JP2005327625A - Solid electrolyte fuel cell - Google Patents

Abstract

<P>PROBLEM TO BE SOLVED: To provide a solid electrolyte fuel cell capable of restraining crossover of fuel. <P>SOLUTION: The solid electrolyte fuel cell, structured of a fuel electrode 2, an oxidant electrode 3, and a solid electrolyte film 4A pinched by the fuel electrode 2 and the oxidant electrode 3, is provided with a substance for catching fuel crossed over between the fuel electrode 2 and the oxidant electrode 3. By providing the substance for catching the fuel crossed over between the fuel electrode 2 and the oxidant electrode 3, the crossover can be attenuated, since the passage of excessive liquid organic fuel is restrained. <P>COPYRIGHT: (C)2006,JPO&NCIPI

Description

  The present invention relates to a solid oxide fuel cell including a fuel electrode, an oxidant electrode, and a solid electrolyte membrane sandwiched between the fuel electrode and the oxidant electrode, and particularly suppresses fuel crossover. The present invention relates to a solid oxide fuel cell.

  A solid oxide fuel cell has a solid polymer electrolyte membrane such as a perfluorosulfonic acid membrane as an electrolyte, and a fuel electrode and an oxidant electrode are joined to both sides of the membrane. It is a device that generates liquid organic fuel by supplying an oxygen to the oxidant electrode and electrochemical reaction.

  Among such fuel cells, those that directly supply liquid organic fuel directly to the fuel electrode without being reformed, as represented by direct methanol fuel cells, have been actively developed in recent years. Yes. The fuel cell that directly supplies the liquid organic fuel to the fuel electrode without reforming has a structure for supplying the liquid organic fuel directly to the fuel electrode, and therefore does not require a device such as a reformer. Therefore, there are advantages that the configuration of the battery is simplified and the entire apparatus can be reduced in size. Moreover, compared with gaseous fuels, such as hydrogen gas and hydrocarbon gas, liquid organic fuel also has the advantage that it can be conveyed easily and safely.

  In general, in a fuel cell using a liquid organic fuel, a solid polymer electrolyte membrane made of a solid polymer ion exchange resin is used as an electrolyte. Here, in order for the fuel cell to function, it is necessary for hydrogen ions to move through the membrane from the fuel electrode to the oxidant electrode, and it is known that this movement of hydrogen ions involves the movement of water. It is necessary that the electrolyte membrane contains a certain amount of moisture.

  However, when a liquid organic fuel such as methanol having a high affinity for water is used, the liquid organic fuel diffuses into the solid polymer electrolyte membrane containing moisture, and further reaches the oxidizer electrode. A phenomenon called over occurs. This crossover is oxidized when the liquid organic fuel that should originally provide electrons at the fuel electrode reaches the oxidizer electrode side, and is no longer used effectively as a fuel, resulting in a decrease in voltage and output, and a decrease in fuel efficiency. cause.

Conventionally, various methods have been reported as measures for avoiding such crossover. For example, an example of using a material that does not easily cross over as a material for the solid electrolyte membrane has been proposed, but it cannot be said that a sufficient effect has been obtained.
JP 2004-26936 A

  Accordingly, an object of the present invention is to provide a solid oxide fuel cell capable of suppressing fuel crossover.

  The solid oxide fuel cell of the present invention is a solid oxide fuel cell comprising a fuel electrode, an oxidant electrode, and a solid electrolyte membrane sandwiched between the fuel electrode and the oxidant electrode. It is characterized in that there is a substance that captures the fuel crossed over with the oxidant electrode.

  In general, a solid electrolyte membrane having high hydrogen ion conductivity, such as Nafion (registered trademark), is used as a solid electrolyte membrane used in a solid oxide fuel cell. The high hydrogen ion conductivity in such a solid electrolyte membrane is manifested by the fact that this solid electrolyte membrane contains moisture. On the other hand, as described above, liquid organic fuel such as methanol becomes water based on the moisture content. It easily dissolves and promotes the development of a crossover that moves through the solid electrolyte membrane and reaches the oxidizer electrode.

  In the present invention, by providing a substance that captures the fuel that has crossed over between the fuel electrode and the oxidant electrode, it is possible to suppress the passage of excess liquid organic fuel, thereby reducing the fuel crossover. Is possible.

