Direct pyrolysis route to GaN quantum dots
Colloidal nanocrystals or “quantum dots” of GaN are directly produced by heating amidogallium dimer, i.e., (Ga 2 [N(CH 3 ) 2 ] 6 ), in the presence of a functional amine. The GaN quantum dots obtained, which comprise isolated particles 2-3 nm in diameter with a relative broad size distribution (e.g., 20% standard deviation) exhibit strong exciton confinement.
1. The process comprising heating an amidogallium oligomer having no more than 10 amidogallium groups in the presence of ammonia, a primary amine, a secondary amine or mixtures thereof in the liquid phase to directly produce colloidal GaN nanocrystals.
2. The process of claim 1 , wherein the amidogallium oligomer is an amidogallium trimer, quatramer, pentamer, hexamer, heptamer or mixture thereof.
3. The process of claim 2 , wherein the amidogallium oligomer is amidogallium dimer.
4. The process of claim 3 , wherein pyrolysis is accomplished by heating the amidogallium oligomer to a temperature of about 250-450° C.
5. The process of claim 4 , wherein the amidogallium oligomer is dissolved in a solvent.
6. The process of claim 5 , wherein the solvent is a C 16 -C 40 hydrocarbon, a primary, secondary and tertiary alkyl amines having a molecular weight of about 150 to 500 Daltons, an alkyl phosphine having a molecular weight of about 150 to 500 Daltons, or a mixture thereof.
7. The process of claim 6 , wherein the solvent is octadecane, trioctylamine, hexadecyl amine, trioctylphosphine or a mixture thereof.
8. The process of claim 4 , wherein a capping ligand is included in the solvent, the capping ligand being a Lewis base.
9. The process of claim 8 , wherein the capping ligand is a thiol, ester, amine, alcohol, aldehyde, ketone or mixture thereof.
10. The process of claim 9 , wherein the capping ligand is trioctylphosphine oxide.
11. The process of claim 1 , wherein the amidogallium oligomer is dissolved in a solvent.
12. The process of claim 11 , wherein the solvent is a C 16 -C 40 hydrocarbon, a primary, secondary and tertiary alkyl amines having a molecular weight of about 150 to 500 Daltons, an alkyl phosphine having a molecular weight of about 150 to 500 Daltons, or a mixture thereof.
13. The process of claim 12 , wherein the solvent is octadecane, trioctylamine, hexadecyl amine, trioctylphosphine or a mixture thereof.
14. The process of claim 1 , wherein a capping ligand is included in the solvent, the capping ligand being a Lewis base.
15. The process of claim 14 , wherein the capping ligand is a thiol, ester, amine, alcohol, aldehyde, ketone or mixture thereof.
16. The process of claim 15 , wherein the capping ligand is trioctylphosphine oxide.