Multi-valence-state vanadium oxide flexible electrode preparation method
A vanadium oxide and flexible electrode technology, which is applied in the field of multivalent vanadium oxide flexible electrode preparation, can solve problems such as difficult operation and complicated process flow, and achieve electrochemical performance improvement, safe and reliable process, and low reaction temperature Effect
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[0025] One aspect of the present invention provides a method for preparing a multivalent vanadium oxide flexible electrode. In an exemplary embodiment of the method for preparing a multivalent vanadium oxide flexible electrode of the present invention, the preparation method may include:
[0026] In step S01, the carbon cloth is activated to obtain an activated carbon cloth.
[0027] In this embodiment, the method for activating the carbon cloth may include arranging the carbon in a container (for example, a reactor) containing hydrogen peroxide for activation treatment. The temperature of the activation treatment may be 120°C to 200°C. Further, the temperature of the activation treatment may be 150°C to 200°C. For example, it can be 180°C. The mass concentration of hydrogen peroxide can be 0.5% to 24.5%. Further, the mass concentration of hydrogen peroxide may be 0.5% to 20.0%. For example, it can be 3%. The appropriate activation temperature and hydrogen peroxide concentrati...
Example
[0044] Example 1
[0045] (1) The interception size is 2.5×6cm 2 , A commercial carbon cloth with a thickness of 350μm, then ultrasonically cleaned with a mixed solution of water / ethanol / nitric acid, washed and dried.
[0046] (2) Put the carbon cloth cleaned in step (1) into the reaction kettle, the concentration of hydrogen peroxide in the reaction kettle is 3wt%, the reaction temperature is set to 200°C, and the reaction time is 12 hours.
[0047] (3) After the reaction, let it cool to room temperature, wash and dry to obtain activated carbon cloth, such as figure 2 Shown.
[0048] (4) Fix the activated carbon cloth obtained in step (3) on the wall of the beaker, and add ethylene glycol and metavanadate at a concentration of 21 mmol / L to the beaker.
[0049] (5) Put the sample obtained in step (4) into an oil bath at 120°C and keep it under stirring for 2 hours until the reaction is complete.
[0050] (6) After the reaction is completed, the product of step (5) is washed and dried, a...
Example
[0052] Example 2
[0053] (1) The interception size is 2.5×6cm 2 , A commercial carbon cloth with a thickness of 350μm, then ultrasonically cleaned with a mixed solution of water / ethanol / nitric acid, washed and dried.
[0054] (2) Put the carbon cloth cleaned in step (1) into a reaction kettle, the concentration of hydrogen peroxide in the reaction kettle is 12.7% by weight, the reaction temperature is set to 200°C, and the reaction time is 12 hours.
[0055] (3) After the reaction, the carbon cloth is cooled to room temperature, washed and dried to obtain the activated carbon cloth.
[0056] (4) Fix the activated carbon cloth obtained in step (3) on the wall of the beaker, and add ethylene glycol and metavanadate at a concentration of 42 mmol / L to the beaker.
[0057] (5) Put the sample obtained in step (4) into an oil bath at 200°C and keep it under stirring for 5 hours until the reaction is complete.
[0058] (6) After the reaction is completed, the product of step (5) is washed and d...
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