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Tuning of dynamic solvation structures via click chemistry for PEO-based solid polymer electrolytes

Abstract:
The Li+-transport mechanisms in both solid polymer electrolytes (SPEs) and liquid electrolytes (LEs) are fundamentally governed by solvation dynamics, requiring an optimal balance between continuous coordination and moderate binding strength. Poly(ethylene oxide) (PEO) is a classic SPE matrix that leverages its –CH2–CH2–O– (EO) segments to provide continuous oxygen coordination for Li+ transport via amorphous regions. While continuous EO segments facilitate the intra-chain Li+-transport, their strong multidentate solvation of Li+ through a chelate effect – each Li+ chelates with 4–6 ethylene oxide (EO) units – significantly hinders the inter-chain Li+ mobility. This effect creates rigid solvation cages that both immobilize Li+ and resist modification by alternative moieties (e.g. carbonate or nitrile groups), resulting in poor room-temperature ionic conductivity (σ) and low Li+ transference number (tLi+). To address these challenges, we developed a series of precise Li+-transport models (LTMs) through click chemistry, strategically combining acrylate-PEG and acrylonitrile to engineer balanced interactions between multidentate (EO) and monodentate (C = O, C ≡ N) coordination sites. This design achieved synergistic enhancement of both inter- and intra-chain transport pathways, demonstrated by significantly improved performance with σ = 6.40 × 10− 5 S/cm and tLi+ = 0.44 at 25 °C. This approach permits tailored control of dynamic solvation structures, offering new opportunities to enhance Li+ transport in PEO-based solid polymer electrolytes.
Publication status:
Published
Peer review status:
Peer reviewed

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Publisher copy:
10.1038/s41598-025-16709-8

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Institution:
University of Oxford
Division:
MPLS
Department:
Engineering Science
Sub department:
Engineering Science
Role:
Author


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Funder identifier:
https://ror.org/01h0zpd94


Publisher:
Nature Research
Journal:
Scientific Reports More from this journal
Volume:
15
Issue:
1
Article number:
34332
Publication date:
2025-10-02
Acceptance date:
2025-08-18
DOI:
EISSN:
2045-2322
ISSN:
2045-2322


Language:
English
Keywords:
Source identifiers:
3337650
Deposit date:
2025-10-02
ARK identifier:
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