TY - JOUR
T1 - Color Tuning of (K1−x,Nax)SrPO4:0.005Eu2+, yTb3+ Blue-Emitting Phosphors via Crystal Field Modulation and Energy Transfer
AU - Dai, Pengpeng
AU - Zhang, Xintong
AU - Bian, Lulu
AU - Lu, Shan
AU - Liu, Yichun
AU - Wang, Xiaojun
PY - 2013/1/1
Y1 - 2013/1/1
N2 - Two series of K1-xNaxSrPO4:0.005Eu 2+ and K0.4Na0.6Sr0.995-yPO 4:0.005Eu2+, yTb3+ phosphors are synthesized via a high-temperature solid-state reaction. Their emission color can be tuned from deep blue to blue-green by modulating the crystal field strength and energy transfer. Partial substitution of K+ with Na+ results in a contraction and distortion of the unit cell of the K1-xNa xSr0.995PO4:0.005Eu2+ host, tuning the emission from 426 to 498 nm. The red-shifted emission is attributed to an increased crystal field splitting for Eu2+ in a lowered symmetry crystal field. The tunable emission is further demonstrated in the cathodoluminescence spectra, which indicates that the luminescence distribution of the K1-xNaxSr0.995PO4:0. 005Eu2+ phosphor is very homogenous. Additionally, utilizing the principle of energy transfer, the emission color can be further tuned by co-doping with Tb3+. The chromaticity coordinates for the co-doped phosphor, K0.4Na0.6Sr0.995-yPO 4:0.005Eu2+, yTb3+, can be adjusted from (0.202, 0.406) for y = 0 to (0.232, 0.420) for y = 0.09. The energy transfer processes from the sensitizer (Eu2+) to the activator (Tb 3+) are studied and demonstrated to have a resonance-type dipole-dipole interaction mechanism, with the critical distance of the energy transfer calculated to be 12.46 Å using a concentration quenching method.
AB - Two series of K1-xNaxSrPO4:0.005Eu 2+ and K0.4Na0.6Sr0.995-yPO 4:0.005Eu2+, yTb3+ phosphors are synthesized via a high-temperature solid-state reaction. Their emission color can be tuned from deep blue to blue-green by modulating the crystal field strength and energy transfer. Partial substitution of K+ with Na+ results in a contraction and distortion of the unit cell of the K1-xNa xSr0.995PO4:0.005Eu2+ host, tuning the emission from 426 to 498 nm. The red-shifted emission is attributed to an increased crystal field splitting for Eu2+ in a lowered symmetry crystal field. The tunable emission is further demonstrated in the cathodoluminescence spectra, which indicates that the luminescence distribution of the K1-xNaxSr0.995PO4:0. 005Eu2+ phosphor is very homogenous. Additionally, utilizing the principle of energy transfer, the emission color can be further tuned by co-doping with Tb3+. The chromaticity coordinates for the co-doped phosphor, K0.4Na0.6Sr0.995-yPO 4:0.005Eu2+, yTb3+, can be adjusted from (0.202, 0.406) for y = 0 to (0.232, 0.420) for y = 0.09. The energy transfer processes from the sensitizer (Eu2+) to the activator (Tb 3+) are studied and demonstrated to have a resonance-type dipole-dipole interaction mechanism, with the critical distance of the energy transfer calculated to be 12.46 Å using a concentration quenching method.
KW - Cathodoluminescence spectra
KW - Crystal field strength
KW - Emission color
KW - High-temperature solid-state reaction
KW - Lowered symmetry crystal field
KW - Luminescence distribution
KW - Phosphors
KW - Red-shifted emission
UR - https://digitalcommons.georgiasouthern.edu/physics-facpubs/40
U2 - 10.1039/C3TC30128A
DO - 10.1039/C3TC30128A
M3 - Article
SN - 2050-7526
VL - 1
JO - Journal of Materials Chemistry C
JF - Journal of Materials Chemistry C
ER -