Abstract: A membrane electrode assembly comprises an anode electrode comprising an anode gas diffusion layer and an anode catalyst layer; a cathode electrode comprising a cathode gas diffusion layer and a cathode catalyst layer; and a polymer electrolyte membrane interposed between the anode catalyst layer and the cathode catalyst layer; wherein the cathode catalyst layer comprises: a first cathode catalyst sublayer adjacent the polymer electrolyte membrane, the first cathode catalyst sublayer comprising a first catalyst supported on a first carbonaceous support and a second catalyst supported on a second carbonaceous support; and a second cathode catalyst sublayer adjacent the cathode gas diffusion layer, the second cathode catalyst sublayer comprising a third catalyst supported on a third carbonaceous support; wherein the first carbonaceous support is carbon black and the second and third carbonaceous supports are graphitized carbon.

Abstract: A membrane electrode assembly comprises an anode electrode comprising an anode gas diffusion layer and an anode catalyst layer; a cathode electrode comprising a cathode gas diffusion layer and a cathode catalyst layer; and a polymer electrolyte membrane interposed between the anode catalyst layer and the cathode catalyst layer; wherein the cathode catalyst layer comprises: a first cathode catalyst sublayer adjacent the polymer electrolyte membrane, the first cathode catalyst sublayer comprising a first catalyst supported on a first carbonaceous support and a second catalyst supported on a second carbonaceous support; and a second cathode catalyst sublayer adjacent the cathode gas diffusion layer, the second cathode catalyst sublayer comprising a third catalyst supported on a third carbonaceous support; wherein the first carbonaceous support is carbon black and the second and third carbonaceous supports are graphitized carbon.

Abstract: A method for removing contaminants in a fuel cell comprises: supplying a hydrogen-based fuel to the anode; supplying a first oxidant to the cathode, wherein the first oxidant comprises at least some sulfur dioxide; drawing a primary load from the fuel cell stack while supplying the hydrogen-based fuel to the anode and the air to the cathode; shutting down the fuel cell when a voltage of the fuel cell is equal to or less than a threshold voltage at which sulfur crosses over from the cathode to the anode, wherein shutting down the fuel cell comprises: performing at least one oxidant starvation while drawing the primary load, removing the primary load after performing the at least one oxidant starvation, and bringing the anode to a high potential after removing the primary load; and thereafter, restarting the fuel cell.

Abstract: A method for removing contaminants in a fuel cell comprises: supplying a hydrogen-based fuel to the anode; supplying a first oxidant to the cathode, wherein the first oxidant comprises at least some sulfur dioxide; drawing a primary load from the fuel cell stack while supplying the hydrogen-based fuel to the anode and the air to the cathode; shutting down the fuel cell when a voltage of the fuel cell is equal to or less than a threshold voltage at which sulfur crosses over from the cathode to the anode, wherein shutting down the fuel cell comprises: performing at least one oxidant starvation while drawing the primary load, removing the primary load after performing the at least one oxidant starvation, and bringing the anode to a high potential after removing the primary load; and thereafter, restarting the fuel cell.

Abstract: Power plant systems and processes are described that enable recovery of at least a portion of the fuel storage energy associated with a storage system for supplying fuel to the power plant systems. A first embodiment of an energy-recovery power plant system includes at least one fuel storage container and at least one expander that can receive fuel from the fuel storage container at a first pressure and provide the fuel to the power plant at a second pressure that is lower than the first pressure. A second embodiment of an energy-recovery power plant system includes a first conduit fluidly coupling the fuel storage container and the power plant for delivering fuel from the fuel storage container to the power plant and at least one regenerative thermodynamic cycle engine thermally coupled to the first conduit such that heat may be exchanged between the fuel and a working fluid for the regenerative thermodynamic cycle engine.

