We explore the potential of Tb- A nd Yb-doped InVO, InTaO, and InNbO for applications as phosphors for light-emitting sources. Doping below 0.2% barely change the crystal structure and Raman spectrum but provide optical excitation and emission properties in the visible and near-infrared (NIR) spectral regions. From optical measurements, the energy of the first/second direct band gaps was determined to be 3.7/4.1 eV in InVO, 4.7/5.3 in InNbO, and 5.6/6.1 eV in InTaO. In the last two cases, these band gaps are larger than the fundamental band gap (being indirect gap materials), while for InVO, a direct band gap semiconductor, the fundamental band gap is at 3.7 eV. As a consequence, this material shows a strong self-activated photoluminescence centered at 2.2 eV. The other two materials have a weak self-activated signal at 2.2 and 2.9 eV. We provide an explanation for the origin of these signals taking into account the analysis of the polyhedral coordination around the pentavalent cations (V, Nb, and Ta). Finally, the characteristic green (D -> F) and NIR (F -> F) emissions of Tb and Yb have been analyzed and explained.

Investigation on the Luminescence Properties of InMO4 (M = V5+, Nb5+, Ta5+) Crystals Doped with Tb3+ or Yb3+ Rare Earth Ions

Enrichi Francesco;
2020

Abstract

We explore the potential of Tb- A nd Yb-doped InVO, InTaO, and InNbO for applications as phosphors for light-emitting sources. Doping below 0.2% barely change the crystal structure and Raman spectrum but provide optical excitation and emission properties in the visible and near-infrared (NIR) spectral regions. From optical measurements, the energy of the first/second direct band gaps was determined to be 3.7/4.1 eV in InVO, 4.7/5.3 in InNbO, and 5.6/6.1 eV in InTaO. In the last two cases, these band gaps are larger than the fundamental band gap (being indirect gap materials), while for InVO, a direct band gap semiconductor, the fundamental band gap is at 3.7 eV. As a consequence, this material shows a strong self-activated photoluminescence centered at 2.2 eV. The other two materials have a weak self-activated signal at 2.2 and 2.9 eV. We provide an explanation for the origin of these signals taking into account the analysis of the polyhedral coordination around the pentavalent cations (V, Nb, and Ta). Finally, the characteristic green (D -> F) and NIR (F -> F) emissions of Tb and Yb have been analyzed and explained.
2020
metal oxides
rare earths
luminescence
crystal structure
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/20.500.14243/384326
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