1.Department of Electrical Engineering, University at Buffalo, The State University of New York, Buffalo, NY 14260, USA
2.Department of Biomedical Engineering, University at Buffalo, The State University of New York, Buffalo, NY 14260, USA
Peter Q. Liu (pqliu@buffalo.edu)
纸质出版日期:2021,
网络出版日期:2021-01-05,
收稿日期:2020-08-12,
修回日期:2020-11-25,
录用日期:2020-12-01
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High-sensitivity nanophotonic sensors with passive trapping of analyte molecules in hot spots[J]. LSA, 2021,10(1):60-70.
Miao, X. L. et al. High-sensitivity nanophotonic sensors with passive trapping of analyte molecules in hot spots. Light: Science & Applications, 10, 60-70 (2021).
High-sensitivity nanophotonic sensors with passive trapping of analyte molecules in hot spots[J]. LSA, 2021,10(1):60-70. DOI: 10.1038/s41377-020-00449-7.
Miao, X. L. et al. High-sensitivity nanophotonic sensors with passive trapping of analyte molecules in hot spots. Light: Science & Applications, 10, 60-70 (2021). DOI: 10.1038/s41377-020-00449-7.
Nanophotonic resonators can confine light to deep-subwavelength volumes with highly enhanced near-field intensity and therefore are widely used for surface-enhanced infrared absorption spectroscopy in various molecular sensing applications. The enhanced signal is mainly contributed by molecules in photonic hot spots
which are regions of a nanophotonic structure with high-field intensity. Therefore
delivery of the majority of
if not all
analyte molecules to hot spots is crucial for fully utilizing the sensing capability of an optical sensor. However
for most optical sensors
simple and straightforward methods of introducing an aqueous analyte to the device
such as applying droplets or spin-coating
cannot achieve targeted delivery of analyte molecules to hot spots. Instead
analyte molecules are usually distributed across the entire device surface
so the majority of the molecules do not experience enhanced field intensity. Here
we present a nanophotonic sensor design with passive molecule trapping functionality. When an analyte solution droplet is introduced to the sensor surface and gradually evaporates
the device structure can effectively trap most precipitated analyte molecules in its hot spots
significantly enhancing the sensor spectral response and sensitivity performance. Specifically
our sensors produce a reflection change of a few percentage points in response to trace amounts of the amino-acid proline or glucose precipitate with a picogram-level mass
which is significantly less than the mass of a molecular monolayer covering the same measurement area. The demonstrated strategy for designing optical sensor structures may also be applied to sensing nano-particles such as exosomes
viruses
and quantum dots.
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