Silicon-carbon composite materials and related processes are disclosed that overcome the challenges for providing amorphous nano-sized silicon entrained within porous carbon. Compared to other, inferior materials and processes described in the prior art, the materials and processes disclosed herein find superior utility in various applications, including energy storage devices such as lithium ion batteries.

An amorphous silicon-carbon composite, a method for preparing the amorphous silicon-carbon composite using a pyrolysis method, a negative electrode for a lithium secondary battery, and a lithium secondary battery including the same.

Disclosed are a secondary battery comprising a negative electrode composed of two or more negative electrode plates and a method of manufacturing the secondary battery, wherein each of the negative electrode plates includes a lithium by-product layer formed through pre-lithiation reaction on a negative electrode current collector coated with a negative electrode active material, wherein an inorganic substance layer is formed on a negative electrode tab that is extended from an end at one side of the negative electrode current collector and is composed of an active material-non-coated portion not coated with the negative electrode active material, and negative electrode tabs of the negative electrode plates are electrically connected with one negative electrode lead to form a negative electrode terminal.

A method for producing an electrode comprising a core-shell nanocomposite material of which the core is made from silicon and the shell from carbon is provided. The method includes A) synthesising the nanocomposite material by pyrolysing a silicon core to form a core and then pyrolysing a a carbon shell precursor to form a carbon shell around the core, wherein the quantities of silicon and carbon precursor are injected in a proportion such that the mass percentage of carbon in the nanocomposite material is greater than or equal to 45%; B) dispersing the nanocomposite material synthesised in step A) in a solvent to form an ink; C) applying this ink to a support intended to form an electricity collector; D) eliminating the solvent from the ink applied to the support in step C) to obtain the electrode; E) pressing or calendaring the electrode.

The present invention relates to a method of forming a cured conductive binder material, to a method of forming a curable binder formulation, to a curable binder formulation, to a cured conductive binder material and to an electrochemical cell. In one embodiment, the method of forming a cured conductive binder material includes the steps of: (i) providing a liquid formulation comprising a liquid carrier, at least one active material, at least one polymeric binder and at least one modified metal coordination complex; and (ii) curing the liquid formulation of step (i), to thereby form a cured conductive binder material.

Silicon-carbon composite matertials and related processes are disclosed that overcome the challenges for providing amorphous nano-sized silicon entrained within porous carbon. Compared to other, inferior materials and processes described in the prior art, the materials and processes disclosed herein find superior utility in various applications, including energy storage devices such as lithium ion batteries.

The present invention provides aqueous chemical mechanical planarization (CMP) polishing compositions having a pH ranging from 2.5 to 5.3 and comprising a mixture of spherical colloidal silica particles and from 30 to 99 wt. %, based on the total weight of silica solids in the aqueous CMP polishing composition, of elongated, bent or nodular silica particles wherein the colloidal and elongated, bent or nodular silica particles differ from each other in weight average particle size (CPS) less than 20 nm, wherein at least one of the spherical colloidal silica particles and the elongated, bent or nodular silica particles contains one or more cationic nitrogen atoms. The present invention further provides methods of using the compositions in high downforce CMP polishing applications.

1. The present invention relates to a method for the purification of halogenated oligosilanes as a pure compound or mixture of compounds each having at least one direct Si—Si bond, the substituents thereof being exclusively halogen or halogen and hydrogen, and the composition thereof being an atom ratio of substituent:silicon of at least 3:2, by the action of at least one purification agent on the halogenated oligosilane and isolation of the halogenated oligosilane with improved purity.

2.1. In the prior art, halogenated monosilanes such as HSiCl.sub.3 are purified by treatment with preferably polymeric organic compounds containing amino groups, and are separated out from these mixtures. This method cannot be used for halogenated oligosilanes because of the contained amino groups, since secondary reactions would lead to decomposition of the products. The new method should provide the desired products in high yield and purity without amino groups being used.

2.2. The purification of the halogenated oligosilanes is carried out in the presence of special purification agents, which convert contaminations such as, for example, FeCl.sub.2 into an insoluble and/or less volatile form. A separation of the products of completes the purification This method gives a high yield and avoids the problems associated with the prior art, such as, for example, long distillation times.

2.3. The method is suitable for the purification of, for example, Si.sub.2Cl.sub.6, Si.sub.3Cl.sub.8, Si.sub.4Cl.sub.10, and higher homologs. These find application, for example, in the deposition of silicon nitride layers in CVD processes.

A method of making mesoporous silicon from silica, the mesoporous silicon obtained by the method, and uses of the mesoporous silicon are described. The mesoporous silicon may be derived from plants, particularly land-based plants.

A mesoporous silicon compound includes a mesoporous silicon phase, a metal silicide phase, and a carbon phase. The metal silicide is embedded in mesoporous silicon particles, the surfaces of which are coated with a carbon layer. A weight ratio of elemental silicon to the metal element is from 2:3 to 900:1. The pores of the mesoporous silicon particles have a size distribution from two nanometers to eighty nanometers.