Showing 3 results for Malek Khachatourian
Z. Abasali Karaj Abad, A. Nemati, A. Malek Khachatourian, M. Golmohammad,
Volume 17, Issue 4 (December 2020)
Abstract
The graphene oxide -TiO2 (GO-TiO2) and pre-reduced graphene oxide -TiO2 (rGO-TiO2) nanocomposites were fabricated successfully by hydrothermal method. The microstructure of synthesized nanocomposites was investigated using field emission scanning electron microscopy (FESEM) equipped with energy dispersive spectroscopy (EDS) analysis. Moreover, galvanostatic charge/discharge (GCD), cyclic voltammetry (CV), and electrochemical impedance spectroscopy (EIS) methods in three electrode system were applied to evaluate electrochemical properties. The results revealed that nanoparticles distributed more uniformly on graphene sheets, at lower concentrations of TiO2. The rGO-TiO2 and GO-TiO2 nanocomposites showed 224 and 32 F/g specific capacitance at 5 mV s-1 scan rate in 1 M KOH aqueous electrolyte, respectively. The pre-reduction of graphene oxide is the main reason for the better electrochemical performance of rGO-TiO2 nanocomposite compared to GO-TiO2 nanocomposite.
Amirhosein Paryab, Toktam Godary, Sorosh Abdollahi, Mohsen Anousheh, Adrine Malek Khachatourian,
Volume 18, Issue 3 (September 2021)
Abstract
Silicon oxycarbide (SiOC) materials derived from silicone attracted great attention for their superior high-temperature behavior. In the present study, Si(Ti)OC and Si(Ti,Al)OC nanocomposites, in which alkoxide precursors were used with the main silicone precursor, have been compared with SiOC material. Although in SiOC, C was bonded with Si in a carbon-rich SiOC phase, X-ray diffraction (XRD) and Fourier transform infrared spectroscopy (FTIR) showed that TiC was the preferred state for C atoms upon adding Ti into the system. This claim was also substantiated by Raman spectroscopy, where adding Ti into the system lowered the intensity of the D band, indicating the high affinity of C to form crystalline TiC. In the Si(Ti,Al)OC nanocomposites synthesized by adding AlCl3 into the Si(Ti)OC system, mullite nanocrystals formed a superlattice structure with TiC. UV-vis spectra of the nanocomposites showed Si(Ti,Al)OC with mullite-TiC superlattice had a larger bandgap compared with Si(Ti)OC with only TiC nanocrystals.
Nazli Aharipour, Adrine Malek Khachatourian, Ali Nemati,
Volume 21, Issue 4 (December 2024)
Abstract
Fe3O4 nanoparticles (NPs) with a continuous and mesoporous silica (m-SiO2) shell were synthesized using a one-step method, sourcing silica from rice husk ash (RHA). The rice husk was thermally treated to obtain ash, from which silica was extracted as sodium silicate and precipitated by pH reduction. This silica powder, combined with iron chloride salts, facilitated the synthesis of the core-shell NPs. Mint extract acted as a capping agent to prevent agglomeration, and CTAB (cetyltrimethylammonium bromide) was used to create the porous SiO2 shell. X-ray diffraction (XRD), Field emission scanning electron microscopy (FESEM), and transmission electron microscopy (TEM) characterization investigated the structure, size, and shell formation. Coating integrity and suspension stability were assessed through Fourier transform infrared spectroscopy (FTIR) and dynamic light scattering (DLS). DLS analysis showed a relatively narrow particle size distribution with an average hydrodynamic size of 72.6 nm. Small-angle X-ray scattering (SAXS) provided insights into the meso- and nanoscale structure, while BET and nitrogen adsorption-desorption isotherms confirmed the mesoporous nature of the silica shell. Magnetization measurements showed superparamagnetic behavior, with specific magnetization values of 57.9 emu/g for Fe3O4 and 27.5 emu/g for Fe3O4@m-SiO2. These results confirm the successful synthesis of superparamagnetic magnetite NPs with a mesoporous silica coating from RHA.
