This invention relates generally to a heat spreader for use with a direct oxidation fuel cell.
Fuel cell power systems that convert an organic fuel such as methanol or ethanol and an oxidant into electricity are generally categorized into two types. In the first type, a fuel reformer is used to convert the organic fuel stream into a fuel stream containing hydrogen gas. The hydrogen gas is fed to the anode of a hydrogen-fueled fuel cell.
The second type is a direct oxidation fuel cell (DOFC) in which the organic fuel is reacted directly at an anode catalyst electrode of a membrane electrode assembly (MEA) of the fuel cell. An example of a direct oxidation fuel cell is the direct methanol fuel cell (DMFC). The half reactions for a DMFC are:
Anode: CH3OH+H2O→CO2+6e−+6H+
Cathode: 6e−+6H++ 3/2O2→3H2O
Many DMFC systems known in the art are liquid-feed systems that circulate a low-molarity methanol/water fuel solution through an anode flow field adjacent to an anode gas diffusion layer (GDL). Carbon dioxide (CO2) that is generated in the anode reaction exits through the anode flow field with the unused fuel solution where it is separated before the unused fuel solution is recirculated through the anode flow field.
Some liquid-feed DMFC systems operate using substantially 100% methanol and employ an active system to manage water in the fuel cell. Water is needed for the anode half reaction (as noted in the above reaction equations). Additionally, the cathode aspect of the membrane must be kept adequately hydrated, but not saturated or flooded. Thus, active water management systems are employed that include techniques for capturing water generated at the cathode and returning it to the anode. This replaces: (i) water lost to the anode reaction, (iii) water leaving the system through the CO2 vent, or (iii) water crossing over the polymer-electrolyte membrane (PEM) from the anode to the cathode. These active water management systems can become complex, adding costs, as well as size and weight, to a system that should be small and lightweight to satisfy commercial applications.
Furthermore, it has been found that DOFCs operate best when fuel and oxygen are delivered uniformly to an adequately-hydrated MEA. In a liquid-feed system, water is mixed with the fuel, which provides hydration of the PEM. In addition, fuel is provided in concentration levels adequate to evenly feed the full active area of the membrane. Concentration of the fuel can be managed so that the beginning of the flow path is not over concentrated and the end of the flow path is not under concentrated. In such cases, the energy required to distribute the fuel across the MEA active area comes from a liquid pump. But, these systems also require water delivery and/or recirculation mechanisms such as pumps and conduits for recirculating unused fuel and water back to the anode of the fuel cell.
It is also known to provide a direct-injection fuel feed DOFC in which liquid fuel is directly injected into the anode chamber of the fuel cell. In this case, any fuel that escapes unused is not captured and circulated back through the anode chamber. For example, U.S. Pat. No. 6,447,942 describes a direct methanol fuel cell in which liquid fuel is introduced to the anode by capillary action to a porous material that acts as a wick and which stays wetted with fuel. Another example of a direct-injection fuel cell system is commonly owned U.S. Pat. No. 6,981,877 of Ren et al, for a SIMPLIFIED DIRECT-OXIDATION FUEL CELL SYSTEM, which describes a direct-injection fuel feed system that feeds substantially 100% methanol to an anode chamber without active collection or pumping of water produced at the cathode. Other DOFCs provide fuel in evaporated methanol form to the anode. For example, commonly owned United States Published Patent Application No. US2005/0170224 of Ren et al, for a CONTROLLED DIRECT LIQUID INJECTION VAPOR FEED, describes a system in which liquid fuel is injected with a pump into an evaporator pad by a device with many injection ports; in another embodiment a dispersion member is placed between the evaporator pad and the anode GDL to effectively disperse the fuel.
Challenges are presented in such designs that include managing hydraulic and gravitational pressure in various orientations, as well as in providing components that adjust for the concentration of fuel in the evaporation pad being highest at the injection ports, in order to more uniformly distribute the fuel.
Notably, these prior techniques for direct injection of fuel feed in a vapor form each describe the liquid-to-vapor transition happening in close proximity to the anode GDL. In such designs, the fuel is distributed from a single point fuel source across the active area of the fuel cell. However, because it is difficult to uniformly distribute the vaporous fuel, water can build up in areas where there is a lower concentration of fuel. Prior techniques attempt to mitigate the water problem by providing a dispersion member between an evaporation pad and the anode catalyst, however this still leaves void spaces in which water can collect. It has been found that the fuel diffuses through water droplets at a diffusion rate that is orders of magnitude lower than fuel diffusing through gas such as CO2. Thus, randomly distributed water droplets in the anode chamber void spaces can still result in a spatially non-uniform distribution of fuel to the anode catalyst which reduces performance.
