Swelling mechanism of polyoxazoline-based gel polymer electrolytes for Lithium-ion batteries
Identifikátory výsledku
Kód výsledku v IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F61389013%3A_____%2F25%3A00617720" target="_blank" >RIV/61389013:_____/25:00617720 - isvavai.cz</a>
Výsledek na webu
<a href="https://pubs.acs.org/doi/10.1021/acsapm.4c03473" target="_blank" >https://pubs.acs.org/doi/10.1021/acsapm.4c03473</a>
DOI - Digital Object Identifier
<a href="http://dx.doi.org/10.1021/acsapm.4c03473" target="_blank" >10.1021/acsapm.4c03473</a>
Alternativní jazyky
Jazyk výsledku
angličtina
Název v původním jazyce
Swelling mechanism of polyoxazoline-based gel polymer electrolytes for Lithium-ion batteries
Popis výsledku v původním jazyce
Gel polymer electrolytes for lithium-ion batteries are typically prepared by swelling a preprepared cross-linked polymer network with a solution of lithium salt. This step of the electrolyte preparation is assumed to be straightforward, and very little attention has been paid to the investigation of the swelling mechanism. We questioned the common assumption that the feed solution swells the polymer network at the same concentration and fed a polyoxazoline network with several concentrations of lithium bis(oxalato)borate and lithium bis(trifluoromethane)sulfonimide solutions in propylene carbonate and diglyme. We thoroughly analyzed the obtained gels using NMR and Raman spectroscopy and evaluated the content of the solvent and salt in the polymer matrix, their mutual interactions, and mobilities. We found that this assumption was invalid and created a model of swelling of a polyoxazoline network with a salt solution. Our model implies the importance of often neglected solvent–polymer interactions or lack thereof. In the context of the function of the polyoxazoline system, our results provide insights into the efficiency of polymer matrices for gel polymer electrolytes, which will help avoid inefficient polymer matrices in the future.
Název v anglickém jazyce
Swelling mechanism of polyoxazoline-based gel polymer electrolytes for Lithium-ion batteries
Popis výsledku anglicky
Gel polymer electrolytes for lithium-ion batteries are typically prepared by swelling a preprepared cross-linked polymer network with a solution of lithium salt. This step of the electrolyte preparation is assumed to be straightforward, and very little attention has been paid to the investigation of the swelling mechanism. We questioned the common assumption that the feed solution swells the polymer network at the same concentration and fed a polyoxazoline network with several concentrations of lithium bis(oxalato)borate and lithium bis(trifluoromethane)sulfonimide solutions in propylene carbonate and diglyme. We thoroughly analyzed the obtained gels using NMR and Raman spectroscopy and evaluated the content of the solvent and salt in the polymer matrix, their mutual interactions, and mobilities. We found that this assumption was invalid and created a model of swelling of a polyoxazoline network with a salt solution. Our model implies the importance of often neglected solvent–polymer interactions or lack thereof. In the context of the function of the polyoxazoline system, our results provide insights into the efficiency of polymer matrices for gel polymer electrolytes, which will help avoid inefficient polymer matrices in the future.
Klasifikace
Druh
J<sub>imp</sub> - Článek v periodiku v databázi Web of Science
CEP obor
—
OECD FORD obor
10404 - Polymer science
Návaznosti výsledku
Projekt
—
Návaznosti
I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace
Ostatní
Rok uplatnění
2025
Kód důvěrnosti údajů
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů
Údaje specifické pro druh výsledku
Název periodika
ACS Applied Polymer Materials
ISSN
2637-6105
e-ISSN
2637-6105
Svazek periodika
7
Číslo periodika v rámci svazku
4
Stát vydavatele periodika
US - Spojené státy americké
Počet stran výsledku
13
Strana od-do
2371-2383
Kód UT WoS článku
001435148400001
EID výsledku v databázi Scopus
2-s2.0-86000387505