Spectroscopic properties of Cr3+ ions in nanocrystalline glass–ceramic composites |
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Institution: | 1. Department of Physics, High Pressure Science and Engineering Center, University of Nevada Las Vegas, Las Vegas, NV 89154-4002, United States;2. Department of Applied Science, UC Davis, Davis, CA 95615, United States;3. Geophysical Laboratory, Carnegie Institution of Washington, Washington DC 20015, United States;4. Department of Electrical Engineering and Bioscience, Waseda University, Shinjuku, Tokyo 169-8555, Japan;1. Department of Materials Science and Engineering, Pennsylvania State University, University Park, PA, USA;2. Department of Materials Science and Engineering, Lehigh University, Bethlehem, PA, USA |
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Abstract: | Luminescence properties of Cr3+ ions in a silica-based precursor glass, and in fabricated optically transparent glass-based nanocrystalline composites, have been investigated. The luminescence spectra of the precursor glass revealed a wide range of crystal fields and showed the 4T2–4A2 broadband emission of Cr3+ ions in a weak crystal field, combined with 2E–4A2 emission characteristic for Cr3+ ions in a strong crystal field. Glass–ceramic nanocomposites, with gallium oxide nanocrystals nucleated in a host glass matrix, indicated the prevailing contribution of the crystal-like 2E–4A2 emissions (R-lines) of Cr3+ ions in a strong crystal field. The low-temperature studies demonstrated that the fluorescence of Cr3+ ions could be altered from sharp R-lines of the 2E–4A2 transition, below 70 K, to a combination of R-lines and their sidebands, above 70 K. Our results indicate that, in the developed glass–ceramic nanocomposites, most of the Cr3+ ions have migrated from the host glass matrix to the nucleated gallium oxide nanocrystalline phase. |
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