural Transition in Confined Pyrrolidinium-Based Ionic Liquids
title_fullStr Monolayer to Bilayer Structural Transition in Confined Pyrrolidinium-Based Ionic Liquids
title_full_unstemmed Monolayer to Bilayer Structural Transition in Confined Pyrrolidinium-Based Ionic Liquids
title_short Monolayer to Bilayer Structural Transition in Confined Pyrrolidinium-Based Ionic Liquids
title_sort monolayer to bilayer structural transition in confined pyrrolidinium based ionic liquids
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