Red-luminescent phosphor with long afterglow and fabrication method thereof
View Patent ↗A red-luminescent long-afterglow phosphor, represented by Mg x Zn y Ge z O 3 : aMn 2+ , bEu 3+ , cR 3+ . The phosphor is a kind of oxide compound based white powder. The phosphor powder synthesis process is environmentally friendly, no sintering-assisted gas required and no harmful gas generated during or after sintering. The phosphor powder can be excited by UV and is chemically stable.
1 . A phosphor having a chemical formula: Mg x Zn y Ge z O 3 : aMn 2+ , bEu 3+ , cR 3+ , wherein R is an element selected from the group consisting of erbium (Er), thulium (Tm), holmium (Ho), samarium (Sm), praseodymium (Pr), ytterbium (Yb) and neodymium (Nd); Mg x Zn y Ge z O 3 is a host material; and x, y, z, a, b and c are each independently a positive number, wherein a is a molar ratio of Mn 2+ to the host material, b is a molar ratio of Eu 3+ to the host material, and c is a molar ratio of R 3+ to the host material, wherein 0.95≤x+y≤0.99, 0.3≤x≤0.7.
2 . The phosphor according to claim 1 , wherein 1.00≤z≤1.5.
3 . The phosphor according to claim 1 , wherein 0.0001≤a≤0.02.
4 . The phosphor according to claim 1 , wherein 0.0001≤b≤0.05.
5 . The phosphor according to claim 1 , wherein 0.0001≤c≤0.005.
6 . The phosphor according to claim 1 , wherein c<b, and b is at least 2 times greater than c.
7 . The phosphor according to claim 1 , wherein 0.95≤x+y≤0.99, 0.3≤x≤0.7, 1.0≤z≤1.5, 0.0001≤a≤0.02, 0.0001≤b≤0.05, 0.0001≤c≤0.005, c<b, wherein b is at least 2 times greater than c.
8 . The phosphor according to claim 1 , wherein R is Tm, 0.50≤x≤0.60, 0.95≤x+y≤0.99, 1.0≤z≤1.3, 0.001≤a≤0.003, 0.006≤b≤0.01, 0.0002≤c≤0.001.
9 . The phosphor according to claim 1 , wherein R is Tm, 0.35≤x≤0.42, 0.95≤x+y≤0.99, 1.0≤z≤1.3, 0.005≤a≤0.02, 0.002≤b≤0.008, 0.0002≤c≤0.001.
10 . The phosphor according to claim 1 , wherein R is Er, 0.35≤x≤0.57, 0.95≤x+y≤0.99, 1.0≤z≤1.3, 0.001≤a≤0.008, 0.005≤b≤0.01, 0.0002≤c≤0.001.
11 . The phosphor according to claim 1 , wherein R is Ho, 0.35≤x≤0.57, 0.95≤x+y≤0.99, 1.0≤z≤1.3, 0.001≤a≤0.008, 0.005≤b≤0.01, 0.0002≤c≤0.001.
12 . The phosphor according to claim 1 , wherein R is Pr, 0.35≤x≤0.57, 0.95≤x+y≤0.99, 1.0≤z≤1.3, 0.001≤a≤0.008, 0.005≤b≤0.01, 0.0002≤c≤0.001.
13 . The phosphor according to claim 1 , wherein R is Nd, 0.35≤x≤0.57, 0.95≤x+y≤0.99, 1.0≤z≤1.3, 0.001≤a≤0.008, 0.005≤b≤0.01, 0.0002≤c≤0.001.
14 . The phosphor according to claim 1 , wherein R is Sm, 0.35≤x≤0.50, 0.95≤x+y≤0.99, 1.0≤z≤1.3, 0.001≤a≤0.008, 0.002≤b≤0.01, 0.0001≤c≤0.002.
15 . The phosphor according to claim 1 , wherein R is Yb, 0.35≤x≤0.50, 0.95≤x+y≤0.99, 1.0≤z≤1.3, 0.001≤a≤0.008, 0.0002≤b≤0.01, 0.0001≤c≤0.001.
16 . The phosphor according to claim 1 , wherein the phosphor is a powder.
17 . The phosphor according to claim 1 , wherein the phosphor has an emission peak between 650-700 nm.
18 . The phosphor according to claim 1 , wherein the phosphor has an emission peak between 670-690 nm.
19 . A method of preparing a phosphor, the method comprising: contacting a Mg 2+ salt of x mol, a Zn 2+ salt of y mol, GeO 2 , a Mn 2+ salt, Eu 2 O 3 , and a metal oxide selected from the group consisting of Er 2 O 3 , Tm 2 O 3 , Ho 2 O 3 , Sm 2 O 3 , Pr 6 O 11 , Yb 2 O 3 and Nd 2 O 3 , wherein each of the Mg 2+ salt and the Zn 2+ salt is independently an oxide, hydroxide, or carbonate salt; and the Mn 2+ salt is an oxide or carbonate salt; thereby forming a mixture; and sintering the mixture thereby forming the phosphor having a chemical formula: Mg x Zn y Ge z O 3 : aMn 2+ , bEu 3+ , cR 3+ ,
wherein R is an element selected from the group consisting of Er, Tm, Ho, Sm, Pr, Yb and Nd; Mg Zn Ge z O 3 is a host material; and x, y, z, a, b and c are each independently a positive number, wherein a is a molar ratio of Mn 2+ to the host material, b is a molar ratio of Eu 3+ to the host material, c is a molar ratio of R 3+ to the host material, 0.95≤x+y≤0.99, and 0.3≤x≤0.7.