Patent Application
20060090317
This application claims priority from a Chinese patent application entitled “Methods for the Fabrication of Membrane Electrode Assemblies of Fuel Cells with Integrated Structure” filed on “Nov. 3, 2004,” having a Chinese Application No. 200410052120.2. The above application is incorporated herein by reference.
This invention relates to fuel cells. Particularly, it relates to the fabrication methods for membrane electrode assemblies of fuel cells with integrated structure.
Fuel cells are energy conversion devices that transform the chemical energy of fuels such as hydrogen and alcohols and oxidants such as oxygen into electric energy. They have a high energy conversion rate and are environmentally friendly. In addition, proton exchange membrane fuel cells (PEMFC) operate at low temperatures and a high specific power. Therefore, PEMFC can be used as an independent power generator as well as a mobile power source in automobile, submarines, and other transportation equipment.
Membrane electrode assemblies (MEA) are the core units for fuel cells where fuels and oxidants chemically react to produce electrical energy. A membrane electrode assembly with only catalyst layers and a proton exchange membrane is called a 3-layered membrane electrode assembly or a catalyst coated membrane (CCM). A membrane electrode assembly with gas diffusion layers, catalyst layers, and a membrane is called a 5-layered membrane electrode assembly.
Traditional 5-layered membrane electrode assemblies are fabricated by directly hot-pressing gas diffusion layers with the proton membrane. In
To solve these problems, attempts have been made to paste a layer of inert protection membrane frame (protection frame) on the surface of the proton exchange membrane that is extended from the membrane electrode assembly. The extended proton exchange membrane and protection membrane frame are bound with a binding agent, usually a hot melt adhesive that is hot-pressed at the same time when the membrane electrode assembly is hot-pressed. This protection frame stabilizes the dimensions of the membrane electrode assembly and reduces the distortion at the edge of the proton exchange membrane. It separates the proton exchange membrane and sealing material and reduces the corrosion of the sealing material by the proton exchange membrane. If the thread sealing method is used, this protection membrane frame can, up to a point, resist the pressure that is concentrated at the sealing thread. However, the proton exchange membrane is still under pressure and can be severely distorted at the seam between the protection membrane frame and the carbon paper such that it can easily crimp. If the proton exchange membrane is thin, it can even be damaged by the pressure. Moreover, it is very difficult to align the protection membrane frame and the carbon paper precisely, particularly when the individual fiber of the of the carbon paper is slightly longer. The protruding carbon fiber can be pressed into the proton exchange membrane, causing damage to the proton exchange membrane. Therefore, despite the protection frame membrane, the life of this type of membrane electrode assembly is still limited.
Chinese patent CN2588552 disclosed a method for fabricating a membrane electrode assembly that includes a sealing area and an active area. The center part is the active area and it includes the proton exchange membrane and the porous gas diffusion electrode coated with catalyst layer. Surrounding it is the sealed area, which is comprised of carbon paper infiltrated by hot melt adhesive, rubber, or resin, and additional hot melt adhesive, rubber, or resin acting as a cushion. This hot melt adhesive, rubber, or resin is infiltrated into the carbon paper during the hot-pressing of the 5-layered membrane assembly, sealing the sealing area of the carbon paper of the sealing area of the carbon paper. The active and sealing area of the carbon paper for the membrane electrode assembly are integrated as one. The sealing area of the carbon paper also protects the protection frame. Therefore, the proton exchange membrane is also protected from damage at the seam between the protection membrane frame and the carbon paper. However, using this fabrication method, it is difficult to control the hot melt adhesive to uniformly melt and infiltrate the carbon paper while hot pressing the 5 layered membrane electrode assembly. In addition, the pressure for directly hot pressing the 5 layered membrane electrode assembly (5-10 MPa) is high. Such a high pressure can cause damage to the proton exchange membrane. It can also easily cause the distortion of the carbon paper at the sealing area.
