JP2793523B2 - Polymer electrolyte fuel cell and method of operating the same - Google Patents

Description

DETAILED DESCRIPTION OF THE INVENTION

[0001]

BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a solid polymer using, as an electrolyte, a polymer film having hydrogen ion conductivity or a composite material comprising an inorganic or organic material powder having hydrogen ion conductivity and a polymer binding material. Fuel cell.

[0002]

2. Description of the Related Art In recent years, fuel cells have attracted attention as high-efficiency energy conversion devices. Depending on the type of electrolyte used for the fuel cell, for example, an alkaline aqueous solution type,
Low-temperature operation fuel cells such as phosphoric acid type and solid polymer type and high temperature operation fuel cells such as molten carbonate type and solid oxide electrolyte type are roughly classified.

[0003] Among these fuel cells, a polymer electrolyte membrane (Polymer Elec) having hydrogen ion conductivity as an electrolyte is used.
polymer electrolyte fuel cell using trolyte membrane)
Because it does not require a pressurized container, it is compact, has a high power density, has excellent start-up properties, and can be operated with a simple system. , For stationary use

As the electrolyte membrane used in the polymer electrolyte fuel cell, a polystyrene-based cation exchange membrane having a sulfonic acid group, a mixed substance of fluorocarbon sulfonic acid and polyvinylidene fluoride, and trifluoroethylene as a fluorocarbon matrix are used. Grafted products are known. Recently, a perfluorocarbon sulfonic acid membrane (for example, Nafion: trade name, manufactured by DuPont) or the like is also used.

A polymer electrolyte fuel cell using such a polymer electrolyte membrane is composed of a pair of porous electrodes having functions as a gas diffusion layer and a catalyst layer, that is, a porous fuel electrode carrying a platinum catalyst and an oxidized fuel electrode. A single cell is formed by sandwiching a polymer electrolyte membrane between the electrode and a current collector provided with a fuel gas flow path and an oxidizing gas flow path outside both electrodes. , A cooling plate and the like.

In a hydrogen ion conduction type fuel cell, on the fuel electrode side and the oxidant electrode side, at the interface between the electrolyte and the electrode in the presence of a platinum catalyst, the fuel electrode: H ₂ → 2H ⁺ + 2e ⁻ . 1) Oxidizer electrode: An electrochemical reaction of 1 / 2O ₂ + 2H ⁺ + 2e ⁻ → H ₂ O (2) occurs.

In the above reaction formula, electrons move from the fuel electrode to the oxidant electrode through an external circuit, and hydrogen ions move in the electrolyte. Then, water is generated as a reaction product on the oxidant electrode side.

In many cases, the fuel gas for such a polymer electrolyte fuel cell is a hydrogen-rich reformed gas obtained by reforming an alcohol fuel such as methanol or a hydrocarbon fuel such as methane gas. Is used. For example,
Taking an example of methanol reforming, as shown in equation (3),
A reaction is performed in which water vapor is added at 200 to 300 ° C. to generate carbon dioxide gas and hydrogen.

CH ₃ OH + H ₂ O → CO ₂ + 3H ₂ (3) In addition to this, a reaction of CH ₃ OH → CO + 2H ₂ (4) also occurs. Generated.

When a reformed gas containing a by-product is directly supplied to the fuel electrode of the battery, a phenomenon occurs in which the contained CO is adsorbed on the platinum catalyst of the fuel electrode, and the platinum catalyst is poisoned. When the catalyst is poisoned by CO, the reaction at the fuel electrode is hindered, and the cell performance is greatly reduced. For this reason,
Normally, the fuel gas discharged from the reformer is further passed through a shift converter or through a CO oxidation removing device (these are referred to as first-stage CO removing devices) to reduce the CO concentration, and then the fuel electrode of the battery is discharged. The method of supplying to the company is adopted.

