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Potentials in Li-Ion Batteries Probed by Operando Ambient Pressure Photoelectron Spectroscopy
[Image: see text] The important electrochemical processes in a battery happen at the solid/liquid interfaces. Operando ambient pressure photoelectron spectroscopy (APPES) is one tool to study these processes with chemical specificity. However, accessing this crucial interface and identifying the int...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2022
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8832392/ https://www.ncbi.nlm.nih.gov/pubmed/35099928 http://dx.doi.org/10.1021/acsami.1c12465 |
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author | Källquist, Ida Ericson, Tove Lindgren, Fredrik Chen, Heyin Shavorskiy, Andrey Maibach, Julia Hahlin, Maria |
author_facet | Källquist, Ida Ericson, Tove Lindgren, Fredrik Chen, Heyin Shavorskiy, Andrey Maibach, Julia Hahlin, Maria |
author_sort | Källquist, Ida |
collection | PubMed |
description | [Image: see text] The important electrochemical processes in a battery happen at the solid/liquid interfaces. Operando ambient pressure photoelectron spectroscopy (APPES) is one tool to study these processes with chemical specificity. However, accessing this crucial interface and identifying the interface signal are not trivial. Therefore, we present a measurement setup, together with a suggested model, exemplifying how APPES can be used to probe potential differences over the electrode/electrolyte interface, even without direct access to the interface. Both the change in electron electrochemical potential over the solid/liquid interface, and the change in Li chemical potential of the working electrode (WE) surface at Li-ion equilibrium can be probed. Using a Li(4)Ti(5)O(12) composite as a WE, our results show that the shifts in kinetic energy of the electrolyte measured by APPES can be correlated to the electrochemical reactions occurring at the WE/electrolyte interface. Different shifts in kinetic energy are seen depending on if a phase transition reaction occurs or if a single phase is lithiated. The developed methodology can be used to evaluate charge transfer over the WE/electrolyte interface as well as the lithiation/delithiation mechanism of the WE. |
format | Online Article Text |
id | pubmed-8832392 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-88323922022-02-11 Potentials in Li-Ion Batteries Probed by Operando Ambient Pressure Photoelectron Spectroscopy Källquist, Ida Ericson, Tove Lindgren, Fredrik Chen, Heyin Shavorskiy, Andrey Maibach, Julia Hahlin, Maria ACS Appl Mater Interfaces [Image: see text] The important electrochemical processes in a battery happen at the solid/liquid interfaces. Operando ambient pressure photoelectron spectroscopy (APPES) is one tool to study these processes with chemical specificity. However, accessing this crucial interface and identifying the interface signal are not trivial. Therefore, we present a measurement setup, together with a suggested model, exemplifying how APPES can be used to probe potential differences over the electrode/electrolyte interface, even without direct access to the interface. Both the change in electron electrochemical potential over the solid/liquid interface, and the change in Li chemical potential of the working electrode (WE) surface at Li-ion equilibrium can be probed. Using a Li(4)Ti(5)O(12) composite as a WE, our results show that the shifts in kinetic energy of the electrolyte measured by APPES can be correlated to the electrochemical reactions occurring at the WE/electrolyte interface. Different shifts in kinetic energy are seen depending on if a phase transition reaction occurs or if a single phase is lithiated. The developed methodology can be used to evaluate charge transfer over the WE/electrolyte interface as well as the lithiation/delithiation mechanism of the WE. American Chemical Society 2022-01-31 2022-02-09 /pmc/articles/PMC8832392/ /pubmed/35099928 http://dx.doi.org/10.1021/acsami.1c12465 Text en © 2022 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by/4.0/Permits the broadest form of re-use including for commercial purposes, provided that author attribution and integrity are maintained (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Källquist, Ida Ericson, Tove Lindgren, Fredrik Chen, Heyin Shavorskiy, Andrey Maibach, Julia Hahlin, Maria Potentials in Li-Ion Batteries Probed by Operando Ambient Pressure Photoelectron Spectroscopy |
title | Potentials
in Li-Ion Batteries Probed by Operando
Ambient Pressure Photoelectron Spectroscopy |
title_full | Potentials
in Li-Ion Batteries Probed by Operando
Ambient Pressure Photoelectron Spectroscopy |
title_fullStr | Potentials
in Li-Ion Batteries Probed by Operando
Ambient Pressure Photoelectron Spectroscopy |
title_full_unstemmed | Potentials
in Li-Ion Batteries Probed by Operando
Ambient Pressure Photoelectron Spectroscopy |
title_short | Potentials
in Li-Ion Batteries Probed by Operando
Ambient Pressure Photoelectron Spectroscopy |
title_sort | potentials
in li-ion batteries probed by operando
ambient pressure photoelectron spectroscopy |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8832392/ https://www.ncbi.nlm.nih.gov/pubmed/35099928 http://dx.doi.org/10.1021/acsami.1c12465 |
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