IP Library Granted Patent US 6,858,162
Granted Patent B2
US 6,858,162 · App. 10/114,410 · Granted Feb 22, 2005

Single molecule realization of the switch and doide combination

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Quick Facts
Patent No.
US 6,858,162
App. No.
10/114,410
Granted
Feb 22, 2005
Kind
B2
Abstract

Diodes and switches are combined in a single molecular species. Thus, the single molecular species is capable of performing more than one function. A single molecular species having both diode and switch functionalities is provided. The molecular species is represented by the formula: where A and B are non-identical conducting moieties, I is an insulating bridge between A and B, CL and CR are connectors to left and right electrodes, respectively, and “+” and “−” represent a rotatable dipolar moiety. Further, a diode-switch combination is provided, comprising the single molecular species. The teachings herein provide a set of principles to combine diodes and switches within one molecular species. Further, with the present teachings, only a single molecular species is needed for the fabrication of viable moletronic devices such as crossbar memory arrays. Consequently, device fabrication is easier and cheaper, and the device itself less faulty and more reliable.

Claims (39)

1. A single molecular species having both diode and switch functionalities, said molecular species represented by the formula:

where A and B are non-identical conducting moieties, I is an insulating bridge between A and B, CL and CR are connectors to left and right electrodes, respectively, and “+” and “−” represent a rotatable dipolar moiety.

2. The molecular species of claim 1 wherein A and B both have a smaller band gap compared to I.

3. The molecular species of claim 2 wherein A and B each have a band gap within a range of about 2 to 6 eV.

4. The molecular species of claim 2 wherein I has a band gap within a range of about 6 to 10 eV.

5. The molecular species of claim 2 wherein A and B are independently selected from the group consisting of conjugated homo-cycle or hetero-cycle aromatics and conjugated hydrocarbon chains.

6. The molecular species of claim 2 wherein I is selected from the group consisting of saturated cyclic and acyclic hydrocarbons.

7. The molecular species of claim 1 wherein I provides sufficient electrical insulation between said two conducting moieties A and B such that hybridization between molecular orbitals of said two conducting moieties A, B is less that 1%.

8. The molecular species of claim 1 wherein said dipolar moiety contains at least one atom capable of hydrogen bonding to at least one hydrogen atom on said molecular species.

9. The molecular species of claim 1 wherein said dipolar moiety has a dipole moment >4 Debye.

10. The molecular species of claim 1 wherein said dipolar moiety is attached to said insulating bridge via a single bond or a triple bond.

11. The molecular species of claim 1 wherein said connectors CL, CR are selected from the group consisting essentially of thiols, thiol-terminated alkenes, and —COOH—terminated chains or groups.

12. The molecular species of claim 1 wherein said electrodes are the same or different and are either metallic or semiconductor.

13. A diode-switch combination comprising a single molecular species having both diode and switch functionalities, said molecular species represented by the formula:

where A and B are non-identical conducting moieties, I is an insulating bridge between A and B, CL and CR are connectors to left and right electrodes, respectively, and “+” and “−” represent a rotatable dipolar moiety.

14. The diode-switch combination of claim 13 wherein A and B both have a smaller band gap compared to I.

15. The diode-switch combination of claim 14 wherein A and B each have a band gap within a range of about 2 to 6 eV.

16. The diode-switch combination of claim 14 wherein I has a band gap within a range of about 6 to 10 eV.

17. The diode-switch combination of claim 13 wherein A and B are independently selected from the group consisting of conjugated homo-cycle or hetero-cycle aromatics and conjugated hydrocarbon chains.

18. The diode-switch combination of claim 13 wherein I is selected from the group consisting of saturated cyclic and acyclic hydrocarbons.

19. The diode-switch combination of claim 13 wherein I provides sufficient electrical insulation between said two conducting moieties A and B such that hybridization between molecular orbitals of said two conducting moieties A, B is less that 1%.

20. The diode-switch combination of claim 13 wherein said dipolar moiety contains at least one atom capable of hydrogen bonding to at least one hydrogen atom on said molecular species.

21. The diode-switch combination of claim 13 wherein said dipolar moiety has a dipole moment >4 Debye.

22. The diode-switch combination of claim 13 wherein said dipolar moiety is attached to said insulating bridge via a single bond or a triple bond.

23. The diode-switch combination of claim 13 wherein said connectors CL, CR are selected from the group consisting essentially of thiols, thiol-terminated alkenes, and —COOH—terminated chains or groups.

24. The diode-switch combination of claim 13 wherein said electrodes are the same or different and are either metallic or semiconductor.

25. A crossbar switch comprising a first plurality of substantially parallel wires and a second plurality of substantially parallel wires, said second plurality of wires crossing said first plurality of wires to form a plurality of junctions, with each junction formed where one wire crosses another, each said junction having a functional diode-switch combination comprising a single molecular species having both diode and switch functionalities, said molecular species represented by the formula:

where A and B are non-identical conducting moieties, I is an insulating bridge between A and B, CL and CR are connectors to left and right electrodes, respectively, and “+” and “−” represent a rotatable dipolar moiety.

26. The crossbar switch of claim 25 wherein A and B both have a smaller band gap compared to I.

27. The crossbar switch of claim 26 wherein A and B each have a band gap within a range of about 2 to 6 eV.

28. The crossbar switch of claim 26 wherein I has a band gap within a range of about 6 to 10 eV.

29. The crossbar switch of claim 25 wherein A and B are independently selected from the group consisting of conjugated homo-cycle or hetero-cycle aromatics and conjugated hydrocarbon chains.

30. The crossbar switch of claim 25 wherein I is selected from the group consisting of saturated cyclic and acyclic hydrocarbons.

31. The crossbar switch of claim 25 wherein I provides sufficient electrical insulation between said two conducting moieties A and B such that hybridization between molecular orbitals of said two conducting moieties A, B is less that 1%.

32. The crossbar switch of claim 25 wherein said dipolar moiety contains at least one atom capable of hydrogen bonding to at least one hydrogen atom on said molecular species.

33. The crossbar switch of claim 25 wherein said dipolar moiety has a dipole moment >4 Debye.

34. The crossbar switch of claim 25 wherein said dipolar moiety is attached to said insulating bridge via a single bond or a triple bond.

35. The crossbar switch of claim 25 wherein said connectors CL, CR are selected from the group consisting essentially of thiols, thiol-terminated alkenes, and —COOH—terminated chains or groups.

36. The crossbar switch of claim 25 wherein said electrodes are the same or different and are either metallic or semiconductor.

Assignments (4)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 12, 2022
From: OT PATENT ESCROW, LLC
To: VALTRUS INNOVATIONS LIMITED
Reel/Frame 060005/0600 →
PATENT ASSIGNMENT, SECURITY INTEREST, AND LIEN AGREEMENT Recorded Jan 26, 2021
From: HEWLETT PACKARD ENTERPRISE DEVELOPMENT LP; HEWLETT PACKARD ENTERPRISE COMPANY
To: OT PATENT ESCROW, LLC
Reel/Frame 055269/0001 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Nov 9, 2015
From: HEWLETT-PACKARD DEVELOPMENT COMPANY, L.P.
To: HEWLETT PACKARD ENTERPRISE DEVELOPMENT LP
Reel/Frame 037079/0001 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 18, 2003
From: HEWLETT-PACKARD COMPANY
To: HEWLETT-PACKARD DEVELOPMENT COMPANY, L.P.
Reel/Frame 013776/0928 →