According to one embodiment, a tungsten oxide material containing potassium is provided. The tungsten oxide material has a shape of particles including a central section and a peripheral section adjacent to the central section, and having an average particle size of 100 nm or less. A periodicity of a crystal varies between the central section and the peripheral section. In addition, a tungsten oxide powder mass for an electrochromic device including 80% by mass to 100% by mass of the tungsten oxide material is provided. Moreover, a slurry for producing an electrochromic device containing the above tungsten oxide material is provided.

An oxide-based solid electrolyte with a high lithium ion conductance is provided. A lithium ion-conducting garnet type oxide includes Li, La, Ga, Zr, a halogen element, and oxygen. A lithium ion conductivity at room temperature is not lower than 1.0×10.sup.−3 S/cm. A proportion of Ga with respect to 1 mole of the oxide may be not larger than 0.5 moles.

The halogen element may be at least one type selected from the group consisting of Cl, Br, and I, and a proportion of Li with respect to 1 mole of the oxide may be not smaller than 6.1 moles and smaller than 6.5 moles.

Preparation of two-dimensional indium selenide, other two-dimensional materials and related compositions via surfactant-free deoxygenated co-solvent systems.

The present invention relates to a lithium composite oxide having improved stability and electrical characteristics as a positive electrode material by inhibiting an interfacial side reaction in the lithium composite oxide and improving the stability of a crystal structure and ion conductivity, and a lithium secondary battery including the same.

A solid electrolyte includes an ion conductor represented by at least one of Formulae 1 to 3,
Li.sub.1+3xM1.sub.1−xO.sub.2  Formula 1
wherein, in Formula 1, M1 is a trivalent element, and 0<x<1,
L.sub.1−yM2O.sub.2−yX.sub.y  Formula 2
wherein, in Formula 2, M2 is a trivalent element, X is at least one of a halogen atom or a pseudohalogen, and 0<y<1,
Li.sub.1−z(a−3)M3.sub.1−zD.sub.zO.sub.2  Formula 3
wherein, in Formula 3, M3 is a trivalent element, D is at least one of a monovalent element to a hexavalent element, and 0<z<1.

The present invention relates to single crystalline RbUO.sub.3, hydrothermal growth processes of making such single crystals and methods of using such single crystals. In particular, Applicants disclose single crystalline RbUO.sub.3 single crystalline RbUO.sub.3 in the Pm-3m space group. Unlike other powdered RbUO.sub.3, Applicants' single crystalline RbUO.sub.3 has a sufficient crystal size to be characterized and used in the fields of neutron detection, radiation-hardened electronics, nuclear forensics, nuclear engineering photovoltaics, lasers, light-emitting diodes, photoelectrolysis and magnetic applications.

The invention relates to Chevrel-phase materials and methods of preparing these materials utilizing a precursor approach. The Chevrel-phase materials are useful in assembling electrodes, e.g., cathodes, for use in electrochemical cells, such as rechargeable batteries. The Chevrel-phase materials have a general formula of Mo.sub.6Z.sub.8 (Z=sulfur) or Mo.sub.6Z.sup.1.sub.8-yZ.sup.2.sub.y (Z.sup.1=sulfur; Z.sup.2=selenium), and partially cuprated Cu.sub.1Mo.sub.6S.sub.8 as well as partially de-cuprated Cu.sub.1-xMg.sub.xMo.sub.6S.sub.8 and the precursors have a general formula of M.sub.xMo.sub.6Z.sub.8 or M.sub.xMo.sub.6Z.sup.1.sub.8-yZ.sup.2.sub.y, M=Cu. The cathode containing the Chevrel-phase material in accordance with the invention can be combined with a magnesium-containing anode and an electrolyte.

Use of nickel in a cathode material of the general formula Li (4/3-2x/3-y/3-z/3)Ni.sub.xCo.sub.yAl.sub.zMn(2/3-x/3-2y/3-2z/3)0.sub.2 wherein x is greater than 0.06 and equal to or less than 0.4; y is equal to or greater than 0 and equal to or less than 0.4; and z is equal to or greater than 0 and equal to or less than 0.05 for suppressing gas evolution during a charge cycle and/or increasing the charge capacity of the material.

This disclosure relates to the manufacture an alkali metal quaternary crystalline nanomaterial. an alkali metal quaternary crystalline nanomaterial having general Formula A (I.sub.2-II-IV-VI.sub.4); and wherein I is sodium (Na) or lithium (Li), II and IV are Zn or Sn, and VI is a chalcogens selected from the group comprising: sulphur (S), selenium (Se) or tellurium (Te). The crystal phase of the alkali metal quaternary crystalline nanomaterial may be a primitive mixed Cu—Au like structure (PMCA) and may have a space group: P42m. The nanomaterials may be adapted to provide a solar cell. Methods of manufacture are also provided.

A positive electrode active material or non-aqueous electrolyte secondary batteries comprises a Co-containing lithium transition metal oxide containing Ni, Mn, and an arbitrary element and having a layered structure, wherein the content ratio of Ni in the lithium transition metal oxide is 75 to 95 mol %, the content ratio of Mn in the lithium transition metal oxide is equal to or greater than the content ratio of Co in the lithium transition metal oxide, the content ratio of Co in the lithium transition metal oxide is 0 to 2 mol %, the content ratio of a metal element other than Li in an Li layer in the layered structure is 1 to 2.5 mol %, and, in the lithium transition metal oxide, the half width n of a diffraction peak for (208) plane of an X-ray diffraction pattern as measured by X-ray diffraction is as follows: 0.30°≤n≤0.50°.