GB2068632A - Sodium-sulphur cell - Google Patents

Sodium-sulphur cell Download PDF

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Publication number
GB2068632A
GB2068632A GB8040587A GB8040587A GB2068632A GB 2068632 A GB2068632 A GB 2068632A GB 8040587 A GB8040587 A GB 8040587A GB 8040587 A GB8040587 A GB 8040587A GB 2068632 A GB2068632 A GB 2068632A
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GB
United Kingdom
Prior art keywords
sulphur cell
cathode current
current collector
conductive metal
sodium sulphur
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Granted
Application number
GB8040587A
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GB2068632B (en
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Chloride Silent Power Ltd
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Chloride Silent Power Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Chloride Silent Power Ltd filed Critical Chloride Silent Power Ltd
Priority to GB8040587A priority Critical patent/GB2068632B/en
Publication of GB2068632A publication Critical patent/GB2068632A/en
Application granted granted Critical
Publication of GB2068632B publication Critical patent/GB2068632B/en
Expired legal-status Critical Current

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    • H—ELECTRICITY
    • H01—ELECTRIC ELEMENTS
    • H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M4/00—Electrodes
    • H01M4/02—Electrodes composed of, or comprising, active material
    • H01M4/64—Carriers or collectors
    • H01M4/66—Selection of materials
    • H01M4/664—Ceramic materials
    • H—ELECTRICITY
    • H01—ELECTRIC ELEMENTS
    • H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M10/00—Secondary cells; Manufacture thereof
    • H01M10/36—Accumulators not provided for in groups H01M10/05-H01M10/34
    • H01M10/39—Accumulators not provided for in groups H01M10/05-H01M10/34 working at high temperature
    • H01M10/3909—Sodium-sulfur cells
    • H—ELECTRICITY
    • H01—ELECTRIC ELEMENTS
    • H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M4/00—Electrodes
    • H01M4/02—Electrodes composed of, or comprising, active material
    • H01M4/64—Carriers or collectors
    • H01M4/66—Selection of materials
    • H01M4/661—Metal or alloys, e.g. alloy coatings
    • H—ELECTRICITY
    • H01—ELECTRIC ELEMENTS
    • H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M4/00—Electrodes
    • H01M4/02—Electrodes composed of, or comprising, active material
    • H01M4/64—Carriers or collectors
    • H01M4/66—Selection of materials
    • H01M4/663—Selection of materials containing carbon or carbonaceous materials as conductive part, e.g. graphite, carbon fibres
    • H—ELECTRICITY
    • H01—ELECTRIC ELEMENTS
    • H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M10/00—Secondary cells; Manufacture thereof
    • H01M10/36—Accumulators not provided for in groups H01M10/05-H01M10/34
    • H01M10/39—Accumulators not provided for in groups H01M10/05-H01M10/34 working at high temperature
    • H01M10/3909—Sodium-sulfur cells
    • H01M10/3954—Sodium-sulfur cells containing additives or special arrangement in the sulfur compartment
    • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02E—REDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
    • Y02E60/00—Enabling technologies; Technologies with a potential or indirect contribution to GHG emissions mitigation
    • Y02E60/10—Energy storage using batteries

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  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Electrochemistry (AREA)
  • General Chemical & Material Sciences (AREA)
  • Materials Engineering (AREA)
  • Ceramic Engineering (AREA)
  • Manufacturing & Machinery (AREA)
  • Secondary Cells (AREA)

Abstract

In a sodium sulphur cell, improved protection of a cathode current collector 14 is obtained by isostatically pressing graphite foil 20 or flakes onto the surface of a substrate 21 of the collector, which surface is preferably roughened or coated with an intermediate conductive layer 22 such as a nickel-chromium alloy or a conductive carbide providing a rough surface. <IMAGE>

