Enhanced gas sensing and photocatalytic activity of reduced graphene oxide loaded TiO2 nanoparticles

In the present study, we have evaluated the gas sensing and photocatalytic activity of reduced graphene oxide (rGO) conjugated titanium dioxide (TiO2) nanoparticles (NPs) formed by the hydrothermal method. The as-synthesized rGO-TiO2 nanocomposite were characterized for the physicochemical properties such as the nature of crystallinity, functionalization, and morphology by making use of the powder X-ray diffraction, Fourier transform-infrared spectroscopy, and scanning electron microscopy, respectively. On testing the gas sensing properties, we found that the rGO-TiO2 nanocomposite can serve as the chemoresistive-type sensor because of its sensitivity and selectivity towards different concentrations of hydrogen and oxygen at room temperature conditions. However, the rGO-TiO2 sensor’s response and recovery speed towards hydrogen and oxygen needs further optimization. Test of photocatalytic activity of TiO2-rGO catalyst for the removal of two model contaminant dyes, RhB and MB showed effective removal, with respective degradation percentages of about 80 and 90% within the first 50 min of irradiation under visible light irradiation. Besides, MB was more effectively degraded using TiO2-rGO than pure TiO2 during the first 30 min of irradiation and this enhanced activity can be attributed to the increased capacity of light absorption, the efficiency of charge carriers separation, and the specific surface area maintained by the rGO-TiO2 nanocomposite to effectively utilize the photo-generated holes (h+) and superoxide radicals (O2−radical dot), responsible for the degradation of the dye. Based on the overall analysis, the formation of rGO-TiO2 nanocomposite can significantly improve the gas sensing and photocatalytic properties of TiO2 NPs and thus can be potential for practical applications in future nanotechnology

Effect of EDTA on the Growth Kinetics and Structural and Optical Properties of KDP Crystal

The solubility of potassium dihydrogen phosphate (KDP) was determined for five different temperatures. Metastable zone width of aqueous solutions of KDP saturated at different temperatures was determined by nucleation method in pure form and adding a well-known chelating agent ethylenediaminetetraacetic acid (0.5 mol% EDTA). The induction period was measured, experiments were performed at selected degrees of supersaturation (C/C∗), and the critical nucleation parameters like interfacial energy () were calculated, based on the classical theory of nucleation. The structural and optical properties of the grown crystals have been investigated. FTIR analysis has been carried out to characterize the grown crystals. Band gap has been calculated from transmission spectra

Synthesis, Growth, and Electrical Transport Properties of Pure and -Doped Triglycine Sulphate Crystal

Pure triglycine sulphate (TGS) and LiSO4-doped TGS crystals were grown from aqueous solution by natural evaporation method. The grown crystals were characterized by UV-vis spectroscopy, electrical conductivity (dc) measurement, dielectric studies, microhardness, and thermogravimetry/differential thermal analysis. Pure TGS and LiSO4-doped TGS crystals were found highly transparent and full faced. The direct current conductivity is found to increase with temperature as well as dopant concentrations. Curie temperature remains the same for pure and doped crystals, but dielectric constant and dielectric loss increase with dopant concentration. The Vicker’s microhardness of the LiSO4-doped TGS crystals along (001) face is found higher than that of pure TGS crystals. Etching studies illustrate the quality of the doped crystal. The experimental results evidence the suitability of the grown crystal for optoelectronic applications

Effect of chromium doping on the band gap tuning of titanium dioxide thin films for solar cell applications

A simple and inexpensive spray pyrolysis deposition (SPD) approach was used to produce TiO2 and Cr (2–8) at.%-doped TiO2 thin films. To explore the morphological features of the films, FE-SEM micrographs were used and found that 6 and 8 at.% TiO2:Cr films had fibrous patterns with diameters of 0.45 and 0.78 μm, respectively, while the remainder of the films were agglomerated particles. From X-ray diffraction investigation, it was found that the TiO2 thin films had an anatase crystal phase (tetragonal) up to 6 at.% Cr doping, while an anatase-rutile mixed crystalline phase was identified for 8 at.% Cr doping. The crystallite size of the pristine TiO2 film was 35 nm, while for TiO2:Cr films, it ranges from 35 to 46 nm. The Fizeau fringes technique was employed to measure the thickness of the TiO2 film and 165 nm was found for pristine TiO2 and 164–180 nm for TiO2:Cr films. UV–visible spectroscopy was used to study optical properties such as absorbance, refractive index, optical band gap, dielectric constant, and optical conductivity. As the Cr concentration increases, the optical band gap decreases from 3.40 eV to 2.70 eV. Using the four-point probe method, it was found that the resistivity changes with temperature and is also affected by the Cr content

Effect of Nickel doping on the Structural, Optical, and electrical properties of titanium dioxide thin films for the application of sensing devices

Thin films of pristine titanium dioxide (TiO2) and doped with different concentrations (0–8) at.% of nickel (Ni) were synthesized onto transparent glass substrates using the spray pyrolysis deposition technique. Field emission scanning electron microscopy revealed the porous and agglomerated surface morphology of the films. X-ray diffractometer demonstrated the anatase crystal structure with a nominal increment of (101) peak. The shifting of peak position revealed the expansion of the unit cell volume from 134.64 to 137.54 (Å)3 whereas crystallite size increased from 34 to 63 nm. Using the Fizeau fringes technique, the thickness of the films was determined between 165 and 190 nm. UV–Vis measurements were employed to examine the optical characteristics of the films. The red shift was observed for 2 at.% Ni content (3.38 eV) while the blue shift was observed for (4–8) at.% Ni content. The wavelength-dependent refractive index and dielectric constant showed anomalous dispersion in the absorption band, representing the transparency of the films. The 4-point probe measurement showed a decreasing trend of resistivity with increasing temperature, whereas the resistivity increased with Ni content. Activation energy indicated a higher amount of adsorbed oxygen in the films due to the high amount of Ni content

4-Fluoro-N-[(E)-3,4,5-trimethoxybenzylidene]aniline

The title compound, C16H16FNO3, exists in a trans configuration with respect to the C=N bond [1.258 (2) Å]. The central methoxy O atom deviates from the plane of the attached benzene ring by 0.0911 (14) Å. The dihedral angle between the aromatic rings is 47.58 (11)°. The crystal structure features C—H...N and C—H...O interactions