High-efficiency organic glass scintillators

Patent metadata

Field	Value
Publication number	US-9845334-B1
Application number	US-201615289611-A
Country	US
Kind code	B1
Filing date	Oct 10, 2016
Priority date	Jun 30, 2016
Publication date	Dec 19, 2017
Grant date	Dec 19, 2017

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.

First claim

It is claimed:

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.

Assignees

• Nat Tech & Eng Solutions Sandia Llc

Inventors

• Feng Patrick L
• Carlson Joseph S

Classifications

• C09K11/06 Primary

  containing organic luminescent materials · CPC title

• C09K2211/1011

  Condensed systems · CPC title

• G01T1/20

  with scintillation detectors · CPC title

• C09K2211/1014

  bridged by heteroatoms, e.g. N, P, Si or B · CPC title

• C07F7/0827

  Syntheses with formation of a Si-C bond · CPC title