Method of Manufacture of an Energy Storage Device

• US 20100188801A1
• Filed: 04/01/2010
• Published: 07/29/2010
• Est. Priority Date: 10/07/2002
• Status: Abandoned Application

• Current Assignee: Alexander Lyubomirskiy, Alexander Mikhailovich Timonov, Dmitriy Ivanovich Pivunov, Nik Shkolnik, Sam Kogan, Sergey Anatolijevich Logvinov, Svetlana Viktorovna Vasiljeva, Valeriy Valentinovich Pavlov
• Original Assignee: Alexander Lyubomirskiy, Alexander Mikhailovich Timonov, Dmitriy Ivanovich Pivunov, Nik Shkolnik, Sam Kogan, Sergey Anatolijevich Logvinov, Svetlana Viktorovna Vasiljeva, Valeriy Valentinovich Pavlov
• Inventors: Shkolnik, Nik, Lyubomirskiy, Alexander, Vasiljeva, Svetlana Viktorovna, Logvinov, Sergey Anatolijevich, Timonov, Alexander Mikhailovich, Pivunov, Dmitriy Ivanovich, Pavlov, Valeriy Valentinovich, Kogan, Sam
• Application Number:
  US12/752,735
• Publication Number:
  US 20100188801A1
• Time in Patent Office: Days
• US Class Current: 361/505
• CPC Class Codes: H01G 11/48 Conductive polymers
• CPC Class Codes: H01G 9/0032 formation of the dielectric layer
• CPC Class Codes: H01G 9/0036 Formation of the solid electrolyte layer
• CPC Class Codes: H01G 9/04 Electrodes or formation of dielectric layers thereon
• CPC Class Codes: H01M 4/0438 by electrochemical processing electroless electrochemical plating C23C18/54
• CPC Class Codes: H01M 4/0466 Electrochemical polymerisation
• CPC Class Codes: H01M 4/137 Electrodes based on electro-active polymers
• CPC Class Codes: H01M 4/60 of organic compounds
• CPC Class Codes: H01M 4/66 Selection of materials
• CPC Class Codes: H01M 4/663 containing carbon or carbonaceous materials as conductive part, e.g. graphite, carbon fibres
• CPC Class Codes: H01M 4/667 in the form of layers, e.g. coatings
• CPC Class Codes: H01M 4/668 Composites of electroconductive material and synthetic resins
• CPC Class Codes: Y02E 60/10 Energy storage using batteries
• CPC Class Codes: Y02E 60/13 Energy storage using capacitors

Abstract

A method of preparing an energy-storage device is disclosed, which involves deposition of a redox polymer of the poly-Me(R-Salen) type onto a conducting substrate by electrochemical polymerization to prepare an electrode for use in the energy-storage device. Polymerization occurs at a voltage applied between the substrate and a counter-electrode, both of which are submerged in an electrolyte. The electrolyte contains an organic solvent, compounds capable of dissolving in the solvent and forming electrochemically inactive ions at concentrations of no less than 0.01 mol/L within the range of potentials from −3.0 V to +1.5 V, and a metal complex polymer represented by the formula poly-[Me(R-Salen)] dissolved at a concentration of no less than 5×10⁻⁵ mol/L, wherein Me is a transition metal having at least two different degrees of oxidation, R is an electron-donating substituent, and Salen is a residue of bis(salicylaldehyde)-ethylenediamine. Deposition of the redox polymer occurs in an electrolyte in which the cations have a diameter that is larger than the diameter of the cations of the electrolyte employed in the energy-storage device for which the electrode is manufactured.

