Carbon fiber-molybdenum selenide nanosheet core-shell composite structure and preparation method thereof
A technology of molybdenum diselenide and composite structure, which is applied in the direction of binary selenium/tellurium compounds, carbon preparation/purification, chemical instruments and methods, etc., and can solve problems such as complex purification and impurity removal, complex chemical reactions, and difficult control. Achieve nanoscale order, high purity, uniform diameter and thickness
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[0030] The preparation method of the carbon fiber@molybdenum diselenide nanosheet core-shell composite structure proposed by the present invention includes the following steps and contents:
[0031] (1) Using commercially available analytically pure selenium powder, MoO 3 Powder and chemically pure pre-oxidized polyacrylonitrile fibers are used as raw materials.
[0032] (2) MoO 3 Powder and absolute ethanol are mixed according to the ratio of (5-80g):(50-100ml), fully stirred to make a uniform suspension; then place the pre-oxidized polyacrylonitrile fiber in it and soak for 10-60min; then dry Dry and set aside.
[0033] (3) In the vacuum tube furnace, place the alumina ceramic crucible with selenium powder on the top of the air flow at a distance of 25-45 cm from the central heating area of the furnace, and fill the crucible soaked with MoO 3 The suspension of pre-oxidized polyacrylonitrile fibers on a quartz substrate is placed in the central heating zone of the furnac...
Embodiment 1
[0039] Embodiment 1: in the vacuum tube furnace, the aluminum oxide ceramic crucible that 3g selenium powder is housed is placed on air flow top distance furnace central heating zone 37cm place, will hold the concentration of warp that is 1g MoO 3 Powder and 5ml of absolute ethanol prepared by soaking and drying the pre-oxidized polyacrylonitrile fiber quartz substrate placed in the central heating area of the furnace.
[0040] Before heating, first use a vacuum pump to evacuate the whole system to below 0.01Pa, then feed high-purity argon gas of more than 99.99vol.% into the system, and repeat 3 times to remove the air in the system. Then the temperature was raised to 400° C. at a rate of 20° C. / min, kept at a temperature of 10 minutes, and then raised to 1110° C. at a rate of 20° C. / min, and kept at a temperature of 3 hours. During the heating process, under the premise that the vacuum system continued to work, argon gas was introduced and the carrier gas flow rate was mai...
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