초록 ▼

One embodiment of the present invention is a method of fabricating an integrated circuit. The method includes providing a substrate having a metal and dielectric damascene metallization layer and depositing substantially on the metal a cap. After deposition of the cap, the substrate is cleaned with

One embodiment of the present invention is a method of fabricating an integrated circuit. The method includes providing a substrate having a metal and dielectric damascene metallization layer and depositing substantially on the metal a cap. After deposition of the cap, the substrate is cleaned with a solution comprising an amine to provide a pH for the cleaning solution of 7 to about 13. Another embodiment of the presented invention is a method of cleaning substrates. Still another embodiment of the present invention is a formulation for a cleaning solution.

대표청구항 ▼

1. A method of cleaning a substrate having copper and dielectric damascene metallization, the surface of the copper having a cap of cobalt, cobalt alloy, nickel, nickel alloy, or cobalt-nickel alloy film, the method comprising: applying a cleaning solution to the substrate to remove at least one of

1. A method of cleaning a substrate having copper and dielectric damascene metallization, the surface of the copper having a cap of cobalt, cobalt alloy, nickel, nickel alloy, or cobalt-nickel alloy film, the method comprising: applying a cleaning solution to the substrate to remove at least one of defects and contamination, wherein the cleaning solution comprises an amine at a concentration from about 1 g/L to about 100 g/L to provide a pH for the cleaning solution of 7 to 13 and all values and subranges subsumed therein; a non-amine complexing agent at a concentration from about 0.5 g/L to about 50 g/L; a corrosion inhibitor at a concentration from about 0.01 g/L to about 20 g/L; a surface active agent at a concentration of 0.02 g/L to 2 g/L; an oxygen scavenger at a concentration from about 0.05 g/L to about 10 g/L, the oxygen scavenger comprising hydroxylamine, diethylhydroxylamine, methyl-ethylketoxime, carbohydrazide, chlorogenic acid, hydrazine, hydrazine salts, derivatives of hydrazine, caffeic acid, phytic acid, luteolin, and/or sulfites; a reducing agent at a concentration from about 0.1 g/L to about 10 g/L, the reducing agent comprising a boron containing reducing agent, a hypophosphite, and/or a thiosulfate; and a water soluble solvent at concentration from about 10 g/L to about 100 g/L. 2. A method of fabricating an integrated circuit, the method comprising: providing a substrate having a metal and dielectric damascene metallization layer using electroless deposition to deposit on the metal a cap comprising at least one of the elements cobalt and nickel;cleaning the substrate after deposition of the cap with a cleaning solution comprising a first amine; a second amine to provide a pH for the cleaning solution of 7 to 13 and all values and subranges subsumed therein; at least one complexing agent; one or more corrosion inhibitors; one or more surface active agents; at least one oxygen scavenger to lower the dissolved oxygen concentration in the cleaning solution to less than 1 ppm; at least one reducing agent selected from the group consisting of boron containing reducing agents, hypophosphites, and thiosulfate; and at least one water-soluble solvent. 3. The method of claim 2, wherein at least one of the one or more complexing agents is a non-amine. 4. The method of claim 2, wherein the one or more corrosion inhibitors protect the cap or retard the dissolution of the cap in the cleaning solution. 5. The method of claim 2, wherein the one or more surface active agents provide adequate wetting of the substrate. 6. The method of claim 2, wherein the concentration of the second amine is from about 1 g/L to about 100 g/L. 7. The method of claim 2, wherein the second amine is selected from the group consisting of primary alkylamines, secondary alkylamines, tertiary alkylamines, quarternary alkylamines, primary arylamines, alkanolamines, secondary alkanolamines, tertiary alkanolamines, ethanolamine, diethanolamine, triethanolamine, choline, amines with mixed alkyl and alkanol functionalities, tetramethylguanidine, and hydroxylamine. 8. The method of claim 2, wherein the at least one complexing agent concentration is from about 0.5 g/L to about 50 g/L. 9. The method of claim 2, wherein the at least one complexing agent concentration is a value from about 0.5 g/L to about 50 g/L, and the at least one complexing agent is selected from the group consisting of carboxylic acids, hydroxycarboxylic acids, amino acids, phosphonic acid, phytic acid, and organic acids wherein Ig K for CoL>2. 10. The method of claim 2, wherein the one or more corrosion inhibitors concentration is between 0.01 g/L to 20 g/L. 11. The method of claim 2, wherein the one or more corrosion inhibitors are selected from the group consisting of triazole, benzotriazole, methyl-benzotriazole, carboxy-benzotriazole, hydroxybenzotriazole, thiazole, mercaptobenzothiazole, polyvinylpyrrolidone, polyvinylalcohol, polyalkylimines, polyethylenimines, long chain alkylamines, tetrazoles, orthophosphates, metaphosphates, phosphites, phosphonates, silicates, alkylphosopohnates, alkoxysilanes, nitrites, and bicycloshexylammonium nitrite. 12. The method of claim 2, wherein the oxygen scavenger concentration is between 0.05 g/L to 10 g/L. 13. The method of claim 2, wherein the at least one oxygen scavenger is selected from the group consisting of hydroxylamine, diethylhydroxylamine, methyl-ethylketoxime, carbohydrazide, L-ascorbic acid, D-ascorbic acid, derivatives of ascorbic acid, chlorogenic acid, hydrazine, hydrazine salts, derivatives of hydrazine, caffeic acid, phytic acid, luteolin, and sulfites. 14. The method of claim 2, wherein the reducing agent concentration is between 0.1 g/L to 10 g/L. 15. The method of claim 2, wherein the cleaning solution further comprises a corrosion inhibitor present in a concentration between 0.01 g/L to about 10 g/L and an oxygen scavenger present in a concentration between about 0.05 g/L to about 10 g/L. 16. The method of claim 2, wherein the at least one corrosion inhibitor concentration is between 0.01 g/L to about 20 g/L and the at least one reducing agent concentration is between about 0.1 g/L to about 10 g/L. 17. The method of claim 2, wherein the oxygen scavenger concentration is between about 0.05 g/L to about 10 g/L and the reducing agent concentration is between about 0.1 g/L to about 10 g/L. 18. The method of claim 2, wherein the one or more corrosion inhibitors concentration is between about 0.01 g/L to about 20 g/L, the at least one oxygen scavenger concentration is between about 0.05 g/L to about 10 g/L, and the at least one reducing agent concentration is between about 0.1 g/L to about 10 g/L. 19. The method of claim 2, wherein the one or more surface active agents are present in a concentration of about 0.02 g/L to about 2 g/L for each of the one or more surface active agents and the one or more surface active agents are anionic, cationic, nonionic, amphoteric, or mixtures thereof. 20. The method of claim 2, wherein the at least one water soluble solvent is present in a concentration from about 10 g/L to about 100 g/L. 21. The method of claim 2, wherein the at least one water soluble solvent comprises primary alcohols, secondary alcohols, tertiary alcohols, polyols, ethylene glycol, dimethylsulfoxide, or propylenecarbonate. 22. The method of claim 2, further comprising applying the cleaning solution to the substrate with a brush. 23. The method of claim 2, further comprising cleaning the substrate with the cleaning solution at a temperature in the range from about 5° C. to about 90° C.