Issue 40, 2013

Blue–white–orange color-tunable luminescence of Ce3+/Mn2+-codoped NaCaBO3via energy transfer: potential single-phase white-light-emitting phosphors

Abstract

Ce3+/Mn2+-codoped NaCaBO3 single-phase color-tunable phosphors were synthesized by solid-state reaction, and their photoluminescence properties were investigated in detail. Under UV excitation, two main emission bands peaking at 400 and 610 nm were realized in the NaCa0.89BO3: 0.01Ce3+, 0.10Mn2+ phosphor on the basis of the energy transfer from Ce3+ to Mn2+ with an efficiency of over 83%. The energy transfer was validated and demonstrated to be a resonant type via a dipole–dipole mechanism, and the critical distance RC values calculated by the quenching concentration method and the spectral overlap method were 22.85 and 19.41 Å, respectively. On examining the Mn2+-concentration-dependent photoluminescence properties, it was observed that the emission color could be tuned from blue (0.162, 0.031) to white-light (0.335, 0.259) and eventually to orange (0.489, 0.246) through energy transfer by changing the Ce3+/Mn2+ ratio. Combining a 370 nm UV chip and a single-phase white-emitting NaCa0.96BO3: 0.01Ce3+, 0.03Mn2+ phosphor produced a white light-emitting diode with CIE chromaticity coordinates of (0.326, 0.274) and an excellent color rendering index of 90.7 at a correlated color temperature of 4046 K. These results indicate that the NaCaBO3: Ce3+, Mn2+ phosphors have potential applications as single-phase white-light-emitting phosphor-converted materials for UV-pumped light-emitting diodes.

Graphical abstract: Blue–white–orange color-tunable luminescence of Ce3+/Mn2+-codoped NaCaBO3 via energy transfer: potential single-phase white-light-emitting phosphors

Article information

Article type
Paper
Submitted
23 May 2013
Accepted
22 Jul 2013
First published
23 Jul 2013

RSC Adv., 2013,3, 18395-18405

Blue–white–orange color-tunable luminescence of Ce3+/Mn2+-codoped NaCaBO3 via energy transfer: potential single-phase white-light-emitting phosphors

J. Sun, Z. Lian, G. Shen and D. Shen, RSC Adv., 2013, 3, 18395 DOI: 10.1039/C3RA42554A

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