WO2016063924A1

WO2016063924A1 - Carbon black for fuel cell

Info

Publication number: WO2016063924A1
Application number: PCT/JP2015/079748
Authority: WO
Inventors: 大貴池田; 祐作原田
Original assignee: デンカ株式会社
Priority date: 2014-10-21
Filing date: 2015-10-21
Publication date: 2016-04-28
Also published as: JPWO2016063924A1; JP6563945B2

Abstract

　Provided is carbon black on which catalytic metal particles can be supported in a highly dispersed manner, and which exhibits excellent oxidation resistance. The carbon black is characterized in having a specific surface area, as measured by the BET method, of 200-500m², a crystal layer thickness Lc, as measured by X ray diffraction, of 20-30Å, and an average primary particle diameter of 15-25nm. The content of volatile matter in the carbon black is preferably 0.10-1.00%. A fuel cell catalyst is obtained by supporting catalytic metal particles on the carbon black.

Description

Carbon black for fuel cells

The present invention relates to carbon black having high oxidation resistance and excellent catalyst supporting properties, and a fuel cell catalyst using the carbon black.

A fuel cell has a structure in which a gas diffusion layer, an electrode catalyst layer, and an electrolyte membrane are sandwiched between separators provided with a gas flow path such as hydrogen or oxygen. There are various configurations of the electrode catalyst layer. For example, it is composed of catalyst metal particles such as platinum and a catalyst carrier, and carbon black having excellent gas diffusibility, electrical conductivity and ion conductivity is used for the catalyst carrier. ing. The electrode catalyst layer is formed by dispersing carbon black or fluorine-based polymer carrying catalyst metal particles such as platinum in a solvent made of water or alcohol, and spraying the dispersion onto a solid electrolyte membrane. .

In recent years, in order to further improve the characteristics of fuel cells, long-term durability of electrode performance and improvement of catalytic activity in the electrode catalyst layer have been demanded.
The electrode performance of a fuel cell is degraded by repeated catalytic reactions during long-term use. This is because carbon black is electrochemically oxidized in the cathode potential range of 1.0 to 0.6 V (.vs NHE), the generation and elimination of surface functional groups proceeds, the surface structure changes, and the support This is because the formed catalytic metal particles aggregate or fall off. Further, when the cathode potential is in the range of 1.5 to 1.0 V (.vs NHE), part of the carbon black reacts with water to become carbon monoxide or carbon dioxide, which corrodes.
In order to improve the oxidation resistance of carbon black, high crystallization (graphitization) is effective. Carbon black is an aggregate of crystallites called “pseudo-graphite structure” in which condensed benzene rings with π-electrons are stacked in multiple layers. However, when heat treatment is performed at 2000 to 3000 ° C. in an inert atmosphere, Rearrangement develops a graphite structure and improves crystallinity (Patent Document 1). The higher the crystallinity, the less the portion that becomes the starting point of the surface oxidation reaction, so that the oxidation resistance of carbon black is improved. However, graphitization of carbon black is accompanied by a decrease in specific surface area at the same time. In other words, too much graphitization with emphasis on oxidation resistance alone reduces the specific surface area to about 50 to 150 m ² / g, so that the catalyst metal particles cannot be supported in a highly dispersed state and the catalytic reaction efficiency decreases (patents). Reference 2).

In addition, in order to improve the catalytic activity, it has been studied to improve the catalytic reaction efficiency by highly dispersing and supporting catalytic metal particles on carbon black having a specific surface area of 500 m ² / g or more (Patent Document 3). .

Special table 2007-505975 Japanese Patent Laid-Open No. 6-140047 JP 2007-112660 A

However, when carbon black having a high specific surface area is used as a support, there is a problem that the oxidation resistance of the carbon black is lowered because the starting point of the surface oxidation reaction is increased. An object of the present invention is to provide a carbon black having high oxidation resistance and excellent catalyst supporting properties.

