Negative electrode material for pseudocapacitor and method for manufacturing same
An anode material and pseudocapacitor technology, applied in the field of anode materials and their preparation, can solve the problems of low conductivity, limited anode material, low output characteristics, etc., and achieve the effect of improving capacitance and output characteristics and improving charge transfer.
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[0056] Specifically, in the preparation method of an anode material for a pseudocapacitor, step 1 is a step of mixing raw materials of a metal oxide, a conductive inorganic material and a doping element with a carboxylic acid complexing agent to react.
[0057] The metal oxide and conductive inorganic material are the same as described above, and may be used in amounts satisfying the above-mentioned content ranges of the metal oxide and conductive inorganic material in the composite. In addition, the metal oxide may be used in a solution state dissolved in a hydrogen peroxide solution or an acid such as hydrochloric acid, and the carbon-based material may be used in a dispersed state dispersed in water or a dispersion medium such as carboxymethylcellulose.
[0058] The raw material of the doping element can be any one or a mixture of two or more selected from sulfate, nitrate, chloride, acetate and carbonate containing the doping element, in this respect, Doping elements are t...
Embodiment 1
[0088] Will 0.9g V 2 o 5 , 30ml deionized water and 20ml H 2 o 2 Put in a round bottom flask and stir. To this was added a dispersion containing 6 g of CNTs in 30 ml of deionized water (CNTs were introduced in the form of a dispersion prepared by dispersing CNTs in CMC (carboxymethyl cellulose), 6 g of CNTs represented the CNT content in the dispersion to be introduced (CNT content in the dispersion = 5% by weight, CNT diameter = 9nm to 11nm), and 0.5mmol of Al as a raw material of the doping element was added thereto 2 (SO 4 ) 3 , followed by mixing. 100 ml of ethanol was added thereto, and to the resulting mixture was added dropwise by mixing 20 ml of L-aspartic acid (4 mol / relative to 100 parts by weight of V 2 o 5 400 parts by weight), 70 ml of deionized water and 5 ml of 6N HCl, and then reflux at 60° C. for 12 hours. The resulting precipitate was separated by centrifuge and washed with deionized water and ethanol to remove impurities. The resulting product was ...
Embodiment 2
[0090] In addition to using 1 mmol of MnSO in Example 1 4 Al instead of 0.5mmol 2 (SO 4 ) 3 Besides, V was prepared in the same manner as in Example 1 2 o 5 Metal oxide-CNT composite anode material doped with Mn.
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