WO2021206175A1 - セルスタック装置、モジュールおよびモジュール収容装置 - Google Patents

セルスタック装置、モジュールおよびモジュール収容装置 Download PDF

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Publication number
WO2021206175A1
WO2021206175A1 PCT/JP2021/015086 JP2021015086W WO2021206175A1 WO 2021206175 A1 WO2021206175 A1 WO 2021206175A1 JP 2021015086 W JP2021015086 W JP 2021015086W WO 2021206175 A1 WO2021206175 A1 WO 2021206175A1
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WIPO (PCT)
Prior art keywords
coating layer
cell
cell stack
metal member
stack device
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.)
Ceased
Application number
PCT/JP2021/015086
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English (en)
French (fr)
Japanese (ja)
Inventor
和也 今仲
史人 古内
佐典 白桃
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.)
Kyocera Corp
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Kyocera Corp
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First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=78022916&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=WO2021206175(A1) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Kyocera Corp filed Critical Kyocera Corp
Priority to US17/916,457 priority Critical patent/US12592400B2/en
Priority to JP2021544179A priority patent/JP7004870B1/ja
Priority to EP21783796.2A priority patent/EP4135079A4/en
Priority to CN202180025685.3A priority patent/CN115398686B/zh
Publication of WO2021206175A1 publication Critical patent/WO2021206175A1/ja
Priority to JP2022000278A priority patent/JP7736578B2/ja
Anticipated expiration legal-status Critical
Priority to JP2025142695A priority patent/JP2025172883A/ja
Ceased 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
    • H01M8/00—Fuel cells; Manufacture thereof
    • H01M8/02—Details
    • H01M8/0271—Sealing or supporting means around electrodes, matrices or membranes
    • H01M8/028—Sealing means characterised by their material
    • H01M8/0282—Inorganic material
    • H—ELECTRICITY
    • H01—ELECTRIC ELEMENTS
    • H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M8/00—Fuel cells; Manufacture thereof
    • H01M8/24—Grouping of fuel cells, e.g. stacking of fuel cells
    • H01M8/2465—Details of groupings of fuel cells
    • H—ELECTRICITY
    • H01—ELECTRIC ELEMENTS
    • H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M50/00—Constructional details or processes of manufacture of the non-active parts of electrochemical cells other than fuel cells, e.g. hybrid cells
    • H01M50/20—Mountings; Secondary casings or frames; Racks, modules or packs; Suspension devices; Shock absorbers; Transport or carrying devices; Holders
    • H01M50/204—Racks, modules or packs for multiple batteries or multiple cells
    • H01M50/207—Racks, modules or packs for multiple batteries or multiple cells characterised by their shape
    • H01M50/209—Racks, modules or packs for multiple batteries or multiple cells characterised by their shape adapted for prismatic or rectangular cells
    • H—ELECTRICITY
    • H01—ELECTRIC ELEMENTS
    • H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M50/00—Constructional details or processes of manufacture of the non-active parts of electrochemical cells other than fuel cells, e.g. hybrid cells
    • H01M50/20—Mountings; Secondary casings or frames; Racks, modules or packs; Suspension devices; Shock absorbers; Transport or carrying devices; Holders
    • H01M50/218—Mountings; Secondary casings or frames; Racks, modules or packs; Suspension devices; Shock absorbers; Transport or carrying devices; Holders characterised by the material
    • H01M50/22—Mountings; Secondary casings or frames; Racks, modules or packs; Suspension devices; Shock absorbers; Transport or carrying devices; Holders characterised by the material of the casings or racks
    • H01M50/222—Inorganic material
    • H01M50/224—Metals
    • H—ELECTRICITY
    • H01—ELECTRIC ELEMENTS
    • H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M8/00—Fuel cells; Manufacture thereof
    • H01M8/02—Details
    • H01M8/0202—Collectors; Separators, e.g. bipolar separators; Interconnectors
    • H01M8/0204—Non-porous and characterised by the material
    • H01M8/0206—Metals or alloys
    • H—ELECTRICITY
    • H01—ELECTRIC ELEMENTS
    • H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M8/00—Fuel cells; Manufacture thereof
    • H01M8/02—Details
    • H01M8/0202—Collectors; Separators, e.g. bipolar separators; Interconnectors
    • H01M8/0204—Non-porous and characterised by the material
    • H01M8/0206—Metals or alloys
    • H01M8/0208—Alloys
    • H01M8/021—Alloys based on iron
    • H—ELECTRICITY
    • H01—ELECTRIC ELEMENTS
    • H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M8/00—Fuel cells; Manufacture thereof
    • H01M8/02—Details
    • H01M8/0202—Collectors; Separators, e.g. bipolar separators; Interconnectors
    • H01M8/0204—Non-porous and characterised by the material
    • H01M8/0215—Glass; Ceramic materials
    • H01M8/0217—Complex oxides, optionally doped, of the type AMO3, A being an alkaline earth metal or rare earth metal and M being a metal, e.g. perovskites
    • H—ELECTRICITY
    • H01—ELECTRIC ELEMENTS
    • H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M8/00—Fuel cells; Manufacture thereof
    • H01M8/02—Details
    • H01M8/0202—Collectors; Separators, e.g. bipolar separators; Interconnectors
    • H01M8/0204—Non-porous and characterised by the material
    • H01M8/0223—Composites
    • H01M8/0228—Composites in the form of layered or coated products
    • H—ELECTRICITY
    • H01—ELECTRIC ELEMENTS
    • H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M8/00—Fuel cells; Manufacture thereof
    • H01M8/02—Details
    • H01M8/0202—Collectors; Separators, e.g. bipolar separators; Interconnectors
    • H01M8/0258—Collectors; Separators, e.g. bipolar separators; Interconnectors characterised by the configuration of channels, e.g. by the flow field of the reactant or coolant
    • H—ELECTRICITY
    • H01—ELECTRIC ELEMENTS
    • H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M8/00—Fuel cells; Manufacture thereof
    • H01M8/02—Details
    • H01M8/0271—Sealing or supporting means around electrodes, matrices or membranes
    • H01M8/0273—Sealing or supporting means around electrodes, matrices or membranes with sealing or supporting means in the form of a frame
    • H—ELECTRICITY
    • H01—ELECTRIC ELEMENTS
    • H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M8/00—Fuel cells; Manufacture thereof
    • H01M8/04—Auxiliary arrangements, e.g. for control of pressure or for circulation of fluids
    • H—ELECTRICITY
    • H01—ELECTRIC ELEMENTS
    • H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M8/00—Fuel cells; Manufacture thereof
    • H01M8/10—Fuel cells with solid electrolytes
    • H01M8/12—Fuel cells with solid electrolytes operating at high temperature, e.g. with stabilised ZrO2 electrolyte
    • H—ELECTRICITY
    • H01—ELECTRIC ELEMENTS
    • H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M8/00—Fuel cells; Manufacture thereof
    • H01M8/24—Grouping of fuel cells, e.g. stacking of fuel cells
    • H01M8/241—Grouping of fuel cells, e.g. stacking of fuel cells with solid or matrix-supported electrolytes
    • H01M8/2425—High-temperature cells with solid electrolytes
    • H—ELECTRICITY
    • H01—ELECTRIC ELEMENTS
    • H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M8/00—Fuel cells; Manufacture thereof
    • H01M8/24—Grouping of fuel cells, e.g. stacking of fuel cells
    • H01M8/241—Grouping of fuel cells, e.g. stacking of fuel cells with solid or matrix-supported electrolytes
    • H01M8/2425—High-temperature cells with solid electrolytes
    • H01M8/2432—Grouping of unit cells of planar configuration
    • H—ELECTRICITY
    • H01—ELECTRIC ELEMENTS
    • H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M8/00—Fuel cells; Manufacture thereof
    • H01M8/24—Grouping of fuel cells, e.g. stacking of fuel cells
    • H01M8/2465—Details of groupings of fuel cells
    • H01M8/247—Arrangements for tightening a stack, for accommodation of a stack in a tank or for assembling different tanks
    • H01M8/2475—Enclosures, casings or containers of fuel cell stacks
    • H—ELECTRICITY
    • H01—ELECTRIC ELEMENTS
    • H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M8/00—Fuel cells; Manufacture thereof
    • H01M8/24—Grouping of fuel cells, e.g. stacking of fuel cells
    • H01M8/2465—Details of groupings of fuel cells
    • H01M8/247—Arrangements for tightening a stack, for accommodation of a stack in a tank or for assembling different tanks
    • H01M8/248—Means for compression of the fuel cell stacks
    • H—ELECTRICITY
    • H01—ELECTRIC ELEMENTS
    • H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M8/00—Fuel cells; Manufacture thereof
    • H01M8/24—Grouping of fuel cells, e.g. stacking of fuel cells
    • H01M8/2465—Details of groupings of fuel cells
    • H01M8/2483—Details of groupings of fuel cells characterised by internal manifolds
    • H—ELECTRICITY
    • H01—ELECTRIC ELEMENTS
    • H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M8/00—Fuel cells; Manufacture thereof
    • H01M8/24—Grouping of fuel cells, e.g. stacking of fuel cells
    • H01M8/2465—Details of groupings of fuel cells
    • H01M8/2484—Details of groupings of fuel cells characterised by external manifolds
    • H01M8/2485—Arrangements for sealing external manifolds; Arrangements for mounting external manifolds around a stack
    • H—ELECTRICITY
    • H01—ELECTRIC ELEMENTS
    • H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M8/00—Fuel cells; Manufacture thereof
    • H01M8/10—Fuel cells with solid electrolytes
    • H01M8/12—Fuel cells with solid electrolytes operating at high temperature, e.g. with stabilised ZrO2 electrolyte
    • H01M2008/1293—Fuel cells with solid oxide electrolytes
    • 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
    • Y02E60/30—Hydrogen technology
    • Y02E60/50—Fuel cells

Definitions

  • the present disclosure relates to cell stack devices, modules and module accommodating devices.
