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LIBRIS Formathandbok  (Information om MARC21)
FältnamnIndikatorerMetadata
00003731naa a2200445 4500
001oai:DiVA.org:umu-224159
003SwePub
008240510s1998 | |||||||||||000 ||eng|
024a https://urn.kb.se/resolve?urn=urn:nbn:se:umu:diva-2241592 URI
024a https://doi.org/10.1063/1.4768442 DOI
040 a (SwePub)umu
041 a engb eng
042 9 SwePub
072 7a ref2 swepub-contenttype
072 7a art2 swepub-publicationtype
100a Ferry, Andersu Umeå universitet,Institutionen för fysik4 aut0 (Swepub:umu)anfe0001
2451 0a Spectroscopic studies of luminescent and ionically conducting Eu[N(CF3SO2)2]3-PPG4000 complexes
264 1b American Institute of Physics (AIP),c 1998
338 a print2 rdacarrier
520 a Alternating current impedance, Fourier transform Raman/infrared (IR), and luminescence excitation (continuous and time-resolved) measurements have been conducted on solutions of poly(propylene glycol) (MW 4000) complexed with Eu[N(CF3SO2)2]3 salt, EuTFSI3, along with differential scanning calorimetry (DSC) studies. From observed frequency shifts of characteristic internal anionic vibrational modes (Raman and IR), we conclude that the salt is solvated by the polymer host. The TFSI anions, however, interact extensively with Eu3+ cations at all concentrations investigated. Ion-polymer interactions are manifested as changes in characteristic vibrational modes of the polymer. Continuous and time-resolved site-selective luminescence data give, respectively, evidence for two different types of chemical environments for solvated Eu3+ cations. In particular, the strongly forbidden non-degenerate 5D0 - 7F0 transition exhibits a structured two-component profile in the spectra. DSC data show that the glass transition temperature, Tg, is only marginally affected by the introduction of a relatively high concentration of salt into the host matrix, whereas the resulting polymer-salt complex is of rubbery character, distinctly different from the pure host polymer, which is a viscous liquid at room temperature. The present findings are interpreted in terms of a phase-segregated microstructure. This conjecture is supported by previous studies on PPG4000-based electrolytes indicating microscopic phase anomalies.
650 7a NATURVETENSKAPx Fysikx Den kondenserade materiens fysik0 (SwePub)103042 hsv//swe
650 7a NATURAL SCIENCESx Physical Sciencesx Condensed Matter Physics0 (SwePub)103042 hsv//eng
653 a low-salt concentrations
653 a polymer electrolytes
653 a physical-properties
653 a ion association
653 a poly(propylene oxide)
653 a microphase separation
653 a photon-correlation
653 a raman-scattering
653 a molecular-weight
653 a decay times
700a Furlani, Mauriziou Department of Physics, Chalmers University of Technology and Göteborg University, S 412 96 Göteborg, Sweden4 aut
700a Franke, Axelu Umeå universitet,Institutionen för fysik4 aut
700a Jacobsson, Peru Umeå universitet,Institutionen för fysik,Department of Physics, Chalmers University of Technology and Göteborg University, S 412 96 Göteborg, Sweden4 aut
700a Mellander, Bengt-Eriku Department of Physics, Chalmers University of Technology and Göteborg University, S 412 96 Göteborg, Sweden4 aut
710a Umeå universitetb Institutionen för fysik4 org
773t Journal of Chemical Physicsd : American Institute of Physics (AIP)g 109:7, s. 2921-2928q 109:7<2921-2928x 0021-9606x 1089-7690
8564 8u https://urn.kb.se/resolve?urn=urn:nbn:se:umu:diva-224159
8564 8u https://doi.org/10.1063/1.476844

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