Electrode for Electrochemical Reduction of Carbon Dioxide to Hydrocarbon and Its Preparation and Application
A hydrocarbon and carbon dioxide technology, applied in battery electrodes, circuits, electrical components, etc., can solve the problems of lower catalyst utilization rate and small specific surface area of Cu nanoparticles, and achieve the effect of simple preparation method
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Embodiment 1
[0037]100um thick 0.3mm copper mesh (purity 99.99%) is used as the substrate. After degreasing treatment in acetone for 30min, at 4.0V voltage, 17.4M H in acidic solution 3 PO 4 Carry out activation treatment for 2min; take out the substrate after washing and drying in 0.01M CuSO 4 In the mixed solution of 0.5M lactic acid, treat it with -0.9V for 3min; after washing and drying, oxidize it at 500°C in an air atmosphere of 120ml / min for ~11h; in 1.0M H 3 PO 4 Reduction treatment was carried out at -3.0V for 10 min; after washing and drying, the prepared electrode was finally obtained. From figure 1 It can be seen that there is a layer of nanoparticles on the surface of the Cu mesh substrate, and a layer of nanowhiskers on the surface of the nanoparticle layer.
Embodiment 2
[0039] 100um thick 0.3mm copper mesh (purity 99.99%) is used as the substrate. After degreasing treatment in acetone for 30min, at 4.0V voltage, 17.4M H in acidic solution 3 PO 4 Carry out activation treatment for 4min; remove the substrate after washing and drying in 0.05M CuSO 4 In the mixed solution of 1M lactic acid, treat it with -1.2V for 3min; after washing and drying, oxidize it at 500°C in an air atmosphere of 120ml / min for ~11h; in 1.0M H 3 PO 4 Reduction treatment was carried out at -3.0V for 10 min; after washing and drying, the prepared electrode was finally obtained.
Embodiment 3
[0041] 1mm thick Cu plate (purity 99.99%) was used as the substrate, after degreasing treatment in acetone for 30min, at 3.0V voltage, 5M H in acidic solution 2 SO 4 Carry out activation treatment for 6 minutes; take out the substrate after washing and drying in 0.01M CuSO 4 In the mixed solution of 0.5M lactic acid, treat it with -0.9V for 3min; after washing and drying, oxidize it at 600°C for 8h in an air atmosphere of 130ml / min; in 1.0M H 2 SO 4 Reduction treatment was carried out at -3.0V for 10 min; after washing and drying, the prepared electrode was finally obtained.
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