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Surface-Enhanced Raman Scattering in Small Noble-Metal Nanoparticles

机译:小贵金属纳米颗粒中的表面增强拉曼散射

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We present a microscopic theory of quantum-size effects in surface-enhanced Raman scattering (SERS) from molecules adsorbed on small metal nanoparticles. In noble-metal nanoparticles, the confining potential has different effect on s-band and d-band electrons. Namely, the spillout of delocalized sp-electrons beyond the classical nanoparticle boundary results in an incomplete embedding of s-electron distribution in the background of localized d-electrons whose density profile follows more closely the classical shape. We demonstrate that a reduction of d-electron screening in the surface layer leads to the enhancement of the surface plasmon local field acting on a molecule located in a close proximity to metal surface. Our numerical calculations of Raman enhancement factor, performed using time-dependent local density approximation, show additional enhancement of the Raman signal which becomes more pronounced for small nanoparticles due to the larger ratio of surface layer to overall nanoparticle size.
机译:我们在吸附在小金属纳米粒子上的分子中,在表面增强的拉曼散射(SERS)中的量子尺寸效应的微观理论。在贵金属纳米粒子中,限制潜力对S波段和D波形电子效果不同。即,超越古典纳米粒子边界的被截止的SP-电子的溢出率导致局部D形电磁背景中的S电子分布的不完全嵌入,其密度曲线更遵循经典形状。我们证明,表面层中的D型电子筛选的减少导致作用在位于金属表面紧密近的分子上的表面等离子体局部场的增强。我们使用时间依赖的局部密度近似进行拉曼增强因子的数值计算,显示了由于表面层与总纳米颗粒尺寸的较大比例而变得更加明显的拉曼信号的额外增强。

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