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NMR and Raman studies of a novel fast-ion-conducting polymer-in-salt electrolyte based on LiCF3SO3 and PAN

Ferry, Anders (författare)
Umeå universitet,Institutionen för fysik,Department of Materials Engineering, Monash University, Clayton, Australia
Edman, Ludvig, 1967- (författare)
Umeå universitet,Institutionen för fysik
Forsyth, Maria (författare)
Department of Materials Engineering, Monash University, Clayton, Australia
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MacFarlane, Douglas R. (författare)
Department of Chemistry, Monash University, Clayton, Australia
Sun, Jianzeng (författare)
Department of Chemistry, Monash University, Clayton, Australia
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 (creator_code:org_t)
Elsevier, 2000
2000
Engelska.
Ingår i: Electrochimica Acta. - : Elsevier. - 0013-4686 .- 1873-3859. ; 45:8-9, s. 1237-1242
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
Stäng  
  • We report spectroscopic results from investigations of a novel solid polymeric fast-ion-conductor based on poly(acrylonitrile), (PAN, of repeat unit [CH2CH(CN)]n), and the salt LiCF3SO3. From NMR studies of the temperature and concentration dependencies of 7Li- and 1H-NMR linewidths, we conclude that significant ionic motion occurs at temperatures close to the glass transition temperature of these polymer-in-salt electrolytes, in accordance with a recent report on the ionic conductivity. In the dilute salt-in-polymer regime, however, ionic motion appears mainly to be confined to local salt-rich domains, as determined from the dramatic composition dependence of the ionic conductivity. FT-Raman spectroscopy is used to directly probe the local chemical anionic environment, as well as the Li+-PAN interaction. The characteristic δs(CF3) mode of the CF3SO3- anion at ∼ 750-780 cm-1 shows that the ionic substructure is highly complex. Notably, no spectroscopic evidence of free anions is found even at relatively salt-depleted compositions (e.g. N:Li ∼ 60-10:1). A strong Li+-PAN interaction is manifested as a pronounced shift of the characteristic polymer C=N stretching mode, found at ∼2244 cm-1 in pure PAN, to ∼ 2275 cm-1 for Li+-coordinated C=N moieties. Our proton-NMR data suggest that upon complexation of PAN with LiCF3SO3, the glass transition occurs at progressively lower temperatures. 

Ämnesord

NATURVETENSKAP  -- Fysik -- Den kondenserade materiens fysik (hsv//swe)
NATURAL SCIENCES  -- Physical Sciences -- Condensed Matter Physics (hsv//eng)

Nyckelord

polymer-in-salt electrolyte
lithium and proton NMR
FT-Raman spectroscopy
poly(acrylonitrile)
LiCF3SO3
TRANSPORT-PROPERTIES
SOLID ELECTROLYTES
POLYACRYLONITRILE
LICLO4
MODEL

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