A high-performance three-dimensional carbon nanotube composite negative electrode material and its preparation method and application
A carbon nanotube composite and negative electrode material technology, applied in the direction of nanotechnology, nanotechnology, nanotechnology for materials and surface science, etc., can solve the problem that the volume effect of high-capacity active materials cannot be effectively improved, and the active materials are not uniform Dispersion, low charge transfer efficiency and other issues, to achieve the effect of good industrialization prospects, improved cycle performance, and convenient industrial production
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Embodiment 1
[0035] 1) Prepare two parts of 200mL aqueous solution containing 1 wt.%PDDA and 0.2M NaCl, and disperse it uniformly by ultrasonic dispersion for 10 minutes; prepare one part of 200 mL aqueous solution of 1 wt.%PSS, and disperse it uniformly by ultrasonic dispersion for 10 minutes ; 1g of Si powder (particle size 100-200 nm) that has undergone surface oxidation treatment is sequentially modified by PDDA-PSS-PDDA, filtered, vacuum-dried at 70 °C for 2 h, ground after drying, and stored with a label;
[0036] 2) Take 0.1 g of the above-mentioned modified Si powder and redisperse it in 200 mL deionized water, and disperse it by ultrasonic for 2 hours to make it evenly dispersed;
[0037] 3) Add 0.02 g of carboxylated carbon nanotubes into 200 mL of deionized water, and disperse ultrasonically for 2 hours to disperse the carboxylated carbon nanotubes evenly;
[0038] 4) In the case of high-speed stirring, take the above-mentioned modified Si powder solution and pour it into the di...
Embodiment 2
[0041] 1) Prepare two parts of 200mL aqueous solution containing 1 wt.%PDDA and 0.2M NaCl, and disperse it uniformly by ultrasonic dispersion for 10 minutes; prepare one part of 200 mL aqueous solution of 1 wt.%PSS, and disperse it uniformly by ultrasonic dispersion for 10 minutes ; 1 g of sintered SnO 2 Nanoparticles (50 nm) were sequentially modified by PDDA-PSS-PDDA treatment, filtered, and vacuum-dried at 70 °C for 2 h. Grind after drying, mark and store;
[0042] 2) Take the above modified SnO 2 Re-disperse 0.2 g of nanoparticles in 200 mL of deionized water, and ultrasonically disperse for 2 hours to make them uniformly dispersed;
[0043] 3) Add 0.02 g of carboxylated carbon nanotubes into 200 mL of deionized water and disperse ultrasonically for 2 hours to disperse the carboxylated carbon nanotubes evenly;
[0044] 4) In the case of high-speed stirring, take the above modified SnO 2 Pour the nanoparticle solution into the dispersion of carboxylated carbon nanotubes...
Embodiment 3
[0047] 1) Prepare two 200 mL aqueous solutions containing 1 wt.%PDDA and 0.2M NaCl, and disperse them by ultrasonic dispersion for 10 minutes to make them uniform; Dispersion; 1g of sintered ZnFe 2 o 4 Nanoparticles (about 50 nm) were sequentially modified by PDDA-PSS-PDDA treatment, filtered, and vacuum-dried at 70 °C for 2 h. Grind after drying, mark and store;
[0048] 2) Take the above modified 0.1g ZnFe 2 o 4 Nanoparticles were redispersed in 200 mL deionized water, and ultrasonically dispersed for 2 hours to make them uniformly dispersed;
[0049] 3) Add 0.01 g of carboxylated carbon nanotubes into 200 mL of deionized water, and ultrasonically disperse for 2 hours to uniformly disperse the carboxylated carbon nanotubes;
[0050] 4) In the case of high-speed stirring, take the above modified 0.1gZnFe 2 o 4 Pour the nanoparticle solution into the dispersion of carbon nanotubes, continue to stir for 2 hours, then let it stand still, use a separatory funnel to take ou...
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