IP Library Patent Application 18832677
Patent Application
App. No. 18/832,677

CHEMICAL MECHANICAL PLANARIZATION SLURRY PROCESSING TECHNIQUES AND SYSTEMS AND METHODS FOR POLISHING SUBSTRATE USING THE SAME

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Patent No.
US None
App. No.
18/832,677
Abstract

A Chemical Mechanical Planarization (CMP) system, apparatus, and method comprising providing a source of CMP slurry; modifying the source of CMP slurry to form a modified CMP slurry by directing a source of at least one of mechanical or electromagnetic wave energy at the source of CMP slurry; applying a flow of the modified CMP slurry to a wafer polishing apparatus at which a substrate is positioned; and performing a polishing operation on the substrate.

Claims (29)

1 . A Chemical Mechanical Planarization (CMP) method, the method comprising:

mixing (1) an aqueous CMP slurry (2) a capsulizing agent that forms a supramolecular structure selected from a group consisting of a vesicle, a micelle, a polyelectrolyte and a liposome and (3) a material additive selected from a group consisting of a ligand, a ligand-metal complex and a non-metal reactive-oxygen species (ROS) catalyst, thereby forming a modified slurry;

directing at least one of mechanical or electromagnetic wave energy at the modified slurry, thereby forming an activated modified slurry; and

planarizing a substrate while the substrate is exposed to the activated modified slurry.

2 . The method as recited in claim 1 , wherein the capsulizing agent is a poloxamer.

3 . The method as recited in claim 1 , wherein the capsulizing agent is an organic quaternary ammonium salt.

4 . The method as recited in claim 1 , wherein the capsulizing agent is selected from a group consisting of a hydrogen trialkane ammonium salt and a sulfate ester salt.

5 . The method as recited in claim 1 , wherein the capsulizing agent is a salt of a carboxylic acid that has at least ten carbons.

6 . The method as recited in claim 1 , wherein the capsulizing agent is selected from a group consisting of a sorbitan ester and a polyethylene glycol sorbitan ester.

7 . The method as recited in claim 1 , wherein the capsulizing agent is selected from a group consisting alginate, chitosan, pectin, polydiallyldimethylammonium halide, polyethyleneimine, polyacrylic acid, polysodium 4-styrenesulfonate, poly(2-dimethylamino)ethyl methacrylate) methyl halide quaternary salt, poly(allylamine) hydrohalide, poly(dialyldimethylammonium halide).

8 . The method as recited in claim 1 , wherein the capsulizing agent is a phospholipid.

9 . The method as recited in claim 1 , wherein the material additive is a ligand that has a water solubility of less than 20 grams per liter when measured at 22° C.

10 . The method as recited in claim 1 , wherein the material additive is a ligand that has a water solubility of less than 10 grams per liter when measured at 22° C.

11 . The method as recited in claim 1 , wherein the material additive is a ligand that is xanthine or hypoxanthine.

12 . The method as recited in claim 1 , wherein the material additive is a ligand selected from a group consisting of salicyhydroxamic acid (SHA), suberohydroxamic acid, tert-butyl N-(benzyloxy)carbamate, bipyridyl, lysine, tryptophan, phenylalanine, tyrosine, ethyl acetohydroxamate, hydroxycarbamide, benzhydroxamic acid, trans-cinnamic acid, adipic acid and caproic acid.

13 . The method as recited in claim 1 , wherein the material additive is a ligand that is a hydroxamic acid.

14 . The method as recited in claim 1 , wherein the material additive is a ligand that is a hydroxamic acid selected from a group consisting of salicyhydroxamic acid (SHA), suberohydroxamic acid, hydroxycarbamide and benzohydroxamic acid.

15 . The method as recited in claim 1 , wherein the material additive is a ligand that is salicyhydroxamic acid (SHA).

16 . The method as recited in claim 1 , wherein the material additive is a ligand that is an amino acid.

17 . The method as recited in claim 1 , wherein the material additive is a ligand that is an amino acid selected from a group consisting of tryptophan and phenylalanine.

18 . The method as recited in claim 1 , wherein the material additive is a ligand-metal complex with a metal ion selected from a group consisting of a magnesium ion, a calcium ion, a barium ion, a nickel ion, a copper ion, a zinc ion, a strontium ion, an iron ion, a cobalt ion, a titanium ion, a vanadium ion, a chromium ion, a molybdenum ion, and a manganese ion.

19 . The method as recited in claim 18 , wherein the ligand has a water solubility of less than 20 grams per liter when measured at 22° C.

20 . The method as recited in claim 18 , wherein the ligand is salicyhydroxamic acid (SHA).

21 . The method as recited in claim 1 , wherein the step of directing directs mechanical wave energy.

22 . A Chemical Mechanical Planarization (CMP) method, the method comprising:

mixing (1) an aqueous CMP slurry (2) a capsulizing agent that forms a supramolecular structure selected from a group consisting of a vesicle, a micelle, a polyelectrolyte and a liposome and (3) a material additive selected from a group consisting of a ligand, a ligand-metal complex and a non-metal reactive-oxygen species (ROS) catalyst, thereby forming a modified slurry, wherein the material additive has a water solubility of less than 20 grams per liter when measured at 22° C.;

directing mechanical wave energy at the modified slurry, thereby forming an activated modified slurry; and

planarizing a substrate while the substrate is exposed to the activated modified slurry.

23 . The method as recited in claim 22 , wherein the material additive is salicyhydroxamic acid (SHA) and the capsulizing agent is a poloxamer.

Assignments (2)
CHANGE OF ADDRESS Recorded Nov 21, 2025
From: ARACA, INC.
To: ARACA, INC.
Reel/Frame 073665/0020 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Sep 24, 2024
From: REDEKER, FRED C.; CAHUE, KIANA A.; KELEHER, JASON J.; SAMPURNO, YASA; PHILIPOSSIAN, ARA
To: ARACA, INC.
Reel/Frame 068673/0566 →