Preparation of high emission efficiency alkaline earth metal thiogallate phosphors

• US 6,544,438 B2
• Filed: 05/17/2001
• Issued: 04/08/2003
• Est. Priority Date: 08/02/2000
• Status: Expired due to Term

• Current Assignee: Lightscape Materials, Inc. (DuPont de Nemours, Inc.)
• Original Assignee: Sarnoff Corporation (SRI International, Inc.)
• Inventors: Yocom, Perry Niel, Zaremba, Diane
• Primary Examiner(s): Wood, Elizabeth D.
• Application Number:
  US09/860,018
• Publication Number:
  US 20020014614A1
• Time in Patent Office: 691 Days
• Field of Search: 252/301.45
• US Class Current: 252/301.40S
• CPC Class Codes: C09K 11/7703 with alkaline earth metals
• CPC Class Codes: C09K 11/7718 with alkaline earth metals
• CPC Class Codes: C09K 11/7731 with alkaline earth metals

Abstract

A method of forming high efficiency emission alkali metal activated gallium sulfide phosphors by including an excess of 1-7% of gallium. A solution of a soluble gallium salt is added to a sulfate precipitate of an alkali metal sulfate and firing in hydrogen sulfide atmosphere at temperatures up to about 900° C.

Claims

1. A method of making a high emission efficiency alkali metal thiogallate phosphor comprising

intimately mixing an alkali metal sulfate having a particle size below about 10 microns coated with an activator with gallium nitrate solution in an amount such that an excess of gallium is present in the final phosphor product, precipitating the activated alkali metal gallium sulfate, and firing in the presence of hydrogen sulfide.

2. A method according to claim 1 wherein an excess of 1 to 7% by weight of gallium is present in the phosphor.

3. A method of making high emission efficiency thiogallate phosphors comprising

a) forming an aqueous solution of a soluble alkali metal salt;

b) adding a sulfate to precipitate an alkali metal sulfate;

c) re-suspending the sulfate in water;

d) adding 2-5 mol % of the sulfate of a soluble activator salt,

e) precipitating the activator sale onto the alkali metal sulfate;

f) adding an excess of from about 0.1-7 percent by weight of a solution of a soluble gallium salt to the precipitate,

g) neutralizing the solution to form a precipitate, and

h) firing the precipitate in hydrogen sulfide to form the corresponding sulfide phosphor.

4. A method according to claim 3 wherein the alkali metal is selected from the group consisting of strontium, calcium and mixtures thereof.

5. A method according to claim 4 wherein the soluble salt is a nitrate.

6. A method according to claim 3 wherein the activator is europium and praseodymium.

7. A method according to claim 3 wherein step h) is carried out by heating at 800°

C. and then at 850°

C.

8. A method according to claim 3 wherein step h) is carried out by heating at 800°

C. and then at 900°

C.

9. A method according to claim 3 wherein an organic solvent is added to the sulfate solution of step f) prior to firing.

10. A high emission efficiency rare earth activated alkaline earth metal (M) thiogallate phosphor comprising

11. A phospor according to claim 10 wherein M is selected from the group consisting of strontium and calcium and mixtures thereof.

12. A phosphor according to claim 10 wherein said rare earth is selected from one or more of the group consisting of europium, cerium and praeseodymium.

13. An activated alkaline earth metal thiogallate phosphor having an excess of gallium of from 0.1 to 7 percent by weight of the alkaline earth metal.

14. A thiogallage phosphor according to claim 13 wherein said alkaline earth is strontium.

15. A thiogallage phosphor according to claim 13 wherein said alkaline earth is calcium.