Abstract: System, method, and circuitry for generating content for a programmable computing device based on user-selected memory regions. Contiguous regions that share memory access attributes are merged, interleaved contiguous regions that share at least one nested attribute are defined into combined regions, and remaining regions are defined as separate independent regions. A memory protection unit (MPU) region size closest to a size of each defined region is identified. If the start address of each region aligns with the address structure of the MPU region size, then those regions are assigned to MPU regions having the MPU region size; otherwise, another MPU size that aligns with the size of the regions is selected and those regions are assigned to MPU regions having that size. Content is generated to configure settings of MPU regions of the programmable computing device for the merged contiguous regions, the combined region, and the independent regions.

Abstract: A P/Metal-N—C hybrid catalyst that includes at least one nitrogen-doped carbonaceous matrix onto which at least one non-precious transition metal is covalently bonded and that includes at least one partially oxidised precious transition metal P of which the weight percentage is less than or equal to 4.0%, and preferably less than or equal to 2.0%, relative to the mass of the P/Metal-N—C hybrid catalyst. Further, an electrochemical device that includes such a device, for example a fuel cell with a polymer electrolyte membrane.

Abstract: A catalyst precursor comprising (A) a microporous support; (B) a non-noble metal precursor; and (C) a pore-filler, wherein the micropores of the microporous support are filled with the pore-filler and the non-noble metal precursor so that the micropore surface area of the catalyst precursor is substantially smaller than the micropore surface area of the support when the pore-filler and the non-noble metal precursor are absent is provided. Also, a catalyst comprising the above catalyst precursor, wherein the catalyst precursor has been pyrolysed so that the micropore surface area of the catalyst is substantially larger than the micropore surface area of catalyst precursor, with the proviso that the pyrolysis is performed in the presence of a gas that is a nitrogen precursor when the microporous support, the non-noble metal precursor and the pore-filler are not nitrogen precursors is also provided. Methods of producing the catalyst precursor and the catalyst are provided.

Abstract: A catalyst precursor is provided having a thermally decomposable porous support; an organic coating/filling compound, and a non-precious metal precursor, wherein the organic coating/filling compound and the non-precious metal catalyst precursor coat and/or fill the pores of the thermally decomposable porous support.

Abstract: A catalyst precursor comprising (A) a microporous support; (B) a non-noble metal precursor; and (C) a pore-filler, wherein the micropores of the microporous support are filled with the pore-filler and the non-noble metal precursor so that the micropore surface area of the catalyst precursor is substantially smaller than the micropore surface area of the support when the pore-filler and the non-noble metal precursor are absent is provided. Also, a catalyst comprising the above catalyst precursor, wherein the catalyst precursor has been pyrolysed so that the micropore surface area of the catalyst is substantially larger than the micropore surface area of catalyst precursor, with the proviso that the pyrolysis is performed in the presence of a gas that is a nitrogen precursor when the microporous support, the non-noble metal precursor and the pore-filler are not nitrogen precursors is also provided. Methods of producing the catalyst precursor and the catalyst are provided.

Abstract: A catalyst precursor comprising (A) a microporous support, (B) a non-noble metal precursor, and (C) a pore-filler, wherein the micropores of the microporous support are filled with the pore-filler and the non-noble metal precursor so that the micropore surface area of the catalyst precursor is substantially smaller than the micropore surface area of the support when the pore-filler and the non-noble metal precursor are absent is provided. Also, a catalyst comprising the above catalyst precursor, wherein the catalyst precursor has been pyrolysed so that the micropore surface area of the catalyst is substantially larger than the micropore surface area of catalyst precursor, with the proviso that the pyrolysis is performed in the presence of a gas that is a nitrogen precursor when the microporous support, the non-noble metal precursor and the pore-filler are not nitrogen precursors is also provided. Methods of producing the catalyst precursor and the catalyst are provided.