Another Chinese patent, CN1476646, disclosed the structure and fabrication method of a type of membrane electrode assembly. The gas diffusion electrode of this membrane electrode assembly is divided into an active area and a sealing area. The area surrounding the carbon paper is the sealing area. This sealing area is immersed in the liquefied rubber. After solidification, the rubber forms a composite structure with a sealing function. A frame that functions as a cushion can be formed at the rim of the carbon paper. The immersed rubber is glued to the frame to form an integrated structure of the gas diffusion layer and the protection membrane frame. The structure is pressed to obtain the membrane electrode assembly. This method does not damage the carbon paper. In addition, the integration of the immersed rubber and carbon paper is better. However, the solidification process of the liquefied rubber is long, taking about 6 to 12 hours. In addition, during the solidification process, the rubber soaked in the carbon paper will shrink to form a gap, resulting in gas leakage. Other sealing structures have to be added to further seal this membrane electrode assembly
U.S. Pat. Nos. 6,159,628 and 6,399,234 disclosed the structure and fabrication method for another membrane electrode assembly. The gas diffusion electrodes of the membrane electrode assemblies are divided into an active area and sealing area. The area surrounding the carbon paper is the sealing area. The sealing area is formed by a plasticization process where a thermoplastic polymer KYNAR® membrane is melted and mold-pressed to infiltrates the gas diffusion layer. This “plasticized” frame acts as a protection membrane frame and seals the carbon paper. The gas diffusion unit and the catalyst coated membrane are bound by a hot melt adhesive membrane to form the membrane electrode assembly unit. A relatively low pressure can be used for the binding thus reducing the potential for damage to the proton membrane. Problems still exist in the fabrication method. The fabrication method is complicated and the efficiency of the equipment for the “plasticization” is very low as each piece of equipment can only “plasticize” one gas diffusion layer at a time. More importantly, the mold pressing technology damages the carbon paper. Therefore, this fabrication method cannot form a good composite structure of the melt permeated KYNAR® membrane and the carbon paper. The “plasticized” frame is weak and has relatively high gas permeability coefficient in the longitudinal direction. This will affect the stability of the membrane electrode assembly during its operation life. In addition, a significant amount of expensive material is discarded and wasted since only the rim of the KYNAR® membrane and the hot melt membrane is used.
Due to the limitations of the prior art, it is therefore desirable to have novel methods of fabricating membrane electrode assemblies of fuel cells that have an integrated structure, are stable and inexpensive.
An object or this invention is to provide methods for fabricating membrane electrode assemblies of fuel cells such that the structure of the membrane electrodes fabricated are stable.
Another object of this invention is to provide fabrication methods that reduce the potential for damage to the proton membrane and increase the lifespan of the membrane.
Another object of this invention is to provide methods for fabricating membrane electrode assemblies of fuels cells that reduce the quantity and cost of the materials used.
Another object of this invention is to improve the efficiency of the fabrication process such that the methods of this invention can be implemented for mass production.
Briefly, the present invention provides methods for fabricating membrane electrode assemblies. The fabrication of a gas diffusion unit for an electrode with a hot melt adhesive layer for a membrane electrode assembly include the steps of: dividing a substrate into an active region and a sealing region; fabricating a gas diffusion layer on said active region; placing a mold for said sealing region on said substrate; pouring a resin material onto said sealing region the aperture of the mold; volatizing said resin material; hot-pressing to form a gas diffusion unit; and fabricating one or more hot melt adhesive layer at the sealing region. The membrane electrode assembly is assembled by hot-pressing the gas diffusion unit for the positive and negative electrodes, the hot-melt adhesive layers for the electrodes, and the catalyst coated proton membrane.
An advantage of the fabrication methods of this invention is that they fabricate membrane electrode assemblies of fuel cells with a stable structure.
Another advantage of the fabrication methods of this invention is that these methods reduce the potential for damage to the proton membrane and increase the lifespan of the membrane.
Another advantage of the fabrication methods of this invention is that they reduce the quantity and cost of materials used.
Another advantage of the fabrication methods of this invention is that the methods are efficient and can be implemented for mass production.