  • a fuel cell is a kind of cell capable of obtaining electric power by using a fuel gas such as a hydrogen-containing gas and an oxygen-containing gas such as air.
  • the cell stack device includes a plurality of cells, a metal member, a coating layer, and a bonding material.
  • the plurality of cells have an element unit and include a first cell.
  • the metal member contains chromium.
  • the coating layer covers the metal member.
  • the bonding material is located between the first cell and the coating layer.
  • the cell stack device satisfies any one of the following (1) to (3).
  • the coating layer has at least two sites having different thicknesses or different surface roughnesses at different positions. (2) The surface roughness of the coating layer is different from the surface roughness of the metal member.
  • At least one element of Mn, Ti, Ca and Al is located at the interface between the metal member and the coating layer, and the content of at least one of Mn, Ti, Ca and Al at the interface is , Mn, Ti, Ca and Al content of the metal member or the coating layer.
  • the module of the present disclosure includes the cell stack device described above and a storage container for accommodating the cell stack device.
  • the module accommodating device of the present disclosure includes the module described above, an auxiliary machine for operating the module, and an outer case for accommodating the module and the auxiliary equipment.
  • FIG. 1A is a cross-sectional view showing an example of a cell according to an embodiment.
  • FIG. 1B is a side view of an example of the cell according to the embodiment as viewed from the air electrode side.
  • FIG. 1C is a side view of an example of the cell according to the embodiment as viewed from the interconnector side.
  • FIG. 2A is a perspective view showing an example of the cell stack device according to the embodiment.
  • FIG. 2B is a cross-sectional view taken along the line XX shown in FIG. 2A.
  • FIG. 2C is a top view showing an example of the cell stack device according to the embodiment.
  • FIG. 3A is a cross-sectional view taken along the line YY shown in FIG. 2C.
  • FIG. 3B is an enlarged cross-sectional view schematically showing a main part of the cell stack shown in FIG. 3A.
  • FIG. 4 is a cross-sectional view taken along the line ZZ shown in FIG. 2C.
  • FIG. 5A is a perspective view showing another example of the metal member.
  • FIG. 5B is a perspective view showing another example of the metal member.
  • FIG. 5C is an enlarged cross-sectional view of another example of the metal member and the joint portion with the cell.
  • FIG. 6A is an enlarged cross-sectional view of the joint portion between the metal member and the cell according to the first modification of the embodiment.
  • FIG. 6B is an enlarged cross-sectional view of the joint portion between the metal member and the cell according to the second modification of the embodiment.
  • FIG. 6C is an enlarged cross-sectional view of the joint portion between the metal member and the cell according to the third modification of the embodiment.
  • FIG. 6D is a cross-sectional view showing a metal member according to the fourth modification of the embodiment.
  • FIG. 6E is a cross-sectional view showing a metal member according to the modified example 5 of the embodiment.
  • FIG. 7A is an enlarged cross-sectional view of the joint portion between the cell and another example of the metal member according to the modified example 6 of the embodiment.
  • FIG. 7B is an enlarged cross-sectional view of the joint portion between the cell and another example of the metal member according to the modified example 7 of the embodiment.
  • FIG. 8A is a front view showing an end current collector member according to a modified example 8 of the embodiment.
  • FIG. 8B is a cross-sectional view showing an end current collector member according to a modified example 9 of the embodiment.
  • FIG. 8C is an enlarged cross-sectional view of the joint portion between the end current collector member and the metal member according to the modified example 10 of the embodiment.
  • FIG. 8D is an enlarged cross-sectional view of the joint portion between the end current collector member and the metal member according to the modified example 11 of the embodiment.
  • FIG. 9 is an external perspective view showing an example of the module according to the embodiment.
  • FIG. 10 is an exploded perspective view schematically showing an example of the module accommodating device according to the embodiment.
  • FIG. 11A is a perspective view showing a flat plate type cell according to the modified example 12 of the embodiment.
  • FIG. 11B is a partial cross-sectional view of the flat plate cell shown in FIG. 11A.
  • FIG. 11C is an enlarged view of the region A shown in FIG. 11B.
  • FIG. 1A is a cross-sectional view showing an example of the cell 1 according to the embodiment
  • FIG. 1B is a side view of an example of the cell 1 according to the embodiment as viewed from the air electrode 5 side
  • FIG. 1C is a side view of the embodiment.
  • FIG. 5 is a side view of an example of the cell 1 according to the above, as viewed from the side of the interconnector 6. It should be noted that FIGS. 1A to 1C show an enlarged part of each configuration of the cell 1.
  • the cell 1 is a hollow flat plate type and has an elongated plate shape.
  • the shape of the entire cell 1 viewed from the side surface is, for example, a side length of 5 cm to 50 cm in the length direction L, and a length W in the width direction orthogonal to the length direction L. Is a rectangle of 1 cm to 10 cm.
  • the thickness of the entire cell 1 in the thickness direction T is, for example, 1 mm to 5 mm.
  • the cell 1 includes a conductive support substrate 2, an element portion, and an interconnector 6.
  • the support substrate 2 is a columnar shape having a pair of opposing flat surfaces n1 and n2 and a pair of arcuate side surfaces m connecting the flat surfaces n1 and n2.
  • the element portion is provided on the flat surface n1 of the support substrate 2.
  • Such an element unit has a fuel electrode 3, a solid electrolyte layer 4, and an air electrode 5.
  • the interconnector 6 is provided on the flat surface n2 of the cell 1.
  • the air electrode 5 does not extend to the upper end and the lower end of the cell 1.
  • the interconnector 6 may extend to the upper end and the lower end of the cell 1.
  • the interconnector 6 and the solid electrolyte layer 4 are exposed on the surface.
  • the solid electrolyte layer 4 is exposed on the surface of the pair of arcuate side surfaces m of the cell 1. The interconnector 6 does not have to extend to the lower end of the cell 1.
  • the support substrate 2 has a gas flow path 2a through which gas flows.
  • the example of the support substrate 2 shown in FIG. 1A has six gas flow paths 2a.
  • the support substrate 2 has gas permeability, and allows the fuel gas flowing in the gas flow path 2a to permeate to the fuel electrode 3.
  • the support substrate 2 may have conductivity.
  • the conductive support substrate 2 collects electricity generated in the element portion into the interconnector 6.
  • the material of the support substrate 2 contains, for example, an iron group metal component and an inorganic oxide.
  • the iron group metal component may be Ni (nickel) and / or NiO.
  • the inorganic oxide may be, for example, a specific rare earth element oxide.
  • the material of the fuel electrode 3 generally known materials can be used.
