The results of experiments on the synthesis of micro- and nano-diamonds by an oxy-acetylene torch on the surface of the pre-deposited copper thin films are presented in this article. The influence of thickness of a buffer copper film and the ratio of the concentrations of oxygen and acetylene on the structure of the deposited samples has been studied in the course of the conducted experiments. The studies by Raman scattering and scanning electron microscopy showed that the synthesis of micro- and nano-diamonds occurs under certain experimental conditions. From the results of the analysis of the obtained samples by the methods of Raman scattering and scanning electron microscopy, it was determined that the deposition time of the copper films and consequently its thickness mainly influence on the structure formation of diamond crystals. On copper films grown for 30 min, the Raman scattering method showed a shift of the diamond peak from the standard (1332 cm‒1) to the low-frequency band (1331.3 cm‒1), which may occur after the presence of stress in the crystals. The results of the investigation showed that with increasing of synthesis time take place smoothing of the facets of crystallites (scanning electron microscopy) and decrease in intensity of the diamond peaks (Raman scattering method).
The results of experiments on the synthesis of SiC and C nanostructures by chemical vapor deposition in microwave plasma are presented in this article. The single crystal silicon plates with orientations [100] and [111] which previously passed chemical purification were used as substrates. Also, the substrates of porous silicon were prepared in order to activate the surface during the synthesis. The synthesis temperature ranged from 700 to 900 °C in steps of 100 °C. The pressure in the chamber was changed depending on the power of the plasma. Studies by scanning electron microscopy (SEM) showed that formed nanostructures have a diameter of 200-350 nm and a rough surface. The formation of nanostructures on the polished Si occurs on the SiC buffer layer. Analysis of SEM images of the samples shows that growth of NS on the surface of porous silicon is more widespread in contrast to the polished Si. The results of X-Ray spectral microanalysis showed that the carbon content in samples of nanostructures on polished Si varies from 10 to 20% and remains constant on porous silicon ~ 25%. The results of studies by Raman scattering confirmed that SiC film with structure of 3C-SiC is formed on the polished Si. Besides, the presence of main carbon peaks on both types of substrates in the range of 1338.2 and 1583 cm -1 should be noted, which correspond to the carbon nanostructures.
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