  In the present invention, the substance that captures the crossover fuel is preferably a compound that forms a complex or molecular compound with the fuel. Examples of the compound that forms a complex or molecular compound with the fuel include organic compounds, inorganic compounds, And one or more selected from the group consisting of organic / inorganic composite compounds. In particular, a compound that forms a molecular compound with a fuel is a monomolecular host compound, a multimolecular host compound, a polymer host compound, an inorganic host compound, or an organic-inorganic hybrid host that forms an inclusion compound with a fuel. One or more selected from the group consisting of compounds are preferred.

  The compound that forms a complex or molecular compound with the fuel may be supported on a porous material.

  In the present invention, the compound that forms a complex or molecular compound with the fuel may be contained in the solid electrolyte membrane. A layer containing a compound that forms a complex or molecular compound with the fuel may be provided between the solid electrolyte membrane and the oxidant electrode.

  The fuel cell of the present invention includes a fuel electrode, an oxidant electrode, and a solid electrolyte membrane sandwiched between the fuel electrode and the oxidant electrode, and a so-called direct organic liquid fuel is directly supplied to the fuel electrode. Type fuel cell. As described above, this direct fuel cell has advantages such as high cell efficiency and the need for a reformer, which can save space, but has a crossover of liquid organic fuel such as methanol. It becomes a problem. According to the present invention, such a crossover problem can be solved, the output of the solid oxide fuel cell can be increased, the fuel efficiency can be improved, and good cell efficiency can be stably maintained over a long period of time. It becomes possible to do.

  Hereinafter, embodiments of the solid oxide fuel cell of the present invention will be described in detail.

  First, a substance that captures crossover fuel, which is a feature of the solid oxide fuel cell of the present invention, will be described.

  In the present invention, the substance that captures the crossover fuel is not particularly limited as long as it is a substance that can capture this fuel, but a compound that forms a complex or molecular compound with the fuel is effective. Hereinafter, a substance that traps the fuel that has crossed over may be referred to as a “fuel trapping substance”, and a compound that forms a complex or molecular compound with the fuel may be referred to as a “trapping compound”.

  The molecular compound referred to in the present invention is a relatively weak interaction other than a covalent bond, in which two or more kinds of compounds that can exist stably alone are represented by hydrogen bonds and van der Waals forces. And includes hydrates, solvates, addition compounds, inclusion compounds, and the like.

  Such a scavenging compound captures the fuel by contact with the fuel.

  Of the compounds that form a molecular compound with the fuel, the host compound that forms the clathrate compound with the fuel is not particularly limited as long as it can clathrate the fuel. Examples of such host compounds include organic compounds, inorganic compounds, or organic / inorganic composite compounds, and monomolecular host compounds, multimolecular host compounds, polymer host compounds, inorganic host compounds, 1 type, or 2 or more types chosen from the group which consists of an organic-inorganic hybrid host compound is mentioned.

  Monomolecular host compounds include cyclodextrins, crown ethers, cryptands, cyclophanes, azacyclophanes, calixarenes, cyclotriveratrilens, spherands, cyclic oligopeptides, etc. .

  The polymolecular host compounds include ureas, thioureas, deoxycholic acids, perhydrotriphenylenes, tri-o-thymotides, bianthryls, spirobifluorenes, cyclophosphazenes, monoalcohols. Diols, acetylene alcohols, hydroxybenzophenones, phenols, bisphenols, trisphenols, tetrakisphenols, polyphenols, naphthols, bisnaphthols, diphenylmethanols, carboxylic acid amides, thioamides, bixanthenes , Carboxylic acids, imidazoles, hydroquinones and the like.

  In addition, examples of the polymer host compound include celluloses, starches, chitins, chitosans, polyvinyl alcohols, polyethylene glycol arm type polymers having 1,1,2,2-tetrakisphenylethane as a core, α, Examples include polyethylene glycol arm type polymers having α, α ′, α′-tetrakisphenylxylene as a core.

  Examples of inorganic host compounds include titanium oxide, graphite, alumina, transition metal dicargogenite, lanthanum fluoride, clay minerals (such as montmorillonite), silver salts, silicates, phosphates, zeolites, silica, porous glass, etc. Is mentioned.

