A non-stoichiometric nanovo for controlling phase transition temperature 2-x Preparation method of powder
A technology of phase change temperature and vo2-x, which is applied in the direction of nanotechnology, nanotechnology, nanotechnology, etc. for materials and surface science, can solve the problem of high cost, high equipment requirements, and the reduction of thermally induced phase transition performance of vanadium dioxide and other problems, to achieve the effect of mild reaction conditions, breakthrough application bottlenecks, and short production cycle
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Embodiment 1
[0023] Add 1.891g of oxalic acid to the beaker, add 75mL of deionized water, and stir magnetically in a water bath at a constant temperature of 30°C for 15 minutes. Stir for 0.5h, put the above-mentioned precursor into the reaction kettle, conduct a hydrothermal reaction at 160°C for 48h, centrifuge the product, wash it with a mixture of absolute ethanol and deionized water with a volume ratio of 1:2, and then put it into vacuum drying The oven was treated at 60°C for 4 hours, and the dried samples were put into the furnace for annealing treatment, and the protective atmosphere was introduced: argon gas 0.5L / min; heat treatment conditions: 30°C heating for 94min to 500°C, constant temperature for 1h, natural cooling in the furnace to room temperature to obtain VO with a phase transition temperature of 63.0°C 2.0 Powder. The phase transition parameters are shown in Table 1, and the differential scanning calorimetry (DSC) spectrum is shown in figure 1 The X-ray diffraction (XR...
Embodiment 2
[0027] Add 1.891g of oxalic acid to the beaker, add 75mL of deionized water, and stir magnetically in a water bath at a constant temperature of 30°C for 15 minutes. Stir for 1 hour, put the above-mentioned precursor into the reaction kettle, conduct a hydrothermal reaction at 280°C for 48 hours, centrifuge the product, wash it with a mixture of absolute ethanol and deionized water with a volume ratio of 1:3, and then put it in a vacuum drying oven Treat at 60°C for 4 hours, put the dried samples into the furnace for annealing treatment, and introduce a protective atmosphere: high-purity nitrogen 0.5L / min; heat treatment conditions: 30°C heating for 114min to 600°C, constant temperature for 2h, natural cooling in the furnace to room temperature to obtain VO with a phase transition temperature of 53.5°C 1.95 Powder. The phase transition parameters are shown in Table 1, and the differential scanning calorimetry (DSC) spectrum is shown in figure 1 The X-ray diffraction (XRD) pat...
Embodiment 3
[0029] Add 1.891g of oxalic acid to the beaker, add 75mL of deionized water, stir in a water bath at a constant temperature of 30°C for 15 minutes, add 2.445g of vanadyl sulfate to the above solution, stir in a water bath at a constant temperature of 30°C for 10 minutes, adjust the temperature of the water bath to 100°C, and stir at a constant temperature 2h, put the above-mentioned precursor into the reaction kettle, hydrothermally react at 280°C for 48h, centrifuge the product, wash it with a mixture of absolute ethanol and deionized water with a volume ratio of 1:5, and then put it in a vacuum drying oven for 60 ℃ treatment for 4 hours, and naturally cooled to room temperature to obtain VO with a phase transition temperature of 55.8℃ 1.96 Powder. Its phase transition parameters are shown in Table 1, and the differential scanning calorimetry (DSC) spectrum is shown in figure 1 The X-ray diffraction (XRD) pattern is shown as figure 2 As shown, the scanning electron microsc...
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