Preparation method of micro-nano structure
A technology of micro-nano structure and equipment, applied in the direction of ion implantation plating, metal material coating process, coating, etc., can solve the problems of inflexible control factors, difficulty in integrating nano-devices, poor crystallinity, etc., and achieve large scalability, Good controllability and good crystallinity
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Embodiment 1
[0029] In this embodiment, the evaporation source is copper phthalocyanine, and the ionic liquid is 1-butyl-3-methyl-imidazole nitrate, in which copper phthalocyanine and 1-butyl-3-methyl-imidazole nitrate are incompatible with each other .
[0030] The specific preparation steps of the copper phthalocyanine micro-nano structure are:
[0031] Step I: Place a quartz boat containing 0.04 g of copper phthalocyanine powder in the heating zone of the physical vapor deposition equipment. Take 2ml of 1-butyl-3-methyl-imidazole nitrate and pour it into another quartz boat and place it in the deposition area of the vapor deposition device. Vacuum the chamber where the deposition area is located, and then pass the protective gas argon, and continue to vacuum for 1 hour to prevent the evaporation source from being oxidized after entering the deposition area. Control the argon pressure to 6×10 -2 pa, adjust the airflow to 100sccm, increase the temperature of the heating zone, make the copp...
Embodiment 2
[0036] The difference between this embodiment and embodiment 1 is that the selected evaporation source is fullerene (C 60 ), the mass is 50mg. Take 2ml of 1,3-dimethylimidazole hexafluorophosphate as the ionic liquid. Under the protection of nitrogen, control the working temperature not higher than C 60 The decomposition temperature is specifically 450℃, and the heating time is 2h.
[0037] After the deposition is complete, use methanol as the cleaning agent to remove excess ionic liquid to obtain figure 2 C shown 60 Micro-nano structure.
Embodiment 3
[0039] The difference between this embodiment and embodiment 1 is that the selected evaporation source is zinc octaethylporphyrin, and the mass is 25 mg. Take 2 ml of N-butyl-3-methylpicolinate methanesulfonate as the ionic liquid. Under the protection of nitrogen, the working temperature is controlled not to be higher than the decomposition temperature of zinc octaethylporphyrin, specifically 400°C, and the heating time is 1.5h.
[0040] After the deposition is completed, water is used as a cleaning agent to remove excess ionic liquid to obtain a zinc octaethylporphyrin micro-nano structure.
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