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Register a new userRaman scattering of plane-wave and twisted light off chiral molecular liquids
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We present an experimental study of the quasi-elastic Raman scattering (QES) of plane-wave and twisted light by liquid crystals. Depending on their temperature, these crystals can exhibit isotropic, nematic and chiral nematic phases. The question is addressed of how the phase of a crystal and the state of incident light can affect the quasi-elastic energy spectra of the scattered radiation, whose shape is usually described by the combination of Lorentzian and Gaussian components. Special attention is paid to the textit{chiral phase}, for which the Raman QES spectrum is dominated by a Lorentzian with reduced linewidth, pointing to diminished disorder and configurational entropy. Moreover, this phase is also known for a regime of iridescence (selective backscattering) which arises when the wavelength of incident light becomes comparable with the chiral pitch length. Detailed measurements, performed in this textit{resonant} regime and by employing twisted light, carrying various projections of the orbital angular momentum (OAM), have indicated a low-energy scattering surplus depending on OAM. We argue that this observation might indicate a transfer of angular momentum between light and the liquid crystal.
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We propose and theoretically analyze a new vibrational spectroscopy, termed electron- and light-induced stimulated Raman (ELISR) scattering, that combines the high spatial resolution of electron microscopy with the molecular sensitivity of surface-enhanced Raman spectroscopy. With ELISR, electron-beam excitation of plasmonic nanoparticles is utilized as a spectrally-broadband but spatially-confined Stokes beam in the presence of a diffraction-limited pump laser. To characterize this technique, we develop a numerical model and conduct full-field electromagnetic simulations to investigate two distinct nanoparticle geometries, nanorods and nanospheres, coated with a Raman-active material. Our results show the significant ($10^6$-$10^7$) stimulated Raman enhancement that is achieved with dual electron and optical excitation of these nanoparticle geometries. Importantly, the spatial resolution of this vibrational spectroscopy for electron microscopy is solely determined by the nanoparticle geometry and the plasmon mode volume. Our results highlight the promise of ELISR for simultaneous high-resolution electron microscopy with sub-diffraction-limited Raman spectroscopy, complementing advances in superresolution microscopy, correlated light and electron microscopy, and vibrational electron energy loss spectroscopy.
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