Preparation method and application of molybdenum selenide-based nano composite material
A nanomaterial, molybdenum selenide-based technology, applied in chemical instruments and methods, chemical/physical processes, physical/chemical process catalysts, etc., can solve problems such as insufficient molybdenum selenide, and achieve good durability, small mechanical stress and Volume change, effect of multiple reactive active sites
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[0039] The invention provides a method for preparing molybdenum selenide-based nanomaterials, comprising: S) mixing an organic molybdenum source, an organic zinc source, and an organic selenium source in an unsaturated amine solvent, and heating and reacting in a stirring and protective atmosphere , to obtain molybdenum selenide-based nanomaterials.
[0040] The present invention uses organometallic sources as precursors to prepare single-layer porous molybdenum selenide nano-heterostructure composite materials modified by zinc selenide quantum dots through a one-step method. The synthesis path is simple, the operation is convenient, and the compound with high activity and high stability Electrochemical hydrogen evolution catalysts and supercapacitor energy storage hosts optimize the structure of active materials and regulate their internal electronic forms, which have good practical prospects.
[0041] The preparation method provided by the invention enables the energy active...
Embodiment 1~3
[0055] Add 0.1mmol (32.6mg) molybdenum dioxide acetylacetonate, 0.1mmol (26.3mg) zinc acetylacetonate, 0.15mmol (51.0mg) dibenzyldiselenide and 5.0ml oleylamine solution into a 100mL three-necked flask. In an atmosphere of magnetic stirring and inert gas, the device was first heated to 130°C at a constant rate of 10°C / min to remove dissolved oxygen and other low-boiling impurities in the reactants. Afterwards, the device was heated to 290°C, 300°C, and 310°C at a rate of 10°C / min and kept for 30 min. After the reaction, the system was cooled down to room temperature by self-heating, and the obtained sample was dark in color, uniformly dispersed in the reaction medium, washed several times with a mixture of absolute ethanol and toluene, and dried overnight in a vacuum oven at 70°C. In order to remove surface oleylamine, the dried sample was placed in a tube furnace with hydrogen (3%) / argon atmosphere, raised to 400°C at a heating rate of 5°C / min, kept for half an hour, and sele...
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