A process of producing a cathode electrocatalyst for metal-air batteries includes providing a carbon source suspension, a metal source solution, and a nitrogen source solution, subjecting the carbon source suspension and the metal source solution to a low-temperature hydrothermal reaction, subjecting a first precursor-containing product thus formed and the nitrogen source solution to a high-temperature hydrothermal reaction, and subjecting a second precursor thus formed to a heating treatment under a protective atmosphere. A cathode electrocatalyst produced by the process is also disclosed.

A design of and the process for forming a rigidly bonded metal supported electro-chemical device stack is provided. The electro-chemical device stack can be a solid oxide fuel cell or solid oxide electrolysis stack. The stack comprises multiple planar cells connected in serial by planar metal interconnects. The cells have metal support layers on both anode and cathode sides. The interconnect has gas channels embedded. Thin ceramic electro-chemical active electrodes and electrolyte are sandwiched between the metal support layers. The cells and interconnects are rigidly bonded to form a rigid body stack. The process comprises the steps of a). forming metal supported electro-chemical device cells with metal supports on both anode and cathode sides, b). sealing the peripherals of porous cell layers with an electrically insulating sealing material such as glass. c). bonding the cells and interconnects through commonly used metal-to-metal bonding methods, such as brazing or laser welding.

A metal metal-air battery includes: an anode layer including a metal, a cathode layer spaced apart from the anode layer and including a hybrid conductive material having both electron conductivity and ionic conductivity; and a separator disposed between the anode layer and the cathode layer, wherein the hybrid conductive material includes a channel for metal ion transfer from the anode layer and a channel for electron transfer between the cathode and the anode.

Disclosed are a metal/carbon-dioxide battery and a hydrogen production and carbon dioxide storage system including the same.

A supported platinum catalyst having a high ratio of a diffraction peak intensity of a Pt (220) plane and having excellent oxidation resistance, obtained by a simple production method without using a polymer. The supported platinum catalyst includes a carbon support and platinum fine particles supported on the carbon support, the platinum fine particles being such that a ratio of a diffraction peak intensity of a (220) plane with respect to a total of diffraction peak intensities of a (111) plane, a (200) plane, and the (220) plane by X-ray diffraction is not less than 0.128.

An oxygen reduction catalyst for use in low-temperature fuel cells and a method for the production thereof. This is in particular carrier-free and free from precious metals. It is based on a conductive polymer produced from a nitrogenous aromatic monomer, which leads to conductive polymers, and an aromatic sulfonic acid, which polymer is pyrolyzed together with one or more transition metal salts and is subsequently acid etched. In one particularly advantageous configuration variant, this involves a polypyrrole produced with sulfanilic acid as a doping agent.

The embodiments herein disclose a system (1000) for managing electrical connections with electrodes in a metal-air fuel cell. The system (1000) includes a cell frame (101) and one or more anode array (102). The one or more anode array (102) is detachably provided with the cell frame (101). The one or more anode array (102) comprises one or more anode. One or more air cathode (103) is provided with the cell frame (101). One or more connector (105) connects the one or more air cathode (103) and the one or more anode array (102). A snap mechanism (106) is used for locking and unlocking the one or more anode array (102) to the cell frame (101).

Provided are a positive electrode active material with which a nonaqueous electrolyte secondary battery having a high energy density can be obtained, a nickel-manganese composite hydroxide suitable as a precursor of the positive electrode active material, and production methods capable of easily producing these in an industrial scale. Provided is a nickel-manganese composite hydroxide represented by General Formula (1): Ni.sub.xMn.sub.yM.sub.z(OH).sub.2+α and containing a secondary particle formed of a plurality of flocculated primary particles. The nickel-manganese composite hydroxide has a half width of a diffraction peak of a (001) plane obtained by X-ray diffraction measurement of at least 0.10° and up to 0.40° and has a degree of sparsity/density represented by [(void area within secondary particle/cross section of secondary particle)×100](%) of at least 0.5% and up to 10%. Also provided is a production method of the nickel-manganese composite hydroxide.

The present invention relates to a flexible electrode, a biofuel cell using the same, and a method for manufacturing the same. The electrode according to the present invention comprises: a non-electrically conductive substrate (10); a base layer (20) disposed on the outer surface of the substrate (10); a nanoparticle layer (31) including metallic nanoparticles and disposed on the outer surface of the base layer (20); and a monomolecular layer (33) including a monomolecular material having an amine group and disposed on the outer surface of the nanoparticle layer (31).

Nanoporous carbon-based scaffolds or structures, and specifically carbon aerogels and their manufacture and use thereof. Embodiments include a cathode material within a lithium-air battery, where the cathode is formed of a binder-free, monolithic, polyimide-derived carbon aerogel. The carbon aerogel includes pores that improve the oxygen transport properties of electrolyte solution and improve the formation of lithium peroxide along the surface and/or within the pores of the carbon aerogel. The cathode and underlying carbon aerogel provide optimal properties for use within the lithium-air battery.