IP Library › Granted Patent US 12,538,727
Granted Patent B2
US 12,538,727 · App. 17/801,964 · Granted Jan 27, 2026

Treatment liquid for semiconductor with ruthenium

Inventors: Tomoaki Sato (Yamaguchi, JP); Yuki Kikkawa (Yamaguchi, JP); Takafumi Shimoda (Yamaguchi, JP); Takayuki Negishi (Yamaguchi, JP)
Assignee: TOKUYAMA CORPORATION
H01L21/32134
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Quick Facts
Patent No.
US 12,538,727
App. No.
17/801,964
Granted
Jan 27, 2026
Kind
B2
Abstract

Provided is a treatment liquid for a semiconductor with ruthenium including a ligand which coordinates to ruthenium, the treatment liquid is a treatment liquid for inhibiting a ruthenium-containing gas generated when contacting a semiconductor wafer including ruthenium with the treatment liquid in a semiconductor forming process. Also provided is an inhibitor for the generation of a ruthenium-containing gas, including a compound having a carbonyl group or a heterocyclic compound. Further provided is a treatment agent for a ruthenium-containing waste liquid, including a compound having a carbonyl group or a heterocyclic compound.

Claims (16)

1 . A treatment liquid for a semiconductor with ruthenium, comprising a ligand which coordinates to ruthenium and an oxidant, wherein

the oxidant is a hypobromite ion,

a concentration of the hypobromite ion is 0.01 to 1.9% by mass,

the ligand which coordinates to ruthenium is a compound having a carbonyl group, and

a concentration of the ligand which coordinates to ruthenium is 0.01 to 35% by mass.

2 . The treatment liquid for a semiconductor with ruthenium according to claim 1 , wherein the ligand which coordinates to ruthenium is at least one selected from the group consisting of ligands represented by the following formulae (1) to (4):

wherein R 1 and R 2 are each independently a hydrocarbon group having carbon number of 1 to 10, optionally containing a hydroxyl group or/and an ether bond, or a hydroxyl group;

wherein R 3 and R 5 are each independently a hydrocarbon group having carbon number of 1 to 10, optionally containing a hydroxyl group or/and an ether bond, or a hydroxyl group, and R 4 is a hydrocarbon group having carbon number of 1 to 10, optionally containing a hydroxyl group or/and an ether bond;

wherein R 6 , R 8 , and R 9 are each independently a hydrocarbon group having carbon number of 1 to 10, optionally containing a hydroxyl group or/and an ether bond, or a hydroxyl group, and R 7 is a hydrocarbon group having carbon number of 1 to 10, optionally containing a hydroxyl group or/and an ether bond;

wherein R 10 and R 12 to 14 are each independently a hydrocarbon group having carbon number of 1 to 10, optionally containing a hydroxyl group or/and an ether bond, or a hydroxyl group, and R 11 is a hydrocarbon group having carbon number of 1 to 10, optionally containing a hydroxyl group or/and an ether bond.

3 . The treatment liquid for a semiconductor with ruthenium according to claim 1 , wherein the ligand which coordinates to ruthenium is a ligand represented by the following formula (5):

wherein R 15 and R 16 are each independently a hydrocarbon group having carbon number of 1 to 10, optionally containing a hydroxyl group or/and an ether bond, or a hydroxyl group.

4 . The treatment liquid for a semiconductor with ruthenium according to claim 2 , wherein the compound having a carbonyl group is oxalic acid, dimethyl oxalate, 1,2,3,4,5,6-cyclohexanehexacarboxylic acid, succinic acid, acetic acid, butane-1,2,3,4-tetracarboxylic acid, dimethylmalonic acid, glutaric acid, diglycolic acid, citric acid, malonic acid, 1,3-adamantane dicarboxylic acid, or 2,2-bis(hydroxymethyl)propionic acid.

5 . The treatment liquid for a semiconductor with ruthenium according to claim 1 , having a pH at 25° C. of 7 or more and 14 or less.

6 . The treatment liquid for a semiconductor with ruthenium according to claim 1 , wherein the concentration of the hypobromite ion is 0.012 to 1.9% by mass.

7 . A method for treating a ruthenium-containing wafer with the treatment liquid according to claim 1 , comprising contacting the ruthenium-containing wafer with the treatment liquid.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Aug 24, 2022
From: SATO, TOMOAKI; KIKKAWA, YUKI; SHIMODA, TAKAFUMI; NEGISHI, TAKAYUKI
To: TOKUYAMA CORPORATION
Reel/Frame 060889/0692 →
Priority Claims (1)
JP 2020-029907 · Feb 25, 2020 · national
Continuity (1)
Related Publication 20230207329A1 · Jun 29, 2023
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