Hierarchical porous separator with excellent isotropic modulus enabling homogeneous Zn2+ flux for stable aqueous Zn battery

被引:13
|
作者
Zhang, Fenglin [1 ]
Huang, Fanyang [2 ]
Huang, Renzhi [1 ]
Dong, Ning [1 ]
Jiao, Shuhong [2 ]
Cao, Ruiguo [2 ]
Pan, Huilin [1 ,3 ]
机构
[1] Zhejiang Univ, Dept Chem, Hangzhou 310027, Peoples R China
[2] Univ Sci & Technol China, Dept Mat Sci & Engn, Hefei 230026, Peoples R China
[3] Zhejiang Univ, State Key Lab Clean Energy Utilizat, Hangzhou 310027, Peoples R China
基金
中国国家自然科学基金;
关键词
aqueous Zn-ion battery; hierarchical porous separator; isotropic mechanical strength; dendrite growth suppression; ELECTROLYTE;
D O I
10.1007/s40843-022-2239-8
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
Low-cost, high-safety aqueous Zn-ion batteries show promise for large-scale energy storage, but the unsatisfactory cycling stability of Zn anodes and the lack of a suitable hydrophilic separator for rechargeable aqueous Zn batteries limit their practical applications. In this work, we report a scalable method for the preparation of a homogenous polyvinylidene fluoride-lithium bistrifluoromethanesulfonimide (LiTFSI) (PVDF-Li)-based separator for aqueous Zn batteries. The homogenously mixed LiTFSI salt interrupted the crystalline framework of PVDF with excellent mechanical strength and led to hierarchical pore structures for the rapid and uniform Zn2+ flux through the separator. Meanwhile, the PVDF-Li separator exhibited excellent wettability toward aqueous Zn electrolytes. With the advanced PVDF-Li separator, the Zn dendrite growth can be suppressed greatly, showing an improved cycle life. The Zn||V2O5 full cell with PVDF-Li separator exhibited a 27% higher initial capacity (324 mA h g(-1)) and considerably better capacity retention than the traditional glass fiber separator due to the uniform reaction on the V2O5 cathode and Zn anode sides. This work provides new insights into the development of high-performance aqueous batteries by regulating the reactions on the cathode and anode through functional separators.
引用
收藏
页码:982 / 991
页数:10
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