WO2009107518A1 - 触媒およびその製造方法ならびにその用途 - Google Patents
触媒およびその製造方法ならびにその用途 Download PDFInfo
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- WO2009107518A1 WO2009107518A1 PCT/JP2009/052696 JP2009052696W WO2009107518A1 WO 2009107518 A1 WO2009107518 A1 WO 2009107518A1 JP 2009052696 W JP2009052696 W JP 2009052696W WO 2009107518 A1 WO2009107518 A1 WO 2009107518A1
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- catalyst
- fuel cell
- titanium
- oxygen
- titanium carbonitride
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- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
- H01M4/00—Electrodes
- H01M4/86—Inert electrodes with catalytic activity, e.g. for fuel cells
- H01M4/90—Selection of catalytic material
- H01M4/9016—Oxides, hydroxides or oxygenated metallic salts
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J21/00—Catalysts comprising the elements, oxides, or hydroxides of magnesium, boron, aluminium, carbon, silicon, titanium, zirconium, or hafnium
- B01J21/06—Silicon, titanium, zirconium or hafnium; Oxides or hydroxides thereof
- B01J21/063—Titanium; Oxides or hydroxides thereof
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J27/00—Catalysts comprising the elements or compounds of halogens, sulfur, selenium, tellurium, phosphorus or nitrogen; Catalysts comprising carbon compounds
- B01J27/24—Nitrogen compounds
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- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
- H01M8/00—Fuel cells; Manufacture thereof
- H01M8/10—Fuel cells with solid electrolytes
- H01M2008/1095—Fuel cells with polymeric electrolytes
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- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02E—REDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
- Y02E60/00—Enabling technologies; Technologies with a potential or indirect contribution to GHG emissions mitigation
- Y02E60/30—Hydrogen technology
- Y02E60/50—Fuel cells
Definitions
- the present invention relates to a catalyst, a production method thereof, and an application thereof.
- Fuel cells are classified into various types according to the type of electrolyte and the type of electrode, and representative types include alkali type, phosphoric acid type, molten carbonate type, solid electrolyte type, and solid polymer type.
- a polymer electrolyte fuel cell that can operate at a low temperature (about ⁇ 40 ° C.) to about 120 ° C. attracts attention, and in recent years, development and practical application as a low-pollution power source for automobiles is progressing.
- a use of the polymer electrolyte fuel cell a vehicle driving source and a stationary power source are being studied. However, in order to be applied to these uses, durability over a long period of time is required.
- a polymer solid electrolyte is sandwiched between an anode and a cathode, fuel is supplied to the anode, oxygen or air is supplied to the cathode, and oxygen is reduced at the cathode to extract electricity.
- Hydrogen or methanol is mainly used as the fuel.
- the fuel cell cathode (air electrode) surface or anode (fuel electrode) surface has a layer containing a catalyst (hereinafter referred to as “for fuel cell”). Also referred to as “catalyst layer”).
- the noble metal used on the cathode surface may be dissolved in an acidic atmosphere, and there is a problem that it is not suitable for applications that require long-term durability. Therefore, there has been a strong demand for the development of a catalyst that does not corrode in an acidic atmosphere, has excellent durability, and has a high oxygen reducing ability.
- Non-Patent Document 1 reports that a ZrOxN compound based on zirconium exhibits oxygen reducing ability.
- Patent Document 1 discloses an oxygen reduction electrode material containing one or more nitrides selected from the group of elements of Group 4, Group 5, and Group 14 of the long periodic table as a platinum substitute material.
- Patent Document 2 discloses that a partially oxidized compound of any one of titanium, lanthanum, tantalum, niobium, and zirconium and any of nitrogen, boron, carbon, or sulfur is used as an electrode catalyst for a fuel cell. ing.
- Patent Document 3 discloses using titanium carbonitride powder as an oxygen electrode catalyst for a polymer electrolyte fuel cell.
- non-metal-containing materials are unstable in an acidic solution or have not obtained a sufficient oxygen reducing ability for practical use as a catalyst, and are not sufficiently active for actual use as a fuel cell. It is.
- Patent Document 4 discloses a carbonitride oxide obtained by mixing carbide, oxide, and nitride and heat-treating them at 500 to 1500 ° C. in a vacuum, inert or non-oxidizing atmosphere.
- Patent Document 4 is a thin film magnetic head ceramic substrate material, and the use of this carbonitrous oxide as a catalyst has not been studied.
- An object of the present invention is to solve such problems in the prior art, and an object of the present invention is to provide a catalyst that does not corrode in an acidic electrolyte or at a high potential, has excellent durability, and has a high oxygen reduction ability. There is.
- a catalyst made of a specific titanium carbonitride oxide does not corrode in an acidic electrolyte or at a high potential, and has excellent durability. It has been found that it has a high oxygen reducing ability.
- the present inventors have found that a catalyst with higher performance can be obtained by controlling the ratio of the number of atoms in titanium carbonitride oxide constituting the catalyst, and have completed the present invention. .
- the present invention relates to the following (1) to (13), for example.
- the composition formula of the titanium oxycarbonitride is TiC x N y O z (where x, y, z represent the ratio of the number of atoms, 0 ⁇ x ⁇ 1.0, 0 ⁇ y ⁇ 1.0, 0.1 ⁇ z ⁇ 2.0, 1.0 ⁇ x + y + z ⁇ 2.0, and 2.0 ⁇ 4x + 3y + 2z.)
