ELECTRODE BINDER USING ALCOHOL BASED SOLVENT FOR POLYMER ELECTROLYTE MEMBRANE FUEL CELL AND METHOD FOR PREPARING THE SAME

Abstract

Disclosed is an alcohol mixture typed hydrocarbon based electrode binder for a polymer electrolyte membrane fuel cell. The binder may be directly applied to a hydrocarbon based electrolyte membrane of the same kind, and may exhibit a superior fuel cell performance over conventional hydrocarbon polymer binders using an organic solvent.

Claims

1. An electrode binder composition for a polymer electrolyte membrane fuel cell, comprising an alcohol based solvent comprising water and an alcohol; and a hydrocarbon based polymer binder.

2. The electrode binder composition for a polymer electrolyte membrane fuel cell according to claim 1, wherein the alcohol has a boiling point of less than 150 C.

3. The electrode binder composition for a polymer electrolyte membrane fuel cell according to claim 2, wherein the alcohol is one or more selected from the group consisting of 1-propanol, isopropanol, and ethanol.

4. The electrode binder composition for a polymer electrolyte membrane fuel cell according to claim 1, wherein the hydrocarbon polymer binder comprises a partially fluorinated hydrocarbon based polymer binder.

5. The electrode binder composition for a polymer electrolyte membrane fuel cell according to claim 1, wherein the hydrocarbon polymer binder is a polymer selected from the group consisting of sulfonated polyarylene ether sulfone, sulfonated polyimide, polysulfone, polyether sulfone, polyarylene ether ketone, polyether ether ketone, polybenzimidazole, polybenzoxazole, polybenzothiazole, and polyphosphazene, a copolymer of the polymer, or a mixture of two or more of the polymer.

6. The electrode binder composition for a polymer electrolyte membrane fuel cell according to claim 1, wherein the alcohol based solvent contains, by weight, 5 to 95% of an alcohol and 95 to 5% of water.

7. The electrode binder composition for a polymer electrolyte membrane fuel cell according to claim 1, wherein the mixture of an alcohol based solvent and a hydrocarbon based polymer binder contains 1 to 20 wt % of the hydrocarbon based polymer binder.

8. A catalyst slurry for a polymer electrolyte membrane fuel cell, comprising a composition of claim 1; and a catalyst.

9. A method for preparing an electrode binder composition for a polymer electrolyte membrane fuel cell, comprising: preparing an alcohol based solvent comprising water and an alcohol; and mixing the alcohol based solvent with a hydrocarbon based polymer binder.

10. The method for preparing an electrode binder composition for a polymer electrolyte membrane fuel cell according to claim 9, wherein the hydrocarbon polymer binder is added to the alcohol based solvent with stirring and heating to a temperature higher than room temperature and less than 60 C.

11. A method for preparing a catalyst slurry for a polymer electrolyte membrane fuel cell, comprising: preparing an alcohol based solvent comprising water and an alcohol; mixing the alcohol based solvent with a hydrocarbon based polymer binder to prepare an electrode binder composition; and mixing the electrode binder composition with a catalyst to prepare a catalyst slurry.

12. A method for preparing a membrane electrode assembly for a polymer electrolyte membrane fuel cell, comprising: directly coating the catalyst slurry for a polymer electrolyte membrane fuel cell according to claim 8 on a hydrocarbon based electrolyte membrane of the same kind as the hydrocarbon based polymer binder of the catalyst slurry.

13. The method for preparing a membrane electrode assembly for a polymer electrolyte membrane fuel cell according to claim 12, wherein the direct coating is performed using a catalyst coated membrane (CCM) method.

Description

BRIEF DESCRIPTION OF THE DRAWINGS

[0020] The above and other aspects, features and advantages of the disclosed example embodiments will be more apparent from the following detailed description taken in conjunction with the accompanying drawings in which:

[0021] FIG. 1A shows a photograph of the alcohol mixture typed electrode binder according to Example of the present invention.

[0022] FIG. 1B shows a photograph of the polymer solution typed electrode binder using an organic solvent of Comparative Example.

