Dioxolanone-Anchored Poly(allyl ether)-Based Cross-Linked Dual-Salt Polymer Electrolytes for High-Voltage Lithium Metal Batteries

被引:35
作者
Vijayakumar, Vidyanand [1 ,2 ,3 ]
Diddens, Diddo [1 ]
Heuer, Andreas [1 ,4 ]
Kurungot, Sreekumar [2 ]
Winter, Martin [1 ,4 ,5 ]
Nair, Jijeesh Ravi [1 ]
机构
[1] Forschungszentrum Julich, Helmholtz Inst Munster, IEK 12, Corrensstr 46, D-48149 Munster, Germany
[2] CSIR, Phys & Mat Chem Div, Natl Chem Lab, Pune 411008, Maharashtra, India
[3] Acad Sci & Innovat Res AcSIR, Sect 19,Kamla Nehru Nagar, Ghaziabad 201002, Uttar Pradesh, India
[4] Univ Munster, Inst Phys Chem, Corrensstr 28-30, D-48149 Munster, Germany
[5] MEET Battery Res Ctr, Corrensstr 46, D-48149 Munster, Germany
关键词
solvent-free photopolymerization; dual-salt electrolyte; cross-linked polymer electrolyte; lithium metal battery; high-voltage cathode; IONIC-CONDUCTIVITY; CORROSION; TEMPERATURE; TRANSPORT; PERFORMANCE; RELAXATION; SOLVATION; COLLECTOR; CARBONATE; MECHANISM;
D O I
10.1021/acsami.9b16348
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
Novel cross-linked polymer electrolytes (XPEs) are synthesized by free-radical copolymerization induced by ultraviolet (UV)-light irradiation of a reactive solution, which is composed of a difunctional poly(ethylene glycol) diallyl ether oligomer (PEGDAE), a monofunctional reactive diluent 4-vinyl-1,3-dioxolan-2-one (VEC), and a stock solution containing lithium salt (lithium bis(trifluoromethanesulfonyl)imide, LiTFSI) in a carbonate-free nonvolatile plasticizer, poly(ethylene glycol) dimethyl ether (PEGDME). The resulting polymer matrix can be represented as a linear polyethylene chain functionalized with cyclic carbonate (dioxolanone) moieties and cross-linked by ethylene oxide units. A series of XPEs are prepared by varying the [O]/[Li] ratio (24 to 3) of the stock solution and thoroughly characterized using physicochemical (thermogravimetric analysis-mass spectrometry, differential scanning calorimetry, NMR, etc.) and electrochemical techniques. In addition, quantum chemical calculations are performed to elucidate the correlation between the electrochemical oxidation potential and the lithium ion-ethylene oxide coordination in the stock solution. Later, lithium bis(fluorosulfonyl)imide (LiFSI) salt is incorporated into the electrolyte system to produce a dual-salt XPE that exhibits improved electrochemical performance, a stable interface against lithium metal, and enhanced physical and chemical characteristics to be employed against high-voltage cathodes. The XPE membranes demonstrated excellent resistance against lithium dendrite growth even after reversibly plating and stripping lithium ions for more than 1000 h with a total capacity of 0.5 mAh cm(-2). Finally, the XPE films are assembled in a lab-scale lithium metal battery configuration by using carbon-coated LiFePO4 (LFP) or LiNi0.8Co0.15Al0.05O2 (NCA) as a cathode and galvanostatically cycled at 20, 40, and 60 degrees C. Remarkably, at 20 degrees C, the NCA-based lithium metal cells displayed excellent cycling stability and good capacity retention (>50%) even after 1000 cycles.
引用
收藏
页码:567 / 579
页数:13
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