- the catalyst according to (1) is TiC x N y O z (where x, y, z represent the ratio of the number of atoms, 0 ⁇ x ⁇ 1.0, 0 ⁇ y ⁇ 1.0, 0.1 ⁇ z ⁇ 2.0, 1.0 ⁇ x + y + z ⁇ 2.0, and 2.0 ⁇ 4x + 3y + 2z.)
- oxygen gas concentration in the inert gas in the step is in the range of 0.1 to 10% by volume.
- a catalyst layer for a fuel cell comprising the catalyst according to any one of (3).
- a membrane electrode assembly having a cathode, an anode, and an electrolyte membrane disposed between the cathode and the anode, wherein the cathode and / or the anode is an electrode according to (10) Membrane electrode assembly.
- a polymer electrolyte fuel cell comprising the membrane electrode assembly according to (11).
- the catalyst of the present invention does not corrode in an acidic electrolyte or at a high potential, is stable, has a high oxygen reducing ability, and is less expensive than platinum. Therefore, the fuel cell including the catalyst is relatively inexpensive and has excellent performance.
- FIG. 2 is a powder X-ray diffraction spectrum of titanium carbonitride of Example 1.
- FIG. 2 is a powder X-ray diffraction spectrum of the catalyst (1) obtained in Example 1. It is the graph which evaluated the oxygen reduction ability of the electrode using a catalyst (1).
- 2 is a powder X-ray diffraction spectrum of the catalyst (2) obtained in Example 2. It is the graph which evaluated the oxygen reduction ability of the electrode using a catalyst (2). It is the graph which evaluated the oxygen reduction ability of the electrode using a catalyst (3).
- 3 is a powder X-ray diffraction spectrum of the catalyst (3) obtained in Example 3. It is an electric current-potential curve of an electrode using a catalyst (4). It is the graph which evaluated the oxygen reduction ability of the electrode using a catalyst (4).
- 3 is a powder X-ray diffraction spectrum of a catalyst (5) obtained in Comparative Example 2. It is the graph which evaluated the oxygen reduction ability of the electrode using a catalyst (5).
- the catalyst of the present invention is characterized by comprising a titanium carbonitride.
- the composition formula of the titanium oxycarbonitride is TiC x N y O z (where x, y, and z represent the ratio of the number of atoms, 0 ⁇ x ⁇ 1.0, 0 ⁇ y ⁇ 1. 0, 0.1 ⁇ z ⁇ 2.0, 1.0 ⁇ x + y + z ⁇ 2.0, and 2.0 ⁇ 4x + 3y + 2z).
- x, y, and z represent the number of C, N, and O atoms when the number of Ti atoms is 1, respectively.
- x + y + z is an index representing a crystal system of a compound of Ti and C, N, and O. If TiC x N y O z is a cubic crystal, x + y + z is a value of 1.0 or less and a value close to 1.0. However, TiC x N y O z Oite, x + y + z to be used in the present invention is 1.0 greater than.
- TiC x N y O z is a mixed system of cubic TiC x N y and tetragonal TiO 2 .
- the value of x + y + z varies depending on the ratio between TiC x N y and TiO 2 .
- the TiC x N y O z used in the present invention has been confirmed to have a rutile structure from the results of analysis by X-ray diffraction. However, it is presumed that a part of O in the crystal lattice is substituted with C and N and further has a rutile structure having lattice defects. In general, titanium oxide having a rutile structure which does not contain C and N hardly shows oxygen reduction activity. The present inventors presume the reason why TiC x N y O z has the above structure as follows.
- TiC is cubic and TiN is also cubic. Since C is tetravalent and N is trivalent, TiC x N y results in a slightly distorted cubic crystal. When this distorted form of TiC x N y is gently oxidized, a plurality of Os are substituted in or around the voids where a part of N or C is removed in TiC x N y , and TiC having a rutile structure with lattice defects. x N y O z is formed. As a result, it is considered that the formed rutile structure TiC x N y O z has an increased unpaired electron density and a high oxygen reducing ability.
- titanium carbonitride When titanium carbonitride is oxidized, an appropriate time, an appropriate temperature, and an appropriate oxygen concentration are required. Even if the time is too long or the temperature is too high, the oxidation proceeds too much, and the catalytic ability is lowered. That is, when oxidizing, a mild oxidation state is required, and a mild oxidation state can be easily achieved by introducing a reducing gas such as hydrogen gas. For example, just mixing TiC x N y and TiO 2 with little distortion does not have a high oxygen reducing ability.
- the oxygen reduction starting potential of the catalyst used in the present invention is preferably 0.7 V (vs. NHE) or more based on the reversible hydrogen electrode.
- the obtained electrode refer to a reversible hydrogen electrode in a sulfuric acid solution of the same concentration at a temperature of 30 ° C. in a 0.5 mol / dm 3 sulfuric acid solution in an oxygen atmosphere and a nitrogen atmosphere.
- the current-potential curve was measured by polarizing the electrode at a potential scanning speed of 5 mV / sec, there was a difference of 0.2 ⁇ A / cm 2 or more between the reduction current in the oxygen atmosphere and the reduction current in the nitrogen atmosphere.
- the potential at which it begins to appear is defined as the oxygen reduction start potential.
- the oxygen reduction starting potential is less than 0.7 V (vs.
- the oxygen reduction starting potential is preferably 0.85 V (vs. NHE) or more in order to suitably reduce oxygen.
- the upper limit of the oxygen reduction start potential is the theoretical value of 1.23 V (vs. NHE).
- the fuel cell catalyst layer of the present invention formed using the above catalyst is preferably used at a potential of 0.4 V (vs. NHE) or more in the acidic electrolyte, and the upper limit of the potential depends on the stability of the electrode. It can be used up to approximately 1.53 (vs. NHE) of the potential at which oxygen is generated.
