Akshay Pimpalkar , Rajesh M. Bhagat , Shruti P. Dhale , Ashok A. Mistry , Nilesh S. Ugemuge , Rujuta Joshi , R. Nithya , Prachita A. Patil , K.M. Nissamudeen
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引用次数: 0
Abstract
The orange red emitting Ca3NbGa3Si2O14: Sm3+, Tb3+ phosphor was synthesized by solid-state reaction (SSR) method at 1280 °C for 10 h followed by annealing at 400 °C for 7hrs. X-ray diffraction pattern confirms the hexagonal structure with P321(No.150) space group. Compound formation, elemental analysis, photoluminescence and energy transfer mechanism from Tb3+ to Sm3+ were studied. Ca3NbGa3Si2O14:Sm3+ phosphor exhibits orange-red emission at 601 nm attributed to 4G5/26H7/2 transition. Ca3NbGa3Si2O14:Tb3+ phosphor exhibits green emission at 544 nm attributed to 5D47F5 transition. The optimum concentration for Sm3+ and Tb3+ is found to be 3.0 and 2.0 mol. % respectively. Lifetime decay measurements of Tb3+ confirms the energy transfer mechanism which was proved to be a quadrupole-quadrupole interaction. The CIE chromaticity coordinates calculated for Sm3+ (0.63, 0.37), Tb3+ (0.27, 0.72) and 2.0 Tb3+, ySm3+ (0.37, 0.40) suggests its potential use for fabrication of optical devices. Higher values of Ω4 indicate centro-symmetric character of the field experienced by Sm3+ ions. This confirms that magnetic dipole transitions are dominant over electric dipole transitions which are analogous to the PL results. Since the obtained values of the branching ratios with respect to transition, 4G5/26H7/2 are around 50 %, this material can be proposed as a potential laser material having emission wavelength around 601 nm.
期刊介绍:
The purpose of the Journal of Luminescence is to provide a means of communication between scientists in different disciplines who share a common interest in the electronic excited states of molecular, ionic and covalent systems, whether crystalline, amorphous, or liquid.
We invite original papers and reviews on such subjects as: exciton and polariton dynamics, dynamics of localized excited states, energy and charge transport in ordered and disordered systems, radiative and non-radiative recombination, relaxation processes, vibronic interactions in electronic excited states, photochemistry in condensed systems, excited state resonance, double resonance, spin dynamics, selective excitation spectroscopy, hole burning, coherent processes in excited states, (e.g. coherent optical transients, photon echoes, transient gratings), multiphoton processes, optical bistability, photochromism, and new techniques for the study of excited states. This list is not intended to be exhaustive. Papers in the traditional areas of optical spectroscopy (absorption, MCD, luminescence, Raman scattering) are welcome. Papers on applications (phosphors, scintillators, electro- and cathodo-luminescence, radiography, bioimaging, solar energy, energy conversion, etc.) are also welcome if they present results of scientific, rather than only technological interest. However, papers containing purely theoretical results, not related to phenomena in the excited states, as well as papers using luminescence spectroscopy to perform routine analytical chemistry or biochemistry procedures, are outside the scope of the journal. Some exceptions will be possible at the discretion of the editors.