IP Library › Granted Patent US 8,129,289
Granted Patent B2
US 8,129,289 · App. 11/543,515 · Granted Mar 6, 2012

Method to deposit conformal low temperature SiO2

Assignee: Micron Technology, Inc.
View Patent ↗
Loading inventors, assignments & file history…
Monitor This Case
Get email alerts when status or documents change.
Order Certified Copies
Most orders are placed with the USPTO same day — all within 24 business hours.
Order via The Patent Place →
Pre-filled with this patent's details
Quick Facts
Patent No.
US 8,129,289
App. No.
11/543,515
Granted
Mar 6, 2012
Kind
B2
Abstract

Methods of controlling critical dimensions of reduced-sized features during semiconductor fabrication through pitch multiplication are disclosed. Pitch multiplication is accomplished by patterning mask structures via conventional photoresist techniques and subsequently transferring the pattern to a sacrificial material. Spacer regions are then formed on the vertical surfaces of the transferred pattern following the deposition of a conformal material via atomic layer deposition. The spacer regions, and therefore the reduced features, are then transferred to a semiconductor substrate.

Claims (31)

1. A method of depositing a conformal silicon dioxide in semiconductor fabrication comprising:

positioning a semiconductor substrate having a sacrificial material adjacent the semiconductor substrate into a deposition region of a deposition apparatus, the semiconductor substrate having a non-planar topography;

exposing the semiconductor substrate to a first mixture comprising a first reactant and a first catalyst wherein the first reactant is hexachlorodisilane (“HCD”) and the first catalyst is pyridine, permitting the formation of a first reactant chemisorbed layer on the semiconductor substrate; and

exposing the semiconductor substrate to a second mixture comprising a second reactant and a second catalyst wherein the second reactant is a compound containing oxygen and hydrogen and the second catalyst is pyridine, permitting the formation of a silicon dioxide monolayer on the semiconductor substrate; wherein the exposings of the semiconductor substrate to the first mixture and the second mixture do not decompose the sacrificial material.

2. The method of claim 1 , further comprising:

exposing the semiconductor substrate to the first reactant and first catalyst;

removing excess first reactant and first catalyst from the deposition region;

purging the deposition region with inert gas;

exposing the semiconductor substrate to the second reactant and second catalyst;

removing excess second reactant and second catalyst from the deposition region; and

purging the deposition region with inert gas.

3. The method of claim 1 , wherein the exposings of the semiconductor substrate to the first mixture and the second mixture are is performed at a temperature in a range of about 30° C. to about 90° C.

4. The method of claim 1 wherein the exposings of the semiconductor substrate to the first mixture and the second mixture are is performed at a temperature in a range of about 65° C. to about 80° C.

5. The method of claim 1 , wherein the deposition region of the deposition apparatus internal temperature is equalized to a temperature in a range of about 30° C. to about 90° C. prior to the exposings of the semiconductor substrate to the first mixture and second mixture.

6. The method of claim 1 , wherein the deposition region of the deposition apparatus internal temperature is equalized to a temperature in a range of about 65° C. to about 80° C. prior to the exposings of the semiconductor substrate to the first mixture and second mixture.

7. The method of claim 1 , wherein the deposition region of the deposition apparatus internal temperature is equalized to a temperature in a range of about 30° C. to about 32° C. prior to the exposings of the semiconductor substrate to the first mixture and second mixture.

8. The method of claim 1 , wherein the first reactant and first catalyst are introduced into the deposition region of the deposition apparatus at a temperature in a range of about 10° C. to about 90° C.

9. The method of claim 1 , wherein the first reactant and first catalyst are introduced into the deposition region of the deposition apparatus at a temperature in a range of about 20° C. to about 60° C.

10. The method of claim 1 , wherein the second reactant and second catalyst are introduced into the deposition region of the deposition apparatus at a temperature in a range of about 10° C. to about 90° C.

11. The method of claim 1 , wherein the second reactant and second catalyst are introduced into the deposition region of the deposition apparatus at a temperature in a range of about 20° C. to about 60° C.

12. The method of claim 1 , wherein the first reactant and first catalyst are introduced into the deposition region of the deposition apparatus at a rate in a range of about 0.1 standard liters per minute (“slm”) to about 2.0 slm.