[0023] FIG. 2 shows the evaluation results of the fuel cell performance of the polymer solution typed electrode binder prepared in Comparative Example of the present invention.

[0024] FIG. 3A shows evaluation results of the fuel cell performance of the alcohol mixture typed electrode binder prepared in Example of the present invention, illustrating the result of a supply of stoichiometric hydrogen and air.

[0025] FIG. 3B shows evaluation results of the fuel cell performance of the alcohol mixture typed electrode binder prepared in Example of the present invention, illustrating the result of a supply of hydrogen and oxygen.

[0026] FIG. 4 shows evaluation results of the performance of a fuel cell in which the alcohol mixture typed electrode binder prepared in Example of the present invention has been applied to a hydrocarbon electrolyte membrane of the same kind.

DETAILED DESCRIPTION

[0027] Exemplary embodiments are described more fully hereinafter. The invention may, however, be embodied in many different forms and should not be construed as limited to the exemplary embodiments set forth herein. Rather, these exemplary embodiments are provided so that this disclosure will be thorough and complete, and will fully convey the scope of the invention to those skilled in the art. In the description, details of features and techniques may be omitted to more clearly disclose exemplary embodiments.

Term Definition

[0028] In the present disclosure, the term hydrocarbon based polymer binder may encompass a partially fluorinated hydrocarbon based polymer binder.

[0029] In the present disclosure, the term hydrocarbon based polymer of the same kind refers that a main chain of a polymer binder has the same structure as a main chain of an electrolyte of the electrolyte membrane.

Description of Exemplary Embodiments

[0030] Hereinafter, exemplary embodiments of the present invention will be described in detail.

[0031] The present inventors have made it possible to directly form an electrode on a hydrocarbon based electrolyte membrane of the same kind as a hydrocarbon based polymer binder using the CCM (catalyst coated membrane) method, by preparing an alcohol mixture typed binder using an alcohol based solvent instead of a conventional organic solvent.

[0032] Specifically, in exemplary embodiments of the present invention, provided is an electrode binder composition for a polymer electrolyte membrane fuel cell, comprising an alcohol based solvent comprising water and an alcohol; and a hydrocarbon based polymer binder.

[0033] In other exemplary embodiments of the present invention, provided is a catalyst slurry for a polymer electrolyte membrane fuel cell, comprising an alcohol based solvent comprising water and an alcohol; and a hydrocarbon based polymer binder.

[0034] Further, in other exemplary embodiments of the present invention, provided is a method for preparing an electrode binder composition for a polymer electrolyte membrane fuel cell, comprising: preparing an alcohol based solvent comprising water and an alcohol; and mixing the alcohol based solvent with a hydrocarbon based polymer binder.

[0035] Further, in other exemplary embodiments of the present invention, provided is a method for preparing a catalyst slurry for a polymer electrolyte membrane fuel cell, comprising: preparing an alcohol based solvent comprising water and an alcohol; mixing the alcohol based solvent with a hydrocarbon based polymer binder to prepare an electrode binder composition; and mixing the electrode binder composition with a catalyst to prepare a catalyst slurry.

[0036] In one exemplary embodiment, the alcohol is not particularly limited, but it preferably has a boiling point of less than 150 C., for example, 10030 C. In a non-limiting example, examples of the alcohol may include 1-propanol, isopropanol and ethanol.

[0037] In a non-limiting example, the alcohol may be, for example, 1-propanol represented by Formula 1. For reference, the boiling point of 1-propanol is 97 C.

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[0038] In one exemplary embodiment, the alcohol may be mixed with water, for example, distilled water, to produce an alcohol based solvent.

[0039] The alcohol is mixed well with water, because water is readily miscible with alcohol and has a boiling point of less than 100 C. In addition, water is preferable because it may disperse hydrocarbon based polymers, particularly polymers substituted with a sulfonic acid group which are used in combination therewith

[0040] In a non-limiting example, 5 to 95% by weight of an alcohol such as 1-propanol etc. is mixed with 95 to 5% by weight of water. When the ratio is outside this range, the polymer may precipitate.

[0041] A hydrocarbon based polymer binder is added to the resultant alcohol based solvent, and the mixture is heated to a room temperature or higher with stirring to prepare a binder.

