Electrode used for vanadium redox flow battery and preparation method for electrode
An all-vanadium redox flow battery and electrode technology, which is applied to battery electrodes, circuits, electrical components, etc., can solve the problems of low voltage efficiency and achieve the effects of improving voltage efficiency, good electrochemical activity, and obvious effects
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[0025] The preparation method of the present invention includes:
[0026] Surface treatment of metal foil / net in advance;
[0027] Mix the nano carbon-based electrode material with the conductive agent and the binder in a weight ratio of 90:1-5:1-5;
[0028] The electrode material is deposited on the surface of the current collector to obtain an electrode for an all-vanadium flow battery.
[0029] In the present invention, the nano carbon-based electrode material is one or more of graphene oxide, reduced graphene, carbide, carbon nitride or carbon / metal nitride composite material; the conductive agent can be acetylene black, Super P, One or more of graphitized carbon fiber and vapor-grown carbon fiber; the binder is polyvinylidene fluoride PVDF, polytetrafluoroethylene PTFE, carboxyl styrene butadiene latex SBR, sodium carboxymethyl cellulose CMC, Nafion solution, etc.
[0030] In the preparation method of the present invention, the deposition method includes electrostatic spraying, ai...
Example Embodiment
[0032] Example 1
[0033] Take 23ml of 98wt% concentrated sulfuric acid and place it in the reaction vessel. Use an ice-water bath to keep the temperature at about 0℃. Add 1g of commercially available artificial graphite and 1NaNO. 3 Add sulfuric acid and stir vigorously for 10 minutes; slowly add 3g KMnO while stirring 4 At the same time, control the reaction temperature below 20°C, remove the ice-water bath after the addition is complete; continue to stir the above mixture in a 35°C water bath for 30 minutes, slowly add 46ml of water, increase the temperature to 98°C and keep it for 10 minutes; use about 50°C warm water Dilute to 140ml, add H 2 O 2 (5wt%), filter while hot, wash twice with 5wt% hydrochloric acid, and then wash with deionized water until there is no SO 4 2- Exist; dry the obtained material in a vacuum oven at 50°C for 24 hours and grind to obtain graphene oxide. The measured specific surface area is 42.7m 2 / g.
[0034] Mix CMC (sodium carboxymethyl cellulose) and ...
Example Embodiment
[0036] Example 2
[0037] The graphene oxide obtained in Example 1 was placed in a tube furnace and heat-treated at 120°C for 12 hours at a heating rate of 5°C min to obtain an electrode material. The measured specific surface area was 56.1m 2 / g.
[0038] The preparation method is the same as in Example 1 except that the electrode vacuum drying temperature is changed to 120° C. for 24 hours. The thickness of the electrode material measured with a micrometer is 30 μm, and the ICP emission spectrum test result shows that the electrode material accounts for 7 wt% of the entire electrode. The battery performance test method is the same as in Example 1, and the results are shown in Table 1.
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