A method for producing a solid electrolyte for an all-solid state battery, the solid electrolyte having the following chemical formula XM.sub.2(PS.sub.4).sub.3, where X is lithium (Li), sodium (Na), silver (Ag) or magnesium (Mg.sub.0.5) and M is titanium (Ti), zirconium (Zr), germanium (Ge), silicon (Si), tin (Sn) or a mixture of X and aluminium (X+Al) and the method including: mixing powders so as to obtain a powder mixture; pressing a component with powder mixture; and sintering component for a period of time equal to or greater than 100 hours so as to obtain the solid electrolyte. The solid electrolyte exhibits the peaks in positions of 2=13.64 (1), 13.76 (1), 14.72 (1), 15.36 (1), 15.90 (1), 16.48 (1), 17.42 (1), 17.56 (1), 18.58 (1), and 22.18 (1) in a X-ray diffraction measurement using CuK line. The disclosure is also related to a method of producing a solid electrolyte.

Cold sintering of materials includes using a process of combining at least one inorganic compound, e.g., ceramic, in particle form with a solvent that can partially solubilize the inorganic compound to form a mixture; and applying pressure and a low temperature to the mixture to evaporate the solvent and densify the at least one inorganic compound to form sintered materials.

Provided herein is a method of manufacturing a nanoscale coated network, which includes providing nanofibers, capable of forming a network in the presence of a liquid vehicle and providing a nanoscale solid substance in the presence of the liquid vehicle. The method may also include forming a network of the nanofibers and the nanoscale solid substance and redistributing at least a portion of the nanoscale solid substance within the network to produce a network of nanofibers coated with the nanoscale solid substance. Also provided herein is a nanoscale coated network with an active material coating that is redistributed to cover and electrochemically isolate the network from materials outside the network.

A precursor of an alumina sintered compact including aluminum, yttrium, and at least one metal selected from iron, zinc, cobalt, manganese, copper, niobium, antimony, tungsten, silver, and gallium. The aluminum content is 98.0% by mass or more as an oxide (Al.sub.2O.sub.3) in 100% by mass of the precursor of an alumina sintered compact; the yttrium content is 0.01 to 1.35 parts by mass as an oxide (Y.sub.2O.sub.3) based on 100 parts by mass of the content of the aluminum as an oxide; the total content of the metals selected from the foregoing group is 0.02 to 1.55 parts by mass as an oxide based on 100 parts by mass of the content of aluminum as an oxide; and the aluminum is contained as -alumina. Also disclosed is an alumina sintered compact, and a method for producing an alumina sintered compact and for producing abrasive grains.

A ceramic composition according to an embodiment of the present invention contains: a main phase component represented by CaMgSi.sub.2O.sub.6 or Ba.sub.4(Re.sub.(1-x), Bi.sub.x).sub.9.33Ti.sub.18O.sub.54; and an additive component containing a Li component and a B component, An observation field, a part of a sectional surface of the ceramic composition, is divided into a plurality of unit observation regions. Among all the unit observation regions, those containing no or little sintering agent component are referred to as the main crystal regions. An area percentage of main crystal regions relative to the observation field is 30% or more, the main crystal regions being the unit observation regions containing 0.5% or less by area of the additive component.

The present disclosure provides a method for preparing a dielectric which can provide a low-dielectric loss dielectric not variable to frequency, wherein the dielectric shows a narrow variation in dielectric characteristics depending on temperature, undergoes no change in dielectric characteristics depending on frequency and thus has a low dielectric loss. The present disclosure also provides a dielectric prepared by the method.

Cold sintering of materials includes using a process of combining at least one inorganic compound, e.g., ceramic, in particle form with a solvent that can partially solubilize the inorganic compound to form a mixture; and applying pressure and a low temperature to the mixture to evaporate the solvent and densify the at least one inorganic compound to form sintered materials.

A method (100) for producing a sintered component being a solid electrolyte and/or an electrode including titanium and sulfur for an all-solid state battery, the method including mixing powders (102) so as to obtain a powder mixture comprising titanium and sulfur, pressing (106) a component with the powder mixture, sintering (108) the component under a partial pressure of sulfur comprised between 200 Pa and 0.2 MPa so as to obtain an intermediate sintered component comprising titanium and sulfur, and sintering (114) the intermediate sintered component under a partial pressure of sulfur equal to or smaller than 150 Pa at a temperature plateau comprised between 200 C. and 400 C. so as to obtain a sintered component comprising titanium and sulfur, the solid electrolyte exhibiting the peaks in positions of 2=15.08 (0.50), 15.28 (0.50), 15.92 (0.50), 17.5 (0.50), 18.24 (0.50), 20.30 (0.50), 23.44 (0.50), 24.48 (0.50), and 26.66 (0.50) in a X-ray diffraction measurement using CuK line.

Disclosed herein are doped perovskite oxides. The doped perovskite oxides may be used as a cathode material in an electrochemical cell to electrochemically generate ammonia from N.sub.2. The doped perovskite oxides may be combined with nitride compounds, for instance iron nitride, to further increase the efficiency of the ammonia production.

A magnesium-based thermoelectric conversion material made of a sintered compact of a magnesium compound, in which, in a cross section of the sintered compact, a Si-rich metallic phase having a higher Si concentration than in magnesium compound grains is unevenly distributed in a crystal grain boundary between the magnesium compound grains, an area ratio of the Si-rich metallic phase is in a range of 2.5% or more and 10% or less, and a number density of the Si-rich metallic phase having an area of 1 m.sup.2 or more is in a range of 1,800/mm.sup.2 or more and 14,000 /mm.sup.2 or less.