  Examples of the organic-inorganic hybrid host compound include calixarene-tungsten oxide clusters. In addition, an organophosphorus compound, an organosilicon compound, etc. are also mentioned. In addition, some organometallic compounds exhibit properties as host compounds, such as organoaluminum compounds, organotitanium compounds, organoboron compounds, organozinc compounds, organoindium compounds, organogallium compounds, organotellurium compounds, organotin compounds. , Organic zirconium compounds, and organic magnesium compounds. Further, it is possible to use a metal salt of an organic carboxylic acid, an organic metal complex, or the like, but it is not particularly limited as long as it is an organic metal compound.

  Of these host compounds, multi-molecular host compounds whose inclusion ability is hardly influenced by the molecular size of the guest compound are preferable.

  Specific examples of the multimolecular host compound include urea, 1,1,6,6-tetraphenylhexa-2,4-diyne-1,6-diol, and 1,1-bis (2,4-dimethyl). Phenyl) -2-propyn-1-ol, 1,1,4,4-tetraphenyl-2-butyne-1,4-diol, 1,1,6,6-tetrakis (2,4-dimethylphenyl)- 2,4-hexadiyne-1,6-diol, 9,10-diphenyl-9,10-dihydroanthracene-9,10-diol, 9,10-bis (4-methylphenyl) -9,10-dihydroanthracene- 9,10-diol, 1,1,2,2-tetraphenylethane-1,2-diol, 4-methoxyphenol, 2,4-dihydroxybenzophenone, 4,4′-dihydroxybenzophenone, 2, 2'-dihydroxybenzophenone, 2,2 ', 4,4'-tetrahydroxybenzophenone, 1,1-bis (4-hydroxyphenyl) cyclohexane, 4,4'-sulfonylbisphenol, 2,2'-methylenebis (4- Methyl-6-tert-butylphenol), 4,4′-ethylidenebisphenol, 4,4′-thiobis (3-methyl-6-tert-butylphenol), 1,1,3-tris (2-methyl-4-hydroxy) -5-t-butylphenyl) butane, 1,1,2,2-tetrakis (4-hydroxyphenyl) ethane, 1,1,2,2-tetrakis (4-hydroxyphenyl) ethylene, 1,1,2, 2-tetrakis (3-methyl-4-hydroxyphenyl) ethane, 1,1,2,2-tetrakis (3-fluoro-4-hydroxyphenyl) Ethane, α, α, α ′, α′-tetrakis (4-hydroxyphenyl) -p-xylene, tetrakis (p-methoxyphenyl) ethylene, 3,6,3 ′, 6′-tetramethoxy-9,9 ′ -Bi-9H-xanthene, 3,6,3 ', 6'-tetraacetoxy-9,9'-bi-9H-xanthene, 3,6,3', 6'-tetrahydroxy-9,9'-bi -9H-xanthene, gallic acid, methyl gallate, catechin, bis-β-naphthol, α, α, α ′, α′-tetraphenyl-1,1′-biphenyl-2,2′-dimethanol, diphenic acid Bisdicyclohexylamide, bisdicyclohexylamide fumarate, cholic acid, deoxycholic acid, 1,1,2,2-tetraphenylethane, tetrakis (p-iodophenyl) ethylene, 9,9′-bianthryl, 1,1,2 , 2- Tetrakis (4-carboxyphenyl) ethane, 1,1,2,2-tetrakis (3-carboxyphenyl) ethane, acetylenedicarboxylic acid, 2,4,5-triphenylimidazole, 1,2,4,5-tetraphenyl Imidazole, 2-phenylphenanthro [9,10-d] imidazole, 2- (o-cyanophenyl) phenanthro [9,10-d] imidazole, 2- (m-cyanophenyl) phenanthro [9,10-d ] Imidazole, 2- (p-cyanophenyl) phenanthro [9,10-d] imidazole, hydroquinone, 2-t-butylhydroquinone, 2,5-di-t-butylhydroquinone, 2,5-bis (2,4 -Dimethylphenyl) hydroquinone, and the like.

