PEO-Based Solid-State Electrolytes Reinforced by High Strength, Interconnected MOF Networks

被引:28
作者
Liu, Xuezhi [1 ]
Liang, Qian [1 ]
Chen, Lining [1 ]
Tang, Junyan [1 ]
Liu, Junjie [1 ]
Tang, Mi [1 ]
Wang, Zhengbang [1 ]
机构
[1] Hubei Univ, Collaborat Innovat Ctr Adv Organ Chem Mat Coconstr, Key Lab Green Preparat & Applicat Funct Mat, Sch Mat Sci & Engn,Minist Educ,Hubei Key Lab Polym, Wuhan 430062, Peoples R China
基金
中国国家自然科学基金; 中国博士后科学基金;
关键词
LITHIUM-METAL BATTERIES; COMPOSITE ELECTROLYTES; POLYMER ELECTROLYTES; IONIC-CONDUCTIVITY;
D O I
10.1021/acsaem.3c00371
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Construction of polymer-based electrolytes with excellent mechanical properties and high ionic conductivity is highly desirable for solid-state lithium-metal batteries. Herein, a scalable strategy is suggested to achieve the high strength and high performance polymer-based solid-state electrolyte via filling polyethylene oxide (PEO)/Li-salt (LiTFSI) electrolyte into an interconnected metal-organic framework (MOF) network based on the typical hot-pressing process, in which the MOF network is grown on the polyacrylonitrile (PAN) electrospun fibrous membrane through an automated layer-by-layer (LbL) assembly spraying technique. The MOF network not only promises excellent mechanical properties and high thermal stability but also enhances ionic conductivity due to the resulting interconnected Li+ transport paths. In addition, such electrolyte also demonstrates a high Li+ transference number (0.68) and a wide electrochemical stability window (5.2 V). As a result, the assembled Li//Li symmetrical cell shows an ultrastable cycling performance even after cycling for 1800 h. Furthermore, its LiFePO4//Li full cell exhibits a high capacity of up to 120 mAh g-1 at 1 C and 30 °C and can maintain a rather high capacity retention of 95% after 160 cycles. This study provides some inspirations for the fabrication of high performance polymer-based solid-state electrolytes in a large scale. © 2023 American Chemical Society.
引用
收藏
页码:4881 / 4891
页数:11
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