Achieving Ultra‐Stable All‐Solid‐State Sodium Metal Batteries with Anion‐Trapping 3D Fiber Network Enhanced Polymer Electrolyte

Author:

Guo Junhong1,Feng Fan2,Zhao Shiqiang3,Wang Rui1,Yang Meng1,Shi Zhenhai1,Ren Yufeng1,Ma Zifeng2,Chen Suli1ORCID,Liu Tianxi1

Affiliation:

1. The Key Laboratory of Synthetic and Biological Colloids Ministry of Education School of Chemical and Material Engineering International Joint Research Laboratory for Nano Energy Composites Jiangnan University Wuxi 214122 P. R. China

2. Shanghai Electrochemical Energy Devices Research Center Department of Chemical Engineering Shanghai Jiao Tong University Shanghai 200240 P. R. China

3. College of Chemistry and Materials Engineering Wenzhou University Wenzhou 325035 P. R. China

Abstract

AbstractAll‐solid‐state sodium metal batteries paired with solid polymer electrolytes (SPEs) are considered a promising candidate for high energy‐density, low‐cost, and high‐safety energy storage systems. However, the low ionic conductivity and inferior interfacial stability with Na metal anode of SPEs severely hinder their practical applications. Herein, an anion‐trapping 3D fiber network enhanced polymer electrolyte (ATFPE) is developed by infusing poly(ethylene oxide) matrix into an electrostatic spun fiber framework loading with an orderly arranged metal‐organic framework (MOF). The 3D continuous channel provides a fast Na+ transport path leading to high ionic conductivity, and simultaneously the rich coordinated unsaturated cation sites exposed on MOF can effectively trap anions, thus regulating Na+ concentration distribution for constructing stable electrolyte/Na anode interface. Based on such advantages, the ATFPE exhibits high ionic conductivity and considerable Na+ transference number, as well as enhanced interfacial stability. Consequently, Na/Na symmetric cells using this ATFPE possess cyclability over 600 h at 0.1 mA cm−2 without discernable Na dendrites. Cooperated with Na3V2(PO4)3 cathode, the all‐solid‐state sodium metal batteries (ASSMBs) demonstrate significantly improved rate and cycle performances, delivering a high discharge capacity of 117.5 mAh g−1 under 0.1 C and rendering high capacity retention of 78.2% after 1000 cycles even at 1 C.

Funder

Natural Science Foundation of Jiangsu Province

Fundamental Research Funds for the Central Universities

National Natural Science Foundation of China

Publisher

Wiley

Subject

Biomaterials,Biotechnology,General Materials Science,General Chemistry

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