The front surface of dielectric passivated silicon wafers were spray coated with polyacrylic acid (PAA) using an ultrasonic coating system. A simple model was proposed to correlate the degree of coverage with the number of spray passes. The sprayed PAA films enabled good etching of the dielectric, using a process referred to as aerosol jet etching (AJE), despite the fact that the PAA thickness was non-uniform over the substrate. The AJE tip-to-substrate distance and diameter of the tip were tuned to balance process throughput and the etched line width. Controlling the level of condensation in the aerosol jet printer (AJP) fluid path was critical for etching 156-mm pseudo square silicon wafers.

Hematite (α-Fe2O3) nanoparticles were diffused of two different shapes (spherical and cubical) in PEDOT:PSS matrices below the percolation threshold. Increases in conductivity within a distinct range in concentration were observed in the dark and under simulated solar illumination. The effect was ascribed to a generalized Poole-Frenkel effect in conjunction with basic properties of heterojunctions and electrostatic dipoles, and verified through data fitting. A difference in behaviour between sphere- and cube-based nanocomposites was also observed.

Silver nanoparticle inks are increasingly applied for the manufacture of inkjet-printed electrically conductive patterns. In order to obtain high conductivity, the printed liquid patterns have to be functionalized by an appropriate post- treatment step. Modern post-treatment methods using e.g. microwaves, intense pulsed light or adopted infrared radiation, are nevertheless the basis of the thermal process. The thermal treatment e.g. in furnaces or on heating plates, is applicable for a great variety of inks and ensures an efficient sintering without major technical efforts. It has been studied intensively wherein the reports mainly focus on reduction of the resistivity by controlling the parameters of the thermal treatment. Our researches exceed these comparative studies by investigating multi-layered patterns, their manufacturing and post-treatment.

Two silver nanoparticle inks were inkjet printed on a rigid and a flexible substrate. The geometry of the patterns was varied. The different drying behaviors of the inks were investigated. In addition, the number of layers which were printed on top of each other was varied. The sintering temperatures and time durations were varied.

The morphology of the patterns is investigated by profilometry and optical microscopy. The microstructure is analyzed by scanning electron microscope and X-ray diffraction. Furthermore, the electrical characteristics were determined by the measurement of the resistance. The results indicate the relation between the manufacture and the resulting microstructure and functionality of the patterns. The knowledge of these parameters enables us to control the industrial manufacturing of similar conductive patterns.

Bismuth selenide (BixSey) films are deposited onto glass substrate using chemical bath deposition at room temperature. The reacting bath contained bismuth nitrate, triethanolamine and sodium selenosulfate as selenium (Se) source. Ammonium hydroxide is used to adjust the pH of the bath. The films deposited in solutions containing Se source solution of 10 ml and 15 ml are characterized by surface morphological, compositional and structural, properties. The optimum deposition time is about 3 hours for both solutions. Films deposited up to 24 hours in bath with 10 ml Se source solution had thickness ranging up to 232 nm. The deposition rate is found to increase up to 61 nm/h for 3-hour deposition. In the case of bath with 15 ml Se source solution, the film thickness ranged from 45 nm to 632 nm for 1-hour to 24-hour deposition, respectively; with a deposition rate increasing up to 123 nm/h for 3-hour deposition. Film roughness of about 6.6 nm to 22.8 nm is measured by atomic force microscope for films deposited in bath containing 10 mL Se source and 15 ml of Se source, respectively. Crack free layers are observed with randomly large plate-like particles on top of the layer for some films. The films with typical composition of Bi21.8Se78.2 are found to be rich in Se when deposited for 6 hours, whereas the composition of a film deposited in the same bath (10 mL Se source) for 3 hours is found at Bi60.3Se39.6. Additionally, structural analysis performed by x-ray diffraction (XRD) did not reveal well-defined XRD patterns, which indicates that BixSey films were constituted mostly of nanocrystalline grains.

A novel approach to fabricate CuIn(S,Se)2 (CIS) thin films through ultrasonically spraying a hydrazine-based precursor solution onto a heated substrate is reported. The effects of the composition of the precursor solutions and the deposition temperature on the CIS film properties were investigated by comparing thin films fabricated using aqueous metal salt solution, anhydrous hydrazine solution, and hydrazine hydrate solution at various deposition temperatures. Crystallite size and texture coefficient in the preferred (112) orientation in the sprayed films increased when the aqueous solution was replaced by hydrazine-based solutions. Additionally, the hydrazine-based precursor solutions resulted in films with better surface smoothness and compositional uniformity than those fabricated using water-based solutions and the hydrazine hydrate solution resulting in the smoothest, most uniform films. The sprayed films were used to fabricate preliminary solar cells that demonstrated a modest photovoltaic response. With optimization, the synthesis of high-quality CIS films by spray pyrolysis from a hydrazine hydrate solution could demonstrate the potential for a low-cost, high-throughput manufacturing process.

