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 |
|