We propose a modified droplet epitaxy method for fabricating self-organized GaAs/AlGaAs quantum dots (QDs) with a high As flux irradiation and a low substrate temperature. By our novel method, GaAs QDs were successfully formed, retaining their pyramidal shape, original base size and density of droplets, and preventing layer-by-layer growth. Quantum size effects of the QDs were distinctly observed by photoluminescence measurements. It was confirmed that this new modified droplet epitaxy method is promising for fabricating a high-quality GaAs/AlGaAs QD system.

The OH reaction rate constants have been measured for CF3CH2OH, CF3CF2CH2OH, and CF3CH(OH)CF3 over the temperature range 250−430K. Kinetic measurements have been carried out using the discharge flow, laser photolysis, and flash photolysis methods, combined respectively with the laser-induced fluorescence technique to monitor the OH radical concentrations. The influence of impurities contained in the sample of CF3CF2CH2OH has been investigated by means of sample purification using gas chromatography. No sizable effect of impurities was found on the measured rate constants of these three fluorinated alcohols. The Arrhenius rate constants have been determined from the respective kinetic data as k(CF3CH2OH) = (2.00 ± 0.37) × 10-12 exp[−(890 ± 60)/T], k(CF3CF2CH2OH) = (1.40 ± 0.27) × 10-12 exp[−(780 ± 60)/T], and k(CF3CH(OH)CF3) = (6.99 ± 1.56) × 10-13 exp[−(990 ± 70)/T] cm3 molecule-1 s-1. A method of predicting the OH reaction rate constants for fluorinated alcohols, hydrofluorocarbons, alkanes, and alcohols has been proposed.

The interactions between condensed molecules at cryogenic temperatures (15–200 K) have been investigated on the basis of secondary ion mass spectrometry. It is demonstrated that the protonated molecular ions, emitted via the proton transfer reactions, provide us unique information about the reorganization of hydrogen-bonded molecules. From the CH3OH molecules adsorbed on the D2O–ice surface, the D+(CH3OH) ions are sputtered predominantly in the temperature range between 100 and 150 K since most of the CH3OH molecules are bound to the D2O layer via hydrogen bonds. A rapid and almost complete H/D exchange, yielding the D+(CH3OD) species, occurs above 150 K due to the enhanced mobility of the surface D2O molecules. Up to the desorption temperature of 180 K, a considerable amount of methanol exists on the surface without mixing with the heavy-water layer due to hydrophobicity of the methyl group. On the methanol–ice surface, the adsorbed D2O molecules form hydrogen bonds preferentially with the CH3OH molecules and tend to be incorporated in the thin-layer bulk of methanol above 120 K.

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We have investigated microscale to nanoscale ferroelectric domain and surface engineering of a near-stoichiometric LiNbO3 crystal by using scanning force microscopy. The single crystals LiNbO3 fixed on metal substrates were polished to a 5 μm thickness. Artificial patterns of inverted-domain structures were fabricated in the samples, where polarization directions of the domains were switched by scanning the samples with a conductive cantilever while applying voltages. Furthermore, the negatively polarized surfaces in the patterns were preferentially etched in HF solution. As a result, cavity and mound-shaped surfaces were fabricated; these structures could be used to create functional templates and devices.