IP Library Granted Patent US 9,751,761
Granted Patent B2
US 9,751,761 · App. 14/442,251 · Granted Sep 5, 2017

Iron chalcogenide nanocomposite and method for preparing same

Inventors: Jae-Beom Lee (Hwaseong-si, KR); Xiang Mao (Miryang-si, KR)
Assignee: PUSAN NATIONAL UNIVERSITY INDUSTRY-UNIVERSITY COOPERATION FOUNDATION
C01B19/04B82Y30/00C01B19/007C09K11/881C01P2002/72C01P2002/84C01P2002/85C01P2002/88C01P2004/01C01P2004/04C01P2004/52C01P2004/64
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Quick Facts
Patent No.
US 9,751,761
App. No.
14/442,251
Granted
Sep 5, 2017
Kind
B2
Abstract

The present invention relates to an iron chalcogenide nanocomposite with photoluminescent properties. The present invention also relates to a method for preparing the iron chalcogenide nanocomposite. The method includes (a) dissolving a Fe precursor in an organic solvent to form a Fe solution, (b) dissolving a chalcogen powder or a chalcogen precursor in an organic solvent to form a chalcogen solution, (c) dropwise injecting the Fe solution into the chalcogen solution to prepare a mixture solution in which an iron chalcogenide is formed, and (d) purifying the iron chalcogenide from the mixture solution.

Claims (17)

1. A method for preparing an iron chalcogenide nanocomposite, comprising

(a) dissolving a Fe precursor in an organic solvent to form a Fe solution,

(b) dissolving a chalcogen powder or a chalcogen precursor in an organic solvent to form a chalcogen solution,

(c) dropwise injecting the Fe solution into the chalcogen solution to prepare a mixture solution in which an iron chalcogenide is formed, and

(d) purifying the iron chalcogenide from the mixture solution.

2. The method according to claim 1 , wherein, in step (a) or (b), the organic solvent is heated to 100 to 140° C.

3. The method according to claim 1 , wherein the organic solvent used in step (a) or (b) is selected from the group consisting of ether-based compounds (CnOCn, Cn: hydrocarbon, 4≦n≦30), hydrocarbons (C n H 2n+2 , 7≦n≦30), unsaturated hydrocarbons (C n H 2n , 7≦n≦30), and organic acids (C n COOH, C n : hydrocarbon, 5≦n≦30).

4. The method according to claim 3 , wherein the ether-based compounds are selected from the group consisting of trioctylphosphine oxide (TOPO), alkylphosphines, octyl ether, benzyl ether, and phenyl ether.

5. The method according to claim 3 , wherein the hydrocarbons are selected from the group consisting of hexadecane, heptadecane, and octadecane.

6. The method according to claim 3 , wherein the unsaturated hydrocarbons are selected from the group consisting of octene, heptadecene, and octadecene.

7. The method according to claim 3 , wherein the organic acids are selected from the group consisting of oleic acid, lauric acid, stearic acid, mysteric acid, and hexadecanoic acid.

8. The method according to claim 3 , wherein, in step (c), the Fe solution is injected dropwise into the chalcogen solution, followed by heating to 250 to 400° C. to prepare a mixture solution in which an iron chalcogenide is formed.

9. The method according to claim 3 , wherein, in step (c), a surfactant is added to and mixed with the mixed solution.

10. The method according to claim 9 , wherein the surfactant is an organic acid selected from the group consisting of oleic acid, lauric acid, stearic acid, mysteric acid, and hexadecanoic acid or is a mixture of these organic acids.

11. The method according to claim 3 , wherein the Fe precursor and the chalcogen precursor are used in a molar ratio of 1:1-2.

12. The method according to claim 3 , wherein the chalcogen is S, Se or Te.

13. The method according to claim 12 , wherein the iron chalcogenide is FeSe or FeSe 2 .

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 12, 2015
From: LEE, JAE-BEOM; MAO, XIANG
To: PUSAN NATIONAL UNIVERSITY INDUSTRY-UNIVERSITY COOPERATION FOUNDATION
Reel/Frame 035618/0976 →
Priority Claims (1)
KR 10-2012-0101089 · Sep 12, 2012 · national
Continuity (1)
Related Publication 20160280543A1 · Sep 29, 2016