  Among the compounds described above, 1,1-bis (4-hydroxyphenyl) cyclohexane, 1,1,2,2-tetrakis (4-hydroxyphenyl) ethane, 1,1,2,2-tetrakis (4 Phenolic host compounds such as -hydroxyphenyl) ethylene are advantageous in terms of economy and inclusion ability.

  One of these trapping compounds such as a host compound may be used alone, or two or more thereof may be used in combination.

  These capturing compounds such as a host compound can also be used as a capturing compound-containing composite material supported on a porous material. In this case, examples of the porous material that supports the capturing compound such as the host compound include silica, zeolites, activated carbons, and intercalation compounds such as clay minerals and montmorillonites, but are not limited thereto. Is not to be done. Such a capturing compound-containing composite material is prepared by dissolving the capturing compound such as the host compound described above in a solvent capable of dissolving the compound, impregnating the solution in a porous material, drying the solvent, and reducing the pressure. It can be produced by a method such as drying. Although there is no restriction | limiting in particular as the load of the trapping compound with respect to a porous substance, Usually, it is about 10 to 80 weight% with respect to a porous substance.

  A configuration of a solid oxide fuel cell according to the present invention including the above-described fuel trapping substance between a fuel electrode and an oxidant electrode will be described below with reference to the drawings.

  1 and 2 are cross-sectional views schematically showing the structure of a solid oxide fuel cell according to an embodiment.

  1 and 2, the electrode-electrolyte assembly 1 includes a fuel electrode 2, an oxidant electrode 3, and solid polymer electrolyte membranes 4 and 4A. The fuel electrode 2 includes a base 2A and a catalyst layer 2B. The oxidant electrode 3 includes a base 3A and a catalyst layer 3B. The plurality of electrode-electrolyte assemblies 1 are electrically connected via the fuel electrode side separator 5 and the oxidant electrode side separator 6 to form fuel cells 10 and 10A.

  In the fuel cells 10 and 10A configured as described above, the fuel 7 is supplied to the fuel electrode 2 of each electrode-electrolyte assembly 1 via the fuel electrode-side separator 5. An oxidant 8 such as air or oxygen is supplied to the oxidant electrode 3 of each electrode-electrolyte assembly 1 through the oxidant electrode side separator 6.

  The solid polymer electrolyte membranes 4 and 4A have a role of separating the fuel electrode 2 and the oxidant electrode 3 and moving hydrogen ions between the two. For this reason, it is preferable that the solid polymer electrolyte membranes 4 and 4A are membranes having high hydrogen ion conductivity. Further, it is preferably chemically stable and has high mechanical strength.

  As a material constituting the solid polymer electrolyte membrane 4 or 4A, an organic polymer having a polar group such as a strong acid group such as a sulfone group, a phosphoric acid group, a phosphone group or a phosphine group or a weak acid group such as a carboxyl group is preferable. Used. Examples of the organic polymer include aromatic-containing polymers such as sulfonated poly (4-phenoxybenzoyl-1,4-phenylene) and alkylsulfonated polybenzimidazole; polystyrene sulfonic acid copolymer, polyvinyl sulfonic acid copolymer, Copolymers such as cross-linked alkyl sulfonic acid derivatives, fluorine resin skeletons and fluorine-containing polymers composed of sulfonic acids; acrylamides such as acrylamide-2-methylpropane sulfonic acid and acrylates such as n-butyl methacrylate Copolymer obtained by polymerization; sulfone group-containing perfluorocarbon (Nafion (registered trademark, manufactured by DuPont), Aciplex (manufactured by Asahi Kasei)); carboxyl group-containing perfluorocarbon (Flemion (registered trademark) S membrane (Asahi Glass Co., Ltd.) Made)); etc. It is shown.

  In the present invention, for example, at the time of manufacturing such solid polymer electrolyte membranes 4 and 4A, a fuel trapping substance is mixed to form a solid polymer electrolyte membrane 4A containing a fuel trapping substance as shown in FIG. As shown in FIG. 2, the fuel trapping material is made into a layer or film and is made to exist as a fuel trapping material layer 9 between the solid polymer electrolyte membrane 4 and the oxidant electrode 3, whereby the fuel electrode 2 and the oxidant electrode 3. A fuel trapping substance is present between the two. The fuel trapping material layer 9 may be provided between the fuel electrode 2 and the solid polymer electrolyte membrane 4, and between the fuel electrode 2 and the solid polymer electrolyte membrane 4, and between the solid polymer electrolyte membrane. 4 and the oxidant electrode 3 may be provided both.

