The present invention relates to a cathode for a metal-air battery, a method for manufacturing the same, and a metal-air battery including the same. The cathode comprises a needle-shaped core including two or more species of metals selected from the group consisting of nickel, cobalt, manganese, zinc, iron, copper, and chrome, or a cobalt oxide; and a flake-shaped shell including an oxide containing two or more species of metals selected from the group consisting of nickel, cobalt, manganese, zinc, iron, copper, and chrome or a cobalt oxide. As such, the core-shell structure may lead to a reduction in the charge voltage of the metal-air battery as well as the taking of the good capacity characteristics of the transition metal oxide. Further, according to the present invention, the cathode for a metal-air battery may be produced without adding carbon or binder.

Method of operating a secondary Metal-Air electrochemical cell with a metal anode and an air cathode including the steps of (a) at start of a charging session, creating in less than 2 seconds an oxygen gas-shield on the electrolyte side of the air-electrode obstructing ion passage between the bulk of the electrolyte and the air-electrode; (b) charging the cell without anodic polarization of the air-electrode with the help of (i) electric conductive material placed between the electrolyte side of air-electrode and the bulk of electrolyte, and, (ii) the oxygen gas-shield obstructing passage of ions of the electrolyte between the electrolyte side of air-electrode and the bulk of electrolyte; (c) removing the oxygen gas-shield at start of a discharging session.

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.

A solid oxide electrochemical device comprises a solid electrolyte layer, the first surface and second surface having surface pores formed therein; a first composite electrolyte layer composed of metal and a solid electrolyte and having a first porosity; a second composite electrolyte layer composed of metal and the solid electrolyte and having the first porosity, the solid electrolyte layer sandwiched between the first composite electrolyte layer and the second composite electrolyte layer; a cathode on one of the first composite electrolyte layer and the second composite electrolyte layer; and an anode on another of the first composite electrolyte layer and the second composite electrolyte layer. The anode comprises an anode metal layer comprising pores; anode active material; and reforming catalyst, wherein the anode active material and the reforming catalyst line walls of the pores in the anode metal layer.

The present specification relates to a carrier-nanoparticle complex, a catalyst including the same, an electrochemical cell or a fuel cell including the catalyst, and a method for preparing the same.

An electrode material includes: (1) a catalyst support; and (2) PtNiN-M nanostructures affixed to the catalyst support, wherein N is a transition metal selected from Group 9 and Group 11 of the Periodic Table, and M is a transition metal selected from Group 5 and Group 6 of the Periodic Table.

Compositions and processes for optimizing oxygen reduction and oxygen evolution reactions are provided. Oxygen reduction and oxygen evolution catalysts include oxide compositions having a general formula a formula A.sub.2-xMO.sub.y, where x is electrochemically tuned to find optimal A content that delivers the best catalytic performance in a chemical system. The process provides the ability to find the optimal catalytic performance by tuning A and hence, the binding strength of O.

The present invention relates to a cathode material for a lithium-air battery and a method of manufacturing a cathode using the same. The cathode material of the present invention includes a solvent component and thus includes an electrolyte in a small amount compared to a conventional cathode material, thereby reducing the weight of a cathode manufactured using the cathode material, ultimately increasing the energy density of a lithium-air battery including the cathode.

A solid oxide electrochemical cell includes a solid oxide electrolyte, a fuel-side electrode located on a first side of the solid oxide electrolyte, and an air-side electrode located on a second side of the solid oxide electrolyte. The air-side electrode includes a strontium getter material, a current collector layer and a functional layer located between the current collector layer and the second side of the solid oxide electrolyte.

A manufacturing method of a proton battery and a proton battery module are provided. The manufacturing method of the proton battery includes the steps of providing a positive electrode, a negative electrode, and a polymer exchange membrane, and assembling the positive electrode, the negative electrode, and the polymer exchange membrane, in which the polymer exchange membrane is interposed between the positive electrode and the negative electrode. The step of providing the negative electrode at least includes forming a carbon layer on a substrate, and performing a polarization process on the carbon layer.