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Characterizing the spectral reproducibility of quartz-bound Au nanoparticle substrates for surface-enhanced Raman spectroscopy

机译:表征用于表面增强拉曼光谱的石英结合金纳米粒子基质的光谱可再现性

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Visible extinction and Surface Enhanced Raman Scattering (SERS) spectra using quartz-bound Au nanoparticle substrates are used to identify substrate production-related sources of spectral variability. Hydrosol Au nanoparticle size distributions are known to affect SERS enhancement, but the effect of spatial orientation and nanoparticle physiosorption during substrate preparation on spectral reproducibility and performance are not well understood. Experiments varying quartz slide orientation and Au nanoparticle delivery method show significant concentration-gradient and physiosorption-related aggregation effects in the substrate extinction spectra and SERS spectra of R6G applied to spatially mapped substrate regions. Additionally, applying multiple Au hydrosol treatments to functionalized quartz substrates reveals interesting relationships between Au nanoparticle thickness and substrate extinction and SERS spectra. Of the many factors affecting substrate spectral reproducibility, minimizing concentration gradients and optimizing the rate of Au nanoparticle-quartz physiosorption allow improvements in SERS active substrate spectral reproducibility.
机译:使用与石英结合的金纳米颗粒基质的可见消光和表面增强拉曼散射(SERS)光谱可用于鉴定与基质生产相关的光谱变异性来源。众所周知,溶胶Au纳米颗粒的粒径分布会影响SERS的增强,但是底物制备过程中空间取向和纳米颗粒的物理吸附对光谱再现性和性能的影响尚不十分清楚。改变石英玻片取向和金纳米粒子传递方法的实验显示,在应用于空间映射的底物区域的R6G的底物消光光谱和SERS光谱中,存在明显的浓度梯度和与物理吸附有关的聚集效应。此外,对功能化石英基板进行多次Au溶胶处理后,发现Au纳米粒子厚度与基板消光和SERS光谱之间有趣的关系。在影响底物光谱可再现性的众多因素中,最小化浓度梯度和优化Au纳米粒子-石英的物理吸收速率可改善SERS活性底物光谱可再现性。

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