Supramolecular Self-Assembly of Nanoconfined Ionic Liquids for Fast Anisotropic Ion Transport

Tutkimustuotos: Lehtiartikkelivertaisarvioitu

Tutkijat

Organisaatiot

  • Univ Paris Saclay, Universite Paris Saclay (ComUE), Centre National de la Recherche Scientifique (CNRS), Universite Paris Sud - Paris 11, Universite Paris Saclay, Lab Phys Solides, CNRS, Univ Paris Sud
  • European Synchrotron Radiat Facil, European Synchrotron Radiation Facility (ESRF)
  • Mohammed VI Polytech Univ, Mohammed VI Polytechnic University, Mat Sci & Nanoengn
  • Univ Grenoble Alpes, CEA, Centre National de la Recherche Scientifique (CNRS), Communaute Universite Grenoble Alpes, Universite Grenoble Alpes (UGA), CNRS, CEA, IRIG SyMMES

Kuvaus

Materials involving nanoconfinement of ionic liquids (ILs) have been pursued for functionalities and ionic devices. However, their complex synthesis, challenges to achieve long-range order, and laborious tunability limit their practical implementation. Herein, these challenges are addressed by complexing surfactants to ILs, yielding a facile, modular, and scalable approach. Based on structural screening, ionic complexation of di-n-nonylamine to the terminal sulfonic acid of 1-(4-sulfobutyl)-3-methylimidazolium hydrogen sulfate IL is selected as a proof of concept. Spontaneous homeotropic smectic order over micrometers is observed, with alternating ionic and alkyl layers. The 1 nm thick ionic layers involve 2D crystalline internal order up to 150 degrees C, strongly promoting anisotropic ion transport (sigma(||)/sigma(perpendicular to) > 6500), and curiously, still allowing fluidity. High ionic conductivity of 35 mS cm(-1) and mesoscopic diffusion coefficient of approximate to 10(-5) cm(2) s(-1) at 150 degrees C along the ionic layers are observed. Fast anisotropic ion transport by simply complexing two components open doors to functional materials and applications.

Yksityiskohdat

AlkuperäiskieliEnglanti
Artikkeli1905054
Sivumäärä8
JulkaisuAdvanced Functional Materials
Varhainen verkossa julkaisun päivämäärä3 lokakuuta 2019
TilaJulkaistu - 2019
OKM-julkaisutyyppiA1 Julkaistu artikkeli, soviteltu

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