研究目的
To study the influence of different capping agents on the structural, morphological, compositional, and photoluminescence properties of SnO2 nanoparticles synthesized by chemical co-precipitation method.
研究成果
SnO2 nanoparticles were successfully prepared by chemical co-precipitation method using different capping agents. XRD and FTIR studies confirmed the tetragonal rutile structure of polycrystalline SnO2 nanoparticles. SEM images showed agglomeration, with EDTA capped samples exhibiting slightly decreased agglomeration. EDAX confirmed the effective composition of the samples. PL studies revealed enhanced luminescence intensity in EDTA capped SnO2 nanoparticles, suggesting potential applications in luminescence-based technologies.
研究不足
The study focuses on the effect of capping agents on SnO2 nanoparticles properties but does not explore the scalability of the synthesis method or the application of these nanoparticles in specific devices.
1:Experimental Design and Method Selection:
SnO2 nanoparticles were synthesized by chemical co-precipitation method using SnCl
2:2H2O as reactant material and different capping agents (EDTA, PVP, PVA). The process involved stirring at 90°C, adjusting pH to 9 with NaOH, washing with de-ionized water, and vacuum drying at 80°C. Sample Selection and Data Sources:
Analytical reagent grade chemicals were used without further purification.
3:List of Experimental Equipment and Materials:
Rigaku D X-ray diffractometer, Fourier transform infrared spectrophotometer (FTIR-4700typeA), Oxford Inca Penta FeTX3 EDAX instrument attached to Carl Zeiss EVO MA 15 scanning electron microscope, PTI (Photon Technology International) Fluorimeter.
4:Experimental Procedures and Operational Workflow:
The synthesis involved dissolving SnCl
5:2H2O in de-ionized water, adding NaOH to adjust pH, stirring, washing, and drying. Data Analysis Methods:
XRD for structural analysis, FTIR for structural confirmation, SEM for morphology, EDAX for compositional analysis, and PL for luminescence properties.
独家科研数据包,助您复现前沿成果,加速创新突破
获取完整内容