Description

SPECIFICATION Sodium sulphur cells and cathode current collectors for such cells This invention relates to sodium sulphur cells and to cathode current collectors for such cells and methods of making such cells and current collectors.
In a sodium sulphur cell, a solid electrolyte material, typically beta alumina, separates molten sodium, constituting the anode, from the cathodic reactant comprising molten sulphur and sodium polysulphides. The cathodic reactant is highly corrosive. The cathode current collector must make electrical contact with the cathodic reactant and many proposals have been made regarding the construction of such current collectors. Although carbon and graphite are widely used because of their corrosion-resistant properties, they do have a very substantially higher electrical resistance than most metals. For this reason, use is made of composite current collectors having a substrate of a relatively highly conductive material with an outer sheath or coating of some material having good corrosionresistant properties.Such an arrangement enables an aluminium substrate to be employed giving the advantages of the high conductivity of that material; aluminium however if exposed to the cathodic reactant in a sodium sulphur cell will form a sulphide coating which is non-conductive. It is important therefore that the outer coating should protect the aluminium from any exposure to the cathodic reactant. Reference is made to U.S. Patent Specifications Nos. 3,982,975; 4,024,320; 4,061,840 and 4,219,690 as examples of composite cathode current collectors for sodium sulphur cells.
According to one aspect of the present invention, a cathode current collector for a sodium sulphur cell is formed of conductive metal having a surface onto which or onto at least part of which a layer of graphite foil or graphite flakes has been isostatically pressed to force the foil or flakes to adhere to the surface.
The isostatic pressing of the graphite foil or flakes may be effected using a pressure in the range of 5,000 to 60,000 p.s.i. Typically a pressure of 40,000 p.s.i. might be employed. Preferably the graphite foil or flakes are pressed onto a rough surface. It has been found that, by such isostatic pressing onto a rough surface, it is possible to obtain a firmly adherent graphite layer which will withstand the conditions in the cathodic region of a sodium sulphur cell. The isostatic pressing not only gives firm adherence to the substrate but provides a further important advantage in that it densifies the graphite material. This material is homogenised and, for example, if graphite foil is wrapped around a cylindrical surface, with an overlap of the foil, then the isostatic pressing causes the overlapping portions to be homogenised.
It has been found that the surface of the conduc tive metal should have a roughness above one micron and preferably above five microns (these being centre line averages on the recognised engineering scale).
The invention furthermore includes within its scope a method of making a cathode current collector for a sodium sulphur cell comprising forming a collector of conductive metal, covering at least part of the surface of the collector with graphite foil or graphite flakes and subjecting the assembly to isostatic pressing to force the graphite foil to adhere to said surface. As stated above preferably the surface, to which the graphite foil or flakes is applied, is a rough surface.
Preferably the conductive metal is aluminium but other metals may be employed, for example, a nickel based alloy containing chromium and iron. Mild steel may be employed with a protective coating of a conductive material chemically inert to the cathodic reactant of a sodium sulphur cell.
The metal surface may be roughened where the graphite foil is to be applied. Such roughening may be effected by applying a surface coating of a conductive material to the metal. This intermediate surface coating is preferably a material resistant to corrosion in the cell environment. This coating may be a conductive carbide such as for example chromium carbide. Very conveniently however an aluminium or aluminium alloy substrate may be coated with a nickel-chromium alloy by flame spraying over the regions where the graphite foil or flakes are to be applied.
The invention includes within its scope a cathode current collector for a sodium sulphur cell made by the above-described method.
The invention furthermore includes within its scope a sodium sulphur cell having a cathode current collector as described above.
In one form of the invention, a sodium sulphur cell has a tubular electrolyte element separating sodium around the outer surface of the electrolyte element from cathodic reactant inside the tubular electrolyte element and there is provided a cathode current collector comprising a conductive metal rod ortube arranged axially within the electrolyte element, this metal rod or tube having a surface covered with graphite foil or graphite flakes isostatically pressed onto the surface of the rod or tube.
