Synthetic method of high-performance one-dimensional nanostructure vanadium oxide lithium ion battery electrode material
A lithium vanadium oxide and nanostructure technology, applied in battery electrodes, vanadium oxide, nanotechnology, etc., to achieve the effect of simple synthesis method, high repeatability and high purity
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Embodiment 1
[0037] First place 0.182g of V 2 o 5 Add it to one cavity of the lining of the high-temperature mixed hydrothermal reactor, and then add 0.378g of oxalic acid to another cavity of the lining;
[0038] Then add 5ml deionized water to the two chambers respectively;
[0039] Then seal the reactor and put it into an oven to heat up. When the temperature rises to 200-260°C, rotate the reactor to mix the reactants in the two inner cavities of the reactor and keep it warm for 2-24 hours;
[0040] Cool to room temperature after reaction finishes;
[0041] Finally, the obtained precipitate was washed several times with deionized water and absolute ethanol, and then dried at 80 °C for 10 h to obtain a metastable phase VO with good dispersibility. 2 (B) Powder.
[0042] Embodiment two:
Embodiment 2
[0044] First place 0.182g of V 2 o 5 Add it to one cavity of the lining of the high-temperature mixed hydrothermal reactor, and then add 0.378g of oxalic acid to another cavity of the lining;
[0045] Then add 5ml deionized water to the two chambers respectively;
[0046] Afterwards, seal the reactor and put it into an oven to heat up. When the temperature rises to 240°C, rotate the reactor to mix the reactants in the two cavities of the reactor and keep it warm for 24-48 hours;
[0047] Cool to room temperature after reaction finishes;
[0048] Finally, the obtained precipitate was washed several times with deionized water and absolute ethanol, and then dried at 80 °C for 10 h to obtain a metastable phase VO with good dispersibility. 2 (A) Powder.
[0049] Embodiment three:
Embodiment 3
[0051] First place 0.182g of V 2 o 5 Add it to one cavity of the lining of the high-temperature mixed hydrothermal reactor, and then add 0.378g of oxalic acid to another cavity of the lining;
[0052] Then add 5ml deionized water to the two chambers respectively;
[0053] Afterwards, seal the reactor and place it in an oven to heat up. When the temperature reaches 240°C, rotate the reactor so that the reactants in the two cavities of the reactor are mixed and kept warm for 1 hour;
[0054] Cool to room temperature after reaction finishes;
[0055] Finally, the obtained precipitate was washed several times with deionized water and absolute ethanol, and dried at 80 °C for 10 h to obtain a stable phase V with better dispersion 3 o 7 ·H 2 O powder.
[0056] like figure 1 , figure 2 and image 3 shown, from figure 1 It is clearly seen in the XRD pattern that VO was synthesized under this experimental condition2 (B), VO 2 (A) and V 3 o 7 ·H 2 O three kinds of vanadi...
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