The study reports green mediated combustion route for the synthesis of Tb(3+) ion activated Y2O3 nanophosphors using Aloe Vera gel as fuel. The concentration of Tb(3+) plays a key role in controlling the morphology of Y2O3 nanostructures. The formation of different morphologies of Y2O3: Tb(3+) nanophosphors were characterized by PXRD, SEM, TEM and HRTEM. PXRD data and Rietveld analysis evident the formation of single phase Y2O3 with cubic crystal structure. The influence of Tb(3+) ion concentration on structural morphology, UV-visible absorption and PL emission were investigated systematically. The PL emission of Y2O3: Tb(3+) (1-11 mol%) nanophosphors were studied in detail under 271 and 304nm excitation wavelengths. The CIE coordinates lies well within green region and correlated color temperature values were found to be 6221 and 5562K under different excitations. Thus, the present phosphor can serve as an excellent candidate for LEDs. Further, prismatic Y2O3: Tb(3+) (3 mol%) nanophosphor showed significant antibacterial activity against Pseudomonas desmolyticum and Staphylococcus aureus. The present study successfully demonstrates Y2O3: Tb(3+) nanophosphors can be used for display applications as well as in medical applications for controlling pathogenic bacteria.
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http://dx.doi.org/10.1016/j.saa.2015.06.081 | DOI Listing |
Tb is extensively employed in magneto-optical devices and luminescent materials owing to its distinctive physical properties. However, under certain conditions, trivalent Tb readily undergoes oxidation to tetravalent Tb, significantly reducing the performance of devices containing Tb. In this Letter, we report a technique called dual-annealing (DA) post-treatment, which effectively solves Tb oxidation issues by utilizing the reducibility of the vacuum environment.
View Article and Find Full Text PDFJ Phys Chem C Nanomater Interfaces
February 2024
Cain Department of Chemical Engineering, Louisiana State University, Baton Rouge, Louisiana 70803, United States.
Anion engineering has proven to be an effective strategy to tailor the physical and chemical properties of metal oxides by modifying their existing crystal structures. In this work, a low-temperature synthesis for rare earth (RE)-doped YOSO and YOS was developed via annealing of Y(OH) intermediates in the presence of elemental sulfur in a sealed tube, followed by a controlled reduction step. The crystal structure patterns (X-ray diffraction) and optical spectra (UV-IR) of YOSO, YOS, and crystalline YO were collected throughout the treatment steps to correlate the structural transformations (via thermogravimetric analysis) with the optical properties.
View Article and Find Full Text PDFBiotechnol Bioeng
March 2024
Department of Biotechnology, Dresden, Germany.
Yttrium is a heavy rare earth element (REE) that acquires remarkable characteristics when it is in oxide form and doped with other REEs. Owing to these characteristics Y O can be used in the manufacture of several products. However, a supply deficit of this mineral is expected in the coming years, contributing to its price fluctuation.
View Article and Find Full Text PDFNanoscale Adv
February 2022
Fraunhofer-CAN Grindelallee 117 20146 Hamburg Germany.
Yttrium oxide (YO) is considered as one of the best host lattices for europium (Eu) based red emitting phosphors because of its unit cell and good photo-saturation properties. As a bulk material, it reaches nearly 100% quantum yield. However, providing high quality nanosized materials for the LED industry is still a challenge and not easily accomplished.
View Article and Find Full Text PDFRSC Adv
December 2021
Institute of Inorganic Chemistry, University of Stuttgart Pfaffenwaldring 55 70569 Stuttgart Germany.
The quaternary halide-containing yttrium(iii) oxidoantimonates(iii) YSbOCl and YSbOBr were synthesised through solid-state reactions from the binary components (YO, SbO and YX, X = Cl and Br) at 750 °C in evacuated fused silica ampoules with eutectic mixtures of NaX and CsX (X = Cl and Br) as fluxing agents. YSbOCl crystallizes tetragonally in the non-centrosymmetric space group 422 with unit-cell parameters of = 773.56(4) pm and = 878.
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