Form of presentation | Articles in international journals and collections |
Year of publication | 2021 |
Язык | английский |
|
Gnezdilov Oleg Ivanovich, author
|
Bibliographic description in the original language |
Khan Inayat Ali, Ion Transport and Electrochemical Properties of Fluorine-Free Lithium-Ion Battery Electrolytes Derived from Biomass / Inayat Ali Khan, O. I. Gnezdilov, A. Filippov, and Faiz Ullah Shah// ACS Sustainable Chem. Eng. - 2021. -N. 9. - P. 7769−7780. |
Annotation |
Unlike conventional electrolytes, ionic liquid (IL)-based electrolytes
o ff er higher thermal stabil ity, acceptab le ionic c onductivit y, and a higher electrochemical stability window (ESW), which are indispensable for the proper functioning of Li-ion batteries. In this study, fl uorine-free electrolytes are prepared by mixing the lithium furan-2-carboxylate [Li(FuA)] salt with the tetra(n -butyl)-phosphonium furan-2-carboxylate [(P4444)(FuA)] IL in diff erent molar ratios. The anion of these electrolytes is produced from biomass and agricultural waste on a large scale and, therefore, this study is a step ahead toward the development of renewable
electrolytes for batteries. The electrolytes are found to have T onset higher than 568 K and acceptable ionic conductivities in a wide temperature range. The pulsed field gradient nuclear magnetic resonance (PFG-NMR) analysis has con firmed that the
(FuA)− anion di ff uses faster than the (P 4444)+ cation in the neat (P 4444)(FuA) IL; however, the anion diff usion becomes slower than cation di ffusion by doping Li salt. The Li + ion interacts strongly with the carboxylate functionality in the (FuA)− anion and diff uses slower than other ions over the whole studied temperature range. The interaction of the Li+ ion with the carboxylate group is also confi rmed by 7 Li NMR and
Fourier transform infrared (FTIR) spectroscopy. The transference number of the Li+ ion is increased with increasing Li salt
concentration. Linear sweep voltammetry (LSV) suggests lithium underpotential deposition and bulk reduction at temperatures
above 313 K. |
Keywords |
renewable electrolytes, furan-2-carboxylate, ionic conductivity, nuclear magnetic resonance, underpotential deposition |
The name of the journal |
ACS Sustainable Chemistry and Engineering
|
URL |
https://pubs.acs.org/10.1021/acssuschemeng.1c00939 |
Please use this ID to quote from or refer to the card |
https://repository.kpfu.ru/eng/?p_id=258155&p_lang=2 |
Resource files | |
|
Full metadata record |
Field DC |
Value |
Language |
dc.contributor.author |
Gnezdilov Oleg Ivanovich |
ru_RU |
dc.date.accessioned |
2021-01-01T00:00:00Z |
ru_RU |
dc.date.available |
2021-01-01T00:00:00Z |
ru_RU |
dc.date.issued |
2021 |
ru_RU |
dc.identifier.citation |
Khan Inayat Ali, Ion Transport and Electrochemical Properties of Fluorine-Free Lithium-Ion Battery Electrolytes Derived from Biomass / Inayat Ali Khan, O. I. Gnezdilov, A. Filippov, and Faiz Ullah Shah// ACS Sustainable Chem. Eng. - 2021. -N. 9. - P. 7769−7780. |
ru_RU |
dc.identifier.uri |
https://repository.kpfu.ru/eng/?p_id=258155&p_lang=2 |
ru_RU |
dc.description.abstract |
ACS Sustainable Chemistry and Engineering |
ru_RU |
dc.description.abstract |
Unlike conventional electrolytes, ionic liquid (IL)-based electrolytes
o ff er higher thermal stabil ity, acceptab le ionic c onductivit y, and a higher electrochemical stability window (ESW), which are indispensable for the proper functioning of Li-ion batteries. In this study, fl uorine-free electrolytes are prepared by mixing the lithium furan-2-carboxylate [Li(FuA)] salt with the tetra(n -butyl)-phosphonium furan-2-carboxylate [(P4444)(FuA)] IL in diff erent molar ratios. The anion of these electrolytes is produced from biomass and agricultural waste on a large scale and, therefore, this study is a step ahead toward the development of renewable
electrolytes for batteries. The electrolytes are found to have T onset higher than 568 K and acceptable ionic conductivities in a wide temperature range. The pulsed field gradient nuclear magnetic resonance (PFG-NMR) analysis has con firmed that the
(FuA)− anion di ff uses faster than the (P 4444)+ cation in the neat (P 4444)(FuA) IL; however, the anion diff usion becomes slower than cation di ffusion by doping Li salt. The Li + ion interacts strongly with the carboxylate functionality in the (FuA)− anion and diff uses slower than other ions over the whole studied temperature range. The interaction of the Li+ ion with the carboxylate group is also confi rmed by 7 Li NMR and
Fourier transform infrared (FTIR) spectroscopy. The transference number of the Li+ ion is increased with increasing Li salt
concentration. Linear sweep voltammetry (LSV) suggests lithium underpotential deposition and bulk reduction at temperatures
above 313 K. |
ru_RU |
dc.language.iso |
ru |
ru_RU |
dc.subject |
renewable electrolytes |
ru_RU |
dc.subject |
furan-2-carboxylate |
ru_RU |
dc.subject |
ionic conductivity |
ru_RU |
dc.subject |
nuclear magnetic resonance |
ru_RU |
dc.subject |
underpotential deposition |
ru_RU |
dc.title |
Ion Transport and Electrochemical Properties of Fluorine-Free
Lithium-Ion Battery Electrolytes Derived from Biomass |
ru_RU |
dc.type |
Articles in international journals and collections |
ru_RU |
|