Tin doped indium oxide (ITO) thin films provide excellent transparency and conductivity for electrodes in displays and photovoltaic systems. Current advances in producing printable ITO inks are reducing the volume of wasted indium during thin film patterning. However, their applicability to flexible electronics is hindered by the need for high temperature processing that results in damage to conventional polymer substrates. Here, we detail the conditions under which laser heating can be used as a replacement for oven and furnace treatments. Measurements of the optical properties of both the printed ITO film and the polymer substrate (polyethylene terephthalate, PET) identify that in the 1.5–2.0 μ m wavelength band there is absorption in the ITO film but good transparency in PET. Hence, laser light that is not absorbed in the film does not go on to add a deleterious energy loading to the substrate. Localization of the energy deposition in the film is further enhanced by using ultrashort laser pulses (~1 ps) thus limiting heat flow during the interaction. Under these conditions, laser processing of the printed ITO films results in an improvement of the conductivity without damage to the PET.

Transparent conducting aluminum doped zinc oxide Al:ZnO (AZO) layers have been deposited by spin coating on glass substrates using two different sols, 1-propanolic solution of Zinc and Aluminum salts (conventional sol) and a suspension of already crystalline AZO nanoparticles redispersed in 1-propanol. The coatings have been sintered in air at 600 degrees C for 15 min. and then post annealed in a reducing atmosphere at 400 degrees C for 90 min. The influence of the aluminum content in the coating sol (sol-gel layer) and in the redispersed nanoparticles (nanoparticulare suspension layer) on the optical properties and electrical resistivity have been investigated. A single step spin coated thin layer is obtained, so that multilayers coating have been used to lower the obtained sheet resistance. The visible transmission of both types of layers is high (T > 80%). The influence of the sintering temperature and the optimum doping concentration are investigated. Seven layers synthesized with Al/Zn = 1 mol.% and submitted to reducing treatment in forming gas (N2:H-2 = 92: 8) exhibited a sheet resistance R = 0.42 k Omega (rho = 7.9x10(-3) Omega center dot cm) with an average transmittance of 80% at 550 nm for layer deposited from conventional sol and 36 k Omega (rho = 2.5x10(-1) Omega center dot cm) for nanoparticles suspension layer.

We describe the fabrication and characterization of organic photodiodes on solution cast ITO (tin doped indium oxide) bottom electrodes. ITO coatings were produced by gravure printing process on PET and PEN substrates. The sheet resistance could be decreased by heat treatment at 120°C under forming gas atmosphere ( N2/ H2) to 1.5 kΩ. The transmission of the ITO coated PET and PEN substrates is more than 80% in the visible range. The printed films were hardened under UV-irradiation at low temperatures (< 130°C) and used as the bottom electrode of an organic photodiode (OPD), consisting of a stacked layer of copper phthalocyanine ( p -type material), perylene tetracarboxylic bisbenzimidazole ( n -type material) and Aluminium tris(8-hydroxyquinoline). The performance of the photodiodes with printed ITO on plastic substrates could be improved by adding a smoothing layer of PEDOT/PSS (Baytron® P) on the ITO coated films and was then similar to the performance of photodiodes with semi-transparent gold as anode. These results demonstrate the suitability of the printed ITO layers as bottom electrode for organic photodiodes. Furthermore the influence of different treatments (forming gas and oxygen plasma treatment) of the ITO bottom electrode on the current-voltage characteristics of the OPDs was studied.

Transparent semiconducting ITO:Ti thin films, prepared by a sol–gel process, has been deposited by spin-coating technique onto alkali-free glass substrates. The as-coated films were annealed in ambient air at 550 °C for 1 h and further annealed in a reducing atmosphere. The influences of the Ti content in the sol on the surface morphology, microstructure, optical properties and electrical resistivity have been investigated. These properties were found to depend on the Ti content in the coating sol. Ti addition led to dense smooth layers with larger crystallite size (20–30 nm). Double layers synthesized with Ti:ITO = 0.53 wt% and submitted to reducing treatment in forming gas exhibited the lowest sheet resistance R□ = 60 Ω□ with an average transmittance of 87% at 550 nm.

