Madiha Sarfraz, Nasar Ahmed, Khizar-ul-Haq, Shabnam Shahida and M. A. Khan
Transition metals, such as chromium (Cr) and manganese (Mn) doped zinc oxide (ZnO) magnetic nanoparticles, were synthesized via sole gel auto-combustion method. The prepared magnetic (Zn1−(x+y)MnxCryO, where x, y = 0, 0.02, 0.075) nanoparticles were calcined in an oven at 6000 °C for 2 hours. The morphologies of the nanoparticles were investigated using different techniques. X-ray diffraction (XRD) analysis revealed that the hexagonal wurtzite structure of the synthesized nanoparticles was unaffected by doping concentration. The crystallite size measured by Scherrer formula was in the range of 32 nm to 38 nm at different doping concentrations. Nanosized particles with well-defined boundaries were observed using a field emission scanning electron microscopy (FE-SEM). Fourier transform infrared (FT-IR) spectra showed a wide absorption band around 1589 cm−1 in all the samples, corresponding to the stretching vibration of zinc and oxygen Zn–O bond. A blue shift in optical band gaps from 3.20 eV for ZnO to 3.08 eV for Zn0.85Mn0.075Cr0.075O nanoparticles was observed in diffuse reflectance spectra, which was attributed to the sp-d exchange interactions. The field-dependent magnetization M-H loops were measured using vibrating sample magnetometer (VSM). The VSM results revealed diamagnetic behavior of the ZnO nanoparticles which changed into ferromagnetic, depending on the doping concentration and particle size. The compositions of Zn, Cr, Mn and O in the prepared samples were confirmed by using the energy dispersive X-ray spectroscopy (EDX). Our results provided an interesting route to improve magnetic properties of ZnO nanoparticles, which may get significant attention for the fabrication of magnetic semiconductors.
In the present work, a new organic second order NLO material: L-isoleucinium p-toluenesulfonate monohydrate (LIPT) is synthesized and reported for the first time. The LIPT is crystallized in a non-centrosymmetric monoclinic space group P21. Structural and hydrogen bond nature of the compound is analyzed using single crystal X-ray diffraction studies. The crystal exhibits very good optical properties such as wide optical transparency in the region of 210 nm to 1100 nm and the ultraviolet wavelength emission (λ = 283 nm). The second harmonic generation efficiency is found to be 1.7 times the standard KDP. Good thermal, mechanical properties and low dielectric constant at high frequency range show that the material may be a potential candidate for optoelectronic applications.
In this communication, we report on Cu2SnS3 quantum dots synthesized by the solvothermal process using different solvents. The optical properties of the quantum dots are analyzed by UV-Vis-NIR and photoluminescence spectroscopy. The results suggest that Cu2SnS3 material has tunable energy bandgap and appropriate wavelength for fabrication of light emitting diodes and laser diodes as sources for fiber optic communication. They exhibit wide absorption in the near infrared range. Further morphological studies with the use of atomic force microscope confirm the surface topography and the existence of quantum dots. The observed characteristics prove the efficiency of Cu2SnS3 quantum dots for O-band wavelength detection used in fiber optic communication and solar cell applications.
This paper attempts to describe an effective method for producing a composite of quantum dots consisting of CdSe (core) with CdS (shell). This nanoparticles composite was synthesized from modified organometallic precursors. The sizes of the nanoparticles were estimated from X-ray diffraction data using Debye-Scherer formula and compared with high resolution electron microscopy (HRTEM) and optical spectra. The shape of CdSe/CdS NPs is nearly spherical and revels that the CdS shell with the thickness ~0.6 nm almost fully covers the CdSe core (higher contrast). Using UV-Vis spectroscopy, a systematic red shift in the absorption and emission spectra was observed after the deposition of CdS which confirms the shell growth over the CdSe core. In the CdSe/CdS core/shell structure, the holes are confined to the core, while the electrons are delocalized as a result of similar electron affinities of the core and the shell. The increased time of synthesis resulted in shell thickness increase. The observed properties of prepared CdSe/CdS QDs demonstrate the capability of the nanocomposite for using in the optoelectronics and photonics devices.
An inorganic coordination complex of single crystal containing sodium and aluminum (SA) was grown at room temperature by slow evaporation technique. The crystal was characterized using single crystal X-ray diffraction (XRD), FT-IR, UV-Vis, SHG, SEM, EDX and TG/DTA analyses. The size of the grown crystal was around 17 mm × 15 mm × 5 mm. Both optical and SEM photographs confirmed that the crystal is transparent with smooth surface. The XRD data showed that the crystal belongs to the BCC crystal structure. The crystal shows excellent transparency in the entire region of visible light (cut-off value is 339 cm−1). The dielectric constant as well as dielectric loss of the sample was calculated by varying frequencies at different temperatures and the presence of low dielectric loss proved that this crystal can be used for the NLO application.
