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Increasing polarization-dependent SERS effects by optimizing the axial symmetry of plasmonic nanostructures

机译:通过优化等离子体纳米结构的轴向对称性来增加偏振相关的SERS效应

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Plasmonic nanoperiodic Ag nanoparticle arrays with hexagonal close-packed structures and different symmetries were synthesized by localized surface plasmon resonance (LSPR) induced chemical growth. When the plasmonic nanostructure was excited by a laser, the neighboring silver nanoparticles generated high local electric field enhancement for surface-enhanced Raman spectroscopy (SERS), which was used to show the relationship between the axisymmetry of the plasmonic nanostructure and the SERS polarization effect. The experimental results indicate that the optimal axisymmetric structure (six-axis symmetric) exhibited the strongest SERS polarization-dependence, whereas the disordered structure with an arbitrary axis exhibited a relatively weak SERS polarization dependence. To clarify the root cause of SERS polarization dependence, the electric field enhancement distribution for the plasmonic nanostructures was numerically simulated based on S-and P-polarization excitation. Most importantly, the fundamental reasons for the polarization dependence of SERS were obtained by the quantitative numerical simulation of the hotspot distribution for the plasmonic nanostructures.
机译:通过局部表面等离振子共振(LSPR)诱导的化学生长合成了具有六角形密堆积结构和不同对称性的等离子纳米周期银纳米颗粒阵列。当等离子体激元纳米结构被激光激发时,相邻的银纳米粒子产生了较高的局部电场增强,以用于表面增强拉曼光谱(SERS),这用于显示等离子体激元纳米结构的轴对称性与SERS极化效应之间的关系。实验结果表明,最佳轴对称结构(六轴对称)表现出最强的SERS偏振依赖性,而无序结构具有任意轴表现出相对较弱的SERS偏振依赖性。为了阐明SERS极化依赖性的根本原因,基于S和P极化激发,对等离子体纳米结构的电场增强分布进行了数值模拟。最重要的是,通过对等离激元纳米结构热点分布的定量数值模拟,获得了SERS极化依赖性的根本原因。

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