Claims

1. A method of manufacturing an energy storage device, wherein the energy storage device is adapted to operate in a first electrolyte comprising cations of a first diameter, the method comprising:

depositing a redox polymer of the formula poly-[Me(R-Salen)] onto a conducting substrate by electrochemical polymerization to provide a polymer-modified electrode, wherein said polymerization is conducted at a voltage between the conducting substrate serving as an anode and a counter electrode serving as a cathode, both the anode and the cathode being submerged in a second electrolyte containing;

an organic solvent,

a compound capable of dissolving in the solvent and producing electrochemically inactive cations and anions at concentrations of no less than 0.01 mol/L within the range of potentials from about −

3.0 V to about +1.5 V, wherein the cations have a second diameter; and

a metal complex [Me(R-Salen)] at a concentration of no less than 5×

10<sup>−

5</sup> mol/L, wherein Me is a transition metal having at least two different degrees of oxidation, R is an electron-donating substituent, and Salen is a residue of bis-(salicylaldehyde)-ethylenediamine;

placing the polymer-modified electrode in a hermetically sealed casing; and

filling the hermetically sealed casing with a first electrolyte comprising cations of a first diameter, wherein the cations in the second electrolyte have a larger diameter than the cations in the first electrolyte.

2. The method of claim 1, wherein the energy storage device is an electrochemical capacitor comprising a positive electrode and a negative electrode, and wherein the polymer-modified electrode functions as either the positive electrode or the negative electrode and the positive electrode and the negative electrode are separated by a porous film.

3. The method of claim 1, wherein the conducting substrate is made of an electronically conductive material which is electrochemically inactive within the range of potentials from −

3.0 V to +1.5 V.

4. The method of claim 3, wherein the conducting substrate is made of a carbon material comprising a metal coating.

5. The method of claim 3, wherein the conducting substrate is made of an electronically conductive polymer in the form of a film, a porous structure, or a solid foam.

6. The method of claim 1, wherein the organic solvent is acetonitrile, dimethyl ketone, or propylene carbonate.

7. The method of claim 1, wherein the compound is a salt of tetrapropyl ammonium or tetrabutyl ammonium, said salt being selected from a tetrafluoroborate, a perchlorate, a hexafluorophosphate, and a trifluoroacetate.

8. The method of claim 1, wherein the transition metal Me is selected from Ni, Pd, Co, Cu, Fe and combinations thereof.

9. The method of claim 1, wherein the electron-donating substituent R is selected from CH₃O—

, C₂H_SO—

, HO—

, —

CH₃ and combinations thereof.

10. The method of claim 1, wherein depositing the redox polymer onto the conducting substrate occurs at a substrate potential no higher than a potential of nonreversible oxidation of the redox polymer.

11. The method of claim 1, further comprising circulating the electrolyte while depositing the redox polymer.

12. The method of claim 1, wherein the cations in the first electrolyte are selected from tetramethyl ammonium and tetraethyl ammonium.

13. The method of claim 1, wherein the first electrolyte comprises anions selected from tetrafluoroborates, perchlorates, and hexafluorophosphates.

14. The method of claim 1, wherein the cations in the first electrolyte have a diameter no greater than about 0.6 nm.

15. The method of claim 1, wherein the cations in the second electrolyte have a diameter of about 0.77 nm or larger.

16. The method of claim 1, wherein the polymer-modified electrode comprises polymer stacks of the redox polymer, and the polymer stacks are separated by a distance.

17. The method of claim 16, wherein the cations in the first electrolyte have a diameter that is smaller than the distance between the polymer stacks.

18. An energy storage device comprising:

an electrode comprising a layer of redox polymer of the formula poly-[Me(R-Salen)] deposited thereon, wherein;

Me is a transition metal having at least two different degrees of oxidation;

R is an electron-donating substituent;

Salen is a residue of bis-(salicylaldehyde)-ethylenediamine; and

the layer of redox polymer comprises polymer stacks separated from each other by a distance; and

an electrolyte comprising cations of a diameter smaller than the distance between the polymer stacks.

19. The device of claim 18, wherein the transition metal Me is selected from Ni, Pd, Co, Cu, Fe and combinations thereof, or wherein the electron-donating substituent R is selected from CH₃O—

, C₂H_SO—

, HO—

, —

CH₃ and combinations thereof.

20. The device of claim 18, wherein the electrolyte comprises cations selected from tetramethyl ammonium and tetraethyl ammonium, and anions selected from tetrafluoroborates, perchlorates, and hexafluorophosphates.