In this study, the photoluminescence (PL) behavior of two aluminosilicate glass series containing alkali-niobates ranging from 0.4 to 20 mol% was investigated. The glasses exhibit an intense visible emission centered at ~18,400 cm for the peralkaline series and at higher energies (~19,300 cm) for the metaluminous glasses. However, the photoluminescence emission intensity varies significantly with the niobate content and the bulk chemistry. PL and fluorescence lifetime measurements indicate that the broad emission bands result from the overlap of different niobate populations, whose distribution changes with niobate content. The distinct PL behavior in the two glass series was related to the structural evolution of the niobate units upon niobium addition. An enhancement of the visible emission was observed for a higher fraction of distorted [NbO] units. Eu-doping was carried out as a structural probe of the glass network, and also to determine if these glasses could be used as potential rare earth element (REE) activators. The crystal field strength around Eu ions is strongly dependent on the bulk chemistry and the niobate content. Furthermore, the peralkaline series showed energy transfer from the host [NbO] to Eu, confirming the feasibility of exploring niobate glasses and glass-ceramics as lanthanide ion-activated luminescent materials. In addition, glass-ceramics (GCs) containing alkali-niobate phases with a perovskite-like structure were developed and studied to verify the optical performance of these materials. It was verified that the bulk chemistry influences crystallization behavior, and also the photoluminescence response. The transparent GC from the metaluminous series exhibits a quenching of the Eu emission, whereas an enhanced emission intensity is observed for the peralkaline GC. The latter shows a strong excitation-dependent PL emission, suggesting energy transfer and migration of electronic excitation from one Eu population to another. Additionally, Eu emissions arising from the D15 and D25 excited states were observed, highlighting the low phonon energy achievable in niobo-aluminosilicate hosts.
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http://dx.doi.org/10.3390/ma17102283 | DOI Listing |
Heliyon
December 2024
Department of Engineering Physics, AUCE (A), Andhra University, Visakhapatnam, India.
Pb₁₋ₓ₋₃BaₓReᵧ³⁺Nb₂O₆ (PBN) ceramics, where x = 0.35 and y = 0.00, 0.
View Article and Find Full Text PDFACS Appl Mater Interfaces
October 2024
College of Materials Science and Engineering, Sichuan University, 610064 Chengdu, China.
The splendid energy storage performances with eminent stability of dielectric ceramics utilized in pulsed power devices have been paid more attention by researchers. This scheme can be basically realized through introducing Li, Bi(MgTa)O, NaNbO, and LiF into KNN-based ceramics. Under the breakdown strength (BDS) of 460 kV/cm, an outstanding energy storage density () of 6.
View Article and Find Full Text PDFMaterials (Basel)
July 2024
Institute of Materials Engineering, Faculty of Science and Technology, University of Silesia in Katowice, 75 Pułku Piechoty 1a, 41-500 Chorzów, Poland.
This article presents the research results of lead-free BaLa(FeNb)O (BFNLa) ceramic materials doped with La ( = 0.00-0.06) obtained via the solid-state reaction method.
View Article and Find Full Text PDFMaterials (Basel)
May 2024
Department of Materials Science and Engineering, Institut für Glas und Keramik, Friedrich-Alexander-Universität Erlangen-Nürnberg, 91058 Erlangen, Germany.
In this study, the photoluminescence (PL) behavior of two aluminosilicate glass series containing alkali-niobates ranging from 0.4 to 20 mol% was investigated. The glasses exhibit an intense visible emission centered at ~18,400 cm for the peralkaline series and at higher energies (~19,300 cm) for the metaluminous glasses.
View Article and Find Full Text PDFACS Appl Nano Mater
May 2024
Department of Chemistry, University of Warwick, Gibbet Hill Road, Coventry CV4 7AL, U.K.
Nanostructured niobium-titanium carbonitrides, (Nb,Ti)CN, with the cubic-rock salt structure are prepared without the use of reactive gases via thermal treatment (700-1200 °C) under nitrogen of mixtures of guanidine carbonate and ammonium niobate (V) oxalate hydrate, with addition of ammonium titanyl oxalate monohydrate as a titanium source. The bulk structure and chemical composition of the materials are characterized using powder X-ray diffraction (XRD) and powder neutron diffraction, elemental homogeneity is studied using energy dispersive spectroscopy (EDS) mapping using transmission electron microscopy (TEM), and surface chemical analysis is examined using X-ray photoelectron spectroscopy (XPS). Nanoscale crystallites of between 10 and 50 nm are observed by TEM, where EDS reveals the homogeneity of metal distribution for the mixed-metal materials.
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