Method of fabricating an organic field transistor

• US 7,534,646 B2
• Filed: 05/31/2006
• Issued: 05/19/2009
• Est. Priority Date: 04/02/2003
• Status: Expired due to Fees

• Current Assignee: Alcatel-Lucent USA, Inc. (Nokia Corporation)
• Original Assignee: Alcatel-Lucent USA, Inc. (Nokia Corporation)
• Inventors: Bao, Zhenan, Yurke, Bernard
• Primary Examiner(s): LE, DUNG ANH
• Application Number:
  US11/421,125
• Publication Number:
  US 20060243969A1
• Time in Patent Office: 1,084 Days
• Field of Search: 438/99, 438/82, 438/562, 438/623, 438/288, 438/414, 257/E51.029, 257/E51.045
• US Class Current: 438/82
• CPC Class Codes: G01N 27/4145 specially adapted for biomolecules, e.g. gate electrode with immobilised receptors

Abstract

The present invention provides an organic field effect transistor and a method of fabricating the transistor. The transistor includes a semiconductive film comprising organic molecules. Probe molecules capable of binding to target molecules are coupled to an outer surface of the semiconductive film such that the interior of the film being substantially free of the probe molecules.

Claims

1. A method of fabricating an organic field effect transistor for the detection of biological target molecules, comprising:

forming a transistor channel, including;

forming a semiconductive film comprising organic molecules between a source and drain; and

coupling a probe molecule to an outer surface of said semiconductive film, said semiconductive film having an interior substantially free of said probe molecule, wherein said organic molecules are hydrophobic and said probe molecules are hydrophilic.

2. The method as recited in claim 1, wherein said semiconductive film is polycrystalline or crystalline.

3. The method as recited in claim 1, wherein said semiconductive film is formed by depositing said organic molecules by a process selected from the group consisting of:

spin coating;

casting;

vapor deposition and printing.

4. The method as recited in claim 1, wherein said organic molecules are functionalized to improve a solubility of said organic molecule in an organic solvent prior to said forming.

5. The method as recited in claim 1, wherein said organic molecules further include a functional group capable of facilitating said coupling.

6. The method as recited in claim 1, wherein said coupling is carried out in an organic solvent selected from the groups consisting of chloroform;

toluene; and

xylene.

7. The method as recited in claim 5, wherein said probe molecules are coupled to ends of said organic molecules that are closest to an exterior surface of said semiconductor film.

8. The method as recited in claim 1, wherein binding a target molecule to said probe molecule results in a change in a conductivity or mobility of said transistor channel.

9. The method as recited in claim 1, wherein said organic molecules are selected from the group consisting of polythiophene and oligothiophene.

10. The method as recited in claim 1, wherein said probe molecules are selected from the group consisting of:

single stranded deoxyribonucleic acid (DNA);

ribonucleic acid (RNA);

aptamers; and

proteins; and

are configured to bind to biological target molecules selected from the group consisting of;

complementary deoxyribonucleic acid (cDNA);

messenger deoxyribonucleic acid (mRNA); and

antibodies.

11. The method as recited in claim 1, wherein said semiconductive film is formed before said probe molecules are coupled to said outer surface.

12. The method as recited in claim 1, further including forming a gate on said substrate, forming an insulating layer on said gate and forming said source and drain on said insulating layer, wherein said semiconductive film is formed on said insulating layer.

13. The method as recited in claim 1, wherein said semiconductive film is between about 20 and about 100 Angstroms thick.

14. The method as recited in claim 1, further including coupling linker molecules to ends of said organic molecules before forming said semiconductive film.

15. The method as recited in claim 14, wherein each of said linker molecules includes an amino or thiol group attached to one end of a spacer group, another end of said spacer group being attached to one of said organic molecules.