Issue 12, 2018, Issue in Progress

High voltage, solvent-free solid polymer electrolyte based on a star-comb PDLLA–PEG copolymer for lithium ion batteries

Abstract

In this work, a novel star-comb copolymer based on poly(d,L-lactide) (PDLLA) macromonomer and poly(ethylene glycol)methyl ether methacrylate (PEGMA) was prepared, and the electrochemical properties were studied, with the aim of using it as a solid polymer electrolyte in lithium ion batteries. The six-arm vinyl functionalized PDLLA macromonomer was synthesized by a ring-opening polymerization (ROP) of D,L-lactide and subsequently an acylation of the hydroxy end-groups. A series of free-standing solid polymer electrolyte membranes from different ratios of PDLLA, PEGMA and LiTFSI were prepared through solvent-free free radical polymerization under UV radiation. The chemical structure of the obtained polymers was confirmed by 1H NMR and FTIR. The as-prepared six-arm star-comb solid polymer electrolytes (PDLLA-SPEs) exhibit good thermal stability with Td5%s of ∼270 °C and low Tgs of −48 to −34 °C. The electrochemical characterization shows that the PDLLA-SPEs possess a wide electrochemical window up to 5.1 V with an optimal ionic conductivity of 9.7 × 10−5 S cm−1 at 60 °C at an EO/Li+ ratio of 16 : 1. Furthermore, the all-solid-state LiFePO4/Li cells display extraordinary cycling and rate performances at 60 °C by curing the PDLLA-SPEs directly on the cathode. These superior properties of the six-arm star-comb PDLLA-SPE make it a promising candidate solid electrolyte for lithium batteries.

Graphical abstract: High voltage, solvent-free solid polymer electrolyte based on a star-comb PDLLA–PEG copolymer for lithium ion batteries

Supplementary files

Article information

Article type
Paper
Submitted
26 Dec 2017
Accepted
01 Feb 2018
First published
08 Feb 2018
This article is Open Access
Creative Commons BY-NC license

RSC Adv., 2018,8, 6373-6380

High voltage, solvent-free solid polymer electrolyte based on a star-comb PDLLA–PEG copolymer for lithium ion batteries

B. Wang, H. Lou, H. Xu, J. Zhao, Q. Wang, Q. Shi and Y. Deng, RSC Adv., 2018, 8, 6373 DOI: 10.1039/C7RA13664A

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