a b s t r a c tSpiro-condensed dithienometalloles (metal ¼ Si, Ge) and dithienothiametallines (metal ¼ Si, Ge, Sn) were prepared by the ring closure reactions of dilithiated bithiophene and dithienyl sulfide with metal tetrachlorides, and their optical properties were studied with respect to the UV absorption and emission spectra. The absorption and emission maxima of them moved to higher energies by increasing the size of the center metal from Si to Ge and Sn, and stepwise oxidation of the ring sulfur atom in the dithienothiasiline system forming sulfoxide and sulfone linkages, making the fine tuning of the electronic states possible.

Effects of carbon impurities and oxygen vacancies in Al2O3 film on the characteristics of Al2O3/GaN MOS capacitors were studied using the different atomic layer deposition (ALD) precursor and high-pressure water vapor annealing (HPWVA). Trimethyl aluminum (TMA: Al(CH3)3) and dimethyl aluminum hydride (DMAH: Al(CH3)2H) were used as ALD precursors to control the carbon impurities. On the other hand, oxygen vacancies in Al2O3 film were suppressed using the HPWVA. The DMAH precursor reduced the concentration of carbon impurities in the ALD Al2O3 film. It was found that the interface trap density (Dit) was mainly affected by the carbon impurities rather than the oxygen vacancies at the Al2O3/GaN interface. On the other hand, voltage stress induced flat band voltage (VFB) shift was attributed to both the carbon impurities and the oxygen vacancies.

Highly photoluminescent acceptor-donor-acceptor (A-D-A) and donor-acceptor (D-A) type compounds with a dithienosilole unit as the donor and perfluorotolyl or dimesitylboryl group(s) as the acceptor were prepared by the reaction of lithiated dithienosilole derivatives with perfluorotoluene or fluorodimesitylborane, respectively. The resulting A-D-A and D-A type compounds showed red-shifted UV absorption and PL bands compared to those of simple dithienosiloles having no acceptor units, reported previously, and were highly photoluminescent in the solid state as well as in solution. Solvatochromic behaviour that would arise from the intramolecular donor-acceptor interaction were observed for the D-A type compounds with respect to the UV absorption and PL spectra. In addition, it was found that bis(dimesitylboryl)dithienosilole and (dimesitylboryl)(methylthio)dithienosilole responded to coexisting fluoride anions, leading to clear UV absorption and PL spectral changes in solutions.

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