研究目的
To synthesize Pt nanoparticles decorated Pt2+-doped α-Fe2O3 nanoplates via a one-step solvothermal process for enhanced photocatalytic O2 evolution in water splitting.
研究成果
The one-step solvothermal synthesis of Pt nanoparticles decorated Pt2+-doped α-Fe2O3 nanoplates significantly enhances photocatalytic O2 evolution due to improved carrier separation from Pt2+ doping and schottky barrier formation from Pt nanoparticle decoration. The optimal sample (Pt/Pt-Fe2O3-0.1) shows the highest activity and stability, making it a promising catalyst for water splitting applications.
研究不足
The study is limited to α-Fe2O3-based materials and Pt doping/decoration; other dopants or methods may yield different results. The photocatalytic performance is dependent on the amount of Pt, with excessive Pt leading to decreased activity due to morphology changes and shielding effects. The method may not be scalable for industrial applications, and the stability under long-term operation needs further investigation.
1:Experimental Design and Method Selection:
A one-step solvothermal method was used to synthesize Pt/Pt-Fe2O3 nanoplates with varying amounts of H2PtCl
2:The method involves reducing chloroplatinic acid with ethanol under high temperature and pressure to incorporate Pt2+ into α-Fe2O3 lattice and deposit Pt nanoparticles on the surface. Sample Selection and Data Sources:
Samples were prepared with 0,
3:05, 1, and 2 ml of H2PtCl6 (4g L-1), named as α-Fe2O3, Pt/Pt-Fe2O3-05, Pt/Pt-Fe2O3-1, and Pt/Pt-Fe2O3-2 NPs. Pt/Fe2O3 NPs were prepared as a contrast using as-prepared α-Fe2O3 NPs and H2PtClList of Experimental Equipment and Materials:
Equipment includes X-ray diffraction (XRD), scanning electron microscope (SEM), transmission electron microscope (TEM), high-resolution TEM (HRTEM), X-ray photoelectron spectroscopy (XPS), UV-visible diffuse-reflectance spectrometer (UV-vis DRS), photoelectrochemical cell (PEC) setup with three-electrode system, and gas chromatography for O2 evolution measurement. Materials include H2PtCl6, ethanol, CoOx nanoparticles as cocatalysts, and other chemicals for synthesis.
4:Experimental Procedures and Operational Workflow:
Solvothermal synthesis was performed at high temperature and pressure. Characterization involved XRD for phase identification, SEM/TEM/HRTEM for morphology and structure, XPS for chemical states, UV-vis DRS for optical properties, photocurrent and open circuit potential measurements for carrier separation, and photocatalytic O2 evolution tests under visible light irradiation with CoOx cocatalysts.
5:Data Analysis Methods:
XRD patterns were indexed to standard JCPDS cards. XPS spectra were analyzed for binding energy shifts. UV-vis DRS data were used with Tauc plots to determine band gaps. Photocurrent and Mott-Schottky plots were analyzed to calculate donor densities and Debye lengths. O2 evolution rates were measured and quantum yields calculated.
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X-ray diffraction
Phase identification of samples
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scanning electron microscope
Morphology analysis
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transmission electron microscope
Structure and morphology analysis
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high-resolution TEM
High-resolution imaging for lattice spacing
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X-ray photoelectron spectroscopy
Chemical state analysis
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UV-visible diffuse-reflectance spectrometer
Optical property measurement
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photoelectrochemical cell
Photocurrent and potential measurements
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gas chromatography
O2 evolution measurement
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Xe lamp
300 W
Light source for irradiation
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