Properties of ZnS1-xFe x thin Films Deposited

Semiconducting ZnS1-xFex thin films were prepared with different substrate temperature on glass substrates from aqueous solution technique. ZnS1-xFex films were prepared, using a aqueous solution containing ethyleneglycol, zinc chloride and sulphur. XRD study shows that the aqueous deposited ZnS1-xFex thin films are polycrystalline hexagonal structure. The effect of Fe concentration on the optical parameters such as absorption coefficient, refractive index, dielectric function, optical conductivity, and reflectivity is also investigated. Results revealed that Cd1-xFexS is a suitable compound for spintronics and optoelectronics devices. A good optical transparency of about 75% in the visible region is observed for all prepared ZnS1-xFex thin films. The direct optical band gap of the deposited ZnS1-xFex thin films with different substrate temperature (380°C – 530°C) were lying in the range 3.27–3.35 eV.

Highly Selective Synthesis of 6-Glyoxylamidoquinoline Derivatives via Palladium-Catalyzed Aminocarbonylation

The aminocarbonylation of 6-iodoquinoline has been investigated in the presence of large series of amine nucleophiles, providing an efficient synthetic route for producing various quinoline-6-carboxamide and quinoline-6-glyoxylamide derivatives. It was shown, after detailed optimization study, that the formation of amides and ketoamides is strongly influenced by the reaction conditions. Performing the reactions at 40 bar of carbon monoxide pressure in the presence of Pd(OAc)2/2 PPh3, the corresponding 2-ketocarboxamides were formed as major products (up to 63%). When the monodentate triphenylphosphine was replaced by the bidentate XantPhos, the quinoline-6-carboxamide derivatives were synthesized almost exclusively under atmospheric conditions (up to 98%). The isolation and characterization of the new carbonylated products of various structures were also accomplished. Furthermore, the structure of three new mono- and double-carbonylated compounds were unambiguously established by using a single-crystal XRD study.

Optical and structural properties of the GaAs heterostructures grown using AlGaAs superlattice buffer layer on compliant Si(100) substrates with the preformed porous-Si (por-Si) layer.

360 nm and 700 nm thick GaAs layers were grown by MO MOCVD growth technique directly on compliant Si (100) substrate and on supper-lattice (SL) AlGaAs buffer layer. The XRD study revealed better structural quality for the sample grown on SL / por-Si buffer. AFM study revealed a smoother sample surface with blocks of more regular rectangular shape and larger size as well. Photoluminescence spectra of the samples revealed an energy shift of PL maximum intensity for both samples. Sample grown on SL buffer also showed higher PL intensity corresponding to better crystalline perfection.

Synthesis and Characterization of Zn-doped CuWO4Nanoparticles and Their Opto-structural Properties

CuWO4 and Zn-doped CuWO4 nanoparticles were prepared by a solid-state reaction method. The XRD study confirms the triclinic crystal structure for both samples and the peak shift is noticed for Zn-doped CuWO4 particles with high crystallinity. The FTIR spectra show metal oxide vibration which arose from the CuWO4 and Zn-doped CuWO4 particles. The optical absorption spectra exhibit strong absorption in the visible region and the band gap of Zn-doped CuWO4 is found to be increased to 2.44 eV compared to that of CuWO4 (2.36 eV), which is due to the elevated conduction band levels after Zn-doping. The SEM images of both CuWO4 and Zn-doped CuWO4 nanoparticles show densely aggregated particles. Keywords: Copper tungstate, Zn-doped CuWO4, Absorption, Nanoparticles.

Powder XRD Study of Changes of Cd2+ Modified Clinoptilolite at Different Stages of the Ion Exchange Process

Cadmium exchange on clinoptilolite is performed and structurally studied for different durations of the ion exchange process (2 h, 24 h, 72 h, 168 h, 12 days, 22 days) at room temperature and 90 °C. The distribution of Cd2+ ions in all samples is elucidated after exchange on clinoptilolite using powder XRD data processed by Rietveld structural software. Clinoptilolite is not selective for cadmium cations, but at 90 °C the exchange is ~2.5 cations per unit cell. At RT it reaches ~1.25 cations per unit cell being twice as low. The obtained maximum exchanged sample for 22 days 90 °C was structurally refined in order to find the cadmium positions in the clinoptilolite voids. The structural refinements of the occupations of the incoming and outgoing cations give an idea of how the intracrystalline diffusion is processed. A good correlation between results obtained by structural refinement of the Cd-exchanged samples and the data of the EDS measurements was achieved.