研究目的
To enhance the photocatalytic hydrogen evolution activity of Cu2O by synthesizing core-shell Cu7S4-coated Cu2O nanocubes to improve light harvesting and electron-hole separation.
研究成果
The Cu2O/Cu7S4 nanocubes exhibit significantly enhanced photocatalytic hydrogen evolution due to improved light absorption and electron-hole separation facilitated by the Cu7S4 cocatalyst, with a high production rate of 1689.00 μmol·g-1·h-1. This approach provides a promising strategy for developing efficient photocatalysts for water splitting.
研究不足
The study may have limitations in scalability, long-term stability under operational conditions, and potential optimization of the Cu7S4 layer thickness or composition for further efficiency improvements.
1:Experimental Design and Method Selection:
The study involved synthesizing Cu2O nanocubes via a solution method and then forming Cu7S4 layers on them through anion exchange to create a core-shell structure. The rationale was to leverage the localized surface plasmon resonance (LSPR) of Cu7S4 to enhance photocatalytic properties.
2:Sample Selection and Data Sources:
Samples included pure Cu2O, Cu7S4, and Cu2O/Cu7S4 nanocubes with varying degrees of sulfuration (e.g., S-x/Cu2O where x is the mole ratio of Na2S to Cu2O). Data were obtained from material characterizations and photocatalytic tests.
3:List of Experimental Equipment and Materials:
Equipment included XRD (Brooker D8 advanced), SEM (JSM-7800F), TEM (JEOL 2100-F), UV-VIS-NIR spectrophotometer (Lambda 750), XPS (Kratos AXIS Ultra DLD), gas chromatography (GC-2014), and electrochemical station (CHI 660D). Materials included CuCl2·2H2O, NaOH, L-ascorbic acid, Na2S·9H2O, Na2SO3, and others from suppliers like Sinopharm Chemical Reagent Co., Ltd.
4:Experimental Procedures and Operational Workflow:
Cu2O nanocubes were synthesized by mixing CuCl2, NaOH, and L-AA solutions, followed by centrifugation and freeze-drying. Cu2O/Cu7S4 NCs were formed by adding Na2S to Cu2O dispersion under stirring, then isolating and washing. Photocatalytic hydrogen evolution tests were conducted in a quartz cell with Na2SO3 as a sacrificial agent under Xe lamp irradiation, with hydrogen measured by GC. Photoelectrochemical measurements used a three-electrode setup with FTO working electrodes.
5:Data Analysis Methods:
Data were analyzed using techniques like Tauc plots for bandgap calculation, Mott-Schottky plots for carrier concentration, and statistical analysis of photocatalytic rates.
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X-ray diffractometer
D8 advanced
Brooker
Recording powder XRD patterns for phase identification.
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Scanning electron microscope
JSM-7800F
JEOL
Taking SEM images for morphology analysis.
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Transmission electron microscope
JEOL 2100-F
JEOL
Conducting TEM, HRTEM, EDS line scan and mapping analyses.
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UV-VIS-NIR spectrophotometer
Lambda 750
Perkin Elmer
Testing UV-VIS-NIR spectra for light absorption analysis.
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Fluorescence spectrometer
RF-5301PC
Perkin Elmer
Confirming defects in semiconductors.
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X-ray photoelectron spectrometer
AXIS Ultra DLD
Kratos
Characterizing surface composition, electronic structure, and valence-band spectra.
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Gas chromatograph
GC-2014
SHIMADZU
Measuring hydrogen evolution amount.
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Xenon lamp
Solaredge 700
China
Providing full-spectrum light irradiation for photocatalytic and photoelectrochemical tests.
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Electrochemical station
CHI 660D
Shanghai Chenhua
Measuring transient photocurrent, LSV, EIS, and Mott-Schottky plots.
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FTO glass
Nippon Sheet Glass
Used as conductive substrate for photoelectrochemical measurements.
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