scholarly journals Enhanced Near-Field Chirality in Periodic Arrays of Si Nanowires for Chiral Sensing

Molecules ◽  
2019 ◽  
Vol 24 (5) ◽  
pp. 853 ◽  
Author(s):  
Emilija Petronijevic ◽  
Concita Sibilia

Nanomaterials can be specially designed to enhance optical chirality and their interaction with chiral molecules can lead to enhanced enantioselectivity. Here we propose periodic arrays of Si nanowires for the generation of enhanced near-field chirality. Such structures confine the incident electromagnetic field into specific resonant modes, which leads to an increase in local optical chirality. We investigate and optimize near-field chirality with respect to the geometric parameters and excitation scheme. Specially, we propose a simple experiment for the enhanced enantioselectivity, and optimize the average chirality depending on the possible position of the chiral molecule. We believe that such a simple achiral nanowire approach can be functionalized to give enhanced chirality in the spectral range of interest and thus lead to better discrimination of enantiomers.

2019 ◽  
Vol 70 (1) ◽  
pp. 275-299 ◽  
Author(s):  
Maximilian J. Urban ◽  
Chenqi Shen ◽  
Xiang-Tian Kong ◽  
Chenggan Zhu ◽  
Alexander O. Govorov ◽  
...  

We present a comprehensive review of recent developments in the field of chiral plasmonics. Significant advances have been made recently in understanding the working principles of chiral plasmonic structures. With advances in micro- and nanofabrication techniques, a variety of chiral plasmonic nanostructures have been experimentally realized; these tailored chiroptical properties vastly outperform those of their molecular counterparts. We focus on chiral plasmonic nanostructures created using bottom-up approaches, which not only allow for rational design and fabrication but most intriguingly in many cases also enable dynamic manipulation and tuning of chiroptical responses. We first discuss plasmon-induced chirality, resulting from the interaction of chiral molecules with plasmonic excitations. Subsequently, we discuss intrinsically chiral colloids, which give rise to optical chirality owing to their chiral shapes. Finally, we discuss plasmonic chirality, achieved by arranging achiral plasmonic particles into handed configurations on static or active templates. Chiral plasmonic nanostructures are very promising candidates for real-life applications owing to their significantly larger optical chirality than natural molecules. In addition, chiral plasmonic nanostructures offer engineerable and dynamic chiroptical responses, which are formidable to achieve in molecular systems. We thus anticipate that the field of chiral plasmonics will attract further widespread attention in applications ranging from enantioselective analysis to chiral sensing, structural determination, and in situ ultrasensitive detection of multiple disease biomarkers, as well as optical monitoring of transmembrane transport and intracellular metabolism.


Research ◽  
2020 ◽  
Vol 2020 ◽  
pp. 1-9 ◽  
Author(s):  
Jiaxin Bao ◽  
Ning Liu ◽  
Hanwei Tian ◽  
Qiang Wang ◽  
Tiejun Cui ◽  
...  

Chiral molecules that do not superimpose on their mirror images are the foundation of all life forms on earth. Chiral molecules exhibit chiroptical responses, i.e., they have different electromagnetic responses to light of different circular polarizations. However, chiroptical responses in natural materials, such as circular dichroism and optical rotation dispersion, are intrinsically small because the size of a chiral molecule is significantly shorter than the wavelength of electromagnetic wave. Conventional technology for enhancing chiroptical signal entails demanding requirements on precise alignment of the chiral molecules to certain nanostructures, which however only leads to a limited performance. Herein, we show a new approach towards enhancement of chiroptical effects through a Fabry–Pérot (FP) cavity formed by two handedness-preserving metamirrors operating in the GHz region. We experimentally show that the FP cavity resonator can enhance the optical activity of the chiral molecule by an order of magnitude. Our approach may pave the way towards state-of-the-art chiral sensing applications.


Nanomaterials ◽  
2020 ◽  
Vol 10 (10) ◽  
pp. 2078
Author(s):  
Saúl A. Rosales ◽  
Francisco González ◽  
Fernando Moreno ◽  
Yael Gutiérrez

Low-loss dielectric nanomaterials are being extensively studied as novel platforms for enhanced light-matter interactions. Dielectric materials are more versatile than metals when nanostructured as they are able to generate simultaneously electric- and magnetic-type resonances. This unique property gives rise to a wide gamut of new phenomena not observed in metal nanostructures such as directional scattering conditions or enhanced optical chirality density. Traditionally studied dielectrics such as Si, Ge or GaP have an operating range constrained to the infrared and/or the visible range. Tuning their resonances up to the UV, where many biological samples of interest exhibit their absorption bands, is not possible due to their increased optical losses via heat generation. Herein, we report a quantitative survey on the UV optical performance of 20 different dielectric nanostructured materials for UV surface light-matter interaction based applications. The near-field intensity and optical chirality density averaged over the surface of the nanoparticles together with the heat generation are studied as figures of merit for this comparative analysis.


