Backscatter WERS for Trace Chemical Analyte Detection Using a Handheld Spectrometer

被引:4
|
作者
Tyndall, N. F. [1 ]
Kozak, D. A. [1 ]
Pruessner, M. W. [1 ]
McGill, R. A. [1 ]
Roberts, C. A. [1 ]
Stievater, T. H. [1 ]
Miller, B. L. [2 ]
Luta, E. [2 ]
Yates, M. Z. [2 ]
Emmons, E. D. [3 ]
Wilcox, P. G. [3 ]
Guicheteau, J. A. [3 ]
机构
[1] US Naval Res Lab, Washington, DC 20375 USA
[2] Univ Rochester, Med Sch, Rochester, NY 14642 USA
[3] US Army CCDC Chem Biol Ctr, Aberdeen Proving Ground, MD 21010 USA
关键词
WERS; Nanophotonics; Raman; Waveguide; Chemical Sensing; ENHANCED RAMAN-SPECTROSCOPY; SPECTRA;
D O I
10.1117/12.2559641
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
Waveguide-enhanced Raman spectroscopy (WERS) enables the detection and identification of trace concentrations of vapor-phase analytes using a functionalized chip-scale photonic circuit. Here, we show that WERS signal can be collected from part-per-billion levels of targeted analytes in a backscatter geometry, which, compared to forward-scatter, simplifies component integration and is more tolerant of waveguide loss and modal interference. In addition, we discuss our progress towards a compact Raman sensing system that incorporates a handheld spectrometer and chip-scale optical filters. We demonstrate that a handheld, thermo-electrically cooled spectrometer can be used for backscatter WERS with a comparable signal-to-noise to that of a liquid-nitrogen cooled benchtop spectrometer. Finally, we describe efforts to integrate the dichroic Raman filter on-chip using arrays of unbalanced Mach-Zehnder interferometers. Measurements show filter performance sufficient for integration with WERS: Transmission of >80% of the laser in the cross port and Stokes signal in the through port; and extinction of the laser by >20 dB in the though port and of Stokes signal by >8 dB in the cross port.
引用
收藏
页数:6
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