研究目的
To develop and characterize a g-C3N4/N-doped CeO2 composite for enhanced photocatalytic degradation of herbicides, specifically diuron, by leveraging nitrogen doping to reduce bandgap and improve efficiency.
研究成果
The synthesis successfully produced a g-C3N4/N-doped CeO2 composite with nitrogen doping confirmed by XPS, leading to a reduced bandgap of 2.8 eV and enhanced photocatalytic activity for diuron degradation. The composite showed good stability over multiple cycles, with superoxide radicals as the dominant active species, indicating potential for environmental applications.
研究不足
The study may have limitations in scalability of the synthesis method, potential variability in nanoparticle size distribution, and the need for further optimization for industrial applications. The photocatalytic efficiency was tested only on diuron, and other contaminants were not evaluated.
1:Experimental Design and Method Selection:
The study employed a facile in-situ synthesis method using l-arginine to synthesize CeO2 nanoparticles on exfoliated g-C3N4 nanosheets, aiming to achieve nitrogen doping and uniform distribution without complex equipment.
2:Sample Selection and Data Sources:
Bulk g-C3N4 was synthesized from melamine, exfoliated via thermal oxidation, and composites were prepared with CeCl3·7H2O and l-arginine in ethanol.
3:List of Experimental Equipment and Materials:
Materials included melamine (Sigma-Aldrich, 99% AR), CeCl3·7H2O, l-arginine, ethanol; equipment included muffle furnace, ultrasonicator, magnetic stirrer, hot air oven, centrifuge, XRD (Bruker D8 advance eco diffractometer), XPS (Thermo Scientific K-Alpha spectrometer), HR-TEM (JEOL JEM 2100), BET (Micromeritics TriStar II), UV-Vis (Varian CARY 300), SEM (JEOL JSM-IT 500), and solar simulator (suntest CPS+).
4:Experimental Procedures and Operational Workflow:
Steps involved synthesis of bulk g-C3N4 by heating melamine at 550°C for 2h, exfoliation at 550°C for 3h, composite synthesis by dispersing exfoliated g-C3N4 in ethanol with l-arginine and CeCl3·7H2O, stirring, heating at 70°C overnight, centrifugation, washing, and drying. Characterization techniques were applied, and photocatalytic tests used a xenon lamp with diuron solution, sampling every 20min for UV-Vis analysis.
5:Data Analysis Methods:
Bandgap calculated using Tauc plot from UV-Vis spectra, surface area via BET method, pore size via BJH method, kinetic analysis using Langmuir-Hinshelwood pseudo-first-order equation, and XPS deconvolution for chemical states.
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melamine
99% AR
Sigma-Aldrich
Precursor for synthesizing bulk g-C3N4
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X-ray diffractometer
D8 advance eco
Bruker
Analyzing crystalline phases of samples
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X-ray photoelectron spectrometer
K-Alpha
Thermo Scientific
Identifying chemical states of samples
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Transmission electron microscope
JEM 2100
JEOL
Taking high-resolution TEM images
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Scanning electron microscope
JSM-IT 500
JEOL
Recording SEM images and elemental mapping
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Surface area analyzer
TriStar II
Micromeritics
Carrying out nitrogen physisorption experiments
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UV-Vis spectrophotometer
CARY 300
Varian
Recording UV-Vis absorption spectra
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Solar simulator
suntest CPS+
Providing light irradiation for photocatalytic tests
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