A negative electrode active material includes a carbon material, where the carbon material has a specific degree of graphitization and aspect ratio distribution. A degree of graphitization Gr of the carbon material measured by an X-ray diffraction analysis method is 0.82 to 0.92, and based on a total quantity of particles of the carbon material, a proportion of particles with an aspect ratio greater than 3.3 in the carbon material is less than 10%. The negative electrode active material helps to improve cycle performance of the electrochemical apparatus. FIG. 1.

A class of compositions that are inclusive of a lithium metal oxide or oxyfluoride compound having a general formula: LiTM[n]OF where TM[n] represents a number of transition metal species inclusive of transitional metal species differentiated by charge or d.sup.0 electron shell conformation, with [n] being at least 4 of said transitional metal species, and wherein said lithium metal oxide or oxyfluoride has a cation-disordered rocksalt (DRX) structure and a mitigated SRO via a high entropy DRX design strategy. Also featured is a method of synthesizing the high entropy DRX lithium metal oxide or oxyfluoride compounds, as well as usage of the same in Li-ion batteries, with particular utility in cathodes of such Li-ion batteries.

Embodiments of the present disclosure generally relate to methods for preparing carbon materials which can be used in battery electrodes. More specifically, embodiments relate to methods for preparing nano-ordered carbon products used as anode materials in metal-ion batteries, such as a lithium-ion battery. In one or more embodiments, a method includes exposing a liquid refinery hydrocarbon product to a first functionalization agent to produce a first solid functionalized product during a first functionalization process and exposing the first solid functionalized product to a second functionalization agent to produce a second solid functionalized product during a second functionalization process. Each of the first and second functionalization agents independently contains an element selected from oxygen, sulfur, phosphorous, nitrogen, or any combination thereof. The method also includes carbonizing the second solid functionalized product at a temperature of about 1,000° C. to about 1,400° C. to produce a solid nano-ordered carbon product during a carbonization process.

Embodiments of the present invention relate to a cathode active material, a method for manufacturing the same, and a lithium secondary battery including the same.

According to an embodiment, a cathode active material can be provided, the cathode active material comprising: a lithium metal oxide including a core and a shell disposed on a surface of the core; and a coating layer disposed on a surface of the lithium metal oxide, wherein a c value that satisfies Equation 1 and is in a range of 0.3 to 0.7, and the core and the shell have a layered crystalline structure.

c=b/a  [Equation 1]

(in Equation 1, a is a peak at 530 to 533 eV and b is a peak at 528 to 531 eV in an XPS spectrum of the coating layer)

A plate-shaped sample with a cross-section perpendicular to a radial direction of a polycrystalline silicon rod as a principal surface is sampled from a region from a center (r=0) of the polycrystalline silicon rod to R/3. Then, the sample is disposed at a position at which a Bragg reflection from a (111) Miller index plane is detected. In-plane rotation with a rotational angle φ on the sample is performed with a center of the sample as a rotational center such that an X-ray irradiation region defined by a slit performs φ-scanning on the principal surface of the sample to obtain a diffraction chart indicating dependency of a Bragg reflection intensity from the (111) Miller index plane on a rotational angle of the sample. A ratio (S.sub.p/S.sub.t) between an area S.sub.p of a peak part appearing in the diffraction chart and a total area S.sub.t of the diffraction chart is calculated.

A non-flaky carbon material having specific optical structures, wherein the ratio between the peak intensity I110 of (110) plane and the peak intensity I004 of (004) plane of a graphite crystal determined by the powder XRD measurement, I110/I004, is 0.10 or more and 0.35 or less; an average circularity is 0.80 or more and 0.95 or less; d002 is 0.337 nm or less; and the total pore volume of pores having a diameter of 0.4 μm or less measured by the nitrogen gas adsorption method is 25.0 μl/g or more and 40.0 μl/g or less. Also disclosed is a method for producing the carbon material, a carbon material for a battery electrode, a paste for an electrode incorporating the carbon material for a battery electrode, an electrode for a lithium battery incorporating a formed body of the paste for an electrode, a lithium-ion secondary battery including the electrode and a method for producing the electrode.

A hydrocarbon adsorbent having high hydrocarbon adsorbing properties even after exposed to a high temperature/high humidity reducing atmosphere, includes a FAU type zeolite having in ESR measurement a spin concentration of a least 1.0 × 10^19 (spins/g) and a ratio of a peak intensity at a magnetic field of at least 260 mT and at most 270 mT to a peak intensity at a magnetic field of at least 300 mT and at most 320 mT of at least 0.25 and at most 0.50 Å and containing bivalent copper. The hydrocarbon adsorbent may be used for a method for adsorbing hydrocarbons to be exposed to a high temperature/high humidity environment, and may be used particularly for a method for adsorbing hydrocarbons in an exhaust gas of an internal combustion engine, such as an automobile exhaust gas.

Several variations of synthetic carbon materials are disclosed. The materials can assume a variety of properties, including high electrical conductivity. The materials also can have favorable structural and mechanical properties. They can form gas impenetrable barriers, form insulating structures, and can have unique optical properties.

The present invention relates to a carbon nanotube composition including entangled-type carbon nanotubes and bundle-type carbon nanotubes, wherein the carbon nanotube composition has a specific surface area of 190 m.sup.2/g to 240 m.sup.2/g and a ratio of specific surface area to bulk density of 0.1 to 5.29.

Described are systems and methods of storing adsorbing diborane on carbon adsorption medium.