Antioxidant for fuel cells and membrane-electrode assembly including the same

Abstract

Disclosed are an antioxidant for fuel cells and a membrane-electrode assembly including the same. The membrane-electrode assembly may have obtained greatly improved durability by using an antioxidant having a novel composition that may provide excellent antioxidant activity and long-term durability.

Claims

1. A membrane-electrode assembly for fuel cells comprising: an electrolyte membrane comprising a perfluorinated sulfonic acid-based ionomer and an antioxidant; and a pair of electrodes formed on both surfaces of the electrolyte membrane, wherein at least one of the electrolyte membrane and the electrodes comprises the antioxidant, wherein the electrolyte membrane comprises the antioxidant in an amount of about 0.05 wt % to 20 wt % based on a total weight of the perfluorinated sulfonic acid-based ionomer and the antioxidant, wherein the antioxidant comprising tin (Sn) and cerium oxide, wherein the cerium oxide is doped with the tin (Sn), and wherein the Sn-doped cerium oxide is represented by the following Formula 1:
SnxCe1-xO2-δ  [Formula 1] wherein x satisfies 0<x≤0.5 and δ is an oxygen vacancy value making the compound of Formula 1 electrically neutral.

2. The membrane-electrode assembly according to claim 1, wherein the electrolyte membrane further comprises a porous reinforcement layer, wherein the electrolyte membrane comprises the perfluorinated sulfonic acid-based ionomer and the antioxidant impregnated into the reinforcement layer.

3. A fuel cell comprising the membrane-electrode assembly according to claim 1.

4. A vehicle comprising the fuel cell according to claim 3.

Description

BRIEF DESCRIPTION OF THE DRAWINGS

(1) The above and other features of the present invention will now be described in detail with reference to certain exemplary embodiments thereof illustrated in the accompanying drawings which are given hereinbelow by way of illustration only, and thus are not limitative of the present invention, and wherein:

(2) FIG. 1 is a sectional view schematically illustrating an exemplary membrane-electrode assembly according to an exemplary embodiment of the present invention;

(3) FIG. 2 is a sectional view schematically illustrating an exemplary configuration of an exemplary electrolyte membrane according to an exemplary embodiment of the present invention;

(4) FIG. 3 is a sectional view schematically illustrating an exemplary configuration of an exemplary electrolyte membrane according to an exemplary embodiment of the present invention;

(5) FIGS. 4A-4C show the results of evaluation of antioxidant activities of Example 1, Comparative Example 1 and Comparative Example 2 of the present invention using a methyl violet method. FIG. 4A shows the result of Example 1, FIG. 4B shows the result of Comparative Example 1, and FIG. 4C shows the result of Comparative Example 2;

(6) FIG. 5 shows the results of evaluation of antioxidant activities of Example 1, Comparative Example 1 and Comparative Example 2 using UV-visible spectroscopy; and

(7) FIG. 6 shows the results of evaluation of the long-term durability of the electrolyte membranes according to an exemplary embodiment (Example 2) of the present invention, Comparative Example 3 and Comparative Example 4.

DETAILED DESCRIPTION

(8) The objects described above, and other objects, features and advantages will be clearly understood from the following preferred embodiments with reference to the annexed drawings. However, the present invention is not limited to the embodiments and will be embodied in different forms. The embodiments are suggested only to offer thorough and complete understanding of the disclosed contents and sufficiently inform those skilled in the art of the technical concept of the present invention.

(9) It will be understood that the terms “comprise”, “include”, “have”, etc. and the like, when used in this specification, specify the presence of stated features, numbers, steps, operations, elements, components or combinations thereof, but do not preclude the presence or addition of one or more other features, numbers, steps, operations, elements, components, or combinations thereof. In addition, it will be understood that, when an element such as a layer, film, region or substrate is referred to as being “on” another element, it can be directly on the other element, or an intervening element may also be present. It will also be understood that, when an element such as a layer, film, region or substrate is referred to as being “under” another element, it can be directly under the other element, or an intervening element may also be present.

(10) As used herein, the singular forms “a,” “an” and “the” are intended to include the plural forms as well, unless the context clearly indicates otherwise.

