研究目的
To synthesize nanocrystalline SnxCd1?xS thin films capped with thioglycerol and methanol (TGM) and study the effects of Sn doping concentration on their optical and structural properties.
研究成果
The synthesis of nanocrystalline SnxCd1?xS thin films with TGM capping was successful, showing high optical transmittance and tunable band gaps with Sn doping. The films exhibited quantum size effects, with particle sizes under 20 nm, and structural changes from hexagonal to cubic phases at certain doping levels. These properties make them suitable for applications like solar cells, but the lack of photoconductivity suggests limitations in electronic devices. Future work could explore higher doping concentrations and alternative capping agents.
研究不足
The study is limited to Sn doping concentrations up to 5% and specific capping agents; photoconductivity was negligible, indicating potential issues for electronic applications. The method may not be scalable for industrial production, and further optimization of doping levels and capping agents could enhance properties.
1:Experimental Design and Method Selection:
The study used a chemical bath deposition method to prepare nanocrystalline SnxCd1?xS thin films on glass substrates, with thioglycerol and methanol as capping agents. The method involved controlling parameters such as pH, temperature, and stirring to achieve desired film properties.
2:Sample Selection and Data Sources:
Glass slides (24 mm x 75 mm) were used as substrates, cleaned with nitric acid and distilled water. Solutions were prepared using hydrated stannous chloride, anhydrous cadmium acetate, thiourea, triethanolamine (TEA), and capping agents in triple distilled water. Sn doping concentrations varied from 0% to 5%.
3:5%. List of Experimental Equipment and Materials:
3. List of Experimental Equipment and Materials: Equipment included a water bath, homogenizer, UV-Vis spectrophotometer (Chemito SPECTRASCAN-UV-2600), photoluminescence spectrometer with UV source and photomultiplier tube, X-ray diffractometer (Bruker AXS D8 Advance), scanning electron microscope (EVO 18), and transmission electron microscope (Joel/JEM 2100). Materials included SnCl2·2H2O, (CH3COO)Cd·2H2O, CS(NH2)2, TEA, thioglycerol, methanol, liquid ammonia, and glass substrates.
4:0). Materials included SnCl2·2H2O, (CH3COO)Cd·2H2O, CS(NH2)2, TEA, thioglycerol, methanol, liquid ammonia, and glass substrates. Experimental Procedures and Operational Workflow:
4. Experimental Procedures and Operational Workflow: Substrates were degreased, cleaned, and dried. Solutions were prepared, pH adjusted to 11 with ammonia, capping agents added, and the mixture stirred and heated to 70°C in a water bath. Films were deposited for 1 hour, washed, and dried. Characterization involved UV-Vis, PL, XRD, SEM, and TEM measurements.
5:Data Analysis Methods:
Optical band gap was determined using Tauc plot from transmission data. Particle size and strain were calculated from XRD using Debye-Scherrer and related equations. SEM and TEM images were analyzed for morphology and size.
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Transmission Electron Microscope
JEM 2100
Joel
Grain size and crystallinity study
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UV-Vis Spectrophotometer
SPECTRASCAN-UV-2600
Chemito
Optical transmittance measurement in the wavelength range 200-1100 nm
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X-ray Diffractometer
D8 Advance
Bruker AXS
Phase confirmation and structural analysis using CuKα radiation
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Scanning Electron Microscope
EVO 18
Surface morphology investigation
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Photomultiplier Tube
RCA 931A
RCA
Detection of emitted light in photoluminescence studies
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Power Supply
EHT-11
Scientific Instruments
Operating the photomultiplier tube
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Digital Pico-ammeter
DPM-121
Scientific Instruments
Recording integrated light output as current
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