Preparation method and application of H4.5Mo5.25O18*( H2O)1.36 hexagonal columnar micrometer rod and application
A hexagonal columnar, micro-rod technology, applied in the field of material chemistry, can solve the problems of poor conductivity and low lithium ion diffusion capacity, and achieve the effects of low cost, simple synthesis process and excellent electrochemical performance.
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Embodiment 1
[0019] with H 4.5 Mo 5.25 o 18 ·(H 2 O) 1.36 A preparation method for hexagonal columnar microrods, comprising the steps of:
[0020] (1) Add 0.2 g of analytically pure ammonium molybdate to 15 ml of deionized water and stir for 20 minutes to dissolve it.
[0021] (2) Add 10 ml of analytically pure formic acid to the solution obtained in step (1), and stir for 20 minutes in a water bath at 80°C.
[0022] (3) Add 0.1 g of analytically pure polyvinylpyrrolidone to the solution obtained in step (2), and continue stirring for 20 minutes.
[0023] (4) Put the solution obtained in step (3) into a 100ml reactor for hydrothermal reaction, and conduct a hydrothermal reaction at 160°C for 14 hours, then naturally cool to room temperature and take out the reactor.
[0024] (5) The product obtained in step (4) was centrifugally filtered, washed 4 times with absolute ethanol, and dried in an oven at 70°C for 24 hours to obtain a blue powder, namely H 4.5 Mo 5.25 o 18 ·(H 2 O) 1....
Embodiment 2
[0029] with H 4.5 Mo 5.25 o 18 ·(H 2 O) 1.36 A preparation method for hexagonal columnar microrods, comprising the steps of:
[0030] (1) Add 0.6 g of analytically pure ammonium molybdate to 30 ml of deionized water and stir for 30 minutes to dissolve it.
[0031] (2) Add 30 ml of analytically pure formic acid to the solution obtained in step (1), and stir for 30 minutes in a water bath at 90°C.
[0032] (3) Add 0.5 g of analytically pure polyvinylpyrrolidone to the solution obtained in step (2), and continue stirring for 30 minutes.
[0033] (4) Put the solution obtained in step (3) into a 100ml reactor for hydrothermal reaction. At 180°C, conduct a hydrothermal reaction for 24 hours, cool naturally to room temperature, and then take out the reactor.
[0034] (5) Centrifuge the product obtained in step (4), wash it with absolute ethanol for 6 times, and dry it in an oven at 70°C for 20 hours to obtain a blue powder, which is 1-3 microns in diameter and 5-20 microns in l...
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