It will be appreciated that the graphite foil or flakes need only be applied over those parts of the surface of the current collector which would be exposed to the cathodic reactant when the cell is in use.
In the following description, reference will be made to the accompanying drawings in which: Figure 1 illustrates diagrammatically a sodium sulphur cell of the central sulphur type; Figure2 illustrates diagrammatically a sodium sulphur cell of the central sodium type; and Figure 3 is a transverse section, to a larger scale, of a cathode collector rod used in the cell of Figure 1.
In a sodium sulphur cell of the central sulphur type, as shown in Figure 1, a tubular member 10 of solid electrolyte material, typically beta-alumina, separates liquid sodium 11 around the outside of the electrolyte tube from a cathodic reactant 12 comprising liquid sulphur/sodium polysulphides within the electrolyte tube. The sodium 11 lies in an annular region between the tube 10 and an outer housing 13 while the cathodic reactant 22 lies in an annular region between the inner surface of the tube 10 and an axially disposed current collector rod 14.
A rod-shaped cathode current collector for use as the current collector rod 14 of a sodium sulphur cell was made by wrapping a thin sheet 20 (Figure 3) of graphite foil (about 0.2 to 0.25 mm thick) around a rod 21 of aluminium alloy having a surface coating 22 of flame-sprayed nickel-chromium alloy. A sheath of soft polymeric material such as rubber or plasticized polyvinylchloride was then placed overthe graphite foil and the assembly was isostatically pressed by sealing the sheathed assembly in an outer pressure container, conveniently using rubber O-rings as seals in a cylindrical assembly, and applying a pressure of 40,000 p.s.i. hydraulically to the outer surface of the polymeric sheath. This pressure caused the graphite foil to adhere to the rough surface of the coated aluminium rod and it has been found that good adhesion can be obtained by this technique.
A rod made as described above was used as a cathode current collector in a sodium sulphur cell of the kind, such as has been described above, having a tubular solid electrolyte element with sodium around the outer surface of the electrolyte element and the cathodic reactant inside the electrolyte element and the annular region between the electrolyte surface and the current collector rod. The cell, with the cathode current collector formed as described above, was subjected to 100 charge and discharge cycles over a period of 100 days at the operating temperature of about 350 C. At the end of this period no visible damage to the surface of the current collector rod could be seen after the cell had been dismantled. No rise in electrical resistance of the cell was observed over this period.In another test, a group of five cells with cathode current collectors of aluminium having a flame-sprayed coating of nickel-chromium alloy and with a 0.25 mm thick layer of isostatically pressed graphite foil were on test for 345 days and completed 680 charge and discharge cycles at an operating temperature of 3500C with no change in resistance.
Instead of using graphite foil, graphite flakes may be isostatically pressed onto the rough surface of the substrate. The flakes are made to form a thin layer completely covering at least that part of the surface which is exposed to the cathodic reactant in the cell.
If the cathodic reactant should, for any reason, penetrate the layer of graphite foil or flakes, the nickel-chromium layer forms a protection for the aluminium against chemical attack by the cathodic reactant.
Aluminium or aluminium alloy is the preferred substrate material because of its high electrical conductivity. Instead of using aluminium, it would be possible to use other metals, e.g. a nickel-based alloy containing chromium and iron. Mild steel may be used provided it has a protective conductive coating, e.g. by chromising.
The invention is applicable to sodium sulphur cells of the central sodium type as well as to cells of the central sulphur type. In a sodium sulphur cell of the central sodium type, as shown in Figure 2, the cathodic reactant 30 lies between the outer surface of an electrolyte tube 31 and the inner surface of the housing 32. The sodium lies inside the electrolyte tube. A similar isostatic pressing technique may be used to press graphite foil 33 or graphite flakes onto the internal surface of the housing 32 which surface is roughened, e.g. by applying a surface coating of a chromium carbide material or nickel-chromium alloy.

