A cathode configured to use oxygen as a cathode active material includes: a porous film including a metal oxide, where a porosity of the porous film is about 50 volume percent to about 95 volume percent, based on a total volume of the porous film, and an amount of an organic component in the porous film is 0 to about 2 weight percent, based on a total weight of the porous film.

Embodiments of the present disclosure are directed to methods of producing a hydrogen-selective oxygen carrier material comprising combining one or more core material precursors and one or more shell material precursors to from a precursor mixture and heat-treating the precursor mixture at a treatment temperature to form the hydrogen-selective oxygen carrier material. The treatment temperature is greater than or equal to 100° C. less than the melting point of a shell material, and the hydrogen-selective oxygen carrier material comprises a core comprising a core material and a shell comprising the shell material. The shell material may be in direct contact with at least a majority of an outer surface of the core material.

A metal-oxide perovskite material having a general formula Ca.sub.1-xCe.sub.xTi.sub.yMn.sub.1-yO.sub.3, where x is in a range of about 0.3 to about 0.35 and y is in a range of about 0.25 to about 0.35. Producing hydrogen and oxygen includes heating the metal-oxide perovskite material; reducing the metal-oxide perovskite material to yield a reduced metal-oxide perovskite material; cooling the reduced metal-oxide perovskite material; and contacting the reduced metal-oxide perovskite material with a re-oxidizing fluid including steam to yield hydrogen and a re-oxidized metal-oxide perovskite material. Producing carbon monoxide and oxygen includes heating the metal-oxide perovskite material; reducing the metal-oxide perovskite material to yield a reduced metal-oxide perovskite material; cooling the reduced metal-oxide perovskite material, and contacting the reduced metal-oxide perovskite material with a re-oxidizing fluid including carbon dioxide to yield carbon monoxide and a re-oxidized metal-oxide perovskite material.

A ceramic member includes a perovskite compound including La, Ca, Mn, and Ti as main components, wherein the amount of Ti is about 5 parts by mole or more and about 20 parts by mole or less, the amount of Ca is about 10 parts by mole or more and about 27 parts by mole or less, and the total amount of La and Ca is about 85 parts by mole or more and about 97 parts by mole or less based on the total amount of Mn and Ti of 100 parts by mole.

The invention provides a ceramic composite oxide of formula (I): (1−x)AaBbOy+xCcDdOz (I) wherein A, B, C and D are each independently selected from the group consisting of Li, Na, Mg, Al, P, K, Ca, Sc, Ti, Cr, Mn, Fe, Co, Ni, Cu, Zn, Ga, Sr, Y, Zr, Nb, Mo, Ru, In, Sn, Ba, La, Ce, Pr, Nd, Sm, Eu, Gd, Er, Tm, Yb, Lu, Ta, W, Bi and mixtures thereof; x is 0.05 to 0.95; y and z are balanced by the charge of the cations; 0≤a, b, c, d≤1; and wherein said ceramic composite oxide has an average particle size diameter of 10 to 700 nm.

A negative thermal expansion material and a preparation method thereof, and a negative thermal expansion film and a preparation method thereof are provided. The negative thermal expansion material includes Eu.sub.0.85Cu.sub.0.15MnO.sub.3-δ, wherein 0≤δ≤2.

An antimicrobial material including a substrate and an antimicrobial mixed metal oxide, mixed metal sulfide, or mixed metal oxysulfide in and/or on the substrate is described, as well as antimicrobial coating materials and coatings formed therefrom. The antimicrobial material may be constituted in an antimicrobial surface of a surface-presenting substrate, to combat transmission and spread of microbial disease, e.g., disease mediated by microbial pathogens such as bacteria, viruses, and fungi. Antimicrobial mixed metal oxide, mixed metal sulfide, or mixed metal oxysulfide as described may be contacted with microorganisms to effect inactivation thereof.

Embodiments of the present disclosure are directed to hydrogen-selective oxygen carrier materials and methods of using hydrogen-selective oxygen carrier materials. The hydrogen-selective oxygen carrier material may comprise a core material, which includes a redox-active transition metal oxide; a shell material, which includes one or more alkali transition metal oxides; and a support material. The shell material may be in direct contact with at least a majority of an outer surface of the core material. At least a portion of the core material may be in direct contact with the support material. The hydrogen-selective oxygen carrier material may be selective to combust hydrogen in an environment that includes hydrogen and hydrocarbons.

Oxide compositions comprising a modified structure which includes the formula ABO.sub.z. The A component may comprise at a cation of least one element selected from the group consisting of Mg, Ca, Sr, Ba, Sc, Y, La, Ce, Pr, Nd, Gd, and Zn, and the B component may comprise a cation of at least one element selected from the group consisting of V, Cr, Mn, Fe, Co, and Ni. Batteries and supercapacitors comprising the oxide compositions of the present disclosure and methods of making the oxide compositions of the present disclosure are also provided.

Embodiments of the present disclosure are directed to methods of producing a hydrogen- selective oxygen carrier material comprising combining one or more core material precursors and one or more shell material precursors to from a precursor mixture and heat-treating the precursor mixture at a treatment temperature to form the hydrogen-selective oxygen carrier material. The treatment temperature is greater than or equal to 100° C. less than the melting point of a shell material, and the hydrogen- selective oxygen carrier material comprises a core comprising a core material and a shell comprising the shell material. The shell material may be in direct contact with at least a majority of an outer surface of the core material.