AgFON结构中的绿色等离子体模式:增强SERS灵敏度的途径

Luis Alfonso Guerra Hernández , Luis Fernando Tapia Payares , Jorge-Enrique Rueda-Parada , Andrés Alejandro Reynoso , Jagger Rivera Julio , Alejandro Fainstein
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引用次数: 0

摘要

在这项工作中,基于聚苯乙烯纳米球有序阵列上沉积的金属薄膜的杂化等离子体纳米结构被设计和表征,目的是推动操作到更短的波长,并优化通过表面增强拉曼光谱(SERS)的超灵敏分子检测。一个关键的发现是在直径为700到800 nm的AgFON系统中发现了高能绿色等离子体模式,这是一种以前未被报道过的共振,它扩展了共振激发范围,提高了SERS灵敏度。此外,我们证明了通过精确调制纳米结构的几何形状来调节等离子体共振的能力,在金和银薄膜系统中都是如此。在数值模拟的支持下,实验结果证实了这些平台作为分子检测应用的高效光学传感器的潜力。以巯基苯甲酸(4-MBA)为探针分子对SERS效率进行了评价,证明了纳米结构在放大拉曼信号方面的有效性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Green plasmonic mode in AgFON structures: A pathway to enhanced SERS sensitivity

Green plasmonic mode in AgFON structures: A pathway to enhanced SERS sensitivity
In this work, hybrid plasmonic nanostructures based on metal films deposited on ordered arrays of polystyrene nanospheres were designed and characterized, with the aim of pushing the operation to shorter wavelengths and optimizing the ultrasensitive molecular detection through Surface-Enhanced Raman Spectroscopy (SERS). A key finding was the identification of a high-energy green plasmonic mode in AgFON systems with diameters ranging from 700 to 800 nm, a resonance previously unreported in the literature, which extends the resonant excitation range and enhances SERS sensitivity. Additionally, we demonstrated the ability to tune the plasmonic resonances by precisely modulating the geometry of the nanostructures, in both gold and silver film systems. Experimental results, supported by numerical simulations, confirm the potential of these platforms as highly efficient optical sensors for molecular detection applications. The SERS efficiency was evaluated using mercaptobenzoic acid (4-MBA) as a probe molecule, demonstrating the effectiveness of the nanostructures in amplifying Raman signals.
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