  As the base 2A of the fuel electrode 2 and the base 3A of the oxidant electrode 3, both the fuel electrode 2 and the oxidant electrode 3 are porous such as carbon paper, carbon molded body, carbon sintered body, sintered metal, and foam metal. A substrate can be used. In addition, a water repellent such as polytetrafluoroethylene can be used for the water repellent treatment of these substrates.

  Examples of the catalyst for the fuel electrode 2 include platinum, rhodium, palladium, iridium, osmium, ruthenium, rhenium, gold, silver, nickel, cobalt, lithium, lanthanum, strontium, yttrium, and the like. More than one type can be used in combination. As the catalyst for the oxidant electrode 3, the same catalyst as that for the fuel electrode 2 can be used, and the above exemplified substances can be used. The catalyst for the fuel electrode 2 and the oxidant electrode 3 may be the same or different.

  Examples of the carbon particles supporting the catalyst include acetylene black (DENKA BLACK (registered trademark, manufactured by Denki Kagaku Kogyo Co., Ltd.), XC72 (manufactured by Vulcan), etc.), ketjen black, carbon nanotube, carbon nanohorn, and the like. . The average particle diameter of the carbon particles is, for example, 0.01 to 0.1 μm, preferably 0.02 to 0.06 μm.

  As the fuel, a liquid organic fuel having a C—H bond is preferably used. For example, alcohols such as methanol, ethanol, and propanol; ethers such as dimethyl ether; cycloparaffins such as cyclohexane; cycloparaffins having a hydrophilic group such as a hydroxyl group, a carboxyl group, an amino group, and an amide group; Substitution or disubstitution; and the like can be used. Here, cycloparaffins refer to cycloparaffins and substituted products thereof, and those other than aromatic compounds are used. Such fuel is usually used as an aqueous solution of about 5 to 90% by weight.

  The method for producing the fuel electrode 2 and the oxidant electrode 3 is not particularly limited, but for example, it can be produced as follows. First, the catalyst for the fuel electrode 2 and the oxidant electrode 3 can be supported on the carbon particles by a generally used impregnation method. Next, the carbon particles carrying the catalyst and the solid polymer electrolyte particles are dispersed in a solvent to form a paste, and this is applied to the substrates 2A and 3A and dried, whereby the fuel electrode 2 and the oxidant electrode 3 are formed. Can be obtained.

  Here, the average particle diameter of the carbon particles is, for example, 0.01 to 0.1 μm as described above. Moreover, the average particle diameter of catalyst particles shall be 1-10 nm, for example. The average particle diameter of the solid polymer electrolyte particles is, for example, 0.05 to 1 μm. For example, the carbon particles and the solid polymer electrolyte particles are used in a weight ratio of 2: 1 to 40: 1. Moreover, the weight ratio of the water and the solute in the paste is, for example, about 1: 2 to 10: 1.

  Although there is no restriction | limiting in particular about the coating method of the paste to a base | substrate, For example, methods, such as brush coating, spray coating, and screen printing, can be used. The paste is applied with a thickness of about 1 μm to 2 mm. After the paste is applied, the fuel electrode 2 or the oxidant electrode 3 is produced by heating at a heating temperature and a heating time according to the fluororesin of the solid polymer electrolyte to be used. The heating temperature and the heating time are appropriately selected depending on the material to be used. For example, the heating temperature may be 100 to 250 ° C., and the heating time may be 30 seconds to 30 minutes.

  The solid polymer electrolyte membranes 4 and 4A in the present invention can be produced by employing an appropriate method depending on the material used. For example, when the solid polymer electrolyte membrane 4 is composed of an organic polymer material, a liquid obtained by dissolving or dispersing the organic polymer material in a solvent is cast on a peelable sheet such as polytetrafluoroethylene and dried. Can be obtained. At the time of manufacturing, the solid polymer electrolyte membrane 4A in which the fuel trapping substance is present can be manufactured by mixing the fuel trapping substance and manufacturing the same. The ratio between the organic polymer material and the fuel trapping substance is used in the range of 100: 0.1 to 100: 10 by weight. Here, if the ratio of the fuel trapping substance is too small, it is not possible to obtain a sufficient crossover suppression effect by trapping the fuel, and if it is too large, it is economically disadvantageous.

