Low temperature thermal conductive inks
View Patent ↗Novel copper alkoxide compound based ink formulations and their chemical syntheses are disclosed. The method of using the ink formulations to print conducting copper metal lines with standard ink jet printing and curing at <150° C. is also disclosed.
1. A precursor containing two or more copper alkoxides having different metallization temperatures, and each alkoxide having a formula Cu—O—R;
wherein —O—R is selected from the group consisting of a radical of a secondary alcohol having an alkyl group of C 4 to C 12 ; a primary alcohol giving CuOCH 2 CH(Me)R′; and mixtures thereof;
wherein R′ is selected from the group consisting of an alkyl having 1 to 8 carbons, an alkenyl having 2 to 8 carbons, an alkynyl having 2 to 8 carbons, and combinations thereof.
2. The precursor of claim 1 wherein the secondary alcohol is an asymmetric, saturated, alkyl group of C 4 to C 12 .
3. The precursor of claim 1 wherein the secondary alcohol is selected from the group consisting of butanol, pentanol, hexanol, heptanol, octanol, nonanol, and mixtures thereof.
4. The precursor of claim 1 wherein the primary alcohol is selected from the group consisting of 2-methylbutanol, 2-methyl-1-propanol, and mixtures thereof.
5. The precursor of claim 1 is selected from the group consisting of copper-2-pentanoxide, copper-2-hexanoxide, copper-2-octanoxide, Cu-2-nonanoxide, copper-3-methyl-2-pentanoxide, copper-4-dimethyl-2-pentanoxide, copper-4-methyl-2-pentanoxide, copper-5-methyl-2-hexanoxide, copper-methyl-1-butanol, copper-2-methyl-1-pentanoxide and mixtures thereof.
6. The precursor of claim 1 has a metallization temperature less than 150° C.
7. The precursor of claim 1 containing a solvent selected from the group consisting of toluene, xylene, polyalkylaromatics, alkoxy aromatics, tertiary amines, hexane, secondary amines, primary amines, diamines, triamines, nitriles, silylnitriles, isocyanates, ethers, ketones, alcohols, diols, triols, phenols, amides, esters, carbamates, carbonates, diketones aldehydes, silanes, pyridines, pyrrolidines, imidazoles, pyrimidines, analines, alkanes, haloalkynes, siloxanes alkenes, dienes, trienes, glymes and mixtures thereof.
8. The precursor of claim 7 wherein the solvent has a boiling temperature higher than metallization temperature of the precursor.
9. A process for synthesizing a precursor containing at least one copper alkoxide comprising reacting an alcohol with a copper compound selected from a group consisting of a bi-nuclear copper organometallic compound; copper mesitylene; copper tertiary alkoxide made from tertiary alcohol; and mixtures thereof.
10. The process of claim 9 wherein the bi-nuclear copper organometallic compound is [—CuNMe 2 SiMe 2 CHSiMe 3 CuNMe 2 SiMe 2 CHSiMe 3 —].
11. The process of claim 9 wherein the tertiary alcohol is an alkyl group of C 4 to C 12 .
12. The process of claim 9 wherein the alcohol is an asymmetric, saturated, alkyl group of C 4 to C 12 .
13. The process of claim 9 wherein the alcohol is a secondary alcohol selected from the group consisting of butanol, pentanol, hexanol, heptanol, octanol, nonanol, and mixtures thereof.
14. The process of claim 9 wherein the alcohol is a primary alcohol selected from the group consisting of 2-methylbutanol, 2-methyl-1-propanol, and mixtures thereof.
15. The process of claim 9 wherein the precursor has a metallization temperature less than 150° C.
16. The process of claim 9 wherein the precursor contains two or more of the at least one copper alkoxide having different metallization temperatures.
17. The process of claim 9 wherein the precursor of claim 1 is selected from the group consisting of copper-2-pentanoxide, copper-2-hexanoxide, copper-2-octanoxide, Cu-2-nonanoxide, copper-3-methyl-2-pentanoxide, copper-4-dimethyl-2-pentanoxide, copper-4-methyl-2-pentanoxide, copper-5-methyl-2-hexanoxide, copper-methyl-1-butanol, copper-2-methyl-1-pentanoxide and mixtures thereof.
18. The process of claim 9 wherein the precursor further contains a solvent selected from the group consisting of toluene, xylene, polyalkylaromatics, alkoxy aromatics, tertiary amines, hexane, secondary amines, primary amines, diamines, triamines, nitriles, silylnitriles, isocyanates, ethers, ketones, alcohols, diols, triols, phenols, amides, esters, carbamates, carbonates, diketones aldehydes, silanes, pyridines, pyrrolidines, imidazoles, pyrimidines, analines, alkanes, haloalkynes, siloxanes alkenes, dienes, trienes, glymes and mixtures thereof.
19. A precursor containing at least one copper alkoxide selected from the group consisting of copper-2-hexanoxide, copper-2-octanoxide, Cu-2-nonanoxide, copper-3-methyl-2-pentanoxide, copper-4-dimethyl-2-pentanoxide, copper-4-methyl-2-pentanoxide, copper-5-methyl-2-hexanoxide, copper-methyl-1-butanol, copper-2-methyl-1-pentanoxide, a copper alkoxide having formula Cu—O—R, and mixtures thereof;
wherein —O—R is a primary alcohol selected from the group consisting of 2-methylbutanol, 2-methyl-1-propanol, and mixtures thereof; and mixtures thereof.
20. The precursor of claim 19 has a metallization temperature less than 150° C.
21. Precursor of claim 19 containing a solvent selected from the group consisting of toluene, xylene, polyalkylaromatics, alkoxy aromatics, tertiary amines, hexane, secondary amines, primary amines, diamines, triamines, nitriles, silylnitriles, isocyanates, ethers, ketones, alcohols, diols, triols, phenols, amides, esters, carbamates, carbonates, diketones aldehydes, silanes, pyridines, pyrrolidines, imidazoles, pyrimidines, analines, alkanes, haloalkynes, siloxanes alkenes, dienes, trienes, glymes and mixtures thereof.
22. The precursor of claim 19 wherein the solvent has a boiling temperature higher than metallization temperature of the precursor.
23. The precursor of claim 19 contains two or more of the at least one copper alkoxide having different metallization temperatures.