Affiliation:
1. Institute of Low-Dimensional Materials Genome Initiative College of Chemistry and Environmental Engineering Shenzhen University Shenzhen 518060 P. R. China
2. Chengdu Institute of Organic Chemistry Chinese Academy of Sciences Chengdu 610041 China
3. Department of Mechanical Engineering The Hong Kong Polytechnic University Hong Kong 100872 China
Abstract
AbstractSolid‐state lithium‐metal batteries are considered as the next generation of high‐energy‐density batteries. However, their solid electrolytes suffer from low ionic conductivity, poor interface performance, and high production costs, restricting their commercial application. Herein, a low‐cost cellulose acetate‐based quasi‐solid composite polymer electrolyte (C‐CLA QPE) was developed with a high Li+ transference number (
) of 0.85 and excellent interface stability. The prepared LiFePO4 (LFP)|C‐CLA QPE|Li batteries exhibited excellent cycle performance with a capacity retention of 97.7 % after 1200 cycles at 1 C and 25 °C. The experimental results and Density Function Theory (DFT) simulation revealed that the partially esterified side groups in the CLA matrix contribute to the migration of Li+ and enhance electrochemical stability. This work provides a promising strategy for fabricating cost‐effective, stable polymer electrolytes for solid‐state lithium batteries.
Funder
National Natural Science Foundation of China
Shenzhen Science and Technology Innovation Program
Cited by
2 articles.
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