JP4815823B2 - Fuel cell catalyst and method for producing the same, fuel cell electrode and fuel cell using the same - Google Patents

Description

  The present invention relates to a fuel cell catalyst using tungsten carbide as a catalyst component, a method for producing the same, a fuel cell electrode using the fuel cell catalyst, and a fuel cell.

  In recent years, in order to further improve energy efficiency and solve environmental problems, attempts have been made to clean exhaust gas by using a fuel cell as a power source for automobiles. ing. In particular, development of a polymer electrolyte fuel cell (PEFC) as a fuel cell for a fuel vehicle (FCHV) has been rapidly progressing.

  A fuel cell is a power generator that supplies fuel to the anode and oxidant to the cathode, takes out the potential difference between the anode and cathode as voltage, and supplies it to the load. Hydrogen is commonly used as the anode fuel, and oxidant is generally used as the oxidant. For this, oxygen in the air is used. A fuel cell is composed of an anode and a cathode and an electrolyte sandwiched between them. In a polymer electrolyte fuel cell, an ion exchange membrane is used as an electrolyte. Specifically, a catalyst layer is formed on both surfaces of an ion exchange membrane as an electrolyte, and an anode gas diffusion layer and a cathode gas / fuel diffusion layer are integrally formed outside the catalyst layer, respectively. The fuel cell is configured by stacking several tens to several hundreds of cells as unit cells composed of a laminate of a partition plate, an electrolyte membrane / electrode assembly, and a partition plate so as to obtain a desired voltage according to the application. Has been.

  In such a fuel cell, when hydrogen reaches the anode catalyst layer, protons and electrons are generated by an electrochemical reaction process. Protons generated here move sequentially in the electrolyte and reach the cathode. On the other hand, electrons are sent to the cathode via an external load. In the cathode catalyst layer, electrons sent via an external load, oxygen in the air as an oxidant, and protons that have moved through the electrolyte combine to form water through an electrochemical reaction process. .

  Conventionally, as a catalyst for such a fuel cell, a catalyst based on a noble metal such as platinum, which is expensive and has a problem in terms of resources, has been used for both the cathode and the anode. The amount of platinum used for the exhaust gas purification catalyst of gasoline cars is considerably larger than that of platinum.

  Therefore, in order to commercialize a fuel cell, development of a fuel cell catalyst that can be used practically at low cost, such as platinum, which is problematic in terms of price and resources, is one of the essential issues. .

  As a fuel cell catalyst that replaces a precious metal-based catalyst, Patent Document 1 describes a fuel cell catalyst in which tungsten carbide (WC) is supported on a carrier, and the average particle diameter of WC is 0.5. 10 nm is preferred.

  Patent Documents 2 and 3 disclose tungsten carbide as an anode and cathode catalyst for a polymer electrolyte fuel cell, preferably having a particle size of 1 to 30 nm, more preferably 1.5 to 10 nm. Preferred is described. Furthermore, examples of the conductive material include carbon materials, and for example, carbon black such as ketjen black is disclosed.

In Patent Documents 4 and 5, diffraction angles 2θ by X-ray diffraction (Cu-K _α- ray) are 37.6 ± 0.3 °, 62.0 ± 0.3 °, and 74.8 ± 0. Tungsten carbide which gives a peak at 3 ° is disclosed in Patent Documents 6 and 7 in which tungsten carbides give peaks at 37.3 to 37.9 °, 61.7 to 62.3 ° and 74.5 to 75.1 °. Is disclosed as a fuel cell catalyst.

In Non-Patent Documents 1, 2 and 3, as a method for producing tungsten carbide, W ₂ N produced by the reaction of WO ₃ and NH ₃ is heat-treated under the flow of CH ₄ and H _2. It is disclosed that WC _1-x (cubic) is formed.
JP 2003-117398 A JP-A-6-342666 JP-A-6-342667 US20030077460A1 US65515569B1 WO0228544A1 WO0228773A1 Studies in Surface Science and Catalysis 130, 989 (2000) Chem. Mater. Volume 12 Page 132 (2000) Applied Catalysis A: General 183, 253 (1999)

  However, none of the above Patent Documents 1 to 7 has a specific description of the catalytic activity as a fuel cell catalyst, and there is no substantial disclosure of a technique for practical use of tungsten carbide as a fuel cell catalyst. .

In addition, Non-Patent Documents 1 to 3 disclose nothing about using the generated WC _1-x as a fuel cell catalyst.

  Thus, it has been known that tungsten carbide is conventionally used as a catalyst for fuel cells. However, the tungsten carbide exhibits sufficient activity as a catalyst for fuel cells, and can be used as a fuel that can be substituted for noble metal catalysts such as platinum. At present, the technology for making a battery catalyst has not been established.

  The present invention provides a tungsten carbide catalyst for a fuel cell that exhibits an excellent catalytic action, which is inexpensive and can be substituted for a noble metal catalyst such as platinum, and a fuel cell electrode and a fuel cell using the fuel cell catalyst. For the purpose.

  As a result of intensive studies in view of the above situation, the present inventors have found that tungsten carbide particles obtained by conversion from a specific tungsten compound have a specific crystal form and can be substituted for a noble metal catalyst such as platinum. It has been found that a fuel cell catalyst having higher practicality can be obtained by using a transition metal catalyst in combination with the catalyst for a fuel cell having the above. The present invention has been completed based on such knowledge.

That is, according to the present invention, the half width of the maximum diffraction peak in a region where the diffraction angle 2θ (± 0.3 °) by X-ray diffraction (Cu-K _α- ray) is 40 ° or more and 60 ° or less is 1.0. A catalyst for a fuel cell containing tungsten carbide having a temperature not less than ° and not more than 16.5 ° , wherein the tungsten carbide is obtained by converting a compound selected from the group consisting of tungsten nitride and tungsten sulfide into tungsten carbide. The present invention resides in a fuel cell catalyst.

  Furthermore, the present invention resides in a fuel cell electrode comprising the fuel cell catalyst.

  The present invention also resides in a fuel cell using the fuel cell electrode.

Furthermore, the present invention is nitrided tungsten, and a compound selected from sulfide tungsten emissions or Ranaru group, in the presence or absence of a carbon-based substrate, by contacting the hydrocarbon or hydrocarbons and hydrogen, tungsten carbide The method for producing a catalyst for a fuel cell, wherein the catalyst is converted into a fuel cell.

  INDUSTRIAL APPLICABILITY According to the present invention, an inexpensive and practical fuel cell catalyst exhibiting a good catalytic action that can be replaced with a catalyst for a noble metal fuel cell such as platinum, which is expensive and has a problem in terms of resources, and for this fuel cell A fuel cell electrode and a fuel cell using a catalyst are provided.

  In addition, since the tungsten carbide according to the present invention exhibits a good catalytic action, it can be used alone, or in combination with a noble metal catalyst such as platinum, resulting in a reduced amount of platinum and the like. Provided are a practical fuel cell catalyst, a fuel cell electrode and a fuel cell using the fuel cell catalyst.

  Hereinafter, embodiments of the present invention will be described in detail. However, the present invention is not limited to the following embodiments, and various modifications can be made within the scope of the gist of the present invention.

[Fuel cell catalyst]
The fuel cell catalyst of the present invention has a maximum half-value width of the maximum diffraction peak in a region where a diffraction angle 2θ (± 0.3 °) by X-ray diffraction (Cu-K _α- ray) is 40 ° or more and 60 ° or less. It contains tungsten carbide that is 0.80 ° or more.

  The fuel cell catalyst of the present invention is also characterized in that a compound selected from the group consisting of tungsten boride, tungsten nitride, tungsten sulfide, tungsten phosphide and tungsten silicide is converted into tungsten carbide.

<Tungsten carbide>
Tungsten carbide has a form in which a tungsten (W) atom and a carbon (C) atom exist as a compound having a bond. For example, WC, WC _1-x (0 <x <1), W ₂ C and the like.

The form of this tungsten carbide can be confirmed by X-ray diffraction (XRD). That is, it can be confirmed by irradiating tungsten carbide with X-rays (Cu- _Kα rays) and observing a diffraction spectrum to give a characteristic peak to tungsten carbide.

Examples of the measurement apparatus and measurement conditions include the following, but the XRD analysis technique for tungsten carbide in the present invention is not limited to the following measurement apparatus and measurement conditions.
(Powder XRD analysis)
Measuring device X-ray powder analysis device / PANallytical PW1700
Measurement conditions X-ray output (Cu-Kα): 40 kV, 30 mA
Scanning axis: θ / 2θ
Measurement range (2θ): 3.0 ° to 70.0 °
Measurement mode: Continuous
Reading width: 0.05 °
Scanning speed: 3.0 ° / min
DS, SS, RS: 1 °, 1 °, 0.20mm
Gonometer radius: 173mm

Specifically, WC is a peak of 2θ (± 0.3 °) of X-ray diffraction, such as 31.513 °, 35.639 °, 48.300 °, 64.016 °, 65.790 °, etc. A characteristic peak is given. WC _1-x is a characteristic peak of 36.977 °, 42.887 °, 62.027 °, 74.198 °, 78.227 °, etc. as a 2θ (± 0.3 °) peak of X-ray diffraction. It gives a peak. In addition, W ₂ C is a peak of 2θ (± 0.3 °) of X-ray diffraction such as 34.535 °, 38.066 °, 39.592 °, 52.332 °, 61.879 °, etc. Giving a positive peak.

In the fuel cell catalyst of the present invention, a region where the diffraction angle 2θ (± 0.3 °) by the X-ray diffraction method (Cu-K _α- ray) is 40 ° or more and 60 ° or less (hereinafter referred to as “specific region”) Tungsten carbide having a half-value width of the maximum diffraction peak of 0.80 ° or more (hereinafter, this condition may be referred to as “specific XRD condition”) is used.

The region where the diffraction angle 2θ (± 0.3 °) by the X-ray diffraction method (Cu-K _α- ray) is 40 ° or more and 60 ° or less corresponds to a crystal plane interval of 0.2252 to 1.5406 nm. The full width at half maximum in this specific area is 0 . The angle of 80 ° or more indicates that the tungsten carbide crystal is miniaturized to a size of 11 nm or less. Although the mechanism that this works well for the catalytic action is not necessarily clear, it is presumed that the surface area as a reaction field increases due to the microcrystal.

  The maximum half-value width of the maximum diffraction peak in this specific region is preferably as large as possible, preferably 1.0 or more, particularly preferably 1.2 or more. However, if it is too large, the stability of tungsten carbide is lowered and deactivated. Therefore, the upper limit of the full width at half maximum is usually about 16.5 ° or less.

  Although there is no restriction | limiting in particular as a shape of tungsten carbide, The most common is a particulate form. In the particulate tungsten carbide, the upper limit of the average particle diameter is usually 100 μm or less, preferably 1000 nm or less, more preferably 500 nm or less, especially 300 nm or less, and the lower limit is usually 0.5 nm or more, preferably 1.0 nm or more. Preferably it is 2.0 nm or more. If the particle size of tungsten carbide is less than this lower limit, it becomes unstable and tends to be deactivated, and if it exceeds the upper limit, it becomes difficult to obtain high activity.

  The average particle size of tungsten carbide is determined by unifying the direction in which the particle size is measured by measuring with a scanning electron microscope (SEM) or transmission electron microscope (TEM). Measured and averaged.

In the measurement by scanning electron microscopy (SEM), the sample surface is visualized by scanning the surface of the sample with an electron beam and detecting secondary electrons generated. Using this technique, the particle size of tungsten carbide can be measured. Examples of the measuring apparatus and measuring method include the following, but the measuring method using the SEM of the tungsten carbide particle size in the present invention is not limited to the following measuring apparatus and measuring method. .
(Measurement by SEM)
Measurement device “S-4100” manufactured by Hitachi, Ltd. is used, and the acceleration voltage of the electron beam is controlled to 15 kV for observation.
Measuring method An appropriate amount of a powder sample is dispersed on a carbon-deposited Si wafer, and methanol is dropped to dry. Specifically, a photograph is observed from a dispersion state of 100 to 1000 times, and a particle diameter is examined from conventional photographs of 10,000 and 100,000 times or more.

  The method for synthesizing tungsten carbide according to the present invention is not particularly limited as long as it satisfies the above-mentioned specific XRD condition, but tungsten oxide that is commonly used industrially as tungsten carbide, As shown in Comparative Example 1 described later, tungsten carbide satisfying a specific XRD condition cannot be obtained.

  Therefore, the tungsten carbide according to the present invention is preferably synthesized by conversion from a specific tungsten compound, as will be described later in the section of the method for producing a catalyst, thereby obtaining tungsten carbide satisfying a specific XRD condition and fuel. Sufficient activity as a battery catalyst can be expressed.

