A nitrogen-containing carbon material includes carbon atoms, nitrogen atoms, and halogen atoms. The nitrogen-containing carbon material has a ratio of a number of moles of pyridinic nitrogen atoms to a total number of moles of the nitrogen atoms that is higher than 59% and a total content ratio of the nitrogen atoms with respect to the nitrogen-containing carbon material that is 7 at % or higher. The nitrogen-containing carbon material includes a fused polycyclic aromatic moiety formed by condensation of three or more aromatic rings, and the fused polycyclic aromatic moiety includes a partial structure for two pyridinic nitrogen atoms to be linked to each other through two carbon atoms.

Sodium-based all solid-state batteries exhibit improved battery cycle life and stability with the use of a new chloride-based sodium solid electrolyte in which sodium diffusivity within the electrolyte is enhanced through substitution of atoms including one or more of Y with Zr, Ti, Hf, Ta, and Na with one or more of Ca and Sr.

Described herein are acidified metal oxide (“AMO”) materials useful in applications such as a battery electrode or photovoltaic component, in which the AMO material is used in conjunction with one or more acidic species. Advantageously, batteries constructed of AMO materials and incorporating acidic species, such as in the electrode or electrolyte components of the battery exhibit improved capacity as compared to a corresponding battery lacking the acidic species.

A method of making a titanium dioxide nanowire array includes contacting a substrate with a solvent comprising a titanium (III) precursor, an acid, and an oxidant while microwave heating the solvent, thereby forming a hydrogen titanate H2Ti2O5.H2O nanowire array. The hydrogen titanate nanowire array is annealed to form a titanium dioxide nanowire array. The substrate is seeded with titanium dioxide before starting the hydrothermal synthesis of the hydrogen titanate nanowire array. The titanium dioxide nanowire array is loaded with a platinum group metal to form an exhaust gas catalyst. The titanium dioxide nanowire array can be used to catalyze oxidation of combustion exhaust.

Composite nanoparticle compositions and associated nanoparticle assemblies exhibit enhancements to one or more thermoelectric properties including increases in electrical conductivity and/or Seebeck coefficient and/or decreases in thermal conductivity. A composite nanoparticle composition comprises a semiconductor nanoparticle including a front face and a back face and sidewalls extending between the front and back faces. Metallic nanoparticles are bonded to at least one of the sidewalls establishing a metal-semiconductor junction.

An object of the present disclosure is to provide an all solid fluoride ion battery that has a favorable capacity property. The present disclosure achieves the object by providing an all solid fluoride ion battery comprising: a cathode layer, an anode layer, and a solid electrolyte layer formed between the cathode layer and the anode layer; wherein the anode layer includes a metal fluoride containing an M1 element, an M2 element, and a F element; the M1 element is a metal element that fluorination and defluorination occur at a potential, versus Pb/PbF.sub.2, of −2.5 V or more; the M2 element is a metal element that neither fluorination nor defluorination occur at a potential, versus Pb/PbF.sub.2, of −2.5 V or more; and the M2 element is a metal element that, when in a form of a fluoride, fluoride ion conductivity is 1×10.sup.−4 S/cm or more at 200° C.

A sulfide solid electrolyte contains a compound that has a crystal phase having an argyrodite-type crystal structure and that is represented by Li.sub.aPS.sub.bX.sub.c, where X is at least one elemental halogen, a represents a number of 3.0 or more and 6.0 or less, b represents a number of 3.5 or more and 4.8 or less, and c represents a number of 0.1 or more and 3.0 or less. The sulfide solid electrolyte has a ratio of A.sub.Li/(A.sub.Li+A.sub.P+A.sub.S+A.sub.X) to a specific surface area (m.sup.2 g.sup.−1) of 3.40 (m.sup.−2g) or more, where A.sub.Li represents the amount of lithium (atom %) quantitatively determined from the Li 1s peak, A.sub.P represents the amount of phosphorus (atom %) quantitatively determined from the P 2p peak, A.sub.S represents the amount of sulfur (atom %) quantitatively determined from the S 2p peak, and A.sub.X represents the amount of halogen (atom %) quantitatively determined from the halogen peak, the peaks being exhibited in X-ray photoelectron spectroscopy (XPS).

There is provided a method for collecting and reusing an active material from positive electrode scrap. The positive electrode active material reuse method of the present disclosure includes (a) thermally treating positive electrode scrap comprising a lithium composite transition metal oxide positive electrode active material layer on a current collector in air at 300 to 650° C. for 1 hour or less for thermal decomposition of a binder and a conductive material in the active material layer, to separate the current collector from the active material layer, and collecting an active material in the active material layer, and (b) annealing the collected active material with an addition of a lithium precursor to obtain a reusable active material.

An active material is provided for use in a solid-state battery. The active material exhibits at least one peak in the range of 0.145 to 0.185 nm and at least one peak in the range of 0.280 to 0.310 nm in a radial distribution function obtained through measurement of an X-ray absorption fine structure thereof. In the particle size distribution, by volume, of the active material obtained through a particle size distribution measurement by laser diffraction scattering method, the ratio of the absolute value of the difference between the mode diameter of the active material and the D.sub.10 of the active material (referred to as the “mode diameter” and the “D.sub.10” respectively) to the mode diameter in percentage terms, (|mode diameter - D.sub.10 / mode diameter) x 100, satisfies 0% < (( | mode diameter - D.sub.10| / mode diameter) x 100) ≤ 58.0%.

Disclosed are a method for preparing a ceramic material including a compound of a formula of A.sub.2B.sub.xO.sub.y and a ceramic material prepared by the method. The method includes: mixing a first oxide of AO.sub.m and a second oxide of BO.sub.n to obtain a mixture, ball-milling the mixture until a particle size of the mixture is not greater than 1 μm with a medium selected from a group consisting of ethanol, acetone, deionized water and a combination thereof, to obtain a powder, drying the powder at a temperature in a range of 60 to 80° C., and sintering the powder with a laser irradiation having a laser wavelength of 980 nm, an irradiation power ranging from 50 to 1500 W and an irradiation period of 3 s to 8 min to obtain the ceramic material.