Asymmetric gel polymer electrolyte with high lithium ion conductivity for dendrite-free lithium metal batteries

Lithium metal has been intensively investigated as a promising anode for next generation rechargeable Li metal batteries (LMBs). However, the safety concern on Li anodes caused by uncontrolled Li dendrite growth in liquid electrolytes hinders their application. Herein, a novel poly(vinylidene fluori...

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Veröffentlicht in:Journal of materials chemistry. A, Materials for energy and sustainability Materials for energy and sustainability, 2020-04, Vol.8 (16), p.833-84
Hauptverfasser: Li, Linge, Wang, Mingchao, Wang, Jian, Ye, Fangmin, Wang, Shaofei, Xu, Yanan, Liu, Jingyu, Xu, Guoguang, Zhang, Yue, Zhang, Yongyi, Yan, Cheng, Medhekar, Nikhil V, Liu, Meinan, Zhang, Yuegang
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container_title Journal of materials chemistry. A, Materials for energy and sustainability
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creator Li, Linge
Wang, Mingchao
Wang, Jian
Ye, Fangmin
Wang, Shaofei
Xu, Yanan
Liu, Jingyu
Xu, Guoguang
Zhang, Yue
Zhang, Yongyi
Yan, Cheng
Medhekar, Nikhil V
Liu, Meinan
Zhang, Yuegang
description Lithium metal has been intensively investigated as a promising anode for next generation rechargeable Li metal batteries (LMBs). However, the safety concern on Li anodes caused by uncontrolled Li dendrite growth in liquid electrolytes hinders their application. Herein, a novel poly(vinylidene fluoride- co -hexafluoropropylene) (PVDF-HFP) based gel polymer electrolyte (GPE) with an asymmetric structure has been designed and developed to effectively retard the growth of lithium dendrites. Atomistic simulations confirm the strong interactions between PF 6 − and dipoles in the polymer matrix, which can anchor PF 6 − in the GPE and slow down its mobility to prevent space charge formation. In addition, this unique asymmetric membrane with a channel upper layer greatly enhances the mobility of Li + in the GPE due to its low tortuosity and high porosity. The synergistic effect of the ion-dipole interaction and asymmetric structure increases the Li + transference number to 0.66 and ionic conductivity to 3.36 mS cm −1 (20 °C). Using this superior asymmetric GPE, Li|Li symmetric cells show more stable cycle performance than those using a liquid electrolyte. Li|LiFePO 4 batteries with the asymmetric GPE also deliver an impressive electrochemical performance, i.e. , coulombic efficiency of 99.5% at 2C after 600 cycles. In consequence, this novel asymmetric GPE possesses potential application in high energy LMBs. An asymmetric gel polymer electrolyte is designed for regulating ions and suppressing Li dendrite growth in high-performance Li metal batteries.
doi_str_mv 10.1039/d0ta01883j
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However, the safety concern on Li anodes caused by uncontrolled Li dendrite growth in liquid electrolytes hinders their application. Herein, a novel poly(vinylidene fluoride- co -hexafluoropropylene) (PVDF-HFP) based gel polymer electrolyte (GPE) with an asymmetric structure has been designed and developed to effectively retard the growth of lithium dendrites. Atomistic simulations confirm the strong interactions between PF 6 − and dipoles in the polymer matrix, which can anchor PF 6 − in the GPE and slow down its mobility to prevent space charge formation. In addition, this unique asymmetric membrane with a channel upper layer greatly enhances the mobility of Li + in the GPE due to its low tortuosity and high porosity. The synergistic effect of the ion-dipole interaction and asymmetric structure increases the Li + transference number to 0.66 and ionic conductivity to 3.36 mS cm −1 (20 °C). Using this superior asymmetric GPE, Li|Li symmetric cells show more stable cycle performance than those using a liquid electrolyte. Li|LiFePO 4 batteries with the asymmetric GPE also deliver an impressive electrochemical performance, i.e. , coulombic efficiency of 99.5% at 2C after 600 cycles. In consequence, this novel asymmetric GPE possesses potential application in high energy LMBs. An asymmetric gel polymer electrolyte is designed for regulating ions and suppressing Li dendrite growth in high-performance Li metal batteries.