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Analysis On The Construction Of Controllable Phase Of Tungsten Oxide Compositing G-C3N4 And Their Photocatalytic Performance

Posted on:2020-12-08Degree:MasterType:Thesis
Country:ChinaCandidate:Y H LiFull Text:PDF
GTID:2381330623963061Subject:Analytical Chemistry
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With the situation of the modern scientific and technological progress,rapid economic and social development,environmental pollution has attracted more and more attention,environmental pollution has become more and more serious.Reducing environmental pollution and building a green China has always been the primary issue for scientific researchers.Since 1972,researchers have found that TiO2 has visible light absorption and has been used as photocatalytic degradation of pollutants.However,there are still many problems in the application of TiO2 as a semiconductor in the field of photocatalysis,such as wide band gap,low utilization rate of solar energy and high photogenerated electron hole recombination rate,which greatly limit its practical application.So scientists began to search for the semiconductor photocatalysts which have the better photocatalytic activity than TiO2.g-C3N4as a non-metallic semiconductor photocatalyst favored by scientists in this century has many advantages:wide visible light absorption,adjustable interband energy levels,high chemical stability,abundant edge N source,non-toxic and harmless.As an environmentally friendly carbon material,g-C3N4 is often used degrade organic pollutants and degrade aquatic hydrogen.Under visible-light photocatalysis,photogenerated electron holes and oxygen generate superoxide radicals and hydroxyl radicals,which can degrade organic pollutants quickly without secondary pollution.It is well known that single-component photocatalysts have many shortcomings for example the rapid combination of photogenerated electrons and holes.While the synthesis of heterojunction composites with suitable band structure by two kinds of semiconductors can improve the separation of charge carriers and the photocatalytic activity and stability of photocatalysts.In this paper,the 2D carbon material g-C3N4 was chosen as the main research object,and WO3 with different phase were synthesized by changing chemical reaction conditions.It could improve the photocatalytic degradation efficiency of g-C3N4 to Rhodamine B under visible light by using the method of solid phase roasting synthesis.The main research results of this paper include:?1?Bulk g-C3N4 and h/m-WO3 were synthesized by pyrolysis of urea and ammonium tungstate at high temperature.Photocatalytic results showed that the catalytic effect of h/m-WO3/g-C3N4 was significantly improved.When the mass ratio of g-C3N4 to h/m-WO3 was 3.0,the degradation rate of 40 mg/L rhodamine B solution could reach 99%within 150 minutes under the irradiation of tungsten iodide lamp.?2?Two different forms of WO3:h-WO3 and m-WO3 were synthesized by changing the calcination temperature and time of precursor Ammonium Tungstate by the same synthesis method and the optimum mass ratio of reactants.Three different forms of WO3:h-WO3,h/m-WO3 and m-WO3 then with g-C3N4 were synthesized to be the heterojunction photocatalysts.Combining with scanning electron microscopy?SEM?,the uncertainty of the influence of different supporting forms of WO3 and g-C3N4 on photocatalytic reaction was eliminated under the same reaction conditions.The results showed that the photocatalytic degradation ability of g-C3N4 was greatly improved after loading hexagonal phase of WO3 under visible light to degradate the organic pollution RhB.According to the SPV characterization of three composite photocatalysts,it can be found that H1G3?h-WO3 and g-C3N4 have a mass ratio of 1:3?has the strongest SPV signal,indicating that the separation and transmission efficiency of photogenerated electron-hole pairs at the interface of H1G3 heterostructure structure is the highest and the photocatalytic activity is the highest.The results are consistent with photocatalytic degradation experiments.?3?Oxygen defect can enlarge the wavelength absorption range of the photocatalyst,promote the separation of the photogenic hole electron pair,and can also be used as electron capture center.In this paper,under the condition of calcined at 400oC in a tubular furnace among the reducing atmosphere,N2,h/m-WO3-oxygen vacancy?h/m-WO3-OV?was synthesized.Then,the heterojunction of h/m-WO3-OV/g-C3N4 was synthesized by the same method.Through the Raman characterization of h/m-WO3-OV,we found that the longer the heterogeneous junction was roasted under N2,the lattice matching of h/m-WO3 increased and then decreased,the half peak width and the photocatalytic performance increased and then decreased,too.Among them,h/m-WO3-60 min-OV crystal lattice has the largest crystal lattice,the widest half-peak width and the largest photocatalytic performance.The SPV characterization results show that h/m-WO3-60min-OV photogenerated electron-hole pair has the highest separation efficiency,indicating that more photogenerated carriers participate in the photocatalytic reaction,thus he photocatalyst degradation efficiency was greatly improved.The RhB degradation experiment of the target pollutant showed that the photodegradation effect of h/m-WO3-60min-OV/g-C3N4 complex was the best.
Keywords/Search Tags:g-C3N4, Heterojunction, Phase, Rhodamine B, Photocatalysis
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