In addition, there is also a temperature dependency that leads to degraded performance. More specifically, as noted, prior designs involve a liquid-to-vapor transition that happens in close proximity to the anode aspect of the MEA. The vapor delivery rate to the anode catalyst in such prior techniques is a function of the vapor pressure of fuel and the porosity of the fuel distribution layers. But the vapor pressure of the fuel is dependent upon the temperature at the area where the evaporation occurs. It has been found that, for a given porosity of layers between the liquid fuel and the anode catalyst, the vapor pressure of the vaporous fuel results in a desired fuel feed rate to the anode catalyst only at a single design point temperature. However, if the temperature in that area of the fuel cell is higher than this single design point temperature, then the vapor pressure is affected and a higher fuel-feed rate occurs. When the temperature is lower than the single design point temperature, then the vapor pressure is such that a lower fuel feed rate results. Thus, the vapor pressure and fuel feed rate are difficult to control due to this temperature dependency.
The temperature dependency can be worsened by the heat of the fuel cell operation itself. As the fuel cell reactions occur, heat can build up which may affect the temperature at the MEA, and cause the cathode to dry out.
Another problem is caused by the heat loss due to vaporization of the fuel acting to cool an area to a temperature that is lower then the membrane and catalyst layers. If the cooling is sufficient, then water generated by the fuel cell reaction at the MEA temperature may have a dew point that is higher than the temperature of the evaporation area of the fuel cell. This can result in condensation of water at the evaporator surface in the anode chamber, thus leading to the problems discussed above regarding build up of water in the active area of the anode.
There remains a need, therefore, for a direct oxidation fuel cell system that removes heat from the fuel cell, maintains an even MEA temperature, and allows sufficient air and water to the cathode aspect of the fuel cell. There remains yet a further need for a direct oxidation fuel cell system having heat and water management features that add minimum complexity, weight, and/or size when integrated into the fuel cell system.
The present invention overcomes the disadvantages of the prior art by providing a multi-function heat spreader assembly for use with a fuel cell. The heat spreader assembly comprises a heat spreader element, and a bulk composite material layer. Preferably, the heat spreader element includes a copper layer sandwiched between two stainless steel layers. The stainless steel layers are roll bonded onto the copper. The bulk composite material layers are then glued to the stainless layers using a similar composite material or conductive thermal set adhesive. The lamination enables heat and electricity to flow from the cathode while maintaining low resistance among other layers of the fuel cell system.
The bulk composite material layers function as a cold side of an enthalpy exchanger and cathode flow field. Both layers include flow channels for evenly distributing air to the cathode and enthalpy exchanger.
The heat spreader assembly performs a number of functions within a fuel cell system. The heat spreader element functions to disperse heat generated by the reactions in the fuel cell. It also functions as a current collector for the electricity generated by the fuel cell, and it acts as a flow field plate for both, the cathode and the cold side of an enthalpy exchanger. The assembly also provides compression for MEA conductivity and integrity of the fuel cell system. With many functions being performed by a single assembly, the present invention reduces the number of components required in the fuel cell system, thereby contributing to a smaller form factor, and simplification of the manufacturing process.
The heat spreader assembly may be produced by either a hot bonding process or an over molding process. Alternatively, the heat spreader assembly may be formed from aluminum and coated with a conductive impermeable coating.
The invention description below refers to the accompanying drawings, of which:
The heat spreader element 190, as shown in
Further, each stainless steel layer is laminated with a thermal set conductive composite material, such as BMCI (Bulk Molding Compounds Inc.). The lamination enables heat and electricity to flow from the cathode while maintaining low resistance among other layers of the fuel cell.
One edge of the heat spread element 190 extends to form a heat switch tab 150, as shown best in
The bulk composite material layer 110 comprises an electrically conductive bulk molding compound, such as BMC 940 or BMC 945 from Bulk Molding Compounds, Inc. The heat spreader element 190 provides desired stiffness and dimensional stability for the fuel cell. In addition, flow channels 115 are formed in the bulk composite material to allow even distribution of incoming air across the surface of the cold side of the enthalpy exchanger. Furthermore, as described below, the bulk composite material layer 110 functions as a cold side component of an enthalpy exchanger system in the fuel cell.
Additionally, the heat spreader assembly 100 may include a cathode flow field plate 175 (shown in
The combination of the heat spreader element 190 and the bulk composite material layer 110 and 175 functions as a heat spreader assembly that disperses heat generated the fuel cell.
In a first embodiment, the bulk composite material layers 110 and 175 are glued to the stainless steel layers 120 and 140 using a composite material similar to the material of the bulk composite material layer 110. The glue is applied to the stainless steel layers 120 and 140 using a roller just prior to the bulk composite material layers 110 and 175 being compressed at a high temperature in a heat press. Additionally, gaskets 160 (from
The heat spreader assemblies 500A, 500B in
In accordance with a further aspect of the invention, as shown in
A fuel distribution structure 650 provides a two way distribution to supply fuel to two fuel cells that are disposed on opposite sides of that structure. A first fuel cell has an MEA 620 and a second fuel cell has a second MEA 622. The fuel distribution structure 650 is, in the illustrative embodiment, a component having a fuel inlet 652, which is coupled in fluid communication with one or more serpentine flow channels 654.