- the current flow when using the catalyst of the present invention is evaluated by the oxygen reduction current density (mA / cm 2 ) when the potential measured according to the measurement method (A) is 0.7 V. Can do.
- the oxygen reduction current density is preferably 0.1 (mA / cm 2 ) or more, and more preferably 0.5 (mA / cm 2 ) or more. When the oxygen reduction current density is less than 0.1 (mA / cm 2 ), the current does not flow so much and its usefulness as a fuel cell catalyst layer is poor.
- the manufacturing method of the said catalyst is not specifically limited, For example, the manufacturing method including the process of obtaining the carbonitrous oxide of titanium by heat-processing titanium carbonitride in the inert gas containing oxygen and hydrogen is mentioned. .
- a method for producing titanium carbonitride by heat-treating a mixture of titanium oxide and carbon in a nitrogen atmosphere, titanium carbide, titanium oxide, and Method (II) for producing titanium carbonitride by heat-treating a mixture of titanium nitride in a nitrogen atmosphere or the like, and producing titanium carbonitride by heat-treating a mixture of titanium carbide and titanium nitride in a nitrogen atmosphere or the like A method (III) is mentioned.
- Production method (I) is a method of producing titanium carbonitride by heat-treating a mixture of titanium oxide and carbon in a nitrogen atmosphere.
- the temperature of the heat treatment for producing titanium carbonitride is usually in the range of 600 to 1800 ° C, preferably in the range of 900 to 1600 ° C.
- the heat treatment temperature is within the above range, it is preferable in terms of good crystallinity and uniformity. If the heat treatment temperature is less than 600 ° C., the crystallinity tends to be poor and the uniformity tends to deteriorate, and if it is 1800 ° C. or more, it tends to be easy to sinter.
- the raw material titanium oxide examples include TiO, TiO 2 and Ti 2 O 3 .
- titanium carbonitride obtained from the oxide is composed of titanium carbonitride obtained by heat treatment in an inert gas containing oxygen gas and hydrogen gas.
- the catalyst has a high oxygen reduction initiation potential and is active.
- the raw material carbon examples include carbon, carbon black, graphite, graphite, activated carbon, carbon nanotube, carbon nanofiber, carbon nanohorn, and fullerene. It is preferable that the particle size of the carbon powder is smaller because the specific surface area is increased and the reaction with the oxide is facilitated.
- carbon black specific surface area: 100 to 300 m 2 / g, such as XC-72 manufactured by Cabot is preferably used.
- titanium carbonitride can be obtained by stoichiometrically controlling the molar ratio of the oxide of titanium and carbon in accordance with the valence of titanium such as 2, 3 or 4 valences.
- the valence of titanium such as 2, 3 or 4 valences.
- 1 to 3 moles of carbon are preferable with respect to 1 mole of titanium oxide.
- 2 to 4 moles of carbon are preferable with respect to 1 mole of titanium oxide. If the upper limit of these ranges is exceeded, titanium carbide tends to be produced, and if the lower limit is not reached, more titanium nitride tends to be produced.
- a divalent titanium oxide 2 to 3 moles of carbon are preferred with respect to 1 mole of titanium oxide.
- 3 to 4 moles of carbon are preferable with respect to 1 mole of titanium oxide.
- Production method (II) is a method of producing titanium carbonitride by heat-treating a mixture of titanium carbide, titanium oxide and titanium nitride in a nitrogen atmosphere or the like.
- the temperature of the heat treatment for producing titanium carbonitride is usually in the range of 600 to 1800 ° C., preferably in the range of 800 to 1600 ° C. When the heat treatment temperature is within the above range, it is preferable in terms of good crystallinity and uniformity. If the heat treatment temperature is less than 600 ° C., the crystallinity tends to be poor and the uniformity tends to deteriorate, and if it is 1800 ° C. or more, it tends to be easy to sinter.
- titanium carbide (TiC), titanium nitride (TiN) and titanium oxide are used as raw materials.
- the raw material titanium oxide examples include TiO, TiO 2 and Ti 2 O 3 . Regardless of which titanium oxide is used, the titanium carbonitride obtained from the oxide, titanium carbide and titanium nitride is heat-treated in an inert gas containing oxygen gas and hydrogen gas. A catalyst made of oxycarbonitride has high oxygen reduction starting potential and is active.
- titanium carbide (TiC), titanium oxide, and titanium nitride (TiN) By controlling the amount (molar ratio) of titanium carbide (TiC), titanium oxide, and titanium nitride (TiN), an appropriate titanium carbonitride can be obtained.
- the blending amount (molar ratio) is usually 0.1 to 500 mol of titanium carbide (TiC) and 0.01 to 50 mol of titanium oxide, preferably 1 mol of titanium nitride (TiN), preferably
- the amount of titanium carbide (TiC) is 1 to 300 mol and the amount of titanium oxide is 0.1 to 30 mol with respect to 1 mol of titanium nitride (TiN).
- titanium carbonitride made at a blending molar ratio satisfying the above range there is a tendency that an oxygen reduction starting potential is high and an active titanium carbonitride oxide is obtained. More preferable amounts (molar ratio) are 10 to 300 mol of titanium carbide and 0.1 to 10 mol of titanium oxide with respect to 1 mol of titanium nitride.
- the ratio of the number of atoms (x, y, z) and titanium carbonitride oxide (TiC x N y O z ) where x + y + z satisfies the above range are used. It is easy to obtain.
- Production method (III) is a method of producing titanium carbonitride by heat-treating a mixture of titanium carbide and titanium nitride in a nitrogen atmosphere or the like.
