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Influence of different synthesis approach on doping behavior of silver nanoparticles onto the iron oxide–silica coreshell surfaces

机译:不同合成方法对氧化铁-二氧化硅核壳表面银纳米颗粒掺杂行为的影响

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摘要

Silver (Ag) nanoparticles with the crystallite size ranging from 13–24 nm were successfully doped onto the surface of iron oxide–silica coreshell particles. In the process, iron oxide particles having a size distribution within 8–19 nm were prepared by using a reverse co-precipitation method followed by the formation of iron oxide-core with silica shell (with 50–150 nm diameter of silica spheres) by using a modified Stöber method. The reduction of Ag ions was done at room temperature in a solution containing polyvinylpyrrolidone and ethanol by using mechanical and ultrasonic mixing. Four different synthesis approaches were used in doping of Ag nanoparticles. The phase, morphology, optical and magnetic properties of the synthesized powders were characterized by using X-ray diffraction, scanning electron microscope (SEM), transmission electron microscope, UV–visible spectrometer (UV–Vis) and vibrating sample magnetometer. Spherical morphology of the Ag nanoparticles was found to deposit on the iron oxide-silica surfaces. The particle size distribution is depending on the synthesis approach used. The UV–Vis absorption peak at 404–410 nm of wavelength confirmed the existence of the Ag nanoparticles.
机译:微晶尺寸范围为13–24 nm的银(Ag)纳米颗粒已成功掺杂到氧化铁-二氧化硅核壳颗粒的表面。在此过程中,采用反向共沉淀法制备尺寸分布在8–19 nm之间的氧化铁颗粒,然后通过以下方法形成带有二氧化硅壳(氧化硅球直径为50–150 nm)的氧化铁核:使用改良的Stöber方法。 Ag离子的还原是在室温下在含有聚乙烯吡咯烷酮和乙醇的溶液中通过机械和超声混合完成的。四种不同的合成方法用于掺杂Ag纳米粒子。利用X射线衍射,扫描电子显微镜(SEM),透射电子显微镜,紫外可见光谱仪(UV-Vis)和振动样品磁力计对合成粉末的相,形貌,光学和磁性进行了表征。发现Ag纳米颗粒的球形形态沉积在氧化铁-二氧化硅表面上。粒度分布取决于所使用的合成方法。在404-410 nm波长处的UV-Vis吸收峰证实了Ag纳米颗粒的存在。

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