  • porous conductive ceramics such as ZrO 2 in which calcium oxide, magnesium oxide, or a rare earth element oxide is solid-dissolved, and ceramics containing Ni and / or NiO may be used.
  • the rare earth element oxide for example, Y 2 O 3 and Yb 2 O 3 are used.
  • Calcium oxide, magnesium oxide or a rare earth element oxide it may be referred to as stabilized zirconia ZrO 2 being dissolved.
  • Stabilized zirconia also includes partially stabilized zirconia.
  • the solid electrolyte layer 4 is an electrolyte and bridges ions between the fuel electrode 3 and the air electrode 5. At the same time, the solid electrolyte layer 4 has a gas blocking property and makes it difficult for a leak between the fuel gas and the oxygen-containing gas to occur.
  • Material of the solid electrolyte layer 4 for example, 3 mol% to 15 mol% of the rare earth oxide may be a ZrO 2 solid-solved.
  • the rare earth element oxide for example, Y 2 O 3 and Yb 2 O 3 are used. As long as it has the above characteristics, other materials may be used as the material of the solid electrolyte layer 4.
  • the material of the air electrode 5 is not particularly limited as long as it is generally used for the air electrode.
  • the material of the air electrode 5 may be, for example, a conductive ceramic such as a so-called ABO 3 type perovskite type oxide.
  • the material of the air electrode 5 may be, for example, a composite oxide in which Sr and La coexist at the A site.
  • a composite oxide La x Sr 1-x Co y Fe 1-y O 3, La x Sr 1-x MnO 3, La x Sr 1-x FeO 3, La x Sr 1-x CoO 3 and the like can be mentioned. Note that x is 0 ⁇ x ⁇ 1 and y is 0 ⁇ y ⁇ 1.
  • the air electrode 5 has gas permeability.
  • the open porosity of the air electrode 5 may be, for example, 20% or more, particularly in the range of 30% to 50%.
  • a lanthanum chromite-based perovskite-type oxide (LaCrO 3- based oxide), a lanthanum strontium titanium-based perovskite-type oxide (LaSrTiO 3- based oxide), or the like may be used. These materials are conductive and are neither reduced nor oxidized when they come into contact with fuel gases such as hydrogen-containing gases and oxygen-containing gases such as air.
  • the interconnector 6 is dense and makes it difficult for the fuel gas flowing through the gas flow path 2a located inside the support substrate 2 and the oxygen-containing gas flowing outside the support substrate 2 to leak.
  • the interconnector 6 may have a relative density of 93% or more, particularly 95% or more.
  • FIGS. 2A to 2C are perspective views showing an example of the cell stack device 10 according to the embodiment
  • FIG. 2B is a cross-sectional view taken along the line AA shown in FIG. 2A
  • FIG. 2C is a cell stack device according to the embodiment. It is a top view which shows an example of 10.
  • the cell stack device 10 includes a cell stack 11 having a plurality of cells 1 arranged (stacked) in the thickness direction T of the cells 1 (see FIG. 1A), and a fixing member 12.
  • the cell stack 11 may have one or more cells 1. Even when only one cell 1 is provided as the first cell, it is referred to as a cell stack 11 and a cell stack device 10 for convenience.
  • the fixing member 12 has a joining member 13 and a supporting member 14.
  • the support member 14 supports the cell 1.
  • the joining material 13 joins the cell 1 and the support member 14.
  • the support member 14 has a support body 15 and a gas tank 16.
  • the support 15 and the gas tank 16 which are the support members 14 are made of metal and have conductivity.
  • the support 15 has an insertion hole 15a into which the lower ends of the plurality of cells 1 are inserted.
  • the lower ends of the plurality of cells 1 and the inner walls of the insertion holes 15a are joined by a joining material 13.
  • the gas tank 16 has an opening for supplying reaction gas to a plurality of cells 1 through the insertion holes 15a, and a concave groove 16a located around the opening.
  • the outer peripheral end of the support 15 is fixed to the gas tank 16 by the fixing material 21 filled in the concave groove 16a of the gas tank 16.
  • the fuel gas is stored in the internal space 22 formed by the support 15 which is the support member 14 and the gas tank 16.
  • a gas flow pipe 20 is connected to the gas tank 16.
  • the fuel gas is supplied to the gas tank 16 through the gas flow pipe 20, and is supplied from the gas tank 16 to the gas flow path 2a (see FIG. 1A) inside the cell 1.
  • the fuel gas supplied to the gas tank 16 is generated by the reformer 102 (see FIG. 9) described later.
  • Hydrogen-rich fuel gas can be generated by steam reforming raw fuel.
  • the fuel gas contains steam.
  • a cell stack 11 having a plurality of cells 1 includes a cell stack 11 in two rows, two supports 15, and a gas tank 16.
  • the two-row cell stack 11 has a plurality of cells 1, respectively.
  • Each cell stack 11 is fixed to each support 15.
  • the gas tank 16 has two through holes on the upper surface.
  • Each support 15 is arranged in each through hole.
  • the internal space 22 is formed by one gas tank 16 and two supports 15.
  • the shape of the insertion hole 15a is, for example, an oval shape when viewed from above.
  • the length of the cell 1 in the arrangement direction that is, the thickness direction T is larger than the distance between the two end current collecting members 17 located at both ends of the cell stack 11.
  • the width of the insertion hole 15a is, for example, larger than the length of the cell 1 in the width direction W (see FIG. 1A).
  • the shape of the insertion hole 15a may be a substantially rectangular shape that is long in the arrangement direction of the cells 1.
  • the joint portion between the inner wall of the insertion hole 15a and the lower end portion of the cell 1 is filled with the joining material 13 and solidified.
  • the inner wall of the insertion hole 15a and the lower end portions of the plurality of cells 1 are joined and fixed, respectively, and the lower end portions of the cell 1 are joined and fixed to each other.
  • the gas flow path 2a of each cell 1 communicates with the internal space 22 of the support member 14 at the lower end portion.
  • the joining material 13 and the fixing material 21 those having low conductivity such as glass can be used.
  • a specific material of the bonding material 13 and the fixing material 21 amorphous glass or the like may be used, and in particular, crystallized glass or the like may be used.
  • the crystallized glass for example, SiO 2 -CaO-based, MgO-B 2 O 3 based, La 2 O 3 -B 2 O 3 -MgO based, La 2 O 3 -B 2 O 3 -ZnO system, SiO 2 it may be used any of materials such as -CaO-ZnO-based, may be especially a material of SiO 2 -MgO system.
  • the conductive member 18 is interposed between the adjacent cells 1 among the plurality of cells 1.
  • the conductive member 18 electrically connects the fuel pole 3 of one adjacent cell 1 and the air pole 5 of the other cell 1 in series. More specifically, the interconnector 6 electrically connected to the fuel pole 3 of one of the adjacent cells 1 and the air pole 5 of the other cell 1 are connected.
  • the end current collecting member 17 is electrically connected to the outermost cell 1 in the arrangement direction of the plurality of cells 1.
  • the end current collecting member 17 is connected to a conductive portion 19 projecting to the outside of the cell stack 11.
  • the conductive portion 19 collects electricity generated by the power generation of the cell 1 and draws it to the outside.
  • the end current collecting member 17 is not shown.
  • the conductive portion 19 of the cell stack device 10 is divided into a positive electrode terminal 19A, a negative electrode terminal 19B, and a connection terminal 19C.
  • the positive electrode terminal 19A is a positive electrode when the electric power generated by the cell stack 11 is output to the outside, and is electrically connected to the end current collecting member 17 on the positive electrode side of the cell stack 11A.
  • the negative electrode terminal 19B is a negative electrode when the electric power generated by the cell stack 11 is output to the outside, and is electrically connected to the end current collecting member 17 on the negative electrode side of the cell stack 11B.
  • connection terminal 19C electrically connects the negative electrode side end current collecting member 17 in the cell stack 11A and the positive electrode side end current collecting member 17 in the cell stack 11B.
  • FIG. 3A is a cross-sectional view taken along the line YY shown in FIG. 2C.
  • FIG. 3B is an enlarged cross-sectional view schematically showing a main part of the cell stack shown in FIG. 3A.
  • the surface of the base material 151 constituting the support 15 is simplified and shown in a planar shape.
  • the support 15 is joined to the cell 1 via the joining member 13.