- the temperature of the heat treatment for producing titanium carbonitride is in the range of 600 to 1800 ° C., preferably in the range of 800 to 1600 ° C.
- the heat treatment temperature is within the above range, it is preferable in terms of good crystallinity and uniformity. If the heat treatment temperature is less than 600 ° C., the crystallinity tends to be poor and the uniformity tends to deteriorate, and if it is 1800 ° C. or more, it tends to be easy to sinter.
- Titanium carbide (TiC) and titanium nitride (TiN) are used as raw materials. By controlling the blending amount (molar ratio) of titanium carbide and titanium nitride, appropriate titanium carbonitride is obtained.
- the blending amount (molar ratio) is usually in the range of 0.01 to 10 moles of titanium nitride (TiN) with respect to 1 mole of titanium carbide (TiC), and preferably with respect to 1 mole of titanium carbide (TiC). Titanium nitride (TiN) is in the range of 0.1 to 10 mol.
- titanium carbonitride obtained at a blending ratio that satisfies the above range When using titanium carbonitride obtained at a blending ratio that satisfies the above range, the ratio of the number of atoms (x, y, z) and titanium carbonitride oxide (TiC x N y O z ) where x + y + z satisfies the above range It is easy to obtain.
- Such a catalyst made of titanium carbonitride (TiC x N y O z ) has a high oxygen reduction starting potential and high activity.
- the inert gas includes helium gas, neon gas, argon gas, krypton gas, xenon gas, radon gas, or nitrogen gas.
- Argon gas, helium gas or nitrogen gas is particularly preferable because it is relatively easy to obtain.
- the oxygen gas concentration in the step depends on the heat treatment time and the heat treatment temperature, but is preferably 0.1 to 10% by volume, particularly preferably 0.5 to 5% by volume.
- the oxygen gas concentration is within the above range, it is preferable in that a uniform carbonitride oxide is formed. Further, when the oxygen gas concentration is less than 0.1% by volume, it tends to be in an unoxidized state, and when it exceeds 10% by volume, oxidation tends to proceed excessively.
- titanium carbonitride obtained by heat-treating titanium carbonitride in an inert gas containing not only oxygen gas but also hydrogen gas has improved electrical conductivity and higher oxygen reducing ability. it can.
- the hydrogen gas concentration is not particularly limited, but is preferably about twice the oxygen gas concentration in the inert gas. That is, since oxygen is 0.1% to 10% by volume, the amount of hydrogen is preferably 0.2% to 20% by volume. However, if the oxygen gas concentration and the hydrogen gas concentration are too high, there is a risk of explosion, so oxygen gas is more preferably 0.5 volume% to 3 volume%, and hydrogen gas is 1 volume% to 6 volume%.
- the temperature of the heat treatment in this step is usually in the range of 400 to 1400 ° C., preferably in the range of 600 to 1200 ° C. When the heat treatment temperature is within the above range, it is preferable in that a uniform carbonitride oxide is formed. When the heat treatment temperature is less than 400 ° C., the oxidation tends not to proceed, and when it is 1400 ° C. or more, the oxidation proceeds too much and grain growth tends to occur.
- Examples of the heat treatment method in the process include a stationary method, a stirring method, a dropping method, and a powder trapping method.
- the furnace is heated to a predetermined heat treatment temperature while flowing an inert gas containing a small amount of oxygen gas and hydrogen gas in the induction furnace, and after maintaining the thermal equilibrium at the temperature, the furnace is heated.
- titanium carbonitride is dropped in a crucible serving as an area and heat treated.
- the dropping method is preferable in that aggregation and growth of titanium carbonitride particles can be suppressed to a minimum.
- the powder trapping method means that titanium carbonitride is suspended in a vertical tube furnace that is kept in a prescribed heat treatment temperature by suspending titanium carbonitride in the inert gas atmosphere containing a small amount of oxygen gas and hydrogen gas. This is a method of trapping and heat-treating.
- the heat treatment time of titanium carbonitride is usually 0.5 to 10 minutes, preferably 0.5 to 3 minutes.
- the heat treatment time is within the above range, a uniform oxycarbonitride tends to be formed, which is preferable. If the heat treatment time is less than 0.5 minutes, oxycarbonitride tends to be partially formed, and if it exceeds 10 minutes, oxidation tends to proceed excessively.
- the heat treatment time of titanium carbonitride is 0.2 second to 1 minute, preferably 0.2 to 10 seconds.
- the heat treatment time is within the above range, a uniform oxycarbonitride tends to be formed, which is preferable.
- the heat treatment time is less than 0.2 seconds, oxycarbonitride tends to be partially formed, and when it exceeds 1 minute, oxidation tends to proceed excessively.
- the heat treatment time of titanium carbonitride is 0.1 to 20 hours, preferably 0.5 to 10 hours.
- the heat treatment time is within the above range, a uniform oxycarbonitride tends to be formed, which is preferable. If the heat treatment time is less than 0.1 hour, oxycarbonitride tends to be partially formed, and if it exceeds 20 hours, oxidation tends to proceed excessively.
- the titanium oxycarbonitride obtained by the above-described production method or the like may be used as it is, but the obtained titanium oxycarbonitride is further pulverized into a finer powder. A thing may be used.
- Examples of the method for crushing titanium carbonitride oxide include a roll rolling mill, a ball mill, a medium agitation mill, an airflow grinder, a mortar, a tank disintegrator, and the like.
- a method using an airflow pulverizer is preferable in that it can be made finer, and a method using a mortar is preferable in that a small amount of processing is easy.
