Abstract: A copper oxide with a hollow porous structure, a preparation method therefor, and a use thereof are provided. The copper oxide with a hollow porous structure is of a hollow octahedral structure, and has a size of 200-400 nm and a specific surface area of 23.5-79.6 m2/g, where the surface of the octahedron is composed of copper oxide nanoparticles having a size of 14-33 nm, and pore structures are formed among the copper oxide nanoparticles. The copper oxide with the hollow porous structure has good conductivity, high hydrophilicity and good catalytic performance, can substantially reduce the detection potential and greatly improve the detection sensitivity and the anti-interference performance when used for the electrochemical detection of pesticides.

Abstract: The present invention provides a method for preparing fluorine/nitrogen co-doped graphitized carbon microspheres with high volumetric specific capacitance, which is a simple process with moderate reaction conditions, high reproducibility, and low costs. The fluorine/nitrogen co-doped graphitized carbon microspheres prepared according to the present invention have a very high density, exhibit good electrochemical properties in an alkaline environment, as well as very high volumetric specific capacitance and good cyclic stability, and is of great importance in improving the properties of the electrode material for a capacitor.

Abstract: A method for preparing fluorine/nitrogen co-doped graphitized carbon microspheres with high volumetric specific capacitance, mainly comprises: successively adding a carbon source, a nitrogen source, a fluorine source and a surfactant to a reactor under a nitrogen atmosphere, and stirring for 10-30 minutes before sealing the reactor; placing the reactor into a crucible furnace, heating at 300-600° C., for 6-48 hours, followed by naturally codling the reactor to room temperature and removing the reaction mixture therefrom; successively washing the resulted reaction mixture with absolute ethanol, 0.1 M-5 M diluted hydrochloride acid and distilled water for 3-6 times, filtering, and placing powder thus obtained in a vacuum oven and drying in vacuum at 60-100° C. for 6-12 hours. The present invention provides a simple process with moderate reaction conditions, high reproducibility, and low costs.