  In particular, in order to synthesize tungsten carbide having the above-mentioned smaller average particle diameter and specific XRD conditions, the production method may be devised as will be described later. Among them, tungsten carbide such as tungsten nitride is provided from the raw material compound described later. Controlling the state of crystal growth by lowering the firing temperature and shortening the firing time during the conversion reaction to the precursor compound and the conversion reaction from the precursor compound such as tungsten nitride to tungsten carbide. .

<Substrate>
In the fuel cell catalyst of the present invention, the substrate is not necessarily essential, but it is preferable that tungsten carbide is applied to the substrate from the viewpoint of maintaining the activity, and among them, the use of a carbon-based substrate is highly conductive. Is suitable in that it is obtained.

  Various carbon-based substrates can be used, and are not particularly limited. For example, carbon black, carbon nanotube, carbon nanohorn, carbon nanocluster, fullerene, pyrolytic carbon, activated carbon, etc. Two or more kinds can be used in combination.

  Among these, carbon black is industrially advantageous in terms of conductivity, availability, and price. Specifically, carbon black includes channel black, furnace black, thermal black, and acetylene black. Oil furnace black, gas furnace black, and the like.

  The form of the substrate is not particularly limited, but the most commonly used is a powder form.

When the powder of the substrate, such as carbon powder, the specific surface area (BET) is usually several tens of ^m 2 / g or more, preferably 200 meters ² / g or more, more preferably 500 meters ² / g or more and usually 5000 m ² / g or less, preferably several thousand m ² / g or less (in the present invention, “number” such as “thousand” or “tens” refers to about “2 to 4”). If the specific surface area is too small, the effective area for depositing tungsten carbide is reduced, and the reaction field is reduced, so that sufficient catalytic activity cannot be obtained. Those having an excessively large specific surface area are expensive, and the object of the present invention to provide an inexpensive fuel cell catalyst is impaired by using tungsten carbide.

<Adhesion of tungsten carbide to the substrate>
In the present invention, the state in which tungsten carbide is deposited on the substrate refers to a state in which both are in contact with each other so as to obtain electrical conductivity between the tungsten carbide and the substrate. Therefore, tungsten carbide can be deposited on the substrate by simply mixing the tungsten carbide and the substrate, but this mixture may be fired. In the following, the state in which the substrate is mixed and then fired and deposited is referred to as “support”.

  As a deposition method, a known method such as a supporting method, a mixing method, an impregnation method, a precipitation method, an adsorption method or the like can be adopted, but the tungsten carbide precursor compound or raw material compound is mixed with the substrate and then tungsten carbide. In the case of performing a conversion reaction for producing, it is usually preferable to perform a baking treatment after producing tungsten carbide.

  The deposition ratio of tungsten carbide to the substrate is not limited, but the lower limit is usually 0.001 or more, preferably 0.01 or more, and the weight ratio of tungsten carbide / (tungsten carbide + substrate). It is 0.05 or more, and the upper limit is usually 0.95 or less, preferably 0.4 or less, and particularly preferably 0.3 or less. If the deposition ratio of tungsten carbide is below this lower limit, the desired activity cannot be obtained, and if it exceeds the upper limit, the effect of improving the activity due to deposition is less likely to occur.

<Other catalyst components>
In the present invention, as long as the effects of the present invention are not impaired, a catalyst component selected from transition metal compounds other than transition metals and tungsten carbide (hereinafter may be referred to as “other catalyst components”) may be used in combination. . The transition metal compound other than tungsten carbide may be a tungsten compound other than tungsten carbide.

The transition metal is an element belonging to the 4th to 6th periods of the groups 3A to 7A, 8 and 1B of the periodic table, and includes titanium (Ti), vanadium (V), chromium (Cr), manganese ( Mn), iron (Fe), cobalt (Co), nickel (Ni), copper (Cu), yttrium (Y), zirconium (Zr), niobium (Nb), molybdenum (Mo), ruthenium (Ru), palladium ( Pd), lanthanum (La), europium (Eu), gold (Au), cerium (Ce), tantalum (Ta), rhenium (Re), praseodymium (Pr), iridium (Ir), neodymium (Nd) are exemplified. It is preferable that the value of the standard electrode potential E ° (25 ° C.) in an aqueous solution is positive, preferably represented by the following electrochemical equilibrium formula: oxidant + ne ⁻ = reduced form. This is because elution due to oxidation is unlikely to occur as a natural property of metals, and there is little deterioration of the catalyst due to it. Specific examples of such materials include gold, iridium, palladium, silver, rhodium, and ruthenium.

  However, in order to make the catalyst more industrially advantageous, it is better to reduce the number of expensive catalyst components as much as possible. Therefore, ruthenium is particularly preferable.

  Of course, platinum (Pt) can be used in combination as a transition metal. However, since platinum is expensive, it is inexpensive and practical to add a small amount while considering the desired catalytic activity. It is desirable to provide a fuel cell catalyst.

  In addition, the following shows the electrochemical equilibrium formula of main transition metals and the standard electrode potential E ° (25 ° C.).

  Examples of transition metal compounds other than tungsten carbide include carbides, nitrides, borides, etc., with carbides being preferred.

Examples of tungsten compounds other than tungsten carbide include tungsten compounds such as WN, W ₂ N, WB, W _1-y Mo _y C _1-z , Ni ₂ W ₄ C, Co ₃ W ₃ C, WP, and WP _2. It is done. In W _1-y Mo _y C _1-z , y is preferably in the range of 0 <y ≦ 0.5, and z is in the range of 0 ≦ z ≦ 0.3. Among these, W _1-y Mo _y C _1-z is preferable in terms of catalytic activity.

  These other catalyst components may be used individually by 1 type, and may use 2 or more types together.

When other catalyst components are used in combination as a cocatalyst, examples of the combined form of the other catalyst components include the following.
(1) Other catalyst components are mixed with the substrate together with tungsten carbide.
(2) Other catalyst components are supported on the substrate together with tungsten carbide.
(3) The tungsten carbide supported on the substrate is mixed with other catalyst components.
(4) Other catalyst components supported on other substrates are mixed with tungsten carbide.
(5) The other catalyst component supported on the other substrate is mixed with the tungsten carbide supported on the substrate.

  When other catalyst components are used, the other catalyst components are generally in the range of 0.001 or more, preferably 0.01 or more as a lower limit in terms of the weight ratio of the total of other catalyst components / tungsten carbide to tungsten carbide. It is preferably 0.05 or more and used so that the upper limit is usually 0.5 or less, preferably 0.4 or less, especially 0.3 or less. If the lower limit is not reached, the desired activity cannot be obtained, and if the upper limit is exceeded, the activity improving effect is hardly obtained.

  The other catalyst component is preferably in the form of powder, and the average particle size in this case is usually 1000 nm or less as an upper limit, preferably 500 nm or less, especially 300 nm or less, and the lower limit is usually 0.5 nm or more. preferable. Below this lower limit, it becomes unstable and easily deactivated, and when it exceeds the upper limit, it becomes difficult to obtain high activity.

  In the fuel cell catalyst of the present invention, even if a metal component other than the transition metal element is contained in an amount of several weight percent or less based on the weight of tungsten carbide, it is acceptable in the object and effect of the present invention. .

  By using such other catalyst components in combination, it is particularly preferable to use the other catalyst components by supporting them on a substrate together with tungsten carbide. Although the details of the action mechanism of the effect of improving the catalytic activity by using other catalyst components in combination, in particular, by supporting the other catalyst components on the substrate together with tungsten carbide are not necessarily clear, the transition metal of the other catalyst components is tungsten carbide. It is estimated that the activity is improved because it functions as a cocatalyst.

<Manufacturing method>
(Manufacture of tungsten carbide)
As a method for producing tungsten carbide, a tungsten compound other than tungsten carbide (hereinafter referred to as “a”) having at least one bond between a typical nonmetallic element having a Pauling electronegativity of 1.8 or more and 3.0 or less and tungsten. And a method of converting the precursor compound to tungsten carbide.

[1] Precursor compounds Typical nonmetallic elements having a Pauling electronegativity of 1.8 or more and 3.0 or less constituting the precursor compound include H (2.1), B (2.0), and N (3. 0), Si (1.8), P (2.1), S (2.5), Cl (3.0), As (2.0) Se (2.4) Br (2.8), Te (2.1), I (2.5), and At (2.2) are included (the electronegativity is in parentheses), and among these, typical non-existence of the second period and the third period of the periodic table B, N, Si, P, and S elements selected from the group consisting of metal elements are preferred for reasons such as low toxicity.

The precursor compound used in the present invention is not particularly limited, _{specifically, WB, WB 4, W 2} B 5 , etc. tungsten boride _of, WN, _{W 2} N, such as WN _2, W 3 _{N 4} Examples include tungsten nitride, tungsten silicide such as WSi ₂ and W ₅ Si ₃ , tungsten sulfide such as WS ₂ and WS ₃ , tungsten phosphide such as WP and WP ₂ , among these, tungsten nitride and phosphide Tungsten and tungsten sulfide are preferred because they are industrially advantageous. These compounds have a form in which tungsten (W) atoms and boron (B), nitrogen (N), silicon (Si), phosphorus (P) or sulfur (S) atoms are directly bonded to each other, and X-ray It can be confirmed by diffraction (XRD).

The reason why tungsten carbide having excellent catalytic activity as a fuel cell catalyst can be obtained by producing tungsten carbide via such a precursor compound is not clear, but is estimated as follows. That is, when tungsten oxide is obtained by converting tungsten oxide (WO ₃ ), which is generally taken conventionally, the W atoms react with hydrocarbons such as methane after all the O atoms are separated from the W atoms. It has been reported that this reaction does not proceed unless the temperature is higher than about 800 ° C. (Catalysis Letters 44, 229 (1997)). On the other hand, the specific typical nonmetallic element of the precursor compound has a low Pauling electronegativity, and therefore binds to tungsten more weakly than oxygen. Since the generated W atom or W compound reacts with the hydrocarbon to form WC, the resulting tungsten carbide microcrystals are difficult to expand, and as a result, suitable as a fuel cell catalyst. It is considered that a tungsten carbide excellent in catalytic activity that produces a simple reaction field can be obtained.

[2] Raw Material Compound The tungsten compound for deriving the precursor compound used in the present invention (hereinafter sometimes referred to as “raw material compound”) is not particularly limited, but specifically, WO ₃ , WO ₂ , H _{2 WO 4, (NH 4)} 10 W 12 O 41 · 5H 2 other tungsten oxides O, _{etc., WF 6, WC l4, WC} l6 and WBr ₅ inorganic tungsten compound such as tungsten halides such as or (NH ₄ ) sulfur-containing tungsten compounds such as ₂ WS ₄ and the like. In addition, a tungsten complex is mentioned as an organic tungsten compound. Specifically, boron atom coordinated tungsten complexes such as ethylborylethylidene ligands, carbons such as carbonyl ligands, cyclopentadienyl ligands, alkyl group ligands, and olefinic ligands. Atom coordinated tungsten complex, nitrogen atom coordinated tungsten complex such as pyridine ligand, acetonitrile ligand, phosphorus atom coordinated tungsten complex coordinated such as phosphine ligand, phosphite ligand, diethylcarbamodithio And a sulfur atom coordinated tungsten complex coordinated with a lato ligand or the like. Further, it may be a complex having a plurality of these ligands or a complex having a plurality of types of ligands. Specifically, a tungsten complex in which a hydride ligand and an olefin ligand are coordinated, W (CO) ₃ (NCCH ₃ ) ₃ , W (CO) ₄ (bipyridyl) in which a carbon atom and a nitrogen atom are coordinated And tungsten complexes.

  Among these, compounds such as carbon atom-coordinated tungsten complex, nitrogen atom-coordinated tungsten complex, and phosphorus atom-coordinated tungsten complex are preferable because they are abundant and easy to handle and industrially advantageous.

  For the raw material compound, the upper limit of the average particle size is usually 100 μm or less, preferably 1000 nm or less, more preferably 500 nm or less, especially 300 nm or less, particularly 100 nm or less, and the lower limit is usually 0.5 nm or more, preferably 1.0 nm or more, More preferably, the thickness is 2.0 nm or more. When the particle size of the raw material compound is less than this lower limit, the tungsten carbide produced becomes unstable and easily deactivated, and when it exceeds the upper limit, it becomes difficult to obtain high activity.

[3] Conversion from raw material compound to precursor compound For the conversion reaction from the raw material compound to the precursor compound, any known method can be used. For example, the conversion reaction from the raw material compounds of tungsten nitride, tungsten sulfide, and tungsten phosphide, which are preferable precursor compounds, can be performed under the following conditions.

(1) Tungsten nitride The method for synthesizing tungsten nitride as the precursor compound is not particularly limited, and can be performed by any known method.

For example, in “Applied Catalysis A: General”, 183, 253 (1999), heating of WO ₃ was started at 270 ° C. under NH ₃ flow, the heating temperature was increased at a rate of 30 ° C. per hour, and the final temperature Although it is disclosed that W ₂ N can be produced by heating at 560 ° C., and that it can be stabilized by forming a passive film by flowing 1% O ₂ / He gas at room temperature. This method can also be adopted.

