2008
DOI: 10.1016/j.jnoncrysol.2007.08.064
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Blue emission of ZrO2:Tm nanocrystals with different crystal structure under UV excitation

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Cited by 49 publications
(19 citation statements)
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“…The band at 3.36 eV is due to the cumulative effect of uneven distribution of Zr 4+ at near surface sites, which arise due to the dangling bonds on the surface of the material and due to the radiative recombination of electrones and holes in gadolinium centers. The green emission at 2.24 eV is due to 6 G J to Gd 3+ transition that arise due to stark level manifolds [32][33][34][35][36]. From PL studies it is found that combination of Gd, Mg and Zr resulted in high oxygen vacancy in the material, this made the Gd:MgZrO 3 a robust photocatalyst for the degradation of RhB.…”
Section: Resultsmentioning
confidence: 99%
“…The band at 3.36 eV is due to the cumulative effect of uneven distribution of Zr 4+ at near surface sites, which arise due to the dangling bonds on the surface of the material and due to the radiative recombination of electrones and holes in gadolinium centers. The green emission at 2.24 eV is due to 6 G J to Gd 3+ transition that arise due to stark level manifolds [32][33][34][35][36]. From PL studies it is found that combination of Gd, Mg and Zr resulted in high oxygen vacancy in the material, this made the Gd:MgZrO 3 a robust photocatalyst for the degradation of RhB.…”
Section: Resultsmentioning
confidence: 99%
“…Zirconia nanocrystals that contain the rare earth element thulium emit blue fluorescence when exposed to UV light 24) . There are reports of fluorescence from pure zirconia (monoclinic phase) that has been doped with Tm 3+ ions or yttria-rich tetragonal phase-stabilized zirconia 25,26) .…”
Section: Discussionmentioning
confidence: 99%
“…This phenomenon can be also explained by the quenching concentration phenomenon of the emission. Indeed, the increase of rare earth activator concentration induces the shortening of the RE 3+ -RE 3+ distance, and it is well known that if the distance of luminescent centers is short enough, energy can transfer among these luminescent centers following a great deal of nonradiative transitions, which leads to the quenching of luminescence [26]. In the other hand, the concentration behaviour of the luminescence is a complex matter, since different energy transfers (mainly cross relaxation) can be involved and several experimental parameters are involved.…”
Section: Photoluminescencementioning
confidence: 99%