IP Library › Granted Patent US 9,966,438
Granted Patent B2
US 9,966,438 · App. 15/418,286 · Granted May 8, 2018

Method of doped germanium formation

Inventors: Yi-Chiau Huang (Fremont, CA); Hua Chung (San Jose, CA); Sheng-Chin Kung (Milpitas, CA); Xuebin Li (Sunnyvale, CA)
Assignee: APPLIED MATERIALS, INC.
H01L29/167H01L21/02057H01L21/0262H01L21/02532H01L21/02636H01L21/02639H01L21/02656H01L21/02667H01L21/2018H01L21/2033H01L21/2053H01L21/2252H01L21/3065H01L21/324H01L29/161
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Quick Facts
Patent No.
US 9,966,438
App. No.
15/418,286
Granted
May 8, 2018
Kind
B2
Abstract

Implementations described herein generally relate to methods and systems for depositing layer on substrates, and more specifically, to methods for forming boron or gallium-doped germanium on silicon-containing surfaces. In one implementation, a method of processing a substrate is provided. The method comprises exposing a substrate having an exposed silicon-germanium surface and an exposed dielectric surface to a pre-treatment process, selectively depositing a boron-doped or a gallium-doped layer on the exposed silicon-germanium surface and exposing the substrate to a post-treatment process.

Claims (62)

1. A method of processing a substrate, comprising:

exposing a substrate having an exposed silicon-germanium surface and an exposed dielectric surface to a pre-treatment process;

selectively depositing a boron-doped germanium layer on the exposed silicon-germanium surface, wherein the selectively depositing the boron-doped germanium layer on the exposed silicon-germanium surface comprises:

co-flowing a germanium source gas and a boron source gas;

stopping the flow of the germanium source gas while continuing to flow the boron source gas to deposit an amorphous boron-doped germanium layer on the exposed silicon-germanium surface and the exposed dielectric surface;

annealing the amorphous boron-doped germanium layer to recrystallize the amorphous boron-doped germanium layer formed on the exposed silicon-germanium surface while the amorphous boron-doped germanium layer formed on the exposed dielectric surface remains amorphous; and

etching the amorphous boron-doped germanium layer formed on the exposed dielectric surface; and

exposing the substrate to a post-treatment process.

2. The method of claim 1 , wherein the pre-treatment process includes at least one of:

an etching process in an integrated dry clean chamber;

an in-situ etching process in reactive gases in a thermal or plasma environment, wherein the reactive gases include halogens, hydrogen halides, or combinations thereof;

depositing a p-type doped or undoped silicon or germanium layer as a sacrificial layer on the exposed silicon-germanium surface;

exposing the substrate to a rapid thermal anneal process; and

exposing the substrate to a wet-clean process.

3. The method of claim 2 , wherein the

germanium source gas is selected from germane (GeH 4 ), germanium dichloride (GeCl 2 ), germanium tetrachloride (GeCl 4 ), dichlorogermane (Cl 2 GeH 2 ), digermane (Ge 2 H 6 ), trigermane (Ge 3 H 8 ), tetragermane (Ge 4 H 10 ), and combinations thereof and

the boron source gas is selected from diborane (B 2 H 6 ), dimethylamine borane, trimethylborane, triethylborane, and combinations thereof.

4. The method of claim 3 , wherein the post-treatment process includes at least one of:

an etching process in an integrated dry clean chamber;

an in-situ etching process in reactive gases in a thermal or plasma environment, wherein the reactive gases include halogens, hydrogen halides, or combinations thereof;

exposing the substrate to a rapid thermal anneal process; and

exposing the substrate to a wet-clean process.

5. The method of claim 4 , wherein the pre-treatment process, the selectively depositing the boron-doped germanium layer, and the post-treatment process are performed without exposing the substrate to atmosphere.

6. The method of claim 1 , wherein the pre-treatment process comprises simultaneously exposing the substrate to NF 3 and Ar plasma by-products.

7. The method of claim 1 , wherein the germanium source gas is selected from digermane (Ge 2 H 6 ), trigermane (Ge 3 H 8 ), tetragermane (Ge 4 H 10 ), and combinations thereof.

8. A method of processing a substrate, comprising:

exposing a substrate having an exposed silicon-germanium surface and an exposed dielectric surface to a pre-treatment process, wherein the pre-treatment process comprises;

simultaneously exposing the substrate to NF 3 and NH 3 plasma by-products;

selectively depositing a boron-doped germanium layer on the exposed silicon-germanium surface, wherein the selectively depositing the boron-doped germanium layer on the exposed silicon-germanium surface comprises:

co-flowing a germanium source gas and a boron source gas;

stopping the flow of the germanium source gas while continuing to flow the boron source gas to deposit an amorphous boron-doped germanium layer on the exposed silicon-germanium surface and the exposed dielectric surface;

annealing the amorphous boron-doped germanium layer to recrystallize the amorphous boron-doped germanium layer formed on the exposed silicon-germanium surface while the amorphous boron-doped germanium layer formed on the exposed dielectric surface remains amorphous; and

etching the amorphous boron-doped germanium layer formed on the exposed dielectric surface; and

exposing the substrate to a post-treatment process.

