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Title: Electronically and ionically conductive gels of ionic liquids and charge-transfer tetrathiafulvalene-tetracyanoquinodimethane
Authors: Mei, X.
Ouyang, J. 
Issue Date: 6-Sep-2011
Citation: Mei, X., Ouyang, J. (2011-09-06). Electronically and ionically conductive gels of ionic liquids and charge-transfer tetrathiafulvalene-tetracyanoquinodimethane. Langmuir 27 (17) : 10953-10961. ScholarBank@NUS Repository.
Abstract: Electronically and ionically conductive gels were fabricated by mixing and mechanically grinding neutral tetrathiafulvalene (TTF) and tetracyanoquinodimethane (TCNQ) in ionic liquids (ILs) like 3-ethyl-1- methylimidazolium dicyanoamide (EMIDCA), 1-ethyl-3-methylimidazolium thiocyanate (EMISCN), 1-ethyl-3-methylimidazolium bis(trifluoromethylsulfonyl)imide (EMITf 2N), trihexyltetradecylphosphonium bis(trifluoromethylsulfonyl) imide (P 14,6,6,6Tf 2N), and methyl-trioctylammonium bis(trifluoromethylsulfonyl)imide (MOATf 2N). Charge-transfer TTF-TCNQ crystallites were generated during the mechanical grinding as indicated by the UV-visibile-near-infrared (UV-vis-NIR) absorption spectroscopy, Fourier transform infrared (FTIR) spectroscopy, and X-ray diffraction. The charge-transfer TTF-TCNQ crystallites have a needle-like shape. They form solid networks to gelate the ILs. The gel behavior is confirmed by the dynamic mechanical measurements. It depends on both the anions and cations of the ILs. In addition, when 1-methyl-3-butylimidazolium tetrafluoroborate (BMIBF 4) and 1-methyl-3-propylimidazolium iodide (PMII) were used, the TTF-TCNQ/IL mixtures did not behave as gels. The TTF-TCNQ/IL gels are both electronically and ionically conductive, because the solid phase formed by the charge-transfer TTF-TCNQ crystallites is electronically conductive, while the ILs are ionically conductive. The gel formation is related to needle-like charge-transfer TTF-TCNQ cyrstallites and the π-π and Coulombic interactions between TTF-TCNQ and ILs. © 2011 American Chemical Society.
Source Title: Langmuir
ISSN: 07437463
DOI: 10.1021/la202465k
Appears in Collections:Staff Publications

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