(11) It is understood that the term “vehicle” or “vehicular” or other similar term as used herein is inclusive of motor vehicles in general such as passenger automobiles including sports utility vehicles (SUV), buses, trucks, various commercial vehicles, watercraft including a variety of boats and ships, aircraft, and the like, and includes hybrid vehicles, electric vehicles, plug-in hybrid electric vehicles, hydrogen-powered vehicles and other alternative fuel vehicles (e.g. fuels derived from resources other than petroleum). As referred to herein, a hybrid vehicle is a vehicle that has two or more sources of power, for example both gasoline-powered and electric-powered vehicles.

(12) Unless mentioned otherwise, all numbers, figures and/or expressions that represent ingredients, reaction conditions, polymer compositions and amounts of mixtures used in the specification are approximations that reflect various uncertainties of measurement occurring inherently in obtaining these figures among other things. For this reason, it should be understood that, in all cases, the term “about” should modify all such numbers, figures and/or expressions. For example, the term “about” is understood as within a range of normal tolerance in the art, for example within 2 standard deviations of the mean. “About” can be understood as within 10%, 9%, 8%, 7%, 6%, 5%, 4%, 3%, 2%, 1%, 0.5%, 0.1%, 0.05%, or 0.01% of the stated value. Unless otherwise clear from the context, all numerical values provided herein are modified by the term “about.” In addition, when numeric ranges are disclosed in the description, these ranges are continuous and include all numbers from the minimum to the maximum including the maximum within each range unless otherwise defined. Furthermore, when a range refers to integer values, it includes all integers from the minimum to the maximum including the maximum within the range, unless otherwise defined.

(13) FIG. 1 is a sectional view schematically illustrating an exemplary membrane-electrode assembly 1 according to an exemplary embodiment of the present invention. The membrane-electrode assembly 1 may include an electrolyte membrane 10 and a pair of electrodes 20 formed on both surfaces of the electrolyte membrane 10. Here, the term “a pair of electrodes” means an anode and a cathode, which face each other based on the electrolyte membrane.

(14) Preferably, at least one of the electrolyte membrane 10 and the pair of electrodes 20 may include an antioxidant.

(15) FIG. 2 is a sectional view schematically illustrating an exemplary configuration of an exemplary electrolyte membrane 10 according to an exemplary embodiment of the present invention. The electrolyte membrane 10 may be a single layer containing a mixture 11 of a perfluorinated sulfonic acid-based ionomer and an antioxidant.

(16) FIG. 3 is a sectional view schematically illustrating an exemplary configuration of an exemplary electrolyte membrane 10 according to an exemplary embodiment of the present invention. The electrolyte membrane 10 may have a tri-layer structure in which a reinforcement layer may be further included to improve mechanical rigidity, and the mixture 11 of a perfluorinated sulfonic acid-based ionomer and an antioxidant may be impregnated into the reinforcement layer.

(17) The reinforcement layer 12 may be a porous membrane containing expanded polytetrafluoroethylene (e-PTFB) and having therein numerous pores.

(18) However, the configuration of the electrolyte membrane 10 in the present invention is not limited to those shown in FIGS. 2 and 3, and any configuration can be used so long as it includes a perfluorosulfonic acid-based ionomer for ion conduction and an antioxidant.

(19) The electrolyte membrane 10 may include the antioxidant in an amount of about 0.05% by weight to about 20% by weight, based on the total weight of the perfluorinated sulfonic acid-based ionomer and the antioxidant. For instance, when the content of the antioxidant is less than about 0.05% by weight, the chemical durability of the electrolyte membrane may not be improved due to the excessively low antioxidant activity, and when the content is greater than about 20% by weight, the proton conductivity of the electrolyte membrane may be decreased and brittleness may be increased.

(20) Preferably, the perfluorinated sulfonic acid-based ionomer may suitably include Nafion. In certain embodiments, the perfluorinated sulfonic acid-based ionomer may be Nafion.

(21) Preferably, the antioxidant may suitably include Sn-doped cerium oxide.