The present invention employs the following means in order to solve the above problems.
(1) The specific surface area measured by the BET method is 200 to 500 m ² / g, the crystal layer thickness Lc measured by X-ray diffraction is 20 to 30 mm, and the average primary particle diameter is 15 to 25 nm. Carbon black.
(2) The carbon black as described in (1) above, which has a volatile content of 0.10 to 1.00%.
(3) A fuel cell catalyst comprising catalyst metal particles supported on the carbon black according to (1) or (2).

The present invention provides a carbon black capable of highly dispersing and supporting catalyst metal particles and having excellent oxidation resistance.

In one embodiment of the present invention, the specific surface area of carbon black is 200 to 500 m ² / g. The specific surface area can be measured by the BET method in accordance with JIS K6217-2: 2001. When the specific surface area exceeds 500 m ² / g, the number of places where the catalytic metal particles can be supported increases, but this position is the starting point of the surface oxidation reaction. However, the oxidation resistance of carbon black is reduced. Further, when the specific surface area is less than 200 m ² / g, the places where the catalyst metal particles are supported are greatly reduced, which causes a reduction in catalytic reaction efficiency. The carbon black of the present invention has a specific surface area sufficient to carry the catalyst metal particles in a highly dispersed manner, and can maintain oxidation resistance. The specific surface area of carbon black is preferably 220 to 380 m ² / g, more preferably 240 to 360 m ² / g.

As a means for increasing the specific surface area of carbon black, there is an activation treatment for making the surface porous, which can be roughly classified into a gas activation method and a chemical activation method. In the present invention, gas activation using air or water vapor is preferable in order to prevent impurities from being mixed into the carbon black powder. The activation treatment is generally performed at 500 to 1000 ° C., but when obtaining the carbon black according to the present invention, it is desirable to perform the treatment at a temperature of 500 to 650 ° C. in order to maintain high crystallinity and productivity.

In one embodiment of the present invention, the carbon black has a crystal layer thickness Lc of 20 to 30 mm. The crystal layer thickness Lc can be determined by X-ray diffraction. Specifically, X-ray diffraction is performed using CuKα rays under the conditions of a measurement range 2θ = 10 to 40 ° and a slit width of 0.5 °. Using the diffraction line of the (002) plane obtained, the crystal layer thickness Lc can be obtained by Scherrer's formula: Lc (Å) = (K × λ) / (β × cos θ). Here, K is a form factor constant of 0.9, λ is an X-ray wavelength of 1.54 mm, θ is an angle indicating a maximum value in the (002) diffraction line absorption band, and β is a half-value width in the (002) diffraction line absorption band. (Radians). The crystal layer thickness Lc is an index indicating the crystallinity of the carbon black, and if it is less than 20%, the portion that becomes the starting point of the surface oxidation reaction increases, so that the oxidation resistance of the carbon black decreases. Further, when graphitization is performed until the crystal layer thickness Lc exceeds 30% in order to improve the oxidation resistance of the carbon black, the edge (edge) in the pseudo-graphite structure, that is, the field where catalyst metal particles are deposited is reduced. The particles cannot be supported in a highly dispersed state. The crystal layer thickness Lc of the carbon black is preferably 22 to 28 mm, more preferably 24 to 26 mm.

In general, carbon black is graphitized by heat treatment at 2000 to 3000 ° C. in an inert atmosphere. The graphitization of the carbon black proceeds by treatment at a high temperature for a long time, and the crystal layer thickness Lc can be increased to about 20 to 100 mm, but the specific surface area decreases. In producing the carbon black in the present invention, it is desirable to treat at a temperature of 1600 to 1800 ° C. in order to achieve both oxidation resistance and catalyst supporting properties.

