研究目的
Investigating the photoelectrocatalytic degradation of Acid Yellow 17 dye using Sn3O4 flower-like thin films supported on Ti substrate under visible light illumination.
研究成果
Sn3O4/TiO2/Ti electrodes effectively degrade and mineralize AY17 dye under visible light, with photoelectrocatalysis showing higher efficiency than photocatalysis. The method is promising for wastewater treatment but requires optimization for film stability and scalability.
研究不足
The Sn3O4 film stability decreases under higher bias potentials in photoelectrocatalysis, leading to leaching and reduced efficiency. The process is less effective at high dye concentrations due to reduced light penetration. Film reusability is limited in PEC compared to PC.
1:Experimental Design and Method Selection:
The study involved synthesizing Sn3O4 nanostructures via microwave-assisted hydrothermal method, depositing them on Ti substrates to form thin films, and evaluating their photocatalytic and photoelectrocatalytic activities for dye degradation under visible light. Theoretical models include semiconductor photocatalysis principles.
2:Sample Selection and Data Sources:
Acid Yellow 17 dye was used as the pollutant model. Samples were prepared in aqueous solutions with Na2SO4 as electrolyte.
3:List of Experimental Equipment and Materials:
Equipment includes microwave-assisted hydrothermal autoclave, FEG-SEM, XRD, TEM, zeta analyzer, potentiostat/galvanostat, UV-Vis spectrophotometer, TOC analyzer, LC-MS/MS, and a homemade glass reactor with a Hg lamp. Materials include SnF2, NaOH, ethanol, titanium foils, PVB, toluene, methanol, 1-pentanol, Na2SO4, H2SO4, and AY17 dye.
4:Experimental Procedures and Operational Workflow:
Synthesis of Sn3O4 involved dissolving SnF2 in water-ethanol, adjusting pH to 6, hydrothermal treatment at 150°C for 2 hours, centrifugation, washing, and drying. Thin films were prepared by spin coating Sn3O4-PVB solution on Ti foils and annealing. Characterization included SEM, XRD, TEM, zeta potential, and photoelectrochemical measurements. Degradation experiments were conducted in a reactor with controlled pH, bias potential, and light conditions, monitoring discoloration and mineralization over time.
5:Data Analysis Methods:
Data analysis involved kinetic rate calculations using pseudo-first-order models, statistical evaluation of degradation efficiency, and identification of intermediates via LC-MS/MS.
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Field Emission Scanning Electron Microscope
JSM-7500F
JEOL
Characterization of material morphology
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X-ray Diffractometer
D-Max 2500
Rigaku
Analysis of crystallinity and phase purity
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Zeta Analyzer
Nano Series
Malvern
Measurement of zeta potential
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Potentiostat/Galvanostat
PGSTAT302N
Autolab
Electrochemical measurements
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UV-Vis Spectrophotometer
Cary 60
Agilent Technologies
Monitoring dye discoloration
Cary 60 UV-Vis Spectrophotometer
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Total Organic Carbon Analyzer
VCPN
Shimadzu
Evaluation of mineralization
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High-Performance Liquid Chromatography
1200
Agilent Technologies
Separation of compounds
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Transmission Electron Microscope
CM200
Philips
Examination of nanostructure crystallinity
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Mass Spectrometer
3200 QTRAP
AB SCIEX
Identification of intermediates
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Radiometer
PMA 2100
Solar Light Co.
Measurement of incident energy density
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High-Pressure Hg Lamp
125 W
Osram
Light source for photocatalysis
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Thermostatic Bath
Quimis
Temperature control in reactor
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Autoclave
Hydrothermal synthesis
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Centrifuge
Separation of synthesized materials
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Spin Coater
Deposition of thin films
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