  • the support 15 has a base material 151 and a coating layer 152.
  • the base material 151 has conductivity and heat resistance.
  • the base material 151 contains chromium.
  • the base material 151 is, for example, stainless steel.
  • the base material 151 is an example of a metal member.
  • the base material 151 may contain, for example, a metal oxide.
  • the coating layer 152 coats the base material 151.
  • the coating layer 152 is located so as to be in contact with the first surface 151a and the second surface 151b of the base material 151.
  • the coating layer 152 has a first surface 152a facing the bonding material 13 and a second surface 152b exposed to an oxidizing atmosphere (external space 23).
  • the first surface 152a is an example of the first outer surface or the third outer surface.
  • the second surface 152b is an example of the second outer surface or the fourth outer surface.
  • the material of the coating layer 152 is, for example, an inorganic oxide.
  • Inorganic oxides include, for example, aluminum oxide (alumina), magnesium oxide (magnesia), silicon oxide (silica), zirconium oxide (zirconia), chromium oxide (chromia), titanium oxide (titania) and composite oxides thereof. There may be.
  • the zirconia may be stabilized zirconia.
  • the composite oxide may be selected from, for example, forsterite and cordierite.
  • the material of the coating layer 152 may be a material having a low conductivity or an insulating material. Since the material of the coating layer 152 is a material having low conductivity or an insulating material, the cell stack device 10 having a high withstand voltage and a high insulation resistance can be obtained.
  • alumina and forsterite have a small difference in the coefficient of thermal expansion from the base material 151, and the thermal stress caused by the temperature difference is small. Therefore, the coating layer 152 can be firmly bonded to the base material 151, and the coating layer 152 is less likely to be peeled off from the base material 151.
  • the coating layer 152 By locating the coating layer 152 between the bonding material 13 and the base material 151, the stress generated between the bonding material 13 and the base material 151 due to, for example, the difference in the coefficient of thermal expansion is relaxed, and the bonding material is relaxed. The occurrence of cracks in 13 is reduced.
  • the external space 23 is a space where the air electrode 5 (see FIG. 1) of the cell 1 is exposed, and is filled with an oxygen-containing gas (air or the like). That is, the external space 23 is an oxidizing atmosphere.
  • the base material 151 contains chromium (Cr).
  • Cr chromium
  • the thickness of the coating layer 152 facing the oxidizing atmosphere can be increased.
  • the thickness t2 of the coating layer 152 where the second surface 152b is located is larger than the thickness t1 of the coating layer 152 where the first surface 152a is located.
  • the durability of the air electrode 5 can be increased, so that the durability of the cell stack device 10 can be increased.
  • the coating layer 152 is bonded to the bonding material 13, and depending on the operating environment, the fuel gas is formed from the gap formed between the support 15 and the bonding material 13 due to the peeling of the coating layer 152 from the bonding material 13. Leaks, which may reduce the durability of the cell stack device 10.
  • the surface roughness of the coating layer 152 can be made larger than the surface roughness of the base material 151.
  • the surface roughness of the first surface 152a of the coating layer 152 may be larger than the surface roughness of the first surface 151a of the base material 151.
  • the adhesion between the coating layer 152 and the bonding material 13 can be improved. Therefore, for example, the support 15 is less likely to peel off from the bonding material 13, and fuel gas leakage can be less likely to occur. Therefore, according to the embodiment, the durability of the support 15 can be increased, so that the durability of the cell stack device 10 can be increased.
  • the surface roughness of the second surface 152b of the coating layer 152 may be the same as or different from the surface roughness of the first surface 152a. Further, the surface roughness of the second surface 151b of the base material 151 may be the same as or different from the surface roughness of the first surface 151a.
  • the bonding strength between the coating layer 152 and the base material 151 may be increased by adjusting the porosity of the coating layer 152. Since the thickness of the coating layer 152 located between the second surface 152b and the base material 151 is larger than the thickness of the coating layer 152 located between the first surface 152a and the base material 151, the thickness of the coating layer 152 is set on the second surface 152b. A large stress is likely to be generated in the covering layer 152 located, and it is easier to peel off from the base material 151 than the covering layer 152 located on the first surface 152a.
  • the coating layer 152 located between the second surface 152b and the base material 151 is formed by the first surface 152a and the base material 151 (the first surface 151a).
  • the porosity can be made larger than that of the coating layer 152 located between them.
  • the coating layer 152 facing the second surface 152b can be enhanced, so that the bonding strength between the coating layer 152 and the base material 151 can be enhanced. Therefore, for example, the coating layer 152 is less likely to be peeled off from the support 15, and the chromium contained in the base material 151 can be less likely to be separated into the oxidizing atmosphere (external space 23). Therefore, according to the embodiment, the durability of the air electrode 5 can be increased, so that the durability of the cell stack device 10 can be increased.
  • the bonding strength between the coating layer 152 and the bonding material 13 may be increased by adjusting the content of the metal element located at the interface between the base material 151 and the coating layer 152.
  • the metal element located at the interface between the base material 151 and the coating layer 152 For example, at least one element of Mn, Ti, Ca and Al is located on the first surface 151a and the second surface 151b corresponding to the interface between the base material 151 and the coating layer 152.
  • the coating layer 152 does not contain any of Mn, Ti, Ca and Al as a main component
  • the content of Mn, Ti, Ca and Al located on the first surface 151a and the second surface 151b is the base material. It may be larger than the content of Mn, Ti, Ca and Al located in 151 and the coating layer 152.
  • These metal elements may be mutually diffused between the base material 151 and the coating layer 152.
  • the adhesion between the base material 151 and the coating layer 152 can be improved. Therefore, for example, the base material 151 and the coating layer 152 are less likely to be peeled off, and fuel gas leakage can be less likely to occur. Therefore, according to the embodiment, the durability of the support 15 can be increased, so that the durability of the cell stack device 10 can be increased.
  • the above-mentioned metal element located at the interface between the base material 151 and the coating layer 152 can be positioned as a simple substance, an alloy, a metal oxide, or a composite oxide. Further, the metal element may be located on either the base material 151 side or the coating layer 152 side, or may be located so as to straddle the base material 151 and the coating layer 152.
  • Mn may be located in the convex portion of the base material 151, or in the concave portion or pore of the coating layer 152.
  • Ti may be located in the recesses of the base material 151 or in the pores of the coating layer 152.
  • Ca may be located in the convex portion of the base material 151, or in the concave portion or pore of the coating layer 152.
  • Al may be located in the convex portion of the base material 151, or in the concave portion or pore of the coating layer 152.
  • FIG. 4 is a cross-sectional view taken along the line ZZ shown in FIG. 2C.
  • the end current collecting member 17 is joined to the support 15 via the joining member 13.
  • the end current collecting member 17 has a base material 171 and a covering material 172.
  • chromium (Cr) contained in the base material 171 can be made difficult to be separated into the oxidizing atmosphere (external space 23) during high temperature operation.
  • the durability of the partial current collecting member 17 can be improved.
  • the base material 171 is, for example, a conductive material containing chromium (Cr).
  • the base material 171 may be, for example, stainless steel.
  • the material of the covering material 172 may be, for example, an inorganic oxide.
  • the coating material 172 may be a conductive oxide containing manganese (Mn) (for example, Mn 1.5 CO 1.5 O 4 , ZnMn CoO 4, etc.).
  • Mn manganese
  • the covering material 172 can be located on the surface of the base material 171 by, for example, electrodeposition coating.
  • the covering material 172 covers the base material 171.
  • the covering material 172 is positioned so as to cover the surfaces 171a and 171b of the base material 171.
  • the covering material 172 has a surface 172a facing the bonding material 13 and a surface 172b exposed to an oxidizing atmosphere (external space 23).
  • the covering material 172 between the joining material 13 and the base material 171, for example, the stress generated between the joining material 13 and the base material 171 due to the difference in the coefficient of thermal expansion is relaxed, and the joining material 172 is used. The occurrence of cracks in 13 is reduced.
  • the base material 171 has a surface 171c adjacent to the surface 171a and facing the bonding material 13. That is, one end (lower end) 172e of the covering material 172 faces the joining material 13 and does not face the internal space 22.
  • the surface roughness of the covering material 172 facing the joining material 13 can be made larger than the surface roughness of the covering material 172 not facing the joining material 13.
