A catalyst particle is composed of an inner particle and an outermost layer that includes platinum and covers the inner particle. The inner particle includes on at least a surface thereof a first oxide having an oxygen defect.

The present invention relates to a secondary aluminum-air electrochemical cell. Therefore, the invention may be framed within the energy storage sector and, in particular, the sector of technologies and industries that require energy accumulators.

Provided is an air electrode/separator assembly including a hydroxide ion conductive dense separator and an air electrode layer provided on one side of the hydroxide ion conductive dense separator. The air electrode layer includes: an internal catalyst layer provided closer to the hydroxide ion conductive dense separator and filled with a mixture containing a hydroxide ion conductive material, an electron conductive material, an organic polymer, and an air electrode catalyst (provided that the hydroxide ion conductive material may be the same material as the air electrode catalyst, and provided that the electron conductive material may be the same material as the air electrode catalyst); and an outermost catalyst layer provided away from the hydroxide ion conductive dense separator having a porosity of 60% or more, composed of a porous current collector and a layered double hydroxide (LDH) covering a surface thereof.

The invention includes a method of making a catalytic electrode for a metal-air cell in which a carbon-catalyst composite is produced by heating a manganese compound in the presence of a particulate carbon material to form manganese oxide catalyst on the surfaces of the particulate carbon, and then adding virgin particulate carbon material to the carbon-catalyst composite to produce a catalytic mixture that is formed into a catalytic layer. A current collector and an air diffusion layer are added to the catalytic layer to produce the catalytic electrode. The catalytic electrode can be combined with a separator and a negative electrode in a cell housing including an air entry port through which air from outside the container can reach the catalytic electrode.

A method is disclosed for regenerating an electrode of a flow battery. The method can be executed during shutdown of the flow battery from an active charge/discharge mode to an inactive, shut-down mode in which neither a negative electrolyte nor a positive electrolyte are circulated through at least one cell of the flow battery. The method includes driving voltage of the least one cell of the flow battery toward zero by converting, in-situ, the negative electrolyte in the at least one cell to a higher oxidation state. The negative electrolyte is in contact with an electrode of the at least one cell. The higher oxidation state negative electrolyte is used to regenerate, in-situ, catalytically active surfaces of the electrode of the at least one cell.

A first proton-donating layer (20a) is a layer having a proton-donative functional group on the surface, for example, a silicon oxide layer. A second proton-donating layer (20b) is also a layer having a proton-donative functional group on the surface, for example, a silicon oxide layer. Negative surface charges are formed on the main surface section of a first base (10a) and the main surface section of a second base (10b), and these negative charges increased the proton conductivity in an aqueous solution fed to a nano channel. Although, in the aqueous solution, proton migration through hopping between water molecules contributes to its diffusion, the negative charges formed on the main surfaces of the bases (10a, 10b) attract protons in the aqueous solution, and the conduction of protons is efficiently achieved in “high-speed transfer regions” formed in the vicinity of the proton-donating layers (20a, 20b).

Provided is an oxygen reduction catalyst having a high oxygen reduction performance. An oxygen reduction catalyst according to the present embodiment includes a transition metal oxide to which an oxygen defect is introduced, and a layer that is provided on the transition metal oxide and that contains an electron conductive substance. A method for producing an oxygen reduction catalyst according to the present embodiment includes heating a transition metal carbonitride as a starting material in an oxygen-containing mixed gas. In addition, a method for producing an oxygen reduction catalyst according to the present embodiment includes heating a transition-metal phthalocyanine and a carbon fiber powder as starting materials in an oxygen-containing mixed gas.

The electrochemical cell according to the present invention has an anode, a cathode, and a solid electrolyte layer disposed between the anode and the cathode. The cathode contains a main phase and a second phase. The main phase is configured with a perovskite oxide which is expressed by the general formula ABO.sub.3 and includes at least one of Sr and La at the A site. The second phase is configured with SrSO.sub.4 and (Co, Fe).sub.3O.sub.4. An occupied surface area ratio of the second phase in a cross section of the cathode is less than or equal to 10.5%.

A catalyst comprising particles of iridium oxide and a metal oxide (M oxide), wherein the metal oxide is selected from the group consisting of a Group 4 metal oxide, a Group 5 metal oxide, a Group 7 metal oxide and antimony oxide, wherein the catalyst is prepared by subjecting a precursor mixture to flame spray pyrolysis, wherein the precursor mixture comprises a solvent, an iridium oxide precursor and a metal oxide precursor is disclosed. The catalyst has particular use in catalysing the oxygen evolution reaction.

A multi-faceted zinc-air electrochemical cell design holistically leverages interactions between components, especially with respect to conductive carbons from differing sources, lamination and the resulting impact it has on the air electrode's surface and other additives that impact the relative hydrophilicity of the membrane and/or performance of the anode, to improve the overall reliability and performance of the resulting battery.