Nanometer forest-shaped V-doped Ni3S2/NF self supporting electrode and preparation method thereof
A self-supporting electrode, forest technology, applied in the direction of electrode, electrode shape/type, electrolysis process, etc., can solve the problems of not being able to perform at the same time, mismatch between hydrogen-producing end and oxygen-producing end, etc., to achieve short reaction time and improve conductivity and electron transfer efficiency, the effect of simple steps
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Embodiment 1
[0017] (1) Immerse the conductive substrate in acetone solution for ultrasonic cleaning for 10 minutes, then transfer it to 2mol / L hydrochloric acid for ultrasonic cleaning for 10 minutes, and finally wash it alternately with ethanol and ultrapure water for 3 times, and then dry it in vacuum at 35°C for 10 hours;
[0018] (2) Configure a precursor solution, which contains nickel chloride at a concentration of 0.05mol / L, vanadium chloride at a concentration of 0.0125mol / L, ammonium fluoride at a concentration of 0.05mol / L and a concentration of 0.125 ) mol / L aqueous solution of urea, magnetically stirred at room temperature for 20 minutes to obtain a clear solution A. Transfer the clarified solution A and the conductive substrate treated in step (1) into a high-temperature and high-pressure hydrothermal kettle, and then react at 100°C for 18 hours, and the reaction filling ratio should be controlled at 40%. After the hydrothermal reaction was completed, the reactor was naturall...
Embodiment 2
[0021] (1) Soak nickel foam of 1cm x 5cm in acetone solution for 10 minutes, then transfer it to 2mol / L hydrochloric acid for 10 minutes, and finally rinse it with ethanol and ultrapure water for 3 times, and then clean it at 35°C. Vacuum drying for 10h;
[0022] (2) Configure a precursor solution, which contains nickel chloride at a concentration of 0.1mol / L, vanadium chloride at a concentration of 0.04mol / L, ammonium fluoride at a concentration of 0.05mol / L and a concentration of 0.2 The aqueous solution of mol / L urea was magnetically stirred at room temperature for 20 minutes to obtain a clear solution A. Transfer the clarified solution A and the conductive substrate treated in step (1) into a high-temperature and high-pressure hydrothermal kettle, and then react at 120°C for 14 hours, and the reaction filling ratio should be controlled at 40%. After the hydrothermal reaction was completed, the reactor was naturally cooled to room temperature, and then the conductive subst...
Embodiment 3
[0025] (1) Sonicate 1cm x 5cm nickel foam in acetone solution for 5 minutes, then immerse foam nickel in 2mol / L hydrochloric acid for 5 minutes, and finally rinse with ethanol and ultrapure water for 3 times respectively. After vacuum drying for 10°C, the treated foamed nickel was obtained;
[0026] (2) Configure a precursor solution, which contains nickel chloride at a concentration of 0.1mol / L, vanadium chloride at a concentration of 0.05mol / L, ammonium fluoride at a concentration of 0.05mol / L and 0.2 The aqueous solution of mol / L urea was magnetically stirred at room temperature for 20 minutes to obtain a clear solution A. Transfer the clarified solution A and the nickel foam treated in step (1) into a high-temperature and high-pressure hydrothermal kettle, and then react at 140°C for 10 hours, and the reaction filling ratio should be controlled at 30%. After the hydrothermal reaction was completed, the reactor was naturally cooled to room temperature, and then the conduct...
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