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In this paper, facile synthesis of water soluble curcumin nanocrystals is reported. Solvent exchange method was applied to synthesize curcumin nanocrystals. Different techniques were used to characterize the structural and photophysical properties of curcumin nanocrystals. We found that nanocurcumin prepared by this method had good chemical and physical stability, could be stored in the powder form at room temperature, and was freely dispersible in water. It was established that the size of curcumin nanocrystals was varied in the range of 20-500 nm. Fourier transform infrared spectroscopy and UV-Vis analyses showed the presence of tetrahydrofuran inside the curcumin nanocrystals. Also, it was found that nanocurcumin emitted photoluminescencewith yellow-green colour. [Projekat Ministarstva nauke Republike Srbije, br. 172003]
Heteropoly acids (HPAs) found wide applications, such as in catalysis, energy conversion and storage, analytical chemistry, clinical medicine, materials science and others, but because of their low surface area and high solubility in water their use is limited. One of the possible ways to overcome these obstacles is to use height specific surface area support for HPAs, such as carbon nanomaterials. Raman spectroscopy was applied for studying study interaction between HPAs and highly ordered pyrolytic graphite (HOPG) as a model of a support. HOPG was exposed to two different HPAs: 12-tungstophosphoric acid and 12-molybodphosphoric acid, at different concentrations. It was noticed that 12-molybodphosphoric acid has stronger effects on HOPG structure causing a weak doping and increase of structural disorder. It is supposed that HOPG interacts with especially external oxygen atoms of 12-molybodphosphoric acid. Atomic force microscopy showed that surface roughness of HOPG treated with 12-molybodphosphoric acid increases with increase of acid concentration, while in the case of HOPG exposed to 12-tungstophosphoric acid the surface roughness is not concentration dependent. The growth trend in measured surface roughness (RMS) is in the agreement with the changes in the intensity ratio ID/IG obtained from Raman spectra of HOPG samples treated with 12-molybdophosphoric acid. [Projekat Ministarstva nauke Republike Srbije, br. 172003 i br. 172043]
Graphene nanoribbons (GNRs) are thin strips of graphene that have captured the interest of scientists due to their unique structure and promising applications in electronics. This paper presents the results of a comparative analysis of morphological properties of graphene nanoribbons synthesized by different methods. Various methods have been reported for graphene nanoribons synthesis. Lithography methods usually include electron-beam (e-beam) lithography, atomic force microscopy (AFM) lithography, and scanning tunnelling microscopy (STM) lithography. Sonochemical and chemical methods exist as well, namely chemical vapour deposition (CVD) and anisotropic etching. Graphene nanoribbons can also be fabricated from unzipping carbon nanotubes (CNTs). We propose a new highly efficient method for graphene nanoribbons production by gamma irradiation of graphene dispersed in cyclopentanone (CPO). Surface morphology of graphene nanoribbons was visualized with atomic force and transmission electron microscopy. It was determined that dimensions of graphene nanoribbons are inversely proportional to applied gamma irradiation dose. It was established that the narrowest nanoribbons were 10-20 nm wide and 1 nm high with regular and smooth edges. In comparison to other synthesis methods, dimensions of graphene nanoribbons synthesized by gamma irradiation are slightly larger, but the yield of nanoribbons is much higher. Fourier transform infrared spectroscopy was used for structural analysis of graphene nanoribbons. Results of photoluminescence spectroscopy revealed for the first time that synthesized nanoribbons showed photoluminescence in the blue region of visible light in contrast to graphene nanoribbons synthesized by other methods. Based on disclosed facts, we believe that our synthesis method has good prospects for potential future mass production of graphene nanoribbons with uniform size, as well as for future investigations of carbon nanomaterials for applications in optoelectronics and biological labeling
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