Preparation method of carbon nanotube @ ternary @ silver composite material of lithium-ion battery
A technology of lithium-ion batteries and carbon nanotubes, which is applied in electrical components, battery electrodes, secondary batteries, etc., can solve the problems such as the difficulty in increasing the specific capacity, and achieve improved electrochemical performance, low energy consumption, and technological conditions. Effect
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Embodiment 1
[0024] Add lithium acetate, nickel acetate, cobalt acetate and manganese acetate into ethylene glycol at a molar ratio of 0.01mol:0.0033mol:0.0033mol:0.0033mol:0.0033mol and stir until the metal salts are completely dissolved; transfer the above ethylene glycol solution into a round bottom flask 0.1 g of CNTs containing functional groups was added, and a coaxial CNTM-alkylate precursor (M=Ni, Co, Mn) was formed by heating and refluxing at 170 °C for 5 h; Calcined at 800°C for 5h to form CNTLiNi 1 / 3 co 1 / 3 mn 1 / 3 o 2 ;CNTLiNi 1 / 3 co 1 / 3 mn 1 / 3 o 2 Add it to the diluted glucose solution and stir it magnetically to form a suspension, then add the diluted ammonia water dropwise to 0.001molAgNO 3 Ag(NH 3 ) 2 OH solution, the above suspension and Ag(NH 3 ) 2 OH solution mixed with magnetic stirring, heated at 60°C, centrifuged, washed and vacuum dried at 60°C to obtain CNTLiNi 1 / 3 co 1 / 3 mn 1 / 3 o 2 Ag.
Embodiment 2
[0026] Add lithium nitrate, nickel nitrate, cobalt nitrate and manganese nitrate into ethylene glycol at a molar ratio of 0.01mol: 0.005mol: 0.003mol: 0.002mol and stir until the metal salts are completely dissolved; transfer the above ethylene glycol solution into a round bottom flask 0.15 g of CNTs containing functional groups were added, and the coaxial CNTM-alkylate precursor (M=Ni, Co, Mn) was formed by heating and refluxing at 170 °C for 5 h; Calcined at 850°C for 5h to form CNTLiNi 0.5 co 0.3 mn 0.2 o 2 ;CNTLiNi 0.5 co 0.3 mn 0.2 o 2 Add it to the diluted glucose solution and stir it magnetically to form a suspension, then add the diluted ammonia water dropwise to 0.001molAgNO 3 Ag(NH 3 ) 2 OH solution, the above suspension and Ag(NH 3 ) 2 OH solution mixed with magnetic stirring, heated at 60°C, centrifuged, washed and vacuum dried at 60°C to obtain CNTLiNi 0.5 co 0.3 mn 0.2 o 2 Ag. figure 2 is CNTLiNi 0.5 co 0.3 mn 0.2 o 2 The rate performance dia...
Embodiment 3
[0028]Add lithium acetate, nickel acetate, cobalt acetate and manganese acetate into glycerin at a molar ratio of 0.01mol: 0.008mol: 0.001mol: 0.001mol and stir until the metal salts are completely dissolved; transfer the above glycerol solution into a round bottom flask, and then add 0.2 g of CNTs containing functional groups were heated and refluxed at 220 °C for 5 h to form a coaxial CNTM-alkylate precursor (M=Ni, Co, Mn); 2 Calcined at 850°C for 5h to form CNTLiNi 0.8 co 0.1 mn 0.1 o 2 ;CNTLiNi 0.8 co 0.1 mn 0.1 o 2 Add it to the diluted maltose solution and stir it magnetically to form a suspension, then add the diluted ammonia water dropwise to 0.002molAgNO 3 Ag(NH 3 ) 2 OH solution, the above suspension and Ag(NH 3 ) 2 OH solution mixed with magnetic stirring, heated at 60°C, centrifuged, washed and vacuum dried at 60°C to obtain CNTLiNi 0.8 co 0.1 mn 0.1 o 2 Ag.
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