  In addition, the following method can also be employed.

The inorganic tungsten compound _{(NH 4) 10 W 12 O} 41 · 5H 2 O and tungsten oxide, an organic medium (e.g., alcohols such as ethanol, carbonyl such as acetone, ethers such as tetrahydrofuran, toluene, etc. Hydrocarbons, chlorides such as methylene chloride) or an aqueous medium (for example, water, etc.), and if necessary, add a desired amount of HCl for complete dissolution, or make a slurry, (Normally 10 minutes or more, preferably 30 minutes or more, usually 50 hours or less, preferably 30 hours or less), and then the solvent is removed by distillation or the like. If necessary, a predetermined temperature (usually 10 minutes or more, usually at 100 ° C. or higher, preferably 200 ° C. or higher, usually 1000 ° C. or lower, preferably 800 ° C. or lower) under a flow of an inert gas such as argon. (Preferably 30 minutes or more, usually 50 hours or less, preferably 30 hours or less) Drying by heating. Thereafter, under the flow of an inert gas containing NH ₃ (usually 10% or more, preferably 30% or more, 100% or less, or 90% or less NH ₃ concentration. High concentration reduces the firing time, but for safety reasons. The concentration may be lowered.) At a predetermined temperature (usually 300 ° C. or higher, preferably 400 ° C. or higher, usually 1000 ° C. or lower, preferably 800 ° C. or lower) for a predetermined time (usually 10 minutes or longer, preferably 30 minutes or longer). (Typically 50 hours or less, preferably 30 hours or less) Tungsten nitride can be produced by heating. In this heating, a predetermined rate (usually 10 ° C./hr or more, preferably 20 ° C./hr or more) from a predetermined temperature (usually room temperature or higher, preferably 100 ° C. or higher, usually 600 ° C. or lower, preferably 400 ° C. or lower). As described above, heating is generally performed at a temperature of 600 ° C./hr or less, preferably 400 ° C./hr or less) to a predetermined temperature (usually 300 ° C. or more, preferably 400 ° C. or more, usually 1000 ° C. or less, preferably 800 ° C. or less). You can go. Furthermore, in an inert gas atmosphere having a low oxygen concentration (for example, an oxygen concentration of about 5% by weight or less, especially about 2% by weight or less), a predetermined time (usually several minutes or more, preferably 30 minutes or more, usually 10 hours or less). In particular, a passivation treatment for forming a passivation film can be performed by treating at a predetermined temperature (usually around room temperature) for 5 hours or less.

Furthermore, tungsten nitride can be synthesized from an organic tungsten compound. Specifically, W (CO) ₃ (CH ₃ CN) ₃ is distributed under an inert gas containing NH ₃ (normally 10% or more, preferably 30% or more, 100% or less, or NH ₃ concentration of 90% or less). If the concentration is high, the firing time is shortened, but the concentration may be lowered for safety.) At a predetermined temperature (usually 200 ° C. or higher, preferably 300 ° C. or higher, usually 1000 ° C. or lower, preferably 800 ° C. or lower). The tungsten nitride can be produced by heating for a predetermined time (usually 10 minutes or more, preferably 30 minutes or more, usually 50 hours or less, preferably 30 hours or less). In this heating, a predetermined rate (usually 10 ° C./hr or more, preferably 20 ° C./hr or more) from a predetermined temperature (usually room temperature or higher, preferably 100 ° C. or higher, usually 600 ° C. or lower, preferably 400 ° C. or lower). As described above, heating is generally performed at a temperature of 600 ° C./hr or less, preferably 400 ° C./hr or less) to a predetermined temperature (usually 300 ° C. or more, preferably 400 ° C. or more, usually 1000 ° C. or less, preferably 800 ° C. or less). You can go. Furthermore, in an inert gas atmosphere having a low oxygen concentration (for example, an oxygen concentration of about 5% by weight or less, especially about 2% by weight or less), a predetermined time (usually several minutes or more, preferably 30 minutes or more, usually 10 hours or less). In particular, a passivation treatment for forming a passivation film can be performed by treating at a predetermined temperature (usually around room temperature) for 5 hours or less.

(2) Tungsten sulfide The shape of tungsten sulfide as a precursor compound is not particularly limited, and it may be nanomaterials such as nanorods, nanotubes, nanotwists, nanoclusters, nanofibers, and sub-microcoils, in addition to those having no specific structure. . Moreover, there is no restriction | limiting in particular also about the synthesis method, It can carry out by well-known arbitrary methods. For example, “Journal of Materials Chemistry Vol. 12, p. 1450 (2002) states that W (CO) ₆ was sonicated in diphenylethane at 90 ° C. in an argon atmosphere in the presence of a slight excess of S. It is reported that WS ₂ nanorods are produced by heating at 800 ° C. in an argon atmosphere.

  In addition, the following method can also be employed.

W (CO) ₆ together with S in an organic medium (for example, alcohols such as ethanol, carbonyls such as acetone, ethers such as tetrahydrofuran, hydrocarbons such as toluene and xylene, chlorides such as methylene chloride) Dissolve or form a slurry, heat or reflux for a predetermined time (usually 10 minutes or more, preferably 30 minutes or more, usually 50 hours or less, preferably 30 hours or less), and collect the precipitate by filtration or distillation of the solvent. If necessary, in order to further remove unreacted W (CO) ₆ , the precipitate is added to a predetermined amount of an organic solvent (for example, a nitrogen-containing organic solvent such as acetonitrile, alcohols such as ethanol, carbonyls such as acetone, tetrahydrofuran, etc. In ethers such as toluene, hydrocarbons such as toluene and xylene, chlorides such as methylene chloride) Predetermined time Te (usually 10 minutes or more, preferably 30 minutes or more, usually at most 50 hours, preferably 30 hours or less) performs heating or reflux, collecting the precipitate by hot filtration and the like. The obtained precipitate is passed through an inert gas such as argon at a predetermined temperature (usually 100 ° C or higher, preferably 200 ° C or higher, usually 1000 ° C or lower, preferably 800 ° C or lower) for a predetermined time (usually 10 minutes or longer). (Preferably 30 minutes or more, usually 50 hours or less, preferably 30 hours or less) Tungsten sulfide is obtained by drying by heating.

(3) Tungsten phosphide The method for synthesizing tungsten phosphide as a precursor compound is not particularly limited, and can be performed by any known method.

For example, “Studies in Surface Science and Catalysis” volume 143, page 247 (2002) includes (NH ₄ ) ₆ H ₂ W ₁₂ O ₄₀ · 18H ₂ O and (HN ₄ ) ₂ HPO ₄ , W and P Is dissolved in water so that the molar ratio thereof becomes 1: 1, and then water is distilled off, followed by heating under air circulation conditions, followed by heat reduction treatment under hydrogen circulation conditions to reduce WP. It is disclosed that it can be stabilized by forming a passive film by flowing 0.5% O ₂ / He gas at room temperature, but this method can also be adopted. .

  Specifically, a tungsten supply compound such as metatungstic acid and a phosphorus supply compound such as diammonium phosphate are mixed in an organic medium (for example, ethanol or the like) at a blending ratio corresponding to a desired molar ratio of tungsten phosphide. Alcohols, carbonyls such as acetone, ethers such as tetrahydrofuran, hydrocarbons such as toluene, chlorides such as methylene chloride) or aqueous media (for example, water, etc.), or dissolved or dispersed for a predetermined time (Normally 10 minutes or more, preferably 30 minutes or more, usually 50 hours or less, preferably 30 hours or less) After standing, the solvent is removed by distillation or the like. Next, under a flow condition of oxygen atmosphere gas, at a predetermined temperature (usually 300 ° C. or more, preferably 400 ° C. or more, usually 1000 ° C. or less, preferably 800 ° C. or less) for a predetermined time (usually 10 minutes or more, preferably 30 minutes). As described above, heating is usually performed for 50 hours or less, preferably 30 hours or less, and then a predetermined temperature (usually 300 ° C. or higher, preferably 400 ° C. or higher, preferably 1000 ° C. or lower) under a reducing atmosphere (for example, under hydrogen gas flow). WP is preferably obtained by heating at 700 ° C. or less for a predetermined time (usually 10 minutes or more, preferably 30 minutes or more, usually 50 hours or less, preferably 30 hours or less). Furthermore, in an inert gas atmosphere having a low oxygen concentration (for example, an oxygen concentration of about 5% by weight or less, especially about 2% by weight or less), a predetermined time (usually several minutes or more, preferably 30 minutes or more, usually 10 hours or less). In particular, a passivation treatment for forming a passivation film can be performed by treating at a predetermined temperature (usually around room temperature) for 5 hours or less.

  Among the conversion reaction from the raw material compound to the precursor compound, a tungsten oxide or a tungsten complex having a carbonyl ligand is used as the raw material compound, and tungsten nitride or tungsten sulfide obtained from the raw material compound is used as the precursor compound of tungsten carbide. It is preferable to use it as a raw material because the raw material is inexpensive and the reaction is easy.

[4] Conversion from precursor compound to tungsten carbide In the present invention, a compound selected from tungsten boride, tungsten nitride, tungsten sulfide, tungsten phosphide, and tungsten silicide is preferably used as a precursor compound, and this is the presence of a substrate. Under or in the absence, it is preferable to convert the hydrocarbon or tungsten to contact with the hydrocarbon under predetermined heating conditions to convert it into tungsten carbide.

  In the case where tungsten carbide is obtained by bringing the precursor compound into contact with hydrocarbon or hydrocarbon and hydrogen in the presence of the substrate, the substrate may be used so as to have the above-mentioned suitable amount of tungsten carbide deposited on the substrate.

  The hydrocarbon is usually methane, ethane, propane, butane, ethylene, propylene, acetylene, preferably methane, ethane, ethylene or a mixed gas thereof, usually at 1 mL / min. Or more, preferably 5 mL / min. As described above, usually 500 mL / min. Hereinafter, preferably 400 mL / min. It is preferable to supply the following. If the amount of hydrocarbon is less than the above lower limit, the carbonization reaction does not proceed easily. By using hydrogen in combination, the effect of preventing the formation of a carbon layer on the tungsten carbide surface can be obtained, but the use ratio is usually 5% or more, preferably the ratio of hydrocarbon in the mixed gas of hydrocarbon and hydrogen. It is preferable to supply 10% or more, usually 90% or less, preferably 30% or less. If the amount of hydrocarbon is less than the above lower limit, the carbonization reaction is difficult to proceed, and if it exceeds the above upper limit, an inactive carbon layer adheres to the tungsten carbide surface, which is not preferable for the reaction.

  The conversion reaction is usually performed at 500 ° C or higher, preferably 600 ° C or higher, usually 1200 ° C or lower, preferably 1000 ° C or lower. If the reaction temperature is lower than the lower limit, the carbonization reaction does not proceed easily. If the reaction temperature is higher than the upper limit, highly active tungsten carbide is difficult to obtain.

  While the reaction time varies depending on the reaction temperature, it is usually 10 minutes or longer, preferably 30 minutes or longer, usually 50 hours or shorter, preferably 30 hours or shorter. If this reaction time is shorter than the above lower limit, the reaction does not proceed completely, and if it is longer than the upper limit, highly active tungsten carbide is difficult to obtain.

  This heating is performed from a predetermined temperature (usually room temperature or higher, preferably 100 ° C. or higher, usually 600 ° C. or lower, preferably 400 ° C. or lower) to a predetermined speed (usually 10 ° C./hr or higher, preferably 20 ° C./hr or higher, usually The temperature may be raised to a predetermined temperature (usually 500 ° C. or more, preferably 600 ° C. or more, usually 1200 ° C. or less, preferably 1000 ° C. or less) at 600 ° C./hr or less, preferably 400 ° C./hr or less. After the formation of tungsten carbide, it is further performed for a predetermined time (usually several tens of minutes or more, preferably 30 minutes) in an inert gas atmosphere having a low oxygen concentration (for example, an oxygen concentration of 5 wt% or less, especially 2 wt% or less). As described above, the passivation treatment for forming a passive film can be performed by treatment at a predetermined temperature (usually around room temperature) usually for 10 hours or less, particularly 5 hours or less.

  Hereinafter, a method for producing tungsten carbide from a precursor compound such as tungsten nitride in the absence of a substrate will be described more specifically, but the present invention is not limited to the following method.

(1) Conversion from tungsten nitride to tungsten carbide There is no particular limitation on the synthesis method for providing tungsten carbide used in the present invention from tungsten nitride, and any known method can be used. For example, in “Applied Catalysis A: General”, 183, page 253 (1999), W ₂ N was started to be heated at 25 ° C. under a flow of methane and hydrogen, and the heating temperature was increased at a rate of 60 ° C. per hour. It is disclosed that WC _1-x can be produced by heating at a final temperature of 750 ° C., and that it can be stabilized by forming a passive film by flowing 1% O ₂ / He gas at room temperature. However, this method can also be adopted.

