Method for producing an air electrode, the electrode thus obtained and its uses

US9799891B2 · US · B2

Patent metadata
FieldValue
Publication numberUS-9799891-B2
Application numberUS-201214003582-A
CountryUS
Kind codeB2
Filing dateMar 7, 2012
Priority dateMar 9, 2011
Publication dateOct 24, 2017
Grant dateOct 24, 2017

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Abstract

Official abstract text for this publication.

This invention relates to a method for preparing an air electrode based on Pr 2-x NiO 4 with 0≦x<2, comprising a step consisting in sintering a ceramic ink comprising Pr 2-x NiO 4 and a pore-forming agent at a temperature above 1000° C. and below or equal to 1150° C. This invention also relates to the air electrode thus obtained and its uses.

First claim

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The invention claimed is: 1. Method for preparing an air electrode based on Pr 2-x NiO 4 with 0≦x<2, comprising sintering a ceramic ink comprising Pr 2-x NiO 4 and a pore-forming agent at a temperature above 1000° C. and below or equal to 1150° C., wherein, before the sintering step, said ceramic ink is brought to the sintering temperature following a temperature rise gradient of between 50 and 400° C./h. 2. Method according to claim 1 , wherein the quantity of Pr 2-x NiO 4 powder with 0≦x<2, expressed by mass relative to the total mass of said ink is comprised between 30 and 70%. 3. Method according to claim 1 , wherein said pore-forming agent is in the form of a powder the particles of which have a median diameter (d50), determined using the Malvern particle size analyser, below 4 μm. 4. Method according to claim 1 , wherein said pore-forming agent is selected from the group consisting of acetylene black, polystyrene, polymethyl methacrylate (PMMA), starch, polyethylene, cyclodextrine, a wax, monosaccharide, oligosaccharide and polysaccharide. 5. Method according to claim 1 , wherein the mass ratio Mp/(Mc+Mp) where Mp is the mass of pore-forming agent and Mc is the mass of Pr 2-x NiO 4 with 0≦x<2 is between 1.5 and 10%. 6. Method according to claim 1 , wherein said ceramic ink comprises at least one solvent and at least one binder and wherein the mass ratio Ml/(Ml+Ms) where Ms is the mass of solvent and Ml is the mass of binder, is between 1 and 10%. 7. Method according to claim 1 , wherein said ceramic ink is subjected to the sintering temperature for a duration of between 1 and 5 h. 8. Method for preparing an air electrode based on Pr 2-x NiO 4 with 0≦x<2, comprising sintering a ceramic ink comprising Pr 2-x NiO 4 and a pore-forming agent at a temperature above 1000° C. and below or equal to 1150° C., wherein, subsequent to the sintering step, said ceramic ink is brought to a temperature of between 10 and 40° C., the layer being brought from the sintering temperature to the cooled temperature along a cooling gradient of between 50 and 400° C./h. 9. Air electrode based on Pr 2-x NiO 4 with 0≦x<2, obtained by sintering a ceramic ink containing Pr 2-x NiO 4 and a pore-forming agent at a temperature above 1000° C. and below or equal to 1150° C., wherein, before the sintering step, said ceramic ink is brought to the sintering temperature following a temperature rise gradient of between 50 and 400° C./h, and wherein the air electrode has a polarisation resistance below 0.06 Ω·cm 2 at 800° C. in air. 10. Air electrode according to claim 9 , wherein the air electrode has an open porosity between 30 and 70%, the percentage being expressed as a volume relative to the total volume of the air electrode. 11. Electrochemical half-cell comprising an air electrode based on Pr 2-x NiO 4 with 0≦x<2, obtained by sintering a ceramic ink containing Pr 2-x NiO 4 and a pore-forming agent at a temperature above 1000° C. and below or equal to 1150° C., wherein, before the sintering step, said ceramic ink is brought to the sintering temperature following a temperature rise gradient of between 50 and 400° C./h, and wherein the air electrode has a polarisation resistance below 0.06 Ω·cm 2 at 800° C. in air. 12. The electrochemical half-cell according to claim 11 , wherein the air electrode has an open porosity between 30 and 70%, the percentage being expressed as a volume relative to the total volume of the air electrode. 13. The electrochemical half-cell according to claim 11 , comprising: i) a dense electrolyte; ii) a barrier layer made from stabilised zirconia and/or from doped ceria, and deposited on said electrolyte; and iii) the air electrode deposited on said barrier layer. 14. The electrochemical half-cell according to claim 13 , wherein the air electrode has an open porosity between 30 and 70%, the percentage being expressed as a volume relative to the total volume of the air electrode. 15. Electrochemical cell comprising an electrochemical half-cell as defined in claim 14 and at least one hydrogen or water electrode and optionally one or more barrier layer(s) separating said hydrogen or water electrode from the electrolyte. 16. The electrochemical half-cell according to claim 13 , wherein the dense electrolyte is a dense Yttrium Stabilized Zirconia (YSZ) and the barrier layer is based on Gadolinia Doped Ceria (GDC) or Yttria Doped Ceria (YDC). 17. Electrochemical cell comprising an electrochemical half-cell as defined in claim 13 and at least one hydrogen or water electrode and optionally one or more barrier layer(s) separating said hydrogen or water electrode from the electrolyte. 18. Method for preparing an electrochemical half-cell comprising an air electrode based on Pr 2-x NiO 4 with 0≦x<2, wherein the air electrode has a polarisation resistance below 0.06 Ω·cm 2 at 800° C. in air, comprising: a) depositing a precursor of a barrier layer on a dense electrolyte; b) depositing a ceramic ink comprising Pr 2-x NiO 4 with 0≦x<2 and a pore-forming agent, on said precursor; and then c) applying to the assembly a sintering step at a temperature above 1000° C. and below or equal to 1150° C., wherein, before the sintering step, said ceramic ink is brought to the sintering temperature following a temperature rise gradient of between 50 and 400° C./h. 19. Method according to claim 18 , wherein the air electrode has an open porosity between 30 and 70%, the percentage being expressed as a volume relative to the total volume of the air electrode.

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Inventors

Classifications

  • Cross-Sectional Technologies · mapped topic

  • Apparatus or processes for treating or working the shaped {or preshaped} articles (specially adapted for tubular articles B28B21/92; decoration or surface treatment in general B05, B44; compacting concrete in situ in connection with building E04G21/06; drying F26) · CPC title

  • H01M4/8885Primary

    Sintering or firing · CPC title

  • the electrolyte containing zirconium oxide · CPC title

  • H01M4/8621Primary

    containing only metallic or ceramic material, e.g. made by sintering or sputtering · CPC title

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What does patent US9799891B2 cover?
This invention relates to a method for preparing an air electrode based on Pr 2-x NiO 4 with 0≦x<2, comprising a step consisting in sintering a ceramic ink comprising Pr 2-x NiO 4 and a pore-forming agent at a temperature above 1000° C. and below or equal to 1150° C. This invention also relates to the air electrode thus obtained and its uses.
Who is the assignee on this patent?
Delahaye Thibaud, Patro Pankaj-Kumar, Commissariat Energie Atomique
What technology area does this patent fall under?
Primary CPC classification H01M4/8885. Mapped technology areas include Electricity.
When was this patent published?
Publication date Tue Oct 24 2017 00:00:00 GMT+0000 (Coordinated Universal Time) (B2). Legal status and post-grant events are not shown on this page.
What related patents are in patentsdb?
We list 8 related publications on this page (citations in our corpus or others sharing the same primary CPC).