catalyst

Abstract

To provide a catalyst that contains an organic nitrogen compound and exhibits improved catalytic performance.SOLUTION: A catalyst has metal particles with oxygen reduction activity, an additive and a binder. The additive is at least one organic nitrogen compound. The organic nitrogen compound is a monomer represented by general formula (1) or a polymer including the monomer in at least a part of it. A ratio of a weight of the additive to a weight of the metal particles is more than 0 and 0.150 or less.SELECTED DRAWING: Figure 1

Description

[Technical Field]

[0001] The present disclosure relates to catalysts. [Background technology]

[0002] Various studies have been conducted on catalysts for electrochemical oxygen reduction, such as that disclosed in Patent Document 1. [Prior art documents] [Patent documents]

[0003] [Patent Document 1] International Publication No. 2019 / 221156 Summary of the Invention [Problem to be solved by the invention]

[0004] When melamine (1,3,5-triazine-2,4,6-triamine) is added as an additive to a catalyst with oxygen reduction activity to improve catalytic performance, it binds with a binder with acidic functional groups, inhibiting the binder's ability to retain water and transport protons, resulting in a lower cell voltage under low-humidity conditions than when no additive is added.

[0005] The present disclosure has been made in view of the above circumstances, and has as its main object to provide a catalyst that contains an organic nitrogen compound and that can improve catalytic performance. [Means for solving the problem]

[0006] The catalyst of the present disclosure comprises metal particles having oxygen reduction activity, an additive, and a binder, wherein the additive is at least one organic nitrogen compound, and the organic nitrogen compound is a monomer represented by the following general formula (1) or a polymer containing at least a portion of the monomer, and the ratio of the weight of the additive to the weight of the metal particles is greater than 0 and not greater than 0.150:

[0007] [ka]

[0008] [In general formula (1), R1, R2, and R3 each represent a hydrogen atom, a halogen atom, or a functional group selected from the group consisting of an amino group, a thiol group, a hydroxyl group, an alkylamino group having 1 to 10 carbon atoms, and an alkyl group having 1 to 10 carbon atoms, and each of the functional groups may have at least one atom selected from the group consisting of an oxygen atom, a sulfur atom, a nitrogen atom, a fluorine atom, a chlorine atom, a bromine atom, an iodine atom, and a hydrogen atom in the molecular chain.]

[0009] In the present disclosure, the additive may be cyanuric acid.

[0010] In the present disclosure, the additive may be a mixture of a first additive and a second additive, the first additive may be cyanuric acid, the second additive may be melamine, and the ratio of the weight of the second additive to the weight of the first additive may be 0.50 or more and 5.0 or less.

[0011] In the present disclosure, the ratio of the weight of the additive to the weight of the metal particles may be 0.010 or more and 0.150 or less.

[0012] In the present disclosure, the metal particles may be platinum-cobalt alloy particles, the carrier may be acetylene black, and the binder may be a perfluorocarbon sulfonic acid polymer. [Effects of the Invention]

[0013] The present disclosure can provide a catalyst that includes an organic nitrogen compound and can improve catalytic performance. [Brief explanation of the drawings]

[0014] [Figure 1]FIG. 1 is a graph showing the cell voltage at low humidity (30% RH) when the weight of additive relative to the weight of metal particles in the catalysts of Examples 1 to 9 and Comparative Examples 1 to 6 is changed. [Figure 2] FIG. 2 is a graph showing the cell voltage at high humidity (80% RH) when the weight of additive relative to the weight of metal particles in the catalysts of Examples 1 to 9 and Comparative Examples 1 to 6 is changed. DETAILED DESCRIPTION OF THE INVENTION

[0015] The catalyst of the present disclosure comprises metal particles having oxygen reduction activity, an additive, and a binder, wherein the additive is at least one organic nitrogen compound, and the organic nitrogen compound is a monomer represented by the following general formula (1) or a polymer containing at least a portion of the monomer, and the ratio of the weight of the additive to the weight of the metal particles is greater than 0 and not greater than 0.150:

