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Vibrational spectra and microstructure of poly(epsilon-caprolactone)/siloxane biohybrids doped with lithium triflate

S. C. Nunes ; V. D. Bermudez ; Denis Ostrovskii (Institutionen för teknisk fysik, Kondenserade materiens fysik) ; N. V. Martins
Journal of Molecular Structure (0022-2860). Vol. 879 (2008), 1-3, p. 72-80.
[Artikel, refereegranskad vetenskaplig]

Fourier Transform infrared (FT-IR) and Raman (FT-Raman) spectroscopies and Scanning Electron Microscopy (SEM) were used to investigate ionic association, hydrogen bonding and morphology in a family of sol-gel derived lithium triflate (LiCF3SO3)-doped di-urethane cross-linked poly(epsilon-caprolactone) (PCL(530))/siloxane hybrid electrolytes. The materials studied, with compositions infinity > n >= 0.5 (where n - composition - expresses the molar ratio of PCL(530) ester repeat units per Li+ ion), are non-porous and homogeneous. The Li+ ions interact with the urethane and ester carbonyl oxygen atoms within the whole range of salt concentration analyzed, promoting the formation of hydrogen-bonded aggregates. The composition dependence of the relative concentration of "free" anions and coordinated anions (weakly coordinated anions, Li+CF3SO3- ion pairs or [Li(CF3SO3)(2)](-) triplets, aggregates I ([Li-2(CF3SO3)](+)) and aggregates II ([Li-3(CF3SO3)](+)) in all the samples is in perfect agreement with the values of the room temperature ionic conductivity reported previously. (C) 2007 Elsevier B.V. All rights reserved.

Nyckelord: sol-gel, poly(epsilon-caprolactone)/siloxane, lithium triflate, vibrational spectra, morphology, AMORPHOUS PHASES, COMPLEXES, ORMOLYTES, SYSTEM, CONDUCTIVITY, CRYSTALLINE, PERCHLORATE, TEMPERATURE, ELECTROLYTE, ENVIRONMENT

Denna post skapades 2009-10-26. Senast ändrad 2016-07-19.
CPL Pubid: 100813


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Institutionen för teknisk fysik, Kondenserade materiens fysik (1900-2015)


Teknisk fysik

Chalmers infrastruktur