In the case of a phosphoric acid type fuel cell, the cell operating temperature is 20
Since the temperature is around 0 ° C., the CO concentration in the fuel gas is several hundreds.
Even about ppm does not substantially affect battery performance.
However, since the operating temperature of the polymer electrolyte fuel cell is usually as low as room temperature to 80 ° C., if the fuel gas contains several hundred ppm of CO, poisoning of the catalyst occurs. Literature (R.
A. Lemons, J. of Power Souurce, vol.29, pp.251-264
(1990)) reports that the allowable concentration of CO when the polymer electrolyte fuel cell is operated at 80 ° C. is 10 ppm. Therefore, in order to remove CO from a reformed gas containing several hundred ppm of CO, the gas that has passed through the first-stage CO removal device is further subjected to second-stage CO such as selective oxidation.
It must be passed through a removal device. However, even if the CO concentration is passed through the second-stage CO removal device, the CO concentration is reliably set to the allowable value of 1.
It is difficult to reduce it to 0 ppm or less. For this reason, it is necessary to further pass through the third stage CO removal device, and there is a problem that the system configuration becomes complicated.

In addition, instead of the third-stage CO removing device, the oxidizing agent is mixed in accordance with the CO concentration in the fuel gas to thereby reduce the CO.
A method of suppressing poisoning (JP-A-6-251786) has also been considered. However, in this method, instead of providing a third-stage CO removal device, a new sensor for detecting the CO concentration in the fuel gas and a gas mixing control device for supplying an oxidant according to the CO concentration are required. Becomes Also, CO
The sensor must be able to follow the concentration fluctuation, and accordingly, an appropriate amount of the oxidizing agent must be supplied by the gas mixing controller. If a malfunction occurs in these devices, there is a new problem that the platinum catalyst of the fuel electrode is poisoned due to insufficient oxidizing agent, and an excessive supply of the oxidizing agent causes an oxidation reaction with hydrogen to lower the battery voltage. Will occur.

[0013]

As described above, in a conventional polymer electrolyte fuel cell, if CO is contained in a fuel gas, the fuel electrode catalyst is poisoned by the CO, and the fuel cell is poisoned. In order to reduce the performance, if a fuel gas that can be used is specified, or if an attempt is made to use a fuel gas obtained by reforming an alcohol-based fuel or a hydrocarbon-based fuel, large-scale incidental facilities will be required. There was a problem that needed.

Therefore, the present invention can suppress the poisoning of the fuel electrode catalyst by CO in the fuel gas despite having a simple structure, and can therefore use the fuel gas without using large-scale auxiliary equipment. It is an object of the present invention to provide a polymer electrolyte fuel cell capable of expanding the range of the above and a method of operating the same.

[0015]

In order to achieve the above object, a polymer electrolyte fuel cell according to the present invention comprises a platinum-ruthenium catalyst having a ruthenium content based on platinum of not less than 50% by weight and not more than 85% by weight. The fuel electrode is provided, and the operating temperature of the battery is between 100 ° C. and 120 ° C.

Although carbon is used as a support for the catalyst, the content of carbon relative to the whole catalyst is 20 to 20%.
Preferably it is 60% by weight.

Further, in order to achieve the above object, in the operating method according to the present invention, the fuel electrode includes a platinum-ruthenium catalyst having a ruthenium content of 50% by weight or more and 85% by weight or less with respect to platinum, and Battery operating temperature is 100
When operating the polymer electrolyte fuel cell at a temperature between 120 ° C. and 120 ° C., an internal humidification method of humidifying the polymer electrolyte membrane via the fuel electrode is employed, and the fuel gas is supplied to the fuel cell at a temperature of 2 ° C.
was supplied at a pressure of ^{kg / cm 2 ~4kg / cm 2} , the oxidant gas is supplied at a pressure of ^{2kg / cm 2 ~4kg / cm 2} , the part is cooling water which is a humidifying water of the internal humidifying system The fuel gas is supplied at a pressure equal to or higher than the supply pressure of the fuel gas.

The platinum-ruthenium catalyst having the above composition is hardly poisoned by CO. Further, when the operating temperature of the battery is raised to the above temperature, it becomes possible to bring the fuel electrode catalyst closer to the direction in which CO is less likely to be poisoned.

