IP Library Granted Patent US 7,211,520
Granted Patent B2
US 7,211,520 · App. 11/066,330 · Granted May 1, 2007

Method for fabricating a field effect transistor

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Quick Facts
Patent No.
US 7,211,520
App. No.
11/066,330
Granted
May 1, 2007
Kind
B2
Abstract

A method for fabricating a field effect transistor, in which, after the etching of the gate electrode, the removal of the etching mask is omitted since the etching mask serves as a gate dielectric. The etching mask or the dielectric has a self-assembled monolayer of an organic compound.

Claims (26)

1. A method for fabricating a field effect transistor, comprising:

a) providing a substrate;

b) depositing a gate electrode onto a whole area of the substrate;

c) bringing the gate electrode into contact with an organic compound in order to obtain a self-assembled monolayer of the organic compound arranged on the gate electrode, wherein the organic compound includes a radical that interacts with a surface of the gate electrode, the radical comprising a constituent selected from the group consisting of: SiCl 3 , SiCl 2 alkyl, SiCl(alkyl) 2 , Si(OR) 3 , Si(OR) 2 alkyl, SiOR(alkyl) 2 , PO(OH) 2 , PO(OR) 2 (alkyl), CHO, CH═CH 2 , COH, CONH 2 , CONHOH, CONHNH 2 , OH, NH 2 , SH, or COOH;

d) etching the gate electrode with the self-assembled monolayer of the organic compound arranged thereon such that the self-assembled monolayer essentially is not removed;

e) depositing a source electrode and a drain electrode without removing the self-assembled monolayer; and

f) depositing a semiconductor material either before or after depositing the source and drain electrodes.

2. The method as claimed in claim 1 , wherein after etching the gate electrode with the self-assembled monolayer of the organic compound arranged thereon, the gate electrode is rewetted with the organic compound.

3. The method as claimed in claim 1 , wherein the gate electrode includes a metal oxide layer at the surface.

4. The method as claimed in claim 3 , wherein the gate electrode is selected from the group consisting of: titanium, titanium nitride, tantalum, tantalum nitride, tungsten, titanium tungsten, tantalum tungsten, tungsten nitride, tungsten carbonitride, iridium oxide, ruthenium oxide, strontium ruthenium oxide, or from a combination of these layers and or materials and, has a layer made of silicon, titanium nitride silicon, silicon oxynitride, silicon oxide, silicon carbide or silicon carbonitride.

5. The method as claimed in claim 1 , wherein the process of bringing the gate electrode into contact with the organic compound is effected by a printing technique.

6. The method as claimed in claim 5 , wherein the process of bringing the gate electrode into contact with the organic compound is effected by microcontact printing.

7. The method as claimed in claim 1 , wherein the organic compound includes a radical that interacts with the surface of the gate electrode.

8. The method as claimed in claim 1 , wherein the etching of the gate electrode with the self-assembled monolayer of the organic compound arranged thereon is effected by wet-chemical etching methods.

9. The method as claimed in claim 8 , wherein the etching is effected by a solution comprising phosphoric acid.

10. The method as claimed in claim 9 , wherein the solution additionally comprises nitric acid.

11. The method as claimed in claim 9 , wherein the solution additionally comprises acetic acid.

12. The method as claimed in claim 1 , wherein the source and drain electrodes, independent of each other, are selected from the group consisting of: gold, silver, copper, platinum, palladium, titanium, titanium nitride, tantalum, tantalum nitride, tungsten, titanium tungsten, tantalum tungsten, tungsten nitride, tungsten carbonitride, iridium oxide, ruthenium oxide, strontium ruthenium oxide, or from a combination of these layers and/or materials and, additionally have a layer made of silicon, titanium nitride silicon, silicon oxynitride, silicon oxide, silicon carbide or silicon carbonitride.

13. The method as claimed in claim 1 , wherein the thickness of the gate electrode is between approximately 20 and 300 nm.

14. The method as claimed in claim 1 , wherein the thickness of the gate electrode is between approximately 20 and 100 nm.

15. The method as claimed in claim 1 , wherein the thickness of the gate electrode is between approximately 20 and 50 nm.

16. The method as claimed in claim 1 , wherein the thickness of the self-assembled monolayer of the organic compound is between approximately 1 and 20 nm.

17. The method as claimed in claim 1 , wherein the thickness of the self-assembled monolayer of the organic compound is between approximately 2 and 10 nm.

18. The method as claimed in claim 1 , wherein the semiconductor material includes an organic semiconductor material.

19. The method as claimed in claim 18 , wherein the organic semiconductor material is selected from the group consisting of pentacene, tetracene and polythiophene.

20. The method as claimed in claim 1 , wherein the radical further comprises a constituent R having a group selected from the group consisting of: n-alkyl (thio)ether, linear aromatic groups of the formula —(C 6 H 4 ) n —, where n is an integer between 2 and 6, and a heteroaromatic group.

Assignments (4)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 19, 2015
From: INFINEON TECHNOLOGIES AG
To: POLARIS INNOVATIONS LIMITED
Reel/Frame 036888/0745 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 8, 2015
From: QIMONDA AG
To: INFINEON TECHNOLOGIES AG
Reel/Frame 035623/0001 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 15, 2010
From: INFINEON TECHNOLOGIES AG
To: QIMONDA AG
Reel/Frame 023853/0001 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 8, 2005
From: ZSCHIESCHANG, UTE; HALIK, MARCUS; KLAUK, HAGEN; SCHMID, GUENTER; BRAUN, STEFAN
To: INFINEON TECHNOLOGIES AG
Reel/Frame 016034/0235 →