[0016] When melamine (1,3,5-triazine-2,4,6-triamine) is used as an additive in a binder-containing catalyst, the presence of the additive causes a problem in that the cell voltage under low humidity conditions is lower than when no additive is added. A catalyst that has high cell performance under both low and high humidity conditions is required. In the present disclosure, by using an additive in which the highly basic amine functional group of melamine is substituted with a less basic functional group such as a hydroxyl group, it is possible to suppress the bonding between the additive and the binder. In addition, in this disclosure, an additive having an amine functional group, such as melamine, and an additive having a hydroxyl group, such as cyanuric acid (1,3,5-triazine-2,4,6-triol), are simultaneously mixed to form a bond between the additives, preferentially and specifically forming a compound called melamine cyanurate, thereby suppressing adhesion between the organic nitrogen compound and the binder. Furthermore, while the water solubility of melamine is 3.5 g / L, melamine cyanurate is insoluble in water, which increases stability inside the battery. According to the present disclosure, not only is voltage drop under low humidification conditions suppressed, but the voltage improvement effect under high humidification conditions is also higher than that of melamine, and catalytic activity can be improved regardless of whether the humidification conditions are low or high, thereby improving cell voltage.

[0017] The catalyst of the present disclosure comprises metal particles having oxygen reduction activity, an additive, and a binder.

[0018] The additive is at least one organic nitrogen compound. At least one organic nitrogen compound is a monomer represented by the following general formula (1) or a polymer containing at least a portion of the monomer.

[0019] [ka]

[0020] [In general formula (1), R1, R2, and R3 each represent a hydrogen atom, a halogen atom, or a functional group selected from the group consisting of an amino group, a thiol group, a hydroxyl group, an alkylamino group having 1 to 10 carbon atoms, and an alkyl group having 1 to 10 carbon atoms, and each of the functional groups may have at least one atom selected from the group consisting of an oxygen atom, a sulfur atom, a nitrogen atom, a fluorine atom, a chlorine atom, a bromine atom, an iodine atom, and a hydrogen atom in the molecular chain.]

[0021] In general formula (1), R1, R2, and R3 may each be a primary amine, a secondary amine, a tertiary amine, a quaternary ammonium cation, or a hydroxyl group.

[0022] As organic nitrogen compounds, the nitrogen equivalent, which represents the dry weight per mole of nitrogen, is 20 to 270 g·eq. -1 It may be a compound that satisfies 20 to 70 g·eq -1 The compound may satisfy the following conditions. The nitrogen equivalent can be calculated from the following formula: In the case of a polymer, the nitrogen equivalent of the monomer is regarded as the nitrogen equivalent of the polymer. Nitrogen equivalent (g·eq -1 ) = molecular weight (g / mol) ÷ amount of nitrogen in the molecule (mol N / mol)

[0023] As the organic nitrogen compound, at least one organic nitrogen compound may be a compound represented by general formula (1), and other organic nitrogen compounds may also be used. Examples of other organic nitrogen compounds include the following, regardless of whether they are compounds represented by general formula (1): melamine (nitrogen equivalent 21 g eq -1 ), thiocyanuric acid (nitrogen equivalent 59g eq -1 ), cyanuric acid (nitrogen equivalent 34g eq -1 ), oleylamine (nitrogen equivalent 267g eq -1 ), tetradecylamine (nitrogen equivalent 213g eq -1 ), 2,4,6-Tris[bis(methoxymethyl)amino]-1,3,5-triazine (nitrogen equivalent 65g·eq -1 ), 6-(Dibutylamino)-1,3,5-triazine-2,4-dithiol (nitrogen equivalent 68 g eq -1 ), 2,4-Diamino-6-butylamino-1,3,5-triazine (nitrogen equivalent 30 g eq -1 ), 2,4,6-Tris(pentafluoroethyl)-1,3,5-triazine (nitrogen equivalent 145g eq -1 ) and polymers containing these as monomers, and Poly(melamine-co-formaldehyde) methylated (nitrogen equivalent: 20-40 g eq) -1 ), and Poly(melamine-co-formaldehyde) isobutylated (nitrogen equivalent: 20-40 g eq) -1 ) etc. In addition, two or more of the above-mentioned additives may be contained.

