Indium-Tin-Oxide (ITO) thin films were deposited on glass substrates using DC magnetron reactive sputtering at different bias voltages and substrate temperatures. Some improvements were obtained on film properties, microstructure and other physical characteristics for different conditions. Amorphous and polycrystalline films can be obtained for various deposition conditions. The transmission, absorption, spectral and diffuse reflection of ITO films were measured in some ranges of UV-Vis-NIR. The refractive index (n), Energy band gap Eg and the surface roughness of the film were derived from the measured spectra data. The carrier density (nc) and the carrier mobility (μ) of the film micro conductive properties were discussed. The films exhibited suitable optical transmittance and conductivity for electrochromic applications. © 2002 Elsevier Science B.V. All rights reserved.

We report, for the first time, results on transparent ZnO:Al thin films deposited on polyester (Mylar type D, 100 μm thickness) substrates at room temperature by magnetron sputtering. The structural, optical and electrical properties of the deposited films have been studied. The samples are polycrystalline with a hexagonal wurtzite structure and a strong crystallographic c-axis orientation (0 0 2) perpendicular to the substrate surface. The ZnO:Al thin films with 83% transmittance in the visible region and a resistivity as low as 3.6 × 10-2 Ωcm have been obtained, as deposited. The obtained results are comparable to those obtained on glass substrates, opening a new field of low cost, light weight, small volume, flexible and unbreakable large area optoelectronic devices. © 2002 Elsevier Science Ltd. All rights reserved.

A new experimental procedure combining usual isothermal DC charging and discharging with non-isothermal current measurements has been recently proposed. It is mainly suitable for very high insulating polymers and it was successfully applied to the study of space charge trapping and transport in low-density polyethylene. The analysis of the isothermal currents revealed the presence of different traps whose characteristic (de)trapping times can be deduced. The isothermal procedures allowed the selective charging of the sample. By choosing the charging field and the ratio of charge/discharge times, non-isothermal analysis permitted the differentiation of three or four peaks (at approximate to50degreesC, approximate to65degreesC, approximate to70degreesC and approximate to85degreesC) associated with charge detrapping from surface or near-surface (<20 mum) traps. These traps have activation energies between 0.21 and 1.54 eV. The mobility at 30degreesC is around 5 x 10(-16) m(2) V-1 s(-1). Samples had to be conditioned before each experiment in order to obtain reproducible results.

A new experimental procedure combining usual isothermal DC charging and discharging with non-isothermal current measurements has been recently proposed. It is mainly suitable for very high insulating polymers and it was successfully applied to the study of space charge trapping and transport in low-density polyethylene. The analysis of the isothermal currents revealed the presence of different traps whose characteristic (de)trapping times can be deduced. The isothermal procedures allowed the selective charging of the sample. By choosing the charging field and the ratio of charge/discharge times, non-isothermal analysis permitted the differentiation of three or four peaks (at approximate to50degreesC, approximate to65degreesC, approximate to70degreesC and approximate to85degreesC) associated with charge detrapping from surface or near-surface (<20 mum) traps. These traps have activation energies between 0.21 and 1.54 eV. The mobility at 30degreesC is around 5 x 10(-16) m(2) V-1 s(-1). Samples had to be conditioned before each experiment in order to obtain reproducible results.

In this work, we study the electro-optical behaviour of cellulose/liquid crystal-based composite systems, in particular the influence of the flexible substrates and its conductive layers in the electro-optical behaviour of these kind of cells. Four cells were made using, respectively, two different substrates (a flexible polymer (poly(ethylene terephthalate) (PET)) and a soda lime glass) and two different conductive layers (indium tin oxide (ITO) and aluminium zinc oxide (AZO)). The conductive layer (AZO) was deposited in both, flexible and rigid substrates, for the same conditions, and the same substrates coated with ITO are commercially available. The cells were prepared from solid films of hydroxypropylcellulose (HPC) (30 μm thick) cross linked with 1,4-diisocyanatobutane (BDI) (7% w/w) and the nematic liquid crystal E7 (Merck, UK). The four different substrates were electrically and morphologically characterised. We have analysed all samples by light transmission and determined the maximum transmission, contrast and Von. We show a comparison of the results obtained for both flexible and rigid cells and discuss them in terms of the proposed working mechanism for these systems. © 2002 Elsevier Science B.V. All rights reserved.

In this work we present results concerning the composition and structure of intrinsic thin film silicon carbide alloys obtained by hot wire and hot wire plasma assisted techniques using ethylene as carbon gas source. The data show that by increasing the percentage of ethylene in the gas mixture from 14% to 60% the optical band gap is enhanced from 1.8 eV to 2.3 eV, for films produced by hot wire technique at a filament temperature of 2123K (1850°C). This is attributed to the increase of carbon incorporation, which was confirmed by the infrared spectra data where an increase is observed in the SiC stretching vibration mode ascribed to the peak located at around 750cm-1. On the other hand, the films produced by combining hot wire and rf plasma show a more efficient carbon incorporation. The SEM photographs of samples produced with hot wire technique reveal an amorphous structure, confirmed by micro-Raman spectroscopy data, while the samples produced with plasma assisting the process show a granular structure with grain sizes in the range of 100-200nm. © 2002 Elsevier Science Ltd. All rights reserved.