Journal
JOURNAL OF MATERIALS CHEMISTRY C
Volume 11, Issue 11, Pages 3865-3874Publisher
ROYAL SOC CHEMISTRY
DOI: 10.1039/d2tc04688a
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The self-reduction of Mn4+ -> Mn2+ and excellent thermal stability of NaY9Si6O26:Mn2+ red phosphors were achieved. The effect of defects on luminescence properties was highlighted, stimulating further research on defect control.
Luminous properties play an essential role in phosphor-converted white light-emitting diodes for high-quality illumination, where the self-reducing behavior of doped activators and their excellent thermal stability have received significant attention. Here, we prepared NaY9Si6O26:Mn2+ red phosphors by a high-temperature solid-state reaction method, which achieved self-reduction of Mn4+ -> Mn2+ and excellent thermal stability (luminous intensity at 420 K is 98% of that at room temperature) under ambient conditions. First-principles calculations and X-ray photoelectron spectroscopy elucidated a self-reduction mechanism from Mn4+ to Mn2+. The defect types were calculated in conjunction with thermoluminescence, verifying that the low thermal quenching properties originated from the transfer of electrons from the defect energy level to the Mn2+ excited state center induced by the cationic vacancy defect, which suppressed the luminescence loss from thermal quenching. In this work, the effect of defects on luminescence properties is highlighted and the further exploration of defect control is stimulated, opening up a new avenue for new types of highly thermally stable materials.
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