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Controlling Gas Generation of Li-Ion Battery through Divinyl Sulfone Electrolyte Additive

The focus of mainstream lithium-ion battery (LIB) research is on increasing the battery’s capacity and performance; however, more effort should be invested in LIB safety for widespread use. One aspect of major concern for LIB cells is the gas generation phenomenon. Following conventional battery eng...

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Autores principales: Choi, Woon Ih, Park, Insun, An, Jae Sik, Kim, Dong Young, Koh, Meiten, Jang, Inkook, Kim, Dae Sin, Kang, Yoon-Sok, Shim, Youngseon
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9267101/
https://www.ncbi.nlm.nih.gov/pubmed/35806333
http://dx.doi.org/10.3390/ijms23137328
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author Choi, Woon Ih
Park, Insun
An, Jae Sik
Kim, Dong Young
Koh, Meiten
Jang, Inkook
Kim, Dae Sin
Kang, Yoon-Sok
Shim, Youngseon
author_facet Choi, Woon Ih
Park, Insun
An, Jae Sik
Kim, Dong Young
Koh, Meiten
Jang, Inkook
Kim, Dae Sin
Kang, Yoon-Sok
Shim, Youngseon
author_sort Choi, Woon Ih
collection PubMed
description The focus of mainstream lithium-ion battery (LIB) research is on increasing the battery’s capacity and performance; however, more effort should be invested in LIB safety for widespread use. One aspect of major concern for LIB cells is the gas generation phenomenon. Following conventional battery engineering practices with electrolyte additives, we examined the potential usage of electrolyte additives to address this specific issue and found a feasible candidate in divinyl sulfone (DVSF). We manufactured four identical battery cells and employed an electrolyte mixture with four different DVSF concentrations (0%, 0.5%, 1.0%, and 2.0%). By measuring the generated gas volume from each battery cell, we demonstrated the potential of DVSF additives as an effective approach for reducing the gas generation in LIB cells. We found that a DVSF concentration of only 1% was necessary to reduce the gas generation by approximately 50% while simultaneously experiencing a negligible impact on the cycle life. To better understand this effect on a molecular level, we examined possible electrochemical reactions through ab initio molecular dynamics (AIMD) based on the density functional theory (DFT). From the electrolyte mixture’s exposure to either an electrochemically reductive or an oxidative environment, we determined the reaction pathways for the generation of CO(2) gas and the mechanism by which DVSF additives effectively blocked the gas’s generation. The key reaction was merging DVSF with cyclic carbonates, such as FEC. Therefore, we concluded that DVSF additives could offer a relatively simplistic and effective approach for controlling the gas generation in lithium-ion batteries.
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spelling pubmed-92671012022-07-09 Controlling Gas Generation of Li-Ion Battery through Divinyl Sulfone Electrolyte Additive Choi, Woon Ih Park, Insun An, Jae Sik Kim, Dong Young Koh, Meiten Jang, Inkook Kim, Dae Sin Kang, Yoon-Sok Shim, Youngseon Int J Mol Sci Communication The focus of mainstream lithium-ion battery (LIB) research is on increasing the battery’s capacity and performance; however, more effort should be invested in LIB safety for widespread use. One aspect of major concern for LIB cells is the gas generation phenomenon. Following conventional battery engineering practices with electrolyte additives, we examined the potential usage of electrolyte additives to address this specific issue and found a feasible candidate in divinyl sulfone (DVSF). We manufactured four identical battery cells and employed an electrolyte mixture with four different DVSF concentrations (0%, 0.5%, 1.0%, and 2.0%). By measuring the generated gas volume from each battery cell, we demonstrated the potential of DVSF additives as an effective approach for reducing the gas generation in LIB cells. We found that a DVSF concentration of only 1% was necessary to reduce the gas generation by approximately 50% while simultaneously experiencing a negligible impact on the cycle life. To better understand this effect on a molecular level, we examined possible electrochemical reactions through ab initio molecular dynamics (AIMD) based on the density functional theory (DFT). From the electrolyte mixture’s exposure to either an electrochemically reductive or an oxidative environment, we determined the reaction pathways for the generation of CO(2) gas and the mechanism by which DVSF additives effectively blocked the gas’s generation. The key reaction was merging DVSF with cyclic carbonates, such as FEC. Therefore, we concluded that DVSF additives could offer a relatively simplistic and effective approach for controlling the gas generation in lithium-ion batteries. MDPI 2022-06-30 /pmc/articles/PMC9267101/ /pubmed/35806333 http://dx.doi.org/10.3390/ijms23137328 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Communication
Choi, Woon Ih
Park, Insun
An, Jae Sik
Kim, Dong Young
Koh, Meiten
Jang, Inkook
Kim, Dae Sin
Kang, Yoon-Sok
Shim, Youngseon
Controlling Gas Generation of Li-Ion Battery through Divinyl Sulfone Electrolyte Additive
title Controlling Gas Generation of Li-Ion Battery through Divinyl Sulfone Electrolyte Additive
title_full Controlling Gas Generation of Li-Ion Battery through Divinyl Sulfone Electrolyte Additive
title_fullStr Controlling Gas Generation of Li-Ion Battery through Divinyl Sulfone Electrolyte Additive
title_full_unstemmed Controlling Gas Generation of Li-Ion Battery through Divinyl Sulfone Electrolyte Additive
title_short Controlling Gas Generation of Li-Ion Battery through Divinyl Sulfone Electrolyte Additive
title_sort controlling gas generation of li-ion battery through divinyl sulfone electrolyte additive
topic Communication
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9267101/
https://www.ncbi.nlm.nih.gov/pubmed/35806333
http://dx.doi.org/10.3390/ijms23137328
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