A negative electrode active material containing a negative electrode active material particle which includes a silicon compound particle containing a silicon compound (SiO.sub.x: 0.5≤x≤1.6). The silicon compound particle has three or more peaks in a chemical shift value ranging from −40 ppm to −120 ppm but has no peak in a chemical shift value within a range of −65±3 ppm in a spectrum obtained from .sup.29Si-MAS-NMR of the silicon compound particle. This provides a negative electrode active material capable of improving cycle characteristics when it is used as a negative electrode active material for a secondary battery.

The invention relates to Chevrel-phase materials and methods of preparing these materials utilizing a precursor approach. The Chevrel-phase materials are useful in assembling electrodes, e.g., cathodes, for use in electrochemical cells, such as rechargeable batteries. The Chevrel-phase materials have a general formula of Mo.sub.6Z.sub.8 (Z=sulfur) or Mo.sub.6Z.sup.1.sub.8-yZ.sup.2.sub.y (Z.sup.1=sulfur; Z.sup.2=selenium), and partially cuprated Cu.sub.1Mo.sub.6S.sub.8 as well as partially de-cuprated Cu.sub.1-xMg.sub.xMo.sub.6S.sub.8 and the precursors have a general formula of M.sub.xMo.sub.6Z.sub.8 or M.sub.xMo.sub.6Z.sup.1.sub.8-yZ.sup.2.sub.y, M=Cu. The cathode containing the Chevrel-phase material in accordance with the invention can be combined with a magnesium-containing anode and an electrolyte.

Systems and methods are provided for high volume roll-to-roll direct coating of electrodes for silicon-dominant anode cells and may include applying a slurry to a current collector film, the slurry comprising silicon particles and a binder material; drying the slurry to form a precursor composite film; rolling the current collector film into a precursor composite roll; and applying a heat treatment to the precursor composite film and the current collector film in a nitrogen gas environment, wherein the heat treatment is configured for converting the precursor composite film to a pyrolyzed composite film. The heat treatment may include one or both of: applying the heat treatment to a roll comprising the precursor composite roll in whole; and applying the heat treatment to the current collector film as it is continuously fed from the precursor composite roll.

The invention provides process for producing a stable Si or Ge electrode structure comprising cycling a Si or Ge nanowire electrode until a structure of the Si nanowires form a continuous porous network of Si or Ge ligaments.

A battery and a method of constructing a battery are disclosed in which a first conductive substrate portion has a first face and a second conductive substrate portion has a second face opposed to the first face. A first electrode material is disposed in electrical contact with the first face, an electrolyte material is disposed in contact with the first electrode material, a second electrode material is disposed in contact with the electrolyte material, and a conductive tab disposed in contact with the second electrode material. The first conductive substrate portion, the first electrode material, and the conductive tab extend outward beyond a particular edge of the second conductive substrate portion.

Various embodiments of the present disclosure describe energy storage devices. In one example, an energy storage device includes an anode having a plurality of active material particles, a cathode having a transition metal oxide material, and an electrolyte including a room temperature ionic liquid to couple the anode to the cathode. Each of the plurality of anode active material particles have a particle size of between about one micrometer and about fifty micrometers. One or more of the plurality of anode active material particles are enclosed by and in contact with a membrane coating permeable to lithium ions.

A negative electrode for a lithium ion secondary battery includes: a negative electrode current collector (11); and a negative electrode active material for a lithium ion secondary battery, which is disposed on the negative electrode current collector and contains a carbon material and an aqueous binder. The carbon material is a graphite particle having a covering layer containing amorphous carbon by 5 wt % or less relative to a total weight of the carbon material.

Provided is a negative electrode for a lithium ion secondary battery including: a negative electrode current collector; and a negative electrode active material for a lithium ion secondary battery which is disposed on the negative electrode current collector and contains a carbon material and an aqueous binder. The carbon material is a graphite particle having a covering layer containing amorphous carbon by 5 wt % or less relative to a total weight of the carbon material

A negative electrode active material including a silicon-containing alloy having a predetermined composition is used in an electric device. A ratio value (B/A) of a diffraction peak intensity B of a (001) plane of Sn to a diffraction peak intensity A of a (111) plane of Si is 0.3 or more and 3.7 or less in an X-ray diffraction measurement of the silicon-containing alloy using a CuKα1 ray. Here, the diffraction peak of the (111) plane of Si is present in a range of 2θ=24 to 33° and the diffraction peak of the (001) plane of Sn is present in a range of 2θ=26 to 35°.

Provided is a carbon material capable of obtaining a non-aqueous secondary battery, which has high capacity, initial efficiency, and low charging resistance and is excellent in productivity. As a result thereof, a high-performance non-aqueous secondary battery is stably provided with efficiency. A composite carbon material for a non-aqueous secondary battery is provided, which contains at least a bulk mesophase artificial graphite particle (A) and graphite particle (B) having an aspect ratio of 5 or greater, and which is capable of absorbing and releasing lithium ions. A graphite crystal layered structure of the graphite particle (B) is arranged in the same direction as a direction of an outer peripheral surface of the bulk mesophase artificial graphite particle (A) at a part of a surface of the bulk mesophase artificial graphite particle (A), and an average circularity of the composite carbon material is 0.9 or greater.