9. The method of claim 8 , wherein the germanium source gas is selected from germane (GeH 4 ), germanium dichloride (GeCl 2 ), germanium tetrachloride (GeCl 4 ), dichlorogermane (Cl 2 GeH 2 ), digermane (Ge 2 H 6 ), trigermane (Ge 3 H 8 ), tetragermane (Ge 4 H 10 ), and combinations thereof.

10. The method of claim 9 , wherein the boron source gas is selected from diborane (B 2 H 6 ), dimethylamine borane, trimethylborane, triethylborane, and combinations thereof.

11. The method of claim 8 , wherein co-flowing the germanium source gas and the boron source gas comprises:

flowing the germanium source gas at a flow rate from about 0.1 sccm to about 1 sccm; and

flowing the boron source gas at a flow rate from about 1 sccm to about 10 sccm.

12. The method of claim 8 , wherein the germanium source gas is selected from digermane (Ge 2 H 6 ), trigermane (Ge 3 H 8 ), tetragermane (Ge 4 H 10 ), and combinations thereof.

13. A method of processing a substrate, comprising:

exposing a substrate having an exposed silicon-germanium surface and an exposed dielectric surface to a pre-treatment process, wherein the pre-treatment process comprises:

depositing a doped or undoped silicon-germanium sacrificial layer on the exposed silicon germanium surface; and

exposing the sacrificial layer to an etchant to remove the sacrificial layer and expose a clean silicon-germanium surface;

selectively depositing a boron-doped germanium layer on the exposed silicon-germanium surface, wherein the selectively depositing the boron-doped germanium layer on the exposed silicon-germanium surface comprises:

co-flowing a germanium source gas and a boron source gas;

stopping the flow of the germanium source gas while continuing to flow the boron source gas to deposit an amorphous boron-doped germanium layer on the exposed silicon-germanium surface and the exposed dielectric surface;

annealing the amorphous boron-doped germanium layer to recrystallize the amorphous boron-doped germanium layer formed on the exposed silicon-germanium surface while the amorphous boron-doped germanium layer formed on the exposed dielectric surface remains amorphous; and

etching the amorphous boron-doped germanium layer formed on the exposed dielectric surface; and

exposing the substrate to a post-treatment process.

14. The method of claim 13 , wherein co-flowing the germanium source gas and the boron source gas comprises:

flowing the germanium source gas at a flow rate from about 0.1 sccm to about 1 sccm; and

flowing the boron source gas at a flow rate from about 1 sccm to about 10 sccm.

15. The method of any of claim 13 , wherein the pre-treatment process, the selectively depositing the boron-doped germanium layer, and the post-treatment process are performed without exposing the substrate to atmosphere.

16. The method of claim 13 , wherein the germanium source gas is selected from germane (GeH 4 ), germanium dichloride (GeCl 2 ), germanium tetrachloride (GeCl 4 ), dichlorogermane (Cl 2 GeH 2 ), digermane (Ge 2 H 6 ), trigermane (Ge 3 H 8 ), tetragermane (Ge 4 H 10 ), and combinations thereof.

17. The method of claim 16 , wherein the boron source gas is selected from diborane (B 2 H 6 ), dimethylamine borane, trimethylborane, triethylborane, and combinations thereof.

18. The method of claim 13 , wherein the post-treatment process includes at least one of:

an etching process in an integrated dry clean chamber;

an in-situ etching process in reactive gases in a thermal or plasma environment, wherein the reactive gases include halogens, hydrogen halides, or combinations thereof;

exposing the substrate to a rapid thermal anneal process; and

exposing the substrate to a wet-clean process.

19. The method of claim 13 , wherein the germanium source gas is selected from digermane (Ge 2 H 6 ), trigermane (Ge 3 H 8 ), tetragermane (Ge 4 H 10 ), and combinations thereof.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 28, 2017
From: HUANG, YI-CHIAU; CHUNG, HUA; KUNG, SHENG-CHIN; LI, XUEBIN
To: APPLIED MATERIALS, INC.
Reel/Frame 042176/0301 →
Continuity (2)
Provisional Application 62396635 · Sep 19, 2016
Related Publication 20180083104A1 · Mar 22, 2018