Nanolithography methods and products therefor and produced thereby
In one aspect, a method of nanolithography is provided using a driving force to control the movement of a deposition compound from a scanning probe microscope tip to a substrate. Another aspect of the invention provides a tip for use in nanolithography having an internal cavity and an aperture restricting movement of a deposition compound from the tip to the substrate. The rate and extent of movement of the deposition compound through the aperture is controlled by a driving force.
1. A method of nanolithography, comprising:
providing a substrate;
providing a tip comprising an internal cavity having an external opening to the surface of said tip, wherein said opening comprises an internal diameter of less than about 200 nanometers
loading said cavity with a deposition compound, wherein said deposition compound does not pass through said external opening in the absence of a driving force; and
subjecting said tip to a driving force to deliver said deposition compound through said external opening to be deposited on said substrate;
wherein said internal cavity comprises a medium semi-permeable to said deposition compound.
2. The method of claim 1 , wherein said deposition compound passes through said medium through the external opening onto said substrate.
3. The method of claim 1 , wherein said medium is at least one of a polymeric gel and a liquid suspension.
4. The method of claim 1 , wherein said deposition compound is a biomolecule.
5. The method of claim 1 , wherein the substrate is gold and the deposition compound is a protein or peptide or has the formula R 1 SH, R 1 SSR 2 , R 1 SR 2 , R 1 SO 2 H, (R 1 ) 3 P, R 1 NC, R 1 CN, (R 1 ) 3 N, R 1 COOH, or ArSH, wherein:
R 1 and R 2 each has the formula X(CH 2 ) n and, if a compound is substituted with both R 1 and R 2 , then R 1 and R 2 can be the same or different;
n is 0-30;
Ar is an aryl;
X is —CH 3 , —CHCH 3 , —COOH, —CO 2 (CH 2 ) m CH 3 , —OH, —CH 2 OH, ethylene glycol, hexa(ethylene glycol), —O(CH 2 ) m CH 3 , —NH 2 , —NH(CH 2 ) m NH 2 , halogen, glucose, maltose, fullerene C60, a nucleic acid, a protein, or a ligand; and
m is 0-30.
6. The method of claim 5 , wherein the deposition compound has the formula R 1 SH or ArSH.
7. The method of claim 1 , wherein the substrate is aluminum, gallium arsenide or titanium dioxide and the deposition compound has the formula R 1 SH, wherein:
R 1 has the formula X(CH 2 ) n ;
n is 0-30;
X is —CH 3 , —CHCH 3 , —COOH, —CO 2 (CH 2 ) m CH 3 , —OH, —CH 2 OH, ethylene glycol, hexa(ethylene glycol), —O(CH 2 ) m CH 3 , —NH 2 , —NH(CH 2 ) m NH 2 , halogen, glucose, maltose, fullerene C60, a nucleic acid, a protein, or a ligand; and
m is 0-30.
8. The method of claim 1 , wherein the deposition compound is selected from the group consisting of 2-mercaptoacetic acid and n-octadecanethiol.
9. The method of claim 1 , wherein the substrate is silicon dioxide and the deposition compound is selected from the group consisting of a protein, a peptide and a compound having the formula R 1 SH or R 1 SiCl 3 , wherein:
R 1 has the formula X(CH 2 ) n ;
n is 0-30;
X is —CH 3 , —CHCH 3 , —COOH, —CO 2 (CH 2 ) m CH 3 , —OH, —CH 2 OH, ethylene glycol, hexa(ethylene glycol), —O(CH 2 ) m CH 3 , —NH 2 , —NH(CH 2 ) m NH 2 , halogen, glucose, maltose, fullerene C60, a nucleic acid, a protein, or a ligand; and
m is 0-30.
10. The method of claim 1 , wherein the deposition compound is 16-mercapto-1-hexadecanoic acid, octadecyltrichlorosilane or 3-(2-aminoethylamino)propyltrimethoxysilane.
11. The method of claim 1 , wherein the substrate is oxidized gallium arsenide or silicon dioxide and the deposition compound is a silazane.
12. The method of claim 1 , wherein said external opening comprises an internal diameter of about 1 nanometers to about 15 nanometers.
13. The method of claim 1 , wherein movement of said deposition compound is achieved by said driving force.
14. The method of claim 13 , wherein said driving force is selected from the group consisting of an electrical, a magnetic and a chemical driving force.
15. The method of claim 14 , wherein said driving force is a chemical driving force created by a substrate having a chemical attraction to said deposition compound.
16. The method of claim 1 , wherein said external opening is a size-specific aperture adaptable to sub-nanometer scale features.
17. The method of claim 16 , wherein said size-specific aperture is produced by a process selected from the group consisting of focused ion beam, mechanical/ion polishing of narrow tip-cones and electron beam drilling.
18. The method of claim 1 , wherein said tip is an atomic force microscope tip.
19. The method of claim 1 , wherein said tip is a near field scanning optical microscope tip.
20. The method of claim 1 , wherein said tip is coated with a hydrophobic compound.
21. The method of claim 20 , wherein the hydrophobic compound has the formula RNH 2 wherein:
R is an alkyl of the formula CH 3 (CH 2 ) n or an aryl; and
n is 0-30.
22. The method of claim 21 , wherein the hydrophobic compound is 1-dodecylamine.
23. The method of claim 1 , wherein said tip is coated with a hydrophilic compound.
24. A method of nanolithography, comprising:
providing a substrate;
providing a tip comprising an internal cavity having an external opening to the surface of said tip, wherein said opening comprises an internal diameter of less than about 200 nanometers
loading said cavity with a deposition compound, wherein said deposition compound does not pass through said external opening in the absence of a driving force; and
subjecting said tip to a driving force to deliver said deposition compound through said external opening to be deposited on said substrate,
wherein said external opening is a size-specific aperture adaptable to sub-nanometer scale features;
wherein said size-specific aperture is produced by a process selected from the group consisting of focused ion beam, mechanical/ion polishing of narrow tip-cones and electron beam drilling; and
wherein said size-specific aperture comprises an ultra-thin membrane.
25. The method of claim 24 , wherein said ultra-thin membrane is about 2 nanometers to about 100 nanometers thick.
26. The method of claim 24 , wherein said ultra-thin membrane comprises a substance selected from the group consisting of SiO 2 , Si 3 N 4 , diamond and amorphous carbon.
27. The method of claim 24 , wherein said ultra-thin membrane comprises a circular aperture.
28. The method of claim 24 , wherein said ultra-thin membrane comprises a square aperture.
29. A method of nanolithography, comprising:
providing a substrate;
providing a tip comprising an internal cavity having an external opening to the surface of said tip, wherein said opening comprises an internal diameter of less than about 200 nanometers
loading said cavity with a deposition compound, wherein said deposition compound does not pass through said external opening in the absence of a driving force; and
subjecting said tip to a driving force to deliver said deposition compound through said external opening to be deposited on said substrate,
wherein said external opening is a size-specific aperture adaptable to sub-nanometer scale features; and
wherein said size-specific aperture comprises an ultra-thin crystalline membrane.
30. The method of claim 29 , wherein said ultra-thin crystalline membrane is selected from the group consisting of magnesium oxide, sapphire, diamond and semiconductors.