Electrodes for use in electrocatalytic processes

• US 4,541,905 A
• Filed: 12/13/1983
• Issued: 09/17/1985
• Est. Priority Date: 12/13/1983
• Status: Expired due to Fees

• Current Assignee: The Ohio State University Research Foundation
• Original Assignee: The Ohio State University Research Foundation
• Inventors: Kao, Wen-Hong, Kuwana, Theodore
• Primary Examiner(s): Niebling, John F.
• Application Number:
  US06/560,832
• Time in Patent Office: 644 Days
• Field of Search: 204/290 R, 204/38 R, 204/38 E, 204/47, 204/14.1, 204/129, 204/38.1, 204/38.7
• US Class Current: 205/105
• CPC Class Codes: C25B 11/095 at least one of the compounds being organic
• CPC Class Codes: C25D 5/56 of plastics
• CPC Class Codes: C25D 5/605 Surface topography of the layers, e.g. rough, dendritic or nodular layers
• CPC Class Codes: C25D 5/617 Crystalline layers
• CPC Class Codes: H01M 4/8853 Electrodeposition
• CPC Class Codes: H01M 4/9016 Oxides, hydroxides or oxygenated metallic salts
• CPC Class Codes: Y02E 60/50 Fuel cells

Abstract

Electrodes having high electrocatalytic activity are prepared by coating a base member of conductive material (preferably glassy carbon) with a layer of a porous polymeric material and then electrodepositing microparticles of metal within the polymeric layer by electrolysis using the electrode in a solution of the appropriate metal. The metal particles deposited within the polymer layer are typically less than about 100 nm. in diameter and their imbedding within the polymeric layer helps prevent poisoning of catalytically active metal by absorbed macromolecules.

Claims

1. A method for producing an electrode, said method comprising:

immersing a base member formed of conductive material and having at least part of its surface covered with a layer of porous, polymeric material, said porous, polymeric material not itself being capable of effecting reduction or oxidation, in a solution of a metal compound capable of being electrolyzed to deposit said metal; and

while said base member is still immersed in said solution, passing current through said base member and said solution, thereby causing electrolysis of said metal salt and deposition of a plurality of discrete particles of said metal dispersed in said layer.

2. A method according to claim 1 wherein said base member comprises glassy carbon.

3. A method according to claim 1 wherein said porous polymeric material comprises polyvinylacetic acid.

4. A method according to claim 3 wherein said layer of polyvinylacetic acid is deposited on said base member by immersing said base member in a refluxing solution of vinylacetic acid monomer.

5. A method according to claim 1 wherein said metal comprises platinum and said solution comprises an acid solution of an alkali metal hexachloroplatinate (IV).

6. A method according to claim 1 wherein said metal comprises palladium and said solution comprises an acid solution of an alkali metal hexachloropalladinate (II).

7. A method according to claim 1 wherein said metal comprises silver and said solution comprises an acid solution of silver sulfate.

8. A method according to claim 1 wherein said metal comprises nickel and said solution comprises a solution of nickel chloride and boric acid.

9. A method according to claim 1 wherein said metal comprises cadmium and said solution comprises a solution of cadmium sulfate and boric acid.

10. A method according to claim 1 wherein said electrolysis is effected by cyclic voltammetry.

11. A method according to claim 1 wherein said electrolysis is effected by single or double potential step electrolysis.

12. A method according to claim 1 wherein the total weight of said metal dispersed in said layer by means of said electrolysis is in the range of about 1 to about 50 micrograms per square centimeter of said base member covered by said layer.

13. A method according to claim 1 wherein at least part of said metal deposited by said electrolysis is thereafter oxidized to form an oxide of said metal.