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      Blue-green tunable color of Ce 3+/Tb 3+ coactivated NaBa 3La 3Si 6O 20 phosphor via energy transfer

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      Scientific Reports
      Nature Publishing Group

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          Abstract

          A series of color tunable phosphors NaBa 3La 3Si 6O 20:Ce 3+, Tb 3+ were synthesized via the high-temperature solid-state method. NaBa 3La 3Si 6O 20 crystallizes in noncentrosymmetric space group Ama2 with the cell parameters of a = 14.9226(4) Å, b = 24.5215(5) Å and c = 5.6241(2) Å by the Rietveld refinement method. The Ce 3+ ions doped NaBa 3La 3Si 6O 20 phosphors have a strong absorption band from 260 to 360 nm and show near ultraviolet emission light centered at 378 nm. The Ce 3+ and Tb 3+ ions coactivated phosphors exhibit color tunable emission light from deep blue to green by adjusting the concentration of the Tb 3+ ions. An energy transfer of Ce 3+ → Tb 3+ investigated by the photoluminescence properties and lifetime decay, is demonstrated to be dipole–quadrupole interaction. These results indicate the NaBa 3La 3Si 6O 20:Ce 3+, Tb 3+ phosphors can be considered as potential candidates for blue-green components for white light emitting diodes.

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          Solid-state light sources getting smart.

          More than a century after the introduction of incandescent lighting and half a century after the introduction of fluorescent lighting, solid-state light sources are revolutionizing an increasing number of applications. Whereas the efficiency of conventional incandescent and fluorescent lights is limited by fundamental factors that cannot be overcome, the efficiency of solid-state sources is limited only by human creativity and imagination. The high efficiency of solid-state sources already provides energy savings and environmental benefits in a number of applications. However, solid-state sources also offer controllability of their spectral power distribution, spatial distribution, color temperature, temporal modulation, and polarization properties. Such "smart" light sources can adjust to specific environments and requirements, a property that could result in tremendous benefits in lighting, automobiles, transportation, communication, imaging, agriculture, and medicine.
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            Narrow-band red-emitting Sr[LiAl3N4]:Eu2+ as a next-generation LED-phosphor material

            To facilitate the next generation of high-power white-light-emitting diodes (white LEDs), the discovery of more efficient red-emitting phosphor materials is essential. In this regard, the hardly explored compound class of nitridoaluminates affords a new material with superior luminescence properties. Doped with Eu(2+), Sr[LiAl3N4] emerged as a new high-performance narrow-band red-emitting phosphor material, which can efficiently be excited by GaN-based blue LEDs. Owing to the highly efficient red emission at λ(max) ~ 650 nm with a full-width at half-maximum of ~1,180 cm(-1) (~50 nm) that shows only very low thermal quenching (>95% relative to the quantum efficiency at 200 °C), a prototype phosphor-converted LED (pc-LED), employing Sr[LiAl3N4]:Eu(2+) as the red-emitting component, already shows an increase of 14% in luminous efficacy compared with a commercially available high colour rendering index (CRI) LED, together with an excellent colour rendition (R(a)8 = 91, R9 = 57). Therefore, we predict great potential for industrial applications in high-power white pc-LEDs.
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              Tunable full-color emitting BaMg2Al6Si9O30:Eu2+, Tb3+, Mn2+ phosphors based on energy transfer.

              A series of single-phase full-color emitting BaMg(2)Al(6)Si(9)O(30):Eu(2+), Tb(3+), Mn(2+) phosphors has been synthesized by solid-state reaction. Energy transfer from Eu(2+) to Tb(3+) and Eu(2+) to Mn(2+) in BaMg(2)Al(6)Si(9)O(30) host matrix is studied by luminescence spectra and energy-transfer efficiency and lifetimes. The wavelength-tunable white light can be realized by coupling the emission bands centered at 450, 542, and 610 nm ascribed to the contribution from Eu(2+) and Tb(3+) and Mn(2+), respectively. By properly tuning the relative composition of Tb(3+)/Mn(2+), chromaticity coordinates of (0.31, 0.30), high color rendering index R(a) = 90, and correlated color temperature (CCT) = 5374 K can be achieved upon excitation of UV light. Thermal quenching properties reveal that BaMg(2)Al(6)Si(9)O(30): Eu(2+), Tb(3+), Mn(2+) exhibits excellent characteristics even better than that of YAG:Ce. Our results indicate our white BaMg(2)Al(6)Si(9)O(30):Eu(2+), Tb(3+), Mn(2+) can serve as a key material for phosphor-converted light-emitting diode and fluorescent lamps. © 2011 American Chemical Society
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                Author and article information

                Journal
                Sci Rep
                Sci Rep
                Scientific Reports
                Nature Publishing Group
                2045-2322
                15 September 2016
                2016
                : 6
                : 33283
                Affiliations
                [1 ]Key Laboratory of Coordination Chemistry and Functional Materials in Universities of Shandong, Dezhou University , Dezhou 253023, PR China
                [2 ]Beijing Center for Crystal Research and Development, Key Laboratory of Functional Crystals and Laser Technology, Technical Institute of Physics and Chemistry, Chinese Academy of Sciences , Beijing 100190, PR China
                [3 ]University of Chinese Academy of Sciences , Beijing 100049, PR China
                Author notes
                Article
                srep33283
                10.1038/srep33283
                5024107
                27628111
                656ff959-6417-4265-9478-da22f62f7de9
                Copyright © 2016, The Author(s)

                This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/

                History
                : 29 April 2016
                : 24 August 2016
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