METHOD FOR PRODUCING A CATALYST-COATED MEMBRANE

Abstract

A method for producing a catalyst-coated membrane includes: preparing and/or providing a first ink having a first ink composition, comprising substrated catalyst particles proton-conducting ionomer and dispersing agent, in which the fraction of the substrated catalyst particles remains behind the fraction of the proton-conducting ionomer; preparing and/or providing at least one second ink having a second ink composition, comprising the substrated catalyst particles, the proton-conducting ionomer and the dispersing agent, in which the fraction of the proton-conducting ionomer remains behind the fraction of the substrated catalyst particles, unwinding a weblike proton-conducting membrane material provided on a roll; applying at least one layer of the first ink with a first application tool onto at least one section of the membrane material; and applying at least one layer of the second ink with a second application tool onto an outermost layer of the first ink deposited onto the membrane material

Claims

1. A method for producing a catalyst-coated membrane, comprising: preparing and/or providing a first ink having a first ink composition, comprising substrated catalyst particles, proton-conducting ionomer and dispersing agent, in which the fraction of the substrated catalyst particles remains behind the fraction of the proton-conducting ionomer; preparing and/or providing at least one second ink having a second ink composition, comprising the substrated catalyst particles, the proton-conducting ionomer and the dispersing agent, in which the fraction of the proton-conducting ionomer remains behind the fraction of the substrated catalyst particles; unwinding a weblike proton-conducting membrane material provided on a roll; applying at least one layer of the first ink with a first application tool onto at least one section of the membrane material; and applying at least one layer of the second ink with a second application tool onto an outermost layer of the first ink, deposited onto the membrane material.

2. The method according to claim 1, wherein the first ink is applied with the first application tool on both sides of the membrane material, and subsequently in time the second ink is applied with the second application tool on both sides of the respectively outermost layer of the first ink deposited onto the membrane material.

3. The method according to claim 1, wherein the membrane material coated with the first ink is taken to an intermediate drying unit, in which the first ink is partially dried to form a dry marginal film of the first ink before the second ink is applied.

4. The method according to claim 1, wherein a layer thickness measurement is performed for the layer of the first ink after the depositing of the first ink.

5. The method according to claim 4, wherein the first ink is applied to subsequent sections of the membrane material in dependence on the measured layer thickness of preceding sections of the membrane material.

6. The method according to claim 4, wherein the second ink is deposited in dependence on the measured layer thickness of the first ink in order to limit an electrode thickness.

7. The method according to claim 1, wherein a layer thickness measurement of the electrode thickness is performed after applying the second ink, and the second ink is deposited on subsequent sections of the membrane material in dependence on the measured electrode thickness.

8. The method according to claim 1, wherein the membrane material coated with the inks is taken to a drying unit, in which the coating is fully dried.

9. The method according to claim 1, wherein a catalyst particle charge of the membrane material coated with the inks is determined by means of an X-ray fluorescence analysis, and the fraction of substrated catalyst particles in the inks is adjusted as a function of the measured catalyst particle charge.

10. The method according to claim 1, wherein the membrane material coated with the inks is cut up into individual catalyst coated membranes.

11. The method according to claim 1, wherein a catalyst content is determined by a layer thickness measurement and/or by a charge measurement.

Description

BRIEF DESCRIPTION OF THE SEVERAL VIEWS OF THE DRAWINGS

[0027] Further benefits, features and details will emerge from the claims, the following description of embodiments, and the drawings.

[0028] FIG. 1 shows a schematic representation of the structure of a fuel cell.

[0029] FIG. 2 shows a merely schematic detail view II of an electrode from FIG. 1.

[0030] FIG. 3 shows a schematic representation of a device for producing a catalyst-coated membrane in a side view.

DETAILED DESCRIPTION

[0031] FIG. 1 shows a fuel cell 1. A semipermeable electrolyte membrane 2 here is covered on a first side 3 with a first electrode 4, in the present case the anode, and on a second side 5 with a second electrode 6, in the present case the cathode. The first electrode 4 and the second electrode 6 comprise substrate particles 14, on which catalyst particles 13 of precious metals or mixtures containing precious metals such as platinum, palladium, ruthenium or the like are arranged or substrated. These catalyst particles 13 serve as reaction accelerants in the electrochemical reaction of the fuel cell 1. The substrate particles 14 may contain carbon. Yet substrate particles 14 may also be considered which are formed from a metal oxide or carbon with an appropriate coating. In such a polymer electrolyte membrane fuel cell (PEM fuel cell), fuel or fuel molecules, especially hydrogen, are split up into protons and electrons at the first electrode 5 (anode). The electrolyte membrane 2 lets through the protons (e.g., H.sup.+), but is impenetrable to the electrons (e.sup.-). The electrolyte membrane 2 in this embodiment is formed from an ionomer, such as a sulfonated tetrafluorethylene polymer (PTFE) or a polymer of perfluorinated sulfonic acid (PFSA). At the anode, the following reaction occurs: 2H.sub.2 ➔ 4H.sup.+ + 4e.sup.- (oxidation/electron surrender).

[0032] While the protons pass through the electrolyte membrane 2 to the second electrode 6 (cathode), the electrons are taken by an external circuit to the cathode or to an energy accumulator. At the cathode, a cathode gas is provided, especially oxygen or oxygen-containing air, so that the following reaction occurs here: O.sub.2 + 4H.sup.+ + 4e.sup.- ➔ 2H.sub.2O (reduction/electron uptake).

