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Preparation Of WO3-based Composite Photocatalysts And Their Photocatalytic Performance

Posted on:2021-05-09Degree:MasterType:Thesis
Country:ChinaCandidate:J H ZhangFull Text:PDF
GTID:2491306470463674Subject:Chemical Engineering and Technology
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With the rapid development of industrialization and urbanization,problems such as energy shortages and environmental pollution have become increasingly serious.It is particularly important to realize sustainable development of society.Visible light photocatalysis technology is an ideal way to generate clean energy and deal with environmental purification problems.WO3nanomaterials,as a photocatalyst that can respond to visible light,have the advantages of non-toxicity,resistance to photocorrosion,and excellent performance,and are a nanomaterial with promising photocatalytic applications.However,the insufficient reduction ability due to the low electron potential of the conduction band of WO3and the excessively high recombination ratio of photogenerated electrons and holes limit its further development and application.In view of the above problems of WO3,this paper modified WO3to construct a direct Z-scheme heterostructure,thereby improving its photocatalytic activity.1.Using the terminal amino group of g-C3N4 to control the morphology of tungsten oxide,a novel Z-scheme W18O49nanowire-g-C3N4nanosheet composite photocatalyst was prepared by solvothermal method.The introduction of g-C3N4improves the absorption of visible light and promotes charge transfer at the interface of the composite.The composites exhibited higher photocatalytic activity than pure W18O49and g-C3N4.When the content of g-C3N4was 50 mg,WCN50 showed the best photocatalytic activity.The corresponding hydrogen production rate was 1.700mmol?g-1?h-1and the conversion of cyclohexane was 7.35%.The improvement of photocatalytic activity is mainly due to the enhancement of visible light absorption capacity,and the Z-scheme charge transfer mechanism promotes interface charge transfer and prolongs the lifetime of photo-generated electrons.2.Z-scheme WO3 nanosheet-carbon quantum dot composites were prepared by loading carbon quantum dots with different terminal amine groups and carboxyl groups on the surface of WO3nanosheets.And compare their micromorphology,structural composition,optical and electrochemical performance.NCDs-loaded composites have lower fluorescence intensity and interface resistance,which means efficient electron transfer.WO3-NCDs composite with a mass content of 9.3%of NCDs showed photocatalytic hydrogen production activity and significantly improved the catalytic activity of cyclohexane oxidation.The highest cyclohexane conversion rate was 7.88%and the selectivity to KA oil was 98.9%.This performance is 1.2times that of WO3-CCDs and 1.5 times that of pure WO3nanosheets.The improvement of the catalytic performance is attributed to the effective Z-scheme charge transfer mechanism and the photo-thermal synergistic catalysis to accelerate chain initiation of cyclohexane oxidation.3.WO3-MoS2-NCDs composites were prepared by solvothermal method.The introduction of MoS2and NCDs makes composites have enhanced visible light absorption capacity,higher photoelectric conversion efficiency and interface charge transfer efficiency.The average hydrogen production rate of WMC composites is16.02μmol?g-1?h-1,which is 87%of the catalytic performance of WC composites using Pt as a cocatalyst,indicating that MoS2has the potential to replace the noble metal Pt as a cocatalyst.WMC composites have both a type II heterostructure and a Z-type heterostructure.The type II heterostructure maximizes the effective use of photogenerated electrons and holes,while the Z-scheme heterostructure maximizes the photo-generated electron’s reducing capacity.The ternary heterostructure enables efficient transfer of photogenerated electrons and holes,thereby significantly improving the photocatalytic hydrogen production capacity.
Keywords/Search Tags:Tungsten trioxide, photocatalysis, Z-scheme heterojunction, carbon quantum dots, g-C3N4
PDF Full Text Request
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