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Preparation Of Ultrathin Bi2O2?OH?xCl2-x Nanosheets And Ultrathin Bi4O5Br2/g-C3N4 Composite Photocatalyst And Their Photocatalytic Properties

Posted on:2019-05-19Degree:MasterType:Thesis
Country:ChinaCandidate:K Q LiFull Text:PDF
GTID:2381330623955765Subject:Environmental Science and Engineering
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In recent years,photocatalytic technology has become more and more widely used in the field of wastewater treatment.However,traditional photocatalytic materials have become the bottleneck of their development because of their narrow spectral response and low quantum efficiency.Ultrathin two-dimensional lanthanide semiconductor materials have bright application prospects due to their special micro-morphology and energy level structure.In view of this,the photocatalytic performance and reaction mechanism of the ultra-thin Bi2O2?OH?xCl2-x and ultra-thin Bi4O5Br2/g-C3N4composite photocatalytic materials were studied.The main contents of this study are as follows:?1?Ultrathin Bi2O2?OH?xCl2-x?0?x?1?nanosheets were prepared by a simple and easy hydrothermal method.The phase composition,morphology and energy level structure of the samples were investigated by various characterization methods.The analysis results show that the use of ethylene glycol and water as the solvent for the hydrothermal reaction is the key factor for the oxygen vacancy?Vo?in the Bi2O2?OH?xCl2-x sample.At the same time,adjusting the pH value during the hydrothermal process can control the content of OH-in the Bi2O2?OH?xCl2-x crystal lattice and control the thickness of Bi2O2?OH?xCl2-x nanosheets.The energy level structure analysis results show that the introduction of OH-and Vo in the Bi2O2?OH?xCl2-x lattice will make its response to the visible spectrum larger.?2?The visible light catalytic performance of different Bi2O2?OH?xCl2-x samples was studied with ciprofloxacin?CIP?solution as the target pollutant.The experimental results show that the Bi2O2?OH?xCl2-x-Vo-8 sample has the best visible light catalytic performance.In addition,the photocatalytic mechanism of Bi2O2?OH?xCl2-x samples was also discussed in this study.The results showed that the hole and superoxide radical?·O2-?play a key role in the photocatalytic degradation of CIP effect.The introduction of OH-in the Bi2O2?OH?xCl2-x lattice makes it more excellent in the ability to separate photogenerated carriers.At the same time,a large amount of Vo on the{001}crystal plane improved its adsorption capacity for O2.It promotes the production of O2-,which effectively enhances its photocatalytic performance.?3?g-C3N4 was prepared by solid-phase method,and g-C3N4 was further added during the hydrothermal synthesis of Bi4O5Br2.Ultrathin Bi4O5Br2/g-C3N4 composite was successfully synthesized.A variety of characterization methods were used to study the phase composition,morphology and energy level structure of the composite samples.The analysis results show that the special two-dimensional morphology of ultra-thin Bi4O5Br2 and g-C3N4 makes it possible to form stable and strong heterogeneous structure,and the composite sample has a wider range of response to the visible spectrum.?4?The photocatalytic activity of the ultrathin Bi4O5Br2/g-C3N4 composite was studied with RhB solution as target contaminant.The experimental results show that the Bi4O5Br2-10wt.%C3N4 sample has better visible light catalysis active.In addition,the photocatalytic mechanism of the ultrathin Bi4O5Br2/g-C3N4 composite photocatalysts was preliminarily discussed.The heterostructure between Bi4O5Br2 and g-C3N4 facilitates the separation of photogenerated electrons and holes.The ultrathin Bi4O5Br2/g-C3N4 composite sample has better visible light catalytic activity than the single Bi4O5Br2 and g-C3N4 samples.The research ultrathin Bi2O2?OH?xCl2-x and ultrathin Bi4O5Br2/g-C3N4 composite photocatalytic materials provides a new idea for the synthesis of ultrathin two-dimensional Bi-based semiconductor materials and their application in the environmental field.
Keywords/Search Tags:Ultrathin, Oxygen vacancy, OH~-, Heterojunction, Photocatalytic mechanism
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