Further, when the content of carbon, which is a carrier of the catalyst, decreases, the metal concentration in the catalyst increases.
Not only is the production cost of the catalyst high, but it is extremely difficult to handle in the production process, for example, it becomes easy to catch fire, and the conductivity of the catalyst is reduced. Therefore, the above range is preferable.

In operating the solid polymer electrolyte fuel cell having the catalyst having the above composition and having the above temperature range in the internal humidification system, the supply pressure of the fuel gas and the oxidizing gas is set to a value lower than the partial pressure of steam. Since it needs to be a large value, 2
kg / cm ² or more is required. Further, when the supply pressure is increased, the pressurizing power is increased, and the efficiency of the entire battery system is reduced. Therefore, it is necessary to suppress the upper limit to 4 kg / cm ² . Further, the pressure of the cooling water, part of which is humidification water of the internal humidification method, needs to be equal to or higher than the supply pressure of the fuel gas in order to stably supply the humidification water.

[0021]

Embodiments of the present invention will be described below with reference to the drawings.

FIG. 1 is an exploded perspective view of a polymer electrolyte fuel cell according to one embodiment of the present invention.

This polymer electrolyte fuel cell has a single cell 21
Are formed in a laminated structure in which a plurality of humidified water permeable plates 22 to be described later and a cooling plate 23 having a cooling water guiding function and a separator function are interposed between each other.

The single cell 21 has a polymer electrolyte membrane 24 formed of the same material as that of a known cell. On both surfaces of the polymer electrolyte membrane 24, a fuel electrode 25 and an oxidizer electrode 26 formed in areas smaller than the polymer electrolyte membrane are arranged in contact with each other. Gas seal packings 27 and 28 formed of a sealing material having substantially the same thickness as each electrode are arranged on the outer peripheral portions of the fuel electrode 25 and the oxidant electrode 26.

Here, the fuel electrode 25 is formed as follows. That is, as shown in FIG. 3A, a slurry of carbon powder and a water repellent is applied to one surface of the carbon porous body 29, and this is sintered at 360 ° C. to form the gas diffusion layer 30. Formed, and platinum (Pt) is formed on the gas diffusion layer 30.
And a catalyst layer 31 made of ruthenium (Ru) and carbon (C). The catalyst layer 31 has, for example, a composition ratio of Pt: Ru: C = 30:
A catalyst slurry for an anode is prepared by mixing a carbon-supported catalyst, a fluoropolymer solution, and water mixed at a ratio of 30:40, and gas diffusion is performed so that the amount of supported platinum becomes 1.5 mg / cm ^2. It is formed by coating on the layer 30. The catalyst layer 31 is arranged so as to be located on the polymer electrolyte membrane 24 side.

On the other hand, as shown in FIG. 3 (b), the oxidant electrode 26 is formed by applying a slurry of carbon powder and a water repellent to one surface of a carbon porous body 29 and firing the slurry at 360.degree. To form a gas diffusion layer 30,
Catalyst layer 3 made of platinum (Pt) and carbon (C) on top
2 is provided. The catalyst layer 32 was prepared by mixing a carbon-supported catalyst having a composition ratio of Pt: C = 50: 50, a fluorinated polymer solution, and water to form an oxidant electrode catalyst slurry, Is 1.5mg / cm
It is formed by coating on the gas diffusion layer 30 so as to be ² . The catalyst layer 32 is arranged so as to be located on the polymer electrolyte membrane 24 side.