13. The method of claim 1 , wherein the first reactant is introduced into the deposition region of the deposition apparatus at a rate in a range of about 0.1 slm to about 0.6 slm.

14. The method of claim 1 , wherein the first catalyst is introduced into the deposition region of the deposition apparatus at a rate in a range of about 0.1 slm to about 0.75 slm.

15. The method of claim 1 , wherein the second reactant is introduced into the deposition region of the deposition apparatus at a rate in a range of about 0.1 slm to about 3.0 slm.

16. The method of claim 1 , wherein the second reactant is introduced into the deposition region of the deposition apparatus at a rate in a range of about 0.1 slm to about 2.0 slm.

17. The method of claim 1 , wherein the second catalyst is introduced into the deposition region of the deposition apparatus at a rate in a range of about 0.1 slm to about 2.0 slm.

18. The method of claim 1 , wherein the second catalyst is introduced into the deposition region of the deposition apparatus at a rate in a range of about 0.1 slm to about 0.8 slm.

19. The method of claim 1 , wherein the depositing a conformal silicon dioxide is performed for approximately 20 to 610 seconds per cycle.

20. The method of claim 1 , wherein the depositing a conformal silicon dioxide is performed for approximately 65 to 125 seconds per cycle.

21. The method of claim 1 , wherein the sacrificial material adjacent the semiconductor substrate is transparent carbon.

22. The method of claim 1 , wherein the sacrificial material adjacent the semiconductor substrate is photoresist.

Assignments (8)
RELEASE OF SECURITY INTEREST Recorded Nov 12, 2019
From: JPMORGAN CHASE BANK, N.A., AS COLLATERAL AGENT
To: MICRON TECHNOLOGY, INC.; MICRON SEMICONDUCTOR PRODUCTS, INC.
Reel/Frame 051028/0001 →
RELEASE OF SECURITY INTEREST Recorded Oct 9, 2019
From: MORGAN STANLEY SENIOR FUNDING, INC., AS COLLATERAL AGENT
To: MICRON TECHNOLOGY, INC.
Reel/Frame 050937/0001 →
RELEASE OF SECURITY INTEREST Recorded Aug 23, 2018
From: U.S. BANK NATIONAL ASSOCIATION, AS COLLATERAL AGENT
To: MICRON TECHNOLOGY, INC.
Reel/Frame 047243/0001 →
SECURITY INTEREST Recorded Jul 13, 2018
From: MICRON TECHNOLOGY, INC.; MICRON SEMICONDUCTOR PRODUCTS, INC.
To: JPMORGAN CHASE BANK, N.A., AS COLLATERAL AGENT
Reel/Frame 047540/0001 →
CORRECTIVE ASSIGNMENT TO CORRECT THE REPLACE ERRONEOUSLY FILED PATENT #7358718 WITH THE CORRECT PATENT #7358178 PREVIOUSLY RECORDED ON REEL 038669 FRAME 0001. ASSIGNOR(S) HEREBY CONFIRMS THE SECURITY INTEREST. Recorded Jun 8, 2017
From: MICRON TECHNOLOGY, INC.
To: U.S. BANK NATIONAL ASSOCIATION, AS COLLATERAL AGENT
Reel/Frame 043079/0001 →
PATENT SECURITY AGREEMENT Recorded Jun 2, 2016
From: MICRON TECHNOLOGY, INC.
To: MORGAN STANLEY SENIOR FUNDING, INC., AS COLLATERAL AGENT
Reel/Frame 038954/0001 →
SECURITY INTEREST Recorded May 12, 2016
From: MICRON TECHNOLOGY, INC.
To: U.S. BANK NATIONAL ASSOCIATION, AS COLLATERAL AGENT
Reel/Frame 038669/0001 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 5, 2006
From: SMYTHE, JOHN A.; SANDHU, GURTEJ S.; COPPA, BRIAN J.; SURTHI, SHYAM; MENG, SHUANG
To: MICRON TECHNOLOGY INC.
Reel/Frame 018394/0060 →
Continuity (1)
Related Publication 20080085612A1 · Apr 10, 2008