  • the surface roughness of the surface 172a of the covering material 172 may be made larger than the surface roughness of the surface 172b.
  • the adhesion between the covering material 172 and the joining material 13 can be improved. Therefore, for example, the end current collecting member 17 is less likely to peel off from the joining member 13, and fuel gas leakage can be less likely to occur. Therefore, according to the embodiment, the durability of the end current collecting member 17 can be increased, so that the durability of the cell stack device 10 can be increased.
  • the surface roughness of the base material 171 facing the joining material 13 can be made larger than the surface roughness of the covering material 172 facing the joining material 13.
  • the surface roughness of the surface 171c of the base material 171 may be made larger than the surface roughness of the surface 172a.
  • the adhesion between the end current collecting member 17 and the joining material 13 can be improved. Therefore, for example, the end current collecting member 17 is less likely to peel off from the joining member 13, and fuel gas leakage can be less likely to occur. Therefore, according to the embodiment, the durability of the end current collecting member 17 can be increased, so that the durability of the cell stack device 10 can be increased.
  • the durability of the end current collecting member 17 can be increased, so that the durability of the cell stack device 10 can be increased.
  • the area of the surface 171c may be smaller than the area of the surface 172a.
  • the area S2 of the surface 171c may be smaller than the area S1 of the surface 172a.
  • the durability of the end current collecting member 17 can be increased, so that the durability of the cell stack device 10 can be increased.
  • the surface roughness of the surface 171b of the base material 171 can be made smaller than the surface roughness of the surface 171a.
  • the surface roughness of the surface 171b is made smaller than the surface roughness of the surface 171a, for example, chromium contained in the base material 171 is desorbed into an oxidizing atmosphere (external space 23) via the surface 171b of the covering material 172 during high temperature operation. It can be made difficult.
  • the surface roughness of the surfaces 171a and 171b may be the same.
  • the base material 171 may have an oxide layer 173 located so as to face the coating material 172 and the bonding material 13.
  • the oxide layer 173 may be, for example, a natural oxide film composed of chromium oxide (Cr 2 O 3).
  • the constituent elements hardly cause a reduction reaction even in a reducing atmosphere.
  • the oxide layer 173 it is possible to make it difficult for the constituent elements of the base material 171 to be detached from the surface exposed to the reducing atmosphere (internal space 22), for example. Therefore, according to the embodiment, the durability of the end current collecting member 17 can be increased, so that the durability of the cell stack device 10 can be increased.
  • the support 15 is located so as to surround the periphery of the joining member 13 that fills the oval-shaped insertion hole 15a in the top view.
  • the insertion hole 15a of the support 15 has a linear portion (first portion 15A) extending linearly along the arrangement direction of the cells 1 as the first direction, that is, the thickness direction T (see FIG. 1A), and from the first direction. It has a bent portion (second portion 15B) that bends.
  • the cell 1 is positioned so as to face the first portion 15A of the support 15, and the end current collecting member 17 is positioned so as to face the second portion 15B of the support 15.
  • the thickness of the coating layer 152 located in the second portion 15B of the support 15 may be larger than the thickness of the coating layer 152 located in the first portion 15A.
  • the thickness t1 (see FIG. 3B) of the coating layer 152 on which the first surface 152a is located is larger in the second portion 15B than in the first portion 15A.
  • the second portion 15B of the support 15 that is bent in the top view, stress due to the difference in thermal expansion of each member is more likely to be concentrated as compared with the first portion 15A.
  • the thickness of the coating layer 152 on which the first surface 152a is located according to the shape of the support 15, particularly the insertion hole 15a viewed from above the stress concentration in the second portion 15B is relaxed, for example. can do. Therefore, according to the embodiment, the durability of the support 15 can be increased, so that the durability of the cell stack device 10 can be increased.
  • the inner surface 151e has been described as being exposed to the reducing atmosphere (internal space 22), but the present invention is not limited to this, and for example, a coating layer located so as to cover the inner surface 151e may be provided. ..
  • FIGS. 5A to 7B are perspective views showing another example of the metal member.
  • the gas tank 16 (see FIG. 2A) is joined to the lower surface or the side surface of the flat plate-shaped support 15 to form an internal space 22 (see FIG. 4C). ) Is formed.
  • the support 15 shown in FIG. 5B has a plurality of insertion holes 15a. In this case, one cell 1 may be inserted into each of the plurality of insertion holes 15a of the support 15, or a plurality of cells 1 may be inserted into each of the plurality of insertion holes 15a of the support 15. You may.
  • FIG. 5C is an enlarged cross-sectional view of another example of the metal member and the joint portion with the cell.
  • the support 15 has a flat plate shape.
  • the support 15 is joined to the cell 1 via a joining member 13.
  • the support 15 has a base material 151 and a coating layer 152.
  • the base material 151 has a first surface 151a, a second surface 151b, and an inner surface 151e.
  • the first surface 151a and the second surface 151b face the covering layer 152.
  • the inner surface 151e faces the reducing atmosphere (internal space 22).
  • the coating layer 152 coats the base material 151.
  • the coating layer 152 is located between the first surface 151a of the base material 151 and the bonding material 13. Further, the coating layer 152 is located between the second surface 151b of the base material 151 and the oxidizing atmosphere (external space 23).
  • the coating layer 152 has a first surface 152a and a second surface 152b.
  • the first surface 151a faces the joining material 13.
  • the second surface 151b faces an oxidizing atmosphere (external space 23).
  • the joining material 13 joins the cell 1 and the support 15.
  • the bonding material 13 is located between the solid electrolyte layer 4 of the cell 1 (see FIG. 1A) and the coating layer 152 of the support 15, and has the cell 1 and the first surface 152a as the first outer surface of the coating layer 152. Join.
  • the thickness t2 of the coating layer 152 on which the second surface 152b of the coating layer 152 exposed to the oxidizing atmosphere (external space 23) is located is such that the first surface 152a facing the bonding material 13 is located. It is larger than the thickness t1 of the coating layer 152 to be formed.
  • the durability of the air electrode 5 can be increased, so that the durability of the cell stack device 10 can be increased.
  • the coating layer 152 is bonded to the bonding material 13, and depending on the operating environment, the fuel gas is formed from the gap formed between the support 15 and the bonding material 13 due to the peeling of the coating layer 152 from the bonding material 13. Leakage may occur and the durability of the cell stack device 10 may be reduced.
  • the surface roughness of the coating layer 152 can be made larger than the surface roughness of the base material 151.
  • the surface roughness of the first surface 152a of the coating layer 152 may be larger than the surface roughness of the first surface 151a and the second surface 151b of the base material 151.
  • the adhesion between the coating layer 152 and the bonding material 13 can be improved. Therefore, for example, the support 15 is less likely to peel off from the bonding material 13, and fuel gas leakage can be less likely to occur. Therefore, according to the embodiment, the durability of the support 15 can be increased, so that the durability of the cell stack device 10 can be increased.
  • the surface roughness of the second surface 151b of the base material 151 may be the same as or different from the surface roughness of the first surface 151a. Further, the surface roughness of the second surface 152b of the coating layer 152 may be the same as or different from the surface roughness of the first surface 152a. For example, the surface roughness of the second surface 152b may be smaller than that of the first surface 152a.
  • Cr chromium
  • the bonding strength between the coating layer 152 and the bonding material 13 may be increased by adjusting the porosity of the coating layer 152.
  • the coating layer 152 located between the second surface 152b and the second surface 151b of the base material 151 is located between the first surface 152a and the first surface 151a of the base material 151.
  • the porosity can be made larger than that of the coating layer 152.
  • the durability of the support 15 can be increased, so that the durability of the cell stack device 10 can be increased.
  • the bonding strength between the coating layer 152 and the bonding material 13 may be increased by adjusting the content of the metal element located at the interface between the base material 151 and the coating layer 152.
  • the metal element located at the interface between the base material 151 and the coating layer 152 For example, at least one element of Mn, Ti, Ca and Al is located on the first surface 151a and the second surface 151b corresponding to the interface between the base material 151 and the coating layer 152.
  • the contents of Mn, Ti, Ca and Al located on the first surface 151a and the second surface 151b are larger than the contents of Mn, Ti, Ca and Al located on the base material 151 and the coating layer 152. May be good.
