Analytical Chemistry · 2024 · 16 citations · 50 references
Natural SciencesMaterials EngineeringMaterials ScienceNanomaterialsNanotechnologyPhotonicsNanomaterial CharacterizationOptical SpectroscopyPlasmonic NanomaterialsPlasmonicsPolarization-based ImagingRaman SpectroscopyIntensity FluctuationsPolarizationRaman ImagingRaman SpectraSuper-resolution ImagingSurface-enhanced Raman ScatteringSurface-enhanced Raman Spectroscopy
Strongly confined electric fields resulting from nanogaps within nanoparticle aggregates give rise to significant enhancement of surface-enhanced Raman scattering (SERS). Nanometer differences in gap sizes lead to drastically different confined field strengths; so much attention has been focused on the development and understanding of nanostructures with controlled gap sizes. In this work, we report a novel petal gap-enhanced Raman tag (GERT) consisting of a bipyramid core and a nitrothiophenol (NTP) spacer to support the growth of hundreds of small petals and compare its SERS emission and localization to a traditional bipyramid aggregate. To do this, we use super resolution spectral SERS imaging that simultaneously captures the SERS images and spectra while varying the incident laser polarization. Intensity fluctuations inherent of SERS enabled super resolution algorithms to be applied, which revealed subdiffraction limited differences in the localization with respect to polarization direction for both particles. Interestingly, however, only the traditional bipyramid aggregates experienced a strong polarization dependence in their SERS intensity and in the plasmon-induced conversion of NTP to dimercaptoazobenzene (DMAB), which was localized with nanometer precision to regions of intense electromagnetic fields. The lack of polarization dependence (validated through electromagnetic simulations) and surface reactions from the bipyramid-GERTs suggests that the emissions arising from the bipyramid-GERTs are less influenced by confined fields.
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Natural Sciences, Chemistry, Physics +17
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