In-situ Fabrication of a Freestanding Acrylate-based Hierarchical Electrolyte for Lithium-sulfur Batteries

被引:78
|
作者
Liu, M. [1 ,2 ,3 ]
Jiang, H. R. [1 ]
Ren, Y. X. [1 ]
Zhou, D. [2 ,3 ]
Kang, F. Y. [2 ,3 ]
Zhao, T. S. [1 ]
机构
[1] Hong Kong Univ Sci & Technol, Dept Mech & Aerosp Engn, Kowloon, Hong Kong, Peoples R China
[2] Tsinghua Univ, Engn Lab Next Generat Power & Energy Storage Batt, Grad Sch Shenzhen, Shenzhen 518055, Peoples R China
[3] Tsinghua Univ, Sch Mat Sci & Engn, Adv Mat Lab, Beijing 100084, Peoples R China
关键词
lithium-sulfur battery; acrylate-based hierarchical electrolyte; ester functional group; in-situ synthesis; quasi-solid; GEL POLYMER ELECTROLYTE; ELECTROCHEMICAL PERFORMANCE; SOLID-ELECTROLYTE; HIGH-CAPACITY; CATHODE; CELLS; POLYSULFIDES; GRAPHENE;
D O I
10.1016/j.electacta.2016.08.015
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
A number of methods have been attempted to suppress the shuttle effect in lithium-sulfur (Li-S) batteries to improve battery performance. Conventional methods, however, reduce the ionic conductivity, sacrifice the overall energy density and increase the cost of production. Here, we report a facile synthesis of an acrylate-based hierarchical electrolyte (AHE). This quasi-solid electrolyte is assembled by in-situ gelation of a pentaerythritol tetraacrylate (PETEA)-based gel polymer electrolyte (GPE) into a polymethyl methacrylate (PMMA)-based electrospun network. The structural similarity and synergetic compatibility between the electrospun network and GPE provide the AHE an ester-rich robust structure with a high ionic conductivity of 1.02 x 10(-3) S cm(-1) due to the strong uptake ability and the elimination of commercial separator. The S/AHE/Li polymer battery also renders a high rate capability of 645 mAh g(-1) at 3C, while maintaining excellent retention at both high and low current densities (80.3% after 500 cycles at 0.3C and 91.9% after 500 cycles at 3C). First-principle calculations reveal that the reduced shuttle effect can be attributed to a strong polysulfide anchoring ability of ester functional groups, while cell modeling shows that the geometric design effectively suppresses polysulfide flux. This in-situ integrated method opens up an avenue for the future development of solid-state and polysulfide redox flow sulfur-based batteries. (C) 2016 Elsevier Ltd. All rights reserved.
引用
收藏
页码:871 / 878
页数:8
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