Utilization of frequency locking for tracking optical resonances of microresonators is an emergent technique, which has relevance in label-free biosensing, owing to its extremely high sensitivity in detecting adsorption on a microcavity’s surface. In this study, we demonstrate the capabilities of a technique known as FLOWER (Frequency Locked Optical Whispering Evanescent Resonator) in a real-life problem: the detection of human chorionic gonadotropin (hCG) in urine samples. hCG, besides being a hormone secreted during pregnancy, is a performance enhancing agent prone to be abused by athletes, and is routinely investigated in doping laboratories. The gold standard in hCG detection is mass spectrometry. As the lowest limit of detection by mass spectrometry is close to the cut-off value for a positive result, various other measurement techniques such as optical interferometry, photoluminescence, or electrochemical sensors have been used to try to enhance measurement sensitivity. These methods, however, do not show a significant improvement in the limit of detection over mass spectrometry and they mostly have a narrow detection range. In addition, measurement selectivity is another issue. Here, we use microtoroidal optical resonators functionalized with antibodies against hCG, and track their resonances using frequency locking upon analyte infusion. Urine samples from pregnant women were measured using our setup. Our results demonstrate that FLOWER can detect the presence of hCG in a large concentration range from 1 fM to 10 nM.
KEYWORDS: Near field scanning optical microscopy, 3D metrology, Plasmonics, Luminescence, Nanostructures, Optical microscopy, Nitrogen, Modulation, Absorbance, Digital recording
We present a dynamic approach to scanning near field optical microscopy that extends the measurement technique to the third dimension, by strobing the illumination in sync with the cantilever oscillation. Nitrogen vacancy (NV) centers in nanodiamonds placed on cantilever tips are used as stable emitters for emission enhancement. Local field enhancement and modulation of optical density states are mapped in three dimensions based on fluorescence intensity and spectrum changes as the tip is scanned over plasmonic nanostructures. The excitation of NV centers is done using a total internal reflection setup. Using a digital phase locked loop to pulse the excitation in various tip sample separations, 2D slices of fluorescence enhancement can be recorded. Alternatively, a conventional SNOM tip can be used to selectively couple wideband excitation to the collection path, with subdiffraction resolution of 60 nm in x and y and 10 nm in z directions. The approach solves the problem of tip-sample separation stabilization over extended periods of measurement time, required to collect data resolved in emission wavelength and three spatial dimensions. The method can provide a unique way of accessing the three dimensional field and mode profiles of nanophotonics structures.
Infrared absorption spectroscopy has greatly benefited from the electromagnetic field enhancement offered by plasmonic surfaces. However, because of the localized nature of plasmonic fields, such field enhancements are limited to nm-scale volumes. Here, we demonstrate that a relatively small, but spatially-uniform field enhancement can yield a superior infrared detection performance compared to the plasmonic field enhancement exhibited by optimized infrared nanoantennas. A specifically designed CaF2/Al thin film surface is shown to enable observation of stronger vibrational signals from the probe material, with wider bandwidth and a deeper spatial extent of the field enhancement as compared to optimized plasmonic surfaces. It is demonstrated that the surface structure presented here can enable chemically specific and label-free detection of organic monolayers using surface enhanced infrared spectroscopy. Also, a low cost hand held infrared absorption measurement setup is demonstrated using a miniature bolometric sensor and a mobile phone. A specifically designed grating in combination with an IR light source yields an IR spectrometer covering 7-12 um range, with about 100 cm-1 resolution. Combining the enhancing substrates with the spectroscopy setup, low cost, high sensitivity mobile infrared sensing is enabled. The results have implications in homeland security and environmental monitoring as well as chemical analysis.
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