The foregoing and other objects, aspects and advantages of the invention will be better understood from the following detailed description of preferred embodiments of this invention when taken in conjunction with the accompanying drawings in which:
Presently preferred methods for fabricating the gas diffusion unit for an electrode of a membrane electrode assembly of the present invention include the following steps: (a) dividing a substrate for the gas diffusion electrode into one or more active and sealing regions; (b) fabricating a gas diffusion layer on the active region or regions; (c) casting a resin material on said sealing regions to form a sealing membrane on top of said sealing regions; and (d) parallel hot-pressing said gas diffusion layer and sealing membrane to form a gas diffusion unit with an integrated structure. Preferably, the hot pressing pressure should be lowered than 0.03 MPa. The substrate for the gas diffusion layer can be carbon paper. In preferred embodiments, the active region is the center of the substrate while the sealed region encompasses the rim of the substrate.
A method for fabricating a membrane electrode assembly includes the steps of: (a) fabricating one or more hot melt adhesive layer at said sealing region or regions on one or both sides of the gas diffusion unit for an electrode to form a gas diffusion unit for an electrode with hot melt adhesive layers; (b) placing the positive and negative gas diffusion unit for an electrode with hot melt adhesive layers of separate sides of proton exchange membrane coated with catalyst layers; and (c) hot-pressing the assembled unit. Preferably, the hot-pressing should be conducted at low pressure. Good results are observed when the hot-pressing pressure is less than 1 MPa and the temperature is between 120° C. and 180° C.
The hot melt adhesive can be fabricated by spraying, coating, screen printing, immersing, soaking or dripping a liquid hot melt adhesive at the sealing region to form the hot melt adhesive layer. In the alternative, the hot melt adhesive membrane can first be transferred to the sealing region of the gas diffusion unit. Then the release membrane of the hot melt adhesive membrane is peeled off to form said hot melt adhesive layer. The hot melt adhesive of said hot melt adhesive layer can be one of the following: polyaminoesters, ethylene-vinyl acetate polymers and polyamides. Preferably, the thickness of said hot melt adhesive layer is between 1 microns and 100 microns.
In preferred methods, the casting of said resin material on the sealing region includes the steps of: (a) placing a mold for the sealing regions on said substrate where the apertures of the mold corresponds to the sealing regions of the substrate; (b) aligning the apertures of the mold to the sealing regions; (c) pouring the resin material onto the sealing region through the aperture in the mold; and volatizing the resin material at a controlled temperature to form said sealing membrane.
Preferably, the resins in the material having solvent should be chemically and thermally stable and soluble in low toxic or nontoxic solvents. Thus, the resin material can comprise of one or more resins selected from the following group: soluble polysulfone, poly-ether-ketones, polyamides, polyimides, polyolefins, fluoropolymers and block polymer. The optimal selection for the resin is polyvinylethylene fluoride resin. the concentration of the resin in said resin material is between 5% and 50%. Preferably, the resin material can also contain of one or more of the following solvents that the resin is dissolved in: ethers, sulfones, ketones or amides. When the resin in the resin material is polyvinylethylene fluoride, the optimal selection for the solvent is dimethyl formamide.
One method for forming the gas diffusion layer include the following steps: (a) spraying or vacuum-infiltrating polytetrafluoroethylene into the active region of the substrate until the concentration of said polytetrafluoroethylene resin in the substrate is between 1% and 60%; (b) drying at a temperature of between 340° C. and 360° C. for 20 minutes to 60 minutes; (c) mixing, preferably with a high speed dispersion equipment, the dispersion of a hydrophobic first resin, carbon, and, alcohol or water in the weight ratio of 1˜5:1˜5:10˜100 for 10˜60 minutes uniformly and treating with ultrasound for 10 minutes to 60 minutes to form an ink-like mixture that does not contain any precipitates; (d) placing the mixture in the active region such that the concentration of the first resin in the substrate is between 0% and 70%. The placing of said mixture can be implemented by the spraying, vacuum-infiltrating, coating, immersing, or immersing with vibration. The optimal method for is by spraying or vacuum infiltration; and (e) drying with heat for 10 to 100 minutes to form a gas diffusion layer that can be 1 micron to 100 microns thick and has a cavity rate of 20-80%.