[0024] Among the above, the additive may be at least one cyanuric acid-based material selected from the group consisting of cyanuric acid, polymers partially containing cyanuric acid, and polymers of cyanuric acid. Isocyanuric acid, a tautomer of cyanuric acid, is also considered to be the same compound. Cyanuric acid and its tautomers may be stabilized with halogen atoms, etc.

[0025] The additive may be a mixture of the first additive and the second additive. The first additive may be at least one cyanuric acid-based material selected from the group consisting of cyanuric acid, a polymer containing cyanuric acid in part, and a polymer of cyanuric acid. The second additive may be at least one melamine-based material selected from the group consisting of melamine, polymers containing melamine in part, and polymers of melamine. In particular, the first additive may be cyanuric acid, and the second additive may be melamine. In the case of a polymer, the polymer is more difficult to desorb after being adsorbed onto the metal particles than a monomer, and therefore the adsorption stability is improved. The polymer may have a degree of polymerization in the range of 1 to 10,000.

[0026] The metal particles may be any metal having oxygen reduction activity (oxygen reduction catalytic activity), such as platinum, ruthenium, iridium, rhodium, palladium, osnium, tungsten, lead, iron, chromium, cobalt, nickel, manganese, vanadium, molybdenum, gallium, aluminum, lanthanum, cerium, praseodymium, neodymium, samarium, gadolinium, and yttrium, or two or more of these metals may be used. Furthermore, the metal may be an oxide, nitride, sulfide, phosphide, or the like. Among the above, the metal particles may be at least one type selected from the group consisting of platinum particles, platinum alloy particles, and composite particles containing platinum. Examples of metals other than platinum contained in platinum alloys and platinum-containing composite particles include ruthenium, iridium, rhodium, palladium, osnium, tungsten, lead, iron, chromium, cobalt, nickel, manganese, vanadium, molybdenum, gallium, aluminum, lanthanum, cerium, praseodymium, neodymium, samarium, gadolinium, and yttrium, and the particles may contain two or more of these metals. The element ratio of metals other than platinum in the platinum alloy is not particularly limited, and may be 0.11 to 50 atm %. The particle size (particle diameter) of the metal particles is not particularly limited and may be 1 to 100 nm.

[0027] In the present disclosure, the particle size is the average crystallite size measured by X-ray diffraction. The particle size of the particles may be determined by measuring the particle sizes of 100 to 1000 particles using an electron microscope and averaging these values ​​to obtain the average particle size. In the present disclosure, particle size was measured by the above two methods.

[0028] The catalyst of the present disclosure may include a support. The metal particles may be supported on a carrier. The particle size of the primary particles of the carrier may be, for example, 5 to 500 nm. The metal loading ratio of the metal particles loaded on the carrier is not particularly limited, and may be 1 to 60%, or may be 18 to 48%. The support may be conductive carbon, oxide, or the like. The carbon may be carbon black (acetylene black, ketjen black, furnace black, etc.), activated carbon, graphite, glassy carbon, graphite, graphene, carbon fiber, carbon nanotubes, carbon nitride, carbon sulfide, carbon phosphide, or a mixture containing at least two of these. The oxide may be titanium oxide, niobium oxide, tin oxide, tungsten oxide, molybdenum oxide, or a mixture containing at least two of these.

[0029] The binder is a polyelectrolyte having ion exchange groups. The binder may be any polymer capable of exchanging ions, and the ion exchange group may be an acidic functional group. The acidic functional group may include sulfonic acid, phosphoric acid, or the like. The binder may be a perfluorocarbon sulfonic acid polymer, an anion exchange polymer, or a polymer primarily composed of polyether ether ketone, polybenzimidazole, or the like.

[0030] The equivalent mass per mole of the acidic functional group of the binder may be 600 g / mol or more and 1100 g / mol or less.

[0031] [Ratio of binder weight to carrier weight] In the catalyst of the present disclosure, the ratio of the weight of the binder to the weight of the support may be 0.50 or more and 0.85 or less. The ratio of the weight of the binder to the weight of the support is defined as (binder weight) / (support weight).