  • the adhesion between the base material 151 and the coating layer 152 can be improved. Therefore, for example, the base material 151 and the coating layer 152 are less likely to be peeled off, and fuel gas leakage can be less likely to occur. Therefore, according to the embodiment, the durability of the support 15 can be increased, so that the durability of the cell stack device 10 can be increased.
  • the above-mentioned metal element located at the interface between the base material 151 and the coating layer 152 can be positioned as a simple substance, an alloy, or a metal oxide. Further, the metal element may be located on either the base material 151 side or the coating layer 152 side, or may be located so as to straddle the base material 151 and the coating layer 152.
  • the insertion hole 15a of the support 15 shown in FIG. 5B has a first portion 15A extending in the width direction W (see FIG. 1A) of the cell 1, a second portion 15B bent from the first direction, and an arrangement of the cell 1. It has a third portion 15C extending in the direction or thickness direction T (see FIG. 1A).
  • the thickness of the coating layer 152 located at the second portion 15B of the support 15 may be larger than the thickness of the coating layer 152 located at the first portion 15A and the third portion 15C.
  • the thickness t1 (see FIG. 5C) of the coating layer 152 on which the first surface 152a is located is larger in the second portion 15B than in the first portion 15A and the third portion 15C.
  • the second portion 15B of the support 15 that is bent in the top view, stress due to the difference in thermal expansion of each member is more likely to be concentrated as compared with the first portion 15A and the third portion 15C.
  • the thickness of the coating layer 152 according to the shape of the support 15, particularly the insertion hole 15a viewed from above, the stress concentration on the first surface 152a is relaxed according to, for example, the second portion 15B. can do. Therefore, according to the embodiment, the durability of the support 15 can be increased, so that the durability of the cell stack device 10 can be increased.
  • 6A to 6E are enlarged cross-sectional views of the joint portion between the metal member and the cell according to the modified examples 1 to 5 of the embodiment.
  • 7A and 7B are enlarged cross-sectional views of the joint between the cell and another example of the metal member according to the modified examples 6 and 7 of the embodiment.
  • the covering layer 152 of the support 15 may further have an intermediate surface 152c located between the first surface 152a and the second surface 152b.
  • the intermediate surface 152c faces the coating layer 152.
  • the surface roughness of the intermediate surface 151c may be smaller than that of the first surface 152a, for example.
  • the intermediate surface 152c is located closer to the oxidizing atmosphere than the first surface 152a.
  • the coating layer 152 facing the bonding material 13 by making the surface roughness of the intermediate surface 152c smaller than that of the first surface 152a located at a portion away from the oxidizing atmosphere, for example, it is included in the base material 151 during high temperature operation. Chromium (Cr) can be prevented from desorbing into the oxidizing atmosphere (external space 23) via the coating layer 152.
  • the durability of the support 15 can be increased, so that the durability of the cell stack device 10 can be increased.
  • the surface roughness of the coating layer 152 located on the intermediate surface 152c may be the same as the surface roughness of the second surface 152b, for example. Further, the intermediate surface 152c may have, for example, an intermediate surface roughness between the first surface 152a and the second surface 152b.
  • the coating layer 152 in which the intermediate surface 152c is located may be thicker than, for example, the coating layer 152 in which the first surface 152a is located.
  • the intermediate surface 152c is located closer to the oxidizing atmosphere than the first surface 152a.
  • the thickness of the intermediate surface 152c larger than that of the first surface 152a located at a portion away from the oxidizing atmosphere in the coating layer 152 facing the bonding material 13, for example, the chromium contained in the base material 151 during high temperature operation. (Cr) can be made difficult to desorb into the oxidizing atmosphere (external space 23) via the coating layer 152. Therefore, according to the embodiment, the durability of the support 15 can be increased, so that the durability of the cell stack device 10 can be increased.
  • the thickness of the coating layer 152 located on the intermediate surface 152c may be the same as, for example, the thickness t2 of the second surface 152b (see FIG. 3B). Further, the intermediate surface 152c may have an intermediate thickness of, for example, thicknesses t1 and t2.
  • the covering layer 152 of the support 15 may further have an intermediate surface 152d located between the first surface 152a and the second surface 152b.
  • the intermediate surface 152d is exposed to an oxidizing atmosphere (external space 23).
  • the intermediate surface 152d has a larger surface roughness than, for example, the second surface 152b. Even when the intermediate surface 152d is provided in this way, it is possible to make it difficult for chromium (Cr) contained in the base material 151 to desorb into the oxidizing atmosphere (external space 23), for example, during high-temperature operation. Therefore, according to the embodiment, the durability of the support 15 can be increased, so that the durability of the cell stack device 10 can be increased.
  • the surface roughness of the intermediate surface 152d may be the same as the surface roughness of the first surface 152a, for example. Further, the intermediate surface 152d may have, for example, an intermediate surface roughness between the first surface 152a and the second surface 152b.
  • the second surface 152b exposed to the oxidizing atmosphere may have surfaces 152b1 and 152b2 having different thicknesses of the coating layer 152.
  • the surface 152b2 is located farther from the element portion of the cell 1 than the surface 152b1.
  • the surface 152b1 close to the element portion tends to have a higher temperature than the surface 152b2 away from the element portion, and chromium (Cr) contained in the base material 151 tends to be desorbed from the oxidizing atmosphere (external space 23). Therefore, the thickness of the coating layer 152 on which the surface 152b1 is located can be made larger than the thickness of the coating layer 152 on which the surface 152b2 away from the element portion is located.
  • the thickness of the coating layer 152 on which the surface 152b1 is located larger than the thickness of the coating layer 152 on which the surface 152b2 is located, for example, during high-temperature operation, chromium (Cr) contained in the base material 151 is oxidized (external space 23). ) Can be made difficult to detach. Therefore, according to the embodiment, the durability of the support 15 can be increased, so that the durability of the cell stack device 10 can be increased.
  • the surface roughness of the surface 152b1 near the element portion may be larger than the surface roughness of the surface 152b2 away from the element portion.
  • the boundary between the surfaces 152b1 and 152b2 was positioned at the upper end portion of the support 15, but the present invention is not limited to this.
  • the upper surface that can be visually recognized when the cell stack device 10 is viewed from above may be the surface 152b1, and the side surface located on the side of the surface 152b1 may be the surface 152b2.
  • the portion where the reached temperature during high temperature operation is equal to or higher than a predetermined value may be designated as the surface 152b1, and the other portion may be designated as the surface 152b2.
  • the portion of the oxygen-containing gas (air) facing the flow path (not shown) may be the surface 152b1, and the other portion may be the surface 152b2.
  • the covering layer 152 of the support 15 may further have a connecting surface 152f located between the first surface 152a and the second surface 152b.
  • the connection surface 152f continuously connects the first surface 152a and the second surface 152b by gradually changing the thickness of the coating layer 152. Since the coating layer 152 has the connection surface 152f in this way, the durability of the support 15 can be enhanced, so that the durability of the cell stack device 10 can be enhanced.
  • the connecting surface 152f may face the joining material 13 together with the first surface 152a. Further, the connecting surface 152f may be exposed to the oxidizing atmosphere (external space 23) together with the second surface 152b. Further, the connecting surface 152f may have a portion facing the bonding material 13 and a portion exposed to an oxidizing atmosphere (external space 23).
  • the thickness of the coating layer 152 may be constant. Even in such a case, the durability of the support 15 can be increased by making the surface roughness of the first surface 152a and the second surface 152b different as described above, so that the durability of the cell stack device 10 can be increased. Can be enhanced. Further, the durability of the support 15 can be enhanced by making the porosity of the coating layer 152 in the portions P1 and P2 where the first surface 152a and the second surface 152b are located different as described above, and thus the cell. The durability of the stacking device 10 can be increased.
  • the surface 152g located between the first surface 152a and the second surface 152b may have a surface roughness intermediate between the first surface 152a and the second surface 152b.
  • the porosity of the portion P3 of the coating layer 152 on which the surface 152 g is located may have an intermediate porosity between the portions P1 and P2.
  • FIG. 8A is a front view showing an end current collecting member according to the modified example 8 of the embodiment.
  • FIG. 8B is a cross-sectional view showing an end current collector member according to a modified example 9 of the embodiment.
