XIA Tian, CAO Wang-he, LUO Xi-xian, TIAN Ying. Combustion Synthesis and Luminescence Characteristic of <em>Ln</em><sub>2</sub>O<sub>2</sub>S:<em>RE</em><sup>3+</sup> (<em>Ln</em>= Gd,La; <em>RE</em>=Eu,Tb) X-ray Phosphors[J]. Chinese Journal of Luminescence, 2005,26(2): 194-198
XIA Tian, CAO Wang-he, LUO Xi-xian, TIAN Ying. Combustion Synthesis and Luminescence Characteristic of <em>Ln</em><sub>2</sub>O<sub>2</sub>S:<em>RE</em><sup>3+</sup> (<em>Ln</em>= Gd,La; <em>RE</em>=Eu,Tb) X-ray Phosphors[J]. Chinese Journal of Luminescence, 2005,26(2): 194-198DOI:
Combustion Synthesis and Luminescence Characteristic of Ln2O2S:RE3+ (Ln= Gd,La; RE=Eu,Tb) X-ray Phosphors
Combustion synthesis technology overcame the disadvantages of high temperature solid-state reaction
and resolved the serious pollution of sulfur for the environment
what's more
phosphor powders of the small particle size were achieved
which could enhance the resolution of imaging system to some extent. X-ray phosphor powders of
Ln
2
O
2
S:
RE
3+
(where
Ln
=La
Gd;
RE
=Eu
Tb)were prepared by combustion reactions. In detail
different kinds of rare earth nitrates were weighed and mixed in stoichiometric amounts
where the doses of the dopant were 0.15%
0.35% and 0.5% in mol fraction
respectively. The nitrates were molten during drying in an oven at 100℃
and during the cooling of these mixed nitrates reactants
appropriate amounts of organic fuel
such as dithio-oxamide were added
mixed and ground along with the nitrates
where molar ratio of dithiooxamide to the rare earth nitrates was 2. The mixtures were heated in an air tube furnace with the ignition temperature of 300~350℃. To evaluate the effects of heat treatment
the combustion-prepared powders were also heated to 500~700℃ in air. The samples were characterized by X-ray diffraction (XRD)
scanning electronic microscope (SEM)
photoluminescence(PL) and X-ray excited luminescence (XEL). XRD results showed the oxide sulfide phases only when the sintering temperatures were lower than 500℃
which avoided the defect of high sintering temperature. SEM results showed a loose
porous agglomeration and a continuous three-dimensional network
and the primary particlesize is not more than 50nm. PL spectra showed the characteristic emission of rare earth activation ions
respectively. To our satisfaction
the PL intensities were nearly the same as some commercial X-ray phosphors. XEL spectra showed the same characteristic emission
although their luminescence principals were different each other. In addition
the absorption coefficients and the dopant concentration doped of these samples weren't the same for X-ray excitation
therefore
their light emission efficiencies were also different.