Molybdenum-based catalysts have high catalytic activity and abundant reserves,which have showed great application potential in photocatalytic degradation,photocatalytic hydrogen evolution,electrocatalysis,battery electrode and other fields.This paper starts from MoO3.On one hand,MoO3 was modified to introduce oxygen vacancies to improve its catalytic performance.On the other hand,MoO3 was used as the precursor to prepare 1T-MoS2 materials,with hydrothermal method used as the preparation method.It is expected to realize the safely and environmentally friendly preparation of 1T-MoS2 materials.The main work contents are as follows:(1)Firstly,MoO3 was prepared by precipitation method.Then,MoO3 was modified by surface reduction modification with ascorbic acid as the modifier,and the contents of oxygen vacancies of MoO3-x was controlled by controlling the modification time.Finally,the photocatalytic degradation activity of the prepared MoO3 and MoO3-x-x were tested using rhodamine B as the simulative pollutant.The degradation efficiency of MoO3-x-x is much higher than that of MoO3.This is because a large number of oxygen vacancies were introduced into MoO3-x after surface reduction modification,which improved MoO3-x’s oxidizability,reduced MoO3-x’s optical band gap energy and reduced the recombination ability of electron hole pairs,and thus improved MoO3-x’s photocatalytic degradation activity.(2)1T-MoS2 was prepared by low-temperature hydrothermal synthesis method with MoO3 serve as raw material and thioacetamide serve as sulfurizing agent.The influence of solvent,reaction temperature and urea addition amount on the morphology,composition and hydrogen evolution performance of MoS2 were discussed.Test results show that MoS2 with high contain of 1T-MoS2 and regular shape was prepared under the condition of water as solvent,200℃as the reaction temperature,and 0.12 g as the of urea addition amount.The prepared MoS2 showed the best hydrogen evolution performance because its smaller size and higher content of 1T-MoS2,which provided more reactive sites for the hydrogen evolution reaction. |