  • the upper end 17a of the end current collecting member 17 that can be visually recognized when viewed from the upper surface may be rounded at the corner 17a1.
  • the lower end 17b of the end current collecting member 17 has an end surface 17f inclined with respect to the direction in which the cells 1 are arranged, so that the width of the end 17e is widened to the end current collecting member 17. It is located so that it is smaller than the thickness of. Therefore, the end current collecting member 17 can be smoothly inserted into the joining material 13 before solidification.
  • 8C and 8D are enlarged cross-sectional views of the joint portion between the end current collector member and the metal member according to the modified examples 10 and 11 of the embodiment.
  • the covering material 172 is located at one end (lower end) 172e of the covering material 172 of the end current collecting member 17, and is a surface 171a (surface 171c) of the base material 171 and a surface 172a of the covering material 172. It may have a surface 172f to connect with.
  • the covering material 172 is located on one end (lower end) 172e side of the covering material 172 of the end current collecting member 17, projects in a direction away from the surface 172a, and faces the joining material 13. It may have a protruding portion 172 g.
  • the covering material 172 has the surface 172f or the protruding portion 172g in this way, the contact area between the covering material 172 and the joining material 13 increases. As a result, the durability of the end current collecting member 17 can be increased, so that the durability of the cell stack device 10 can be increased.
  • the covering material 172 is shown as having a surface 172f or a protruding portion 172g in FIGS. 8C and 8D, the covering material 172 may have a surface 172f and a protruding portion 172g.
  • the thickness of each surface of the support 15 and the end current collecting member 17 described above and each surface described later is calculated by image analysis of a cross section perpendicular to each surface.
  • the support 15 and the bonding material 13, or the end current collecting member 17 and the bonding material 13 are cut out and embedded in resin, and a cross section perpendicular to the surface for measuring surface roughness is formed with abrasive grains and a wrapping film (# 8000). (Degree) or the like to polish to obtain a mirror-finished cross section.
  • the obtained cross section is photographed using an SEM (scanning electron microscope), an optical microscope, or the like, and the thickness of each surface can be measured by image analysis of the obtained image.
  • the magnitude of the surface roughness of each surface of the support 15 and the end current collecting member 17 described above and each surface described later can be determined based on the arithmetic mean roughness Ra specified in JIS B0633; 2001. can.
  • the arithmetic mean roughness Ra can be calculated by image analysis of a cross section perpendicular to each surface in the same manner as the thickness of each surface.
  • the porosity of each part of the coating layer 152 is determined by, for example, an image analysis of an image obtained by observing a cross section of each part of the coating layer 152 with an SEM (scanning electron microscope), and the total area of pores with respect to the total area of the image. It can be calculated as a ratio.
  • the content of Mn, Ti, Ca and Al in each part of the support 15 can be confirmed by elemental analysis such as ICP emission spectroscopic analysis by cutting or scraping each part of the support 15 from cell 1, for example.
  • the cross section of the support 15 can be calculated by elemental analysis using an electron probe microanalyzer (EPMA), wavelength dispersion type X-ray spectroscopy (WDS), energy dispersion type X-ray spectroscopy (EDS), or the like.
  • EPMA electron probe microanalyzer
  • WDS wavelength dispersion type X-ray spectroscopy
  • EDS energy dispersion type X-ray spectroscopy
  • the thickness of the coating layer 152 calculated as described above can be, for example, 2 ⁇ m to 400 ⁇ m on average for the entire support 15.
  • the surface roughness (arithmetic mean roughness Ra) of each surface calculated as described above may be, for example, 0.1 ⁇ m to 30 ⁇ m.
  • the surface roughness (arithmetic mean roughness Ra) of one of the first surface 152a and the second surface 152b may be, for example, 0.1 ⁇ m to 30 ⁇ m.
  • each surface described later can also have the same surface roughness (arithmetic mean roughness Ra) as each surface described above.
  • the porosity of the coating layer 152 and the coating layer described later calculated as described above can be, for example, 10 area% to 40 area% on average of the entire support 15.
  • the coating layer 152 may have cracks having an opening width of 10 ⁇ m or less, for example. Further, the bonding material 13 may be located inside the crack. By locating the joining member 13 inside the crack, for example, the durability of the support 15 can be increased, so that the durability of the cell stack device 10 can be increased.
  • the contents of Mn, Ti, Ca and Al in the support 15 and the support member described later calculated as described above are, for example, 0.01% by mass to 10% by mass on average of the entire support 15. be able to. Further, the contents of Mn, Ti, Ca and Al in the interface between the base material 151 and the coating layer 152, the base material 151 and the coating layer 152 are, for example, 0.1% by mass to 30% by mass (intersection) and 0. It can be 01% by mass to 10% by mass (base material 151) and 0.01% by mass to 10% by mass (coating layer 152).
  • the coating layer 152 can be positioned by a method such as a thermal spraying method, a vapor deposition method, an electrodeposition method, or a sputtering method. Further, for example, the surface of the base material 151 may be coated with a coating material and then fired to form a coating layer 152.
  • first surface 152a and the second surface 152b of the coating layer 152 differ in the surface roughness of the first surface 151a and the second surface 151b of the base material 151 corresponding to the first surface 152a and the second surface 152b, for example. Can be formed based on. Further, the thickness of the portion corresponding to the second surface 152b may be made larger than the thickness of the portion corresponding to the first surface 152a. Further, for example, the second surface 152b may be formed by polishing the portion of the surface of the coating layer 152 corresponding to the second surface 152b, and the remaining portion may be used as the first surface 152a.
  • first surface 152a and the second surface 152b may be formed by changing various conditions at the time of forming the covering layer 152 described above. Further, the other surfaces can also be formed by appropriately combining the above-mentioned production methods of the first surface 152a and the second surface 152b and known methods.
  • FIG. 9 is an external perspective view showing the module according to the embodiment, in which the front surface and the rear surface, which are a part of the storage container 101, are removed, and the cell stack device 10 of the fuel cell stored inside is taken out to the rear. Shown.
  • the module 100 includes a storage container 101 and a cell stack device 10 housed in the storage container 101.
  • a reformer 102 is arranged above the cell stack device 10.
  • the reformer 102 reforms raw fuels such as natural gas and kerosene to generate fuel gas, which is supplied to cell 1.
  • the raw fuel is supplied to the reformer 102 through the raw fuel supply pipe 103.
  • the reformer 102 may include a vaporizing unit 102a for vaporizing water and a reforming unit 102b.
  • the reforming unit 102b includes a reforming catalyst (not shown), and reforms the raw material fuel into a fuel gas.
  • Such a reformer 102 can perform steam reforming, which is a highly efficient reforming reaction.
  • the fuel gas generated by the reformer 102 is supplied to the gas flow path 2a (see FIG. 1A) of the cell 1 through the gas flow pipe 20, the gas tank 16, and the support member 14.
  • the temperature inside the module 100 at the time of normal power generation becomes about 500 ° C. to 1000 ° C. due to the combustion of gas and the power generation of the cell 1.
  • the module 100 that reduces the deterioration of the battery performance can be obtained by accommodating the cell stack device 10 that reduces the deterioration of the battery performance.
  • FIG. 10 is an exploded perspective view showing an example of the module accommodating device according to the embodiment.
  • the module accommodating device 110 according to the embodiment includes an outer case 111, a module 100 shown in FIG. 11, and an auxiliary machine (not shown).
  • the auxiliary device operates the module 100.
  • the module 100 and auxiliary equipment are housed in the outer case 111. In FIG. 10, a part of the configuration is omitted.
  • the exterior case 111 of the module accommodating device 110 shown in FIG. 10 has a support column 112 and an exterior plate 113.
  • the partition plate 114 divides the inside of the outer case 111 into upper and lower parts.
  • the space above the partition plate 114 in the outer case 111 is the module storage chamber 115 for accommodating the module 100, and the space below the partition plate 114 in the outer case 111 accommodates the auxiliary equipment for operating the module 100.
  • the auxiliary machine accommodated in the auxiliary machine accommodating chamber 116 is omitted.
  • the partition plate 114 has an air flow port 117 for flowing the air of the auxiliary machine accommodating chamber 116 to the module accommodating chamber 115 side.
  • the exterior plate 113 constituting the module accommodating chamber 115 has an exhaust port 118 for exhausting the air in the module accommodating chamber 115.
