A method of forming an activated carbon sorbent from a seagrass. The method involves treating a seagrass with a base solution to form an intermediate solid, drying the intermediate solid to form a precursor, and pyrolyzing the precursor at 600 to 1000° C. to form the activated carbon sorbent. Preferably the seagrass is Halodule uninervis. The activated carbon sorbent is used in a method of removing an organic pollutant from a contaminated water. Preferred organic pollutants removed are phenols, specifically 2,4-dimethylphenol and 2,4-dichlorophenol.

There is provided a method for producing lithium difluorophosphate in which difluorophosphate ester reacts with a lithium salt compound in a nonaqueous organic solvent without using water as a raw material, a method for producing a difluoro phosphate ester including a step of allowing a dihalophosphate ester to react with a fluorinating agent having a concentration of contained hydrogen fluoride of 15 mol % or less in a nonaqueous organic solvent; lithium difluorophosphate in which a value of a relational expression (d90-d10)/MV represented by d90 which is a particle size at which a volume cumulative distribution is 90%, d10 which is a particle size at which a volume cumulative distribution is 10%, and MV which is a volume average particle size is 10 or less; and methods for producing a nonaqueous electrolytic solution and a nonaqueous secondary battery using the production method described above.

An alumina grain has a single-crystal structure and has an approximate regular octahedral stereoscopic morphology. Eight sides of the alumina grain belong to the {111} family of crystal planes of γ-state alumina, and the grain size is 5-100 μm. The alumina grain is unique in crystal plane exposure and distribution, simple and feasible in preparation, and low in cost, and has higher operability, and thus has good application prospect in the field of catalysis and adsorption.

A whitlockite preparation method includes: determining a size of the whitlockite crystal to be prepared; determining a first amount of a first cation other than calcium ion on the basis of the determined size of the crystal, wherein when the determined size of the whitlockite crystal is a first size, the first amount is determined to be a first value, wherein when the determined size is a second size larger than the first size, the first amount is determined to be a second value; mixing calcium ion and phosphate ion in order to prepare a first phosphate crystal, wherein the determined first amount of the cation other than calcium ion is also mixed therewith; mixing a second amount of cation other than calcium ion with phosphate ion to prepare a second phosphate crystal; and aging a solution containing the first phosphate crystal and the second phosphate crystal.

A cathode active material for a lithium secondary battery includes a core portion comprising a lithium metal oxide particle, and a coating layer at least partially covering a surface of the core portion and including a lithium boron composite oxide. The lithium boron composite oxide is included in an amount from 100 ppm to 1,500 ppm based on a total weight of the cathode active material. A lithium secondary battery having improved structural stability and electrical property is provided using the cathode active material.

Passivated Li.sub.7La.sub.3Zr.sub.2O.sub.12 (LLZO) particles, tape casting powders and slip compositions including the particles, methods of forming the particles, methods of tape casting using the particles, green tapes including the particles, cast LLZO films formed from the particles, and lithium batteries including the cast LLZO film. A passivated LLZO particle includes an LLZO core, wherein the LLZO is optionally doped with one or more elements. The passivated LLZO particle also includes a shell including H-LLZO, H.sub.3O.sup.+-LLZO, and/or Li.sub.2CO.sub.3.

A preparation method of fluorocarbon-coated VSe.sub.2 composite (VSe.sub.2@CF) anode electrode material, including: weighting and dissolving an acetylacetone oxovanadium (VO(acac).sub.2) and a selenium dioxide in a solvent to prepare a first solution with a concentration of 0.5-2 mol/L, and stirring the first solution for 0.5 h to obtain a dark green solution; adding the dark green solution with an organic acid to obtain a second solution; transferring the second solution to a polytetrafluoroethylene-lined high-pressure hydrothermal reactor, and holding at a heat insulation temperature for 15-30 h to obtain a third solution; after the third solution is cooled, suction filtering the cooled third solution, and washing the filtered third solution repeatedly to obtain a precipitate; drying the precipitate to obtain a black powder; co-mixing a citric acid solution with the black powder, stirring, ball milling, and drying; and heating up, holding, and finally cooling naturally to room temperature under inert atmosphere.

The disclosure relates to a method for preparing a 3D sponge structured carbonitride coated VSe.sub.2 composite (3D-VSe.sub.2@CN), belonging to the technical fields of electrode materials and preparation of batteries. In the disclosure, carbon, nitrogen and VSe.sub.2 are composited by using NaCl as a template so as to construct a 3D sponge structured carbonitride coated VSe.sub.2 composite. The 3D sponge structure can increase the structure stability of the material in the cyclic process, and the carbocanitride can increase the electron conductivity and activity sites of the material, so as to allow easier diffusion of potassium ions. Meanwhile, the stable structure can cause the clustering of VSe.sub.2 all the time. Thus, the prepared composite has good and stable rate capability and cycle stability. The process method is simple, low in cost, environmental-friendly, and suitable for large-scale industrial production.

The present disclosure relates to production of electrodes. The present disclosure particularly relates to production of graphene based transparent conducting electrode (TCE). The disclosure provides a simple and environmental friendly process for producing said graphene based TCE by coating of graphene on a modified or non-modified substrate. Said electrode provides large area metal network with reduced non-uniformity of conducting film, visible transparency and low or reduced sheet resistance. The disclosure further relates to a graphene based transparent conductive electrode (TCE).

The present invention relates to a process for preparing a rodlike magnetic ferroferric oxide (Fe.sub.3O.sub.4) material and use thereof. The preparation includes the following steps: step 1: magnetic Fe3O4 nanoparticle preparation; and step 2: self-assembly of magnetic Fe3O4@SiO2 nanoparticles into a rodlike magnetic material. When in use, the rodlike magnetic Fe.sub.3O.sub.4 material prepared by the process according to claim 1 is used in micro- and nano-motors, which can implement rotation and deflection in an external magnetic field. The present invention provides a process for preparing a rodlike magnetic Fe.sub.3O.sub.4 material. The rodlike magnetic ferroferric oxide material prepared by the process is suitable for mass production on an industrial scale, featuring identifiable direction of the magnetic moment, strong magnetism, good magnetic response, simple process, and low cost.