A composite nanomaterial of ZnO impregnated by, e.g., a green copper phthalocyanine compound (CuPc) can be an efficient solar light photocatalyst for water remediation. The composite may include hollow shell microspheres and hollow nanospheres of CuPc-ZnO. CuPc may function as a templating and/or structure modifying agent, e.g., for forming hollow microspheres and/or nanospheres of ZnO particles. The composite can photocatalyze the degradation of organic pollutants such as crystal violet (CV) and 2,4-dichlorophenoxyacetic acid as well as microbes in water under solar light irradiation. The ZnO-CuPc composite can be stable and recyclable under solar irradiation.

The present invention relates to a method of preparing an iron-chromium oxide using an ion-exchange resin. Moreover, the present invention relates to a method of preparing an iron-chromium oxide that can be used as a cathode material for lithium-ion batteries. According to one aspect of the present invention, it has the effect of providing a cathode material for lithium-ion batteries with a high capacitance, while exhibiting a voltage similar to that of a transition-metal oxide (2-4.5 V vs Li.sup.+/Li).

The present disclosure provides an irreversible additive contained in a cathode material for a secondary battery, wherein the irreversible additive is an oxide represented by the following chemical Formula 1, and wherein the oxide has a trigonal structure, a cathode material including the irreversible additive, and a secondary battery including the cathode material:

Li.sub.2+aNi.sub.1-bMo.sub.bO.sub.2+c  (1) in Formula 1, −0.2≤a≤0.2, 0<b≤0.2, 0≤c≤0.2.

The present invention relates to a MXene electrode for electronic products having excellent oxidation stability and flexibility and a method for manufacturing the same, and more specifically to a MXene electrode which has excellent stability from changes such as oxidation in a driving environment, excellent transparency and mechanical properties and high electrical conductivity such that it is appropriate to be used as a transparent electrode in electronic devices, and a method for manufacturing the same.

One aspect of the present invention is a solid electrolyte containing lithium, phosphorus, sulfur, halogen, and tin as constituent elements and having a crystal structure.

A layered-oxide positive electrode active material may have a molecular formula of Na.sub.xMn.sub.aFe.sub.bNi.sub.cM.sub.dN.sub.eO.sub.2-δQ.sub.f, where a doping element M is selected from at least one of Cu, Li, Ti, Zr, K, Sb, Nb, Mg, Ca, Mo, Zn, Cr, W, Bi, Sn, Ge, or Al, a doping element N is selected from at least one of Si, P, B, S, or Se, a doping element Q is selected from at least one of F, Cl, or N, 0.66≤x≤1, 0<a≤0.70, 0<b≤0.70, 0<c≤0.23, 0≤d<0.30, 0≤e≤0.30, 0≤f≤0.30, 0≤δ≤0.30, a+b+c+d+e=1, 0<e+f≤0.30, 0<(e+f)/a≤0.30, 0.20≤d+e+f≤0.30, and (b+c)/a≤1.5.

An electrode material of the present disclosure is an electrode material that includes a compound represented by the chemical formula BaZr.sub.1-x-yM.sub.xCo.sub.yO.sub.3-δ. M is In or Yb, and the chemical formula satisfies 0<x<1, 0<y<1, 0<(x+y)<1, and 0<δ<1. A membrane electrode assembly of the present disclosure includes a first electrode including the electrode material, and an electrolyte membrane provided on a first main surface of the first electrode.

The solid electrolyte material of the present disclosure includes Li, Ca, Y, Sm, X, and O, where Xis at least one selected from the group consisting of F, Cl, Br, and I; and the molar ratio of O to the sum of Y and Sm in a surface area of the solid electrolyte material is higher than the molar ratio of O to the sum of Y and Sm in the entire solid electrolyte material.

Several variations of synthetic carbon materials are disclosed. The materials can assume a variety of properties, including high electrical conductivity. The materials also can have favorable structural and mechanical properties. They can form gas impenetrable barriers, form insulating structures, and can have unique optical properties.

The invention relates to a process for the preparation of a vanadium-carbon phosphate composite material, a vanadium-carbon phosphate composite material obtained according to the process, and to the uses of the composite material, especially as a precursor for the synthesis of electrochemically-active materials, electrode or active anode material.