IP Library Granted Patent US 8,481,245
Granted Patent B2
US 8,481,245 · App. 13/333,109 · Granted Jul 9, 2013

System, method and apparatus for pattern clean-up during fabrication of patterned media using forced assembly of molecules

Inventors: Qing Dai (San Jose, CA); Dan Saylor Kercher (Santa Cruz, CA); Huey-Ming Tzeng (San Jose, CA)
Assignee: HGST Netherlands B.V.
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Quick Facts
Patent No.
US 8,481,245
App. No.
13/333,109
Granted
Jul 9, 2013
Kind
B2
Abstract

A pattern clean-up for fabrication of patterned media using a forced assembly of molecules is disclosed. E-beam lithography is initially used to write the initial patterned bit media structures, which have size and positioning errors. Nano-sized protein molecules are then forced to assemble of on top of the bits. The protein molecules have a very uniform size distribution and assemble into a lattice structure above the e-beam patterned areas. The protein molecules reduce the size and position errors in e-beam patterned structures. This process cleans the signal from the e-beam lithography and lowers the noise in the magnetic reading and writing. This process may be used to fabricate patterned bit media directly on hard disk, or to create a nano-imprint master for mass production of patterned bit media disks.

Claims (36)

1. A method of forming a pattern, comprising:

(a) providing a substrate with resist;

(b) exposing and developing the resist on the substrate;

(c) depositing a metal on the developed resist and substrate;

(d) removing the resist and metal on the resist from the substrate such that metal features remain on the substrate;

(e) attaching nano-sized particles to the metal features;

(f) using the nano-sized particles as a mask to protect selected portions of the substrate while exposed portions of the substrate are etched; and

(g) removing the nano-sized particles and the metal features from the etched substrate to form a topographically patterned substrate.

2. A method according to claim 1 , wherein step (b) comprises forming holes in the resist, and step (c) comprises directionally evaporating the metal on the developed resist and substrate to form a coating thereon.

3. A method according to claim 1 , wherein step (d) comprises a lift off metallization process to strip the resist and metal on the resist from the substrate such that the metal features remain on the substrate.

4. A method according to claim 1 , wherein the metal features are at or beyond a resolution of a lithography tool used to form the metal features such that the metal features have irregular shapes and are not symmetrically arrayed.

5. A method according to claim 1 , wherein the nano-sized particles are protein molecules that assemble into a lattice structure above the metal features in step (e), such that the protein molecules reduce size and position errors in the patterned media.

6. A method according to claim 1 , wherein step (e) comprises attaching a chaperonin molecule to each of the metal features, and step (f) comprises reactive ion etching (RIE) the substrate.

7. A method according to claim 1 , further comprising removing the nano-sized particles and the metal features from the substrate to form the topographically patterned substrate.

8. A method according to claim 1 , wherein step (e) further comprises agitating the nano-sized particles to facilitate self-assembly onto the metal features.

9. A method according to claim 1 , wherein step (e) further comprises bonding the nano-sized particles to the metal features.

10. A method according to claim 1 , wherein the nano-sized particles are magnetic biological agents, and step (e) comprises using magnetic fields to facilitate self-assembly onto the metal features.

11. A method according to claim 1 , wherein step (e) comprises facilitating self-assembly of the nano-sized particles onto the metal features.

12. A method according to claim 1 , wherein nano-sized particles comprise chaperonin, and step (e) comprises using a monolayer of alkanethiols to facilitate self-assembly of the nano-sized particles onto the metal features.

13. A method of fabricating a patterned device, comprising:

(a) providing a substrate with e-beam resist;

(b) exposing and developing the e-beam resist on the substrate;

(c) depositing a noble metal on the developed e-beam resist and substrate;

(d) removing the e-beam resist and noble metal on the e-beam resist from the substrate such that noble metal features remain on the substrate;

(e) attaching molecules to the noble metal features;

(f) using the molecules as a mask to protect selected portions of the substrate while exposed portions of the substrate are etched; and

(g) removing the molecules and the noble metal features from the etched substrate to form a topographically patterned substrate.

14. A method according to claim 13 , wherein step (b) comprises forming holes in the resist, and step (c) comprises directionally evaporating the noble metal on the developed e-beam resist and substrate to form a coating thereon.

15. A method according to claim 13 , wherein step (d) comprises a lift off metallization process to strip the e-beam resist and noble metal on the e-beam resist from the substrate such that noble metal features remain on the substrate.

16. A method according to claim 13 , wherein the molecules are protein molecules having a uniform size distribution that assemble into a lattice structure above the noble metal features in step (e), such that the protein molecules reduce size and position errors in the patterned media.

17. A method according to claim 13 , wherein step (e) comprises attaching a chaperonin molecule to each of the noble metal features, and step (f) comprises reactive ion etching (RIE) the substrate.

18. A method according to claim 13 , further comprising removing the molecules and the noble metal features from the substrate to form the topographically patterned substrate.

19. A method according to claim 13 , wherein step (e) further comprises agitating the molecules to facilitate self-assembly onto the noble metal features.

20. A method according to claim 13 , wherein step (e) further comprises bonding the molecules to the noble metal features.

21. A method according to claim 13 , wherein the molecules are magnetic biological agents, and step (e) comprises using magnetic fields to facilitate self-assembly onto the noble metal features.

22. A method according to claim 13 , wherein the molecules comprise chaperonin, and step (e) comprises using a monolayer of alkanethiols to facilitate self-assembly of the molecules onto the noble metal features.

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Dec 6, 2016
From: HGST NETHERLANDS B.V.
To: WESTERN DIGITAL TECHNOLOGIES, INC.
Reel/Frame 040826/0327 →
CHANGE OF NAME Recorded Oct 25, 2012
From: HITACHI GLOBAL STORAGE TECHNOLOGIES NETHERLANDS B.V.
To: HGST NETHERLANDS B.V.
Reel/Frame 029341/0777 →
Continuity (2)
Continuation 11946423 · Nov 28, 2007
Related Publication 20120091096A1 · Apr 19, 2012