One feature of the carbon black in one embodiment of the present invention is that the average primary particle size is as small as 15 to 25 nm in order to achieve both oxidation resistance and catalyst supporting properties. The average primary particle diameter can be obtained by measuring the primary particle diameter of 100 carbon blacks from a 50,000-magnification image of a transmission electron microscope (TEM) and calculating the average value. The primary particles of carbon black have a small aspect ratio and a shape close to a true sphere, but are not perfect spheres. Therefore, the largest of the line segments connecting the two outer peripheral points of the primary particles in the TEM image is the primary particle diameter of carbon black. In general, the specific surface area of many powders containing carbon black depends on the particle size and surface roughness. That is, the smaller the particle diameter and the rougher the surface, the higher the specific surface area. As one of means for increasing the specific surface area of carbon black, there is an activation treatment for making the surface porous, whereby the specific surface area of the powder is increased by, for example, twice or more. The inventor has found that when the activation treatment is performed under the same conditions, the increase rate of the specific surface area is improved as the average primary particle size is smaller. Although the rate of increase of the specific surface area can be controlled by changing the activation conditions such as the treatment temperature and time, the crystallinity and productivity decrease as the treatment is performed at a high temperature for a long time. If the average primary particle diameter exceeds 25 nm, the specific surface area cannot be increased to 200 m ² / g or more while maintaining the crystallinity, and the catalyst metal particles cannot be supported in a highly dispersed state. In the case of porous carbon black having a hollow structure, even if the average primary particle diameter exceeds 25 nm, the specific surface area can be increased to 200 m ² / g or more. It will enter the interior and the catalytic reaction efficiency will decrease. On the other hand, if the average primary particle diameter is less than 15 nm, even if the specific surface area is high, the supported catalytic metal particles are likely to come into contact with each other and aggregate, and the catalytic reaction efficiency is lowered. The average primary particle diameter of carbon black is preferably 16 to 24 nm, and more preferably 18 to 22 nm.

It is thought that the surface oxidation reaction of carbon black by the cathode potential proceeds as follows. That is, single-bond surface functional groups such as phenolic hydroxyl groups are generated in the first stage, and they are oxidized to double-bond surface functional groups such as carboxyl groups in the second stage. Desorbs as carbon. Therefore, as the amount of surface functional groups on the carbon black increases, the reaction of the second and third stages proceeds easily without going through the first-stage surface functional group generation process, thus promoting the surface oxidation reaction. End up.
One means for evaluating the surface functional group species present on the carbon black is a temperature programmed desorption (TPD) method. The TPD method is a method for measuring the amount of CO, CO ₂ and H ₂ O that are desorbed when a previously dried sample is heated in an inert atmosphere at a constant heating rate. The surface functional group species can be estimated from the profile of the desorbed gas amount. As a result of TPD measurement, it is known that oxygen-containing functional groups such as phenolic hydroxyl groups, ether groups, carboxyl groups, carbonyl groups, and lactone groups exist on carbon black.

The volatile content of carbon black in the present invention is preferably 0.10 to 1.00%. Here, the volatile matter is an index for evaluating the amount of surface functional groups present on the carbon black. The volatile matter can be measured from a weight change when a sample which has been dried at 105 ° C. for 1 hour to remove moisture is heated in vacuum at 950 ° C. for 5 minutes. As a result of intensive studies, the present inventors have found that the surface oxidation reaction of carbon black is strongly dependent on the amount of surface functional groups as long as it is an oxygen-containing functional group, regardless of the type of surface functional group. If the volatile content exceeds 1.00%, the amount of surface functional groups increases, so that the surface oxidation reaction of carbon black by the cathode potential tends to proceed, and the oxidation resistance tends to decrease. On the other hand, if the volatile content is less than 0.10%, the amount of surface functional groups decreases, and thus hydrophilicity tends to be remarkably lowered. For this reason, it is difficult to disperse the catalyst metal particles on the carbon black in the precursor solution, and the catalyst metal particles may not be supported in a highly dispersed state. Volatiles are reduced by the graphitization treatment heated in an inert atmosphere, and increased by the activation treatment heated in an oxygen-containing atmosphere. The volatile content of carbon black is preferably 0.20 to 0.80%, and more preferably 0.30 to 0.70%.

The carbon black production method of the present invention is characterized in that the raw material carbon black having a controlled average primary particle size is graphitized at 1600 to 1800 ° C. and then activated at 500 to 650 ° C. By performing the activation treatment after the graphitization treatment, it is possible to preferentially burn the amorphous carbon that has not been sufficiently crystallized, as well as to increase the specific surface area, thereby enabling further crystallization.