  The solid polymer electrolyte membrane 4A produced as described above is sandwiched between the fuel electrode 2 and the oxidant electrode 3 and hot pressed to obtain the electrode-electrolyte assembly 1. At this time, the surface on which the catalyst of both electrodes is provided is brought into contact with the solid polymer electrolyte membrane 4A.

  When the fuel trapping material layer 9 is provided, for example, a fuel trapping material film prepared by separately forming is used, and the fuel electrode 2, the solid polymer electrolyte membrane 4, the fuel trapping material layer 9, and the oxidant electrode 3 are used in this order. Laminate and hot press to obtain the electrode-electrolyte assembly 1. In this case, the thickness of the fuel trapping material layer 9 is preferably about 1 to 10% with respect to the thickness of the solid polymer electrolyte membrane 4. If the thickness of the fuel trapping material layer 9 is too thin, a sufficient crossover suppression effect due to fuel trapping cannot be obtained, and if it is too thick, it is economically disadvantageous.

  Needless to say, the fuel trapping substance-containing solid polymer electrolyte membrane 4A and the fuel trapping substance layer 9 may be laminated and used, but in this case, the fuel trapping substance-containing solid polymer electrolyte membrane 4A described above is used. It is preferable that the ratio of the fuel trapping material is slightly less than the above and the fuel trapping material layer 9 is thinly provided.

The conditions for hot pressing are selected according to the material. When the solid polymer electrolyte membranes 4 and 4A and the electrolyte membrane on the electrode surface are composed of organic polymers, the softening temperature and glass transition temperature of these polymers are set. The temperature can be exceeded. Specifically, the conditions of a temperature of 100 to 250 ° C., a pressure of 5 to 100 kgf / cm ² (0.49 to 9.8 MPa), and a time of 10 to 300 seconds are employed.

  Hereinafter, the present invention will be described more specifically with reference to examples and comparative examples. However, the present invention is not limited to the following examples as long as the gist thereof is not exceeded.

(Example 1)
A solid oxide fuel cell according to this example will be described with reference to FIG.

  First, 10 g of acetylene black (Denka Black (registered trademark); manufactured by Denki Kagaku Kogyo Co., Ltd.) is mixed with 500 g of a dinitrodiamine platinum nitric acid solution containing 3% by weight of platinum as a catalyst in the fuel electrode 2 and the oxidizer electrode 3 and stirred. Then, 60 mL of 98% ethanol was added as a reducing agent. This solution was stirred and mixed at about 95 ° C. for 8 hours, and platinum fine particles were supported on acetylene black particles. Then, this solution was filtered and dried to obtain platinum-supported carbon particles. The amount of platinum supported was about 50% by weight with respect to the weight of acetylene black.

Next, 200 mg of platinum-supported carbon particles and 3.5 mL of 5% Nafion (registered trademark) solution (alcohol solution, manufactured by Aldrich Chemical Co.) are mixed and stirred to adsorb Nafion (registered trademark) on the surface of platinum and carbon particles. It was. The dispersion thus obtained was made into a paste by dispersing with an ultrasonic disperser at 50 ° C. for 3 hours. 2 mg / cm ^{2 of} this paste was applied on carbon paper (Toray Industries, Inc .: TGP-H-120) by screen printing, and dried at 120 ° C. to obtain an electrode.

As the solid polymer electrolyte membrane 4A, a Nafion membrane (thickness 150 μm) containing 1% by weight of 1,1-bis (4-hydroxyphenyl) cyclohexane as a fuel trapping material was prepared and used. The fuel-capturing substance-containing solid polymer electrolyte membrane 4A is sandwiched between the polymer electrolyte membrane 4A with the electrode obtained above as the fuel electrode 2 and the oxidizer electrode 3 and thermocompression-bonded at 120 ° C. The electrode-electrolyte assembly 1 was produced by hot pressing under conditions of a pressure of 10 kgf / cm ² (0.98 MPa) for 10 seconds.