On the lower surface side of the fuel electrode 25 in FIG.
A fuel electrode-side current collector plate 33 that has a function of supplying fuel gas to the fuel cell 5 and a function of collecting current is disposed in contact with the fuel electrode 5. The fuel electrode side current collector 33 is formed of a hydrophilic carbon porous plate. As shown in FIG. 2, a plurality of guide grooves 34 for passing fuel gas are formed on the contact surface of the fuel electrode side current collector plate 33 with the fuel electrode 25. Similarly, oxidizer electrode 2
6 on the upper surface side in FIG. 1, an oxidant electrode-side current collector plate 35 that exhibits a function of supplying an oxidant gas to the oxidant electrode 26 and a current collecting function.
Are arranged in contact. This oxidant electrode side current collector plate 35
It is formed of a dense carbon plate. As shown in FIG. 2, a plurality of guide grooves 36 for allowing the oxidant gas to flow are formed on the contact surface of the oxidant electrode side current collector plate 35 with the oxidant electrode 26.

On the other hand, the above-mentioned humidified water permeable plate 22 is disposed in contact with the lower surface side of the fuel electrode side current collector plate 33 in FIG.
A cooling plate 23 is arranged in contact with the humidified water permeable plate 22 on the lower surface side in FIG. The humidification water permeable plate 22 is formed of a hydrophilic carbon porous thin plate, and the cooling plate 23 is formed of a dense carbon plate or a metal plate. Cooling plate 2
A plurality of guide grooves 37 for guiding the cooling water are formed on the surface of the third humidified water permeable plate 22 side.

Both sides of the humidified water permeable plate 22, both sides of the cooling plate 23, both sides of the polymer electrolyte membrane 24, the packing 2
As shown in FIG. 1, holes 50 and 51 for supplying / discharging the fuel gas are provided on both sides of the fuel cells 7 and 28, respectively (however,
The holes 51 are not shown), the holes 52 and 53 for supplying / discharging the cooling water, and the holes 54 and 55 for supplying / discharging the oxidizing gas are provided so as to communicate in the stacking direction. .

The guide groove 34 provided on the fuel electrode side current collector 33 has holes 50 for supplying / discharging the fuel gas.
The guide groove 36 provided in the oxidant electrode side current collector plate 35 is provided with holes 54 and 55 for supplying / discharging the oxidant gas.
The guide groove 37 provided in the cooling plate 23 communicates with holes 52 and 53 for supplying / discharging cooling water.

The fuel cell stack 70 is formed by stacking a plurality of the single cells 21, the humidified water permeable plate 22, and the cooling plate 23 thus configured. Conductive end plates 71, 7 are provided on both end faces of the fuel cell stack 70 in the stacking direction.
2 and the end plates 71, 7
A clamping plate (not shown) wider than the end plate is applied to the outer surface of the second plate, and both clamping plates are clamped in the laminating direction with insulating rods under the condition that a spring is interposed at the peripheral edge of these clamping plates. ing.

The upper surface of the end plate 71 is provided with a fuel supply pipe 73 and a fuel discharge pipe 74 for supplying / discharging the fuel gas through the holes 50 and 51 and the holes 52 and 53 described above. A cooling water supply pipe 75 and a cooling water discharge pipe 76 for supplying / discharging the cooling water through the
An oxidizing gas supply pipe 77 and an oxidizing gas discharge pipe 78 for supplying / discharging the oxidizing gas via the holes 4 and 55 are provided in such a manner as to communicate with the corresponding holes.

With such a configuration, the fuel supply pipe 73
Gas supplied through the fuel (supply pressure 2 to 4 kg / c
m ² ) flows through each guide groove 34 provided in the fuel electrode side current collector 33 in each unit cell 21. Then, a part thereof is diffused to the fuel electrode 25 and used for power generation, and the remaining part flows to the hole 51 and then flows to the fuel discharge pipe 74. The oxidizing gas supplied through the oxidizing agent supply pipe 77 (supply pressure 2 to 4 k
g / cm ² ) flows through each guide groove 36 provided in the oxidant electrode side current collector 35 in each single cell 21. Then, a part is diffused to the oxidizer electrode 26 and is used for power generation, and the rest is
After flowing to 5, it flows to the oxidant discharge pipe 78.