The method for producing the raw material carbon black according to the present invention is not particularly limited. For example, a raw material gas such as hydrocarbon is supplied from a nozzle installed at the top of the reactor, and a pyrolysis reaction and / or a partial combustion reaction is performed. Can produce carbon black and collect it from the bag filter directly connected to the bottom of the reactor. The raw material gas to be used is not particularly limited, and gaseous hydrocarbons such as acetylene, methane, ethane, propane, ethylene, propylene, and butadiene, and oils such as toluene, benzene, xylene, gasoline, kerosene, light oil, and heavy oil Gasified hydrocarbons can be used. A plurality of these can also be mixed and used. Among them, it is preferable to use acetylene gas having a small amount of impurities such as sulfur. As one means for controlling the average primary particle size of the raw material carbon black, there is a method of reducing the particle size by adding an oxidizing gas such as air together with the raw material gas into the reaction furnace and causing incomplete combustion. Furthermore, if the carbon black is rapidly cooled immediately after generation by giving a swirling flow in the reactor and greatly shortening the residence time in a high temperature field, it is suitable for reducing the particle size. It is preferable to use water vapor, hydrogen, nitrogen, or the like as the swirling gas, and the water vapor content is 10 to 20 vol%. Although water vapor has a cooling effect and an activation effect, if the content rate of the water vapor in the swirling gas exceeds 20 vol%, the activation effect increases, so that the crystallinity of the generated carbon black is significantly lowered.

When performing the graphitization treatment, a crucible such as graphite, alumina, or silicon carbide can be used as a container for filling the raw material carbon black. In producing the carbon black according to the present invention, it is preferable to perform the graphitization treatment in a state where the filling density of the raw material carbon black into the crucible is 0.05 g / ml or less. Thereby, crystallization between particles can be prevented, and a decrease in specific surface area can be suppressed. The packing density can be determined from the weight of the raw material carbon black to be filled and the volume of the crucible. When the packing density exceeds 0.05 g / ml, the specific surface area is remarkably lowered and the catalytic metal particles are increased because the crystallization between the particles progresses not only within the particles due to the increased degree of contact between the particles. It becomes impossible to carry the dispersion. The packing density of the raw material carbon black into the crucible is preferably 0.04 g / ml or less, and more preferably 0.03 g / ml or less. However, if this packing density is too small, the productivity is lowered, so that it is preferably 0.01 g / ml or more.
Further, the crystal layer thickness Lc of the raw material carbon black before the graphitization treatment is preferably 15 mm or more, and more preferably 16 mm or more. If the crystal layer thickness Lc of the raw material carbon black is less than 15 mm, graphitization at a high temperature exceeding 1800 ° C. is required, and the specific surface area is extremely reduced. The crystal layer thickness Lc of the raw material carbon black can be changed depending on the reaction temperature at the time of carbon black synthesis.

In producing the carbon black according to the present invention, the temperature of the activation treatment is preferably 500 to 650 ° C. Since the average primary particle diameter of the raw material carbon black is small, there is a sufficient specific surface area increasing effect even if the activation treatment temperature is set at a relatively low temperature. Further, the volatile content of the carbon black after the activation treatment can be reduced to, for example, 1.00% or less.

The catalyst for a fuel cell of the present invention is obtained by carrying highly dispersed metal catalyst particles on the surface of the carbon black of the present invention. As a kind of the catalyst metal, it is preferable to use platinum alloy in addition to platinum. Examples of the platinum alloy-forming metal include palladium, rhodium, iridium, ruthenium, iron, titanium, nickel, cobalt, gold, silver, copper, chromium, manganese, molybdenum, tungsten, aluminum, silicon, rhenium, zinc, and tin. When used in a polymer electrolyte fuel cell, platinum-ruthenium or a platinum-cobalt alloy is preferable because it is effective in preventing carbon monoxide poisoning. The platinum alloy composition is preferably 30 to 90% by mass of platinum. The size of the catalyst metal particles is preferably 10 to 50 mm for platinum, for example.

