Graft copolymer-based lithium-ion battery for high-temperature operation

被引:79
作者
Hu, Qichao [1 ,2 ]
Osswald, Sebastian [1 ,3 ]
Daniel, Reece [1 ]
Zhu, Yan [1 ]
Wesel, Steven [1 ]
Ortiz, Luis [1 ]
Sadoway, Donald R. [1 ]
机构
[1] MIT, Dept Mat Sci & Engn, Cambridge, MA 02139 USA
[2] Harvard Univ, Sch Engn & Appl Sci, Dept Appl Phys, Cambridge, MA 02138 USA
[3] USN, Postgrad Sch, Dept Phys, Grad Sch Engn & Appl Sci, Monterey, CA 93943 USA
关键词
Graft copolymer; Polymer electrolyte; PEO; Lithium-ion battery; LiFePO4; High temperature; PROPYLENE CARBONATE SOLUTIONS; THERMAL-STABILITY; POLYMER ELECTROLYTES; ROOM-TEMPERATURE; IMPEDANCE SPECTROSCOPY; ELECTROCHEMICAL IMPEDANCE; LIXCOO2; CATHODE; SOLID-STATE; LIFEPO4; ELECTRODES;
D O I
10.1016/j.jpowsour.2011.03.001
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
The use of conventional lithium-ion batteries in high temperature applications (>50 degrees C) is currently inhibited by the high reactivity and volatility of liquid electrolytes. Solvent-free, solid-state polymer electrolytes allow for safe and stable operation of lithium-ion batteries, even at elevated temperatures. Recent advances in polymer synthesis have led to the development of novel materials that exhibit solid-like mechanical behavior while providing the ionic conductivities approaching that of liquid electrolytes. Here we report the successful charge and discharge cycling of a graft copolymer electrolyte (GCE)-based lithium-ion battery at temperatures up to 120 degrees C. The GCE consists of poly(oxyethylene) methacrylate-g-poly(dimethyl siloxane) (POEM-g-PDMS) doped with lithium triflate. Using electrochemical impedance spectroscopy (EIS), we analyze the temperature stability and cycling behavior of GCE-based lithium-ion batteries comprised of a LiFePO4 cathode, a metallic lithium anode, and an electrolyte consisting of a 20-mu m-thick layer of lithium triflate-doped POEM-g-PDMS. Our results demonstrate the great potential of GCE-based Li-ion batteries for high-temperature applications. (C) 2011 Elsevier B.V. All rights reserved.
引用
收藏
页码:5604 / 5610
页数:7
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