Abstract: A polymer electrolyte electrochemical device includes an anode current collector (1), a membrane electrode assembly (2) with anode and cathode gas backings (3, 4), and a cathode current collector (5), wherein the membrane electrode assembly is sealed and attached at least to the anode current collector by adhesive elements, thereby creating an anode gas chamber, and optionally attached to the cathode current collector by adhesive elements, the adhesive elements being electrically conducting or electrically non-conducting. The invention also relates to polymer electrolyte electrochemical device components adapted for use in a single cell electrochemical device and a series arrangement electrochemical device.

Abstract: A catalyst precursor comprising (A) a microporous support, (B) a non-noble metal precursor, and (C) a pore-filler, wherein the micropores of the microporous support are filled with the pore-filler and the non-noble metal precursor so that the micropore surface area of the catalyst precursor is substantially smaller than the micropore surface area of the support when the pore-filler and the non-noble metal precursor are absent is provided. Also, a catalyst comprising the above catalyst precursor, wherein the catalyst precursor has been pyrolysed so that the micropore surface area of the catalyst is substantially larger than the micropore surface area of catalyst precursor, with the proviso that the pyrolysis is performed in the presence of a gas that is a nitrogen precursor when the microporous support, the non-noble metal precursor and the pore-filler are not nitrogen precursors is also provided. Methods of producing the catalyst precursor and the catalyst are provided.

Abstract: A polymer electrolyte fuel cell structure includes a proton exchange membrane (4). An anode catalyst layer (1,16) is located on one side of the proton exchange membrane. A cathode catalyst layer (7) is located on the opposite side of the proton exchange membrane, and a gas distribution layer (3,5) is arranged on each side of the proton exchange membrane (4). The anode side gas distribution layer (3) is a flat, porous structure having water channels (3a) formed in the surface facing the membrane (4). The anode side gas distribution layer (3) is enclosed by a coplanar, sealing plate (2) with water inlet channels coupled to the water channels (3a) in the gas distribution layer.

Abstract: A polymer electrolyte electrochemical device includes an anode current collector (1), a membrane electrode assembly (2) with anode and cathode gas backings (3, 4), and a cathode current collector (5), wherein the membrane electrode assembly is sealed and attached at least to the anode current collector by adhesive elements, thereby creating an anode gas chamber, and optionally attached to the cathode current collector by adhesive elements, the adhesive elements being electrically conducting or electrically non-conducting. The invention also relates to polymer electrolyte electrochemical device components adapted for use in a single cell electrochemical device and a series arrangement electrochemical device.

Abstract: A cathode layer structure for a solid polymer fuel cell is disclosed. It comprises a composite cathode layer (48) of catalyst (11), anion ion conducting polymer (12) and cation conducting polymer (14). The interface between the anion ion conducting polymer (12) and the cation conducting polymer (14) is located entirely within the cathode layer (48). In particular the catalyst (11) is embedded in the anion conducting polymer (12), and the cation conducting polymer (14) encloses regions of the anion conducting polymer (12).

Abstract: A cathode layer structure for a solid polymer fuel cell is disclosed. It comprises a composite cathode layer (48) of catalyst (11), anion ion conducting polymer (12) and cation conducting polymer (14). The interface between the anion ion conducting polymer (12) and the cation conducting polymer (14) is located entirely within the cathode layer (48). In particular the catalyst (11) is embedded in the anion conducting polymer (12), and the cation conducting polymer (14) encloses regions of the anion conducting polymer (12).

Abstract: A polymer electrolyte fuel cell structure includes a proton exchange membrane (4). An anode catalyst layer (1,16) is located on one side of the proton exchange membrane. A cathode catalyst layer (7) is located on the opposite side of the proton exchange membrane, and a gas distribution layer (3,5) is arranged on each side of the proton exchange membrane (4). The anode side gas distribution layer (3) is a flat, porous structure having water channels (3a) formed in the surface facing the membrane (4). The anode side gas distribution layer (3) is enclosed by a coplanar, sealing plate (2) with water inlet channels coupled to the water channels (3a) in the gas distribution layer.