[0032] [Ratio of total weight of additives to weight of metal particles] In the catalyst of the present disclosure, the ratio of the total weight of the additives to the weight of the metal particles may be greater than 0 and not greater than 0.150, and may be 0.010 or greater and 0.150 or less. The ratio of the weight of the additive to the weight of the metal particles is defined as (weight of additive) / (weight of metal particles). When a mixture of a first additive and a second additive is used as the additive, the weight of the additive is the total weight of the first additive and the second additive.

[0033] [Ratio of the weight of the second additive to the weight of the first additive] When a mixture of at least one cyanuric acid-based material selected from the group consisting of cyanuric acid (1,3,5-triazine-2,4,6-triol), a polymer containing cyanuric acid in part, or a polymer of cyanuric acid is used as the first additive, and melamine (1,3,5-triazine-2,4,6-triamine), a polymer containing melamine in part, or a polymer of melamine is used as the second additive, the weight ratio of the second additive to the weight of the first additive may be 0 to 5.0 or 0.50 to 5.0. Note that when a polymer containing cyanuric acid in part or a polymer of cyanuric acid is used as the first additive, and a polymer containing melamine in part or a polymer of melamine is used as the second additive, the weight ratio is expressed as a weight ratio converted into monomers. The ratio of the weight of the second additive to the weight of the first additive is defined as (weight of the second additive) / (weight of the first additive).

[0034] [Evaluation method for weight of additives] Methods for evaluating the weight of the additive contained in the catalyst of the present disclosure include a method for measuring the nitrogen content by CHN elemental analysis, and a method for extracting the additive from the catalyst and measuring the additive directly.

[0035] [Method for evaluating metal particle weight, carrier weight, and binder weight] Methods for evaluating the weight of the metal particles, the weight of the carrier, and the weight of the binder contained in the catalyst of the present disclosure include thermogravimetric analysis (TG), high-frequency inductively coupled plasma emission spectroscopy (ICP), and the like.

[0036] The catalyst of the present disclosure may be used for a fuel cell or a metal-air battery. The catalyst of the present disclosure may be used in the cathode of a fuel cell, the anode of a fuel cell, or the air electrode of a metal-air battery. The fuel cell and metal-air battery of the present disclosure may include a cathode containing the catalyst of the present disclosure.

[0037] The catalyst of the present disclosure may have a layered shape. That is, the catalyst of the present disclosure may be a catalyst layer. Examples of methods for forming the catalyst layer include the following methods.

[0038] [Catalyst ink preparation process] First, a predetermined amount of a carrier carrying metal particles (metal particle-carrying carrier), a binder, an additive, and a solvent is placed in a container, and these are stirred using a stirrer to prepare a catalyst ink. The type of solvent is not particularly limited, and any liquid can be used, and may be water, alcohol, or a mixed solution of at least one alcohol and water. Examples of the alcohol include methanol, diacetone alcohol, ethanol, 1-propanol, 2-propanol, tert-butyl alcohol, ethylene glycol, and propylene glycol. Examples of the stirrer include an ultrasonic homogenizer, a jet mill, a bead mill, a ball mill, a high-shear mill, a Filmix, etc. The stirring conditions, such as the stirring speed, stirring time, and rotation speed, are not particularly limited and can be set appropriately. Thereafter, a vacuum degassing treatment may be carried out. There is no limit to the time for leaving the mixture to stand, and it may be left to stand for one day. It is also possible to use the mixture without leaving it to stand. It is also possible to carry out a vacuum degassing treatment again.

