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      Measuring optical activity in the far-field from a racemic nanomaterial: diffraction spectroscopy from plasmonic nanogratings

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          Abstract

          Photograph of the experimental setup with light diffracting from a racemic nanoarray. The diffracted spectra change depending on the direction of circularly polarized illumination.

          Abstract

          Recent progress in nanofabrication has redrawn the boundaries of the applicability of chiroptical (chiral optical) effects. Chirality, often expressed as a twist in biomolecules, is crucial for pharmaceuticals, where it can result in extremely different chemical properties. Because chiroptical effects are typically very weak in molecules, plasmonic nanomaterials are often proposed as a promising platform to significantly enhance these effects. Unfortunately, the ideal plasmonic nanomaterial has conflicting requirements: its chirality should enhance that of the chiral molecules and yet it should have no chiroptical response on its own. Here, we propose a unique reconciliation to satisfy the requirements: a racemic plasmonic nanomaterial, consisting of equal amounts of opposite chiral unit cells. We show how diffraction spectroscopy can be used to unveil the presence of chirality in such racemic nanogratings in the far-field. Our experiments are supported by numerical simulations and yield a circular intensity difference of up to 15%. The physical origin is demonstrated by full wave simulations in combination with a Green's function – group-theory-based analysis. Contributions from Circular Dichroism in the Angular Distribution of Photoelectrons (CDAD) and pseudo/extrinsic chirality are ruled out. Our findings enable the far-field measurement and tuning of racemic nanomaterials, which is crucial for hyper-sensitive chiral molecular characterization.

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          Most cited references44

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          Optical Constants of the Noble Metals

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            DNA Origami: Scaffolds for Creating Higher Order Structures.

            DNA has become one of the most extensively used molecular building blocks for engineering self-assembling materials. DNA origami is a technique that uses hundreds of short DNA oligonucleotides, called staple strands, to fold a long single-stranded DNA, which is called a scaffold strand, into various designer nanoscale architectures. DNA origami has dramatically improved the complexity and scalability of DNA nanostructures. Due to its high degree of customization and spatial addressability, DNA origami provides a versatile platform with which to engineer nanoscale structures and devices that can sense, compute, and actuate. These capabilities open up opportunities for a broad range of applications in chemistry, biology, physics, material science, and computer science that have often required programmed spatial control of molecules and atoms in three-dimensional (3D) space. This review provides a comprehensive survey of recent developments in DNA origami structure, design, assembly, and directed self-assembly, as well as its broad applications.
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              Chirality and chiroptical effects in plasmonic nanostructures: fundamentals, recent progress, and outlook.

              Strong chiroptical effects recently reported result from the interaction of light with chiral plasmonic nanostructures. Such nanostructures can be used to enhance the chiroptical response of chiral molecules and could also significantly increase the enantiomeric excess of direct asymmetric synthesis and catalysis. Moreover, in optical metamaterials, chirality leads to negative refractive index and all the promising applications thereof. In this Progress Report, we highlight four different strategies which have been used to achieve giant chiroptical effects in chiral nanostructures. These strategies consecutively highlight the importance of chirality in the nanostructures (for linear and nonlinear chiroptical effects), in the experimental setup and in the light itself. Because, in the future, manipulating chirality will play an important role, we present two examples of chiral switches. Whereas in the first one, switching the chirality of incoming light causes a reversal of the handedness in the nanostructures, in the second one, switching the handedness of the nanostructures causes a reversal in the chirality of outgoing light. Copyright © 2013 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.
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                Author and article information

                Journal
                NHAOAW
                Nanoscale Horizons
                Nanoscale Horiz.
                Royal Society of Chemistry (RSC)
                2055-6756
                2055-6764
                August 19 2019
                2019
                : 4
                : 5
                : 1056-1062
                Affiliations
                [1 ]Centre for Photonics and Photonic Materials and Centre for Nanoscience and Nanotechnology, University of Bath
                [2 ]Bath
                [3 ]UK
                [4 ]Department of Electrical Engineering (ESAT-TELEMIC), KU Leuven
                [5 ]Heverlee
                [6 ]Belgium
                [7 ]Electrical Engineering Division, Department of Engineering, University of Cambridge
                [8 ]Cambridge
                [9 ]Centre for Nanoscience and Nanotechnology, University of Bath
                Article
                10.1039/C9NH00067D
                b0c0548b-71dd-4eea-a9c5-464cefdcc5c9
                © 2019

                http://creativecommons.org/licenses/by/3.0/

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