  In addition, tungsten nitride is used in a predetermined hydrocarbon gas (usually methane, ethane, propane, butane, ethylene, propylene, acetylene, preferably methane, ethane, ethylene) or a mixed gas thereof and hydrogen gas (usually a mixed gas). The mixing ratio of the hydrocarbon gas is usually 5% or more, preferably 10% or more, usually 90% or less, preferably 30% or less), a predetermined temperature (usually 500 ° C or more, preferably 600 ° C or more, usually 1000 ° C). Tungsten carbide can be produced by heating for a predetermined time (usually 10 minutes or more, preferably 30 minutes or more, preferably 50 minutes or less, preferably 30 hours or less) preferably at 900 ° C. or less. In this heating, as described above, a predetermined rate (usually 10 ° C./hr or more, preferably 100 ° C. or more, preferably 600 ° C. or less, preferably 400 ° C. or less), from a predetermined temperature (usually 10 ° C./hr or more, preferably 20 ° C / hr or higher, usually 600 ° C / hr or lower, preferably 400 ° C / hr or lower) to a predetermined temperature (usually 500 ° C or higher, preferably 600 ° C or higher, usually 1000 ° C or lower, preferably 900 ° C or lower). You may heat with temperature. Furthermore, in an inert gas atmosphere having a low oxygen concentration (for example, an oxygen concentration of about 5% by weight or less, especially about 2% by weight or less), a predetermined time (usually several minutes or more, preferably 30 minutes or more, usually 10 hours or less). In particular, a passivation treatment for forming a passivation film can be performed by treating at a predetermined temperature (usually around room temperature) for 5 hours or less.

(2) Conversion from tungsten sulfide to tungsten carbide There is no particular limitation on the synthesis method for providing tungsten carbide used in the present invention from tungsten sulfide, and any method can be used.

  Specifically, tungsten sulfide is converted into a predetermined hydrocarbon gas (usually methane, ethane, propane, butane, ethylene, propylene, acetylene, preferably methane, ethane, ethylene) or a mixed gas thereof and hydrogen gas (usually The mixing ratio of the hydrocarbon gas in the mixed gas is usually 5% or more, preferably 10% or more, usually 90% or less, preferably 30% or less), a predetermined temperature (usually 550 ° C. or more, preferably 650 ° C. or more, Tungsten carbide can be generated by heating for a predetermined time (usually 10 minutes or more, preferably 30 minutes or more, usually 50 hours or less, preferably 30 hours or less) at 1100 ° C. or less, preferably 1000 ° C. or less. . In this heating, as described above, a predetermined rate (usually 10 ° C./hr or more, preferably 100 ° C. or more, preferably 600 ° C. or less, preferably 400 ° C. or less), from a predetermined temperature (usually 10 ° C./hr or more, preferably 20 ° C / hr or more, usually 600 ° C / hr or less, preferably 400 ° C / hr or less) to a predetermined temperature (usually 550 ° C or more, preferably 650 ° C or more, usually 1100 ° C or less, preferably 1000 ° C or less) You may heat with temperature. Furthermore, in an inert gas atmosphere having a low oxygen concentration (for example, an oxygen concentration of about 5% by weight or less, especially about 2% by weight or less), a predetermined time (usually several minutes or more, preferably 30 minutes or more, usually 10 hours or less). In particular, a passivation treatment for forming a passivation film can be performed by treating at a predetermined temperature (usually around room temperature) for 5 hours or less.

(3) Conversion from tungsten phosphide to tungsten carbide There is no particular limitation on the synthesis method for providing tungsten carbide used in the present invention from tungsten phosphide, and any method can be used. Tungsten carbide can be obtained under the same reaction conditions as the conversion reaction to tungsten.

[5] Production of Tungsten Carbide / Substrate-deposited Catalyst When producing the fuel cell catalyst of the present invention in which tungsten carbide is deposited on a substrate, the timing of applying the substrate in the synthesis process of tungsten carbide is arbitrary. For example, the following method is mentioned.
(1) After the substrate is mixed with the raw material compound, the conversion reaction of the raw material compound to the precursor compound is performed, and then the conversion reaction of the precursor compound to tungsten carbide is further performed.
(2) After mixing the substrate with the precursor compound, the conversion reaction of the precursor compound to tungsten carbide is performed.
(3) After preparing the tungsten carbide, the substrate is mixed with the tungsten carbide, and further subjected to a firing treatment or the like as desired.

In the case of (1) above, for example, after dissolving the raw material compound in a solvent such as an aqueous solution, dissolved or dispersed in a solvent such as an aqueous solution together with the substrate, and after removing the solvent, if necessary, under an inert gas flow Then, drying is performed by heating at a desired temperature and time, and then W ₂ N supported on the substrate can be obtained by heating under a flow of NH ₃ . Furthermore, by heating at a desired temperature and time under a flow of hydrocarbon gas and hydrogen, a fuel cell catalyst in which the tungsten carbide disclosed in the present invention is deposited on the substrate is produced. Further, a passivation treatment may be performed in which a passivation film is formed by processing at a predetermined temperature and time (usually around room temperature) in an inert gas atmosphere having a desired low oxygen concentration.

_{Specifically, (NH 4)} a _{10 W 12 O 41 · 5H 2} O, organic medium (e.g., alcohols such as ethanol, carbonyl such as acetone, ethers such as tetrahydrofuran, hydrocarbons such as toluene, Chlorides such as methylene chloride) or in an aqueous medium (for example, water), and if necessary, add a desired amount of HCl for complete dissolution, or make a slurry, and add carbon black A predetermined amount of the substrate is mixed and allowed to stand for a predetermined time (usually 10 minutes or more, preferably 30 minutes or more, usually 50 hours or less, preferably 30 hours or less), and then the solvent is removed by distillation or the like. If necessary, a predetermined temperature (usually 10 minutes or more, usually at 100 ° C. or higher, preferably 200 ° C. or higher, usually 1000 ° C. or lower, preferably 800 ° C. or lower) under a flow of an inert gas such as argon. (Preferably 30 minutes or more, usually 50 hours or less, preferably 30 hours or less) Drying by heating. Thereafter, under the flow of an inert gas containing NH ₃ (usually 10% or more, preferably 30% or more, 100% or less, or 90% or less NH ₃ concentration. High concentration reduces the firing time, but for safety reasons. The concentration may be lowered.) At a predetermined temperature (usually 300 ° C. or higher, preferably 400 ° C. or higher, usually 1000 ° C. or lower, preferably 800 ° C. or lower) for a predetermined time (usually 10 minutes or longer, preferably 30 minutes or longer). (Typically 50 hours or less, preferably 30 hours or less) By heating, tungsten nitride can be generated and supported on the substrate. In this heating, a predetermined rate (usually 10 ° C./hr or more, preferably 20 ° C./hr or more) from a predetermined temperature (usually room temperature or higher, preferably 100 ° C. or higher, usually 600 ° C. or lower, preferably 400 ° C. or lower). As described above, heating is generally performed at a temperature of 600 ° C./hr or less, preferably 400 ° C./hr or less) to a predetermined temperature (usually 300 ° C. or more, preferably 400 ° C. or more, usually 1000 ° C. or less, preferably 800 ° C. or less). You can go.

  Next, tungsten nitride is mixed with a predetermined hydrocarbon gas (usually methane, ethane, propane, butane, ethylene, propylene, acetylene, preferably methane, ethane, ethylene) or a mixed gas thereof and hydrogen gas (usually mixed). The mixing ratio of hydrocarbon gas in the gas is usually 5% or more, preferably 10% or more, usually 90% or less, preferably 30% or less), a predetermined temperature (usually 500 ° C. or more, preferably 600 ° C. or more, usually 1000). Tungsten carbide is deposited on the substrate by heating at a temperature of ℃ or less, preferably 900 ℃ or less for a predetermined time (usually 10 minutes or more, preferably 30 minutes or more, usually 50 hours or less, preferably 30 hours or less). The fuel cell catalyst is produced. In this heating, as described above, a predetermined rate (usually 10 ° C./hr or more, preferably 100 ° C. or more, preferably 600 ° C. or less, preferably 400 ° C. or less), from a predetermined temperature (usually 10 ° C./hr or more, preferably 20 ° C / hr or higher, usually 600 ° C / hr or lower, preferably 400 ° C / hr or lower) to a predetermined temperature (usually 500 ° C or higher, preferably 600 ° C or higher, usually 1000 ° C or lower, preferably 900 ° C or lower). You may heat with temperature. Furthermore, in an inert gas atmosphere having a low oxygen concentration (for example, an oxygen concentration of about 5% by weight or less, especially about 2% by weight or less), a predetermined time (usually several minutes or more, preferably 30 minutes or more, usually 10 hours or less). In particular, a passivation treatment for forming a passivation film can be performed by treating at a predetermined temperature (usually around room temperature) for 5 hours or less.

In addition, WO ₃ and other tungsten compounds are physically mixed with a carrier such as carbon black in a predetermined amount, and when necessary, a predetermined temperature (usually 100 ° C. or higher, preferably 200 ° C. or higher, usually 1500 under oxygen-containing gas flow conditions). ° C. or less, preferably 1000 ° C. or less) a predetermined time (usually 10 minutes or more, not preferably 30 minutes or more, usually at most 50 hours, preferably 30 hours or less) was heated, as above, the NH ₃ By heating under active gas flow, tungsten nitride can be generated and supported on the substrate. This heating may be performed by raising the temperature. Next, in the same manner as described above, a fuel cell catalyst is produced in which tungsten carbide is deposited on the substrate by heating at a predetermined temperature and for a predetermined time under a flow of hydrocarbon gas and hydrogen. This heating may be performed by raising the temperature. Further, a passivation treatment may be performed in which a passivation film is formed by processing at a predetermined temperature and time (usually around room temperature) in an inert gas atmosphere having a desired low oxygen concentration.

[6] Production of catalyst containing other catalyst components When producing the fuel cell catalyst of the present invention containing other catalyst components, other catalyst components or substances that produce other catalyst components during the synthesis of tungsten carbide ( Hereinafter, the timing of applying “other catalyst component source” is not particularly limited, but the following method is usually employed.
(1) After mixing other catalyst components or other catalyst component sources into the raw material compound or the mixture of the raw material compound and the substrate, the conversion reaction of the raw material compound into the precursor compound is performed, and then the precursor compound is further converted into tungsten carbide. Perform the conversion reaction. Further, mixing with the substrate is performed as necessary.
(2) After mixing another catalyst component or another catalyst component source into the precursor compound or a mixture of the precursor compound and the substrate, the conversion reaction of the precursor compound to tungsten carbide is performed. Further, mixing with the substrate is performed as necessary.
(3) After preparing tungsten carbide or tungsten carbide adhering to the substrate, another catalyst component or another catalyst component source is mixed with this, and further subjected to a calcination treatment or the like as desired.

  Among these, the method (3) is preferable because it is expected that the amount of other catalyst components deposited on the catalyst surface is large.

  Other catalyst component sources include the above transition metal oxides, inorganic acid salts such as nitrates, sulfates and carbonates, organic acid salts such as acetates, halides, hydrides, carbonyl compounds, Examples thereof include amine compounds, olefin coordination compounds, phosphine coordination compounds, and phosphite coordination compounds. Preferred are oxides, carbonates, organic acid salts, carbonyl compounds, and olefin coordination compounds that do not contain halogen elements or nitrogen elements.

When carrying out the above method (3), for example, the raw material compound is dissolved in a solvent such as an aqueous solution, dissolved or dispersed in a solvent such as an aqueous solution together with the substrate, the solvent is removed, and if necessary, It can be dried by heating at a desired temperature and time under a flow of active gas, and then heated under a flow of NH ₃ to obtain W ₂ N supported on the substrate. Furthermore, a catalyst in which tungsten carbide is deposited on the substrate is produced by heating at a desired temperature and time under a flow of hydrocarbon gas and hydrogen. Next, the obtained catalyst is added to a solution such as an aqueous solution in which a transition metal chloride or the like as another catalyst component source is dissolved or dispersed, left for a desired time, after removing the solvent, if necessary, Dried by heating at a desired temperature and time under an inert gas flow, and then heated at a desired temperature and time under a hydrogen flow to deposit other catalyst component sources and tungsten carbide on the substrate. A catalyst is produced. Further, a passivation treatment may be performed in which a passivation film is formed by processing at a predetermined temperature and time (usually around room temperature) in an inert gas atmosphere having a desired low oxygen concentration.

