A negative electrode active material including lithium titanium oxide particles, wherein the lithium titanium oxide particles have a Na content of 50 ppm-300 ppm, a K content of 500 ppm-2400 ppm and a crystallite size of 100-200 nm, and a lithium secondary battery including the same.

A method of manufacturing a mixed metal oxide powder is provided. The method includes steps of mixing two or more metal precursors in a solvent to form a dispersion of the metal precursors in the solvent; drying the dispersion to obtain a dried mixed metal precursor powder; jet milling the dried mixed metal precursor powder to obtain particles having a size distribution in a range of 0.2-20 micrometers; and exposing the particles to a hydrocarbon flame or oxygen plasma to provide the mixed metal oxide powder. Mixed metal oxide powders produced by the disclosed methods are also provided.

Provided is a potassium titanate powder that can avoid safety and health concerns and concurrently, during use in a friction material, can give excellent frictional properties. A potassium titanate powder is a powder formed of bar-like potassium titanate particles having an average length of 30 μm or more, an average breadth of 10 μm or more, and an average aspect ratio of 1.5 or more, wherein the bar-like potassium titanate particles are represented by a composition formula K.sub.2Ti.sub.nO.sub.2n+1 (where n=5.5 to 6.5).

A lithium titanate/titanium niobate core-shell composite material includes a core which comprises lithium titanate; and a shell which is cladded over the core and comprises titanium niobate. A preparation method of lithium titanate/titanium niobate core-shell composite material includes (A) mixing lithium titanate powder and titanium niobate powder; and (B) granulating the mixture produced by step (A) through a spray granulation process to obtain a lithium titanate/titanium niobate composite material with titanium niobate cladding over lithium titanate. The lithium titanate/titanium niobate core-shell composite material and the preparation method thereof can be applied to a battery.

Resistive switching devices that contain lithium, including resistive switching devices containing a lithium titanate, and associated systems and methods are generally described. In some cases, the resistive switching device contains a lithium titanate-containing domain, a first electrode, and a second electrode. In some cases, the application of an electrical potential to the resistive switching device causes a change in resistance state of the lithium titanate-containing domain. The resistive switching devices described herein may be useful as memristors, and in applications that include Resistive-random access memory and neuromorphic computing.

Provided is a particulate alkaline earth metal ion adsorbent having a large adsorption capacity. The particulate alkaline earth metal ion adsorbent comprising: a potassium hydrogen dititanate hydrate represented by a chemical formula K.sub.2-xH.sub.xO.Math.2TiO.sub.2.Math.nH.sub.2O, wherein x is 0.5 or more and 1.3 or less, and n is greater than 0; and no binder, wherein the particulate alkaline earth metal ion adsorbent has a particle size range of 150 μm or more and 1000 μm or less.

The present invention provides a linear porous lithium titanate material, preparation and product thereof. The material comprises a lithium titanate material having a crystal phase which is a spinel type, wherein the lithium titanate material has a linear structure having an aspect ratio of greater than 10, and the linear lithium titanate material has a porous structure; wherein the linear porous lithium titanate material has a structure composed of a plurality of particles having an oriented growth direction. The material has a long-axis structure which facilitates the effective migration of electrons, a porous structure which facilitates the rapid intercalation and deintercalation process of lithium ions, sodium ions or potassium ions, and a large specific surface area which facilitates the contact area between the electrolyte solution and the electrodes and reduces the current density, thus is excellent in a rapid charge-discharge performance of the battery.

A process for the preparation of non-fibrous alkaline titanates comprising the steps of: melting alkaline titanate in a furnace at a temperature ranging from 1300° C. to 1500° C. to form a molten product; cooling said molten product by placing it in contact with a material having a temperature equal to or lower than 15° C.

There is demand for a lithium ion capacitor positive electrode that can improve the battery characteristics (and, in particular, the rate characteristics) of a lithium ion capacitor. This lithium ion capacitor positive electrode is characterized by containing, in a positive electrode active material, at least one titanate selected from among Li.sub.2TiO.sub.3, Li.sub.4Ti.sub.5O.sub.12, Na.sub.2TiO.sub.3, and K.sub.2Ti.sub.2O.sub.5.

There is demand for a power storage device composition that: compared to past lithium compounds, can suppress development of conductivity caused by blue discoloration (reduction), even when used in a reducing atmosphere; and can inhibit the generation of gases, such as carbon dioxide gas, hydrogen gas, and fluoride gas, that has been a problem in past power storage devices during use and with aging. This power storage device composition is characterized by including, as a principal component, Li.sub.2TiO.sub.3 that has an x-ray diffraction pattern for which the intensity ratio (A/B) of the peak intensity (A) at a diffraction angle of 2θ=18.4±0.1° and the peak intensity (B) at a diffraction angle of 2θ=43.7±0.1° is at least 1.10.