[0033] In the present case, the electrodes 4, 6 are each associated with a gas diffusion layer 7, 8, one gas diffusion layer 7 being associated with the anode and the other gas diffusion layer 8 with the cathode. Moreover, the anode-side gas diffusion layer 7 is associated with a flow field plate, shaped as a bipolar plate 9, for supply of the fuel gas, having a fuel flow field 11. By means of the fuel flow field 11, the fuel is supplied through the gas diffusion layer 7 to the electrode 4. At the cathode side, the gas diffusion layer 8 is associated with a flow field plate having a cathode gas flow field 12, likewise shaped as bipolar plate 10, for supply of the cathode gas to the electrode 6.

[0034] The electrodes 4, 6 in the present instance are formed with a multitude of catalyst particles 13, which can be formed as nanoparticles, such as “core-shell nanoparticles.” These have the advantage of a large surface, while the precious metal or the precious metal alloy is arranged only on the surface, and a less valuable metal, such as nickel or copper, forms the core of the nanoparticle

[0035] The catalyst particles 13 are arranged or substrated on a multitude of electrically conducting substrate particles 14. Furthermore, between the substrate particles 14 and/or the catalyst particles 13 there is present an ionomer binder 15, which may be formed from the same material as the membrane 2. This ionomer binder 15 may be formed as a polymer or ionomer containing a perfluorinated sulfonic acid. The ionomer binder 15 in the present case is in porous form, having a porosity of more than 30 percent. This ensures, especially on the cathode side, that the oxygen diffusion resistance is not increased, thus making possible a lower charging of the catalyst particle 13 with precious metal or a lower charging of the substrate particle 14 with catalyst particles 13 (FIG. 2).

[0036] In the following, a method will be described for producing a catalyst-coated membrane (CCM). At first, a first ink 16 is prepared and/or provided, comprising a first ink composition containing substrated catalyst particles 13, proton-conducting ionomer 15 and dispersing agent. The ionomer 15 may be formed from the same material as the membrane 2. The dispersing agent can be isopropanol or acetone, for example. In this first ink 16, the fraction of the substrated catalyst particles remains behind the fraction of the proton-conducting ionomer 15. Moreover, a second ink 18 is prepared or provided, comprising an ink composition containing the substrated catalyst particle 13, the proton-conducting ionomer 15 and the dispersing agent. In this second ink 18, the fraction of the proton-conducting ionomer 15 remains behind the fraction of the substrated catalyst particles 13. “Remaining behind” may mean a difference in the fractions of at least 10 percent, at least 30 percent, or at least 50 percent.

[0037] As shown by FIG. 3, a weblike proton-conducting membrane material provided on a roll 22 is unwound and taken in a delivery direction 21 at first to a foil cleaning unit 25, where the membrane material 20 is made free of dust and deposits. After this, the membrane material 20 is transported further in the delivery direction 21 to a first application tool 17, with which the first ink 16 is deposited on at least one section, such as on the entire membrane material 20. After the first application tool 17 in the delivery direction 21 there is performed a layer thickness measurement of the layer of the first ink 16 by means of a layer thickness meter 27. After the first application tool 17 in the delivery direction 21 there is provided an intermediate drying unit 23, in order to dry the first ink 16 before it is imprinted with an additional ink. The intermediate drying unit 23 shown in the present case is designed to dry the first ink 16 only partly, so as to form there a dry marginal film of the first ink 16 before the second ink 18 is then deposited in the delivery direction 21 with a second application tool 19 onto an outermost layer of the first ink 16 deposited on the membrane material 20. After the second application tool 19 in the delivery direction 21 there is once again a layer thickness meter 27, in order to measure the electrodes 4, 6 formed from the first ink 16 and the second ink 18. With this layer thickness meter 27, a measurement of the wet film thickness can be done. After the second application tool 19 in the delivery direction 21 there is provided a drying unit 24, which is designed to fully dry the membrane material 20 coated with the inks 16, 18. After the drying unit 24 in the delivery direction 21 there is arranged a further layer thickness meter 27, which can measure the dried electrode film, for example, by means of an optical layer thickness measuring head. In addition, there is an X-ray fluorescence analysis unit 26, which determines the catalyst particle charge of the membrane material 20 coated with the inks 16, 18, whereupon the fraction of substrated catalyst particles 13 in the inks 16, 18 can then be adjusted in dependence on the measured catalyst particle charge. Before the coated membrane material 20 is rolled up once more on the further roll 22, it is taken past a unit for defect marking 28, with which any holes in the electrode layers or such defects can be marked, so that during the subsequent cutting up of the membrane material into individual catalyst-coated membranes it is ensured that these do not have a defective coating.

[0038] As a result, it is possible with the method described herein to produce on an industrial scale membrane electrode assemblies which are coated with catalyst pastes or inks 16, 18, so that these can be prepared in large lot numbers. The catalyst-coated membrane produced as described herein is characterized by an improved water management. Furthermore, the method can be carried out quickly with reduced cycle time to produce the individual fuel cells.

[0039] In general, in the following claims, the terms used should not be construed to limit the claims to the specific embodiments disclosed in the specification and the claims, but should be construed to include all possible embodiments along with the full scope of equivalents to which such claims are entitled.