More specifically, the W ₂ N catalyst supported on the substrate synthesized by the above method is used as an organic medium in which RuCl ₃ is dissolved or in a slurry state (for example, alcohols such as ethanol, carbonyls such as acetone, and the like). , Ethers such as tetrahydrofuran, hydrocarbons such as toluene, chlorides such as methylene chloride) or an aqueous medium (for example, water, etc.), and a predetermined amount is mixed for a predetermined time (usually 10 minutes or more, preferably For 30 minutes or longer, usually 50 hours or shorter, preferably 30 hours or shorter), and then the solvent is removed by distillation or the like. If necessary, a predetermined temperature (usually 10 minutes or more, usually at 100 ° C. or higher, preferably 200 ° C. or higher, usually 1000 ° C. or lower, preferably 800 ° C. or lower) under a flow of an inert gas such as argon. (Preferably 30 minutes or more, usually 50 hours or less, preferably 30 hours or less) Drying by heating. Next, under a hydrogen gas flow, at a predetermined temperature (usually 100 ° C. or more, preferably 200 ° C. or more, usually 1000 ° C. or less, preferably 900 ° C. or less) for a predetermined time (usually 10 minutes or more, preferably 30 minutes or more, (Normally 50 hours or less, preferably 30 hours or less) By heating, a fuel cell catalyst in which tungsten carbide and Ru are deposited on the substrate is produced. In this reduction process by hydrogen circulation, a predetermined rate (usually 10 ° C./hr or more, preferably 100 ° C. or more, preferably 600 ° C. or less, preferably 400 ° C. or less) from a predetermined temperature (usually room temperature or more, preferably 100 ° C. or more, preferably 400 ° C. or less, preferably 400 ° C. or less, 20 ° C / hr or higher, usually 600 ° C / hr or lower, preferably 400 ° C / hr or lower) to a predetermined temperature (usually 200 ° C or higher, preferably 300 ° C or higher, usually 1000 ° C or lower, preferably 900 ° C or lower). You may heat with temperature. Furthermore, in an inert gas atmosphere having a low oxygen concentration (for example, an oxygen concentration of about 5% by weight or less, especially about 2% by weight or less), a predetermined time (usually several minutes or more, preferably 30 minutes or more, usually 10 hours or less). In particular, a passivation treatment for forming a passivation film can be performed by treating at a predetermined temperature (usually around room temperature) for 5 hours or less.

Further, when Pd is used in combination, PdCl ₂ is used instead of RuCl ₃ , and when Pt is used in combination, H ₂ PtCl ₄ is used, and the W ₂ N catalyst supported on the substrate synthesized by the above method is used. In an organic medium in which PdCl ₂ or H ₂ PtCl ₄ is dissolved or in a slurry state (for example, alcohols such as ethanol, carbonyls such as acetone, ethers such as tetrahydrofuran, hydrocarbons such as toluene, methylene chloride, etc. In the following, a catalyst containing Pd or Pt can be prepared in the same manner as in the case of Ru, by mixing a predetermined amount with an aqueous medium (for example, water).

[7] Surface treatment of catalyst The catalyst activity can be further improved by heating the catalyst of the present invention under a hydrogen flow to perform a reduction treatment. This is because the inactive carbon layer adhering to the catalyst surface is removed as CH ₄ or the like, and the active WC surface is exposed.

  Hydrogen to be circulated may be circulated only with hydrogen, or may be circulated together with an inert gas such as argon or nitrogen. The hydrogen to be circulated is usually 1 mL / min. Or more, preferably 5 mL / min. As described above, usually 500 mL / min. Hereinafter, preferably 400 mL / min. It is preferable to supply the following. If the amount of hydrogen to be circulated is less than the above lower limit, removal of the inactive carbon layer attached to the catalyst surface is difficult to proceed. .

  The treatment temperature depends on the particle size of the catalyst and the nature of the attached carbon layer, but is usually 100 ° C. or higher, preferably 200 ° C. or higher, usually 1200 ° C. or lower, preferably 1000 ° C. or lower. When the treatment temperature is lower than the lower limit, removal of the inactive carbon layer attached to the catalyst surface is difficult to proceed, and when the treatment temperature is higher than the upper limit, desorption of carbon from the catalyst WC itself proceeds. Decreases.

  The treatment time varies depending on the treatment temperature, but is usually 5 minutes or more, preferably 10 minutes or more, usually 50 hours or less, preferably 30 hours or less. If this treatment time is shorter than the above lower limit, the reaction is difficult to proceed completely, and if it is longer than the upper limit, it becomes difficult to obtain a highly active catalyst.

Moreover, catalytic activity can also be improved by making the catalyst of this invention contact alkaline solutions, such as sodium hydroxide aqueous solution and ammonia water. This is due to a decrease in the inactive WO ₂ layer present on the catalyst surface.

  This alkali treatment is preferably carried out by charging the catalyst into an alkali solution and maintaining it under reflux conditions. The treatment time varies depending on the type of alkali used, but is usually 5 minutes or more, preferably 10 minutes. As described above, it is usually 50 hours or less, preferably 30 hours or less. If this treatment time is shorter than the above lower limit, the reaction is difficult to proceed completely, and if it is longer than the upper limit, it becomes difficult to obtain a highly active catalyst.

  Furthermore, a highly active WC catalyst can be obtained by performing the reduction treatment in combination with the alkali treatment.

[Fuel cell electrode and fuel cell]
The fuel cell electrode of the present invention is characterized by containing the above-described fuel cell catalyst of the present invention. The fuel cell of the present invention is characterized by using such a fuel cell electrode of the present invention.

  The fuel cell according to the present invention is a power generator that supplies fuel to the anode and oxidant to the cathode, takes out the potential difference between the anode and cathode as a voltage, and supplies it to the load as described above. In a polymer electrolyte fuel cell, an ion exchange membrane is used as an electrolyte. That is, an electrolyte membrane / electrode assembly in which a catalyst layer is formed on both surfaces of an ion exchange membrane as an electrolyte, and an anode gas diffusion layer and a cathode gas / fuel diffusion layer are integrally formed on the outside of the catalyst layer, respectively. ing. The electrolyte membrane / electrode assembly has a partition plate disposed on the diffusion layer side, and several tens of cells until the unit cell of the partition plate, electrolyte membrane / electrode assembly, and partition plate has a desired voltage according to the application. Several hundred cells are stacked to form a fuel cell.

  In the present invention, the aforementioned fuel cell catalyst of the present invention is used as a catalyst for forming the catalyst layer of the electrolyte membrane / electrode assembly.

  An ion exchange membrane as an electrolyte is only required to have a cation exchange capacity, but it is practically desired to withstand an oxidation-reduction atmosphere at a temperature of about 80 to 100 ° C., which is a use temperature of a fuel cell. Alkyl sulfonic acid resins are exclusively used. Specific examples include perfluoroalkylsulfonic acid resin membranes such as Nafion (registered trademark manufactured by DuPont), Flemion (registered trademark manufactured by Asahi Glass Co., Ltd.), and Aciplex (registered trademark manufactured by Asahi Kasei Co., Ltd.).

  As the thickness of the ion exchange membrane, a thickness of about 10 μm or more and about several 100 μm or less is used, but it is desirable to make the thickness thinner in order to lower the electric resistance. Taking Nafion as an example, Nafion 115 having a thickness of about 120 μm is often used. However, an electrolyte having a thickness of 30 to 50 μm has begun to be developed, and these can be used in the same manner.

  As the constituent material of the diffusion layer, hydrogen is supplied to the anode and air is supplied to the cathode, and also has a function as a current collector for taking out the generated voltage. A material that allows both gases of air to flow and withstands the use atmosphere is selected. As a material constituting the anode fuel diffusion layer and the cathode gas / fuel diffusion layer, a carbon porous body such as carbon paper or carbon cloth having a thickness of usually about 100 to 500 μm, preferably about 100 to 200 μm is used.

  When an electrolyte membrane / electrode assembly is used in a fuel cell, a partition plate made of a material such as carbon, and in some cases, stainless steel, titanium, etc. is usually disposed behind the membrane to prevent hydrogen and air from mixing. In general, the partition plate is formed with grooves for the purpose of uniform and stable supply of hydrogen and air.

  Although there is no restriction | limiting in particular as a method of producing the electrolyte membrane / electrode assembly of a fuel cell by forming a catalyst layer using the catalyst for fuel cells of this invention, For example, the following methods are mentioned.

  Although there is no restriction | limiting in particular about the method of producing a cathode side catalyst layer and an anode side catalyst layer, For example, it can produce as follows. First, the fuel cell catalyst of the present invention obtained by depositing tungsten carbide on a substrate is placed in a suitable container and dispersed in a medium such as alcohol or water to prepare a catalyst slurry. At this time, it is more preferable to apply ultrasonic vibration in order to promote the dispersion well. In order to obtain a desired dispersibility, the catalyst concentration for a fuel cell of the present invention in the catalyst slurry is preferably about 1 to 50 g / L. Of course, a binder such as polytetrafluoroethylene (PTFE) can be added to the slurry in the range of about 3 to 30% by weight for the purpose of providing water repellency or preventing the catalyst layer from peeling off. is there. Further, when the contents are aggregated to make a paste, a lower alcohol such as ethanol or isopropyl alcohol having 2 to 5 carbon atoms, preferably about 2 to 4 carbon atoms, has a ratio of 0.25 to 1.0 with respect to water. In addition, it can be aggregated.

  The catalyst slurry thus obtained may be dried to form the cathode side catalyst layer and the anode side catalyst layer of the electrolyte membrane / electrode assembly. For example, the catalyst layer may be placed on the ion exchange membrane. A method of laminating the gas / fuel diffusion layer material after the formation and a method of laminating the ion exchange membrane after forming the catalyst layer on the gas / fuel diffusion layer material are exemplified.

Specifically, the cathode side catalyst layer and the anode side catalyst layer are respectively formed on the ion exchange membrane or the gas diffusion electrode material by the following methods.
(1) Spray on the ion exchange membrane to be used and dry.
(2) Spray the catalyst slurry on a gas diffusion electrode material such as carbon paper and dry.
(3) The catalyst slurry is sprayed onto a transfer film material such as a tetrafluoroethylene-hexafluoropropylene copolymer (FEP) film (development treatment) and dried, and the surface opposite to the transfer film surface is made of Nafion, etc. The catalyst layer is transferred onto the desired ion exchange membrane by appropriately pressing.
(4) As in (3), after the catalyst slurry is spread on the FEP film, the slurry is covered with a gas diffusion electrode material such as carbon paper and dried.

Both the cathode side catalyst layer and the anode side catalyst layer are generally 0.5 mg / cm ² or more, preferably 1 mg / cm ² or more, and several g / cm ² or less, preferably 1 g / cm ^{2 in} terms of tungsten carbide adhesion amount (weight per unit area). It is preferably formed so as to have an amount of about cm ² or less. If the tungsten carbide adhesion amount is less than the above lower limit, sufficient catalytic activity cannot be obtained, and if it exceeds the upper limit, it is difficult to form an electrolyte membrane / electrode assembly.

  After each forming step of the cathode side catalyst layer and the anode side catalyst layer, preliminary pressure molding is appropriately performed, and then the final electrolyte membrane / electrode assembly, that is, the surface on one side of the ion exchange membrane is described above. A cathode-side catalyst layer is formed, and an anode-side catalyst layer is laminated on the opposite surface of the ion-exchange membrane, and a gas / fuel diffusion layer constituting the anode and the cathode is laminated outside the both catalyst layers. Then, an electrolyte membrane / electrode assembly is produced by press-heating using a press machine.

  In addition, as conditions for preliminary pressure molding, it is preferable to set the temperature and pressure lower and the time shorter than the conditions of the main molding performed later within a range in which the catalyst layer can be prevented from collapsing. This is because the catalyst particles and gas / fuel diffusion layer porous body do not cause compressive fracture.

  EXAMPLES Next, although an Example and a comparative example are given and this invention is demonstrated further more concretely, this invention is not limited by a following example, unless the summary is exceeded.

  In the following examples and comparative examples, the performance (catalytic activity) of the produced anode electrode was measured by the following cyclic voltammetry (CV) measurement.

[CV measurement]
Cyclic voltammetry (CV) measurement was performed using a stopper capable of maintaining hermeticity in the electrolytic cell, and bubbling nitrogen or hydrogen into the electrolytic solution, but under conditions where hydrogen was not supplied. In addition, in order to remove the surface oxygen of the catalyst components such as WC that had been passivated prior to the measurement, an application treatment was performed at −0.99 V for 1000 seconds. The measurement conditions are as follows.
Electrolyte: 1.0 MH ₂ SO ₄ aqueous solution Scan speed: 10 mV / sec Scan range: 0 to 900 mV
Counter electrode: Pt
Reference electrode: Standard hydrogen electrode (SHE)

If the potential of the electrode is noble relative to the standard hydrogen electrode, H ₂ = 2H ⁺ + 2e ⁻ between the working electrode and the Pt counter electrode.
It is recognized that the hydrogen oxidation current due to. Measured current value flowing at 450 mV (SHE standard) when scanned in your direction, and converted the measured current value to the current value per unit weight (1 g) of WC or WC and Ru contained in the catalyst The catalytic activity was evaluated.