  • the module accommodating device 110 that reduces the deterioration of the battery performance is provided by providing the module 100 that reduces the deterioration of the battery performance in the module accommodating chamber 115. Can be done.
  • a so-called “vertical stripe type” in which only one element portion including a fuel electrode, a solid electrolyte layer, and an air electrode is provided on the surface of the support substrate is exemplified, but a plurality of elements separated from each other on the surface of the support substrate are illustrated. It can be applied to a horizontal stripe type cell stack device in which element portions are provided at each location and so-called “horizontal stripe type” cells in which adjacent element portions are electrically connected are stacked.
  • a hollow flat plate type support substrate is used, but it can also be applied to a cell stack device using a cylindrical support substrate. Further, as will be described later, it can also be applied to a flat plate type cell stack device in which so-called "flat plate type” cells are stacked in the thickness direction.
  • the example in which the fuel electrode is provided on the support substrate and the air electrode is arranged on the surface of the cell is shown, but the opposite arrangement, that is, the air electrode is provided on the support substrate. It can also be applied to cell stacking devices where the fuel poles are located on the surface of the cell.
  • the fuel cell, the fuel cell stack device, the fuel cell module, and the fuel cell device are shown as examples of the “cell”, the “cell stack device”, the “module”, and the “module accommodating device”.
  • Other examples may be an electrolytic cell, an electrolytic cell stacking device, an electrolytic module and an electrolytic device, respectively.
  • FIG. 11A is a perspective view showing a flat plate type cell according to the modified example 12 of the embodiment.
  • FIG. 11B is a partial cross-sectional view of the flat plate cell shown in FIG. 11A.
  • FIG. 11C is an enlarged view of the region A shown in FIG. 11B.
  • the cell stack device has a cell 1A in which a fuel electrode 3, a solid electrolyte layer 4, and an air electrode 5 are laminated. Further, as shown in FIG. 11B, the cell 1A has an element portion 90 in which the solid electrolyte layer 4 is sandwiched between the fuel electrode 3 and the air electrode 5.
  • each element portion 90 of the plurality of cells 1A is electrically connected by conductive members 91 and 92 which are metal layers adjacent to each other.
  • the conductive members 91 and 92 electrically connect the element portions 90 of the adjacent cells 1A to each other, and have a gas flow path for supplying gas to the fuel pole 3 or the air pole 5.
  • the flat plate type cell stack has a sealing material that airtightly seals the flow path 98 of the fuel gas and the flow path 97 of the oxygen-containing gas.
  • the sealing material is a cell fixing member 96, and has a joining material 93 and support members 94 and 95 which are frames.
  • the bonding material 93 may be glass or a metal material such as silver wax.
  • the support member 94 may be a so-called separator that separates the fuel gas flow path 98 and the oxygen-containing gas flow path 97.
  • the materials of the support members 94 and 95 may be, for example, a conductive metal or an insulating ceramic.
  • the bonding material 93 is an insulating material such as glass
  • both the support members 94 and 95 may be made of metal, or one of the supporting members 94 and 95 may be made of an insulating material.
  • the bonding material 93 is a conductive metal
  • the support members 94 and 95 may be made of an insulating material.
  • the support members 94 and 95 may be integrated with the conductive member 92.
  • One of the joining material 93 and the supporting members 94 and 95 is insulating, and the two conductive members 91 and 92 sandwiching the flat plate type cell are electrically insulated from each other.
  • the flat plate type cell includes a support member 94 and a joining material 93.
  • the support member 94 has a base material 941 and a coating layer 942.
  • the base material 941 has a first surface 941a and a second surface 941b, and contains chromium.
  • the coating layer 942 covers the first surface 941a and the second surface 941b of the base material 941.
  • the bonding material 93 is located between the solid electrolyte layer 4 of the element portion 90 and the first surface 942a of the coating layer 942.
  • the second surface 942b of the coating layer 942 is exposed to the oxidizing atmosphere (flow path 97).
  • the thickness of the coating layer 942 on which the second surface 942b is located is larger than the thickness of the coating layer 942 on which the first surface 942a is located.
  • Cr chromium
  • the surface roughness of the first surface 942a may be larger than the surface roughness of the second surface 942b.
  • the coating layer 942 can be prevented from being peeled off from the bonding material 93, or the bonding material 93 can be broken and the fuel gas can be prevented from leaking. Therefore, according to the embodiment, the durability of the support member 94 can be improved.
  • the porosity of the coating layer 942 on which the second surface 942b is located may be larger than the porosity of the coating layer 942 where the first surface 942a is located. This makes it difficult for chromium (Cr) contained in the base material 941 to desorb into the oxidizing atmosphere (flow path 97) via the coating layer 942 during high-temperature operation. Therefore, according to the embodiment, the durability of the support member 94 can be increased, so that the durability of the cell stack device can be increased.
  • the coating layer 942 is positioned so as to cover the surface 941e of the base material 941 facing the reducing atmosphere (flow path 98), but the present invention is not limited to this, and the surface 941e is positioned as the reducing atmosphere. It may be exposed to (flow path 98).
  • the cell stack device 10 includes a plurality of cells 1, a metal member (base material 151), a coating layer 152, and a bonding material 13.
  • the plurality of cells 1 have an element unit and include a first cell.
  • the metal member (base material 151) contains chromium.
  • the coating layer 152 covers the metal member (base material 151).
  • the bonding material 13 is located between the first cell and the coating layer 152.
  • the cell stack device 10 satisfies any one of (1) to (3).
  • the coating layer 152 has at least two sites having different thicknesses or different surface roughnesses at different positions. (2) The surface roughness of the coating layer 152 is different from the surface roughness of the metal member.
  • At least one element of Mn, Ti, Ca and Al is located at the interface between the metal member and the coating layer, and the content of at least one of Mn, Ti, Ca and Al at the interface is the metal member or It is different from the Mn, Ti, Ca and Al contents of the coating layer. This makes it possible to increase the durability of the cell stack device 10.
  • the module 100 includes the cell stack device 10 described above and a storage container 101 for accommodating the cell stack device 10. As a result, the module 100 can be made to reduce the deterioration of the battery performance.
  • the module accommodating device 110 includes the module 100 described above, an auxiliary machine for operating the module 100, and an outer case for accommodating the module 100 and the auxiliary equipment. As a result, the module accommodating device 110 can be obtained to reduce the deterioration of the battery performance.

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  • General Chemical & Material Sciences (AREA)
  • Electrochemistry (AREA)
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  • Sustainable Energy (AREA)
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  • Materials Engineering (AREA)
  • Ceramic Engineering (AREA)
  • Composite Materials (AREA)
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  • Electrolytic Production Of Non-Metals, Compounds, Apparatuses Therefor (AREA)
  • Other Surface Treatments For Metallic Materials (AREA)
PCT/JP2021/015086 2020-04-09 2021-04-09 セルスタック装置、モジュールおよびモジュール収容装置 Ceased WO2021206175A1 (ja)

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US17/916,457 US12592400B2 (en) 2020-04-09 2021-04-09 Cell stack device, module, and module housing device
JP2021544179A JP7004870B1 (ja) 2020-04-09 2021-04-09 セルスタック装置、モジュールおよびモジュール収容装置
EP21783796.2A EP4135079A4 (en) 2020-04-09 2021-04-09 ELEMENT STACKING DEVICE, MODULE AND MODULE RECEIVING APPARATUS
CN202180025685.3A CN115398686B (zh) 2020-04-09 2021-04-09 电池堆装置、模块、模块收容装置以及带涂层的金属构件
JP2022000278A JP7736578B2 (ja) 2020-04-09 2022-01-04 被覆層付き金属部材
JP2025142695A JP2025172883A (ja) 2020-04-09 2025-08-28 被覆層付き金属部材

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WO2026071253A1 (ja) * 2024-09-30 2026-04-02 京セラ株式会社 金属部材、電気化学セル装置、モジュールおよびモジュール収容装置

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JP2022060212A (ja) 2022-04-14
CN115398686B (zh) 2025-03-04
US12592400B2 (en) 2026-03-31
EP4135079A1 (en) 2023-02-15
CN115398686A (zh) 2022-11-25
US20230223565A1 (en) 2023-07-13
JP7004870B1 (ja) 2022-02-04

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