An object of the present invention is to provide ferrite particles for supporting a catalyst having a small apparent density, various properties are maintained in a controllable state and a specified volume is filled with a small weight, and a catalyst using the ferrite particles for supporting a catalyst. To achieve the object, ferrite particles for supporting a catalyst provided with an outer shell structure containing Ti oxide, a catalyst using the ferrite particles for supporting a catalyst are employed.

A simple one pot sol-gel method for the synthesis of bi-metal nanostructures is based on non-noble metals (Fe, Co and Sn) and titanium. The method involves the synthesis of mixed metal nanoscale composites using low cost precursors which allow for the synthesis of desired nanocomposite materials with self-scarifying titanium or silica supports. The procedure does not require any surfactant or any need for pH controlled step. Applicants' method involves the in-situ generation of precursors and their simultaneous entrapment in a gel. This simple one pot synthesis allows for the synthesis of homogenous size, shape and distribution of targeted nanostructures. Further, this method can be applied for the preparation of various nanocomposite materials using different choices of metals and self-scarifying supports. Applicants also show that Pd, the noble metal based nanocomposite is feasible.

A process for preparing a stable Li.sub.xK.sub.yMn.sub.2-zMe.sub.zO.sub.4 is provided. The general formula of the potassium A site and Group VIII Period 4 (Fe, Co and Ni) B site modified lithium manganese-based AB.sub.2O.sub.4 spinel is Li.sub.xK.sub.yMn.sub.2-zMe.sub.zO.sub.4 where Me is Fe, Co, or Ni. In addition, a Li.sub.xK.sub.yMn.sub.2-zMe.sub.zO.sub.4 cathode material for electrochemical systems is provided. Furthermore, a lithium or lithium-ion rechargeable electrochemical cell is provided, incorporating the Li.sub.xK.sub.yMn.sub.2-zMe.sub.zO.sub.4 cathode material in a positive electrode.

A ferrite sintered magnet includes a composition expressed by a formula (1) of Ca.sub.1-w-xLa.sub.wA.sub.xFe.sub.zCo.sub.mMn.sub.aO.sub.19. In the formula (1), w, x, z, m, and a satisfy a formula (2) of 0.21w0.62, a formula (3) of 0.02x0.46, a formula (4) of 7.43z11.03, a formula (5) of 0.18m0.41, and a formula (6) of 0.046a0.188. In the formula (1), A is at least one kind of element selected from a group consisting of Sr and Ba.

An object of the present invention is to provide a ferrite carrier core material for an electrophotographic developer having desired resistance properties and charging properties with small environmental variation of resistivity and charge amount while maintaining the advantages of ferrite carriers, a ferrite carrier for an electrophotographic developer, an electrophotographic developer using the ferrite carrier, and a method for manufacturing the ferrite carrier core material for an electrophotographic developer. In order to solve the problem, a ferrite carrier core material comprising ferrite particles containing 15 mass % or more and 25 mass % or less of Mn, 0.5 mass % or more and 5.0 mass % or less of Mg, 0.05 mass % or more and 4.0 mass % of Sr, and 45 mass % or more and 55 mass % or less of Fe, with Si localized in the surface thereof is used.

A disordered rocksalt lithium metal oxide and oxyfluoride as in manganese-vanadium oxides and oxyfluorides well suited for use in high capacity lithium-ion battery electrodes such as those found in lithium-ion rechargeable batteries. A lithium metal oxide or oxyfluoride example is one having a general formula: Li.sub.xM.sub.aM.sub.bO.sub.2-yF.sub.y, with the lithium metal oxide or oxyfluoride having a cation-disordered rocksalt structure of one of (a) or (b), with (a) 1.09?x?1.35, 0.1?a?0.7, 0.1?b?0.7, and 0?y<0.7; M is a low valent transition metal and M is a high-valent transition metal; and (b) 1.1?x?1.33, 0.1?a?0.41, 0.39?b?0.67, and 0?y?0.3; M is Mn; and M is V or Mo. The oxides or oxyfluorides balance accessible Li capacity and transition metal capacity. An immediate application example is for high energy density Li-cathode battery materials, where the cathode energy is a key limiting factor to overall performance. The second structure (b) is optimized for maximal accessible Li capacity.

Provided is a material that can be used as a potassium secondary battery positive electrode active material (particularly a potassium ion secondary battery positive electrode active material), other than Prussian blue, by using a potassium compound and a potassium ion secondary battery positive electrode active material comprising the potassium compound, the potassium compound being represented by general formula (1):

K.sub.nA.sub.kBO.sub.m,

wherein A is a positive divalent element in groups 7 to 11 of the periodic table; B is positive tetravalent silicon, germanium, titanium or manganese, excluding a case in which A is manganese and B is titanium, and a case in which A is cobalt and B is silicon; n is 1.5 to 2.5; and m is 3.5 to 4.5.

Provided are a ferrite material, a composite magnetic body, a coil component, and a power supply device, having high magnetic permeability. Ferrite is ferromagnetic and is expressed by a chemical formula Mn.sub.xSi.sub.yFe.sub.zO.sub.4-, where 0<x<1, y>0, z>0, x+y+z=3, and 0.5.

The present disclosure provides for compositions of magnetic nanoparticles and methods of making magnetic nano-particles with large magnetic diameters.

Methods, systems, and devices are disclosed for fabricating and implementing optically absorbing coatings. In one aspect, an optically selective coating includes a substrate formed of a solar energy absorbing material, and a nanostructure material formed over the substrate as a coating capable of absorbing solar energy in a selected spectrum and reflecting the solar energy in another selected spectrum. A concentrating solar power (CSP) system includes heat transfer fluids (HTFs); thermal energy storage system (TES); and solar receivers in communication with HTFs and including a light absorbing coating layer based on cobalt oxide nanoparticles.