Abstract: A voltage reversal tolerant fuel cell anode structure that includes a gas diffusion layer is prepared by a method that comprises: (a) applying to the gas diffusion layer a first carbon component comprising a sacrificial carbon component having substantially no resistance to corrosion during cell reversal at fuel cell operating temperatures, and (b) applying to the gas diffusion layer a second carbon component. The first carbon material has a BET surface area of at least 350 m2g?1. The second carbon component supports an electrocatalyst material and has substantially more resistance to corrosion during cell reversal at fuel cell operating temperatures than the first carbon component.

Abstract: A significant problem in PEM fuel cell durability is in premature failure of the ion-exchange membrane and in particular by the degradation of the ion-exchange membrane by reactive hydrogen peroxide species. Such degradation can be reduced or eliminated by the presence of an additive in the anode, cathode or ion-exchange membrane. The additive may be a radical scavenger, a membrane cross-linker, a hydrogen peroxide decomposition catalyst and/or a hydrogen peroxide stabilizer. The presence of the additive in the membrane electrode assembly (MEA) may however result in reduced performance of the PEM fuel cell. Accordingly, it may be desirable to restrict the location of the additive to locations of increased susceptibility to membrane degradation such as the inlet and/or outlet regions of the MEA.

Abstract: In a solid polymer fuel cell series, various circumstances can result in a fuel cell being driven into voltage reversal. For instance, cell voltage reversal can occur if that cell receives an inadequate supply of fuel. In order to pass current, reactions other than fuel oxidation may take place at the fuel cell anode, including water electrolysis and oxidation of anode components. The latter may result in significant degradation of the anode, particularly if the anode employs a carbon black supported catalyst. Such fuel cells can be made more tolerant to cell reversal by using higher catalyst loading or coverage on the anode catalyst support or a more oxidation resistant anode catalyst support, such as a more graphitic carbon or Ti4O7.

Abstract: An electrochemical fuel cell stack comprises a plurality of fuel cell assemblies, wherein, each fuel cell assembly comprises a cell compressed between a pair of flow field plates, a perimeter seal circumscribing the cell and interposed between the pair of flow field plates, and a first diode, having an aspect ratio greater than 10:1, positioned adjacent to, and outside of, the perimeter seal along a first edge of the cell and interposed between the pair of flow field plates.

Abstract: A solid polymer electrolyte fuel cell stack having a plurality of fuel cells, wherein at least one cell of the fuel cell stack has a resistance to corrosion that is greater than a significant portion of the other fuel cells of the stack. In one embodiment, the at least one fuel cell of the fuel cell stack that is more resistant to corrosion is one or both end cells of the stack. Also disclosed is a fuel cell system containing such a stack, as well as methods for reducing degradation of the same during operation.

Abstract: In a solid polymer fuel cell series, various circumstances can result in the fuel cell being driven into voltage reversal. For instance, cell voltage reversal can occur if that cell receives an inadequate supply of fuel (for example, fuel starvation). In order to pass current during fuel starvation, reactions other than fuel oxidation may take place at the fuel cell anode, including water electrolysis and oxidation of anode components. The latter may result in significant degradation of the anode. Such fuel cells can be made more tolerant to cell reversal by promoting water electrolysis over anode component oxidation at the anode. This can be accomplished by incorporating a catalyst composition at the anode to promote the water electrolysis reaction, in addition to the typical anode electrocatalyst for promoting fuel oxidation.

Abstract: Various systems, method and apparatuses are disclosed that include a pressure swing adsorption apparatus coupled to a fuel cell, wherein the fuel cell receives at least a portion of a product gas from the pressure swing adsorption and powers the pressure swing adsorption apparatus. Also disclosed is a portable gas separator that include a housing that houses a rotary pressure swing adsorption apparatus.