The following embodiments further describe this invention.
Fabrication of the Gas Diffusion Layer
In this embodiment, the substrate is TORRY carbon paper TCP-H-090. This substrate is divided into a predetermined sealing region and an active region. The sealing region, at the rim of the substrate is reserved for later treatment. The gas diffusion layer is fabricated as follows:
spray-coating a 10 wt. % concentration of polytetrafluoroethylene dispersion onto the center active region until the concentration of the polytetrafluoroethylene is 10%;
drying the carbon paper with heat at a temperature of 350° C. for 15 minutes,
cooling naturally;
mixing 1 unit (by weight) of the polytetrafluoroethylene dispersion, 3 units (by weight) of black carbon powder and 100 units (by weight) of deionized water uniformly by using a ball mill for 30 minutes;
treating with ultrasound for 20 minutes to form a stable, “ink-like” mixture that does not contain any precipitates;
roll-coating said ink-like mixture onto the center active region of the substrate to form a micro-pore thin layer 25 microns thick with a cavity ratio of 60%;
drying with heat at a temperature of 350° C. for 20 minutes; and
cooling naturally.
Fabrication of the Gas Diffusion Unit
The fabrication of the gas diffusion unit includes the following steps:
dissolving 1 unit (by weight) of polyvinylethylene fluoride resin in 10 units (by weight) of the solvent dimethyl formamide;
placing a mold on the substrate with the gas diffusion layer and aligning the reserved sealing region of the substrate casting area (aperture) of the mold;
pouring the polyvinylidene fluoride resin solution at the casting area of the mold;
volatilizing the solvent at a temperature of 110° C. to form sealing membrane on said sealing region;
hot-pressing the gas diffusion layer with sealing membrane at a temperature to 190° C. and a pressure of 0.02 MPa for 5 minutes;
removing and cooling to obtain the gas diffusion unit with a stable integrated structure.
Assembly of the 5-Layered Membrane Electrode Assembly
The method for the assembly includes:
spray-coating the hot melt coat onto the gas diffusion unit at the sealing regions on the same side of the gas diffusion unit and the gas diffusion layer.
hot-pressing the gas diffusion unit of the positive and negative electrodes with the catalyst coated membrane for 3 minutes at a temperature of 130° C. and pressure of 0.1 MPa to obtain the 5-layered membrane electrode assembly with the integrated structure.
The diagram of the structure of the membrane electrode assembly fabricated by the methods of Embodiment 1 is illustrated in
Fabrication of the Gas Diffusion Layer
In this embodiment, the substrate is TORRY carbon paper TCP-H-060. This substrate is divided into a predetermined sealing region and an active region. The sealing region, at the rim of the substrate is reserved for later treatment. The gas diffusion layer is fabricated as follows:
vacuum infiltrating at a pressure of 0.01 MPa to uniformly coat a 10 wt. % concentration of polytetrafluoroethylene dispersion onto the center active region until the concentration of the polytetrafluoroethylene is 10%;
drying the carbon paper with heat at a temperature of 350° C. for 15 minutes,
cooling naturally;
mixing 1 unit (by weight) of the polytetrafluoroethylene dispersion, 3 units (by weight) of Vulcan-XC-72 carbon powder and 100 units (by weight) of deionized water for 30 minutes until uniformly mixed;
treating with ultrasound for 20 minutes to form a stable, “ink-like” mixture that does not contain any precipitates;
coating said ink-like mixture onto the center active region of the substrate with a scraper to form a micro-pore thin layer that is 22 microns thick with a cavity ratio of 50%;
drying with heat at a temperature of 350° C. for 20 minutes; and
cooling naturally.
