Preparation method of nano mesoporous gold film loaded copper oxide cluster material and application of nano mesoporous gold film loaded copper oxide cluster material in preparation of ethanol
A technology of copper oxide and mesoporous gold, which is applied in metal material coating process, liquid chemical plating, ion implantation plating, etc., can solve the problems of low catalyst activity and poor product selectivity, so as to reduce the activation energy barrier, The effect of promoting reactivity and increasing reaction temperature
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Embodiment 1
[0025] Au / Ag double-layer films with a thickness of 5nm Au / 20nm Ag were deposited on the ITO substrate by electron beam evaporation technology, and a heat treatment was carried out at 900 °C for 15 minutes in an argon atmosphere to induce dehumidification. Then, the dehumidified Au-Ag alloy particles on the substrate were immersed in nitric acid solution (65 wt% HNO 3 solution) to remove Ag, and carry out dealloying treatment; the nanometer mesoporous gold thin film material (NP-Au) is prepared, and the physical map and different magnifications are observed in the scanning electron microscope to obtain figure 2 ( figure 2 ), with a good mesoporous structure.
Embodiment 2
[0027] The preparation process is the same as in Example 1, the only difference is that the concentration is 10mM hydrazine hydrate solution and 5mM copper acetate solution, respectively as a reducing agent and a copper precursor: then soak the NP-Au sample prepared in Example 1 in a hydration solution at room temperature Hydrazine solution for 30 minutes, the reducing agent is adsorbed by capillary effect, and then rinsed with deionized water to remove excess hydrazine hydrate solution on the surface. Then, soak the nanometer mesoporous gold film electrode adsorbed with hydrazine hydrate in copper acetate solution at room temperature for 30min, so that Cu 2+ After reduction, it was washed with deionized water again, so that the copper oxide clusters were supported on the nano-mesoporous gold film sample, and finally dried in a vacuum oven at 100°C for 2 hours. Prepared to get NP-Au-CuO X The -1C electrode material has no obvious difference from the microstructure of NP-Au ob...
Embodiment 3
[0029] The preparation process is the same as in Example 2, the only difference is that the NP-Au sample is soaked in hydrazine hydrate solution for 3 times and washed, and then soaked in copper acetate solution at room temperature for 30 minutes to increase the loading capacity of copper oxide clusters. NP-Au-CuO X -3C.
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