TY - JOUR
T1 - The Structure of the polymer electrolyte Poly(ethylene oxide)6:LiAsF6
AU - MacGlashan, G
AU - Andreev, Yuri Georgievich
AU - Bruce, Peter George
PY - 1999/4/29
Y1 - 1999/4/29
N2 - 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.
AB - 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.
KW - CRYSTAL-STRUCTURE
KW - COMPLEX
KW - SALTS
UR - http://www.scopus.com/inward/record.url?scp=0033614305&partnerID=8YFLogxK
M3 - Article
SN - 0028-0836
VL - 398
SP - 792
EP - 794
JO - Nature
JF - Nature
ER -