Fabrication of the Gas Diffusion Unit
The fabrication of the gas diffusion unit includes the following steps:
dissolving 1 unit (by weight) of polyvinylethylene fluoride resin in 4 units (by weight) of the solvent N-methyl pyrrolidinone (NMP);
placing a mold on the substrate with the gas diffusion layer and aligning the reserved sealing region of the substrate casting area (aperture) of the mold;
pouring the polyvinylidene fluoride resin solution at the casting area of the mold;
volatilizing the solvent at a temperature of 110° C. to form sealing membrane on said sealing region;
hot-pressing the gas diffusion layer with sealing membrane at a temperature to 170° C. and a pressure of 0.03 MPa for 5 minutes;
removing and cooling to obtain the gas diffusion unit with a stable integrated structure.
Assembly of the 5-Layered Membrane Electrode Assembly
The method for the assembly includes:
cutting a hot melt adhesive membrane TBF-615 (or other 3M Corporation's hot melt adhesive membrane) to the same shape and size as the sealing region;
aligning the hot melt adhesive membrane to the sealing region;
hot-pressing the membrane onto the gas diffusion unit at the sealing region at 130° C. to transfer the membrane to the sealing region;
hot-pressing the gas diffusion unit of the positive and negative electrodes with the catalyst coated membrane for 1 minute at a temperature of 130° C. and pressure of 0.1 MPa to obtain the 5-layered membrane electrode assembly with the integrated structure.
Fabrication of the Gas Diffusion Layer
In this embodiment, the substrate is carbon paper GDL 30 BA from SGL Company. This substrate is divided into a predetermined sealing region and an active region. The sealing region, at the rim of the substrate is reserved for later treatment. The gas diffusion layer is fabricated as follows:
mixing 1 unit (by weight) of the polytetrafluoroethylene dispersion, 3 units (by weight) of Vulcan-XC-72 carbon powder, and 100 units (by weight) of deionized water for 30 minutes until uniformly mixed;
treating with ultrasound for 20 minutes to form a stable, “ink-like” mixture that does not contain any precipitates;
coating said ink-like mixture onto the center active region of the substrate with a scraper to form a micro-pore thin layer that is 22 microns thick with a cavity ratio of 50%;
drying with heat at a temperature of 350° C. for 20 minutes; and
cooling naturally.
Fabrication of the Gas Diffusion Unit
The fabrication of the gas diffusion unit includes the following steps:
dissolving 1 unit (by weight) of polynaphtfol diphenylether polysulfides resin in 9 units (by weight) of the solvent dimethyl acetamide (DMAc);
placing a mold on the substrate with the gas diffusion layer and aligning the reserved sealing region of the substrate casting area (aperture) of the mold;
pouring the polynaphtfol diphenylether polysulfides resin solution at the casting area of the mold;
volatilizing the solvent at a temperature of 110° C. to form sealing membrane on said sealing region;
hot-pressing the gas diffusion layer with sealing membrane at a temperature to 250° C. and a pressure of 0.02 MPa for 5 minutes;
removing and cooling to obtain the gas diffusion unit with a stable integrated structure.
Assembly of the 5-Layered Membrane Electrode Assembly
The method for the assembly includes:
cutting a hot melt adhesive membrane TBF-845EG (or other 3M Corporation's hot melt adhesive membrane) to the same shape and size as the sealing region;
aligning the hot melt adhesive membrane to the sealing region;
hot-pressing the membrane onto the gas diffusion unit at the sealing region at 130° C. to transfer the membrane to the sealing region;
hot-pressing the gas diffusion unit of the positive and negative electrodes with the catalyst coated membrane for 0.5 minutes at a temperature of 130° C. and pressure of 0.1 MPa to obtain the 5-layered membrane electrode assembly with the integrated structure.
While the present invention has been described with reference to certain preferred embodiments, it is to be understood that the present invention is not limited to such specific embodiments. Rather, it is the inventor's contention that the invention be understood and construed in its broadest meaning as reflected by the following claims. Thus, these claims are to be understood as incorporating not only the preferred embodiments described herein but all those other and further alterations and modifications as would be apparent to those of ordinary skilled in the art.
| Number | Date | Country | Kind |
|---|---|---|---|
| 200410052120.2 | Nov 2004 | CN | national |
