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Coating time effect on surface structures of silica-encapsulated gold nanoparticles

机译:涂覆时间对二氧化硅包裹的金纳米颗粒表面结构的影响

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This paper reports the silica density, surface structures and optical properties of gold nanoparticles coated with different thickness of silica shells. The gold nanoparticles encapsulated with amorphous silica shells were prepared in a slight modification of Stǒber method. The silica-shell thickness could be varied from 20 to 50 nm by controlling the experimental conditions, such as reaction time. Transmission Electron Microscopy (TEM) and UV-Visible absorption spectroscopy were employed to characterize the size, shell density, surface structures and the optical properties of these silica-coated gold nanoparticles. The TEM images demonstrated that the density of the silica shell were depended on the reaction time, and the surface morphology was changed from porous structures in the initial coating to the final continuous and smooth silica surface. With the increasing of the reaction time, the silica-coated gold nanoparticles became more and more round and monodispersed. UV-Vis spectra showed that surface plasmon absorption peak had a red-shifted of 3~12 nm on increasing the thickness of silica shell from 20 to 50 nm. A possible mechanism of silica formation on gold nanoparticles was proposed on the basis of silica shell density and the shift of absorption peak of coated gold nanoparticles.
机译:本文报道了涂覆有不同厚度的二氧化硅壳的金纳米颗粒的二氧化硅密度,表面结构和光学性质。用Stǒber方法稍加修改即可制备包裹有无定形二氧化硅壳的金纳米颗粒。通过控制实验条件,例如反应时间,可以使硅壳厚度在20至50 nm之间变化。透射电子显微镜(TEM)和紫外可见吸收光谱用于表征这些二氧化硅涂层的金纳米颗粒的尺寸,壳密度,表面结构和光学性质。 TEM图像表明,二氧化硅壳的密度取决于反应时间,并且表面形态从初始涂层中的多孔结构改变为最终连续且光滑的二氧化硅表面。随着反应时间的增加,二氧化硅包覆的金纳米颗粒变得越来越圆和单分散。 UV-Vis光谱表明,随着二氧化硅壳厚度从20nm增加到50nm,表面等离子体吸收峰出现3〜12nm的红移。根据硅壳密度和包覆金纳米颗粒的吸收峰位移,提出了在金纳米颗粒上形成二氧化硅的可能机理。

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