(22) The Sn-doped cerium oxide may have increased oxygen vacancy and thus provide improved redox reactivity of cerium ions by substituting at least a portion of cerium (IV) ions (Ce.sup.4′) in cerium oxide (CeO.sub.2) having a fluorite structure with tin ions (Sn.sup.2+).

(23) The Sn-doped cerium oxide may be represented by the following Formula 1.
Sn.sub.xCe.sub.1−xO.sub.2−δ  [Formula 1]

(24) wherein x satisfies 0<x≤0.5 and δ is an oxygen vacancy value making the compound of Formula 1 electrically neutral, for example, 0<δ≤0.5.

(25) When x is greater than 0.5, the inherent structural properties of cerium oxide may be deteriorated. For this reason, x is preferably within the range.

(26) The antioxidant may be synthesized by various methods such as a hydrothermal synthesis method, a flame hydrolysis deposition method, and a sol-gel autocombustion method. Preferably, the antioxidant may be synthesized by hydrothermal synthesis under a hydrogen atmosphere for cerium reduction. The method of synthesizing a tin-doped cerium oxide nanopowder may include dissolving a cerium salt and a tin salt in distilled water at an appropriate stoichiometric ratio, followed by reacting and mixing for about 2 hours, adding a nitric acid solution thereto to maintain the pH at 9, forming a tin-doped cerium oxide precipitate, washing the tin-doped cerium oxide precipitate, and performing calcination in a hydrogen-containing atmosphere at a temperature of 100 to 750° C.

Example

(27) Hereinafter, the antioxidant according to various exemplary embodiments of the present invention will be described in more detail with reference to the following Examples. However, these examples are provided only for illustration of the present invention and should not be construed as limiting the scope of the present invention.

(28) Antioxidant Activity Evaluation—Methyl Violet Method

(29) A methyl violet method offering rapid naked eye inspection was used to evaluate antioxidant activities.

(30) Methyl violet was mixed with iron (II) sulfate heptahydrate (FeSO.sub.4.7H.sub.2O), hydrogen peroxide and an antioxidant and then changes in color were observed.

(31) As the antioxidant activity of the antioxidant increases, violet, the original color of methyl violet, is maintained, and as the antioxidant activity decreases, the violet turns pale and finally changes to colorless.

(32) First, methyl violet, iron sulfate heptahydrate and hydrogen peroxide were mixed at a molar ratio of 1:40:40 to prepare a methyl violet test solution.

(33) In Example 1, about 3 mg of tin-doped cerium oxide (Sn.sub.0.25Ce.sub.0.75O.sub.2−δ, wherein δ is an oxygen vacancy value making the antioxidant electrically neutral) synthesized under a hydrogen atmosphere was added as an antioxidant to the methyl violet test solution. In Comparative Example 1, no antioxidant was added. In Comparative Example 2, about 3 mg of cerium oxide (CeO.sub.2), synthesized in a hydrogen atmosphere, was added as an antioxidant.

(34) The results of evaluation of antioxidant activities of Example 1, Comparative Example 1 and Comparative Example 2 through a methyl violet method are shown in FIGS. 4A to 4C. FIG. 4A shows the result of Example 1, FIG. 4B shows the result of Comparative Example 1, and FIG. 4C shows the result of Comparative Example 2.

(35) As shown in FIG. 4B, the methyl violet test solution of Comparative Example 1 with no antioxidant added thereto gradually became colorless. As shown in FIG. 4C, the methyl violet test solution of Comparative Example 2, when cerium oxide (CeO.sub.2) was present as an antioxidant, turned much paler.

(36) On the other hand, as shown in FIG. 4A, Example 1, when the tin-doped cerium oxide according to an exemplary embodiment of the present invention was present as an antioxidant, maintained its original violet color very well.

(37) Accordingly, the tin-doped cerium oxide according to the present invention may exhibit the best antioxidant activity.

(38) 2) Antioxidant Activity Evaluation—UV-Visible Spectroscopy

(39) The absorbance intensities of the methyl violet test solutions of Example 1, Comparative Example 1 and Comparative Example 2 were measured using a UV-visible spectrometer (UV-3600, Shimadzu Corporation, Japan) to more accurately evaluate the antioxidant activity.

