A process for producing a surface-modified particulate lithium nickel metal oxide material is provided. The process comprises the dry mixing lithium nickel metal oxide particles with at least one metal-containing compound using acoustic energy and then calcining the mixture at a temperature of less than or equal to 800 # C.

A copper oxide crystallite having an average particle size that is greater than or equal to 5 nm and less than or equal to 15 nm, a ratio of (−111)/(111) greater than or equal to 0.5 and less than or equal to 1.5, and a blackness My greater than or equal to 130 and less than or equal to 170. The copper oxide crystallite has a reflectivity in the visible spectrum of electromagnetic radiation that is less than or equal to 10.0%, and a reflectivity in the near-IR and LiDAR spectrum of electromagnetic radiation that is greater than or equal to 10%.

This disclosure provides systems, methods, and apparatus related to lithium-ion batteries. In one aspect, a method includes synthesizing an intermediate selected from a group of a nickel-manganese-cobalt nitrate, a nickel-manganese-cobalt acetate, a nickel-manganese-cobalt sulfate, a nickel-manganese-cobalt chloride, and a nickel-manganese-cobalt phosphate. The intermediate is mixed with a lithium salt selected from a group of LiOH, LiCl, LiNO.sub.3, LiSO.sub.4, LiF, LiBr, Li.sub.3PO.sub.4, Li.sub.2CO.sub.3, and combinations thereof to form a mixture. The mixture is annealed at a sequence of temperatures and times to form a plurality of single crystals of a lithium nickel-manganese-cobalt oxide, with no cooling of the mixture between operations of the sequence of temperatures and times.

Provided is a method of manufacturing MoS.sub.2 having a 1T crystal structure. The method includes performing phase transition from a 2H crystal structure of MoS.sub.2 to the 1T crystal structure by reacting MoS.sub.2 having the 2H crystal structure with CO gas. The phase transition includes annealing the MoS.sub.2 having the 2H crystal structure in an atmosphere including CO gas.

The present invention relates to a laser additive comprising core/shell particles, to a process for the preparation of a laser additive of this type, and to the use thereof, in particular as laser absorber in plastics and plastic-containing coatings of articles.

Dy.sub.2O.sub.3 particles of a nanoparticle scale have beneficial properties for ceramic and electronic uses. Disclosed herein are moderately dispersed Dy.sub.2O.sub.3 particles having regular morphology and lateral size ranging from about 10 nm to 1 μm. The Dy.sub.2O.sub.3 particles may exhibit a narrow particle size distribution such that the difference between D.sub.10 and D.sub.90 is about 0.1 μm to 1 μm. Further disclosed are processes of producing these moderately dispersed Dy.sub.2O.sub.3 particles. These processes do not include grinding to obtain the particles. Also disclosed herein are uses for these Dy.sub.2O.sub.3μ particles.

The present exemplary embodiments relate to a cathode active material, a manufacturing method thereof, and a lithium secondary battery including the same. A cathode active material according to an exemplary embodiment is a lithium metal oxide particle in the form of a secondary particle including a primary particle, a coating layer including a boron compound is positioned on at least a portion of a surface of the primary particle, and the boron compound includes an amorphous structure.

A lithium battery positive active material precursor, a preparation method therefor and the use thereof are provided. The precursor has a chemical formula of Ni.sub.xCo.sub.yM.sub.z(OH).sub.2, wherein M is at least one metal selected from the group consisting of Fe, Cr, Cu, Ti, Mg, W, Mo, Nb, Zn, Sn, Zr, Ga, Mn and Al, 0.3≤x≤1, 0<y≤0.5, 0<z≤0.3; and the precursor comprises aggregates of platy monocrystals and polyhedral monocrystal particles. In the XRD pattern of the precursor, I(001), I(100) and I(101) satisfy the following relationship: I(001)/I(100) is not less than about 1.5, and I(001)/I(101) is not less than about 1.2.

The present invention comprises, in lithium composite oxide particles, an overlithiated oxide having a layered crystal structure and represented by chemical formula 1 below, and comprises a lithium manganese oxide represented by chemical formula 2 below outside the lithium composite oxide particles, wherein the overlithiated oxide included in the particles and the lithium manganese oxide included outside the particles have different Li/IM values. [Chemical formula 1] rLi.sub.2MnO.sub.3.(1-r)Li.sub.aNi.sub.xCo.sub.yMn.sub.zM1.sub.1-(x+y+z)O.sub.2 (wherein, in chemical formula 1, 0<r≤0.6, 0<a≤1, 0≤x≤1, 0≤y<1, 0≤z<1, and 0<x+y+z≤1, and M1 is at least any one selected from Na, K, Mg, Al, Fe, Cr, Y, Sn, Ti, B, P, Zr, Ru, Nb, W, Ba, Sr, La, Ga, Mg, Gd, Sin, Ca, Ce, Fe, Al, Ta, Mo, Se, Zn, Nb, Cu, in, S, B, and Bi) [Chemical formula 2] Li.sub.bMn.sub.pO.sub.q (wherein, in chemical formula 2, 0.1≤b/p≤2.5 and 0<q≤15).

A method of preparing iron oxide nanoparticles using an herbal mixture comprising Capparis spinosa, Cichorium intybus, Solanum nigrum, Cassia occidentalis, Terminalia arjuna, Achillea millefolium, and Tamarix gallica. The method produces crystalline γ-Fe.sub.2O.sub.3 nanoparticles which are superparamagnetic. The iron oxide nanoparticles are used in a method of killing or inhibiting the growth of a bacteria and/or fungus, particularly in the form of a biofilm. The nanoparticles are also used in a method of treating colon cancer.