Solvent-Free Superionic Polymer Conductors from a Bicontinuous Network Nanostructure

In traditional ion conducting polymers, the lithium-ion transport is strongly coupled with segmental motion of a polymer chain. The resulted severe weakness of room-temperature ion conductivity and mechanical strength necessitates the development of superionic conductors, which decouple lithium-ion conduction from polymer segmental relaxation. Here, we demonstrate a simple and efficient superionic lithium conductor system based on polyacrylonitrile (PAN)-grafted ferroelectric poly(vinylidene fluoride) (PVDF), i.e., PVDF-g-PAN. A bicontinuous network nanostructure is constructed through the microphase segregation. The ferroelectric PVDF network not only presents a high dielectric constant, facilitating dissociation of high-concentration lithium salts, but also strongly interacts with fluorinated anions to enhance the lithium transference number (>0.6). The PAN-rich network with abundant polar nitrile groups and high glass transition temperature serves as the Li+ hopping channels, enabling high ion conductivity (5.8 × 10–4 S cm–1, 30 °C), low activation energy (0.21 eV), as well as excellent mechanical strength (>200 MPa). In particular, a nearly solvent-free condition is realized, enabling long-term stability of ion conducting performance.

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Publication Details

Journal
Macromolecules
Published
2025-06-19
DOI
https://doi.org/10.1021/acs.macromol.5c00294
Citations
4
Primary Topic
Advanced Battery Materials and Technologies
Type
article
Field-Weighted Citation Impact
2.92

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article

Solvent-Free Superionic Polymer Conductors from a Bicontinuous Network Nanostructure

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4 citations
Macromolecules
Advanced Battery Materials and Technologies
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article

Solvent-Free Superionic Polymer Conductors from a Bicontinuous Network Nanostructure

Yongmei Zhu, Xinghan Li, Weijiang Xue, Rongchun Zhang, Xian Kong, Mingjun Huang, Jinyi Cui, Jinxin Xie, Shuqi Dai, Xueying Yuan, Zhiwei Yan
article en
4 citations

Abstract

In traditional ion conducting polymers, the lithium-ion transport is strongly coupled with segmental motion of a polymer chain. The resulted severe weakness of room-temperature ion conductivity and mechanical strength necessitates the development of superionic conductors, which decouple lithium-ion conduction from polymer segmental relaxation. Here, we demonstrate a simple and efficient superionic lithium conductor system based on polyacrylonitrile (PAN)-grafted ferroelectric poly(vinylidene fluoride) (PVDF), i.e., PVDF-g-PAN. A bicontinuous network nanostructure is constructed through the microphase segregation. The ferroelectric PVDF network not only presents a high dielectric constant, facilitating dissociation of high-concentration lithium salts, but also strongly interacts with fluorinated anions to enhance the lithium transference number (>0.6). The PAN-rich network with abundant polar nitrile groups and high glass transition temperature serves as the Li+ hopping channels, enabling high ion conductivity (5.8 × 10–4 S cm–1, 30 °C), low activation energy (0.21 eV), as well as excellent mechanical strength (>200 MPa). In particular, a nearly solvent-free condition is realized, enabling long-term stability of ion conducting performance.

MacromoleculesVol. 58(13)
Pulp and Paper Research Institute (SK), State Key Laboratory of Pulp and Paper Engineering, Xi'an Jiaotong University (CN), South China University of Technology (CN)
National Natural Science Foundation of China, Natural Science Foundation of Guangdong Province, State Key Laboratory of Polymer Materials Engineering, State Key Laboratory of Pulp and Paper Engineering, Higher Education Discipline Innovation Project, Fundamental Research Funds for the Central Universities
Openalex Percentile: Top 9%
Advanced Battery Materials and Technologies
2.92
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