Method of preparing metallic oxide phosphor

1. A method for preparing a metal oxide phosphor, the method comprising the steps of:

(a) preparing a solution comprising a metal precursor compound and an ionic material; and

(b) heating the solution under pressure using microwaves.

2. The method of claim 1 , wherein the metal precursor compound is selected from among the group consisting of a carbonate, a nitrate, a chloride, a hydroxide, an oxalate, an acetate, or alkoxide of one of Mg, Ca, Sr, Ba, Zn, Mn, Al, Ga, B, Y, La, Ce, Gd, Eu, Ce, Pr, Dy, Tm, Tb, Er, Yb, Sm, Er, Bi, Sb, Ge, Si, and Sn; tetraethyl orthosilicate (TEOS); tetramethyl orthosilicate (TMOS); H 3 BO 3 ; NH 4 B 5 O 8 ; H 3 PO 4 ; NH 4 H 2 PO 4 ; (NH 4 ) 2 HPO 4 ; NH 4 H 2 PO 4 ; (NH 4 ) 3 PO 4 ; VO(SO 4 ); Na 3 VO 4 ; NaVO 3 ; NH 4 VO 3 ; Na 2 (NH 4 ) 4 V 10 O 28 ; and compounds of at least two materials selected from those listed above.

3. The method of claim 1 , wherein a dipole moment of the ionic material is in a range of approximately 5 debye to approximately 80 debye.

4. The method of claim 1 , wherein the ionic material comprises at least one ion selected from the group consisting of alkylpyridinium, (trifluoromethane sulfonyl)imide ([N(SO 2 CF 3 ) 2 ] − ), (1-alkyl-3-methylimidazolium) + , and alkylsulfonate and a counter anion or counter cation of the ion.

5. The method of claim 1 , wherein a solvent of the solution comprises at least one selected from the group consisting of water, methanol, ethanol, ethylene glycol, diethylene glycol, glycerol, and 1,4-butylene glycol.

6. The method of claim 1 , wherein a molar ratio of the metal precursor compound to the ionic material is in a range of approximately 100:1 to approximately 1:10 in the solution comprising the metal precursor compound and the ionic material.

7. The method of claim 1 , wherein the solution further comprises a surfactant.

8. The method of claim 7 , wherein the surfactant comprises at least one selected from the group consisting of citric acid, acetic acid (CH 3 COOH), sodium acetate (NaCOOCH 3 ), ammonium acetate (NH 4 COOCH 3 ), oleic acid, sodium oleate (C 17 H 33 COONa), ammonium oleate (C 17 H 33 COONH 4 ), ammonium succinate (NH 4 COOCH 2 CH 2 COONH 4 ), polyacrylate, glycine, acylglutamate and sodium dodecylbenzenesulfonate.

9. The method of claim 1 , wherein a frequency of the microwave is in a range of approximately 300 MHz to approximately 300 GHz.

10. The method of claim 1 , wherein the heating is conducted for approximately 5 minutes to 60 minutes using microwaves in step (b).

11. The method of claim 1 , wherein the heating is conducted at approximately 20 PSI to approximately 800 PSI using microwave in step (b).

12. The method of claim 1 , comprised of the heating being conducted at approximately 150° C. to 300° C. using microwaves in step (b).

13. The method of claim 1 , further comprising heat-treating the resultant of step (b).

14. The method of claim 13 , wherein the heat-treatment is performed at approximately 500° C. to approximately 1500° C.

15. The method of claim 1 , wherein the particle size of the metallic oxide is in the range of approximately 20 nm to approximately 1000 nm.

16. The method of claim 1 , wherein the metal oxide phosphor has particles in a spherical shape.

17. The method of claim 1 , wherein the metallic oxide phosphor is selected from the group consisting of (Gd,Y,Sc,Lu,La)BO 3 :Eu 3+ , (Gd,Y,Sc,Lu,La) 2 O 3 :Eu 3+ , (Gd,Y,Sc,Lu,La)(P,V)O 4 :Eu 3+ , (Ca,Sr,Ba) 2 P 2 O 7 :Eu 2+ ,Mn 2+ , (Ca,Sr,Ba) 5 (PO 4 ) 3 (Cl,FlBr,OH):Eu 2+ , Mn 2+ , ZnSiO 3 :Mn 2+ , (Ca,Sr,Ba)MgAl 10 O 17 :Eu 2+ ,Mn 2+ , (Ca,Sr,Ba)Al 2 O 4 :Eu 2+ , (Ca,Sr,Ba)BPO 5 :Eu 2+ ,Mn 2+ , Y 3 Al 5 O 12 :Ce 3+ , (Ca,Sr,Ba) 2 SiO 4 :Eu 2+ , and (Ca,Sr,Ba) 3 SiO 5 :Eu 2+ .