Phonon Investigations in YVO4: Eu3+ Nanopowders

In this work two methods of preparation of yttrium orthovanadate nanopowders were presented: Solid State Reaction (top – down approach) and Solution Combustion Synthesis (bottom – up approach). For starting structural characterization, X – Ray Powder Diffraction (XPRD) and Field Emission Scanning Electron Microscopy (FESEM) were used. We report the change in reflection spectra in europium doped YVO4 nanopowders with comparison to its bulk analog. In UV – Vis reflection spectra we consider the change in values of band gap in these structures, after resizing it from bulk to nanomaterial. In Far – Infrared (FIR) reflection spectra, we registered the existence of Surface Optical Phonon (SOP) and different multi – phonon processes which alter the reflection spectra of bulk YVO4 . The influence of Eu ions is reflected through multi – phonon processes that occur and are connected with energy transfer from YVO4 lattice to Eu ions. All IR spectra were modeled using classical oscillator model with Drude part added which takes into account the free carrier contribution. Since our samples are distinctively inhomogeneous materials, we use Effective Medium theory in Maxwell Garnett approximation to model its effective dieletric function.IX Serbian Ceramic Society Conference - Advanced Ceramics and Application : new frontiers in multifunctional material science and processing : program and the book of abstracts; September 20-21, 2021; Belgrad

Supplementary information for the article: Milović, M.D., Vasić Anićijević, D.D., Jugović, D., Anićijević, V.J., Veselinović, L., Mitrić, M., Uskoković, D., 2019. On the presence of antisite defect in monoclinic Li2FeSiO4 – A combined X-Ray diffraction and DFT study. Solid State Sciences 87, 81–86. https://doi.org/10.1016/j.solidstatesciences.2018.11.008

Supplementary information for: [https://doi.org/10.1016/j.solidstatesciences.2018.11.008]Related to: [http://dais.sanu.ac.rs/123456789/4552

Colloidal-chemistry based synthesis of quantized CuInS2/Se2 nanoparticles

Ternary chalcogenide nanoparticles, CuInS2 and CuInSe2, were synthesized in high- temperature boiling organic non-polar solvent. The X-ray diffraction analysis revealed that both materials have tetragonal (chalcopyrite) crystal structure. Morphology of the obtained materials was revealed by using transmission electron microscopy. Agglomerated spherical CuInS2 nanoparticles with broad size distribution in the range from 2 to 20 nm were obtained. In the case of CuInSe2, isolated particles with spherical or prismatic shape in the size range from 10 to 25 nm were obtained, as well as agglomerates consisting of much smaller particles with diameter of about 2-5 nm. The particles with the smallest diameters of both materials exhibit quantum size effect

Electrochemical tuning of capacitive response of graphene oxide

Increasing energy demands of modern society requires deep understanding of the properties of energy storage materials as well as their performance tuning. We show that the capacitance of graphene oxide (GO) can be precisely tuned using a simple electrochemical reduction route. In situ resistance measurements, combined with cyclic voltammetry measurement and Raman spectroscopy, have shown that upon the reduction GO is irreversibly deoxygenated which is further accompanied with structural ordering and increasing of electrical conductivity. The capacitance is maximized when the concentration of oxygen functional groups is properly balanced with the conductivity. Any further reduction and de-oxygenation leads to the gradual loss of the capacitance. The observed trend is independent on the preparation route and on the exact chemical and structural properties of GO. It is proposed that an improvement of capacitive properties of any GO can be achieved by optimization of its reduction conditions.Comment: 23 pages, 7 figures, 59 reference

Isomer specific spectroscopy of metal clusters trapped in a matrix: Ag9

Clusters of metal atoms at a fixed size can assume different structural arrangements, known as isomers, which may have nearly the same energy. Therefore at given experimental conditions distribution of these isomers can be present. While the size selection is a relatively common technique, the isomer selection is not; it is therefore more difficult to obtain information about a single isomer. We report here on isomer specific spectroscopy of Ag9 clusters together with ab initio calculations allowing to identify the isomer responsible for the measured excitation pattern and fluorescence

Investigation of properties of electrochemically synthesizediron oxide nano-powders

