Very intense visible green photoluminescence ͑PL͒ was observed at room temperature in structurally ordered-disordered BaZrO 3 powders. Ab initio calculations, ultraviolet-visible absorption spectroscopy, electron paramagnetic resonance, and PL were performed. Theoretical and experimental results showed that local defects in the cubic structure caused byplay an important role in the formation of hole-electron pairs, giving rise to a charge gradient in the structure which is responsible for PL emission.
Violet-blue photoluminescence was produced at room temperature in a structurally disordered SrZrO3 perovskite structure with a 350.7nm excitation line. The intensity of this emission was higher than that of any other perovskites previously studied. The authors discuss the role of structural order-disorder that favors the self-trapping of electrons and charge transference, as well as a model to elucidate the mechanism that triggers photoluminescence. In this model the wide band model, the most important events occur before excitation.
This paper describes a new amorphous wide-band gap semiconductor with photoluminescence (PL) at room temperature. The amorphous PbTiO 3 was prepared by a sol-gel-like process in powder and thin film form. The optical property and the PL behaviour showed a direct relation to the amorphous structure. The PL peak energy can be controlled by the change of the exciting surge energy. Copyright $ Weak PL was observed in BaTiO 2 only at cryogenic tempera! tures\ see Ref[ 3[ E[ R[ LEITE ET AL[
A complimentary combination of experimental work and first principle calculations, based on the Density Functional Theory (DFT) method, has been used to increase our limited understanding of the enhanced photocatalytic activity of PbMoO 4 powders with predominant (111), (100), (011), and (110) facets.In this work, PbMoO 4 powders were prepared by the co-precipitation method and processed on a hydrothermal reactor at 100 o C/10 minutes. The variation of different types of modifier such as acetylacetone (acac) or polyvinylpyrrolidone (PVP) is found to play a crucial role in controlling the particle size and morphology of products and their photocatalytic properties.The structure and morphology of these crystals were characterized by X-ray diffraction (XRD), micro-Raman (MR) spectroscopy, field-emission gun scanning electron microscopy (FEG-SEM), and ultraviolet visible (UV-vis) absorption spectroscopy. Furthermore, the assynthesized PbMoO 4 micro-octahedrons without presence of (001) surface exhibit enhanced activity for the photodegradation of rhodamine B (RhB) under ultraviolet-visible light irradiation.Based on the theoretical and experimental results, we provide a complete assignment of the micro-Raman spectra of PbMoO 4 , while a growth mechanism for the formation of PbMoO 4 micro-octahedrons was systematically discussed, and a schematic illustration of the probable formation of morphologies in the whole of the synthetic process was also proposed, which reveals that the high photocatalytic activity is attributed to the absence of (001) facet.
This letter reports on a process to prepare nanostructured PbTiO3 (PT) at room temperature with photoluminescence (PL) emission in the visible range. This process is based on the high-energy mechanical milling of ultrafine PbTiO3 powder. The results suggest that high-energy mechanical milling modifies the particle’s structure, resulting in localized states in an interfacial region between the crystalline PT and the amorphous PT. These localized states are believed to be responsible for the PL obtained with short milling times. When long milling times are employed, the amorphous phase that is formed causes PL behavior. An alternative method to process nanostructured wide-band-gap semiconductors with active optical properties such as PL is described in this letter.
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