研究目的
To develop a novel Mn-doped Fe2O3/g-C3N4 composite photocatalyst for overall visible-light driven water splitting without additional sacrificial reagents.
研究成果
The Mn-doped Fe2O3/g-C3N4 composite exhibits enhanced photocatalytic activity for water splitting under visible light, with optimal performance at a 10:1 ratio (FMC-10), achieving H2 evolution of 51 μmol h?1. The improvement is due to synergistic effects enhancing charge separation and transfer. Future studies could explore other dopants or composite structures.
研究不足
The photocatalytic performance decreases at higher Mn-doped Fe2O3 contents due to increased opacity and light scattering. The study is limited to visible light conditions and specific composite ratios; further optimization and scalability may be needed.
1:Experimental Design and Method Selection:
A facile hydrothermal route was used to synthesize Mn-doped Fe2O3 nanocubes supported on g-C3N4 sheets. The method involved thermal polymerization for g-C3N4 preparation and hydrothermal synthesis for the composite.
2:Sample Selection and Data Sources:
Various mass ratios of g-C3N4 to Mn-doped Fe2O3 (20:1, 10:1, 5:1) were prepared to optimize photocatalytic performance. Pure g-C3N4 and Fe2O3/C3N4 samples were used for comparison.
3:List of Experimental Equipment and Materials:
Chemicals included FeCl3·6H2O, MnCl2·4H2O, PVP, urea, NaAc, ethylenediamine. Equipment included X' Pert Pro XRD system, AXIS Ultra DLD XPS, JEOL JSM-6700 FESEM, JEM-2100 F TEM, Tristar 3010 isothermal nitrogen sorption analyzer, Lambda 750 spectrophotometer, Lambda LS55 PL spectrometer, 300 W Xe lamp, gas chromatograph.
4:Experimental Procedures and Operational Workflow:
g-C3N4 was prepared by heating urea at 550°C in N2. The composite was synthesized by dispersing g-C3N4 in water, adding precursors, and hydrothermal treatment at 200°C for 10 h. Photocatalytic activity was tested in a lab-made reactor with visible light irradiation and gas analysis.
5:The composite was synthesized by dispersing g-C3N4 in water, adding precursors, and hydrothermal treatment at 200°C for 10 h. Photocatalytic activity was tested in a lab-made reactor with visible light irradiation and gas analysis. Data Analysis Methods:
5. Data Analysis Methods: XRD, XPS, FESEM, TEM, BET surface area analysis, UV-vis DRS, PL spectra, photocurrent measurements, and gas chromatography were used for characterization and performance evaluation.
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X-ray photoelectron spectroscopy
AXIS Ultra DLD
Kratos
Recording chemical composition
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Field-emission scanning electron microscope
JSM-6700
JEOL
Determining morphology
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Transmission electron microscope
JEM-2100 F
JEOL
High-resolution imaging
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Spectrophotometer
Lambda 750
PerkinElmer
Performing diffuse reflectance UV–vis spectra
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Photoluminescence spectrometer
Lambda LS55
PerkinElmer
Recording PL spectra
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X-ray diffraction system
X' Pert Pro
Characterization of crystallographic information
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Isothermal nitrogen sorption analyzer
Tristar 3010
Micromeritics
Measuring texture properties
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Xe lamp
300 W
Providing visible light irradiation
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Gas chromatograph
Analyzing reaction-evolved gases
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