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Optical and structural properties of silver nanoparticles in glass matrix formed by thermal annealing of field assisted film dissolution

机译:场辅助膜溶解的热退火形成的玻璃基质中银纳米颗粒的光学和结构性质

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摘要

A two-step procedure for the formation of silver nanoparticles embedded in a glass matrix is studied. The procedure consists of: (i) the inclusion of silver ions in the glass matrix by electric field assisted dissolution of Ag film deposited on the glass and (ii) the aggregation of silver by thermal annealing. The optical properties of the sample, dominated by the surface plasmon resonance of metal nanoparticles in the visible spectral range, are studied by optical spectroscopy. The structural characterization is carried out by grazing-incidence small-angle X-ray scattering measurements performed at the Synchrotron Elettra (Italy) and silver depth profiles are determined using Rutherford backscattering. The results suggest that the depth profile of Ag might be tailored by modification of the parameters of metal film dissolution (electric field and temperature). Variation of thermal annealing parameters (temperature and time) allows control of the nanoparticles size. Thus, the surface plasmon absorption intensity and line shape are changed, enabling tuning of the optical properties of the sample.
机译:研究了嵌入在玻璃基质中的银纳米颗粒形成的两步过程。该程序包括:(i)通过电场辅助溶解沉积在玻璃上的Ag膜,通过电场辅助将银离子包含在玻璃基质中,以及(ii)通过热退火使银聚集。通过光谱学研究了样品的光学性质,该光谱性质由金属纳米颗粒在可见光谱范围内的表面等离子体共振引起。通过在同步加速器Elettra(意大利)进行的掠入射小角X射线散射测量进行结构表征,并使用卢瑟福反向散射确定银的深度分布。结果表明,可以通过修改金属膜溶解参数(电场和温度)来调整Ag的深度分布。热退火参数(温度和时间)的变化允许控制纳米颗粒的尺寸。因此,改变了表面等离子体激元吸收强度和线形,从而能够调节样品的光学性质。

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