Электронная библиотека (репозиторий) Томского государственного университета
Gavrilova, Tatiana A.

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Source: Journal of crystal growth. 2019. Vol. 518. P. 103-107
Type: статьи в журналах
Date: 2019
Description: The Sn-rich islands with a Si pedestal on the Si(1 0 0) substrate were obtained by the molecular-beam epitaxy technique. Initially, Sn films of different thicknesses were formed on the Si surface and ... More
Source: Materials and design. 2018. Vol. 140. P. 488-494
Type: статьи в журналах
Date: 2018
Description: New noncentrosymmetric double borate Rb3EuB6O12 was designed and synthesized by the solid state reaction method, and its crystallographic parameters were obtained by Rietveld analysis. This borate cry ... More
Source: Inorganic chemistry. 2017. Vol. 56, № 6. P. 3276-3286
Type: статьи в журналах
Date: 2017
Description: Cs2Pb(MoO4)2 crystals were prepared by crystallization from their own melt, and the crystal structure has been studied in detail. At 296 K, the molybdate crystallizes in the low-temperature α-form and ... More
Source: The Journal of Physical Chemistry C. 2016. Vol. 120, № 9. P. 5114-5123
Type: статьи в журналах
Date: 2016
Description: The barium hexaferrite, BaFe12O19, microcrystals were obtained by the flux crystal growth method and were characterized by XRD, SEM, and TEM methods. XPS measurements were carried out on a powder samp ... More
Source: Journal of physics and chemistry of solids. 2015. Vol. 77, № 2. P. 101-108
Type: статьи в журналах
Date: 2015
Description: β-RbNd(MoO4)2 microplates have been prepared by the multistage solid state synthesis method. The phase composition and micromorphology of the final product have been evaluated by XRD and SEM methods. ... More
Source: Dalton transactions. 2015. Vol. 44, № 4. P. 1805-1815
Type: статьи в журналах
Date: 2015
Description: Microcrystals of orthorhombic rubidium samarium molybdate, β-RbSm(MoO4)2, have been fabricated by solid state synthesis at T = 450 °C, 70 h, and at T = 600 °C, 150 h. The crystal structure has been re ... More
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