A quantum dot luminescent material and a method of producing thereof. The quantum dot luminescent material includes a hole injection layer, a hole transport layer, a quantum dot light emitting layer, an electron transport layer, and an electron injection layer. The quantum dot luminescent layer is located on the hole transport layer, and the quantum dot luminescent layer includes uniformly distributed perovskite nanodots.

There is provided a core-shell composite comprising a core which comprises zinc metal and a shell that at least partially encapsulates the core, wherein the shell comprises a salt of the zinc metal as a cation with a sulphur-containing anion. There is also provided a method of forming a core-shell composite comprising the step of heating a mixture of zinc metal particle with elemental sulphur to form the core-shell composite, wherein the zinc metal particle forms the core of the core-shell composite, and wherein the shell of the said core-shell composite at least partially encapsulates the core and comprises a salt of the zinc metal as a cation with a sulphur-containing anion. There is also provided a method of killing or inhibiting the growth of a microbe, comprising the step of subjecting the microbe to the as-disclosed core-shell composite. There is also provided an anti-microbial coating on a substrate surface or an additive in a composition or a formulation comprising the as-disclosed core-shell composite.

A negative electrode for a secondary battery including: a negative electrode current collector; and a negative electrode active material layer present on the negative electrode current collector. The negative electrode active material layer includes a negative electrode active material, wherein the negative electrode active material for a secondary battery includes natural graphite, and has a sphericity of 0.58 to 1, a tap density of 1.08 g/cc to 1.32 g/cc, and D.sub.max−D.sub.min of 16 μm to 19 μm, wherein D.sub.max−D.sub.min is a difference between a maximum particle diameter D.sub.max and a minimum particle diameter D.sub.min in a particle size distribution.

The present invention relates to spherical, dense micrometre-sized particles comprising colourants. The invention also relates to a material comprising these particles intended for use in papermaking, paint, agri-food, cosmetics or pharmaceuticals. It also relates to the process for preparing these particles and their incorporation in a matrix.

A silicon nanoparticle-containing hydrogen polysilsesquioxane sintered product-metal oxide complex comprising a silicon nanoparticle-containing hydrogen polysilsesquioxane sintered product and a metal oxide, wherein the silicon nanoparticle-containing hydrogen polysilsesquioxane sintered product contains 5 wt % to 95 wt % of silicon nanoparticles having a volume-based mean particle size of more than 10 nm but less than 500 nm, and a hydrogen polysilsesquioxane-derived silicon oxide structure that coats the silicon nanoparticles and is chemically bonded to the surfaces of the silicon nanoparticles. The silicon nanoparticle-containing hydrogen polysilsesquioxane sintered product is represented by the general formula SiO.sub.xH.sub.y (0.01<x<1.35, 0<y<0.35) and has Si—H bonds. The metal oxide consists of one or more metals selected from titanium, zinc, zirconium, aluminum, and iron.

According to one embodiment, an electrode is provided. The electrode includes an active material-containing layer. The active material-containing layer includes an active material and a conductive agent. The active material contains primary particles of a niobium-titanium composite oxide. The conductive agent contains fibrous carbon. The primary particles have an average particle size of 0.3 μm or more and 2 μm or less. At least a part of a surface of the primary particles is coated with the fibrous carbon. A covering ratio of the primary particles by the fibrous carbon is 0.01% or more and 40% or less.

Semiconductor structures having a nanocrystalline core and corresponding nanocrystalline shell and insulator coating, wherein the semiconductor structure includes an anisotropic nanocrystalline core composed of a first semiconductor material, and an anisotropic nanocrystalline shell composed of a second, different, semiconductor material surrounding the anisotropic nanocrystalline core. The anisotropic nanocrystalline core and the anisotropic nanocrystalline shell form a quantum dot. An insulator layer encapsulates the nanocrystalline shell and anisotropic nanocrystalline core.

This invention provides a membrane electrode material and its preparation method, as well as the application of the material into lithium extraction by adsorption-electrochemical coupling method. The membrane electrode material is described as MnO@C. The preparation steps are as follows: LiMn.sub.2O.sub.4 is firstly obtained by calcining lithium carbonate and manganese carbonate, which is then dispersed in hydrochloric acid solution. After stirring and separating, the solid products are dried to obtain λ-MnO.sub.2. The λMnO.sub.2 is added to the raw material of Mn-MOF-74, and then the Mn-MOF-74 coated λ-MnO.sub.2 can be obtained by hydrothermal reaction. By further calcining Mn-MOF-74 coated λ-MnO.sub.2 in nitrogen atmosphere, the membrane capacitor/electrode material can be obtained as MnO@C. The material is fabricated into an adsorption film electrode plate and assembled into an adsorption-electrochemical coupling lithium extraction device. The pure lithium solution can be obtained in the recovery pool through the combined lithium extraction and lithium recovery process. In this invention, the thickness of the carbon coating layer in the electrode material is adjustable. Adsorption-electrochemical coupling technology takes the advantages of both adsorption and electrochemical lithium intercalation, which can extract and recover lithium resources with high capacity. Thus, this invention not only achieves high-efficiency separation of lithium resources, but also opens up a new way for the extraction of lithium resources.

Hybrid particles having improved electrical conductivity and thermal and chemical stabilities are disclosed. The hybrid particles are for use in conductive pastes. The hybrid particles include a nanoparticle selected from a graphene-containing material, a dichalcogenide material, a conducting polymer, or a combination thereof encapsulated in a conducting metal. The hybrid particles include a nanoparticle selected from a graphene-containing material, a dichalcogenide material, or a combination thereof encapsulated in a conducting polymer, and optionally further in a conducting metal. Suitable conducting metals include nickel or silver. Suitable conducting polymers include polyaniline, polypyrrole, or polythiophene. Suitable dichalcogenide materials include MoS.sub.2 or MoSe.sub.2. The hybrid particles can further include a conducting polymer layer on an outer surface of the conducting metal. Methods of making the hybrid particles are also disclosed.

The present disclosure is directed to a negative electrode active material for lithium secondary batteries, to a method for preparing the same, and to a lithium secondary battery including the same, the negative electrode active material including a porous core in which scaly silicon fragments are connected in an entangled manner; and a shell layer covering the core, where the shell layer includes a carbon-based material and silicon.