[0039] [Catalyst ink coating process] The prepared catalyst ink is coated onto a substrate, and the solvent is then removed after coating. For example, the catalyst ink is coated onto a substrate such as polytetrafluoroethylene (PTFE), and the coated catalyst ink is heated to dry and remove the solvent. The coating method may be any method that can uniformly coat the catalyst ink on the substrate, and examples thereof include die coating, spin coating, screen printing, doctor blade, squeegee, spray coating, and applicator methods. The heating rate and heating time can be appropriately set depending on the type of solvent, etc. The removal rate may also be increased by degassing simultaneously with heating. The coating thickness may be 5 to 30 μm. The amount of platinum in the coating may be 0.1 to 0.6 mg cm. -2 The catalyst ink may be applied so as to satisfy the above condition. [Example]

[0040] Example 1 Platinum-cobalt alloy particles (metal particle diameter 3–4 nm) were used as the metal particles, 1,3,5-triazine-2,4,6-triol (cyanuric acid, Fujifilm Wako Pure Chemical Industries, Ltd.) was used as the additive, carbon (acetylene black) was used as the support, and perfluorocarbon sulfonic acid polymer (DE2020, Chemours Corporation) was used as the binder. A catalyst layer containing these materials was formed using the following method. The equivalent mass per mole of acidic functional groups in the binder was 1100 g / mol. The binder weight relative to the support weight in the catalyst was 0.85. The additive weight relative to the metal particle weight in the catalyst was 0.010.

[0041] [Catalyst layer formation method] A predetermined amount of a carrier carrying metal particles (metal particle-carrying carrier, metal loading ratio 50 wt%), a binder, an additive, and water and diacetone alcohol as a solvent were placed in a container and stirred at 300 rpm using a bead mill for a total of 4 hours to prepare a catalyst ink. The catalyst ink was subjected to a vacuum degassing treatment and left to stand for one day. Thereafter, the catalyst ink was subjected to a vacuum degassing treatment again. The prepared catalyst ink was applied to a polytetrafluoroethylene (PTFE) substrate using a die coating method, and the applied catalyst ink was heated to dry and remove the solvent, forming a catalyst layer. The amount of platinum contained in the catalyst layer was 0.20 mg cm. -2 The coating was applied so that the

[0042] (Examples 2 and 3) A layer made of catalyst (catalyst layer) was formed under the same conditions as in Example 1, except that the weight of additives relative to the weight of metal particles in the catalyst was changed as shown in Table 1.

[0043] (Examples 4 to 9, Comparative Example 2) A layer made of catalyst (catalyst layer) was formed under the same conditions as in Example 1, except that 1,3,5-triazine-2,4,6-triol (cyanuric acid, manufactured by Fujifilm Wako Pure Chemical Industries, Ltd.) was used as the first additive and 1,3,5-triazine-2,4,6-triamine (melamine, manufactured by Fujifilm Wako Pure Chemical Industries, Ltd.) was used as the second additive, and the weight of the first additive relative to the weight of the metal particles in the catalyst, the weight of the second additive relative to the weight of the metal particles in the catalyst, the total weight of additives relative to the weight of the metal particles in the catalyst, and the weight of the second additive relative to the weight of the first additive in the catalyst were set to the values ​​shown in Tables 2 and 3.

[0044] (Comparative Example 1) A layer made of a catalyst (catalyst layer) was formed under the same conditions as in Example 1, except that no additive was used.

[0045] (Comparative Examples 3 to 6) A layer made of catalyst (catalyst layer) was formed under the same conditions as in Example 1, except that 1,3,5-triazine-2,4,6-triamine (melamine, Fujifilm Wako Pure Chemical Industries, Ltd.) was used as the additive and the weight of the additive relative to the weight of the metal particles in the catalyst was changed as shown in Table 4.

[0046] [Method for producing membrane-electrode gas diffusion layer assembly] Each catalyst layer produced in Examples 1 to 9 and Comparative Examples 1 to 6 was prepared as a cathode catalyst layer. An electrolyte membrane (Nafion NR211) was prepared, and an anode catalyst layer containing TEC10E50E manufactured by Tanaka Kikinzoku Kogyo Kogyo was prepared as an anode catalyst. The electrolyte membrane was sandwiched between the cathode catalyst layer and the anode catalyst layer, and a temperature (130°C) and pressure (3 MPa) were applied to thermocompression bond the cathode catalyst layer, electrolyte membrane, and anode catalyst layer to produce a membrane-electrode assembly. Two carbon fiber gas diffusion layers (GDL 22BB manufactured by SGL) were prepared and placed on both sides of the membrane-electrode assembly to produce a membrane-electrode gas diffusion layer assembly for Examples 1 to 9 and Comparative Examples 1 to 6.