(40) When the antioxidant activity of the antioxidant is exerted, an absorbance intensity is present at 582 nm, which is the inherent absorbance wavelength of methyl violet, whereas, when antioxidant activity is not exerted, no absorbance intensity is present at the corresponding wavelength.

(41) The methyl violet test solutions according to Example 1, Comparative Example 1 and Comparative Example 2 were stirred for 24 hours and then the antioxidants were removed through a centrifugation process. The absorbance intensities of the remaining solutions were measured. The results are shown in FIG. 5.

(42) As shown in FIG. 5, Comparative Example 1, with no antioxidant added thereto, did not show an absorbance peak, whereas Example 1, in which the tin-doped cerium oxide according to an exemplary embodiment of the present invention was present as an antioxidant, maintained a higher absorbance intensity at a wavelength of about 582 nm than Comparative Example 2, in which cerium oxide (CeO.sub.2) was present as an antioxidant.

(43) Long-Term Durability Evaluation

(44) An electrolyte membrane including the tin-doped cerium oxide according to an exemplary embodiment of the present invention as an antioxidant was produced as follows:

(45) (Example 2) 2% by weight of Sn.sub.0.25Ce.sub.0.75O.sub.2−δ (wherein δ is an oxygen vacancy value making the compound of Formula 1 electrically neutral) as an antioxidant was mixed with a perfluorinated sulfonic acid ionomer dispersion (Nafion D2021, DuPont Co., USA), and the resulting mixture was subjected to bar coating to produce an electrolyte membrane. The electrolyte membrane had a thickness of 30 μm.

(46) (Comparative Example 3) An electrolyte membrane was produced in the same manner as in Example 2, except that no antioxidant was added.

(47) (Comparative Example 4) An electrolyte membrane was prepared in the same manner as in Example 2, except that cerium oxide (CeO.sub.2) was used as an antioxidant.

(48) The long-term durability of the electrolyte membranes according to Example 2, Comparative Example 3 and Comparative Example 4 were evaluated as follows.

(49) Deionized water and hydrogen peroxide were mixed at a weight ratio of 1:0.43, and 30 ppm of iron sulfate heptahydrate was added to the resulting mixture to prepare a Fenton solution. The electrolyte membranes according to Example 2, Comparative Example 3, and Comparative Example 4 were immersed in the Fenton solution and reacted at temperature of about 80° C., and the fluorine ion concentration was measured at various time points during the reaction.

(50) The electrolyte membranes were degraded by radicals contained in the Fenton solution to release fluorine ions (F.sup.−). When the antioxidant is added to the electrolyte membrane, the antioxidant may remove radicals, thereby suppressing the release of the fluorine ions. Thus, by measuring the concentration of the released fluorine ions, the antioxidant activity of the antioxidant and the durability of the electrolyte membrane can be evaluated.

(51) The results are shown in FIG. 6. Based on the results of the reaction time of 300 hours, the fluorine ion concentration of Example 2 including the tin-doped cerium oxide according to an exemplary embodiment of the present invention as an antioxidant was about 1/13 of that of Comparative Example 3 with no antioxidant added thereto, and was about ⅓ of that of Comparative Example 4, containing the cerium oxide as an antioxidant.

(52) Accordingly, the tin-doped cerium oxide according to exemplary embodiments of the present invention may have high antioxidant activity and the electrolyte membrane including the tin-doped cerium oxide has excellent long-term durability.

(53) As apparent from the foregoing, the present invention provides a novel antioxidant having excellent antioxidant activity as well as superior long-term stability, and thus a membrane-electrode assembly to which the antioxidant is introduced is capable of exhibiting greatly improved durability.

(54) The effects of the present invention are not limited to those mentioned above. It should be understood that the effects of the present invention include all effects that can be inferred from the foregoing description of the present invention.

(55) The invention has been described in detail with reference to various exemplary embodiments thereof. However, it will be appreciated by those skilled in the art that changes may be made in these embodiments without departing from the principles and spirit of the invention, the scope of which is defined in the appended claims and their equivalents.