[0042] In one exemplary embodiment, for example, sulfonated polyarylene ether sulfone may be used as the hydrocarbon polymer binder, although not particularly limited thereto. Further, sulfonated polyimide, polysulfone, polyether sulfone, polyarylene ether ketone, polyether ether ketone, polybenzimidazole, polybenzoxazole, polybenzothiazole, polyphosphazene, and polymer materials made of copolymers and blends thereof may be used as the hydrocarbon based polymer binder.

[0043] In a non-limiting example, the concentration of a polymer binder in the mixture of an alcohol based solvent and a binder may be, for example, 1 to 20 wt %, for example 5 wt %. When the solution has a concentration within the above range, the viscosity of the solution may be about 1000 cp or less, which makes it easy to prepare catalyst slurry.

[0044] In a non-limiting example, for example, a hydrocarbon polymer binder may be added to an alcohol based solvent and stirred while heating to a temperature higher than room temperature, for example, to 40 to 60 C. If the temperature is higher than 60 C., it may promote a volatilization of the alcohol based solvent. The solvent and the polymer are mixed over time, resulting in an opaque milky color.

[0045] Then, the resultant electrode binder, together with a commercial catalyst, may be prepared into catalyst ink or catalyst slurry, and an electrode layer may be formed on a hydrocarbon based electrolyte membrane by the CCM (catalyst coated membrane) method to form a membrane electrode assembly. Then, a fuel cell may be constructed therefrom.

[0046] Thus, in other exemplary embodiments of the present invention, provided is a method for preparing a membrane electrode assembly for a polymer electrolyte membrane fuel cell, comprising: directly coating the catalyst slurry for a polymer electrolyte membrane fuel cell on a hydrocarbon based electrolyte membrane of the same kind as the hydrocarbon based polymer binder using the catalyst coated membrane (CCM) method.

[0047] Further, in other exemplary embodiments of the present invention, provided is an electrode for a polymer electrolyte membrane fuel cell, prepared from a catalyst slurry for a polymer electrolyte membrane fuel cell comprising a catalyst; an alcohol based solvent comprising water and an alcohol; and a hydrocarbon based polymer binder.

[0048] In addition, in other exemplary embodiments of the present invention, provided is a membrane electrode assembly for a polymer electrolyte membrane fuel cell, prepared by directly coating a catalyst slurry for a polymer electrolyte membrane fuel cell on a hydrocarbon electrolyte membrane of the same kind as the polymer binder, using the catalyst coated membrane (CCM) method.

[0049] In addition, in other exemplary embodiments of the present invention, a polymer electrolyte membrane fuel cell comprising the membrane electrode assembly is provided.

[0050] Hereinafter, a specific example according to exemplary embodiments of the present invention will be described in more detail. It should be understood, however, that the invention is not limited to the following example, but that various changes may be made without departing from the scope of the appended claims. It is to be understood that the following example is provided merely to make the disclosure complete and to facilitate the practice of the invention by those skilled in the art.

SYNTHESIS EXAMPLES

Example

Preparation of an Electrode Binder using an Alcohol Based Solvent

[0051] 0.05 g of polyarylene ether sulfone polymer substituted with a sulfonic acid group is added to a solvent obtained by mixing 0.633 g of 1-propanol and 0.317 g of distilled water, and the mixture is stirred at 40 C. As a result, a mixture having an opaque milk color is prepared.

Comparative Example

Preparation of an Electrode Binder using an Organic Solvent

[0052] The same binder preparation method as the above example is used except that 0.95 g of an organic solvent (dimethylacetamide) is used instead of an alcohol mixture solvent, and that 0.05 g of the same polymer is dissolved at 60 C. with stirring. As a result, a pale yellow transparent polymer solution is prepared.