- the catalyst of the present invention can be used as an alternative catalyst for a platinum catalyst.
- it can be used as a fuel cell catalyst, exhaust gas treatment catalyst or organic synthesis catalyst.
- the fuel cell catalyst layer of the present invention is characterized by containing the catalyst.
- the fuel cell catalyst layer includes an anode catalyst layer and a cathode catalyst layer, and the catalyst can be used for both. Since the catalyst is excellent in durability and has a large oxygen reducing ability, it is preferably used in the cathode catalyst layer.
- the fuel cell catalyst layer of the present invention preferably further contains electron conductive particles.
- the reduction current can be further increased.
- the electron conductive particles are considered to increase the reduction current because they generate an electrical contact for inducing an electrochemical reaction in the catalyst.
- the electron conductive particles are usually used as a catalyst carrier.
- the material constituting the electron conductive particles examples include carbon, conductive polymers, conductive ceramics, metals, and conductive inorganic oxides such as tungsten oxide or iridium oxide, which can be used alone or in combination. .
- carbon particles having a large specific surface area alone or a mixture of carbon particles having a large specific surface area and other electron conductive particles are preferable. That is, the fuel cell catalyst layer preferably includes the catalyst and carbon particles having a large specific surface area.
- carbon carbon black, graphite, graphite, activated carbon, carbon nanotube, carbon nanofiber, carbon nanohorn, fullerene and the like can be used. If the particle size of the carbon is too small, it becomes difficult to form an electron conduction path, and if it is too large, the gas diffusibility of the catalyst layer for the fuel cell tends to be reduced or the utilization factor of the catalyst tends to be reduced. A range of 1000 nm is preferable, and a range of 10 to 100 nm is more preferable.
- the mass ratio of the catalyst to carbon is preferably 4: 1 to 1000: 1.
- the conductive polymer is not particularly limited.
- polypyrrole, polyaniline, and polythiophene are preferable, and polypyrrole is more preferable.
- the polymer electrolyte is not particularly limited as long as it is generally used in a fuel cell catalyst layer.
- a perfluorocarbon polymer having a sulfonic acid group for example, Nafion (DuPont 5% Nafion solution (DE521))
- a hydrocarbon polymer compound having a sulfonic acid group for example, an inorganic acid such as phosphoric acid.
- Nafion DuPont 5% Nafion solution (DE521)
- DE521 Nafion (DuPont 5% Nafion solution
- the fuel cell catalyst layer of the present invention can be used for either an anode catalyst layer or a cathode catalyst layer.
- the catalyst layer for a fuel cell of the present invention includes a catalyst layer (catalyst catalyst for cathode) provided on the cathode of a fuel cell because it contains a catalyst having high oxygen reducing ability and hardly corroded even in a high potential in an acidic electrolyte. Layer).
- a catalyst layer provided on the cathode of a membrane electrode assembly provided in a polymer electrolyte fuel cell.
- Examples of the method for dispersing the catalyst on the electron conductive particles as a support include air flow dispersion and dispersion in liquid. Dispersion in liquid is preferable because a catalyst and electron conductive particles dispersed in a solvent can be used in the fuel cell catalyst layer forming step. Examples of the dispersion in the liquid include a method using an orifice contraction flow, a method using a rotating shear flow, and a method using an ultrasonic wave.
- the solvent used for dispersion in the liquid is not particularly limited as long as it does not erode the catalyst or electron conductive particles and can be dispersed, but a volatile liquid organic solvent or water is generally used.
- the electrolyte and the dispersant may be further dispersed at the same time.
- the method for forming the catalyst layer for the fuel cell is not particularly limited. For example, a method of applying a suspension containing the catalyst, the electron conductive particles, and the electrolyte to the electrolyte membrane or the gas diffusion layer to be described later. It is done. Examples of the application method include a dipping method, a screen printing method, a roll coating method, and a spray method. In addition, after forming a catalyst layer for a fuel cell on a base material by a coating method or a filtration method using a suspension containing the catalyst, electron conductive particles, and an electrolyte, the catalyst layer for a fuel cell is formed on the electrolyte membrane by a transfer method. The method of forming is mentioned.
- the electrode of the present invention is characterized by having the fuel cell catalyst layer and a porous support layer.
- the electrode of the present invention can be used as either a cathode or an anode. Since the electrode of the present invention is excellent in durability and has a large catalytic ability, it is more effective when used for a cathode.
- a fuel cell is formed by providing a gas diffusion layer between a current collector outside an anode and a cathode electrode sandwiched between solid electrolytes (membrane electrode assembly) and an electrode catalyst.
- a device for improving the efficiency of the fuel cell by increasing the diffusibility of the oxidizing gas is made.
- a carbon-based porous material such as carbon paper or carbon cloth, or an aluminum foil coated with stainless steel or a corrosion-resistant material for weight reduction is used for the gas diffusion layer.
- the membrane electrode assembly of the present invention is a membrane electrode assembly having a cathode, an anode, and an electrolyte membrane disposed between the cathode and the anode, wherein the cathode and / or the anode is the electrode. It is characterized by that.
- an electrolyte membrane using a perfluorosulfonic acid system or a hydrocarbon electrolyte membrane is generally used.
- a membrane or porous body in which a polymer microporous membrane is impregnated with a liquid electrolyte is impregnated with a liquid electrolyte.
- a membrane filled with a polymer electrolyte may be used.
- the fuel cell of the present invention is characterized by comprising the membrane electrode assembly.
- Fuel cell electrode reactions occur at the so-called three-phase interface (electrolyte-electrode catalyst-reaction gas).