On the other hand, the cooling water (supply pressure 2 kg / cm ² or more) supplied through the cooling water supply pipe 75 is
3 flows through each guide groove 37 provided in the guide groove 3. Then, a part of the water passes through the humidified water permeable plate 23, the fuel electrode side current collector 33, and the fuel electrode 25, and is used for humidifying the polymer electrolyte membrane 24,
The remainder flows into the holes 53 after absorbing heat through the cooling plate 23, and then flows to the cooling water discharge pipe 76.

At this time, the temperature of the fuel cell stack 70 is maintained between 100 ° C. and 120 ° C. by a heater (not shown).

As described above, the function of the battery is exhibited by the supply of the fuel gas, the oxidizing gas and the cooling water.
In this case, the fuel electrode 25 is provided with the catalyst layer 31 having the above-described composition, that is, the carbon-supported catalyst layer 31 in which the content of Ru with respect to Pt is set to 50% by weight or more and 85% by weight or less. And the fact that the operating temperature of the battery is set between 100 ° C. and 120 ° C., so that even if the fuel gas contains CO, the poisoning of platinum in the catalyst layer 31 is prevented. Is suppressed, and stable power generation performance can be exhibited over a long period of time.

An experimental example confirming this fact will be described below.

Experimental Example 1 Regarding the fuel electrode 25, a slurry of carbon powder and a water repellent was applied to one surface of the carbon porous body 29, and this was sintered at 360 ° C. to form the gas diffusion layer 30. did. Further, a carbon-supported catalyst having a composition ratio of Pt: Ru: C = 30: 30: 40, a fluorine-based polymer solution, and water were mixed to prepare a fuel electrode catalyst slurry. The slurry is applied to the gas diffusion layer 30 so that the platinum loading is 1.5 mg / cm ^2.
The catalyst layer 31 was formed by coating on the upper surface.

On the other hand, with respect to the oxidizer electrode 26, a slurry of carbon powder and a water repellent is applied to one surface of the carbon porous body 29, and this is sintered at 360 ° C. to form the gas diffusion layer 30. did. Further, the composition ratio is Pt: C = 50: 5.
The carbon-supported catalyst, the fluoropolymer solution, and water were mixed to prepare an oxidant electrode catalyst slurry. This slurry was applied on the gas diffusion layer 30 so that the amount of supported platinum was 1.5 mg / cm ² , to form a catalyst layer 32.

[0040] sandwiched a fluorinated polymer membrane Nafion ^R 117 manufactured by DuPont in the these fuel electrode oxidant electrode was fabricated unit cell of the electrode area 100 cm ² by hot pressing.

The manufactured unit battery was sealed with Viton packing, sandwiched by a holder provided with a gas flow path, and battery temperature 1
A power generation test was performed at 10 ° C. and by an internal humidification method. At this time, the fuel electrode gas pressure was set to 4 kg / cm ^2, and a mixed gas of H ₂ + CO (50 ppm) was used as the fuel gas.
The mixture was bubbled at 30 ° C. and flowed at a gas utilization of 30%. On the oxidant electrode side, the gas pressure was 4 kg / cm ^2, and air flowed at a gas utilization of 50%.

A change in the battery voltage with time when the battery was operated at a current density of 0.4 A / cm ² is indicated by A in FIG. In addition,
For reference, the characteristics when operated at 80 ° C. are shown in FIG.
Indicated by When operating at 80 ° C., the battery voltage dropped significantly in a few hours, compared to 20 hours at 110 ° C.
Even after 00 hours, the voltage dropped by 1%.

Experimental Example 2 In the preparation process of the catalyst slurry for fuel electrode in Experimental Example 1,
A slurry of a carbon-supported catalyst having a composition ratio of Pt: Ru: C = 40: 20: 40 was prepared, and this was used to prepare a fuel electrode having a catalyst layer having a platinum support amount of 1.5 mg / cm ² .
In between this and the oxidant electrode of the platinum supported catalysts thermocompression bonding by hot pressing to sandwich the fluorinated polymer membrane Nafion ^R 117 manufactured by DuPont, was fabricated unit cell.