Fuel Cell Construction and Evaluation of Characteristics Thereof

[0053] The respective binders of Example and Comparative Example are used. The composition of the catalyst electrode slurry is as follows: 64.3 mg of 46.7 wt % Pt/C, 12 ml of isopropanol, and 321.2 mg of a binder. Nafion NR212 and a polymer electrolyte membrane of poly(arylene ether sulfone) substituted with a sulfonic acid group is used as electrolyte membranes. An electrode assembly is prepared by coating a catalyst layer with an area of 25 cm.sup.2 on an electrolyte membrane using the CCM method so that the amount of platinum catalyst per unit area is 0.4 mg/cm.sup.2. The performance of the fuel cell is evaluated by measuring the voltage at a current while increasing the current from 0 A by 0.5 A, and expressing the measurements as current densities and power densities.

[0054] FIGS. 1A and 1B show the photographs of the electrode binders with a concentration of 5 wt % of Example and Comparative Example of the present invention, prepared using an alcohol based solvent and an organic solvent, respectively.

[0055] The alcohol mixture typed binder of Example (FIG. 1A) exhibits an opaque milky color, and the binder using an organic solvent of Comparative Example (FIG. 1B), is prepared as a pale yellow transparent polymer solution.

[0056] FIG. 2 is a current-voltage polarization curve drawn by evaluating the fuel cell performance of the polymer solution typed binder of Comparative Example.

[0057] The fuel cell is operated at a cell temperature of 65 C. and a relative humidity of 95% with a supply of stoichiometric hydrogen and air. The results show that the current density is 62 mA/cm.sup.2 at 0.6 V and the maximum power density is 46 mW/cm.sup.2.

[0058] FIGS. 3A and 3B are current-voltage polarization curves drawn by evaluating the fuel cell performance of the alcohol mixture typed binder prepared in Example of the present invention.

[0059] The fuel cell is operated at a cell temperature of 80 C. and a relative humidity of 95% with a supply of stoichiometric hydrogen and air. The results shows that the current density is 385 mA/cm.sup.2 at 0.6 V and the maximum power density is 267 mW/cm.sup.2 (FIG. 3A).

[0060] On the other hand, when oxygen is sufficiently supplied instead of air, the current density is 840 mA/cm.sup.2 at 0.6 V and the maximum power density is 618 mW/cm.sup.2 (FIG. 3B).

[0061] FIG. 4 shows the comparison results of the performance of fuel cells obtained by applying the alcohol mixture typed binder prepared in Example of the present invention to a Nafion electrolyte membrane from DuPont, which is a commercial membrane, and a hydrocarbon membrane of polyarylene ether sulfone substituted with a sulfonic acid, respectively.

[0062] The fuel cell is operated at a cell temperature of 80 C. and a relative humidity of 95% with a supply of hydrogen and oxygen. The results show that when the prepared electrode binder is applied to a hydrocarbon electrolyte membrane of the same kind, it exhibits the maximum power density of about 500 mW/cm.sup.2 although it has a power density about 100 mW/cm.sup.2 lower than a case where a Nafion electrolyte membrane is applied, which in turn demonstrates that an excellent performance is achieved in the Example.

[0063] According to exemplary embodiments of the present invention, a hydrocarbon based electrode binder mixed with an alcohol may achieve good bonding without formation of pinholes, etc. when applied to a hydrocarbon based electrolyte membrane of the same kind, and it is easy to handle and prepare. When an organic solvent is used, there is a possibility of pinhole formation, in which an electrolyte membrane may be partially dissolved, due to the residual organic solvent. However, when alcohol is used, it does not dissolve the electrolyte membrane. In addition, the use of alcohol may facilitate handling and preparation because it has a higher volatility than organic solvents.

[0064] Accordingly, it is possible to apply the catalyst coated membrane (CCM) method, in which an electrode layer is directly formed on a hydrocarbon based electrolyte membrane of the same kind using a hydrocarbon based electrode binder, without using an organic solvent. In addition, there is no problem of formation of pinholes in the electrolyte membrane of a polymer electrolyte membrane fuel cell or the accompanying deterioration of the durability of the fuel cell. Further, it is possible to achieve a superior fuel cell performance over the case of using a polymer solution typed binder using an organic solvent.

[0065] While the present invention has been described with respect to the specific embodiments, it will be apparent to those skilled in the art that various changes and modifications may be made without departing from the spirit and scope of the invention as defined in the following claims.