FROM THE GREEN COLOR OF ESKOLAITE TO THE RED COLOR OF RUBY: AN X-RAY ABSORPTION SPECTROSCOPY STUDY

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dc.contributor.author Gaudry É.
dc.contributor.author Sainctavit Ph.
dc.contributor.author Juillot F.
dc.contributor.author Bondioli F.
dc.contributor.author Ohresser Ph.
dc.contributor.author Letard I.
dc.date.accessioned 2025-04-19T06:19:52Z
dc.date.available 2025-04-19T06:19:52Z
dc.date.issued 2006
dc.identifier https://elibrary.ru/item.asp?id=51094653
dc.identifier.citation Physics and Chemistry of Minerals, 2006, 32, 10, 710-720
dc.identifier.issn 0342-1791
dc.identifier.uri https://repository.geologyscience.ru/handle/123456789/49017
dc.description.abstract The best known cause for colors in insulating minerals is due to transition metal ions as impurities. As an example, Cr3+ is responsible for the red color of ruby (α-Al2O3:Cr3+) and the green color of eskolaite (α-Cr2O3). Using X-ray absorption measurements, we connect the colors of the Cr x Al2−x O3 series with the structural and electronic local environment around Cr. UV–VIS electronic parameters, such as the crystal field and the Racah parameter B, are related to those deduced from the analysis of the isotropic and XMCD spectra at the Cr L2,3-edges in Cr0.07Al1.93O3 and eskolaite. The Cr–O bond lengths are extracted by EXAFS at the Cr K-edge in the whole Cr x Al2−x O3 (0.07≤x< 2) solid solution series. The variation of the mean Cr–O distance between Cr0.07Al1.93O3 and α-Cr2O3 is evaluated to be 0.015 Å (≈1%). The variation of the crystal field in the Cr x Al2−x O3 series is discussed in relation with the variation of the averaged Cr–O distances.
dc.subject XAFS
dc.subject RUBY
dc.subject COLOR OF MINERALS
dc.title FROM THE GREEN COLOR OF ESKOLAITE TO THE RED COLOR OF RUBY: AN X-RAY ABSORPTION SPECTROSCOPY STUDY
dc.type Статья
dc.identifier.doi 10.1007/s00269-005-0046-x


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