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Preparation and Characterization of Silver Nanoparticles Embedded in Silica Sol Particles

机译:包埋在二氧化硅溶胶颗粒中的银纳米颗粒的制备与表征

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Silver nanoparticles coated with silica can be obtained by the reduction of AgNO3 with hydrazine in the presence of NaOH-stabilized, active silicic acid (polysilicic acid). The size of the silver nanoparticles and the silica shell thicknesses were affected by varying the hydrazine content, the active silicic acid content and the experimental method (e.g. hydrothermal method). Typically, silver nanoparticles sized around 40 nm were aggregated, connected by silica. The presence of peaks centered around 400 nm in UV-vis spectra corresponds to the surface plasmon resonance of silver nanoparticles. The size of the aggregated silver nanoparticles increased with increasing hydrazine concentration. Under hydrothermal conditions at 150 °C the formation of individual silica particles was observed and the sizes of the silver nanoparticles were reduced. The hydrothermal treatment of silver nanoparticles at 180 °C gives a well-defined Ag@SiO2 core-shell in aggregated silica sol particles. The absorption band observed at around 412 nm were red-shifted with respect to the uncoated silver nanoparticles (λmax = 399 nm) due to the larger refractive index of silica compared to that of water. The formation of silver nanoparticles coated with silica is confirmed by UV-visible absorption spectra, transmission electron microscopy (TEM) and energy-dispersive spectroscopy (EDS) data.
机译:涂有二氧化硅的银纳米颗粒可通过在NaOH稳定的活性硅酸(聚硅酸)存在下用肼还原AgNO3来获得。通过改变肼含量,活性硅酸含量和实验方法(例如水热法)来影响银纳米颗粒的尺寸和二氧化硅壳的厚度。通常,聚集大小约为40 nm的银纳米颗粒,并通过二氧化硅连接。 UV-vis光谱中以400 nm为中心的峰的存在与银纳米粒子的表面等离振子共振相对应。随着肼浓度的增加,聚集的银纳米颗粒的尺寸增加。在150°C的水热条件下,观察到了单个二氧化硅颗粒的形成,并且银纳米颗粒的尺寸减小了。银纳米颗粒在180°C的水热处理可在聚集的硅溶胶颗粒中得到定义明确的Ag @ SiO2核壳。相对于未涂覆的银纳米颗粒(λmax= 399 nm),在412 nm处观察到的吸收带发生了红移,这是因为二氧化硅的折射率比水的折射率大。紫外可见吸收光谱,透射电子显微镜(TEM)和能量色散光谱(EDS)数据证实了涂有二氧化硅的银纳米颗粒的形成。

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