- Fuel cells are classified into several types depending on the electrolyte used, etc., and include molten carbonate type (MCFC), phosphoric acid type (PAFC), solid oxide type (SOFC), and solid polymer type (PEFC).
- MCFC molten carbonate type
- PAFC phosphoric acid type
- SOFC solid oxide type
- PEFC solid polymer type
- the catalyst of the present invention can be used as an alternative to platinum, it can be used regardless of the type of fuel cell. Among them, the effect is even greater when used in a polymer electrolyte fuel cell.
- Powder X-ray diffraction Samples were subjected to powder X-ray diffraction using a rotor flex made by Rigaku Corporation.
- Nitrogen / oxygen About 0.1 g of a sample was weighed and sealed in Ni-Cup, and then measured with an ON analyzer.
- Titanium About 0.1 g of a sample was weighed on a platinum dish, and nitric acid-hydrofluoric acid was added for thermal decomposition. This thermally decomposed product was fixed, diluted, and quantified by ICP-MS.
- Example 1 Preparation of catalyst 5.10 g (85 mmol) of titanium carbide (TiC), 0.80 g (10 mmol) of titanium oxide (TiO 2 ), and 0.31 g (5 mmol) of titanium nitride (TiN) were mixed well at 1800 ° C. for 3 hours. By heating in a nitrogen atmosphere, 5.73 g of titanium carbonitride was obtained. In order to become a sintered body, the obtained titanium carbonitride was pulverized with an automatic mortar.
- TiC titanium carbide
- TiO 2 titanium oxide
- TiN titanium nitride
- Table 1 shows the elemental analysis results of the obtained titanium carbonitride.
- Titanium carbonitride oxidation was performed by heating 298 mg of the obtained titanium carbonitride in a tubular furnace at 1000 ° C. for 10 hours while flowing nitrogen gas containing 1 vol% oxygen gas and 4 vol% hydrogen gas. 393 mg of a product (hereinafter also referred to as “catalyst (1)”) was obtained.
- Table 1 shows the results of elemental analysis of the catalyst (1).
- Nafion DuPont 5% Nafion solution (DE521)
- the prepared fuel cell electrode (1) was polarized in an oxygen atmosphere and a nitrogen atmosphere in a 0.5 mol / dm 3 sulfuric acid solution at 30 ° C. and a potential scanning rate of 5 mV / sec, and a current-potential curve was obtained. It was measured. At that time, a reversible hydrogen electrode in a sulfuric acid solution having the same concentration was used as a reference electrode.
- the potential at which a difference of 0.2 ⁇ A / cm 2 or more appears between the reduction current in the oxygen atmosphere and the reduction current in the nitrogen atmosphere was defined as the oxygen reduction start potential, and the difference between the two was defined as the oxygen reduction current.
- the catalytic ability (oxygen reducing ability) of the fuel cell electrode (1) produced by this oxygen reduction starting potential and oxygen reducing current was evaluated.
- FIG. 3 shows the results of examining the oxygen reducing ability of the electrode using the catalyst (1).
- the oxygen reduction starting potential of this electrode was 0.85 V (vs. NHE), and it was found to have a high oxygen reducing ability.
- Example 2 Catalyst Preparation 314 mg of titanium carbonitride obtained in Example 1 was heated at 1000 ° C. for 3 hours in a tubular furnace while flowing nitrogen gas containing 1.5 vol% oxygen gas and 4 vol% hydrogen gas. As a result, 411 mg of titanium carbonitride (hereinafter also referred to as “catalyst (2)”) was obtained.
- Table 1 shows the results of elemental analysis of the catalyst (2).
- a fuel cell electrode (2) was obtained in the same manner as in Example 1 except that the catalyst (2) was used.
- FIG. 5 shows a current-potential curve obtained by the measurement.
- Example 2 It was found that the fuel cell electrode (2) produced in Example 2 had an oxygen reduction starting potential of 0.83 V (vs. NHE) and high oxygen reducing ability.
- Example 3 Preparation of Catalyst 314 mg of titanium carbonitride obtained in Example 1 was passed through a tubular furnace at 1000 ° C. for 3 hours while flowing nitrogen gas containing 1.0 vol% oxygen gas and 1.3 vol% hydrogen gas. By heating, 415 mg of titanium carbonitride (hereinafter also referred to as “catalyst (3)”) was obtained.
- FIG. 7 shows a powder X-ray diffraction spectrum of the obtained catalyst (3).
- Table 1 shows the elemental analysis results of the catalyst (3).
- a fuel cell electrode (3) was obtained in the same manner as in Example 1 except that the catalyst (3) was used.
- FIG. 6 shows a current-potential curve obtained by the measurement.
- Example 3 It was found that the fuel cell electrode (3) produced in Example 3 had an oxygen reduction starting potential of 0.90 V (vs. NHE) and high oxygen reducing ability.
- a fuel cell electrode (4) was obtained in the same manner as in Example 1 except that the catalyst (4) was used.
- FIG. 9 shows a current-potential curve obtained by the measurement.
- the electrode for fuel cell (4) produced in Comparative Example 1 had an oxygen reduction starting potential of 0.6 V (vs. NHE).
- FIG. 8 shows the current-potential curve in FIG. 9, and after leaving for several hours at the open potential, sweeps to 0.05 V in the reduction direction, turns back and sweeps in the oxidation direction to 1.15 V.
- FIG. 6 is a current-potential curve when returning to the first open-circuit potential. From FIG. 8, it was found that the electrode for fuel cell produced in Comparative Example 1 had an electrode corrosion current flowing from around 1 V (vs. NHE) when the potential was scanned on the anode side, and the corrosion resistance of the electrode was poor.
