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Interplay between chromium content and lattice disorder on persistent luminescence of ZnGa(2)O(4):Cr3+ for in vivo imaging

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dc.contributor.author Sharma, S.K.
dc.contributor.author Bessiere, A.
dc.contributor.author Basavaraju, N.
dc.contributor.author Priolkar, K.R.
dc.contributor.author Binet, L.
dc.contributor.author Viana, B.
dc.contributor.author Gourier, D.
dc.date.accessioned 2015-06-04T05:10:50Z
dc.date.available 2015-06-04T05:10:50Z
dc.date.issued 2014
dc.identifier.citation Journal of Luminescence. 155; 2014; 251-256. en_US
dc.identifier.uri http://dx.doi.org/10.1016/j.jlumin.2014.06.056
dc.identifier.uri http://irgu.unigoa.ac.in/drs/handle/unigoa/3174
dc.description.abstract In the quest of bright and long persistent far-red/near-infrared phosphors for in vivo optical imaging, the interest in the family of ZnGa(2)O(4) spinel compounds doped with Cr3+ has been aroused in the most recent years. We show that the dopant concentration plays an important role in the total persistent luminescence output of the material. ZnGa2O4 doped with 0.25 percent, 0.50 percent and 0.75 percent Cr relative to (Ga+Cr) was prepared by solid state synthesis. 0.50 percent Cr was found optimal to obtain the most intense persistent luminescence after matrix excitation with X-rays or localized excitation in Cr3+ absorption band with 550nm wavelength. Up to 0.5 percent Cr content, persistent luminescence increases as a consequence of an increased number of Cr3+ luminescent centers and associated defects. With 0.75 percent Cr content, a too large number of defects locally concentrated around Cr3+ ions are detrimental to the long-term persistent luminescence intensity. We supplement long lasting phosphorescence investigation with laser excited photoluminescence and thermally stimulated luminescence results. en_US
dc.publisher Elsevier en_US
dc.subject Physics en_US
dc.title Interplay between chromium content and lattice disorder on persistent luminescence of ZnGa(2)O(4):Cr3+ for in vivo imaging en_US
dc.type Journal article en_US
dc.identifier.impf y


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