The first fuel cell (which is the upper fuel cell in the figure, however, it should be understood that the assembly is orientation independent and thus will operate in orientations other that that shown in
The first fuel cell has an anode current collector assembly 625 which is adjacent to an anode aspect of the MEA 620. Adjacent to a cathode aspect of the MEA 620 is an enthalpy exchanger and heat management assembly which is generally designated by reference number 618. The enthalpy exchanger and heat management assembly 618 includes a heat spreader assembly 100A that functions as a cold side element and a cathode flow field. An enthalpy exchange membrane 615 is located between the heat spreader assembly 100A and hot side element 610.
Similarly, the second fuel cell includes a second methanol delivery film (MDF) 642 and a second PVDF layer 632. In addition, the second fuel cell has an anode current collector assembly 627 which is adjacent to the anode aspect of the MEA 622 of that fuel cell. On the cathode side of the second fuel cell, is a second enthalpy exchanger and heat management assembly 616 which has a heat spreader assembly 100B that functions as a cold side element and a cathode flow field. An enthalpy exchange membrane 617 is located between the heat spreader assembly 100B and the hot side element 612.
In operation, fuel is delivered to fuel inlet 652 of the fuel distribution structure 654. Typically, the fuel is in a liquid form when it is delivered to the fuel inlet 652. In the meantime, the heat spreader elements 190 provide adequate heat for vaporizing the fuel. The heat needed to vaporize the fuel is about 5-10% of waste reaction heat. The vapor pressure caused as the fuel vaporizes acts to deliver the fuel to the MDF layers 640 and 642 in a generally uniform and even manner. The MDF layers help to further distribute the fuel through each anode current collector 625 and 627, to the respective anode aspects of the MEAs 620 and 622. The CO2 resulting from the anode reaction is vented to the ambient which in turn causes the pressure in anode void spaces to be at ambient pressure. Because the vapor pressure of the fuel is higher than the ambient pressure, fuel tends to flow freely to fill any anode void spaces. The vapor pressure of the fuel allows it to fill such spaces, further adding to the uniformity of fuel distribution.
At the cathode side of each fuel cell, pressurized air is delivered to the cathode portion of the fuel cell through air inlet 611, 614. The enthalpy exchanger and heat spreader assembly 618 includes a heat spreader assembly 100A which has a bulk composite material layer 110 that is an electrically conductive element that also has flow channels formed therein. The bulk composite material layer 110 also functions as the cold side of the enthalpy exchanger.
A cold side element receives incoming pressurized air and directs the air towards the cathode aspect of the MEA 620. As is understood by those skilled in the art, oxygen in the air reacts with the hydrogen ions that cross the membrane to form water. The water is typically in vapor form. A microporous layer (not shown in
In turn, water vapor that is not pushed back to the anode side (mixed with unreacted air) is directed through the hot side of the enthalpy exchanger, along the enthalpy exchange membrane 615 that is disposed adjacent to the heat spreader assembly 100. The enthalpy exchange membrane 615 passes exhaust heat and water vapor to the incoming pressurized air that is directed by the cold side element. This allows the incoming air to be humidified, thereby avoiding cathode membrane dry out. In accordance with another aspect of the invention, the flow from the anode exhaust can be sent back into the hot side of the enthalpy exchanger to use the water from the anode to further humidify the incoming air stream.
A heat spreader assembly 100A is a thermally conductive assembly that provides the heat to vaporize the fuel, or to maintain a desired operating temperature in the MEA 620. The heat spreader assembly 100A acts to uniformly distribute air across the cathode aspect of the MEA 620.
Similarly, the second fuel cell has MEA 622 has an enthalpy exchanger and heat spreader assembly 616 that includes a heat spreader assembly 100B like that described above. Assembly 616 functions, in part, to uniformly distribute air across the cathode aspect of the MEA 622.
It should be understood that the heat spreader assembly of the present invention performs a number of functions within the fuel cell system. It acts as a current collector for the electricity generated by the fuel cell, and it acts as a flow field plate for the cathode and cold side of the enthalpy exchanger. The internal layer of the heat spreader assembly is the heat spreader layer. The lower layer is the cathode flow field plate 175 which distributes the air evenly across the cathode aspect of the MEA. It also provides compression for stabilization and integrity of the fuel cell system. With many functions being performed by a single component, this further reduces the number of components required in the fuel cell system, thereby contributing to the smaller form factor, and simplification of the manufacturing process.
The foregoing description has been directed to specific embodiments of the invention. It will be apparent, however, that other variations and modifications may be made to the described embodiments, with the attainment of some or all of the advantages of such. Accordingly this description is to be taken only by way of example and not to otherwise limit the scope of the invention. Therefore, it is the object of the appended claims to cover all such variations and modifications as come within the true spirit and scope of the invention.
This application is related to commonly owned United States Patent Application of Leach, et al. entitled DIRECT OXIDATION FUEL CELL SYSTEM WITH UNIFORM VAPOR DELIVERY OF FUEL which is being filed on even date herewith and is identified by Attorney Docket No. 107044-0077, and which is presently incorporated by reference herein in its entirety.