The title compound is the only known organic superconductor (Tc = 0.8 K) with an a-phase crystal structure, in which the conducting plane contains single BEDT-TT F molecules with alternating orientation, rather than the pairs of molecules found in the higher Tc Ie-phase compounds. We have measured the polarized reflectivity of protonated and deuterated ., from 80 cm-1 to 8000 cm-l , at temperatures between 6.5 K and 300 K. The overall shape of these spectra are discussed. The optical conductivity obtained after a Kramers-Kronig analysis shows no maximum in the mid-infrared as known from the compounds of the Ie-phase due to the lack of dimerization of the BEDT-TTF molecules. This causes an accentuation of the far-infrared intraband conductivity. The vibrational features are assigned and discussed.
INTRODUCTIONEven if the first popular BEDT-TTF (bia--(ethylenedithio) tetrathiafulvalene) radical ion salt was a- , no superconductivity in an a-phase crystal of this familiy was found. Various efforts to observe ambient pressure superconductivity in an a-phase BEDT-TTF salt like a-(BEDT-TTFhI 3 or related components a-(BEDT-TTFhAuI2 have failed: Doping of a-(BE-DT-TTFhI 3 ·with iodine does not cause a partial supression of the metal-insulator transition at 135 K and superconducting behaviour at T ~ 3 K as reported [2], but only gives a slight rise of the high-frequency conductivity in the insulating phase after extreme doping of several hours [3].