Transparent, conductive oxides (TCOs) applied as coatings find multiple applications in various areas such as flat panel display setups, as electrodes in touch-screen panels, electrochromic devices, slar cells and in architectural applications for example as IR reflectors. The favored material in the class of TCOs is still ITO - Sn-doped In2O3 - due to its unique combination of high transparency and electrical conductivity. Though already very good, the potneital of the ITO coatings with regard to their conductivity leaves some space for future improvements. Also ITO as a material has some serious drawbacks, such as limitied availability and high costs. This work presents some strategies to overcome these obstacles. One way to enhance the conductivities of alternative materials is to use carbon nanotubes as a dopant. This strategy was tested for ATO (Antimony-doped Tin Oxide), Titan dioxide and AZO (Aluminium-doped Zinc oxide). The results for these materials are presented. In coatings of ITO on glass or polymeric foils usually silica-based binders are used. They have the disadvantage to reduce the contact between the highly conducting grains and thus reduce overall conductivity in the composite. The matrix between the nanoparticles can be improved by serveral measures. Experiments with relevance in this direction are discussed. A third strategy aims at the reduction of costs in the process of ITO fabrication. Here one way to go is to use in electrochemical synthesis method. Results of the line of development are presented. Other strategies comprise the suitable processing of materials with a lower intrinsic conductivity or the search for materials with high intrinsic conductivity close to that of ITO. Exmples are presented and discussed.

ITO (tin doped indium oxide) coatings were produced by gravure printing process on PET and PEN foils. The printing paste consists of ITO nanoparticles, which are dispersed in a solvent and mixed with a binder. By modification of the printing paste, the sheet resistance (R/sq) of the ITO coatings after hardening under UV-irradiation at low temperatures (<130 degrees C) could be decreased to 1 k Omega/sq. R/sq could be further reduced down to 0.5 k Omega/sq by heat treatment under forming gas atmosphere (N-2/H-2), the transmission of the ITO coated foils still being more than 80% in the visible range. The application of these ITO films as a bottom electrode in organic photodiodes (OPDs) is shown, and the current density-voltage characteristics of the OPDs are presented. (C) 2009 Elsevier B.V. All rights reserved.

The fabrication of organic photodiodes on solution cast indium tin oxide (ITO) bottom electrodes on flexible substrates is described. ITO coatings with a sheet resistance of 2 to 3 k Omega/sq are produced by gravure printing process on PEN (polyethylene 2,6-naphthalate) films. The ITO films are directly used as transparent bottom electrodes for organic photodiodes (OPD). Furthermore, first experiments to integrate one of these OPDs in an all-organic opto-chemical sensor are successfully demonstrated. The implementation of OPDs as detectors in applications such as integrated sensors demands a fabrication of these devices on flexible substrates. For these applications the OPDs on printed ITO on PEN are especially suitable. (C) 2009 Elsevier B.V. All rights reserved.

6×8cm2 electrochromic devices (ECDs) with the configuration K-glass/EC-layer/electrolyte/ion-storage (IS) layer/K-glass, have been assembled using Nb2O5:Mo EC layers, a (CeO2)0.81–TiO2 IS-layer and a new gelatin electrolyte containing Li+ ions. The structure of the electrolyte is X-ray amorphous. Its ionic conductivity passed by a maximum of 1.5×10−5S/cm for a lithium concentration of 0.3g/15ml. The value increases with temperature and follows an Arrhenius law with an activation energy of 49.5kJ/mol. All solid-state devices show a reversible gray coloration, a long-term stability of more than 25,000 switching cycles (±2.0V/90s), a transmission change at 550nm between 60% (bleached state) and 40% (colored state) corresponding to a change of the optical density (ΔOD=0.15) with a coloration efficiency increasing from 10cm2/C (initial cycle) to 23cm2/C (25,000th cycle).

ITO (tin doped indium oxide) coatings with a sheet resistance of 2 to 3 kΩ(square) were produced by gravure printing process on PET and PEN foil. The printing paste consisted of ITO nanoparticles which were dispersed in a solvent by using a surfactant. The dispersion was mixed with a binder and a photo initiator before printing. The printed films were hardened under UV-irradiation at low temperatures (< 130°C). The sheet resistance could be decreased by heat treatment at 120°C under forming gas atmosphere (N2/H2) to 1.5 kΩ(square). The transmission of the ITO coated PET and PEN foils is more than 80 % in the visible range. The ITO films were directly used as the bottom electrode in an organic photodiode (OPD). The setup of the OPD originates from the well known Tang photodiode, consisting of a stacked layer of copper phthalocyanine (p-type material) and perylene tetracarboxylic bisbenzimidazole (n-type material). The photodiodes are characterised via current-voltage (I-V) characteristics. The performance of the photodiodes with printed ITO on plastic substrates could be improved by the deposition of a PEDOT/PSS layer (Baytron(R) P) on the ITO coated foils and was then comparable to the performance of photodiodes with semi-transparent gold as anode on PET substrates. These results demonstrate the suitability of the printed ITO layers as anode for organic photodiodes.