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Issue 119, 2015
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Dual energy transfer controlled photoluminescence evolution in Eu and Mn co-activated β-Ca2.7Sr0.3(PO4)2 phosphors for solid-state lighting

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Abstract

Photoluminescence evolution in single-composition phosphors for solid state lighting can be realized through an energy transfer strategy, which is commonly based on one sensitizer and one activator. In this work, we focus on a dual energy transfer process, that is, energy transfers from the sensitizer Eu2+ at two different cation sites to the activator Mn2+ at another site in whitlockite-type β-Ca2.7Sr0.3(PO4)2. Firstly, we refined the crystal structure of the β-Ca2.7Sr0.3(PO4)2 host by a Rietveld method. Then we studied the phase, morphology and photoluminescence of Eu and Mn co-activated β-Ca2.7Sr0.3(PO4)2 phosphors, which are synthesized by a conventional solid-state reaction. By adjusting the ratio of Eu2+/Mn2+, the emission hue can be controlled from cyan (0.211, 0.281) to white-light (0.332, 0.290) and eventually to red (0.543, 0.276). The dual energy transfers from Eu2+ to Mn2+ are demonstrated to be dipole–dipole and quadrupole–quadrupole mechanisms, respectively. Moreover, white light-emitting diodes (LEDs) were fabricated through the integration of a 375 nm NUV chip and the white-emitting phosphor Ca2.7Sr0.3(PO4)2:0.008Eu2+, 0.03Mn2+ into a single package, which shows a warm white light with color coordinates of (0.40, 0.41) and correlated color temperature of 3731 K.

Graphical abstract: Dual energy transfer controlled photoluminescence evolution in Eu and Mn co-activated β-Ca2.7Sr0.3(PO4)2 phosphors for solid-state lighting

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Publication details

The article was received on 03 Sep 2015, accepted on 09 Nov 2015 and first published on 11 Nov 2015


Article type: Paper
DOI: 10.1039/C5RA17877K
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RSC Adv., 2015,5, 98026-98032

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    Dual energy transfer controlled photoluminescence evolution in Eu and Mn co-activated β-Ca2.7Sr0.3(PO4)2 phosphors for solid-state lighting

    J. Han, F. Pan, W. Zhou, Z. Qiu, M. Tang, J. Wang and S. Lian, RSC Adv., 2015, 5, 98026
    DOI: 10.1039/C5RA17877K

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