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Superionicity by design: high proton conductivity in a fluorine-free protic ionic liquid.

Authors :
Schütz, Hanno Maria
Nejrotti, Stefano
Adenusi, Henry
Mariani, Alessandro
Bodo, Enrico
Bonomo, Matteo
Innocenti, Alessandro
Barolo, Claudia
Gao, Xinpei
Passerini, Stefano
Source :
Journal of Materials Chemistry A; 8/7/2024, Vol. 12 Issue 29, p18412-18422, 11p
Publication Year :
2024

Abstract

In this study, the protic ionic liquid N,N-diethyl-3-sulfopropan-1-ammonium hydrogen methanedisulfonate is synthesized and characterized with the aim of elucidating its transport properties. A unique feature of this ionic liquid are the exchangeable acidic protons present on the anion and the cation, both of which contain low proton affinity sulfonic groups. The pronounced superionicity of this liquid, highlighted in the Walden-plot (ΔW > 0.8), indicates the decoupling of the conductivity from ionic diffusion. To explicate this enhanced proton mobility, the diffusion coefficients of the protons were measured by Pulsed-Field Gradient Spin-Echo NMR experiments at different temperatures. Below 373 K the diffusion coefficients of the cationic and anionic exchangeable protons are comparable with the ones of the other protons of the respective ions, indicating a vehicular transport mechanism. However, in the temperature range 383–413 K the diffusion coefficient of one of the exchangeable protons exceeds the diffusion of both ions by an unprecedented factor between 2 and 3. This temperature-induced switch in the proton transport mechanism is the result of a mixed-ion proton-transfer chain, as also supported by computational simulations. Both experimental and theoretical findings suggest the existence of a Grotthuss(-like) proton transport mechanism at high temperature in this system. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
20507488
Volume :
12
Issue :
29
Database :
Complementary Index
Journal :
Journal of Materials Chemistry A
Publication Type :
Academic Journal
Accession number :
178594595
Full Text :
https://doi.org/10.1039/d4ta02880e