[Example 1]
<Synthesis of WC>
1.0 g WO ₃ manufactured by Kishida Chemical Co., Ltd. was put in a quartz tube and NH ₃ gas 30 ml / min. Then, the temperature was increased from 300 to 630 ° C. over 7 hours at a temperature increase rate of 49 ° C./hr, and further reduced and nitrided by holding at 630 ° C. for 0.5 hr to obtain a W ₂ N black powder. 1.0 g of W ₂ N thus obtained was put in a quartz tube, and 70 ml / min. Of a mixed gas of CH ₄ / H ₂ (mixing ratio 2/8). Was reduced and carbonized at 777 ° C. for 6 hours to obtain an α-WC black powder. After cooling to room temperature, the inside of the firing tube was replaced with argon gas, and then the mixture was passivated with 2% O ₂ -98% N ₂ mixed gas for 1.5 hr and taken out into the air.
The raw material compound used had a WO ₃ particle size (average particle size) of approximately 250 nm.

  This compound was confirmed by XRD analysis to have an α-WC structure (2θ values peaked at 31.649 °, 35.801 °, 48.251 °, and 65.598 °). . The half width of the 48.251 ° peak was 1.888 °.

<Creation of anode electrode>
20 mg of the obtained α-WC powder and 80 mg of carbon black (VULCAN XC-72R (manufactured by Cabot, specific surface area (BET) 254 m ² / g)) were mixed in a mortar, and 42.41 mg thereof was mixed with 5 mL of ethanol, After sufficiently stirring with an ultrasonic cleaner, it was dropped with a microsyringe onto a glassy carbon electrode as a working electrode so that α-WC would be 0.30 mg / cm ² and dried by standing. Next, a commercially available Nafion solution in which a Nafion membrane manufactured by DuPont was dissolved in a solvent was dropped, dried by standing, and then further dried under vacuum to obtain an anode electrode.

  CV measurement was performed on this anode electrode, and the evaluation results of catalyst activity are shown in Table 2.

[Example 2]
In the same manner as in Example 1, except that 135 mg of the same α-WC powder as used in Example 1 and 15 mg of the same carbon black were mixed in a mortar and 47.1 mg thereof was mixed in 5 mL of ethanol. An anode electrode was prepared so that the amount of α-WC supported on the substrate was 0.30 mg / cm ² , evaluation was performed in the same manner, and the results are shown in Table 2.

[Example 3]
<WC surface treatment>
500 mg of the same α-WC powder as used in Example 1 was put in a quartz-made baking tube, and H ₂ gas at 50 ml / min. Then, reduction treatment was performed at 400 ° C. for 3 hours. After cooling to room temperature, the inside of the firing tube was replaced with argon gas, and then the mixture was passivated with 2% O ₂ -98% N ₂ mixed gas for 1.5 hr and taken out into the air.

  This compound was confirmed by XRD analysis to have an α-WC structure (2θ values peaked at 31.649 °, 35.801 °, 48.251 °, and 65.598 °). . The half width of the 48.251 ° peak was 1.888 °.

<Creation of anode electrode>
Instead of the α-WC powder used in Example 1, the α-WC supported amount on the electrode was set to 0. 0 by the same method as in Example 1 except that the α-WC powder subjected to the surface treatment was used. An anode electrode was prepared so as to be 30 mg / cm ² , evaluation was performed in the same manner, and the results are shown in Table 2.

[Example 4]
<WC surface treatment>
500 mg of the same α-WC powder as used in Example 1 was added to 25 ml of 1N NaOH aqueous solution and refluxed for 3 hours. Next, the treated α-WC powder was placed in a quartz firing tube, and hydrogen gas at 50 ml / min. Then, reduction treatment was performed at 400 ° C. for 2 hours. After cooling to room temperature, the inside of the firing tube was replaced with argon gas, and then the mixture was passivated with 2% O ₂ -98% N ₂ mixed gas for 1.5 hr and taken out into the air.

  This compound was confirmed by XRD analysis to have an α-WC structure (2θ values were peaks at 31.404 °, 35.699 °, 48.400 °, and 65.550 °). . The half width of the peak at 48.400 ° was 1.799 °.

<Creation of anode electrode>
Instead of the α-WC powder used in Example 1, the α-WC supported amount on the electrode was set to 0. 0 by the same method as in Example 1 except that the α-WC powder subjected to the surface treatment was used. An anode electrode was prepared so as to be 30 mg / cm ² , evaluation was performed in the same manner, and the results are shown in Table 2.

[Example 5]
<Synthesis of WC>
1.0 g WO ₃ manufactured by Kishida Chemical Co., Ltd. was put in a quartz tube and NH ₃ gas 30 ml / min. Then, the temperature was raised to 300 to 680 ° C. over 7 hours at a heating rate of 54 ° C./hr, and further reduced and nitrided by holding at 680 ° C. for 0.5 hr to obtain a W ₂ N black powder. 1.0 g of W ₂ N thus obtained was put in a quartz tube, and 70 ml / min. Of a mixed gas of CH ₄ / H ₂ (mixing ratio 2/8). Was reduced and carbonized at 777 ° C. for 6 hours to obtain an α-WC black powder. After cooling to room temperature, the inside of the firing tube was replaced with argon gas, and then the mixture was passivated with 2% O ₂ -98% N ₂ mixed gas for 1.5 hr and taken out into the air.

  This compound was confirmed by XRD analysis to have an α-WC structure (values of 2θ were peaks at 31.552 °, 35.699 °, 48.400 °, and 65.157 °). . The half width of the 48.400 ° peak was 1.912 °.

<Creation of anode electrode>
Instead of the α-WC powder used in Example 2, the α-WC supported amount on the electrode was 3 by the same method as in Example 2 except that the α-WC powder obtained by the above synthesis method was used. An anode electrode was prepared to be 0.000 mg / cm ² and evaluated in the same manner, and the results are shown in Table 2.

[Example 6]
<Synthesis of WC>
1.0 g of WO ₃ manufactured by Aldrich (catalog number 23,278-5) was put in a quartz firing tube, and NH ₃ gas 30 ml / min. Then, the temperature was raised to 300 to 680 ° C. over 7 hours at a heating rate of 54 ° C./hr, and further reduced and nitrided by holding at 680 ° C. for 0.5 hr to obtain a W ₂ N black powder. 1.0 g of W ₂ N thus obtained was put in a quartz tube, and 70 ml / min. Of a mixed gas of CH ₄ / H ₂ (mixing ratio 2/8). Was reduced and carbonized at 777 ° C. for 2 hours to obtain an α-WC black powder. After cooling to room temperature, the inside of the firing tube was replaced with argon gas, and then the mixture was passivated with 2% O ₂ -98% N ₂ mixed gas for 1.5 hr and taken out into the air.

  This compound was confirmed by XRD analysis to have an α-WC structure (the values of 2θ peaked at 31.548 °, 35.848 °, 48.498 °, and 65.247 °). . The half width of the peak at 48.498 ° was 1.722 °.

<Creation of anode electrode>
Instead of the α-WC powder used in Example 1, the amount of α-WC supported on the electrode was 0 by the same method as in Example 1 except that the α-WC powder obtained by the above synthesis method was used. An anode electrode was prepared so as to be 30 mg / cm ² , evaluation was performed in the same manner, and the results are shown in Table 2.

[Example 7]
<Synthesis of WC>
1.0 g of WO ₃ manufactured by Aldrich (catalog number 23,278-5) was placed in a quartz baking tube, and argon 80 ml / min. H2 20 ml / min. , H ₂ S gas 20 ml / min. Then, the temperature was raised and treated at 850 ° C. for 2.0 hours. 0.3 g of WS ₂ obtained in this way was put in a quartz-made calcining tube, and a mixed gas of CH ₄ / H ₂ (mixing ratio 2/8) was 70 ml / min. Was reduced and carbonized at 840 ° C. for 13 hours to obtain an α-WC black powder. After cooling to room temperature, the inside of the firing tube was replaced with argon gas, and then the mixture was passivated with 2% O ₂ -98% N ₂ mixed gas for 1.5 hr and taken out into the air.

  This compound was confirmed to have an α-WC structure by XRD analysis (the values of 2θ gave peaks at 31.356 °, 35.552 °, 48.202 °, 63.944 °). . The half width of the 48.202 ° peak was 1.493 °.

<Creation of anode electrode>
Instead of the α-WC powder used in Example 1, the amount of α-WC supported on the electrode was 0 by the same method as in Example 1 except that the α-WC powder obtained by the above synthesis method was used. An anode electrode was prepared so as to be 30 mg / cm ² , evaluation was performed in the same manner, and the results are shown in Table 2.

[Example 8]
<Synthesis of WC>
0.5 g of WO ₃ manufactured by Aldrich (nanopowder, catalog number 55,008-6) was placed in a quartz firing tube, and NH ₃ gas 30 ml / min. Then, the temperature was increased from 300 to 680 ° C. over 7 hours at a temperature increase rate of 54 ° C./hr, and further maintained at 680 ° C. for 0.5 hr for reduction and nitriding to obtain a W ₂ N black powder. 0.5 g of W ₂ N obtained in this way was put in a quartz firing tube, and 70 ml / min. Of a mixed gas of CH ₄ / H ₂ (mixing ratio 2/8). Was reduced and carbonized at 777 ° C. for 6 hours to obtain an α-WC black powder. After cooling to room temperature, the inside of the firing tube was replaced with argon gas, and then the mixture was passivated with 2% O ₂ -98% N ₂ mixed gas for 1.5 hr and taken out into the air.
The raw material compound used had a WO ₃ particle size (average particle size) of approximately 50 nm.

  This compound was confirmed by XRD analysis to have an α-WC structure (the values of 2θ gave peaks at 31.252 °, 35.602 °, 48.201 °, and 65.098 °). . The half width of the 48.201 ° peak was 1.569 °.

<Creation of anode electrode>
Instead of the α-WC powder used in Example 1, the amount of α-WC supported on the electrode was 0 by the same method as in Example 1 except that the α-WC powder obtained by the above synthesis method was used. An anode electrode was prepared so as to be 30 mg / cm ² , evaluation was performed in the same manner, and the results are shown in Table 2.

[Example 9]
<Synthesis of WC>
0.6 g (nanopowder, catalog number 55,008-6) of WO ₃ manufactured by Aldrich was put in a quartz baking tube, and argon 80 ml / min. , H ₂ S gas 20 ml / min. Then, the temperature was raised and the mixture was fired at 800 ° C. for 2.5 hours. 0.3 g of WS ₂ obtained in this way was put in a quartz-made calcining tube, and a mixed gas of CH ₄ / H ₂ (mixing ratio 2/8) was 70 ml / min. Was reduced and carbonized at 840 ° C. for 17 hours to obtain an α-WC black powder. After cooling to room temperature, the inside of the firing tube was replaced with argon gas, and then the mixture was passivated with 2% O ₂ -98% N ₂ mixed gas for 1.5 hr and taken out into the air.

  This compound was confirmed by XRD analysis to have an α-WC structure (the values of 2θ gave peaks at 31.550 °, 35.502 °, 48.301 °, and 63.945 °). . The half width of the peak at 48.301 ° was 1.846 °.

<Creation of anode electrode>
Instead of the α-WC powder used in Example 1, the amount of α-WC supported on the electrode was 0 by the same method as in Example 1 except that the α-WC powder obtained by the above synthesis method was used. An anode electrode was prepared so as to be 30 mg / cm ² , evaluation was performed in the same manner, and the results are shown in Table 2.

[Example 10]
<Synthesis of WC>
1.0 g of WO ₃ manufactured by Aldrich (nanopowder, catalog number 55,008-6) was placed in a quartz baking tube, and argon 80 ml / min. H ₂ gas 20 ml / min. , H ₂ S gas 20 ml / min. Then, the temperature was raised and treated at 850 ° C. for 2.0 hours. 0.3 g of WS ₂ obtained in this way was put in a quartz-made calcining tube, and a mixed gas of CH ₄ / H ₂ (mixing ratio 2/8) was 70 ml / min. Was reduced and carbonized at 840 ° C. for 8 hours to obtain an α-WC black powder. After cooling to room temperature, the inside of the firing tube was replaced with argon gas, and then the mixture was passivated with 2% O ₂ -98% N ₂ mixed gas for 1.5 hr and taken out into the air.

  This compound was confirmed by XRD analysis to have an α-WC structure (values of 2θ gave peaks at 31.451 °, 35.647 °, 48.199 °, and 64.389 °). . The half width of the peak at 48.199 ° was 1.507 °.

<Creation of anode electrode>
Instead of the α-WC powder used in Example 1, the amount of α-WC supported on the electrode was 0 by the same method as in Example 1 except that the α-WC powder obtained by the above synthesis method was used. An anode electrode was prepared so as to be 30 mg / cm ² , evaluation was performed in the same manner, and the results are shown in Table 2.