Under the same gas pressure conditions as in Experimental Example 1, a mixed gas of H ₂ + CO (100 ppm) was flowed through the fuel electrode.
Humidification by internal humidification method, battery operating temperature 120 ° C,
A power generation test was performed at a load of 0.4 A / cm ² . A battery using a catalyst supporting only platinum as a fuel electrode has a voltage drop of 20% in a few hours from the start of power generation, whereas a battery using a platinum-ruthenium catalyst has a voltage of only 4% even after 2000 hours. It just dropped.

EXPERIMENTAL EXAMPLE 3 In order to investigate the effect of the ruthenium content in the catalyst, the carbon weight ratio was fixed at 50% by weight, and the platinum-ruthenium-supported carbon catalyst having a ruthenium content with respect to platinum different from 20 to 90% by weight. The amount of supported platinum is 0.6
A fuel electrode was prepared in the same procedure as in Experimental Example 1 so as to obtain mg / cm ² . The electrode area of the fuel electrode, the oxidizer electrode, and the fluorine polymer membrane Nafion ^R 117 manufactured by DuPont is 10
Each unit battery of 0 cm ² was manufactured, and the battery temperature was 110
° C, gas pressure 2kg /
cm ² and H ₂ + CO (100 pp) on the fuel electrode side.
m) was flowed at a gas utilization of 40%, and air was flowed at a gas utilization of 50% to the oxidant electrode side, and a power generation test was performed by an internal humidification method.

Table 1 shows the initial battery voltage and 200
The battery voltage under a load of 0.4 A / cm ² after 0 hours is shown.

[0047]

[Table 1]

As can be seen from Table 1, as the content of ruthenium increases, the battery voltage decreases less, and good results are shown when the content of ruthenium with respect to platinum is in the range of 50 to 80% by weight. In particular, it can be seen that the voltage drop of the battery using the catalyst having a ruthenium content of 78% by weight is small. However, when the ruthenium content exceeds 85% by weight, the initial battery voltage decreases. This is thought to be due to the insufficient amount of platinum contributing to the reaction at the fuel electrode.

When the ruthenium content reaches 90% by weight,
This tendency was significant, and the battery voltage dropped to 20%.
From these results, it can be said that the ruthenium content suitable for the catalyst of the fuel electrode is in the range of 50 to 85% by weight based on platinum.

Experimental Example 4 The composition ratio was Pt: Ru: C = 20: 10: 70 (ruthenium content based on platinum: 67% by weight), and Pt: Ru: C =
25:15:60 (ruthenium content 63 with respect to platinum)
Experimental Example 1 using a platinum-ruthenium catalyst having a Pt: Ru: C ratio of 40:20:40 (ruthenium content based on platinum: 67% by weight) and a platinum-supported amount of 1.0 mg / cm ^2. Fuel electrodes having different carbon weight ratios were prepared in the same manner as described above.

From the initial performance of the unit cells manufactured using these fuel electrodes, the effect of the carbon weight ratio in the catalyst was examined. The operating conditions are the same as in Experimental Example 3. When the weight ratio of carbon to the entire catalyst is 60% by weight and 40% by weight, the battery voltage under a load of 0.4 A / cm ^{2 is} 0.1%.
Although good initial performances of 7 V and 0.729 V were obtained, the battery voltage at a load of 0.4 A / cm ² was 0.55 V at a load of 0.4 A / cm ² at a battery voltage of 70% by weight due to the influence of material diffusion control. It was remarkably low.

Thus, for example, those having a high carbon weight ratio, such as the composition ratio of the fuel electrode catalyst (carbon weight ratio is 80 to 90% by weight) of the phosphoric acid type fuel cell, are used for the polymer electrolyte fuel cell. When used as an electrode catalyst, the function as a catalyst cannot be sufficiently obtained, and the carbon weight ratio of the catalyst is 6%.
It was found that the content was desirably 0% by weight or less.

Conversely, for a catalyst having a small carbon weight ratio,
Since the metal concentration in the catalyst is increased, not only the production cost of the catalyst is increased, but also it is extremely difficult to handle in the production process such as easy ignition, and the conductivity of the catalyst is reduced. From this, it is considered that the carbon weight ratio suitable for the anode catalyst is 20 to 60% by weight.