Although the manufacturing method of the catalyst for fuel cells is not particularly limited, examples of the case where the catalyst metal particles are platinum include the following methods. First, an aqueous solution of hexachloroplatinic acid (IV) is added to a dispersion in which carbon black is suspended in water to obtain a mixed solution A, to which 10 times equivalent sodium borohydride is added (reduction treatment) to platinum. Then, after depositing platinum particles on the surface of carbon black, a catalyst for a fuel cell can be produced by filtration, washing and drying.
When the catalyst metal particles are a platinum alloy, a mixed solution containing platinum and an alloy-forming metal is used. For example, when ruthenium is used as the alloy-forming metal, a mixed solution B is prepared by adding a ruthenium (III) trichloride aqueous solution containing a predetermined amount of ruthenium to the mixed solution A. Next, 10 times equivalent of sodium borohydride with respect to the platinum alloy is added to the mixed solution B (reduction treatment), and after the platinum alloy particles are precipitated on the surface of the carbon black, the fuel cell is filtered, washed and dried. Catalysts can be produced.

The polymer electrolyte fuel cell using the fuel cell catalyst of the present invention can be produced, for example, as follows. That is, a fuel cell catalyst is mixed with a tetrafluoroethylene resin powder, and a paste obtained by adding alcohol is applied to one side of carbon paper to form a catalyst layer. And a Nafion solution is uniformly apply | coated to the surface of a catalyst layer, and it is set as an electrode. The electrodes are stacked on both sides of a Nafion membrane (perfluorosulfonic acid electrolyte membrane) so as to be in contact with each other, and are hot-pressed by hot pressing to obtain a membrane electrode assembly (MEA). When the MEA is sandwiched between the separator and the current collector plate, a single fuel cell is completed, and the fuel cell can be evaluated by connecting an electronic load device and a gas supply device.

Example 1
A raw material carbon black having a specific surface area of 392 m ² / g, a crystal layer thickness Lc of 17 mm, and an average primary particle diameter of 19 nm obtained by pyrolyzing acetylene gas at 2000 ° C. is graphitized at 1700 ° C. for 1 hour in a nitrogen atmosphere. Then, activation treatment was performed at 550 ° C. for 30 minutes. The packing density into the alumina container during the graphitization treatment was 0.03 g / ml.
The obtained carbon black was measured for the following physical properties. The evaluation results are shown in Table 1.
(1) Specific surface area: Measured according to JIS K 6217-2.
(2) Crystal layer thickness Lc: X-ray diffraction is performed with an X-ray diffractometer (“D8ADVANCE” manufactured by Brucker) using CuKα rays in a measurement range of 2θ = 10 to 40 ° and a slit width of 0.5 °. It was. For calibration of the measurement angle, silicon for X-ray standard (metal silicon manufactured by Mitsuwa Chemicals) was used. Using the diffraction line of the (002) plane obtained, the crystal layer thickness Lc was determined by Scherrer's formula: Lc (Å) = (K × λ) / (β × cos θ). Here, K is a form factor constant of 0.9, λ is an X-ray wavelength of 1.54 mm, θ is an angle indicating a maximum value in the (002) diffraction line absorption band, and β is a half-value width in the (002) diffraction line absorption band. (Radians).
(3) Average primary particle diameter: 100 primary particle diameters of carbon black were measured from a 50,000 times image of a transmission electron microscope (TEM), and an average value was calculated.
(4) Volatile content: A sample obtained by previously drying at 105 ° C. for 1 hour to remove moisture was measured from a change in weight when heat-treated in vacuum at 950 ° C. for 5 minutes.

The obtained carbon black was mixed with a chloroplatinic acid aqueous solution. The mixing ratio was mass ratio, and carbon black / platinum = 70/30. The mixture was stirred at 80 ° C. for 30 minutes and then cooled to room temperature. 0.5M sodium borohydride was added in 5 portions to precipitate platinum, filtered, washed and dried to obtain a fuel cell catalyst. The platinum weight contained in the obtained platinum-supported carbon black was quantified using an inductively coupled plasma mass spectrometer (ICP-MS), and the platinum weight ratio (platinum support ratio) per unit weight of the platinum-supported carbon black was calculated. did. The calculated platinum loading is shown in Table 1.

