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dc.contributor.author | Samigullina R. | |
dc.contributor.author | Tyutyunnik А. | |
dc.contributor.author | Gracheva I. | |
dc.contributor.author | Krasnenko Т. | |
dc.contributor.author | Zaitseva N. | |
dc.contributor.author | Onufrieva T. | |
dc.date.accessioned | 2018-09-19T20:23:29Z | |
dc.date.available | 2018-09-19T20:23:29Z | |
dc.date.issued | 2017 | |
dc.identifier.issn | 0025-5408 | |
dc.identifier.uri | https://dspace.kpfu.ru/xmlui/handle/net/142857 | |
dc.description.abstract | © 2016 Elsevier LtdThe monophase morphologically homogeneous phosphor α-Zn2SiO4:V has been produced by the hydrothermal method. With the use of energy-dispersive analysis and X-ray powder diffraction analysis, it was established that the ratio of cations Zn:Si:V corresponded to the formula Zn2Si0.9V0.1O4. The charge state of vanadium ions was determined by the spectroscopic methods. Maxima of the bands in the luminescence spectra correspond to V5+ (523 nm) and V3+ (720 nm) centers. The small width of the EPR signal hyperfine structure components indicates the presence of single V4+ centers, their contribution is not greater than 0.1% of the total vanadium content. The presence of a broad structureless component in the EPR spectrum was explained by the fact that the main amount of the dopant ion was united in the areas containing V5+, V4+ and V3+ ions. V4+ ions and V5+ ions with high probability occupy silicon positions in the lattice. | |
dc.relation.ispartofseries | Materials Research Bulletin | |
dc.subject | A. Oxides | |
dc.subject | C. Electron microscopy | |
dc.subject | C. X-ray diffraction | |
dc.subject | D. Crystal structure | |
dc.subject | D. Electronic paramagnetic resonance (EPR) | |
dc.title | Hydrothermal synthesis of α-Zn<inf>2</inf>SiO<inf>4</inf>:V phosphor, determination of oxidation states and structural localization of vanadium ions | |
dc.type | Article | |
dc.relation.ispartofseries-volume | 87 | |
dc.collection | Публикации сотрудников КФУ | |
dc.relation.startpage | 27 | |
dc.source.id | SCOPUS00255408-2017-87-SID84996938703 |