Structure of the polymer electrolyte poly(ethylene oxide)6:LiAsF6

被引:420
作者
MacGlashan, GS [1 ]
Andreev, YG [1 ]
Bruce, PG [1 ]
机构
[1] Univ St Andrews, Sch Chem, St Andrews KY16 9ST, Fife, Scotland
关键词
D O I
10.1038/19730
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Polymer electrolytes-salts (such as LiCF3SO3) dissolved in solid, high-molar-mass polymers (for example, poly(ethylene oxide), PEO)(1-3)-hold the key to the development of all-solid-state rechargeable Lithium batteries(4). They also represent an unusual class of coordination compounds in the solid state(5). Conductivities of up to 10(-4) S cm(-1) may be obtained, but higher levels are needed for applications in batteries(5-7). To achieve such levels requires a better understanding of the conduction mechanism, and crucial to this is a knowledge of polymer-electrolyte structure. Crystalline forms of polymer electrolytes are obtained at only a few discrete compositions. The structures of 3 : 1 and 4: 1 complexes (denoting the ratio of ether oxygens to cations) have been determined(5,8,9). But the 6:1 complex is of greater interest as the conductivity of polymer electrolytes increases significantly on raising the polymer content from 3:1 to 6: 1 (refs 10, 11). Furthermore, many highly conducting polymer-electrolytes) stems form crystalline 6:1 complexes whereas those with lower conductivities do not. Here we report the structure of the PEO:LiAsF6 complex with a 6:1 composition. Determination of the structure was carried out ab initio by employing a method for flexible molecular structures, involving full profile fitting to the X-ray powder diffraction data by simulated annealing(12). Whereas in the 3:1 complexes the polymer chains form helices, those in the 6:1 complex form double non-helical chains which interlock to form a cylinder. The lithium ions reside inside these cylinders and, in contrast to other complexes, are not coordinated by the anions.
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页码:792 / 794
页数:3
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