Deciphering the role of tetrahydrofuran residue in the poly(ethylene oxide)/LiTFSI hybrid used for secondary battery electrolyte
Residual solvent in polymer electrolytes recently has attracted great attention since it influences the performance and safety of the polymer-electrolyte based batteries and electric vehicles. In this work, we did a systematic study of exploring the role of the residual solvent in lithium-ion second...
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doaj-2435042dd41e49439b962a7f9ac7a31a2021-05-14T04:20:14ZengElsevierGiant2666-54252021-06-016100056Deciphering the role of tetrahydrofuran residue in the poly(ethylene oxide)/LiTFSI hybrid used for secondary battery electrolyteZekun Zhou0Ruike Zou1Zhen Liu2Peng Zhang3School of Materials Science and Engineering, PCFM Lab, Sun Yat-sen University, Guangzhou 510275, ChinaSchool of Materials Science and Engineering, PCFM Lab, Sun Yat-sen University, Guangzhou 510275, ChinaSchool of Materials Science and Engineering, PCFM Lab, Sun Yat-sen University, Guangzhou 510275, ChinaCorresponding author.; School of Materials Science and Engineering, PCFM Lab, Sun Yat-sen University, Guangzhou 510275, ChinaResidual solvent in polymer electrolytes recently has attracted great attention since it influences the performance and safety of the polymer-electrolyte based batteries and electric vehicles. In this work, we did a systematic study of exploring the role of the residual solvent in lithium-ion secondary battery electrolyte beyond the traditional understanding of plasticizing effect, based on the typical polymer electrolyte system of polyethylene oxide/tetrahydrofuran/lithium bis(trifluoromethanesulfonyl)imide (PEO/THF/LiTFSI). A series of complementary characterization techniques, i.e., small-angle neutron scattering (SANS), wide-angle X-ray scattering (WAXS), Raman, infrared, nuclear magnetic resonance, thermogravimetric analysis and electrochemical impedance spectroscopy, were applied to decipher the structure-function relationship. We found that the PEO/LiTFSI hybrid formed a complex with the THF residue, which was further confirmed by the Gaussian simulation. By using the oxygen-free solvent, acetonitrile, as a reference, we demonstrated that THF provided ambient oxygen bonding sites among PEO and LiTFSI, which leaded to PEO/LiTFSI/THF clusters and endowed the hybrid a ionic conductivity value of 1.1 × 10−4 S cm−1 at 30 °C. The battery showed a discharge capacitance of 905 mAh g−1 at 0.1C in a Li-S cell. Moreover, both ionic conductivity and cell performance deteriorate significantly with vigorous drying of the polymer electrolyte membrane in vacuum oven at 120 °C and argon-purged glove box at room temperature, although there are still around 10 wt% THF residues found in the dried membranes. It seems to be that the vigorous drying caused damage to the PEO/LiTFSI/THF clusters and the ion conductive network, especially around the electrode/electrolyte interfaces. Our findings shed light on improving the ionic conductivity of polymer electrolyte for lithium-ion secondary battery by carefully tailoring the solvent residue.http://www.sciencedirect.com/science/article/pii/S2666542521000126Polymer electrolyteLithium-ion secondary batteryCoordinating structureStructure-function relationship |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Zekun Zhou Ruike Zou Zhen Liu Peng Zhang |
spellingShingle |
Zekun Zhou Ruike Zou Zhen Liu Peng Zhang Deciphering the role of tetrahydrofuran residue in the poly(ethylene oxide)/LiTFSI hybrid used for secondary battery electrolyte Giant Polymer electrolyte Lithium-ion secondary battery Coordinating structure Structure-function relationship |
author_facet |
Zekun Zhou Ruike Zou Zhen Liu Peng Zhang |
author_sort |
Zekun Zhou |
title |
Deciphering the role of tetrahydrofuran residue in the poly(ethylene oxide)/LiTFSI hybrid used for secondary battery electrolyte |
title_short |
Deciphering the role of tetrahydrofuran residue in the poly(ethylene oxide)/LiTFSI hybrid used for secondary battery electrolyte |
title_full |
Deciphering the role of tetrahydrofuran residue in the poly(ethylene oxide)/LiTFSI hybrid used for secondary battery electrolyte |
title_fullStr |
Deciphering the role of tetrahydrofuran residue in the poly(ethylene oxide)/LiTFSI hybrid used for secondary battery electrolyte |
title_full_unstemmed |
Deciphering the role of tetrahydrofuran residue in the poly(ethylene oxide)/LiTFSI hybrid used for secondary battery electrolyte |
title_sort |
deciphering the role of tetrahydrofuran residue in the poly(ethylene oxide)/litfsi hybrid used for secondary battery electrolyte |
publisher |
Elsevier |
series |
Giant |
issn |
2666-5425 |
publishDate |
2021-06-01 |
description |
Residual solvent in polymer electrolytes recently has attracted great attention since it influences the performance and safety of the polymer-electrolyte based batteries and electric vehicles. In this work, we did a systematic study of exploring the role of the residual solvent in lithium-ion secondary battery electrolyte beyond the traditional understanding of plasticizing effect, based on the typical polymer electrolyte system of polyethylene oxide/tetrahydrofuran/lithium bis(trifluoromethanesulfonyl)imide (PEO/THF/LiTFSI). A series of complementary characterization techniques, i.e., small-angle neutron scattering (SANS), wide-angle X-ray scattering (WAXS), Raman, infrared, nuclear magnetic resonance, thermogravimetric analysis and electrochemical impedance spectroscopy, were applied to decipher the structure-function relationship. We found that the PEO/LiTFSI hybrid formed a complex with the THF residue, which was further confirmed by the Gaussian simulation. By using the oxygen-free solvent, acetonitrile, as a reference, we demonstrated that THF provided ambient oxygen bonding sites among PEO and LiTFSI, which leaded to PEO/LiTFSI/THF clusters and endowed the hybrid a ionic conductivity value of 1.1 × 10−4 S cm−1 at 30 °C. The battery showed a discharge capacitance of 905 mAh g−1 at 0.1C in a Li-S cell. Moreover, both ionic conductivity and cell performance deteriorate significantly with vigorous drying of the polymer electrolyte membrane in vacuum oven at 120 °C and argon-purged glove box at room temperature, although there are still around 10 wt% THF residues found in the dried membranes. It seems to be that the vigorous drying caused damage to the PEO/LiTFSI/THF clusters and the ion conductive network, especially around the electrode/electrolyte interfaces. Our findings shed light on improving the ionic conductivity of polymer electrolyte for lithium-ion secondary battery by carefully tailoring the solvent residue. |
topic |
Polymer electrolyte Lithium-ion secondary battery Coordinating structure Structure-function relationship |
url |
http://www.sciencedirect.com/science/article/pii/S2666542521000126 |
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