Provided is a friction modifier giving excellent formability in producing a friction material and capable of reducing rust formation on a rotor even when the moisture-absorbed friction material is left pressed against the rotor for a long. The friction modifier is made of a titanate compound having a layered crystal structure, wherein the titanate compound has a rate of chlorine ion dissolution of 0.5 ppm to 400 ppm.

The present invention provides an EMI shielding device including a flame retarding, thermal interface material composite with a through plane thermal conductivity of no less than 30 W/mK and a dielectric withstanding voltage of no less than 1 kV/mm, where the composite includes at least one dielectric layer of self-aligned, carbon-based materials associated with superparamagnetic particles and at least one layer of fillers including a blend of dielectric heat transfer materials with a thermal or UV curable polymer or phase change polymer. The anisotropic heat transfer carbon-based materials associated with superparamagnetic materials are aligned under a low magnetic field strength of less than 1 Tesla to an orientation that results in a high thermal conductivity direction which can conduct the maximum heat from the adjacent device of the present composite. The present invention also provides a method for preparing the composite.

Nanostructured carbide chemical compound is used to convert carbide to carbon. A method comprising: providing at least one carbide chemical compound and reducing a metal cation with use of the carbide chemical compound to form elemental carbon, wherein the carbide chemical compound is nanostructured. The nanostructured carbide chemical compound can be in the form of a nanoparticle, a nanowire, a nanotube, a nanofilm, a nanoline. The reactant can be a metal salt. Electrochemical reaction, or reaction in the melt or in solution, can be used to form the carbon. The nanostructured carbide chemical compound can be an electrode.

A nano-thin Bi.sub.xO.sub.ySe.sub.z low-temperature oxygen transporter membrane for oxygen transport, separation, and two-dimensional (2D) material manipulation comprising a material comprising a compound of Bi.sub.xO.sub.ySe.sub.z and R3m bismuth oxide (Bi.sub.2O.sub.3). A method of making a nano-thin Bi.sub.xO.sub.ySe.sub.z low-temperature oxygen transporter membrane for oxygen transport, separation, and two-dimensional (2D) material manipulation comprising providing an oxygen environment, providing Bi.sub.2Se.sub.3, processing the Bi.sub.2Se.sub.3 in the oxygen environment, incorporating oxygen, removing selenium, creating a structural change, and creating a compound of Bi.sub.xO.sub.ySe.sub.z and R3m bismuth oxide (Bi.sub.2O.sub.3), wherein the material transports oxygen at room temperature.

A display substrate having a transparent electrode and manufacturing method thereof includes a transparent substrate, and a patterned channel is disposed on the transparent substrate; a transparent electrode including a composite material of MXene material and polyvinylpyrrolidone, and the transparent electrode is filled in the patterned channel. The transparent electrode of embodiments of the present disclosure has advantages of high transmittance, high conductivity, great machinability, great substrate affinity, great ductility, etc.

A nickel-based active material precursor includes a particulate structure including a core portion, an intermediate layer portion on the core portion, and a shell portion on the intermediate layer portion, wherein the intermediate layer portion and the shell portion include primary particles radially arranged on the core portion, and each of the core portion and the intermediate layer portion includes a cation or anion different from that of the shell portion. The cation includes at least one selected from boron (B), magnesium (Mg), calcium (Ca), strontium (Sr), barium (Ba), titanium (Ti), vanadium (V), tungsten (W), chromium (Cr), iron (Fe), copper (Cu), zirconium (Zr), and aluminium (Al), and the anion includes at least one selected from phosphate (PO.sub.4), BO.sub.2, B.sub.4O.sub.7, B.sub.3O.sub.5, and F.

The titanium phosphate powder of the present invention includes plate-shaped crystalline particles of titanium phosphate, an average thickness of the plate-shaped crystalline particles is 0.01 μm or more and less than 0.10 μm, and an aspect ratio, which is a value obtained by dividing an average primary particle diameter of the plate-shaped crystalline particles by the average thickness, is 5 or more. In the method for producing a titanium phosphate powder of the present invention, a raw material containing titanium and phosphorus is caused to react by a hydrothermal synthesis method, and when the titanium phosphate powder including plate-shaped crystalline particles of titanium phosphate is produced, a mixture of titanium sulfate and phosphoric acid is used as the raw material.

A reducing material including a two-dimensional hydrogen boride-containing sheet having a two-dimensional network composed of (BH).sub.n (n≥4).

A composite including a two-dimensional hydrogen boride-containing sheet having a two-dimensional network composed of (BH).sub.n (n≥4) and a metal nanoparticle.

A reduction method including: a step of dispersing the reducing material according to any one of Claims 1 to 5 in an organic solvent to prepare a dispersion liquid containing the reducing material; and a step of reducing a metal ion having a redox potential which is given as a standard electrode potential of −0.26 V/SHE or higher by mixing the dispersion liquid with the metal ion.

Methods for making of nanomaterials from a bulk source material involve heating the material in an inert atmosphere, whereby a material having at least one nanometer scale dimension is formed on a nearby substrate surface. The heated bulk source material forms a vapor phase which is deposited in the form of the nanomaterial on a growth surface of the substrate. The methods require no complex machinery or devices, unlike chemical vapor deposition, and can be tuned to provide different forms of nanomaterials, such as two-dimensional or other crystalline forms. The methods can be used to make two-dimensional semiconductor materials and semiconductor devices.

A nickel (Ni)-based active material precursor for a lithium secondary battery, a preparing method thereof, a Ni-based active material obtained therefrom, and a lithium secondary battery including a positive electrode including the same, are provided. The Ni-based active material precursor includes a secondary particle including a plurality of particulate structures, wherein each of the particulate structures includes a porous core portion; and a shell portion including primary particles radially arranged on the porous core portion. Phosphorus (P) may be present in the porous core portion, between the plurality of primary particles, and on the surface of the secondary particle, and the content of the phosphorus may be in a range of 0.01 wt % to 2 wt % based on a total weight of the Ni-based active material precursor.