Annealing effect of hybrid solar cells based on poly (3-hexylthiophene) and zinc-oxide nanostructures

The structural growth and optical and photovoltaic properties of the organic–inorganic hybrid structures of zinc oxide (ZnO)-nanorods/poly-3-hexylthiophene (P3HT) and two variations of organic polymer blends of ZnO/ P3HT:C60 fullerene and ZnO/P3HT:6,6]-phenyl C61 butyric acid methyl ester were studied in detail during thermal annealing. The ordering of the P3HT nanocrystals increased during annealing, which also improved hole transport in the hybrid structures. The optical constants of the ZnO/P3HT:[6,6]-phenyl C61 butyric acid methyl ester (PCBM) films elevated with annealing temperature due to the improved crystallisation induced by the formation of P3HT crystalline domains. As a result, a maximum power conversion efficiency of approximately 1.03% was achieved for the annealed ZnO/P3HT:PCBM device at 140 °C. These findings indicate that ZnO-nanorods/P3HT:PCBM films are stable at temperatures up to 160 °C.Web of Scienc

Self-catalytic growth of tin oxide nanowires by chemical vapor deposition process

We report on the synthesis of tin oxide (SnO2) nanowires by a chemical vapor deposition (CVD) process. Commercially bought SnO nanopowders were vaporized at 1050∘C for 30 minutes with argon gas continuously passing through the system. The assynthesized products were characterized using UV-visible absorption spectroscopy, X-ray diffraction (XRD), scanning electron microscopy (SEM), and high-resolution transmission electron microscopy (HRTEM). The band gap of the nanowires determined from UV-visible absorption was around 3.7 eV.The SEM micrographs revealed “wool-like” structure which contains nanoribbons and nanowires with liquid droplets at the tips. Nanowires typically have diameter in the range of 50–200nm and length 10–100 m. These nanowires followed the vapor-liquid-solid (VLS) growth mechanism

Characterization of silicon nitride thin films deposited by hot-wire CVD at low gas flow rates

We examined the chemical, structural, mechanical and optical properties of amorphous hydrogenatedsilicon nitride thin films deposited by hot-wire chemical vapour deposition using SiH4, NH3and H2gases at total flow rates below 33 sccm. Time of flight secondary ion mass spectroscopy reveal that thefilm surfaces consist of predominantly Si with hydrogenated SixNyOzspecies. Energy dispersive X-rayspectroscopy and X-ray photoelectron spectroscopy corroborate on the N/Si ratio. Electron energy lossspectroscopy discloses that the thickness of the nitrogen rich oxidized interface between the SiNxfilmsand the c-Si substrate decrease with an enhancing NH3flow rate. By varying the NH3flow rate, denseSiNxfilms can be realized with hydrogen content between 16 and 9 at.%, a refractive index between 3.5and 1.9 and optical band gap ranging from 2 to 4.5 eV. The SiNxfilm stress is compressive for N/Si 0.55. Mechanisms relating the HWCVD conditions and the film structure andproperties are proposed.Web of Scienc

Chemical Vapor Deposited Mixed Metal Halide Perovskite Thin Films

In this article, we used a two-step chemical vapor deposition (CVD) method to synthesize methylammonium lead-tin triiodide perovskite films, MAPb1−xSnxI3, with x varying from 0 to 1. We successfully controlled the concentration of Sn in the perovskite films and used Rutherford backscattering spectroscopy (RBS) to quantify the composition of the precursor films for conversion into perovskite films. According to the RBS results, increasing the SnCl2 source amount in the reaction chamber translate into an increase in Sn concentration in the films. The crystal structure and the optical properties of perovskite films were examined by X-ray diffraction (XRD) and UV-Vis spectrometry. All the perovskite films depicted similar XRD patterns corresponding to a tetragonal structure with I4cm space group despite the precursor films having different crystal structures. The increasing concentration of Sn in the perovskite films linearly decreased the unit volume from about 988.4 Å3 for MAPbI3 to about 983.3 Å3 for MAPb0 .39Sn0 .61I3, which consequently influenced the optical properties of the films manifested by the decrease in energy bandgap (Eg) and an increase in the disorder in the band gap. The SEM micrographs depicted improvements in the grain size (0.3–1 μm) and surface coverage of the perovskite films compared with the precursor films

Controlled deposition of lead iodide and lead chloride thin films by low-pressure chemical vapor deposition

Lead halide thin films, such as lead iodide (PbI2) and lead chloride (PbCl2), are used as precursor films for perovskite preparation, which is frequently achieved by vacuum thermal evaporation but rarely by the low-pressure chemical vapor deposition (CVD) method. Here, we report on the deposition of PbI2 and PbCl2 thin films on glass substrates by employing the low-pressure CVD method. The effect of the substrate temperature on the structure and morphology of the lead halide films is investigated. Crystalline films were realized for both lead halides, with PbI2 films showing high texture compared to the reduced texture of the PbCl2 films. Large lateral grain sizes were observed for the PbI2 films with a flat platelet grain morphology and an average grain size up to 734.2 ± 144.8 nm. PbCl2 films have columnar grains with an average grain size up to 386.7 ± 119.5 nm. The PbI2 films showed a band gap of about 2.4 eV, confirming its semiconducting properties, and the PbCl2 had a wide band gap of 4.3 eV, which shows the insulating properties of this material

