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Electrolyte contact changes nano-Li(4)Ti(5)O(12) bulk properties via surface polarons

It is of general interest to combine the faradaic processes based high energy density of a battery with the non-faradaic processes based high power density of a capacitor in one cell. Surface area and functional groups of electrode materials strongly affect these properties. For the anode material L...

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Autores principales: Schleker, P. Philipp M., Grosu, Cristina, Paulus, Marc, Jakes, Peter, Schlögl, Robert, Eichel, Rüdiger-A., Scheurer, Christoph, Granwehr, Josef
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10247714/
https://www.ncbi.nlm.nih.gov/pubmed/37286703
http://dx.doi.org/10.1038/s42004-023-00913-6
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author Schleker, P. Philipp M.
Grosu, Cristina
Paulus, Marc
Jakes, Peter
Schlögl, Robert
Eichel, Rüdiger-A.
Scheurer, Christoph
Granwehr, Josef
author_facet Schleker, P. Philipp M.
Grosu, Cristina
Paulus, Marc
Jakes, Peter
Schlögl, Robert
Eichel, Rüdiger-A.
Scheurer, Christoph
Granwehr, Josef
author_sort Schleker, P. Philipp M.
collection PubMed
description It is of general interest to combine the faradaic processes based high energy density of a battery with the non-faradaic processes based high power density of a capacitor in one cell. Surface area and functional groups of electrode materials strongly affect these properties. For the anode material Li(4)Ti(5)O(12) (LTO), we suggest a polaron based mechanism that influences Li ion uptake and mobility. Here we show electrolytes containing a lithium salt induce an observable change in the bulk NMR relaxation properties of LTO nano particles. The longitudinal (7)Li NMR relaxation time of bulk LTO can change by almost an order of magnitude and, therefore, reacts very sensitively to the cation and its concentration in the surrounding electrolyte. The reversible effect is largely independent of the used anions and of potential anion decomposition products. It is concluded that lithium salt containing electrolytes increase the mobility of surface polarons. These polarons and additional lithium cations from the electrolyte can now diffuse through the bulk, induce the observed enhanced relaxation rate and enable the non-faradaic process. This picture of a Li(+) ion equilibrium between electrolyte and solid may help with improving the charging properties of electrode materials.
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spelling pubmed-102477142023-06-09 Electrolyte contact changes nano-Li(4)Ti(5)O(12) bulk properties via surface polarons Schleker, P. Philipp M. Grosu, Cristina Paulus, Marc Jakes, Peter Schlögl, Robert Eichel, Rüdiger-A. Scheurer, Christoph Granwehr, Josef Commun Chem Article It is of general interest to combine the faradaic processes based high energy density of a battery with the non-faradaic processes based high power density of a capacitor in one cell. Surface area and functional groups of electrode materials strongly affect these properties. For the anode material Li(4)Ti(5)O(12) (LTO), we suggest a polaron based mechanism that influences Li ion uptake and mobility. Here we show electrolytes containing a lithium salt induce an observable change in the bulk NMR relaxation properties of LTO nano particles. The longitudinal (7)Li NMR relaxation time of bulk LTO can change by almost an order of magnitude and, therefore, reacts very sensitively to the cation and its concentration in the surrounding electrolyte. The reversible effect is largely independent of the used anions and of potential anion decomposition products. It is concluded that lithium salt containing electrolytes increase the mobility of surface polarons. These polarons and additional lithium cations from the electrolyte can now diffuse through the bulk, induce the observed enhanced relaxation rate and enable the non-faradaic process. This picture of a Li(+) ion equilibrium between electrolyte and solid may help with improving the charging properties of electrode materials. Nature Publishing Group UK 2023-06-07 /pmc/articles/PMC10247714/ /pubmed/37286703 http://dx.doi.org/10.1038/s42004-023-00913-6 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Schleker, P. Philipp M.
Grosu, Cristina
Paulus, Marc
Jakes, Peter
Schlögl, Robert
Eichel, Rüdiger-A.
Scheurer, Christoph
Granwehr, Josef
Electrolyte contact changes nano-Li(4)Ti(5)O(12) bulk properties via surface polarons
title Electrolyte contact changes nano-Li(4)Ti(5)O(12) bulk properties via surface polarons
title_full Electrolyte contact changes nano-Li(4)Ti(5)O(12) bulk properties via surface polarons
title_fullStr Electrolyte contact changes nano-Li(4)Ti(5)O(12) bulk properties via surface polarons
title_full_unstemmed Electrolyte contact changes nano-Li(4)Ti(5)O(12) bulk properties via surface polarons
title_short Electrolyte contact changes nano-Li(4)Ti(5)O(12) bulk properties via surface polarons
title_sort electrolyte contact changes nano-li(4)ti(5)o(12) bulk properties via surface polarons
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10247714/
https://www.ncbi.nlm.nih.gov/pubmed/37286703
http://dx.doi.org/10.1038/s42004-023-00913-6
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