Claims (30)

1. A cathode current collector for a sodium sulphur cell formed of a conductive metal having a surface onto which or onto at least part of the surface of which a layer of graphite foil or graphite flakes has been isostatically pressed to force the foil or flakes to adhere to the surface.
2. A cathode current collector as claimed in claim 1 wherein the conductive metal is aluminium or an aluminium alloy.
3. A cathode current collector as claimed in claim 1 wherein the conductive metal is a nickel-based alloy containing chromium and iron.
4. A cathode current collector as claimed in claim 1 and for use in a sodium sulphur cell wherein the conductive metal is mild steel with a protective coating of an electrically conductive material chemically inert to the cathodic reactant of a sodium sulphur cell.
5. A cathode current collector as claimed in any of the preceding claims wherein said conductive metal has a rough surface onto which the layer of graphite foil or flakes is applied.
6. A cathode current collector as claimed in claim 5 wherein the rough surface is constituted by a layer of conductive material between the conductive metal and the graphite foil or flakes.
7. A cathode current collector as claimed in claim 6wherein the conductive material is a nickel chromium alloy.
8. A cathode current collector as claimed in claim 6 wherein the conductive material is a conductive carbide.
9. A method of making a cathode current collec tor for a sodium sulphur cell comprising forming a collector of a conductive metal, covering at least part of the surface of the collector with graphite foil or graphite flakes and subjecting the assembly to isostatic pressing to force the graphite foil or flakes to adhere to said surface.
10. A method as claimed in claim 9 wherein the conductive metal is aluminium or an aluminium alloy.
11. A method as claimed in claim 9 wherein the conductive metal is a nickel-based alloy containing chromium and iron.
12. A method as claimed in claim 9 wherein the conductive metal is mild steel with a protective coating of an electrically conductive material chemically inert to the cathodic reactant of the sodium sulphur cell.
13. A method as claimed in claim 10 wherein a surface coating of a conductive material is applied to the aluminium or aluminium alloy to form a rough surface on the aluminium or aluminium alloy.
14. A method as claimed in claim 13 wherein the surface coating is of a nickel-chromium alloy.
15. A method as claimed in any of claims 9 to 14 wherein said conductive metal has a rough surface onto which the graphite foil or flakes is applied.
16. A method as claimed in claim 15 wherein the rough surface is constituted by an intermediate layer of conductive material.
17. A method as claimed in claim 16 wherein said intermediate layer is a layer of material resistant to corrosion in the cell environment.
18. A method as claimed in claim 16 wherein the intermediate layer is a nickel-chromium alloy.
19. A method as claimed in claim 16 wherein said intermediate material is a conductive carbide.
20. A method as claimed in any of claims 9 to 19 wherein the isostatic pressing is effected at a pressure in the range of 5,000 to 60,000 p.s.i.
21. Asodium sulphur cell having atubular electrolyte element separating sodium around the outer surface of the electrolyte element from cathodic reactant inside the tubular electrolyte element and wherein there is provided a cathode current collector comprising a conductive metal rod or tube arranged axially within the electrolyte element, this metal rod or tube having a surface covered with graphite foil or graphite flakes isostatically pressed onto the surface of the rod ortube.
22. A sodium sulphur cell as claimed in claim 21 wherein said surface is a rough surface as herein be fore defined.
23. A sodium sulphur cell as claimed in either claim 21 or claim 23 wherein the conductive metal rod or tube is of aluminium or aluminium alloy.
24. A sodium sulphur cell as claimed in either claim 21 or claim 22 wherein the rod or tube has a surface coating of a nickel-chromium alloy, onto which is isostatically pressed the graphite foil or graphite flakes.
25. A sodium sulphur cell as claimed in either claim 21 or claim 22 wherein the rod or tube has a surface coating of a conductive carbide onto which is isostatically pressed the graphite foil or graphite flakes.
26. A sodium sulphur cell as claimed in either claim 21 or claim 22 wherein the conductive metal is a nickel-based alloy containing chromium and iron.
27. A sodium sulphur cell as claimed in either claim 21 or claim 22 wherein the conductive metal is mild steel with a protective coating of an electrically conductive material chemically inert to the cathodic reactant of the sodium sulphur cell.
28. A cathode current collector for a sodium sulphur cell substantially as hereinbefore described with reference to the accompanying drawings.
29. A method of making a cathode current collector for a sodium sulphur cell substantially as hereinbefore described with reference to the accompanying drawings.
30. A sodium sulphur cell having a cathode current collector as claimed in claim 28 or as made by the method of claim 29.
GB8040587A 1979-12-24 1980-12-18 Sodium-sulphur cell Expired GB2068632B (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
GB8040587A GB2068632B (en) 1979-12-24 1980-12-18 Sodium-sulphur cell

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
GB7944348 1979-12-24
GB8040587A GB2068632B (en) 1979-12-24 1980-12-18 Sodium-sulphur cell

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GB2068632A true GB2068632A (en) 1981-08-12
GB2068632B GB2068632B (en) 1983-02-16

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Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5234778A (en) * 1990-04-09 1993-08-10 Aabh Patent Holdings Societe Anonyme Electrochemical cell
US5396694A (en) * 1990-05-16 1995-03-14 Silent Power Gmbh Fur Energiespeichertechnik Method of manufacturing a graphite foil coated reservoir
GB2340295A (en) * 1998-07-28 2000-02-16 Aabh Patent Holdings Electrochemical Cell

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5234778A (en) * 1990-04-09 1993-08-10 Aabh Patent Holdings Societe Anonyme Electrochemical cell
US5396694A (en) * 1990-05-16 1995-03-14 Silent Power Gmbh Fur Energiespeichertechnik Method of manufacturing a graphite foil coated reservoir
GB2340295A (en) * 1998-07-28 2000-02-16 Aabh Patent Holdings Electrochemical Cell

Also Published As

Publication number Publication date
GB2068632B (en) 1983-02-16

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Legal Events

Date Code Title Description
732E Amendments to the register in respect of changes of name or changes affecting rights (sect. 32/1977)
PCNP Patent ceased through non-payment of renewal fee

Effective date: 19951218