construction of an ultra-thin and flexible polymer electrolyte for stable all-solid-state lithium-metal batteries
Solid polymer electrolytes (SPEs) with low density, high flexibility and excellent processability have been attracting broad interest in constructing high energy density and safe all-solid-state batteries. However, the poor lithium-ion (Li + ) migration kinetics should be addressed before their larg...
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Published in | Journal of materials chemistry. A, Materials for energy and sustainability Vol. 12; no. 16; pp. 9469 - 9477 |
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Main Authors | , , , , , , , , |
Format | Journal Article |
Published |
23.04.2024
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Online Access | Get full text |
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Abstract | Solid polymer electrolytes (SPEs) with low density, high flexibility and excellent processability have been attracting broad interest in constructing high energy density and safe all-solid-state batteries. However, the poor lithium-ion (Li
+
) migration kinetics should be addressed before their large-scale applications. Reducing the thickness can efficiently shorten the Li
+
diffusion distance and time, making the low ionic conductivity of electrolytes still applicable for practical applications. Herein, by integrating polyethylene fiber (PEF) with an
in situ
polymerized network,
i.e
., poly[(poly(ethylene glycol) methyl ether methacrylate)-
r
-(vinyl ethylene carbonate)-
r
-(dimethyl aminopropyl methacrylamide)-
r
-(polyethylene glycol dimethacrylate)] (PPVD), an ultra-thin, flexible and mechanically robust SPE with a thickness of 5 μm was developed. With an ionic conductivity of 2.0 × 10
−2
mS cm
−1
, such an
in situ
constructed ultra-thin SPE still exhibits a high ionic conductance of 0.1 S, providing sufficient Li
+
conductance for operable batteries at room temperature. As a result, the assembled Li|PPVD@PEF|Li symmetric cell delivers stable cycling performance over 800 h. The Li|PPVD@PEF|LiFePO
4
full cell exhibits excellent cycling stability with a capacity retention of 85.7% over 500 cycles. The current design of the
in situ
constructed ultra-thin SPE not only decreases the electrolyte/electrode interfacial resistance but also sheds light on breaking the bottleneck of ionic conductivity for SPEs towards high energy density batteries.
By integrating polyethylene fiber and a rationally designed,
in situ
formed polymer network, an ultra-thin, flexible and high mechanical robustness solid polymer electrolyte with a thickness of 5 μm is constructed. |
---|---|
AbstractList | Solid polymer electrolytes (SPEs) with low density, high flexibility and excellent processability have been attracting broad interest in constructing high energy density and safe all-solid-state batteries. However, the poor lithium-ion (Li
+
) migration kinetics should be addressed before their large-scale applications. Reducing the thickness can efficiently shorten the Li
+
diffusion distance and time, making the low ionic conductivity of electrolytes still applicable for practical applications. Herein, by integrating polyethylene fiber (PEF) with an
in situ
polymerized network,
i.e
., poly[(poly(ethylene glycol) methyl ether methacrylate)-
r
-(vinyl ethylene carbonate)-
r
-(dimethyl aminopropyl methacrylamide)-
r
-(polyethylene glycol dimethacrylate)] (PPVD), an ultra-thin, flexible and mechanically robust SPE with a thickness of 5 μm was developed. With an ionic conductivity of 2.0 × 10
−2
mS cm
−1
, such an
in situ
constructed ultra-thin SPE still exhibits a high ionic conductance of 0.1 S, providing sufficient Li
+
conductance for operable batteries at room temperature. As a result, the assembled Li|PPVD@PEF|Li symmetric cell delivers stable cycling performance over 800 h. The Li|PPVD@PEF|LiFePO
4
full cell exhibits excellent cycling stability with a capacity retention of 85.7% over 500 cycles. The current design of the
in situ
constructed ultra-thin SPE not only decreases the electrolyte/electrode interfacial resistance but also sheds light on breaking the bottleneck of ionic conductivity for SPEs towards high energy density batteries.
By integrating polyethylene fiber and a rationally designed,
in situ
formed polymer network, an ultra-thin, flexible and high mechanical robustness solid polymer electrolyte with a thickness of 5 μm is constructed. |
Author | Li, Lin Zhang, Youjia Yang, Dandan He, Yayue Cao, Peng-Fei Ma, Mengxiang Zhu, Shuangshuang Gao, Shilun Yang, Huabin |
AuthorAffiliation | State Key Laboratory of Organic-Inorganic Composites Tianjin Key Laboratory of Metal and Molecular Based Material Chemistry School of Integrated Circuit Science and Engineering Experimental Teaching Center of Materials Science School of Materials Science and Engineering Nankai University Institute of New Energy Material Chemistry Tianjin University of Technology Beijing University of Chemical Technology |
AuthorAffiliation_xml | – name: Experimental Teaching Center of Materials Science – name: Institute of New Energy Material Chemistry – name: Tianjin Key Laboratory of Metal and Molecular Based Material Chemistry – name: Tianjin University of Technology – name: School of Materials Science and Engineering – name: State Key Laboratory of Organic-Inorganic Composites – name: Beijing University of Chemical Technology – name: Nankai University – name: School of Integrated Circuit Science and Engineering |
Author_xml | – sequence: 1 givenname: Shilun surname: Gao fullname: Gao, Shilun – sequence: 2 givenname: Mengxiang surname: Ma fullname: Ma, Mengxiang – sequence: 3 givenname: Youjia surname: Zhang fullname: Zhang, Youjia – sequence: 4 givenname: Lin surname: Li fullname: Li, Lin – sequence: 5 givenname: Shuangshuang surname: Zhu fullname: Zhu, Shuangshuang – sequence: 6 givenname: Yayue surname: He fullname: He, Yayue – sequence: 7 givenname: Dandan surname: Yang fullname: Yang, Dandan – sequence: 8 givenname: Huabin surname: Yang fullname: Yang, Huabin – sequence: 9 givenname: Peng-Fei surname: Cao fullname: Cao, Peng-Fei |
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