M. C. TERRILE

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  • Artigo IPEN-doc 19540
    Spectroscopic properties and quantum cutting in Tb3+-Yb3+ co-doped ZrO2 nanocrystals
    2013 - TERRA, I.A.A.; BORRERO GONZALEZ, L.J.; CARVALHO, J.M.; TERRILE, M.C.; FELINTO, M.C.F.C.; BRITO, H.F.; NUNES, L.A.O.
    Ultraviolet-visible to near-infrared quantum cutting (QC) materials are a promising tool to enhance the efficiency of conventional crystalline silicon solar cells. The spectroscopic properties of Tb3Ć¾ā€“Yb3Ć¾ co-doped ZrO2 nanocrystals are presented, and the QC mechanisms in these nanocrystals are investigated. The materials were fabricated using the sol gel method and characterized using X-ray powder diffraction, X-ray absorption near edge structure, and luminescence spectroscopy. The incorporation of Yb3Ć¾ ions into the host induced a crystalline phase change of ZrO2 from monoclinic to tetragonal to cubic symmetry and influenced the Tb valence state. The Tb3Ć¾ visible emission, excitation intensity (monitored by the Tb3Ć¾: 5 D4 emission), decay time of the Tb3Ć¾: 5 D4 emitter level, and down-conversion (DC) emission intensity increased with Yb3Ć¾ concentration. Furthermore, a sublinear dependence of the DC intensity on the excitation power at the Tb3Ć¾: 5 D4 level indicated the coexistence of two different QC mechanisms from Tb3Ć¾ ! Yb3Ć¾. The first one is a linear process in which one Tb3Ć¾ ion transfers its energy simultaneously to two Yb3Ć¾ ions, known as cooperative energy transfer, and the second one is a non-linear process involving an intermediated virtual level in the Tb3Ć¾ ion.