This investigation is a comprehensive study of the effect of ammonium acetate on the electrical, optical, morphology and microstructure of CdS thin films grown by Chemical Bath Deposition method (CBD). Two sets of CdS thin films (A and B) were deposited on glass substrates at 60°C for 60 min. The films were deposited using chemical bath solution that consists of cadmium acetate, ammonium hydroxide, and thiourea. However, ammonium acetate was added into the chemical bath used to deposit set (B), where ammonium acetate was eliminated from bath solution used to deposit set (A). The films’ morphology was examined by Field Emission Scanning Electron Microscopy (FE-SEM), whereas, the chemical composition was investigated by Electron Probe Micro-Analyzer (EPMA). The X-Ray Diffraction (XRD) θ/2θ technique was applied to study the structure of the films. Atomic Force Microscopy (AFM) was used to measure the average surface roughness of the films, and Dektak Profilometer was used to determine the CdS films thickness. The optical and electrical properties for the films were determined using UV-Vis-NIR Spectrometer, and the Hall Effect technique, respectively. The highest carrier mobility was obtained for the films deposited in an ammonium acetate free bath. However, both films were polycrystalline with hexagonal structure exhibiting a tendency toward <002> texture, that increase with increasing the pH value of the chemical bath.

In this work, spherical copper (core) - silver (shell) nanoparticles with diameter of 40-50 nm were synthesized through polyol successive reduction process in glycerol with addition of sodium hydroxide (NaOH). The process involves microwave-assisted reduction of copper nitrate by glycerol under atmospheric conditions and successive reduction of silver nitrate at the surface of copper nanoparticles synthesized. We investigated the influence of synthesis parameters including molar ratio of NaOH:Cu (0:1, 1:1, 3:1 and 5:1), the molar ratio of Ag:Cu (0.01:1, 0.05:1, 0.10:1, 0.15:1 and 0.20:1) on the size, structure and composition of the resulting particles. High-resolution transmission electron microscopy with energy dispersive X-ray spectroscopy (TEM/EDS), scanning electron microscopy (SEM) and X-ray diffraction (XRD) analysis were used to characterize the particles obtained. The average size of the nanoparticles decreased with increasing of the ratio of sodium hydroxide. With the molar ratio of Ag:Cu greater than 0.05:1, the silver protective shell can prevent forming of copper oxide on the surface of nanoparticles.

High-energy flash cure lamps process thick film materials (<10 um) over large areas (<100 cm2) within milliseconds and are capable to deliver higher energy and power densities (20 J/cm2 and 20 kW/cm2) allowing for a more complete curing and elimination of flaws that would exist in conventional treatment. Click reactions are especially attractive for patterned devices as they have minimal shape change during curing and have a more predictable structure compared to free radical acrylate polymerization. Pentaerythritol tetrakis(3-mercaptopropionate) and 2,4,6-Triallyloxy-1,3,5-triazine were combined at 3:4 by weight and then spin coated on copper foil substrates. The solutions were processed both thermally and with exposure to a xenon flash bulb. Thermal treatment consisted of heating the sample at 80°C on a hot plate over night. Flash curing was accomplished using a Novacentrix Pulseforge 1300 system. The flash lamp curing fluence and intensities were varied to determine their effects on degree of cross-linking, dielectric constant, breakdown field and energy storage. The degree of cross-linking was determined through comparative FTIR studies. Dielectric constant was measured using an Agilent 4294a impedance analyzer from 100 Hz-100 MHz with a two terminal setup. Breakdown strength and energy density measurements were taken using Radiant Technology's Precision Ferroelectric tester with a 10 kV source. The printed films averaged 1-3 microns thick as observed by an SEM cross section measurement. It was found that dielectric constant varies with both treatment intensity and fluence. Energy densities were calculated using the ideal capacitor equation and ranged from 1.5-4.8 J/cm3.

The present study describes the effect of ageing time during the synthesis of oleic acid capped cadmium selenide quantum dots synthesized by the hot injection route and their use in the fabrication of a hybrid quantum dot light emitting device (QD-LED). This hot injection process has been carried out at the lower synthesis temperature of 140°C compared to the conventional temperature of ∼300°C. Fluorescent monodisperse quantum dots of size 3-5 nm and 8-10 nm have been obtained at an ageing time of 2 and 3 hours respectively. An attempt to fabricate a QD-LED has been carried out. Current versus voltage studies show a turn on voltage at 3.06 V with a current of ∼ 87 nA.

The effect of Y dopant incorporated into ZTO with different Y ratios in Y-ZTO system on the performances of ZTO-based TFTs is investigated by using sol-gel process. The proper Y doped ZTO present both high film crystallization temperature and superior electrical properties as an active channel layer of TFTs. The fabricated YZTO-based TFTs with 11% Y show the excellent devices performance such as the channel field effect mobility of 1.756 cm2/Vs, SS of 2.13 V/dec, threshold voltage of 0.8V and on/off ratio of 3.12×106.