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Register a new userDisordered Cellulose-based Nanostructures for Enhanced Light-scattering
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Cellulose is the most abundant bio-polymer on earth. Cellulose fibres, such as the one extracted form cotton or woodpulp, have been used by humankind for hundreds of years to make textiles and paper. Here we show how, by engineering light matter-interaction, we can optimise light scattering using exclusively cellulose nanocrystals. The produced material is sustainable, biocompatible and, when compared to ordinary microfibre-based paper, it shows enhanced scattering strength (x4) yielding a transport mean free path as low as 3.5 um in the visible light range. The experimental results are in a good agreement with the theoretical predictions obtained with a diffusive model for light propagation.
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A key concept underlying the specific functionalities of metasurfaces, i.e. arrays of subwavelength nanoparticles, is the use of constituent components to shape the wavefront of the light, on-demand. Metasurfaces are versatile and novel platforms to manipulate the scattering, colour, phase or the intensity of the light. Currently, one of the typical approaches for designing a metasurface is to optimize one or two variables, among a vast number of fixed parameters, such as various materials properties and coupling effects, as well as the geometrical parameters. Ideally, it would require a multi-dimensional space optimization through direct numerical simulations. Recently, an alternative approach became quite popular allowing to reduce the computational cost significantly based on a deep-learning-assisted method. In this paper, we utilize a deep-learning approach for obtaining high-quality factor (high-Q) resonances with desired characteristics, such as linewidth, amplitude and spectral position. We exploit such high-Q resonances for the enhanced light-matter interaction in nonlinear optical metasurfaces and optomechanical vibrations, simultaneously. We demonstrate that optimized metasurfaces lead up to 400+ folds enhancement of the third harmonic generation (THG); at the same time, they also contribute to 100+ folds enhancement in optomechanical vibrations. This approach can be further used to realize structures with unconventional scattering responses.
The optics of correlated disordered media is a fascinating research topic emerging at the interface between the physics of waves in complex media and nanophotonics. Inspired by photonic structures in nature and enabled by advances in nanofabrication processes, recent investigations have unveiled how the design of structural correlations down to the subwavelength scale could be exploited to control the scattering, transport and localization of light in matter. From optical transparency to superdiffusive light transport to photonic gaps, the optics of correlated disordered media challenges our physical intuition and offers new perspectives for applications. This article reviews the theoretical foundations, state-of-the-art experimental techniques and major achievements in the study of light interaction with correlated disorder, covering a wide range of systems -- from short-range correlated photonic liquids, to Levy glasses containing fractal heterogeneities, to hyperuniform disordered photonic materials. The mechanisms underlying light scattering and transport phenomena are elucidated on the basis of rigorous theoretical arguments. We overview the exciting ongoing research on mesoscopic phenomena, such as transport phase transitions and speckle statistics, and the current development of disorder engineering for applications such as light-energy management and visual appearance design. Special efforts are finally made to identify the main theoretical and experimental challenges to address in the near future.
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.
Chiral fields with large optical chirality are very important in chiral molecules analysis, sensing and other measurements. Plasmonic nanostructures have been proposed to realize such super chiral fields for enhancing weak chiral signals. However, most of them cannot provide uniform chiral near-fields close to the structures, which makes these nanostructures not so efficient for applications. Plasmonic helical nanostructures and blocked squares have been proved to provide uniform chiral near-fields, but structure fabrication is a challenge. In this paper, we show that very simple plasmonic dimer structures can provide uniform chiral fields in the gaps with large enhancement of both near electric fields and chiral fields under linearly polarized light illumination with polarization off the dimer axis at dipole resonance. An analytical dipole model is utilized to explain this behavior theoretically. 30 times of volume averaged chiral field enhancement is gotten in the whole gap. Chiral fields with opposite handedness can be obtained simply by changing the polarization to the other side of the dimer axis. It is especially useful in Raman optical activity measurement and chiral sensing of small quantity of chiral molecule.
We theoretically demonstrate direction-dependent polarization conversion efficiency, yielding unidirectional light transmission, through a two-layer nanostructure by using the angular spectrum representation of optical near-fields. The theory provides results that are consistent with electromagnetic numerical simulations. This study reveals that optical near-field interactions among nanostructured matter can provide unique optical properties, such as the unidirectionality observed here, and offers fundamental guiding principles for understanding and engineering nanostructures for realizing novel functionalities.
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