Provided herein are processes for producing positive electrode active substance particles for non-aqueous electrolyte secondary batteries which is excellent in life characteristics of a battery with respect to a repeated charging and discharging performance thereof, as well as a non-aqueous electrolyte secondary battery. In particular, provided herein are processes for producing a positive electrode active substance for non-aqueous electrolyte secondary batteries comprising lithium transition metal layered oxide having a composition represented by the formula: Li.sub.a(Ni.sub.xCo.sub.yMn.sub.1-x-y)O.sub.2 wherein a is 1.0≤a≤1.15; x is 0<x<1; and y is 0<y<1, in which the positive electrode active substance is in the form of secondary particles formed by aggregating primary particles thereof, and a coefficient of variation of a compositional ratio: Li/Me wherein Me is a sum of Ni, Co and Mn as measured on a section of the secondary particle is not more than 25%.

A positive active material for a rechargeable lithium battery includes a lithium nickel-based composite oxide including a secondary particle in which a plurality of plate-shaped primary particles are agglomerated; and a lithium manganese composite oxide having at least two crystal lattice structures, wherein the secondary particle has a regular array structure in which (003) planes of the primary particles are oriented in a vertical direction with respect to the surface of the secondary particle.

A negative active material includes a carbon material. The carbon material satisfies the following relationship: 6<Gr/K<16, Gr is a graphitization degree of the carbon material, measured by X-ray diffraction; and K is a ratio Id/Ig of a peak intensity Id of the carbon material at a wavenumber of 1250 cm.sup.−1 to 1650 cm.sup.−1 to a peak intensity Ig of the carbon material at a wavenumber of 1500 cm.sup.−1 to 1650 cm.sup.−1, and is measured by using Raman spectroscopy, and K is 0.06 to 0.15.

This positive electrode active material for a non-aqueous electrolyte secondary battery contains a lithium-transition metal composite oxide that has a rock salt-related structure and is represented by the compositional formula Li.sub.aMn.sub.bM.sub.cO.sub.2-xF.sub.x (in the formula: M is at least one metal element excluding Li and Mn; 2.000<a+b+c≤2.195; 1.0<a≤1.4; 0.4≤b≤0.9; 0≤c≤0.2; and 0.2≤x≤0.6). The metal element M preferably is at least one selected from Ni, Sn, Mo, Ti, W, Zn, and Al.

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.

The present invention provides the compound LiMn.sub.2--x-yNa.sub.xM.sub.yO.sub.4/Na.sub.1-zMnLi.sub.zM.sub.tO.sub.2/Na.sub.2CO.sub.3, to be used as a positive electrode for rechargeable lithium ion battery, where M is a metal or metalloid, 0.0≤x≤0.5; 0.0≤y≤0.5; 0.1≤z≤0.5; 0.0≤t≤0.3; as well as the method for producing it. The synthesis process includes disolving or mixing the precursor metals and then calcining them in air or controlled atmosphere in a temperature range between 250° C. and 1000° C., and for a time range of 0.5 h to 72 h to obtain the composite proposed with the interaction of its three present phases, presenting a high retention capacity during repeated loading/unloading cycles and excellent discharge capacity both at room temperature and up to 55° C.

A rechargeable battery using a solution of an aluminum salt as an electrolyte is disclosed, as well as methods of making the battery and methods of using the battery.

A positive-electrode active material contains a lithium composite oxide containing manganese. The crystal structure of the lithium composite oxide belongs to a space group Fd-3m. The integrated intensity ratio I.sub.(111)/I.sub.(400) of a first peak I.sub.(111) on the (111) plane to a second peak I.sub.(400) on the (400) plane in an XRD pattern of the lithium composite oxide satisfies 0.05≤I.sub.(111)/I.sub.(400)≤0.90.

A method of producing an inorganic material (S10) according to the present invention includes a vitrification step (S12) of applying shearing stress and compressive stress to a mixed powder (MP) of a plurality of kinds of inorganic compound powders by using a ring ball mill mechanism (70) to vitrify at least a part of the mixed powder (MP); and a dispersion step (S13) of dispersing the vitrified mixed powder (MP) after the vitrification step (S12), where a combined step of the vitrification step (S12) and the dispersion step (S13) is performed a plurality of times to obtain a vitrified inorganic material powder from the mixed powder.

The present disclosure relates to methodologies, systems and apparatus for generating lithium ion battery materials. Starting materials are combined to form a homogeneous precursor solution including lithium, and a droplet maker is used to generate droplets of the precursor solution having controlled size. These droplets are introduced into a microwave generated plasma, where micron or sub-micron scale lithium-containing particles are formed. These lithium-containing particles are collected and formed into a slurry to form lithium ion battery materials.