Abstract: The electrochemical performance of an ion-exchange membrane in a fuel cell system may be improved by impregnating therein a perfluoroamine. The amine may be primary, secondary or tertiary. Further, the amine is preferably water insoluble or only slightly water soluble. For example, the amine may be perfluorotriamylamine or perfluorotributylamine. Use of such a membrane system within a fuel cell may allow high or low temperature operation (i.e. at temperatures greater than 100° C. or less than 0° C.) as well as operation at low relative humidity.

Abstract: A solid polymer electrolyte fuel cell stack having a plurality of fuel cells, wherein at least one cell of the fuel cell stack has a resistance to corrosion that is greater than a significant portion of the other fuel cells of the stack. In one embodiment, the at least one fuel cell of the fuel cell stack that is more resistant to corrosion is one or both end cells of the stack. Also disclosed is a fuel cell system containing such a stack, as well as methods for reducing degradation of the same during operation.

Abstract: An improved fuel cell anode structure comprises a substrate and a first carbon-based component. The first carbon-based component exhibits little or no resistance to corrosion. When said anode structure is incorporated into a membrane electrode assembly, the membrane electrode assembly is tolerant to incidences of cell voltage reversal.

Abstract: In a solid polymer fuel cell series, various circumstances can result in a fuel cell being driven into voltage reversal. For instance, cell voltage reversal can occur if that cell receives an inadequate supply of fuel. In order to pass current, reactions other than fuel oxidation may take place at the fuel cell anode, including water electrolysis and oxidation of anode components. The latter may result in significant degradation of the anode, particularly if the anode employs a carbon black supported catalyst. Such fuel cells can be made more tolerant to cell reversal by using higher catalyst loading or coverage on the anode catalyst support or a more oxidation resistant anode catalyst support, such as a more graphitic carbon or Ti4O7.

Abstract: Water management is improved in solid polymer electrolyte fuel cells by employing capillary channels or wicks in the lands that separate the reactant distribution channels in the flow fields. Capillary action moves water within these micro-sized capillary channels or wicks. Appropriate designs can be used to assist in the removal of water from the cell and/or in the redistribution of water from relatively wet regions in the cell to relatively dry regions.

Abstract: The electrochemical performance of an ion-exchange membrane in a fuel cell system may be improved by impregnating therein a perfluoroamine. The amine may be primary, secondary or tertiary. Further, the amine is preferably water insoluble or only slightly water soluble. For example, the amine may be perfluorotriamylamine or perfluorotributylamine. Use of such a membrane system within a fuel cell may allow high or low temperature operation (i.e. at temperatures greater than 100° C. or less than 0° C.) as well as operation at low relative humidity.

Abstract: An electrochemical fuel cell stack includes a plurality of fuel cells. At least one of the fuel cells is a sensor cell. The sensor cell has at least one structural dissimilarity with respect to the remaining fuel cells of the plurality. The structural dissimilarity may include, for example, a reduced sensor cell electrochemically active area, reduced electrocatalyst loading, modified anode or cathode flow field, different electrocatalyst composition, or a modified coolant flow field configuration. The sensor cell operates under substantially the same conditions as the remaining cells in the stack. However, in response to a change in a particular stack operating condition, an electrical or thermal response, preferably a voltage change, is induced in the sensor cell which is not simultaneously induced in the remaining fuel cells. Thus, the sensor cell can detect undesirable conditions and its response can be used to initiate corrective action.

Abstract: In a solid polymer fuel cell series, various circumstances can result in a fuel cell being driven into voltage reversal by other cells in the series stack. For instance, cell voltage reversal can occur if that cell receives an inadequate supply of fuel (for example, fuel starvation). In order to pass current during fuel starvation, reactions other than fuel oxidation may take place at the fuel cell anode, including water electrolysis and oxidation of anode components. The latter may result in significant degradation of the anode. Such fuel cells can be made more tolerant to cell reversal by promoting water electrolysis over anode component oxidation at the anode. This can be accomplished by enhancing the presence of water in the anode catalyst layer through modifications to the anode structure or anode composition near or in the catalyst layer.