The role of focused laser plasmonics in shaping SERS spectra of molecules on nanostructured surfaces

IF 4.6 3区 材料科学 Q2 CHEMISTRY, MULTIDISCIPLINARY
Fran Nekvapil and Cosmin Farcău
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Abstract

Over fifty years have passed since the groundbreaking discovery of Surface Enhanced Raman Scattering (SERS), yet many aspects of this phenomenon remain elusive. In this study, we unveil novel observations concerning the spatial variation of SERS signal profiles through vertical (Z axis) scans, performed by varying the distance between the laser focus and a solid, planar, nanostructured SERS substrate. The signal strength profile manifests a Lorentzian shape during axial scans along the Z direction, consistently peaking above the actual sample surface. More intriguingly, the intensity ratio of various spectral regions—including SERS bands and background—exhibits significant non-constancy along the Z axis. Finite-Difference Time-Domain (FDTD) simulations suggest that these variations can be attributed to specific plasmonic near-field responses induced by the focused/defocused beam at the SERS substrate. This research highlights the critical need to consider that focus imprecision can alter spectral profiles in SERS analyses on solid nanostructured SERS substrates, particularly when devising quantitative assays based on band intensity ratios.

Abstract Image

聚焦激光等离子体在纳米结构表面分子SERS谱中的作用。
自从突破性地发现表面增强拉曼散射(SERS)以来,已经过去了50多年,但这种现象的许多方面仍然难以捉摸。在这项研究中,我们通过垂直(Z轴)扫描,通过改变激光焦点与固体、平面、纳米结构的SERS衬底之间的距离,揭示了关于SERS信号剖面空间变化的新观察结果。在沿Z方向轴向扫描期间,信号强度剖面呈现洛伦兹形状,在实际样品表面上方始终达到峰值。更有趣的是,各个光谱区域(包括SERS波段和背景)的强度比沿Z轴表现出显著的非恒定性。时域有限差分(FDTD)模拟表明,这些变化可归因于特定的等离子体近场响应,这些响应是由聚焦/散焦光束在SERS衬底上引起的。这项研究强调了在固体纳米结构SERS衬底上,聚焦不精确会改变SERS分析中的光谱轮廓,特别是在设计基于波段强度比的定量分析时,需要考虑到这一点。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Nanoscale Advances
Nanoscale Advances Multiple-
CiteScore
8.00
自引率
2.10%
发文量
461
审稿时长
9 weeks
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