[0047] [Actual 1cm 2 Cell Evaluation] The electrode part is 1cm 2Using each membrane-electrode gas diffusion layer assembly, cell evaluation was carried out. The current-voltage characteristics were evaluated under low humidity conditions (30% RH) and high humidity conditions (80% RH). The current-voltage characteristics were acquired using an anodic sweep at a sweep rate of 20 mA / s. The cell temperature was 80°C, the pressure was 150 kPa_ABS, the cathode gas was air, the cathode gas flow rate was 2.0 L / min, the anode gas was hydrogen, and the anode gas flow rate was 1.0 L / min. From the results of the current-voltage characteristics evaluation, the cell voltage (mV) under low humidity conditions (30% RH) and high humidity conditions (80% RH) was calculated. These results are shown in Tables 1 to 4. The evaluation criteria for cell voltage under low humidity conditions (30% RH) were as follows: if the cell voltage was 773 mV or higher, it was rated as 1 (Excellent); if it was 703 mV or higher but less than 773 mV, it was rated as 2 (Good); if it was 634 mV or higher but less than 703 mV, it was rated as 3 (Average); and if it was less than 634 mV, it was rated as 4 (Poor). The evaluation criteria for cell voltage under highly humidified conditions (80% RH) were as follows: if the cell voltage was 846 mV or higher, it was rated as 1 (Excellent); if it was 843 mV or higher but less than 846 mV, it was rated as 2 (Good); if it was 836 mV or higher but less than 843 mV, it was rated as 3 (Average); and if it was less than 836 mV, it was rated as 4 (Poor).

[0048] [Table 1]

[0049] [Table 2]

[0050] [Table 3]

[0051] [Table 4]

[0052] [Evaluation results] FIG. 1 is a graph showing the cell voltage at low humidity (30% RH) when the weight of additive relative to the weight of metal particles in the catalysts of Examples 1 to 9 and Comparative Examples 1 to 6 is changed. FIG. 2 is a graph showing the cell voltage at high humidity (80% RH) when the weight of additive relative to the weight of metal particles in the catalysts of Examples 1 to 9 and Comparative Examples 1 to 6 is changed. As shown in Figures 1 and 2 and Tables 1 to 4, the cells using the catalysts of Examples 1 to 9 have higher cell voltages under both low humidification conditions (30% RH) and high humidification conditions (80% RH) than the cells using the corresponding catalysts of Comparative Examples 2 to 6.

Claims

1. A catalyst for electrochemical oxygen reduction, comprising: The catalyst comprises metal particles having oxygen reduction activity, a support, an additive, and a binder; the metal particles are supported on the support, the additive is cyanuric acid, a ratio of the weight of the additive to the weight of the metal particles is 0.050 or more and 0.150 or less; the metal particles are at least one selected from the group consisting of platinum particles, platinum alloy particles, and platinum-containing composite particles; A catalyst, wherein the support is electrically conductive carbon.

2. A catalyst for electrochemical oxygen reduction, comprising: The catalyst comprises metal particles having oxygen reduction activity, a support, an additive, and a binder; the metal particles are supported on the support, the additive is a mixture of a first additive and a second additive; the first additive is cyanuric acid; the second additive is melamine; a ratio of the weight of the second additive to the weight of the first additive is 0.50 or more and 5.0 or less; a ratio of the weight of the additive to the weight of the metal particles is 0.050 or more and 0.150 or less; the metal particles are at least one selected from the group consisting of platinum particles, platinum alloy particles, and platinum-containing composite particles; A catalyst, wherein the support is electrically conductive carbon.

3. 2. The catalyst according to claim 1, wherein the ratio of the weight of the additive to the weight of the metal particles is 0.050 or more and 0.100 or less.

4. the metal particles are platinum-cobalt alloy particles, the carrier is acetylene black, 10. The catalyst of claim 1, wherein the binder is a perfluorocarbon sulfonic acid polymer.

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