[Example 11]
<Synthesis of WC>
When Aldrich W (CO) ₆ 4.22 g, Kishida S0.832 g, and xylene 80 ml were added to a glass Kolbe and refluxed for 4 hours with stirring, black particles were precipitated. After completion of the reaction, the precipitate was collected by filtration. Further, in order to remove unreacted W (CO) ₆ , the precipitate was refluxed with 60 ml of CH ₃ CN for 2 hours, followed by hot filtration. The obtained precipitate was finally heat-treated at 350 ° C. for 3 hours under an argon stream to obtain WS ₂ . 0.3 g of WS ₂ obtained in this way was put in a quartz-made calcining tube, and a mixed gas of CH ₄ / H ₂ (mixing ratio 2/8) was 70 ml / min. Was reduced and carbonized at 810 ° C. for 24 hours to obtain an α-WC black powder. After cooling to room temperature, the inside of the firing tube was replaced with argon gas, and then the mixture was passivated with 2% O ₂ -98% N ₂ mixed gas for 1.5 hr and taken out into the air.

  This compound was confirmed by XRD analysis to have an α-WC structure (2θ values gave peaks at 31.499 °, 35.654 °, 48.252 °, and 65.101 °). . The half width of the 48.252 ° peak was 1.187 °.

<Creation of anode electrode>
Instead of the α-WC powder used in Example 1, the amount of α-WC supported on the electrode was 0 by the same method as in Example 1 except that the α-WC powder obtained by the above synthesis method was used. An anode electrode was prepared so as to be 30 mg / cm ² , evaluation was performed in the same manner, and the results are shown in Table 2.

[Example 12]
<Synthesis of WC>
When Aldrich W (CO) ₆ 4.22 g, Kishida S0.832 g, and xylene 80 ml were added to a glass Kolbe and refluxed for 4 hours with stirring, black particles were precipitated. After completion of the reaction, the precipitate was collected by filtration. Further, in order to remove unreacted W (CO) ₆ , the precipitate was refluxed with 60 ml of CH ₃ CN for 2 hours, followed by hot filtration. The obtained precipitate was finally heat-treated at 350 ° C. for 3 hours under an argon stream to obtain WS ₂ . 0.5 g of WS ₂ obtained in this way was put in a quartz firing tube, and 70 ml / min. Of a mixed gas of CH ₄ / H ₂ (mixing ratio 2/8). Was reduced and carbonized at 840 ° C. for 11 hours to obtain an α-WC black powder. After cooling to room temperature, the inside of the firing tube was replaced with argon gas, and then the mixture was passivated with 2% O ₂ -98% N ₂ mixed gas for 1.5 hr and taken out into the air.

  This compound was confirmed by XRD analysis to have an α-WC structure (the values of 2θ gave peaks at 31.613 °, 35.525 °, 48.186 °, 63.854 °). . The half width of the peak at 48.186 ° was 2.205 °.

<Creation of anode electrode>
Instead of the α-WC powder used in Example 2, the α-WC supported amount on the electrode was 3 by the same method as in Example 2 except that the α-WC powder obtained by the above synthesis method was used. An anode electrode was prepared to be 0.000 mg / cm ² and evaluated in the same manner, and the results are shown in Table 2.

[Example 13]
<Synthesis of WC>
When Aldrich W (CO) ₆ 4.22 g, Kishida S0.832 g, and xylene 80 ml were added to a glass Kolbe and refluxed for 4 hours with stirring, black particles were precipitated. After completion of the reaction, the precipitate was collected by filtration. Further, in order to remove unreacted W (CO) ₆ , the precipitate was refluxed with 60 ml of CH ₃ CN for 2 hours, followed by hot filtration. The obtained precipitate was finally heat-treated at 350 ° C. for 3 hours under an argon stream to obtain WS ₂ . 0.5 g of WS ₂ obtained in this way was put in a quartz firing tube, and 70 ml / min. Of a mixed gas of CH ₄ / H ₂ (mixing ratio 2/8). The carbon was reduced and carbonized at 900 ° C. for 7 hours under an air current of α to obtain a black powder of α-WC. After cooling to room temperature, the inside of the firing tube was replaced with argon gas, and then the mixture was passivated with 2% O ₂ -98% N ₂ mixed gas for 1.5 hr and taken out into the air.

  This compound was confirmed by XRD analysis to have an α-WC structure (2θ values were peaks at 31.500 °, 35.501 °, 48.200 °, 63.849 °). . The half width of the peak at 48.200 ° was 1.912 °.

<Creation of anode electrode>
Instead of the α-WC powder used in Example 2, the amount of α-WC supported on the electrode was 0 by the same method as in Example 2 except that the α-WC powder obtained by the synthesis method was used. An anode electrode was prepared so as to be .75 mg / cm ² and evaluated in the same manner, and the results are shown in Table 2.

[Example 14]
<Synthesis of WC>
Aldrich W (CO) ₃ (CH ₃ CN) ₃ 0.6 g was placed in a quartz firing tube, and NH ₃ gas 30 ml / min. Then, the temperature was increased from 200 to 500 ° C. over 5 hours at a temperature increase rate of 60 ° C./hr, and further maintained at 500 ° C. for 2 hours for reduction and nitridation to obtain a W ₂ N black powder. 0.3 g of W ₂ N obtained in this way was put in a quartz firing tube, and a mixed gas of CH ₄ / H ₂ (mixing ratio 2/8) was 70 ml / min. Was reduced and carbonized at 777 ° C. for 6 hours to obtain an α-WC black powder. After cooling to room temperature, the inside of the firing tube was replaced with argon gas, and then the mixture was passivated with 2% O ₂ -98% N ₂ mixed gas for 1.5 hr and taken out into the air.

  This compound was confirmed by XRD analysis to have an α-WC structure (values of 2θ were 31.401 °, 35.551 °, 48.248 °, 62.027 °, 64.761 °). Gave a peak). The half width of the peak at 48.248 ° was 1.760 °.

<Creation of anode electrode>
Instead of the α-WC powder used in Example 1, 20 mg of the α-WC powder obtained by the above synthesis method and 80 mg of the same carbon black were mixed in a mortar, and 35.3 mg thereof was mixed with 5 mL of ethanol. An anode electrode was prepared by the same method as in Example 1 so that the amount of α-WC supported on the electrode was 0.10 mg / cm ² , evaluation was performed in the same manner, and the results are shown in Table 2.

[Example 15]
<Synthesis of WC>
0.7 g of WCl ₄ manufactured by Kishida Chemical Co., Ltd. was put in a quartz baking tube, and NH ₃ gas 30 ml / min. Then, the temperature was increased from 300 to 630 ° C. over 5 hours at a temperature increase rate of 66 ° C./hr, further maintained at 630 ° C. for 0.5 hr, reduced and nitrided to obtain W ₂ N black powder. 0.3 g of W ₂ N obtained in this way was put in a quartz tube, and 70 ml / min. Of a mixed gas of CH ₄ / H ₂ (mixing ratio 2/8). Was reduced and carbonized at 777 ° C. for 2 hours to obtain an α-WC black powder. After cooling to room temperature, the inside of the firing tube was replaced with argon gas, and then the mixture was passivated with 2% O ₂ -98% N ₂ mixed gas for 1.5 hr and taken out into the air.

  This compound was confirmed by XRD analysis to have an α-WC structure (values of 2θ gave peaks at 31.443 °, 35.649 °, 48.246 °, 64.725 °). . The half width of the peak at 48.246 ° was 1.876 °.

<Creation of anode electrode>
Instead of the α-WC powder used in Example 1, the amount of α-WC supported on the electrode was 0 by the same method as in Example 1 except that the α-WC powder obtained by the above synthesis method was used. An anode electrode was prepared so as to be 30 mg / cm ² , evaluation was performed in the same manner, and the results are shown in Table 2.

[Example 16]
<Synthesis of WC>
Aldrich (NH ₄ ) ₂ WS ₄ (0.5 g) was placed in a quartz firing tube and placed in a glass reaction tube filled with thiophene at 25 ml / min. While bubble of _{H 2} gas, 600 ° C. while introducing _{H 2} gas to the calcining tube by entraining thiophene was 0.5hr reaction. The obtained WS ₂ was placed in a quartz fired tube, and a CH ₄ / H ₂ (2/8) gas of 70 ml / min. An α-WC black powder was obtained by firing and carbonization at 840 ° C. for 8 hours in an air stream. After cooling to room temperature, the inside of the firing tube was replaced with argon gas, and then the mixture was passivated with 2% O ₂ -98% N ₂ mixed gas for 1.5 hr and taken out into the air.

  This compound was confirmed to have an α-WC structure by XRD analysis (2θ values gave peaks at 31.405 °, 35.548 °, 48.298 °, and 63.906 °). . The half width of the peak at 48.298 ° was 2.105 °.

<Creation of anode electrode>
Instead of the α-WC powder used in Example 1, the amount of α-WC supported on the electrode was 0 by the same method as in Example 1 except that the α-WC powder obtained by the above synthesis method was used. An anode electrode was prepared so as to be 30 mg / cm ² , evaluation was performed in the same manner, and the results are shown in Table 3.

[Example 17]
<Synthesis of WC-Ru>
A catalyst solution prepared by dissolving 1.04 g of RuCl ₃ manufactured by NE Chemcat in 10 ml of demineralized water was added to 0.4 g of WC obtained in Example 1, 1 ml and 5 ml of demineralized water were added, and the mixture was allowed to stand overnight. Was removed. The dried product was dried at 200 ° C. under an argon stream for 3 hours. After cooling to room temperature, it was switched from argon to hydrogen and reduced at 350 ° C. for 1.5 hr. After cooling to room temperature, the inside of the firing tube was replaced with argon gas, and then the mixture was passivated with 2% O ₂ -98% N ₂ mixed gas for 1.5 hr and taken out into the air.

  This compound was confirmed by XRD analysis to have an α-WC structure (values of 2θ were 31.499 °, 35.652 °, 48.348 °, 64.511 ° and 65.500 °). Gave a peak). The half width of the peak at 48.348 ° was 1.761 °.

<Creation of anode electrode>
Instead of the α-WC powder used in Example 1, 20 mg of α-WC powder coated with Ru obtained by the above synthesis method and 80 mg of the same carbon black were mixed in a mortar, and 35.3 mg thereof was mixed with 5 mL of ethanol. In the same manner as in Example 1 except that the anode electrode was prepared so that the amount of α-WC supported by the Ru deposited on the electrode was 0.10 mg / cm ^2, and the same evaluation was performed. The results are shown in Table 3.

[Example 18]
<Synthesis of WC-Pd>
1 ml of a catalyst solution prepared by dissolving 0.89 g of PdCl ₂ manufactured by NE Chemcat in 10 ml of demineralized water was added to 0.4 g of WC obtained in Example 1, and the mixture was allowed to stand overnight. Was removed. The dried product was dried at 200 ° C. under an argon stream for 3 hours. After cooling to room temperature, it was switched from argon to hydrogen and reduced at 350 ° C. for 1.5 hr. After cooling to room temperature, the inside of the firing tube was replaced with argon gas, and then the mixture was passivated with 2% O ₂ -98% N ₂ mixed gas for 1.5 hr and taken out into the air.

  This compound was confirmed by XRD analysis to have an α-WC structure (values of 2θ were 31.595 °, 35.895 °, 40.151 ° (Pd), 46.702 ° (Pd). 48.303 °, 65.097 °, 68.202 ° (Pd). The half width of the peak at 48.303 ° was 1.722 °.

<Creation of anode electrode>
In place of the α-WC powder used in Example 1, 90 mg of the same carbon black as 10 mg of α-WC powder coated with Pd obtained by the above synthesis method was mixed in a mortar, and the same as the resulting mixture of 10 mg. 90 mg of carbon black was again mixed in a mortar, 28.3 mg thereof was mixed with 5 mL of ethanol, and the amount of α-WC supported by Pd deposited on the electrode was 0.00 by the same method as in Example 1. An anode electrode was prepared so as to be 01 mg / cm ² , evaluation was performed in the same manner, and the results are shown in Table 3.

[Example 19]
<Synthesis of WC-Pt>
A catalyst solution prepared by dissolving 1.70 g of H ₂ PtCl ₄ manufactured by NE Chemcat in 10 ml of demineralized water was added to 0.4 g of WC obtained in Example 1, 1 ml and 5 ml of demineralized water were added, and the mixture was allowed to stand overnight. To remove water. The dried product was dried at 200 ° C. under an argon stream for 3 hours. After cooling to room temperature, it was switched from argon to hydrogen and reduced at 350 ° C. for 1.5 hr. After cooling to room temperature, the inside of the firing tube was replaced with argon gas, and then the mixture was passivated with 2% O ₂ -98% N ₂ mixed gas for 1.5 hr and taken out into the air.

