Photoluminescence Properties of a-SiC:H Films Grown by Plasma Enhanced Chemical Vapor Deposition from SiH_(4)+C_(2)H_(2) Gas Mixtures

The films of a-SiC:H were deposited by plasma enhanced chemical vapor deposition system from SiH_(4)+C_(2)H_(2) gas mixtures.The C-rich a-SiC:H films were easily obtained by using C_(2)H_(2) gases due to the low dissociation energy of C_(2)H_(2) molecule in the plasma.Thus,the carbon was effectively incorporated into a-Si:H network.Although the defect state densities were proportional to carbon content in a-SiC:H films,the photoluminescence intensities were not directly related with defect density,yet increased with the carbon content increasing.The infrared spectra indicated that CHn groups as clusters were incorporated mainly into a-SiC:H network.The little correlation of the PL integrated intensity with defect state density suggested that luminescence was associated with clusters as a largely intracluster process.

Langmuir-Blodgett Films from Schiff Base Aluminium (Ⅲ) Complex

The characteristics of the LB films of Schiff base aluminium(Ⅲ), tris(2-hydroxy-5-nitro-N-dodecyl-benzylideneaminato) aluminium(Ⅲ)[Al(TA12)_3], were studied. The surface pressure-area(π-A) isotherm of Al(TA12)_3 in the pure water subphase was investigated. The molecular area, 0.48 nm^2, is one-third of the expected value that indicates the formation of an aggregate. The Langmuir-Blodgett(LB) films of Al(TA12)_3 were transferred and characterized. The UV-Vis spectra and the AFM image both confirmed that the J-aggregates formed. The polarized UV-Vis spectra indicated that the complex plane had to be oriented with an angle of about 30° to the substrate surface. The IR spectra suggested that the complexation took place between aluminium ions and the oxygen atoms of the ligand rather than the nitrogen atom.

Photoelectrochemical Character of TiO_2 Nanocrystalline Electrodes Sensitized by Aluminum Phthalocyanines Modified with Sulfonate Groups

Particular kinds of TiO2 nanocrystalline electrodes were sensitized by aluminum phthalocyanines modified with sulfonate groups [ Al（OH） PcSm ]. It was found that in the red region, the electrodes show obvious photoelectrical responses. The surface photovoltage spectra and photocurrent action spectra indicate that in the red region, the monomers of aluminum phthalocyanines have a greater influence on the determination of the photoelectrical response of TiO2 electrodes than the dimers. The dye-sensitized solar cells were obtained by using the aluminum phthalocyaninessensitized TiO2 electrodes and Pt electrodes, which have an open circuit photovoltage of 360 mV, a short circuit photocurrent of 39. 4 μA/cm^2 , a fill factor of 0. 54 and a maximum power output of 7.65 μW/cm^2 under a light intensity of 50 mW/cm^2.

UV-Vis and Surface Photovoltage Spectra of Fe_2O_3/Polystyrene Composite Microspheres

Fe_2O_3 sol with the particle diameter of 3-5 nm was flocculated by the addition of SDS, and the flocculate formed was redispersed by the further addition of that surfactant. Thus the surfactant bilayer was formed on the surface of Fe_2O_3. The emulsion polymerization of styrene(St) adsolubilized on the surfactant adsorbed bilayer was carried out by initiator potassium persulfate(KPS). The UV-Vis and surface photovoltage spectra(SPS) indicate that the Fe_2O_3 particles were encapsulated in polystyrene(PSt) successfully.

C-V Characterization of α-Fe_2O_3/Block-Copolymer Composite Particulate Films

α-Fe_2O_3 nanocrystal was encapsulated by a block-copolymer, hydroxylated poly (styrene-b- butadiene-styrene) (HO-SBS) to fabricate composite microspheres with α-Fe_2O_3 cores and HOSBS shell. Its film fabricated on n-Si wafer acts as the insulator layer in the metal-insulator- semiconductor(MIS) structure. The capacitance-voltage (C-V) properties were measured to characterize the composite particulate films.