等离子纳米粒子光学化学台上配体相互作用的偏振和疏散导波表面增强拉曼光谱学

Biosensors Pub Date : 2024-08-23 DOI:10.3390/bios14090409
Xining Chen, Mark P. Andrews
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引用次数: 0

摘要

本研究探讨了偏振蒸发导波表面增强拉曼光谱在确定小分子和配体修饰纳米粒子的结合和取向方面的应用,以及该技术与芯片实验室、表面等离子体极化子和其他类型的拉曼生物传感相关场增强技术的关联性。本文提供了一个简化的导波拉曼光谱教程,介绍了等离子纳米粒子场增强的概念,即在一个简单的等离子纳米粒子板状波导基底上放大原本微弱的TE和TM极化蒸发场,以实现拉曼散射。该波导结构被称为光学化学工作台(OCB),以强调其对制备光学生物传感器所需的各种表面化学物质的适应性。当 OCB 集成到定制的拉曼光谱仪中时,就形成了一个完整的光谱平台。通过在多模玻璃波导基底表面附着多孔的 Au@Ag 核壳纳米颗粒地毯,实现了等离子体对蒸发场的增强。我们通过确定吸附的 4-巯基吡啶和 4-氨基苯甲酸的 SER 光谱对蒸发场的 TE/TM 偏振状态的依赖性来校准 OCB。我们将 OCB 结构与更复杂的光子芯片设备进行了对比,后者同样受益于增强的蒸发场,但没有使用等离子体。我们组装了物质层次,通过跟踪 4MPy 在配位阳离子时 SER 光谱的变化,表明 OCB 可以在 OCB 的纳米级界面上解析来自水中的 Fe2+ 离子的结合。对磁弹子学的简要介绍为一项研究奠定了基础,该研究解决了客体磁铁矿纳米粒子吸附到与 OCB 结合的主电浆 Au@Ag 纳米粒子之间的 4ABA 配体界面问题。在某些情况下,蒸发波 TM 极化被强烈衰减,这很可能是由于惯性电荷载流子的阻尼作用,在质子纳米粒子密集组装的情况下,惯性电荷载流子有利于这种极化状态的光学损耗。OCB 提供了一种为界面(生物)传感提供振动和取向信息的方法,这种方法可以补充蒸发波方法的信息含量,后者依赖于蒸发波区域折射率的扰动。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Polarized and Evanescent Guided Wave Surface-Enhanced Raman Spectroscopy of Ligand Interactions on a Plasmonic Nanoparticle Optical Chemical Bench
This study examined applications of polarized evanescent guided wave surface-enhanced Raman spectroscopy to determine the binding and orientation of small molecules and ligand-modified nanoparticles, and the relevance of this technique to lab-on-a-chip, surface plasmon polariton and other types of field enhancement techniques relevant to Raman biosensing. A simplified tutorial on guided-wave Raman spectroscopy is provided that introduces the notion of plasmonic nanoparticle field enhancements to magnify the otherwise weak TE- and TM-polarized evanescent fields for Raman scattering on a simple plasmonic nanoparticle slab waveguide substrate. The waveguide construct is called an optical chemical bench (OCB) to emphasize its adaptability to different kinds of surface chemistries that can be envisaged to prepare optical biosensors. The OCB forms a complete spectroscopy platform when integrated into a custom-built Raman spectrograph. Plasmonic enhancement of the evanescent field is achieved by attaching porous carpets of Au@Ag core shell nanoparticles to the surface of a multi-mode glass waveguide substrate. We calibrated the OCB by establishing the dependence of SER spectra of adsorbed 4-mercaptopyridine and 4-aminobenzoic acid on the TE/TM polarization state of the evanescent field. We contrasted the OCB construct with more elaborate photonic chip devices that also benefit from enhanced evanescent fields, but without the use of plasmonics. We assemble hierarchies of matter to show that the OCB can resolve the binding of Fe2+ ions from water at the nanoscale interface of the OCB by following the changes in the SER spectra of 4MPy as it coordinates the cation. A brief introduction to magnetoplasmonics sets the stage for a study that resolves the 4ABA ligand interface between guest magnetite nanoparticles adsorbed onto host plasmonic Au@Ag nanoparticles bound to the OCB. In some cases, the evanescent wave TM polarization was strongly attenuated, most likely due to damping by inertial charge carriers that favor optical loss for this polarization state in the presence of dense assemblies of plasmonic nanoparticles. The OCB offers an approach that provides vibrational and orientational information for (bio)sensing at interfaces that may supplement the information content of evanescent wave methods that rely on perturbations in the refractive index in the region of the evanescent wave.
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