  This compound was confirmed by XRD analysis to have an α-WC structure (values of 2θ were 31.502 °, 35.750 °, 39.801 ° (Pt), 46.349 ° (Pt). 48.204 °, 65.251 ° and 67.511 ° (Pt). The half width of the 48.204 ° peak was 1.800 °.

<Creation of anode electrode>
Instead of the α-WC powder used in Example 1, 10 mg of α-WC powder coated with Pt obtained by the above synthesis method and 90 mg of the same carbon black were mixed in a mortar, and the same as the resulting mixture of 10 mg. 90 mg of carbon black was again mixed in a mortar, 28.3 mg thereof was mixed with 5 mL of ethanol, and the amount of α-WC supported by Pt deposited on the electrode was 0.00 by the same method as in Example 1. An anode electrode was prepared so as to be 01 mg / cm ² , evaluation was performed in the same manner, and the results are shown in Table 3.

[Example 20]
<Synthesis of WC-Ru>
In place of the α-WC synthesized in Example 1, α-WC synthesized in Example 13 was used, and α-WC coated with Ru was obtained in the same manner as in Example 17.

  This compound was confirmed by XRD analysis to have an α-WC structure (values of 2θ peaked at 31.649 °, 35.600 °, 48.199 °, 63.753 °). . The half width of the peak at 48.199 ° was 1.876 °.

<Creation of anode electrode>
In place of α-WC coated with Ru used in Example 17, α-WC coated with Ru obtained by the above synthesis method was used in the same manner as in Example 17 to the electrode. An anode electrode was prepared so that the amount of α-WC supported to which Ru was deposited was 0.10 mg / cm ² , evaluation was performed in the same manner, and the results are shown in Table 3.

[Example 21]
<Synthesis of WC-Pd>
Α-WC coated with Pd was obtained in the same manner as in Example 18 except that α-WC synthesized in Example 13 was used instead of α-WC synthesized in Example 1.

  This compound was confirmed by XRD analysis to have an α-WC structure (values of 2θ were 31.404 °, 35.449 °, 40.153 ° (Pd), 46.802 ° (Pd)). , 48.250 °, 65.555 °, 68.157 ° (Pd). The half width of the 48.250 ° peak was 2.220 °.

<Creation of anode electrode>
In place of α-WC coated with Pd used in Example 18, α-WC coated with Pd obtained by the above synthesis method was used in the same manner as in Example 18 to the electrode. An anode electrode was prepared so that the amount of α-WC supported by the Pd deposited was 0.01 mg / cm ² , evaluated in the same manner, and the results are shown in Table 3.

[Example 22]
<Synthesis of WC-Pt>
Α-WC coated with Pt was obtained in the same manner as in Example 19 except that α-WC synthesized in Example 13 was used instead of α-WC synthesized in Example 1.

  This compound was confirmed by XRD analysis to have an α-WC structure (values of 2θ were 31.551 °, 35.452 °, 39.899 ° (Pt), 46.400 ° (Pt). 48.150 °, 63.703 °, and 67.555 ° (Pt)). The half width of the peak at 48.150 ° was 2.105 °.

<Creation of anode electrode>
In place of α-WC coated with Pt used in Example 19, α-WC coated with Pt obtained by the above synthesis method was used in the same manner as in Example 19 to the electrode. An anode electrode was prepared so that the amount of α-WC supported to which Pt was deposited was 0.01 mg / cm ² , evaluated in the same manner, and the results are shown in Table 3.

[Example 23]
<Synthesis of WC-Ru>
In place of α-WC synthesized in Example 1, α-WC synthesized in Example 16 was used, except that α-WC coated with Ru was obtained in the same manner as in Example 17.

  This compound was confirmed to have an α-WC structure by XRD analysis (2θ values gave peaks at 31.405 °, 35.548 °, 48.298 °, and 63.906 °). . The half width of the peak at 48.298 ° was 2.105 °.

<Creation of anode electrode>
In place of α-WC coated with Ru used in Example 17, α-WC coated with Ru obtained by the above synthesis method was used in the same manner as in Example 17 to the electrode. An anode electrode was prepared so that the amount of α-WC supported to which Ru was deposited was 0.10 mg / cm ² , evaluation was performed in the same manner, and the results are shown in Table 3.

[Example 24]
<Synthesis of WC-Pt>
Α-WC coated with Pt was obtained in the same manner as in Example 19 except that α-WC synthesized in Example 16 was used instead of α-WC synthesized in Example 1.

  This compound was confirmed to have an α-WC structure by XRD analysis (2θ values gave peaks at 31.405 °, 35.548 °, 48.298 °, and 63.906 °). . The half width of the peak at 48.298 ° was 2.105 °.

<Creation of anode electrode>
In place of α-WC coated with Pt used in Example 19, α-WC coated with Pt obtained by the above synthesis method was used in the same manner as in Example 19 to the electrode. An anode electrode was prepared so that the amount of α-WC supported to which Pt was deposited was 0.01 mg / cm ² , evaluated in the same manner, and the results are shown in Table 3.

[Comparative Example 1]
<Synthesis of WC>
Kishida Chemical Ltd. _WO 3 1.2 g were placed in a quartz calcining _tube, CH 4 / _{H 2} mixed gas (mixing ratio 2/8) 70ml / min. Then, reduction and carbonization were performed at 877 ° C. for 6 hours to obtain an α-WC black powder. After cooling to room temperature, the inside of the firing tube was replaced with argon gas, and then the mixture was passivated with 2% O ₂ -98% N ₂ mixed gas for 1.5 hr and taken out into the air.

  This compound was confirmed to have an α-WC structure by XRD analysis (the values of 2θ peaked at 31.404 °, 35.652 °, 48.254 °, and 64.278 °). . The half width of the peak at 48.254 ° was 0.570 °.

<Creation of anode electrode>
The amount of α-WC supported on the electrode was 0. 0 by the same method as in Example 1 except that the α-WC powder obtained by the above synthesis method was used instead of the α-WC powder used in Example 1. An anode electrode was prepared to 75 mg / cm ² and evaluated in the same manner, and the results are shown in Table 3.

[Comparative Example 2]
The same α-WC powder 135 mg as in Comparative Example 1 and 15 mg of the same carbon black were mixed in a mortar, 47.1 mg thereof was mixed in 5 mL of ethanol, and the α- An anode electrode was prepared so that the amount of WC supported was 0.75 mg / cm ² , evaluation was performed in the same manner, and the results are shown in Table 3.

[Comparative Example 3]
<Synthesis of WC-Ru>
In place of the α-WC synthesized in Example 1, α-WC synthesized in Comparative Example 1 was used, except that α-WC coated with Ru was obtained in the same manner as in Example 17. This compound was confirmed by XRD analysis to have an α-WC structure (values of 2θ were 31.400 °, 35.648 °, 40.111 °, 48.299 °, 63.777 °, Gave a peak at 64.153 °). The half width of the peak at 48.299 ° was 0.624 °.

<Creation of anode electrode>
In place of α-WC coated with Ru used in Example 17, α-WC coated with Ru obtained by the above synthesis method was used in the same manner as in Example 17 to the electrode. An anode electrode was prepared so that the amount of α-WC supported to which Ru was deposited was 0.10 mg / cm ² , evaluation was performed in the same manner, and the results are shown in Table 3.

[Comparative Example 4]
<Synthesis of WC-Pd>
Α-WC coated with Pd was obtained in the same manner as in Example 18 except that α-WC synthesized in Comparative Example 1 was used instead of α-WC synthesized in Example 1. This compound was confirmed by XRD analysis to have an α-WC structure (values of 2θ were 31.400 °, 35.649 °, 40.305 ° (Pd), 46.608 ° (Pd)). 48.254 °, 58.349 °, 64.297 °, 65.393 ° and 68.376 ° (Pd)). The half width of the 48.254 ° peak was 0.562 °.

<Creation of anode electrode>
In place of α-WC coated with Pd used in Example 18, α-WC coated with Pd obtained by the above synthesis method was used in the same manner as in Example 18 to the electrode. An anode electrode was prepared so that the amount of α-WC supported by the Pd deposited was 0.01 mg / cm ² , evaluated in the same manner, and the results are shown in Table 3.

[Comparative Example 5]
<Synthesis of WC-Pt>
Α-WC coated with Pt was obtained in the same manner as in Example 19 except that α-WC synthesized in Comparative Example 1 was used instead of α-WC synthesized in Example 1. This compound was confirmed by XRD analysis to have an α-WC structure (values of 2θ were 31.401 °, 35.605 °, 39.800 ° (Pt), 40.342 °, 46. 253 ° (Pt), 48.254 °, 58.311 °, 64.350 ° and 67.690 ° (Pt). The half width of the 48.254 ° peak was 0.566 °.

<Creation of anode electrode>
In place of α-WC coated with Pt used in Example 19, α-WC coated with Pt obtained by the above synthesis method was used in the same manner as in Example 19 to the electrode. An anode electrode was prepared so that the amount of α-WC supported to which Pt was deposited was 0.01 mg / cm ² , evaluated in the same manner, and the results are shown in Table 3.

As is clear from Tables 2 and 3, among the examples, Examples 1 to 6, 8, 14, and 15 synthesized via W ₂ N were synthesized via WC and WS _2. The WCs of Examples 7, 9 to 13 and 16 have a wider half-value width of the peak of 48.186 ° to 48.498 ° than the WCs of Comparative Examples 1 and 2 synthesized from WO ₃ , and clearly High catalytic activity. In addition, the half width of WC of Example 17 in which Ru is further supported on a WC synthesized from W ₂ N, and Examples 20 and 23 in which Ru is further supported on a WC synthesized from WS ₂ are the same as those of WC synthesized from WO ₃ It is wider than the half width of WC of Comparative Example 3 supporting Ru, and the catalytic activity is also clearly improved. Further, Examples 18 and 19 in which Pd or Pt is further supported on a WC synthesized from W ₂ N, respectively, and WC half widths in Examples 21 and 22, and 24 in which Pd or Pt is further supported on a WC synthesized from WS ₂ respectively. The value is wider than the half width value of WC of Comparative Examples 4 and 5 in which Pd or Pt is supported on WC synthesized from WO ₃ , and the catalytic activity is also clearly improved.

From Examples 1 to 24, it can be seen that according to the fuel cell catalyst of the present invention using WC that satisfies a specific XRD condition synthesized via W ₂ N, WS _{2 and the} like, high catalytic activity can be obtained. .

Furthermore, from Examples 17 to 24, it can be seen that the catalytic activity can be further enhanced by using other catalyst components such as Ru, Pd or Pt in combination.
By comparing Example 1 and Example 3, it can be seen that the activity is improved when reduction treatment is performed by heating in a hydrogen gas stream. Moreover, by comparing Example 3 and Example 4, it can be seen that the activity is further improved by contacting with an aqueous NaOH solution in addition to the reduction treatment.
By comparing Example 1 and Example 8, the WC prepared using the raw material compound WO ₃ having a particle size of about 50 nm is more WC than the WC prepared using the raw material compound WO ₃ having a particle size of about 250 nm. It can be seen that the activity is high.

  According to the present invention, since a fuel cell using an inexpensive fuel cell catalyst is provided, the expansion and practical use of fuel cells such as fuel vehicles are promoted.

Claims (9)

The half-width of the maximum diffraction peak in the region where the diffraction angle 2θ (± 0.3 °) by X-ray diffraction method (Cu-K _α- ray) is 40 ° or more and 60 ° or less is 1.0 ° or more and 16.5 °. A fuel cell catalyst containing tungsten carbide , which is:
The tungsten carbide is obtained by converting a compound selected from the group consisting of tungsten nitride and tungsten sulfide into tungsten carbide . 2. The fuel cell catalyst according to claim 1 , wherein the tungsten carbide is deposited on a substrate. The fuel cell catalyst according to claim 1 or 2 , wherein the tungsten carbide has an average particle size of 0.1 nm or more and 1000 nm or less. In the catalyst for a fuel cell according to claim 2 or 3, the catalyst for a fuel cell which said substrate is characterized in that it is a carbon-based substrate. 5. The fuel cell catalyst according to claim 4 , wherein the carbon-based substrate has a specific surface area of 200 m ² / g or more and 5000 m ² / g or less. The fuel cell catalyst according to any one of claims 1 to 5 , further comprising at least one selected from the group consisting of a transition metal and a transition metal compound other than tungsten carbide. Battery catalyst. A fuel cell electrode comprising the fuel cell catalyst according to any one of claims 1 to 6 . A fuel cell using the fuel cell electrode according to claim 7 . A method for producing a catalyst for a fuel cell containing tungsten carbide as claimed in any one of claims 1 to 6, nitriding tungsten, and a compound selected from sulfide tungsten emissions or Ranaru group, the carbon-based substrate A method for producing a catalyst for a fuel cell, wherein the catalyst is converted into tungsten carbide by contacting with hydrocarbon or hydrocarbon and hydrogen in the presence or absence.