Effect of the annealing atmosphere on the layer interdiffusion in Pd/Ti/Pd multilayer stacks deposited on pure Ti and Ti-alloy substrates

Pd(50 nm)/Ti(25 nm)/Pd(50 nm) multilayer stack has been deposited on Ti and Ti6Al4V substrates; we have studied the intermixing of layers upon annealing at the hydrogenation temperature of 550 °C, under vacuum, H/Ar gas mixture and pure hydrogen atmospheres. Scanning electron microscopy (SEM) micrographs indicated surface roughening in samples annealed under vacuum and H/Ar gas mixture while those annealed under pure H2 remained relatively smoother. Rutherford backscattering spectrometry (RBS) revealed intermixing of layers as evidenced by the diffusion of Pd toward the bulk, while XRD indicated the formation of PdTi2 phase in the samples annealed under vacuum and H/Ar gas mixture atmosphere. In-situ, real-time RBS showed that the annealing under pure H2 preserves the integrity of the Pd catalyst. No indication of the PdTi2 formation in the pure H2 annealed samples was observed; instead only the TiH2 phase appeared, indicating the absorption of H into the system

Visible and IR photoluminescence of c-FeSi@a–Si core–shell nano-fibres produced by vapour transport

The procedures for the synthesis of amorphous ε-FeSi/Sicore–shell nanofibres by vapour transport in a CVD configuration are reported. Crystallite studies by the Williamson-Hall method show the sizes to be typically about 8.0nm which agrees with TEM value of 7.9nm fibre diameter with a compressive strain of about 0.04. Features in the photoluminescence of these FeSi core–shells in both visible and IR are at 410nm,1062nm,1414nm and 1772nm and absorption feature at 1000cm−1 from FTIR are explained from density functional theory(DFT) abinitio calculations. PL confirms the intra-band transition whereas FTIR agrees perfectly with the band-to-band transition whose band gap energy is 0.13eV for FeSi. FTIR also unveils inter-bandtransition which DFT calculation could not predict. Raman spectroscopy data confirm FeSi and nano-Sipresence.Web of Scienc

Influence of Synthesis Method on Structural, Morphological, Magnetic, and Antimicrobial Properties of Fe-Ag Nanoparticles

This contribution reports on the development of two versatile and efficient methods, namely the green and gamma radiolysis for Fe-Ag nanoparticles (NPs) synthesis, characterization, and further their growth inhibition potential on some spoilage microorganisms. Green Ag/Fe2O3 NPs were obtained at Fe-Ag [3:1], annealing temperature of 800 °C for 2 h, and gamma irradiated Ag/Fe3O4 NPs were obtained at Fe-Ag [7:1], a 50 kGy dose. The characterization techniques were performed with these two samples whereby the sizes from crystallographic and microscopic analyses were 39.59 and 20.00 nm for Ag/Fe2O3 NPs, 28.57 and 15.37 nm for Ag/Fe3O4 NPs, respectively. The polycrystallinity nature observed from X-ray diffraction was in accordance with the selected area electron diffraction. The vibrational properties confirmed the presence of bimetallic Fe-Ag NPs with the depiction of chemical bonds, Fe–O and Ag–O from attenuated total reflection-Fourier transform infrared spectroscopy and elements Ag, Fe, O from energy-dispersive X-ray spectroscopy analyses. The magnetic properties carried out using a vibrating sample magnetometer suggested a superparamagnetic behavior for the Ag/Fe2O3 NPs and a ferromagnetic behavior for the Ag/Fe3O4 NPs. Overall, the green Ag/Fe2O3 NPs successfully inhibited the growth of spoilage yeasts Candida guilliermondii, Zygosaccharomyces fermentati, Zygosaccharomyces florentinus, and spoilage molds Botrytis cinerea, Penicillium expansum, Alternaria alstroemeriae

Self-Catalytic Growth of Tin Oxide Nanowires by Chemical Vapor Deposition Process

We report on the synthesis of tin oxide (SnO 2 ) nanowires by a chemical vapor deposition (CVD) process. Commercially bought SnO nanopowders were vaporized at 1050 ∘ C for 30 minutes with argon gas continuously passing through the system. The assynthesized products were characterized using UV-visible absorption spectroscopy, X-ray diffraction (XRD), scanning electron microscopy (SEM), and high-resolution transmission electron microscopy (HRTEM). The band gap of the nanowires determined from UV-visible absorption was around 3.7 eV. The SEM micrographs revealed "wool-like" structure which contains nanoribbons and nanowires with liquid droplets at the tips. Nanowires typically have diameter in the range of 50-200 nm and length 10-100 m. These nanowires followed the vapor-liquid-solid (VLS) growth mechanism

Grain structure orientational change in Ti6Al4V alloys induced by sea water quenching and novel stress relief annealing process

We report on the microstructures and properties of Ti6Al4V alloys, which were achieved upon quenching in sea water medium with potential high cooling rate. The Ti6Al4V alloys were quenched at 1000 and 1100 ◦C, respectively. Moreover, the effect of post-quenching annealing performed at 900 ◦C was analyzed. As a result, the quenched alloy experienced surface thermal stress, due to rapid cooling and thermal shock, due to exposure to high temperature annealing