Particles with suitable properties may be generated using systems and methods provided herein. The particles may include carbon particles.

The present disclosure is directed to novel germanosilicate compositions and methods of producing and using the same. In particular, this disclosure describes new germanosilicates of CIT-14 topology. The disclosure also describes methods of preparing and using these new germanosilicate compositions as well as the compositions themselves.

Provided herein are high throughput continuous or semi-continuous reactors and processes for manufacturing graphenic materials, such as graphene. Such processes are suitable for manufacturing graphenic materials at rates that are up to hundreds of times faster than conventional techniques, and have little batch-to-batch variation. Also provided herein are graphenic compositions of matter, including large, high quality and/or highly uniform graphene.

A method of preparing a soft carbon material for high-voltage supercapacitors includes: providing an initial soft carbon material characterized by: (A) a first carbon layer spacing greater than 0.345 nm but less than 0.360 nm; (B) a crystal plane (002) with a length (L.sub.c) less than 6 nm; (C) a crystal plane (101) with a length (L.sub.a) less than 6 nm; and (D) an intensity ratio (I.sub.(002)/I.sub.(101)) of the crystal plane (002) to the crystal plane (101) obtained by XRD analysis being less than 60; performing an alkaline activation on the initial soft carbon material with an alkaline activator to obtain a first processing carbon material; and performing an electrochemical activation on the first processing carbon material with an electrolyte to obtain the soft carbon material for the high-voltage supercapacitors.

A SiC single crystal, including: a seed crystal; a first growth portion formed in a direction that is substantially orthogonal to a <0001> direction; a second growth portion formed in a direction that is substantially orthogonal to the <0001> direction and substantially orthogonal to the direction in which the first growth portion is formed; a third growth portion that is formed on a surface of the seed crystal opposite the first growth portion; and a fourth growth portion that is formed on a surface of the seed crystal opposite the second growth portion.

The present invention provides a carbonaceous material suitable for a negative electrode active material for non-aqueous electrolyte secondary batteries (e.g., lithium ion secondary batteries, sodium ion secondary batteries, lithium sulfur batteries, lithium air batteries) having high charge/discharge capacities, and preferably high charge/discharge efficiency and low resistance, a negative electrode comprising the carbonaceous material, a non-aqueous electrolyte secondary battery comprising the negative electrode, and a production method of the carbonaceous material. The present invention relates to a carbonaceous material having a nitrogen content obtained by elemental analysis of 3.5 mass % or more, a ratio of nitrogen content and hydrogen content (R.sub.N/H) of 6 or more and 100 or less, a ratio of oxygen content and nitrogen content (R.sub.O/N) of 0.1 or more and 1.0 or less, and a carbon interplanar spacing (d.sub.002) observed by X-ray diffraction measurement of 3.70 Å or more.

The present invention relates to a method for producing a magnetic powder, including: preparing a precursor solution containing an iron precursor and a silica precursor; spraying the precursor solution to form iron/silica precursor droplets; drying the iron/silica precursor droplets to produce iron/silica precursor particles; and heat treating the iron/silica precursor particles to produce an iron oxide/silica composite powder in which iron oxide particles are embedded in a silica matrix. The present invention also relates to a magnetic powder produced by the method. The present invention may provide an iron oxide magnetic powder that does not use rare earth elements and a method for producing the same.

An electromagnetic wave absorbing particle dispersoid is provided that includes at least electromagnetic wave absorbing particles and a thermoplastic resin, wherein the electromagnetic wave absorbing particles contain hexagonal tungsten bronze having oxygen deficiency, wherein the tungsten bronze is expressed by a general formula: M.sub.xWO.sub.3-y (where one or more elements M include at least one or more species selected from among K, Rb, and Cs, 0.15≤x≤0.33, and 0<y≤0.46), and wherein oxygen vacancy concentration N.sub.V in the electromagnetic wave absorbing particles is greater than or equal to 4.3×10.sup.14 cm.sup.−3 and less than or equal to 8.0×10.sup.21 cm.sup.−3.

The technology subject of the present application concerns methods and systems for manufacturing and producing stable polarized or ferroelectric layered materials.

The present invention discloses a layer-number-controllable graphene derived from natural biomass and a preparation method thereof. The preparation method includes pulverizing 1-100 g of biomass to obtain a 50- to 300-mesh biomass scrap, and drying the biomass scrap at 60-100° C. to obtain a biomass precursor; mixing the biomass precursor with a Bronsted acid solution in a solid-liquid ratio of 0.1:10 to 2:100 g/mL, conducting sealing after discharging oxygen and introducing nitrogen, and then conducting heating for a reaction at 75-95° C. for 1-6 hours to obtain a graphene suspension; and conducting post-treatment on the graphene suspension to obtain a stable graphene dispersion, and then drying the stable graphene dispersion to obtain a graphene powder, where the post-treatment includes one or more of filtration washing, dialysis or ultrasonic treatment. According to the preparation method, the layer-number-controllable graphene is prepared by a mild chemical strategy at relatively low temperature with the biomass having high selectivity as a carbon source. The present invention further provides a layer-number-controllable graphene prepared by the method.