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Correlated dynamics in aqueous proton diffusion

The aqueous proton displays an anomalously large diffusion coefficient that is up to 7 times that of similarly sized cations. There is general consensus that the proton achieves its high diffusion through the Grotthuss mechanism, whereby protons hop from one molecule to the next. A main assumption c...

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Detalles Bibliográficos
Autores principales: Fischer, Sean A., Dunlap, Brett I., Gunlycke, Daniel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Royal Society of Chemistry 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6137442/
https://www.ncbi.nlm.nih.gov/pubmed/30310634
http://dx.doi.org/10.1039/c8sc01253a
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author Fischer, Sean A.
Dunlap, Brett I.
Gunlycke, Daniel
author_facet Fischer, Sean A.
Dunlap, Brett I.
Gunlycke, Daniel
author_sort Fischer, Sean A.
collection PubMed
description The aqueous proton displays an anomalously large diffusion coefficient that is up to 7 times that of similarly sized cations. There is general consensus that the proton achieves its high diffusion through the Grotthuss mechanism, whereby protons hop from one molecule to the next. A main assumption concerning the extraction of the timescale of the Grotthuss mechanism from experimental results has been that, on average, there is an equal probability for the proton to hop to any of its neighboring water molecules. Herein, we present ab initio simulations that show this assumption is not generally valid. Specifically, we observe that there is an increased probability for the proton to revert back to its previous location. These correlations indicate that the interpretation of the experimental results need to be re-examined and suggest that the timescale of the Grotthuss mechanism is significantly shorter than was previously thought.
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spelling pubmed-61374422018-10-11 Correlated dynamics in aqueous proton diffusion Fischer, Sean A. Dunlap, Brett I. Gunlycke, Daniel Chem Sci Chemistry The aqueous proton displays an anomalously large diffusion coefficient that is up to 7 times that of similarly sized cations. There is general consensus that the proton achieves its high diffusion through the Grotthuss mechanism, whereby protons hop from one molecule to the next. A main assumption concerning the extraction of the timescale of the Grotthuss mechanism from experimental results has been that, on average, there is an equal probability for the proton to hop to any of its neighboring water molecules. Herein, we present ab initio simulations that show this assumption is not generally valid. Specifically, we observe that there is an increased probability for the proton to revert back to its previous location. These correlations indicate that the interpretation of the experimental results need to be re-examined and suggest that the timescale of the Grotthuss mechanism is significantly shorter than was previously thought. Royal Society of Chemistry 2018-07-30 /pmc/articles/PMC6137442/ /pubmed/30310634 http://dx.doi.org/10.1039/c8sc01253a Text en This journal is © The Royal Society of Chemistry 2018 http://creativecommons.org/licenses/by/3.0/ This article is freely available. This article is licensed under a Creative Commons Attribution 3.0 Unported Licence (CC BY 3.0)
spellingShingle Chemistry
Fischer, Sean A.
Dunlap, Brett I.
Gunlycke, Daniel
Correlated dynamics in aqueous proton diffusion
title Correlated dynamics in aqueous proton diffusion
title_full Correlated dynamics in aqueous proton diffusion
title_fullStr Correlated dynamics in aqueous proton diffusion
title_full_unstemmed Correlated dynamics in aqueous proton diffusion
title_short Correlated dynamics in aqueous proton diffusion
title_sort correlated dynamics in aqueous proton diffusion
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6137442/
https://www.ncbi.nlm.nih.gov/pubmed/30310634
http://dx.doi.org/10.1039/c8sc01253a
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