- Example 2 A fuel cell electrode (5) was produced in the same manner as in Example 1 except that commercially available rutile-type titanium dioxide (TiO 2 ) (manufactured by Cabot) was used as the catalyst (5). The oxygen reducing ability of 5) was evaluated.
- FIG. 11 shows a current-potential curve obtained by the measurement.
- the fuel cell electrode (5) produced in Comparative Example 2 had an oxygen reduction starting potential of 0.45 V (vs. NHE) and almost no reducing ability.
- the powder X-ray diffraction spectrum of the catalyst (5) is shown in FIG.
- the crystal form was rutile.
- the catalyst of the present invention does not corrode in an acidic electrolyte or at a high potential, has excellent durability, and has a high oxygen reducing ability. Therefore, a catalyst layer for a fuel cell, an electrode, an electrode assembly, or a gas diffusion for a fuel cell or salt electrolysis It can be used for electrodes and other oxygen reduction electrodes.
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Abstract
Description
チタンの炭窒酸化物からなる触媒。
前記チタンの炭窒酸化物の組成式が、TiCxNyOz(ただし、x、y、zは原子数の比を表し、0<x≦1.0、 0<y≦1.0、 0.1≦z<2.0、 1.0<x+y+z≦2.0、かつ2.0≦4x+3y+2zである。)で表される(1)に記載の触媒。
燃料電池用である(1)または(2)に記載の触媒。
炭窒化チタンを、酸素ガス及び水素ガスを含む、不活性ガス中で熱処理することにより、チタンの炭窒酸化物を得る工程を含むことを特徴とするチタンの炭窒酸化物からなる触媒の製造方法。
前記工程における熱処理の温度が400~1400℃の範囲であることを特徴とする(4)に記載の製造方法。
前記工程における不活性ガス中の酸素ガス濃度が0.1~10容量%の範囲であることを特徴とする(4)または(5)に記載の製造方法。
前記工程における不活性ガス中の水素ガス濃度が0.2~20容量%の範囲であることを特徴とする(4)~(6)のいずれかに記載の製造方法。
(1)~(3)のいずれかに記載の触媒を含むことを特徴とする燃料電池用触媒層。
さらに電子伝導性粒子を含むことを特徴とする(8)に記載の燃料電池用触媒層。
燃料電池用触媒層と多孔質支持層とを有する電極であって、前記燃料電池用触媒層が(8)または(9)に記載の燃料電池用触媒層であることを特徴とする電極。
カソードとアノードと前記カソードおよび前記アノードの間に配置された電解質膜とを有する膜電極接合体であって、前記カソードおよび/または前記アノードが(10)に記載の電極であることを特徴とする膜電極接合体。
(11)に記載の膜電極接合体を備えることを特徴とする燃料電池。
(11)に記載の膜電極接合体を備えることを特徴とする固体高分子形燃料電池。
本発明の触媒は、チタンの炭窒酸化物からなることを特徴としている。また、前記チタンの炭窒酸化物の組成式は、TiCxNyOz(ただし、x、y、zは原子数の比を表し、0<x≦1.0、 0<y≦1.0、 0.1≦z<2.0、 1.0<x+y+z≦2.0、かつ2.0≦4x+3y+2zである。)で表されることが好ましい。上記組成式において、0.05≦x≦0.6、 0.005≦y≦0.6、 0.4≦z≦1.945、 1.0<x+y+z≦2.0、かつ3.5≦4x+3y+2z≦4.5であることがより好ましい。各原子数の比が、前記範囲を満たすと、酸素還元能が著しく高くなるので好ましい。
電子伝導性粒子であるカーボンに分散させた触媒が1質量%となるように、該触媒およびカーボンを溶剤中に入れ、超音波で撹拌し懸濁液を得る。なお、カーボンとしては、カーボンブラック(比表面積:100~300m2/g)(例えばキャボット社製 XC-72)を用い、触媒とカーボンとが質量比で95:5になるように分散させる。また、溶剤としては、イソプロピルアルコール:水(質量比)=2:1を用いる。
上記酸素還元開始電位が0.7V(vs.NHE)未満であると、前記触媒を燃料電池のカソード用の触媒として用いた際に過酸化水素を発生することがある。また酸素還元開始電位は0.85V(vs.NHE)以上であることが、好適に酸素を還元するために好ましい。また、酸素還元開始電位は高い程好ましく、特に上限は無いが、酸素還元開始電位の上限は、理論値の1.23V(vs.NHE)である。
上記触媒の製造方法は特に限定されないが、例えば、炭窒化チタンを、酸素及び水素を含む、不活性ガス中で熱処理することにより、チタンの炭窒酸化物を得る工程を含む製造方法が挙げられる。
製造方法(I)は、チタンの酸化物と炭素との混合物を、窒素雰囲気中で熱処理することにより炭窒化チタンを製造する方法である。
製造方法(II)は、炭化チタン、酸化チタンおよび窒化チタンの混合物を、窒素雰囲気中などで熱処理することにより炭窒化チタンを製造する方法である。
