A kind of porous-hollow composite negative electrode material, preparation method and application thereof
A negative electrode material and hollow technology, which is applied in the field of high-performance porous-hollow composite negative electrode material and its preparation, can solve the problems of poor electrode cycle stability and low electrical conductivity, and achieves cheap preparation of raw materials, high yield, and excellent charge-discharge performance. Effect
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Embodiment 1
[0032] 1) Take 1.0g of Si powder and treat it in a muffle furnace at 600°C for 1h to prepare SiO 2 Layer-coated Si material;
[0033] 2) Take 0.2 g containing SiO 2 The layer-coated Si material was dispersed in an aqueous solution mixed with 100 mL of 28.6 mL of deionized water and 71.4 mL of ethanol, and stirred ultrasonically for 1 h. Add 1.2 g of cetyltrimethylammonium bromide (CTAB), 0.175 g of resorcinol, and 0.1 mL of ammonia water into the above solution, and stir ultrasonically for 30 min. Then put it in an oil bath at 45°C and stir for 30 minutes, add 0.15 mL of formaldehyde solution to the above mixed solution, keep stirring at 45°C for 1 hour, immediately filter with suction, wash with deionized water 3 times, and dry in vacuum at 70°C for 3 hours , preparing a composite material coated with a phenolic resin layer;
[0034] 3) Redisperse 0.1 g of the composite material coated with phenolic resin layer prepared above into 50 mL of deionized water, and ultrasonical...
Embodiment 2
[0039] 1) Take SnO 2 Nanoparticles (50-70 nm) 0.5g, prepared by Stober method containing SiO 2 layer-coated SnO 2 Material;
[0040] 2) Take 0.4 g containing SiO 2 layer-coated SnO 2 Materials The material was dispersed in an aqueous solution of 100 mL of 28.6 mL of deionized water and 71.4 mL of ethanol, and was stirred ultrasonically for 1 h. Add 2.4 g of cetyltrimethylammonium bromide, 0.35 g of resorcinol, and 0.1 mL of ammonia water into the above solution, and stir ultrasonically for 60 min. Then put it in an oil bath at 45°C and stir for 60 minutes, add 0.3 mL of formaldehyde solution to the above mixed solution, keep stirring at 45°C for 1 hour, immediately filter with suction, wash with deionized water 3 times, and dry in vacuum at 70°C for 5 hours. A composite material covered with a phenolic resin layer is prepared;
[0041] 3) Redisperse 0.2 g of the composite material coated with the phenolic resin layer prepared above into 50 mL of deionized water, and disp...
Embodiment 3
[0046] 1) Take 0.5 g of zinc ferrite nanoparticles (50 nm) and prepare SiO-containing 2 Layer-coated zinc ferrite material;
[0047] 2) Take 0.4 g containing SiO 2 The layer-coated zinc ferrite material was dispersed in an aqueous solution mixed with 100 mL of 28.6 mL of deionized water and 71.4 mL of ethanol, and stirred ultrasonically for 1 h. Add 2.4 g of cetyltrimethylammonium bromide (CTAB), 0.35 g of resorcinol, and 0.1 mL of ammonia water into the above solution, and stir ultrasonically for 45 min. Then put it in an oil bath at 45°C and stir for 45 minutes, add 0.3 mL of formaldehyde solution to the above mixed solution, keep stirring at 45°C for 1 hour, immediately filter with suction, wash with deionized water 3 times, and dry in vacuum at 70°C for 3 hours , preparing a composite material coated with a phenolic resin layer;
[0048] 3) Re-disperse 0.2 g of the prepared composite material coated with phenolic resin layer into 50 mL of deionized water, and disperse i...
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