Nanoparticles of calcium hydroxide having a dumbbell shape, wherein the dumbbell shape has rounded ends separated by a narrow central portion, wherein a ratio of a largest width of the central portion to a largest width of the rounded ends is 0.30 to 0.75, a length is in the range of 500 nm to 1100 nm, the largest width of the narrow central portion is 100 to 250 nm, and the largest width of the narrow central portion is 100 to 250 nm. The nanoparticles have a mesoporous structure and are made up of subparticles that have a size of 5 to 75 nm. A method of making the nanoparticles from calcined calcium carbonate sources is disclosed. Also disclosed is an enhanced fuel containing the nanoparticles.

Silica sand agglomerates for silicon metal production according to the present invention may be formed in the form of lumps by mixing clay, a liquid adhesive, and silica sand having a particle size in a certain range, and thus be maintained in shape during reduction in a high-temperature carbothermal reduction furnace to facilitate heat transfer and gas circulation.

The present invention is directed to a nanoporous cerium oxide nanoparticle (NCeONP) macro-structure containing a plurality of the cerium oxide nanoparticles which define a plurality of macro-structure pores. The NCeONP macro structure may be used to improve pigment and/or dye performance.

Methods of preparing graphene/graphene oxide particulates under mild conditions, comprising reacting pristine graphene with hydrogen peroxide and a source of iron to oxidize the outer surface of the pristine graphene particulates in solution and yield graphene/graphene oxide particulates. Methods and articles incorporating the same are also disclosed.

The present application provides a method for preparing a zinc oxide nanoparticle structure synthesized using a microfluidic device and a self-assembled porous three-dimensional zinc oxide nanoparticle structure prepared therefrom. The self-assembled porous three-dimensional zinc oxide nanoparticle structure of the present application is a three-dimensional structure in which micropores, mesopores and macropores are created, and has excellent reactivity.

This application provides a silicon-based material, a preparation method thereof, and a secondary battery, a battery module, a battery pack, and an apparatus associated therewith. The silicon-based material includes a core structure and a coating layer provided on at least partial surface of the core structure, where the core structure includes both a silicon phase and a lithium metasilicate phase, and a particle size P of the lithium metasilicate phase is ≥30 nm. The silicon-based material of this application can not only increase energy density of a secondary battery with the silicon phase, but also improve structural stability and chemical stability of the silicon-based material, so that the secondary battery can deliver satisfactory and balanced cycling performance and first-cycle coulombic efficiency in overall.

A positive electrode active material for a lithium secondary battery comprising a compound represented by Chemical Formula 1 is introduced.

Li.sub.1+mNi.sub.1-w-x-y-zCo.sub.wMn.sub.xM1.sub.yM2.sub.zO.sub.2-pX.sub.p  [Chemical Formula 1] (In the Chemical Formula 1, M1 and M2 are different from each other, and any one element selected from the group consisting of Al, Mg, Zr, Sn, Ca, Ge, Ti, Cr, Fe, Zn, Y, Ba, La, Ce, Sm, Gd, Yb, Sr, Cu and Ga respectively, X is any one element selected from the group consisting of F, N, S, and P, w, x, y, z, p and m are respectively 0.125<w<0.202, 0.153<x<0.225, 0≤y≤0.1, 0≤z≤0.1, 0.34≤w+x≤0.36, 0≤p≤0.1, and −0.1≤m≤0.2.)

Particles are disclosed. Methods of making and using the particles are also disclosed.

A positive-electrode active material precursor for a nonaqueous electrolyte secondary battery is provided that includes a nickel-cobalt-manganese carbonate composite represented by general formula Ni.sub.xCo.sub.yMn.sub.zM.sub.tCO.sub.3 (where x+y+z+t=1, 0.05≤x≤0.3, 0.1≤y≤0.4, 0.55≤z≤0.8, 0≤t≤0.1, and M denotes at least one additional element selected from a group consisting of Mg, Ca, Al, Ti, V, Cr, Zr, Nb, Mo, and W) and a hydrogen-containing functional group, wherein H/Me representing the ratio of the amount of hydrogen to the amount of metal components Me included in the positive-electrode active material precursor is greater than or equal to 1.60.

A negative electrode material for a lithium-ion secondary battery includes composite particles, each of the composite particles having a structure in which plural flat graphite particles are stacked, wherein the composite particles have a particle size distribution D90/D10 of from 2.0 to 5.0, or wherein the plural flat graphite particles have a particle size distribution D90/D10 of from 2.0 to 4.4.