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Near IR Scanning Angle Total Internal Reflection Raman Spectroscopy at Smooth Gold Films

机译:光滑金膜的近红外扫描角全内反射拉曼光谱

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Total internal reflection (TIR) Raman and reflectivity spectra were collected for nonresonant analytes as a function of incident angle at sapphire or sapphire/smooth 50 nm gold interfaces using 785 nm excitation. For both interfaces, the Raman signal as a function of incident angle is well-modeled by the calculated interfacial mean square electric field (MSEF) relative to the incident field times the thickness of the layer being probed in the Raman measurement (D_(RS)). The Raman scatter was reproducibly enhanced at the interface containing a gold film relative to the sapphire interface by a factor of 4.3-4.6 for aqueous pyridine or 2.2-3.7 for neat nitrobenzene, depending on the analyzed vibrational mode. The mechanism for the increased Raman signal is the enhanced MSEF at incident angles where propagating surface plasmons are excited in the metal film. The background from the TIR prism was reduced by 89-95percent with the addition of the gold film, and the percent relative uncertainty in peak area was reduced from 15 to 1.7percent for the 1347 cm~(-1) mode of nitrobenzene. Single monolayers of benzenethiol (S/N velence 6.8) and 4-mercaptopyridine (S/N velence 16.5) on gold films were measured by TIR Raman spectroscopy with 785 nm excitation (210 mW) without resonant enhancement in 1 min.
机译:使用785 nm激发,收集非共振分析物的全内反射(TIR)拉曼光谱和反射率光谱,作为蓝宝石或蓝宝石/光滑50 nm金界面处入射角的函数。对于两个接口,通过相对于入射场的计算的界面均方电场(MSEF)相对于入射场乘以在拉曼测量中被探测层的厚度(D_(RS) )。拉曼散射在包含金膜的界面上相对于蓝宝石界面可再现地增强,对于吡啶水溶液而言为4.3-4.6,对于纯硝基苯而言为2.2-3.7,这取决于所分析的振动模式。增加拉曼信号的机制是在入射角处金属表面中传播的表面等离子体激元受到激发的情况下MSEF增强。通过添加金膜,TIR棱镜的背景降低了89-95%,对于1347 cm〜(-1)硝基苯模式,峰面积的相对不确定度百分比从15%降低到1.7%。通过TIR拉曼光谱法在785 nm激发(210 mW)下在1分钟内没有共振增强的情况下测量了金膜上苯硫醇(S / N velence 6.8)和4-巯基吡啶(S / N velence 16.5)的单层膜。

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