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      Novel persistent phosphors of lanthanide–chromium co-doped yttrium aluminum gallium garnet: design concept with vacuum referred binding energy diagram

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          Abstract

          We have developed Pr 3+–Cr 3+ and Tb 3+–Cr 3+ co-doped Y 3Al 2Ga 3O 12 (YAG G) persistent phosphors with orange (Pr 3+) and light green (Tb 3+) persistent luminescence.

          Abstract

          We have developed Pr 3+–Cr 3+ and Tb 3+–Cr 3+ co-doped Y 3Al 2Ga 3O 12 (YAG G) persistent phosphors with orange (Pr 3+) and light green (Tb 3+) persistent luminescence. The duration of their persistent luminance (of 0.32 mcd m −2) can last up to about 8 h and 12 h, respectively. On the other hand, the persistent luminescence intensities of Nd 3+–Cr 3+ and Dy 3+–Cr 3+ co-doped YAG G samples are much weaker than those of the Pr 3+–Cr 3+ and Tb 3+–Cr 3+ co-doped ones, and the dominant persistent luminescence is mainly due to the deep-red transition of Cr 3+. The mechanisms of different persistent luminescence behaviors of these four samples can be explained by the vacuum referred binding energy (VRBE) diagram of lanthanide ions in the YAG G host. The stability of hole traps at the ground states of Pr 3+, Nd 3+, Tb 3+ and Dy 3+ ions and the possibility to collaborate with Cr 3+ electron traps to induce persistent luminescence are discussed in detail.

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          Most cited references33

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          A New Long Phosphorescent Phosphor with High Brightness, SrAl[sub 2]O[sub 4]:Eu[sup 2+],Dy[sup 3+]

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            The in vivo activation of persistent nanophosphors for optical imaging of vascularization, tumours and grafted cells.

            Optical imaging for biological applications requires more sensitive tools. Near-infrared persistent luminescence nanoparticles enable highly sensitive in vivo optical detection and complete avoidance of tissue autofluorescence. However, the actual generation of persistent luminescence nanoparticles necessitates ex vivo activation before systemic administration, which prevents long-term imaging in living animals. Here, we introduce a new generation of optical nanoprobes, based on chromium-doped zinc gallate, whose persistent luminescence can be activated in vivo through living tissues using highly penetrating low-energy red photons. Surface functionalization of this photonic probe can be adjusted to favour multiple biomedical applications such as tumour targeting. Notably, we show that cells can endocytose these nanoparticles in vitro and that, after intravenous injection, we can track labelled cells in vivo and follow their biodistribution by a simple whole animal optical detection, opening new perspectives for cell therapy research and for a variety of diagnosis applications.
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              Persistent Luminescence in Eu2+-Doped Compounds: A Review

              In 1996, Matsuzawa et al. reported on the extremely long-lasting afterglow of SrAl2O4:Eu2+ codoped with Dy3+ ions, which was more than 10-times brighter than the previously widely used ZnS:Cu,Co. Since then, research for stable and efficient persistent phosphors has continuously gained popularity. However, even today - almost 15 years after the discovery of SrAl2O4:Eu2+, Dy3+ - the number of persistent luminescent materials is still relatively low. Furthermore, the mechanism behind this phenomenon is still unclear. Although most authors agree on the general features, such as the existence of long-lived trap levels, many details are still shrouded in mystery. In this review, we present an overview of the important classes of known persistent luminescent materials based on Eu2+-emission and how they were prepared, and we take a closer look at the models and mechanisms that have been suggested to explain bright afterglow in various compounds.
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                Author and article information

                Journal
                JMCCCX
                Journal of Materials Chemistry C
                J. Mater. Chem. C
                Royal Society of Chemistry (RSC)
                2050-7526
                2050-7534
                2016
                2016
                : 4
                : 20
                : 4380-4386
                Affiliations
                [1 ]Graduate School of Human and Environmental Studies
                [2 ]Kyoto University
                [3 ]Kyoto 606-8501
                [4 ]Japan
                Article
                10.1039/C6TC00802J
                a27f2f65-a004-4a96-a627-9f226981b9c1
                © 2016
                History

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