製造方法(III)は、炭化チタンおよび窒化チタンの混合物を、窒素雰囲気中などで熱処理することにより炭窒化チタンを製造する方法である。
次に、炭窒化チタンを、酸素ガス及び水素ガスを含む、不活性ガス中で熱処理することにより、チタンの炭窒酸化物を得る工程について説明する。
本発明の触媒は、白金触媒の代替触媒として使用することができる。
理学電機株式会社製 ロータフレックスを用いて、試料の粉末X線回折を行った。
炭素:試料約0.1gを量り取り、堀場製作所 EMIA-110で測定を行った。
1.触媒の調製
炭化チタン(TiC)5.10g(85mmol)、酸化チタン(TiO2)0.80g(10mmol)、窒化チタン(TiN)0.31g(5mmol)をよく混合して、1800℃で3時間、窒素雰囲気中で加熱することにより、炭窒化チタン5.73gが得られた。焼結体になるため、得られた炭窒化チタンを自動乳鉢で粉砕した。
酸素還元能の測定は、次のように行った。触媒(1)95mgおよびカーボン(キャボット社製 XC-72)5mgをイソプロピルアルコール:純水=2:1の質量比で混合した溶液10gに入れ、超音波で撹拌、懸濁して混合した。この混合物30μlをグラッシーカーボン電極(東海カーボン社製、直径:5.2mm)に塗布し、120℃で1時間乾燥した。さらに、ナフィオン(デュポン社 5%ナフィオン溶液(DE521))を10倍に純水で希釈したもの10μlを塗布し、120℃で1時間乾燥し、燃料電池用電極(1)を得た。
このようにして作製した燃料電池用電極(1)の触媒能(酸素還元能)を以下の方法で評価した。
1.触媒の調製
実施例1で得られた炭窒化チタン314mgを、1.5容量%の酸素ガスおよび4容量%水素ガスを含む、窒素ガスを流しながら、管状炉で、1000℃で3時間加熱することにより、チタンの炭窒酸化物(以下「触媒(2)」とも記す。)411mgが得られた。
前記触媒(2)を用いた以外は実施例1と同様にして燃料電池用電極(2)を得た。
前記燃料電池用電極(2)を用いた以外は実施例1と同様にして触媒能(酸素還元能)を評価した。
1.触媒の調製
実施例1で得られた炭窒化チタン314mgを、1.0容量%の酸素ガスおよび1.3容量%水素ガスを含む、窒素ガスを流しながら、管状炉で、1000℃で3時間加熱することにより、チタンの炭窒酸化物(以下「触媒(3)」とも記す。)415mgが得られた。
前記触媒(3)を用いた以外は実施例1と同様にして燃料電池用電極(3)を得た。
前記燃料電池用電極(3)を用いた以外は実施例1と同様にして触媒能(酸素還元能)を評価した。
1.触媒の調製
実施例1で得られた炭窒化チタンを触媒(以下「触媒(4)」とも記す。)として使用した。
前記触媒(4)を用いた以外は実施例1と同様にして燃料電池用電極(4)を得た。
前記燃料電池用電極(4)を用いた以外は実施例1と同様にして触媒能(酸素還元能)を評価した。
市販のルチル型二酸化チタン(TiO2)(キャボット社製)を触媒(5)として用いた以外は実施例1と同様にして、燃料電池用電極(5)を製造し、該燃料電池用電極(5)の酸素還元能を評価した。図11に、当該測定により得られた電流-電位曲線を示す。
Claims (13)
- チタンの炭窒酸化物からなる触媒。
- 前記チタンの炭窒酸化物の組成式が、TiCxNyOz(ただし、x、y、zは原子数の比を表し、0<x≦1.0、 0<y≦1.0、 0.1≦z<2.0、 1.0<x+y+z≦2.0、かつ2.0≦4x+3y+2zである。)で表される請求項1に記載の触媒。
- 燃料電池用である請求項1または2に記載の触媒。
- 炭窒化チタンを、酸素ガス及び水素ガスを含む、不活性ガス中で熱処理することにより、チタンの炭窒酸化物を得る工程を含むことを特徴とするチタンの炭窒酸化物からなる触媒の製造方法。
- 前記工程における熱処理の温度が400~1400℃の範囲であることを特徴とする請求項4に記載の製造方法。
- 前記工程における不活性ガス中の酸素ガス濃度が0.1~10容量%の範囲であることを特徴とする請求項4または5に記載の製造方法。
- 前記工程における不活性ガス中の水素ガス濃度が0.2~20容量%の範囲であることを特徴とする請求項4~6のいずれかに記載の製造方法。
- 請求項1~3のいずれかに記載の触媒を含むことを特徴とする燃料電池用触媒層。
- さらに電子伝導性粒子を含むことを特徴とする請求項8に記載の燃料電池用触媒層。
- 燃料電池用触媒層と多孔質支持層とを有する電極であって、前記燃料電池用触媒層が請求項8または9に記載の燃料電池用触媒層であることを特徴とする電極。
- カソードとアノードと前記カソードおよび前記アノードの間に配置された電解質膜とを有する膜電極接合体であって、前記カソードおよび/または前記アノードが請求項10に記載の電極であることを特徴とする膜電極接合体。
- 請求項11に記載の膜電極接合体を備えることを特徴とする燃料電池。
- 請求項11に記載の膜電極接合体を備えることを特徴とする固体高分子形燃料電池。
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Also Published As
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CA2722083A1 (en) | 2009-09-03 |
JP2014087793A (ja) | 2014-05-15 |
CN101959599A (zh) | 2011-01-26 |
US20110008709A1 (en) | 2011-01-13 |
KR20100115809A (ko) | 2010-10-28 |
EP2251081B1 (en) | 2017-09-13 |
JPWO2009107518A1 (ja) | 2011-06-30 |
JP5411123B2 (ja) | 2014-02-12 |
EP2251081A1 (en) | 2010-11-17 |
EP2251081A4 (en) | 2012-04-04 |
KR101202104B1 (ko) | 2012-11-15 |
CN101959599B (zh) | 2013-05-15 |
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