In the embodiment shown in FIG. 1, the fuel gas and the oxidizing gas flow in a co-current system, but they may flow in a counter-current system or a cross-current system. Further, the humidification method is not limited to the embodiment shown in FIG. But,
When the internal humidification method as shown in FIG. 1 is adopted, the effect of suppressing the poisoning of the platinum catalyst at the fuel electrode is large.

As the electrode catalyst for the oxidant electrode, an alloy catalyst may be used in addition to the platinum catalyst.

[0056]

According to the present invention, a platinum-ruthenium catalyst layer which is hardly poisoned by CO is provided on the fuel electrode, and the battery is operated at 100 ° C. or higher, so that an environment in which the fuel electrode catalyst is hardly poisoned by CO is created. CO concentration is 10
Even if a fuel gas exceeding ppm is supplied, stable battery characteristics can be exhibited over a long period of time. Therefore, an additional facility for reducing the CO concentration in the fuel gas to 10 ppm or less can be eliminated, which contributes to simplification of the fuel cell system.

[Brief description of the drawings]

FIG. 1 is an exploded perspective view of a polymer electrolyte fuel cell according to an embodiment of the present invention.

FIG. 2 is a sectional view partially showing the fuel cell;

FIG. 3 is a configuration explanatory view of a fuel electrode and an oxidizer electrode incorporated in the fuel cell.

FIG. 4 is a diagram showing the aging characteristics of the fuel cell in comparison with a reference example.

[Explanation of symbols]

 DESCRIPTION OF SYMBOLS 21 ... Single cell 22 ... Humidified water permeable plate 23 ... Cooling plate 24 ... Polymer electrolyte membrane 25 ... Fuel electrode 26 ... Oxidizer electrode 27, 28 ... Packing 29 ... Carbon porous body 30 ... Gas diffusion layers 31, 32 ... Catalyst Layer 33: Fuel electrode side current collectors 34, 36, 37 ... Guide grooves 35 ... Oxidizer electrode side current collectors 50, 51 ... Holes for supplying / discharging fuel gas 52, 53 ... Supply / discharge of cooling water Holes 54, 55 ... holes for supplying / discharging the oxidizing gas 71, 72 ... end plates

──────────────────────────────────────────────────の Continued on the front page (58) Field surveyed (Int. Cl. ⁶ , DB name) H01M 4/90-4/92 B01J 23/46 301 H01M 8/00-8/24

Claims (3)

(57) [Claims] 1. A fuel electrode comprising a platinum-ruthenium catalyst having a ruthenium content based on platinum of not less than 50% by weight and not more than 85% by weight, and operating temperature of the battery is 100 ° C. to 1%.
A polymer electrolyte fuel cell, wherein the temperature is between 20 ° C. 2. A composition comprising platinum, ruthenium, and carbon, wherein the content of ruthenium with respect to platinum is not less than 50% by weight and not more than 85% by weight, and the content of carbon with respect to the whole is from 20 to 85% by weight.
A polymer electrolyte fuel cell, characterized in that the fuel electrode has a catalyst of 60% by weight and the operating temperature of the cell is between 100 ° C and 120 ° C. 3. A fuel electrode comprising a platinum-ruthenium catalyst having a ruthenium content based on platinum of not less than 50% by weight and not more than 85% by weight, and having an operating temperature of the battery of 100 ° C. to 1%.
In operating the polymer electrolyte fuel cell at a temperature between 20 ° C., an internal humidification method of humidifying the polymer electrolyte membrane through the fuel electrode is employed, and the fuel gas is supplied at 2 kg / c.
m ² -4 kg / cm ² , and oxidant gas
was supplied at a pressure of ^{kg / cm 2 ~4kg / cm 2} , so a portion of which supplies cooling water to be humidifying water of the internal humidifying system at equal to or higher pressure to the feed pressure of the fuel gas A method for operating a polymer electrolyte fuel cell, comprising: