Abstract: The present invention relates to the technical field of catalysts, and discloses a yolk/shell-type CoxCu1-xCo2O4@CoyCu1-yCo2O4 catalyst as well as a preparation method and application thereof to catalytic hydrogen generation. The preparation method of the yolk/shell-type CoxCu1-xCo2O4@CoyCu1-yCo2O4 catalyst includes the steps of: successfully synthesizing, by applying a hydrothermal synthesis method, a [Co(C6H12N4)2](NO3)2 solid sphere complex from a cobalt salt and hexamethyleneteramine serving as an alkali source; and then, performing calcination to obtain a yolk/shell-type Co3O4 microsphere structure, adsorbing Cu2+ on a surface in a physical adsorption manner, and performing calcination again to form yolk/shell-type CoxCu1-xCo2O4@CoyCu1-yCo2O4.

Abstract: An automatic high-speed stacking machine is disclosed, including a loading unit, a precision positioning unit, a stacking unit, a grabbing unit and a feeding unit. The feeding unit includes a platen configured to place silicon steel sheet stack; a material warehouse configured to store the platen containing the silicon steel sheet stack. An area of a side of the material warehouse is defined as a reclaiming area, and an area of a side of the loading unit is defined as a loading area. A skip car moving back and forth between the reclaiming area and the loading area is configured to take out and send the platen containing the silicon steel sheet stack from the material warehouse to the loading area, or send an empty platen back to the material warehouse.

Abstract: A method for preparing copper-nickel cobaltate nanowires includes steps of: (1) dissolving a soluble nickel salt, cobalt salt and copper salt in ultrapure water, and preparing same into a mixed salt solution A; (2) adding 1-4 mmol of sodium dodecyl sulfate to solution A, and dissolving same with stirring; (3) dissolving 12-30 mmol of hexamethylenetetramine in 20 mL of ultrapure water to form solution B; (4) slowly dropwise adding solution B to solution A via a separatory funnel to form solution C, and stirring same for 0.5-1 h; and (5) further transferring same into a 100 mL reaction vessel, reacting same at 100-160° C. for 8-20 h, suction filtration and washing, and drying same at 40-60° C. in a vacuum oven, and further reacting same at 350-800° C. for 1-4 h in a muffle furnace.

Abstract: The present invention relates to the technical field of catalysts, and discloses a yolk/shell-type CoxCu1-xCo2O4@CoyCu1-yCo2O4 catalyst as well as a preparation method and application thereof to catalytic hydrogen generation. The preparation method of the yolk/shell-type CoxCu1-xCo2O4@CoyCu1-yCo2O4 catalyst includes the steps of: successfully synthesizing, by applying a hydrothermal synthesis method, a [Co(C6H12N4)2](NO3)2 solid sphere complex from a cobalt salt and hexamethyleneteramine serving as an alkali source; and then, performing calcination to obtain a yolk/shell-type Co3O4 microsphere structure, adsorbing Cu2+ on a surface in a physical adsorption manner, and performing calcination again to form yolk/shell-type CoxCu1-xCo2O4@CoyCu1-yCo2O4.

Abstract: A method of preparing hollow molybdate composite microspheres includes steps of: (1) dissolving 1-4 mmol of MCl2 in 20 ml of water to obtain a solution A and dissolving 1-4 mmol. of molybdic acid in 20 ml of water to obtain a solution B, followed by mixing the solution A and the solution B, in which M is Co, Ni, or Cu; (2) dissolving 10-40 mmol of urea in 40 ml of water, adding the mixed solution of step (1) and stirring uniformly; (3) placing the mixed solution of step (2) into a reaction vessel and reacting at 120-160° C. for 6-12 hours; (4) suction filtrating and water washing, followed by drying in a vacuum oven at 40-60° C.; (5) calcination at 350-500° C. for 2-4 hours in a Muffle furnace.

Abstract: A lithium ion battery comprising (i) at least one anode, (ii) at least one cathode containing a cathode active material selected from lithium ion containing transition metal compounds having a content of Manganese of from 50 to 100 wt.

Abstract: A method of preparing hollow molybdate composite microspheres includes steps of: (1) dissolving 1-4 mmol of MCl2 in 20 ml of water to obtain a solution A and dissolving 1-4 mmol. of molybdic acid in 20 ml of water to obtain a solution B, followed by mixing the solution A and the solution B, in which M is Co, Ni, or Cu; (2) dissolving 10-40 mmol of urea in 40 ml of water, adding the mixed solution of step (1) and stirring uniformly; (3) placing the mixed solution of step (2) into a reaction vessel and reacting at 120-160° C. for 6-12 hours; (4) suction filtrating and water washing, followed by drying in a vacuum oven at 40-60° C.; (5) calcination at 350-500° C. for 2-4 hours in a Muffle furnace.

Abstract: A method for preparing copper-nickel cobaltate nanowires includes steps of: (1) dissolving a soluble nickel salt, cobalt salt and copper salt in ultrapure water, and preparing same into a mixed salt solution A; (2) adding 1-4 mmol of sodium dodecyl sulfate to solution A, and dissolving same with stirring; (3) dissolving 12-30 mmol of hexamethylenetetramine in 20 mL of ultrapure water to form solution B; (4) slowly dropwise adding solution B to solution A via a separatory funnel to form solution C, and stirring same for 0.5-1 h; and (5) further transferring same into a 100 mL reaction vessel, reacting same at 100-160° C. for 8-20 h, suction filtration and washing, and drying same at 40-60° C. in a vacuum oven, and further reacting same at 350-800° C. for 1-4 h in a muffle furnace.

Abstract: A lithium ion battery comprising (i) at least one anode, (ii) at least one cathode containing a cathode active material selected from lithium ion containing transition metal compounds having a content of Manganese of from 50 to 100% wt. based on the total weight of transition metal in the lithium ion containing transition metal compound, and (iii) at least one electrolyte composition containing •(A) at least one aprotic organic solvent, •(B) 0.01 up to less than 5% wt. based on the total weight of the electrolyte composition of at least one compound selected from the group consisting of lithium bis(oxalato)borate, lithium difluoro(oxalato)borate, lithium tetrafluoro(oxalato)phosphate, lithium oxalate, lithium (malonato oxalato)borate, lithium (salicylato oxalato)borate, lithium tris(oxalato)phosphate and vinylene carbonate compounds of formula (I), •(C) 0.01 up to less than 5% wt.