Two-terminal voltammetric microsensors

• US 5,223,117 A
• Filed: 05/03/1991
• Issued: 06/29/1993
• Est. Priority Date: 05/03/1991
• Status: Expired due to Fees

• Current Assignee: Harvard University, Massachusetts Institute of Technology
• Original Assignee: Harvard University, Massachusetts Institute of Technology
• Inventors: Valentine, James R., Laibinis, Paul E., Whitesides, George M., Mirkin, Chad A., Hickman, James J., Ofer, David, Wrighton, Mark S.
• Primary Examiner(s): Niebling, John
• Assistant Examiner(s): Bell, Bruce F.
• Application Number:
  US07/695,254
• Time in Patent Office: 788 Days
• Field of Search: 204/415, 204/416, 204/418, 204/419, 204/431, 204/433, 204/435
• US Class Current: 204/415
• CPC Class Codes: B82Y 15/00 Nanotechnology for interacting, sensing or actuating, e.g. quantum dots as markers in protein assays or molecular motors
• CPC Class Codes: B82Y 30/00 Nanotechnology for materials or surface science, e.g. nanocomposites
• CPC Class Codes: G01N 27/3277 being a redox reaction, e.g. detection by cyclic voltammetry voltammetry per se G01N27/42, G01N27/48

Abstract

Self-assembly of a chemically insensitive redox material, such as ferrocenyl thiol, and a chemically sensitive redox material, such as a quinone thiol, onto microelectrodes forms the basis for a two-terminal, voltammetric microsensor having reference and sensor functions on the same electrode. Detection is based on measuring the potential difference of current peaks for oxidation and reduction of the reference (ferrocene) and indicator (quinone) in aqueous electrolyte in a two-terminal, linear sweep voltammogram using a counterelectrode of relatively large surface area. Use of microelectrodes modified with monolayer coverages of reference and indicator molecules minimizes the size of the counterelectrode and the perturbation of the solution interrogated. Key advantages are that the sensor requires no separate reference electrode and the sensor functions as long as current peaks can be located for reference and indicator molecules.

Claims

1. An two-terminal voltammetric electrochemical sensor comprising:

a working, electrode comprising surface confined chemically sensitive redox material and chemically insensitive redox material in a thickness functionally equivalent to that of a monolayer, wherein the two materials act as terminals and

a counterelectrode having a surface area at least 10² larger than the surface area of the working electrode.

2. The sensor of claim 1 further comprising means for measuring a difference in redox potential between the chemically sensitive redox material and the chemically insensitive redox material.

3. The sensor of claim 2 wherein the measuring means applies a linear sweep of applied voltage to the sensor and detects the difference in separations between changes in potential of the two redox materials.

4. The sensor of claim 1 wherein the conductivity of the chemically sensitive redox material changes in response to changes in pH and the conductivity of the chemically insensitive redox material does not measurably change in response to changes in pH.

5. The sensor of claim 1 comprising more than one different chemically sensitive redox materials.

6. The sensor of claim 1 wherein the electrode is formed on an inert, electrically conductive material selected from the group consisting of platinum, gold, silver, palladium, carbon, tin doped indium oxide, tin oxide and combinations thereof.

7. The sensor of claim 1 wherein the electrode is formed of an inert, electrically conductive material on a chemically inert, electrically insulating material.

8. The sensor of claim 1 wherein the redox materials are electroactive molecules with functional groups that bind or coordinate to the electrode surface.

9. The sensor of claim 1 wherein the redox materials bind or coordinate to another material confined to the electrode surface.

10. A method for making a two-terminal voltammetric sensor comprising

forming a working electrode having a chemically sensitive redox material and a chemically insensitive redox material confined on the surface of an electrically conductive substrate in a thickness functionally equivalent to that of a monolayer, wherein the two materials act as terminals, and a counter electrode having a surface area at least 10² larger than the surface area of the working electrode.

11. The method of claim 10 further comprising placing the electrode in an environment where a change in chemical concentration is to be detected, applying means for measuring a difference in redox potential between the chemically sensitive redox material and the chemically insensitive redox material to the electrode, and measuring a difference in redox potential as a function of the change in chemical concentration at the electrode.

12. The method of claim 11 further wherein a linear sweep of voltage is applied to the sensor and the difference in separations between changes in potential of the two redox materials is measured.

13. The method of claim 10 wherein the conductivity of the chemically sensitive redox material changes in response to changes in pH and the conductivity of the chemically insensitive redox material does not measurably change in response to changes in pH, further comprising detecting changes in pH.

14. The method of claim 10 wherein the microelectrode comprises more than one different chemically sensitive redox materials, further comprising measuring changes in chemical concentration of more than one species.