A kind of core double-shell structure negative electrode nanomaterial for nickel-iron battery and its preparation method and application
A composite nanomaterial, shell structure technology, applied in battery electrodes, nanotechnology for materials and surface science, negative electrodes, etc. The electrochemical properties of the interface, the improvement of high-rate discharge performance, and the effects of tight and uniform coating
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Embodiment 1
[0024] Embodiment 1: (undoped nickel)
[0025] Weigh 3.15g of citric acid and dissolve in 35ml of absolute ethanol solution. Then weigh 2.02g of ferric nitrate and add it to the above solution, stir at room temperature for 30min, then raise the temperature to 40°C for 1h, continue to raise the temperature to 80°C, stir and evaporate to dryness to obtain the precursor powder. Placed in a tube furnace, with a 60cm 3 min -1 Continuous injection of argon protective gas at the flow rate, after half an hour, at 5°C min -1 The heating rate was heated to 600°C for 2h at a constant temperature. Then naturally cooled to room temperature to obtain the target product.
[0026]The negative electrode sheet of the iron electrode was produced by rolling sheet method. The mass ratio of active material, conductive agent acetylene black and binder polytetrafluoroethylene is 8:1:1. First, weigh the active material and acetylene black according to the above ratio. After mixing evenly, trans...
Embodiment 2
[0029] Weigh 3.15g of citric acid and dissolve in 35ml of absolute ethanol solution. Then weigh 2.02g of iron nitrate and 0.15g of nickel nitrate into the above solution, stir at room temperature for 30min, then raise the temperature to 40°C for 1h, continue to raise the temperature to 80°C, stir and evaporate to dryness to obtain the precursor powder. Placed in a tube furnace, with a 60cm 3 min -1 Continuous injection of argon protective gas at the flow rate, after half an hour, at 5°C min -1 The heating rate was heated to 600°C for 2h at a constant temperature. Then naturally cooled to room temperature to obtain the target product.
[0030] The electrode manufacturing process and battery electrochemical performance test are the same as in Example 1. Table 2 records the specific surface area data of the product, and its specific surface area is 51.2m 2 g -1 , slightly larger than that of Example 1 (without adding nickel source). figure 1 The XRD curve of the sample is ...
Embodiment 3
[0032] Weigh 3.15g of citric acid and dissolve in 35ml of absolute ethanol solution. Then weigh 2.02g of ferric nitrate and 0.29g of nickel nitrate and add to the above solution, stir at room temperature for 30min, then raise the temperature to 40°C for 1h, continue to raise the temperature to 80°C, stir and evaporate to dryness to obtain the precursor powder. Placed in a tube furnace, with a 60cm 3 min -1 Continuous injection of argon protective gas at the flow rate, after half an hour, at 5°C min -1 The heating rate was heated to 600°C for 2h at a constant temperature. Then naturally cooled to room temperature to obtain the target product.
[0033] The electrode manufacturing process and battery electrochemical performance test are the same as in Example 1. Record the specific surface area data of gained sample in table 2, its specific surface area is 52.8m 2 g -1 , which is also larger than the samples in Example 1 and Example 2. figure 1 Recorded the XRD pattern of ...
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