The present invention relates to fuel cell systems, and more particularly, to a development of high energy surfaces on stainless steels to improve wettability.
Electrochemical cells, such as fuel cells, generate electrical power through the electrochemical reaction of a fuel and an oxidant. An exemplary fuel cell has a membrane electrode assembly (MEA) with catalytic electrodes and a proton exchange membrane (PEM) sandwiched between the electrodes. In PEM type fuel cells, hydrogen can be supplied as a reductant to an anode and oxygen can be supplied as an oxidant to a cathode. PEM fuel cells reduce oxygen at the cathodes and generate an energy supply for various applications, including vehicles.
It is well established that channel water accumulation, in both the anode and cathode flow field plates, significantly influences fuel cell performance at low loads. When the gas velocities are relatively low (i.e., less than about 5 meters per second), the water transported through diffusion media favors the formation of liquid droplets that occupy a significant portion of the channel cross-section. These droplets increase the gas flow resistance in particular channels, thereby diverting flow to neighboring channels and essentially starving the local active area of necessary reactants. Various means of circumventing this potential problem have been explored and have included altering the physical characteristics of the channels, including the channel geometry, specifically the size and shape. There remains a need for improved water management to improve fuel cell performance, efficiency, and lifespan.
The present invention provides a bi-polar plate for a fuel cell stack. The bi-polar plate has improved surface wettability. The bi-polar plate includes a body comprising at least approximately 90 percent by weight of a metal and defining at least one flow channel. At least about 0.05 percent and up to 6 percent by weight of the bi-polar plate material is silicon which will enrich the passive film on the metallic bi-polar plates with silicon dioxide. The latter creates a high energy surface for the bi-polar plate. The presence of silicon is pre-determined based on a desired wettability of the high energy surface of the at least one flow channel.
Further areas of applicability of the present invention will become apparent from the detailed description provided hereinafter. It should be understood that the detailed description and specific examples, while indicating the preferred embodiment of the invention, are intended for purposes of illustration only and are not intended to limit the scope of the invention.
The present invention will become more fully understood from the detailed description and the accompanying drawings, wherein:
The following description of various embodiments is merely exemplary in nature and is in no way intended to limit the invention, its application, or uses. Although the following exemplary description refers to the development of a high energy surface material with improved wettability for a fuel cell system in a vehicle, it will be understood that the present invention may be applicable to other systems/components and may be appropriate for use in a variety of different mechanisms. In addition, the foregoing description details the use of silicon to increase the surface energy of a metallic material, however, it will be understood that any suitable additive could be used to increase the surface energy of the metallic material. It will be further understood that while the following description will relate to the use of a hydrogen feed gas for a fuel cell system, it should be noted that numerous other fuels could be employed, and further, the foregoing description is understood to not limit the appended claims.
Referring now to
With continuing reference to
During the reaction of the feed gas and oxidant gas, water is produced. The water droplets W may form on surfaces 30 of the flow channels 26 and thus restrict the flow of the feed gas and oxidant gas through the flow channels 26 as best shown in
With continuing reference to
Generally, the amount of silicon Si added to the metallic material M may range from about 0.5 percent to 10 percent by weight, but could range from about 1.5 percent to 6 percent by weight, depending on the desired metallic material M. It is desired that the surface has up to 100 percent silicon disposed thereon in order to achieve lower water contact angle values. If stainless steel is the desired metallic material M, the amount of silicon Si in the stainless steel may range from 4 percent to 6 percent and in another embodiment from 3 percent to 4 percent, and is preferably 1.5 percent to 3 percent by weight.
With reference now to
The incorporation of silicon S into the metallic material M used for forming the bi-polar plates 20 will increase the wettability of the surfaces 30 of the flow channels 26 of the bi-polar plates 20, and thus improve the efficiency of the flow of water and thereby improve the flow of the oxidant gas and feed gases through the flow channels 26 of the bi-polar plates 20. The improvement in the flow of the feed gas and oxidant gas through the bi-polar plates 20 in turn increases the efficiency of the fuel cell stack 12. It will be understood that any appropriate technique could be used to form the silicon rich layer on the surfaces 30 besides the techniques disclosed herein.
The description of the invention is merely exemplary in nature and, thus, variations that do not depart from the gist of the invention are intended to be within the scope of the invention. Such variations are not to be regarded as a departure from the spirit and scope of the invention.
Number | Name | Date | Kind |
---|---|---|---|
3663215 | Tanczyn | May 1972 | A |
4039356 | Schumacher et al. | Aug 1977 | A |
4279648 | Ito et al. | Jul 1981 | A |
4653684 | Saito et al. | Mar 1987 | A |
5565167 | Fujimoto et al. | Oct 1996 | A |
5942347 | Koncar et al. | Aug 1999 | A |
20040224212 | Wakahoi et al. | Nov 2004 | A1 |
20050109434 | Seung et al. | May 2005 | A1 |
20050164070 | Krajewski et al. | Jul 2005 | A1 |
20060194095 | Vyas et al. | Aug 2006 | A1 |
Number | Date | Country |
---|---|---|
2001207243 | Jul 2001 | JP |
2004124197 | Apr 2004 | JP |
Number | Date | Country | |
---|---|---|---|
20070178356 A1 | Aug 2007 | US |