Božana Čolović, Danilo Kisić, Bojan Jokanović, Zlatko Rakočević, Ilija Nasov, Anka Trajkovska Petkoska and Vukoman Jokanović
Thin films of titanium oxides, titanium oxynitrides and titanium nitrides were deposited on glass substrates by the methods of direct current (DC) and pulsed magnetron sputtering and cathodic arc evaporation. Phase analysis of the deposited films by X-ray diffraction (XRD) and Fourier-transform infrared spectroscopy (FT-IR) showed the presence of phases with various Ti oxidative states, which indicated a high concentration of oxygen vacancies. The films morphology was investigated by scanning electron microscopy (SEM). Investigations of the films wettability, either with water or ethylene glycol, showed that it depends directly on the concentration of oxygen vacancies. The wettability mechanism was particularly discussed.
Nanostructured CdO thin films have been prepared on glass substrates by spray pyrolysis technique using perfume atomizer from fresh and aged (1, 2, 3 and 4 days) precursor solutions. XRD studies confirm that all the films exhibit cubic crystal structure with a (1 1 1) preferential orientation. The preferential orientation factor f(1 1 1) increases with an increase in aging the period of precursor solution. The 2θ value of the (1 1 1) plane shifts towards lower Bragg angles with aging inferring an expansion in the lattice volume of the aged films. Increased crystallite size is observed for the 3-days aged film for which minimum strain and dislocation density values are obtained. Optical transparency increases with an increase in aging period of the precursor solution and the optical band gap exhibits a red shift from 2.48 eV to 2.32 eV. Minimum resistivity of 0.78 × 10−2 Ω·cm is observed for the CdO film prepared from 3-days aged solution. The obtained results infer that the CdO film prepared from 3-days aged solution exhibits better physical properties than the others.
Pure CdO nanopowder and CdO-Fe3O4 nanocomposite were synthesized by a cost effective chemical method, and the samples were characterized by XRD, SEM, TEM, FT-IR, UV-Vis-NIR and PL. Also, magnetic and photocatalytic properties of the synthesized samples were studied. XRD patterns of the composite confirm the presence of diffraction peaks related to both CdO and Fe3O4. EDX spectrum confirms the presence of the elements Cd, O and Fe in the composite. Peaks related to Cd–O and Fe–O bonds were observed respectively at 688 cm−1 and 592 cm−1 in the FT-IR spectrum. The paramagnetic behavior of pure CdO becomes ferromagnetic when coupled with Fe3O4. The composite exhibited a high photodegradation efficiency of 92.85 % against the degradation of methylene blue dye under visible light radiation.
In this study, CdZnO films prepared at different ratios of dopants (CdO:ZnO = 5:5, CdO:ZnO = 6:4, and CdO:ZnO = 8:2) were coated on glass surface by using the sol-gel spin coating technique. After this process, surface structure and optical properties of the CdZnO films was investigated by atomic force microscopy (AFM) and UV-Vis spectroscopy. The surface structure of the CdZnO films depended on the content of ZnO and CdO in the films. Low percentage of CdO films were very similar to the ZnO film but higher amount of CdO resuted in granular structures together with pure structure of ZnO in the films. Eg values of produced CdZnOs depended on the additions of CdO and ZnO. The obtained Eg values of the produced CdO:ZnO = 5:5 (S3), CdO:ZnO = 6:4 (S4), and CdO:ZnO = 8:2 (S5) films are 2.5 eV, 2.49 eV, and 2.4 eV, respectively.
Nanocomposite silica thin films made using the sol-gel method were studied. The nano-silica films were prepared using a mixture of tetraethyl orthosilicate (TEOS), deionized water, ethanol, and ammonia solution. To control the growth of the particles inside the film, the nanocomposite silica film was prepared using a mixture of the nano-silica sol and the silica sol. The change in the particle size with the heat treatment temperature ranging from 450 °C to 1100 °C was investigated. X-ray diffraction (XRD), atomic force microscopy (AFM), scanning electron microscopy (SEM), NKD (refractive index-N, extinction coefficient-K, and thickness-D) and ultraviolet-visible (UV-Vis) spectrophotometry were used for characterization purposes. The XRD studies showed that the nano-silica thin films were amorphous at all annealing temperatures except for 1100 °C. The_-cristobalite crystal structure formed at the annealing temperature of 1100 °C. Optical parameters, such as refractive indices and extinction coefficients, were obtained using the NKD analyzer with respect to the annealing temperature of the films. The activation energy and enthalpy of the nanocomposite silica film were evaluated as 22.3 kJ/mol and 14.7 kJ/mol, respectively. The cut-off wavelength values were calculated by means of extrapolation of the absorbance spectra estimated using the UV-Vis spectroscopy measurements. A red shift in the absorption threshold of the nanocomposite silica films indicated that the size of the silica nanoparticles increased with an increase of the annealing temperatures from 450 °C to 900 °C, and this confirms the quantum confinement effect in the nanoparticles.