2.5 g of Nafion was mixed with 1 g of the obtained fuel cell catalyst to form a paste, which was applied to carbon paper and then dried at 80 ° C. to form an air electrode. Commercially available platinum-supported carbon black (“TEC10E40E” manufactured by Tanaka Kikinzoku Co., Ltd.) is used as the fuel electrode, and the Nafion membrane is sandwiched between the air electrode and pressed at 135 ° C. for 10 minutes at 9.8 MPa. MEA) was obtained. A fuel cell single cell was constructed by sandwiching and integrating with a separator and a current collector plate. This fuel cell single cell was introduced at a temperature of 90 ° C., 10 ml / min of nitrogen was introduced into both electrodes, and cyclic voltammetry measurement was performed in a potential range of 1.0 V to 0.1 V (vs. NHE). The effective specific surface area (ECSA) of the platinum catalyst was calculated from the adsorption wave.

Next, this fuel cell single cell was introduced at a temperature of 90 ° C. with 4 ml / min of hydrogen and 60 ml / min of air, and a constant potential scan of 1.0 V to 0.6 V (vs. NHE) at 20 mV / s. After repeating 5000 cycles, cyclic voltammetry measurement was performed in a nitrogen atmosphere in the same manner as described above, and the effective specific surface area (ECSA) of the platinum catalyst was calculated from the obtained hydrogen adsorption wave. As an indicator of catalyst durability, the ECSA reduction rate before and after the constant potential scanning cycle was determined. Here, since surface oxidation and corrosion occur on carbon black having low oxidation resistance, the ECSA reduction rate becomes large. The evaluation results are shown in Table 1.

Comparative Example 1
A fuel cell catalyst and a single fuel cell were prepared and evaluated using commercially available carbon black (“VULCAN (registered trademark) XC72” manufactured by CABOT). The evaluation results are shown in Table 2.

Comparative Example 2
A fuel cell catalyst and a fuel cell single cell were prepared and evaluated using the steam activated graphitized carbon black described in the examples of paragraphs (0009) to (0010) of Patent Document 2. The evaluation results are shown in Table 2.

Examples 2 to 8 and Comparative Examples 3 to 12
Carbon black was obtained in the same manner as in Example 1 except that the raw material carbon black used, the graphitization temperature, and the activation temperature were changed to the conditions shown in Tables 1 and 2. In Comparative Example 3, graphitization treatment and activation treatment were performed, in Comparative Example 4, activation treatment was not performed, and in Comparative Example 5, no graphitization treatment was performed. In Comparative Example 6, the packing density into the alumina container during the graphitization treatment was 0.08 g / ml, and in Comparative Example 12, porous carbon black having a hollow structure was used as the raw material carbon black. The evaluation results are shown in Tables 1 and 2.

From Table 1, the carbon black of the present invention showed a high platinum loading and retained the effective specific surface area (ECSA) of the platinum catalyst for a long time.

The carbon black of the present invention can be used as a catalyst carrier for various fuel cells. This makes it possible to produce a fuel cell with high power generation performance and excellent long-term durability.

Claims

Carbon black having a specific surface area measured by BET method of 200 to 500 m 2 / g, a crystal layer thickness Lc measured by X-ray diffraction of 20 to 30 mm, and an average primary particle diameter of 15 to 25 nm.
2. The carbon black according to claim 1, wherein the volatile content is 0.10 to 1.00%.
A fuel cell catalyst comprising catalyst carbon particles supported on the carbon black according to claim 1.
A fuel cell catalyst comprising catalyst metal particles supported on the carbon black according to claim 2.
A fuel cell comprising the fuel cell catalyst according to claim 3.
A fuel cell comprising the fuel cell catalyst according to claim 4.