  Next, a fuel flow channel 21 made of tetrafluoroethylene resin was provided on the fuel electrode 2 in order to supply fuel to the fuel electrode 2. The fuel channel 21 is provided with a fuel tank 22 and a waste liquid tank 23. The fuel tank 22 is provided with a pump so that methanol can be continuously supplied to the fuel electrode 2 as indicated by an arrow in the figure.

  Further, in order to supply the oxidant to the oxidant electrode 3, a tetrafluoroethylene resinous oxidant flow path 24 was provided on the oxidant electrode 3. The oxidant flow path 24 is provided with an oxygen compressor 25 and an exhaust port 26 so that oxygen can be continuously supplied to the oxidant electrode 3 as indicated by arrows in the figure.

  The fuel tank 22 was charged with a 10% by weight aqueous methanol solution as fuel. This fuel was supplied to the fuel electrode 2 at 2 mL / min. The oxidizer electrode 3 was supplied with oxygen at 1.1 atm (0.11 MPa) and 25 ° C. by an oxygen compressor 25.

The operation was performed under such conditions, the current-voltage characteristics of the unit cells were measured, and the results are shown in Table 1.
(Comparative Example 1)
A solid oxide fuel cell was assembled in the same manner as in Example 1 except that a Nafion membrane (thickness 150 μm) containing no fuel-trapping substance was used as the solid polymer electrolyte membrane, and the current of the unit cell under the same conditions The voltage characteristics were measured and the results are shown in Table 1.

  From Table 1, it is clear that the unit cell in Example 1 is superior to the unit cell in Comparative Example 1 in terms of open circuit voltage, short circuit current, and maximum power.

It is sectional drawing which represented typically the structure of an example of the solid oxide fuel cell of this invention. It is sectional drawing which represented typically the structure of the other example of the solid oxide fuel cell of this invention. It is explanatory drawing of the fuel supply system of the solid oxide fuel cell in an Example.

Explanation of symbols

1 Electrode-Electrolyte Assembly 2 Fuel Electrode 2A Base 2B Catalyst Layer 3 Oxidant Electrode 3A Base 3B Catalyst Layer 4 Solid Polymer Electrolyte Membrane 4A Fuel Capturing Substance-Containing Solid Polymer Electrolyte 5 Fuel Electrode Side Separator 6 Oxidant Electrode Side Separator 7 Fuel 8 Oxidant 9 Fuel capture material layer 10, 10A Fuel cell 21 Fuel flow path 22 Fuel tank 23 Waste liquid tank 24 Oxidant flow path 25 Oxygen compressor 26 Exhaust port

Claims (7)

  In a solid oxide fuel cell comprising a fuel electrode, an oxidant electrode, and a solid electrolyte membrane sandwiched between the fuel electrode and the oxidant electrode, a crossover occurs between the fuel electrode and the oxidant electrode A solid oxide fuel cell characterized in that a substance for capturing fuel is present.   2. The solid oxide fuel cell according to claim 1, wherein the substance that captures the crossover fuel includes a compound that forms a complex or a molecular compound with the fuel.   3. The solid oxide fuel cell according to claim 1, wherein the compound that forms a complex or molecular compound with the fuel is one or two selected from the group consisting of an organic compound, an inorganic compound, and an organic / inorganic composite compound. A solid oxide fuel cell characterized in that it is a seed or more.   4. The solid oxide fuel cell according to claim 1, wherein the compound that forms a molecular compound with the fuel forms a clathrate compound with the fuel. A solid oxide fuel cell, which is one or more selected from the group consisting of a host compound, a polymer host compound, an inorganic host compound, and an organic-inorganic hybrid host compound.   5. The solid electrolyte fuel cell according to claim 1, wherein a compound that forms a complex or a molecular compound with the fuel is supported on a porous material. 6.   6. The solid oxide fuel cell according to claim 1, wherein a compound that forms a complex or a molecular compound with the fuel is contained in the solid electrolyte membrane. battery.   7. The solid oxide fuel cell according to claim 1, wherein a layer containing a compound that forms a complex or a molecular compound with the fuel is provided between the solid electrolyte membrane and an oxidant electrode. A solid oxide fuel cell.

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