Nano-sized powders of iron oxides have been synthesized electrochemically at temperatures in the range of 295-361 K, and current densities in the range of 200-1000 mA dm(-2). The structure and morphology of the powders were investigated by X-ray diffraction and scanning electron and transmission electron microscopy techniques. Their infrared absorption spectra, specific heat C(p)(T) and magnetic susceptibility chi(T) temperature dependences are also determined. The obtained powders consist of two phases, each possessing distinguished characteristics: the one formed of large plates and the other of whiskers. By appropriate adjustment of the synthesis conditions, it is possible to change features and relative abundances of the two phases, and that way to control morphology and other powder properties. Relaxation and transformation of the phases under external influences was also investigated, and the optimal procedure for preparation and stabilization of iron oxide nano-sized powders with desired characteristics was established

Electrochemical tuning of capacitive response of graphene oxide

The increasing energy demands of modern society require a deep understanding of the properties of energy storage materials, as well as the tuning of their performance. We show that the capacitance of graphene oxide (GO) can be precisely tuned using a simple electrochemical reduction route. In situ resistance measurements, in combination with cyclic voltammetry measurements and Raman spectroscopy, have shown that upon reduction GO is irreversibly deoxygenated, which is further accompanied by structural ordering and an increase in electrical conductivity. The capacitance is maximized when the concentration of oxygen functional groups is properly balanced with the conductivity. Any further reduction and deoxygenation leads to a gradual loss of capacitance. The observed trend is independent of the preparation route and the exact chemical and structural properties of GO. It is proposed that an improvement in the capacitive properties of any GO can be achieved by optimization of its reduction conditions.This is the peer-reviewed version of the following article: Gutić, Sanjin J., Dževad Kozlica, Fehim Korać, Danica Bajuk-Bogdanović, Miodrag Mitrić, Vladimir M. Mirsky, Slavko V. Mentus, and Igor A. Pašti. "Electrochemical tuning of capacitive response of graphene oxide." (2018). [https://doi.org/10.1039/C8CP03631D]Published version available at: [http://vinar.vin.bg.ac.rs/handle/123456789/7877

Determination of Microstructural Changes By Severely Plastically Deformed Copper-Aluminum Alloy: Optical Study

Our work deals with the problem of producing a complex metal-ceramic composite using the processes of internal oxidation (IO) and severe plastic deformation. For this purpose, Cu-Al alloy with 0.4wt.% of Al was used. IO of sample serves in the first step of the processing as a means for attaining a fine dispersion of nanosized oxide particles in the metal matrix. Production technology continues with repeated application of severe plastic deformation (SPD) of the resulting metal-matrix composite to produce the bulk nanoscaled structural material. SPD was carried out with equal channel angular pressing (ECAP), which allowed that the material could be subjected to an intense plastic strain through simple shear. Microstructural characteristics of one phase and multiphase material was studied on internally oxidized Cu with 0.4wt.% of Al sample composed of one phase copper-aluminum solid solution in the core and fine dispersed oxide particles in the same matrix in the mantle region. In this manner AFM, X-ray diffraction and Raman spectroscopy were used. Local structures in plastically deformed samples reflect presence of Cu, CuO, Cu2O, Cu4O3 or Al2O3 structural characteristics, depending on type of sample

Structural investigation of mechanically activated ZnO powder

Commercially available ZnO powder was mechanically activated in a planetary ball mill. In order to investigate the specific surface area, pore volume and microstructure of non-activated and mechanically activated ZnO powders the authors performed N-2 physisorption, SEM and TEM. Crystallite size and lattice microstrain were analyzed by X-ray diffraction method. XRD patterns indicate that peak intensities are getting lower and expend with activation time. The reduction in crystallite size and increasing of lattice microstrain with prolonged milling time were determined applying the Rietveld's method. The difference between non-activated and the activated powder has been also observed by X-ray photoelectron spectroscopy (XPS). XPS is used for investigating the chemical bonding of ZnO powder by analyzing the energy of photoelectrons. The lattice vibration spectra were obtained using Raman spectroscopy. In Raman spectra some changes along with atypical resonant scattering were noticed, which were caused by mechanical activation

Time Resolved Photoelectron Spectroscopy of Thioflavin T Photoisomerization: A Simulation Study

The excited state isomerization of thioflavin T (ThT) is responsible for the quenching of its fluorescence in a non-restricted environment. The fluorescence quantum yield increases substantially upon binding to amyloid fibers. Simulations reveal that the variation of the twisting angle between benzothiazole and benzene groups (ϕ(1)) is responsible for the sub-picosecond fluorescence quenching. The evolution of the twisting process can be directly probed by photoelectron emission with energies ε ≥ 1.0 eV before the molecule reaches the ϕ(1)-twisted configuration (~300 fs)