Storage element and method for the production thereof

Patent metadata

Field	Value
Publication number	US-9570782-B2
Application number	US-201214239141-A
Country	US
Kind code	B2
Filing date	Sep 3, 2012
Priority date	Sep 27, 2011
Publication date	Feb 14, 2017
Grant date	Feb 14, 2017

Abstract

A storage element for a solid electrolyte battery is provided. The storage element has a main member having a porous matrix of sintered ceramic particles in which particles that are made of a metal and/or a metal oxide and jointly form a redox couple are embedded. Along a preferred direction, the storage element has a certain concentration gradient of the particles made of the metal and/or the metal oxide and/or a certain gradient of a pore density and/or a pore size, thereby allowing the diffusion behavior of oxygen ions within the main member to be controlled and thus the charge and discharge kinetics, the life and the capacity of the battery to be improved.

First claim

The invention claimed is:

1. A storage element for a solid electrolyte battery, having:
a base body comprising a porous matrix of sintered ceramic particles, in which particles of a metal and/or a metal oxide, which together form a redox pair, are incorporated,
wherein along a preferred direction, the base body has a concentration gradient of the particles of the metal and/or the metal oxide, and/or a concentration gradient of a pore density and/or a pore size,
wherein the storage element has a peripheral metal layer, to which the preferred direction forms a surface normal, and
wherein the peripheral metal layer is surrounded on both sides with ceramic layers which are at least predominantly free of pores and of the particles of the metal and/or the metal oxide.

2. The storage element as claimed in claim 1 ,
wherein the concentration gradient and/or the concentration gradient of the pore density and/or the pore size are stepped concentration gradients.

3. The storage element as claimed in claim 1 ,
wherein the ceramic particles comprise a redox-inert material.

4. The storage element as claimed in claim 1 ,
wherein the ceramic particles have a median particle size d50 of less than 1 μm.

5. The storage element as claimed in claim 1 ,
wherein the particles of the metal and/or the metal oxide comprise Fe, Ni or Mn and/or the respective oxides.

6. The storage element as claimed in claim 1 ,
wherein the particles of the metal and/or the metal oxide have a median particle size d50 of from 1 to 10 μm.

7. A method for the production of a storage element for a solid electrolyte battery, comprising
shaping a first slip of ceramic particles and particles of a metal and/or a metal oxide, which together form a redox pair, as well as a pore forming agent to form a green body which is subsequently sintered,
wherein at least one further slip of ceramic particles and the particles of the metal and/or the metal oxide, as well as a pore forming agent, are used, which differs from the first slip in a proportion of pore forming agents and in a proportion of the metal and/or the metal oxide,
wherein one subregion of the green body is formed from the first slip, and at east one subregion of the green body is formed from the at least one further slip,
forming a protective metal sheet made from a protective metal slip exclusively comprising the particles of the metal, and surrounding the protective metal sheet on both sides with ceramic sheets made from ceramic slips exclusively comprising ceramic particles and which are at least predominantly free of pores and of the particles of the metal and/or the metal oxide,
wherein along a preferred direction, the storage element has a concentration gradient of the particles of the metal and/or the metal oxide, and/or a concentration gradient of a pore density and/or a pore size, and
wherein the preferred direction forms a surface normal to the protective metal sheet.

8. The method as claimed in claim 7 ,
wherein in order to form the green body, a first green sheet is initially produced on a support by sheet casting of the first slip, and at least one further green sheet is produced on a support by sheet casting of the at least one further slip, the respective supports are subsequently removed and a multiplicity of green sheet sections are stacked to form the green body and subsequently laminated and debindered, a first subregion of the green body being formed by stacking sheet sections of the first green sheet and at least one further subregion of the green body being formed by stacking sheet sections of the at least one further green sheet.

9. The method as claimed in claim 8 ,
wherein in total three green sheets are formed from respectively assigned slips.

10. The method as claimed in claim 9 ,
wherein the first slip contains 50 vol % of the metal and/or the metal oxide and 10 vol % of the pore forming agent, the at least one further slip contains 35 vol % of the metal and/or the metal oxide and 20 vol % of the pore forming agent, and a third slip contains 20 vol % of the metal and/or the metal oxide and 30 vol % of the pore forming agent.

11. The method as claimed in claim 10 ,
wherein in order to form the green body, first a multiplicity of sheet sections of the first green sheet followed by a multiplicity of sheet sections of the at least one further green sheet, followed by a multiplicity of sheet sections of a third green sheet comprising the third slip are stacked.

12. The method as claimed in claim 7 ,
wherein the protective metal sheet comprises a multiplicity of the protective metal sheets, and wherein the both sides of the protective metal sheets are surrounded with a multiplicity of the ceramic sheets which are at least predominantly free of pores and of the particles of the metal and/or the metal oxide.

13. The method as claimed in claim 7 ,
wherein ceramic particles comprising a redox-inert material having a median particle size d50 of less than 1 μm, are used.

14. The method as claimed in claim 7 ,
wherein particles of Fe, Ni or Mn and/or the respective oxides, with a median particle size d50 of from 1 to 10 μm, are used as the particles of the metal and/or the metal oxide.

15. The method as claimed in claim 7 ,
wherein natural fibers, carbon particles or cellulose particles, having a median particle size d50 of from 10 to 50 μm, are used as pore forming agents.

16. The storage element as claimed in claim 3 , wherein the redox-inert material comprises Al 2 O 3 , MgO or ZrO 2 .

17. The method as claimed in claim 13 , wherein the redox-inert material comprises Al 2 O 3 , MgO or ZrO 2 .

18. The storage element as claimed in claim 1 ,
wherein along the preferred direction, the concentration gradient of the particle of the metal and/or the metal oxide increases and the pore density and/or the pore size decrease.

Assignees

• Schuh Carsten
• Soller Thomas
• Siemens Ag

Inventors

• Schuh Carsten
• Soller Thomas

Classifications

• H01M2004/021

  Physical characteristics, e.g. porosity, surface area · CPC title

• H01M12/08 Primary

  composed of a half-cell of a fuel-cell type and a half-cell of the secondary-cell type · CPC title

• H01M4/801

  Sintered carriers · CPC title

• H01M10/39

  working at high temperature · CPC title

• H01M4/803

  of only powdered material · CPC title