IP Library Granted Patent US 9,845,334
Granted Patent B1
US 9,845,334 · App. 15/289,611 · Granted Dec 19, 2017

High-efficiency organic glass scintillators

Inventors: Patrick L. Feng (Livermore, CA); Joseph S. Carlson (Morgan Hill, CA)
Assignee: National Technology & Engineering Solutions of Sandia, LLC
C07F9/46C07C209/08C07C211/54C07F7/0809C07F7/0827C09K11/06G01T1/20G01T3/06C09K2211/1011C09K2211/1014
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Quick Facts
Patent No.
US 9,845,334
App. No.
15/289,611
Granted
Dec 19, 2017
Kind
B1
Abstract

A new family of neutron/gamma discriminating scintillators is disclosed that comprises stable organic glasses that may be melt-cast into transparent monoliths. These materials have been shown to provide light yields greater than solution-grown trans-stilbene crystals and efficient PSD capabilities when combined with 0.01 to 0.05% by weight of the total composition of a wavelength-shifting fluorophore. Photoluminescence measurements reveal fluorescence quantum yields that are 2 to 5 times greater than conventional plastic or liquid scintillator matrices, which accounts for the superior light yield of these glasses. The unique combination of high scintillation light-yields, efficient neutron/gamma PSD, and straightforward scale-up via melt-casting distinguishes the developed organic glasses from existing scintillators.

Claims (35)

1. A glass scintillator material comprising:

a compound, including:

a central species selected from the group consisting of: silicon, phosphorus, nitrogen, tin, germanium; an oxide, salt, or alkyl salt of silicon, phosphorus, nitrogen, tin, or germanium; or a rotationally symmetric organic species, or combination of any of the these;

a luminescent organic group bonded to the central species or to an optional organic linker group;

the optional organic linker group, if present, is bonded to the central species and the luminescent organic group;

wherein the compound is in the form of an amorphous glass and is capable of generating luminescence in the presence of ionizing radiation.

2. The glass scintillator material of claim 1 , wherein the luminescent organic group is selected from the group consisting of: quaterphenyl, terphenyl, trans-stilbene, naphthalene, anthracene, truxene, triphenylene, 1,3,5-triphenylbenzene, spirobifluorene, fluorene, carbazole, coumarin, anthracene, naphthalene, biphenyl, coumarin, phenyloxazole, phenyloxadiazole, 2,5-diphenyloxazole, 9,9′-dialkylfluorene, 9,9′-diarylfluorene, 2-aryl-9,9′-dialkylfluorene, 2-aryl-9,9′-diarylfluorene, 7-aryl-9,9′-dialkylfluorene, 7-aryl-9,9′-diarylfluorene, 7-alkyl-9,9′-dialkylfluorene, 7-alkyl-9,9′-diarylfluorene, 9,10-diphenylanthracene, 2,5-diphenyl-1,3,4-oxadiazole, p-terphenyl, salicylic acid, and methyl salicylate and analogs thereof.

3. The glass scintillator material of claim 1 , wherein the central species is adamantane, benzene, truxene, triphenylene, spiro-bifluorene, and analogs thereof.

4. The glass scintillator material of claim 1 , wherein the central species and the luminescent organic group are selected to inhibit pi-pi stacking in the compound and an overall three-dimensional structure of the compound inhibits pi-pi stacking.

5. The glass scintillator material of claim 1 , wherein the central species is selected from phosphine oxide, tin, or silicon, and the luminescent organic group is an aromatic group.

6. The glass scintillator material of claim 1 , wherein the luminescent organic group is a polycyclic group comprising one or more benzylic carbons and at least one benzylic carbon is substituted with an organic group.

7. The glass scintillator material of claim 6 , wherein the organic group contains a fluorene or biphenyl sub-unit possessing alkylation at a benzylic, or double benzylic position.

8. The glass scintillator material of claim 1 , wherein the central atom or species bonds to the luminescent organic groups in a tripodal or tetrahedral geometry.

9. The glass scintillator material of claim 6 , wherein the compound has C3 rotational symmetry.

10. The glass scintillator material of claim 1 , wherein the compound produces a light yield of 15,000 photons/MeVee to 40,000 photons/MeVee with a trans-stilbene reference.

11. The glass scintillator material of claim 1 , wherein the compound has a glass transition temperature of 25° C. to 300° C.

12. The glass scintillator material of claim 1 , further comprising a wavelength shifter.

13. The glass scintillator material of claim 1 , wherein the amorphous glass has a thickness of 1 micrometer to 1 meter.

14. The glass scintillator material of claim 1 , wherein the amorphous glass is capable of neutron and gamma pulse-shape discrimination, at 33 keVee to 30 MeVee.

15. A method of making a compound, comprising:

functionalizing a luminescent organic group;

reacting the functionalized luminescent organic group with a central species to produce a compound with tripodal or tetrahedral geometry wherein one or more of the luminescent organic groups are bonded to the central species;

wherein the central species is selected from the group consisting of: silicon, phosphorus, nitrogen, tin, germanium; an oxide, salt, or alkyl salt of silicon, phosphorus, nitrogen, tin, or germanium; or a rotationally symmetric organic species, or combination of any of these;

wherein the luminescent organic group is selected to inhibit pi-pi stacking of the compound.

16. The method of claim 15 , further comprising melting the compound and cooling the compound or sublimating the compound and condensing the compound to form an amorphous glass.

17. The method of claim 15 , wherein the luminescent organic group is a polycyclic group comprising one or more benzylic carbons and at least one benzylic carbon is substituted with an organic group that is selected to inhibit pi-pi stacking in the compound.

18. The method of claim 16 , further comprising adding a wavelength shifter to the material prior to the cooling step.

19. A method for conducting scintillation, the method comprising:

generating luminescence with a glass scintillating compound in the presence of ionizing radiation, the glass scintillating compound including:

a central species selected from the group consisting of: silicon, phosphorus, nitrogen, tin, germanium; an oxide, salt, or alkyl salt of silicon, phosphorus, nitrogen, tin, or germanium; or a rotationally symmetric organic species, or combination of any of these;

a luminescent organic group bonded to the central species or to an optional organic linker group;

the optional organic linker group if present is bonded to the central species and the luminescent organic group;

wherein the compound is in the form of an amorphous glass and is capable of scintillation;

detecting photons from the glass scintillating compound with a photodetector.

20. The method of claim 19 , further comprising conducting neutron and gamma pulse-shape discrimination with the glass scintillating compound at 33 keVee to 30 MeVee.

Assignments (3)
CHANGE OF NAME Recorded Sep 20, 2017
From: SANDIA CORPORATION
To: NATIONAL TECHNOLOGY & ENGINEERING SOLUTIONS OF SANDIA, LLC
Reel/Frame 043923/0649 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 15, 2017
From: FENG, PATRICK L.; CARLSON, JOSEPH S.
To: SANDIA CORPORATION
Reel/Frame 041580/0876 →
CONFIRMATORY LICENSE Recorded Mar 15, 2017
From: SANDIA CORPORATION
To: U.S. DEPARTMENT OF ENERGY
Reel/Frame 041582/0557 →
Continuity (1)
Provisional Application 62356996 · Jun 30, 2016