The development of laser-based polarimetric detectors for high-performance liquid chromatography (HPLC) (Yeung et al . 1980; Bobbitt & Yeung 1986) with noise levels in the range of 0.1-10 p° has provided a significant advance in the quantitation of chiral molecules. We have designed an instrument based on an 820 nm diode laser which has the advantages of low source flicker noise and compact design (Lloyd et al . 1989). Detection limits were found to be in the range 0.1-2 pg, dependent on the specific rotation of the chiral molecule and the chromatographic peak width (Goodall et al. 1990).


Nanophotonics ◽  
2019 ◽  
Vol 8 (5) ◽  
pp. 941-948 ◽  
Author(s):  
Jungho Mun ◽  
Junsuk Rho

AbstractSurface-enhanced circular dichroism (SECD) of chiral molecules adsorbed on plasmonic nanostructures can substantially enhance chiroptical molecular signals by several orders, which is otherwise very weak to be directly measured. Several mechanisms were proposed to explain this extreme enhancement, but the exact mechanism is still controversial. We investigate strong higher-order multipole contribution to SECD near plasmonic nanostructures using the superposition T-matrix method and discuss how 3-dimensional full-field simulations implementing a homogeneous chiral medium have succeeded in the reconstruction of the extreme enhancement. We also discuss how theoretical studies modeling chiral molecules based on dipole approximation have failed to reconstruct the extreme enhancement and show that SECD enhancement of such chiral dipoles is directly governed by optical chirality enhancement. In addition, strong multipolar transitions in subwavelength chiral plasmonic nanoparticles are discussed based on the T-matrix. This work reviews theoretical frameworks describing chiral molecules, demonstrates significant contribution of a multipolar transition on the extreme SECD enhancement near plasmonic nanostructures, and emphasizes the importance of a multipolar transition in chiral nearfield interaction.


2019 ◽  
Vol 7 (15) ◽  
pp. 1900617 ◽  
Author(s):  
Ming Lun Tseng ◽  
Zhan‐Hong Lin ◽  
Hsin Yu Kuo ◽  
Tzu‐Ting Huang ◽  
Yi‐Teng Huang ◽  
...  
Keyword(s):  

Author(s):  
Robin Le Poidevin

According to classical stereochemistry, the molecules of some substances have doubles, in the sense of incongruent mirror-image counterparts. This is the phenomenon of optical isomerism, first identified 150 years ago by Pasteur. In some cases, the double occurs naturally; in others, it has to be artificially synthesized. These molecules thus share a geometrical feature with such familiar objects as our hands, and, indeed, it is this connection that gives the feature its technical name: chirality (from the Greek for hand, kheir). Instances of chirality in chemistry are numerous, especially in living things: examples of chiral molecules include adrenaline, glucose, and DNA. Optical isomerism is interesting, both historically—it played a crucial role in the emergence of structural chemistry and in the attempt to link chemistry with physics— and, I believe, philosophically. I should like to take this opportunity to revisit the scene of an earlier article of mine (Le Poidevin, 1994) in which I examined the implications optical isomerism has for a philosophical debate concerning the nature of space. In that article I argued that chirality in chemistry reinforces a conclusion that Graham Nerlich (1994), in a brilliant reconstruction of a famous argument of Kant’s, had derived from more visible instances of chirality: that we should be realists about the geometrical properties of space. I did not, however, want to follow Nerlich (and Kant) in drawing a more radical conclusion: that we should be realists about the existence of space. That may sound paradoxical, but it is possible (or so I thought) to regard space as a logical construction from its contents and still think of it, qua construction, as possessing certain intrinsic properties that we do not merely impose on it by convention. Since then, I have become more sympathetic to Nerlich’s position. Chirality is best understood by thinking of space as an entity in its own right. So chemistry has some lessons for the philosophy of space. But the pedagogical relation goes the other way, too: the philosophy of space has interesting implications for chemistry.


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