The invention can be more fully understood by reading the subsequent detailed description and examples with references made to the accompanying drawings, wherein:
The following description is of the best-contemplated mode of carrying out the invention. This description is made for the purpose of illustrating the general principles of the invention and should not be taken in a limiting sense. The scope of the invention is best determined by reference to the appended claims.
Referring to
The membrane electrode assembly 110 comprises a proton exchange membrane 111, a cathode electrode 112, and an anode electrode 113. The proton exchange membrane 111 is disposed between the cathode electrode 112 and the anode electrode 113. Specifically, the cathode electrode 112 comprises a cathode catalyst layer 112a and a cathode gas diffusion layer 112b, and the anode electrode 113 comprises an anode catalyst layer 113a and an anode gas diffusion layer 113b. The proton exchange membrane 111 is disposed between the cathode catalyst layer 112a and the anode catalyst layer 113a. The cathode gas diffusion layer 112b is disposed on the cathode catalyst layer 112a. The anode gas diffusion layer 113b is disposed on the anode catalyst layer 113a.
The cathode porous current collector 120 is disposed on the cathode electrode 112. Specifically, the cathode porous current collector 120 is disposed on the cathode gas diffusion layer 112b of the cathode electrode 112.
The anode porous current collector 130 is disposed on the anode electrode 113. Specifically, the anode porous current collector 130 is disposed on the anode gas diffusion layer 113b of the anode electrode 113 and opposite the cathode porous current collector 120.
The cathode water-absorptive layer 140 is disposed on the cathode porous current collector 120. Compared to the cathode porous current collector 120, the cathode water-absorptive layer 140 is hydrophilic and can rapidly absorb water or guide water to other areas, preventing the water from being accumulated at the cathode porous current collector 120 or cathode electrode 112. The cathode water-absorptive layer 140 may comprise porous hydrophilic material, such as a hydrophilic thread, a lampwick, woven fabrics, non-woven fabrics, paper, foam sponge, or foaming PU. The porous hydrophilic material, such as foaming PU, may be directly attached to the cathode porous current collector 120 by coating. Specifically, disposed in the exterior of the cathode porous current collector 120, the cathode water-absorptive layer 140 does not adversely affect electrical contact between the cathode porous current collector 120 and the cathode gas diffusion layer 112b. Thus, the total resistance in the fuel cell 100 is not increased. Moreover, the cathode water-absorptive layer 140 is provided with sufficient capillary surface area. Small size and a large amount of capillary surface are preferred. To effectively promote permeability of air, the size of the capillary surface or through holes is determined by surface energy provided by the cathode water-absorptive layer 140 without formation of any water film, such that oxygen can easily enter the cathode electrode 112. Specifically, the radius of the capillary surface or through holes must exceed the thickness of the cathode water-absorptive layer 140, such that water droplets on the edges thereof do not connect to each other and form water films to clog up the capillary surface or through holes.
Elements corresponding to those in the first embodiment share the same reference numerals.
Referring to
Structure, disposition, and function of other elements in the fuel cell 100′ are the same as those in the fuel cell 100, and explanation thereof is omitted for simplicity.
Elements corresponding to those in the first embodiment share the same reference numerals.
Referring to
Structure, disposition, and function of other elements in the fuel cell 100″ are the same as those in the fuel cell 100, and explanation thereof is omitted for simplicity.
Accordingly, in the fuel cell 100″, the excess water at the cathode electrode 112 and adversely affecting the redox reaction is effectively recycled or transported to the anode electrode 113 for reaction. Thus, the fuel cell 100″ can provide long-term operation.
While the invention has been described by way of example and in terms of preferred embodiment, it is to be understood that the invention is not limited thereto. To the contrary, it is intended to cover various modifications and similar arrangements (as would be apparent to those skilled in the art). Therefore, the scope of the appended claims should be accorded the broadest interpretation so as to encompass all such modifications and similar arrangements.
Number | Date | Country | Kind |
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TW95132721 | Sep 2006 | TW | national |