| Water pollution has become one of the most important issues to be addressed in today’s society.Zinc stannate(Zn2SnO4)photocatalysts are widely used for the degradation of organic pollutants in water.However,the wide band gap of Zn2SnO4 and the rapid compounding of photogenerated carriers limit its application in photocatalysis.To improve its performance of photocatalysis,two kinds of Zn2SnO4 and a derivative of Zn2SnO4heterojunction photocatalysts are constructed in this paper.And their morphology,structure,photoelectrochemical properties,degradation performance and mechanism of catalytic degradation are investigated.The details are as follows.(1)SnS/Zn2SnO4 photocatalyst(SZS-x)is synthesized by a one-step hydrothermal method.The results show that SnS is successfully attached to the surface of Zn2SnO4,and there is a Z-scheme heterojunction between SnS and Zn2SnO4.The optimized SZS-6sample exhibits good photocatalytic degradation activity and photogenerated carrier separation ability.It is demonstrated that the Z-scheme heterojunction is formed between SnS and Zn2SnO4,and the present of SnS effectively shortens the band gap of Zn2SnO4.And their synergistic effect enhances the light absorption capacity of SZS-6.Meanwhile,SZS-6 shows a stable photocatalytic activity under different pollutants,catalyst amounts,ion concentrations,p H and temperature environments.The degradation mechanism study demonstrates that the hole(h+)and superoxide free radical(?O2-)produced by this catalyst under light are the main active species for methylene blue(MB)degradation of SZS-6.(2)Zn-Sn-Mo trimetallic sulfides(ZSM-x)are fabricated by direct vulcanizing Zn2SnO4 by using ammonium molybdate as the molybdenum source.TEM analysis indicates that the lamellar Mo S2 is uniformly loaded with Zn S/SnS nanoparticles,and their interfaces are tightly combined.Results demonstrate that the formation of Zn S/SnS/Mo S2double heterojunctions within ZSM-x accelerates the charge separation and transfer of ZSM-x catalysts to increase the electron transfer rate.The degradation experiments shows that ZSM-x exhibits great degradation activity for MB under visible light.The ZSM-15 has the best performance.Its removal rate of MB achieves 99.5%within 50 min,corresponding to 0.0994 min-1 of rate constant k.The mechanism study shows that the electrons(e-)and hydroxyl radicals(·OH)dominate the degradation of MB.(3)Zn2SnO4/Ti3C2(ZTC-x)is prepared by electrostatic adsorption of positively charged Zn2SnO4 polyhedral nanoparticles and negatively charged Ti3C2 ultra-thin nanosheets via an ultrasound-assisted method.The degradation experiment displays that the degradation rate of ZTC-4 is 0.0537 min-1 for MB,which is approximately 16.8 times that of Ti3C2 and 26.8 times that of Zn2SnO4.This is due to the good light response capacity and metal-like property of black Ti3C2 itself,which enhances the light trapping ability and electrical conductivity of ZTC-4.Meanwhile,the Schottky barrier between Ti3C2 and Zn2SnO4 effectively accumulates electrons,and enhances the carrier transfer rate of Zn2SnO4,inhibits the rapid recombination of photogenerated electron-hole and greatly improves the photocatalytic degradation activity of Zn2SnO4. |