</description><identifier>ISSN: 2050-7488</identifier><identifier>EISSN: 2050-7496</identifier><identifier>DOI: 10.1039/d0ta01883j</identifier><language>eng</language><publisher>CAMBRIDGE: Royal Soc Chemistry</publisher><subject>Anodes ; Asymmetric structures ; Chemistry ; Chemistry, Physical ; Conductivity ; Crystallization ; Dendrites ; Dipole interactions ; Electrochemical analysis ; Electrochemistry ; Electrolytes ; Electrolytic cells ; Energy &amp; Fuels ; Ion currents ; Lithium ; Lithium ions ; Materials Science ; Materials Science, Multidisciplinary ; Mobility ; Physical Sciences ; Polymers ; Porosity ; Rechargeable batteries ; Science &amp; Technology ; Space charge ; Synergistic effect ; Technology ; Tortuosity ; Vinylidene ; Vinylidene fluoride</subject><ispartof>Journal of materials chemistry. 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A, Materials for energy and sustainability</title><addtitle>J MATER CHEM A</addtitle><description>Lithium metal has been intensively investigated as a promising anode for next generation rechargeable Li metal batteries (LMBs). However, the safety concern on Li anodes caused by uncontrolled Li dendrite growth in liquid electrolytes hinders their application. Herein, a novel poly(vinylidene fluoride- co -hexafluoropropylene) (PVDF-HFP) based gel polymer electrolyte (GPE) with an asymmetric structure has been designed and developed to effectively retard the growth of lithium dendrites. Atomistic simulations confirm the strong interactions between PF 6 − and dipoles in the polymer matrix, which can anchor PF 6 − in the GPE and slow down its mobility to prevent space charge formation. In addition, this unique asymmetric membrane with a channel upper layer greatly enhances the mobility of Li + in the GPE due to its low tortuosity and high porosity. The synergistic effect of the ion-dipole interaction and asymmetric structure increases the Li + transference number to 0.66 and ionic conductivity to 3.36 mS cm −1 (20 °C). Using this superior asymmetric GPE, Li|Li symmetric cells show more stable cycle performance than those using a liquid electrolyte. Li|LiFePO 4 batteries with the asymmetric GPE also deliver an impressive electrochemical performance, i.e. , coulombic efficiency of 99.5% at 2C after 600 cycles. In consequence, this novel asymmetric GPE possesses potential application in high energy LMBs. 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A, Materials for energy and sustainability</jtitle><stitle>J MATER CHEM A</stitle><date>2020-04-28</date><risdate>2020</risdate><volume>8</volume><issue>16</issue><spage>833</spage><epage>84</epage><pages>833-84</pages><issn>2050-7488</issn><eissn>2050-7496</eissn><abstract>Lithium metal has been intensively investigated as a promising anode for next generation rechargeable Li metal batteries (LMBs). However, the safety concern on Li anodes caused by uncontrolled Li dendrite growth in liquid electrolytes hinders their application. Herein, a novel poly(vinylidene fluoride- co -hexafluoropropylene) (PVDF-HFP) based gel polymer electrolyte (GPE) with an asymmetric structure has been designed and developed to effectively retard the growth of lithium dendrites. Atomistic simulations confirm the strong interactions between PF 6 − and dipoles in the polymer matrix, which can anchor PF 6 − in the GPE and slow down its mobility to prevent space charge formation. In addition, this unique asymmetric membrane with a channel upper layer greatly enhances the mobility of Li + in the GPE due to its low tortuosity and high porosity. The synergistic effect of the ion-dipole interaction and asymmetric structure increases the Li + transference number to 0.66 and ionic conductivity to 3.36 mS cm −1 (20 °C). Using this superior asymmetric GPE, Li|Li symmetric cells show more stable cycle performance than those using a liquid electrolyte. Li|LiFePO 4 batteries with the asymmetric GPE also deliver an impressive electrochemical performance, i.e. , coulombic efficiency of 99.5% at 2C after 600 cycles. In consequence, this novel asymmetric GPE possesses potential application in high energy LMBs. 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subjects Anodes
Asymmetric structures
Chemistry
Chemistry, Physical
Conductivity
Crystallization
Dendrites
Dipole interactions
Electrochemical analysis
Electrochemistry
Electrolytes
Electrolytic cells
Energy & Fuels
Ion currents
Lithium
Lithium ions
Materials Science
Materials Science, Multidisciplinary
Mobility
Physical Sciences
Polymers
Porosity
Rechargeable batteries
Science & Technology
Space charge
Synergistic effect
Technology
Tortuosity
Vinylidene
Vinylidene fluoride
title Asymmetric gel polymer electrolyte with high lithium ion conductivity for dendrite-free lithium metal batteries
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