Collectively Enhanced Giant Circular Dichroism of Germanium Nanohelix Square Lattice Arrays

Circular dichroism is a unique chiroptical signature of the chirality of a system and is a prevalent way to characterize and distinguish systems on a fundamental level and for their technological applicability. Thus, engineering and maximizing the chiroptical response of a single chiral object or a...

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Bibliographic Details
Published in:Advanced photonics research Vol. 4; no. 10
Main Authors: Ellrott, Günter, Beck, Paul, Sultanov, Vitaliy, Rothau, Sergej, Lindlein, Norbert, Chekhova, Maria, Krstić, Vojislav
Format: Journal Article
Language:English
Published: Hoboken John Wiley & Sons, Inc 01-10-2023
Wiley-VCH
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Summary:Circular dichroism is a unique chiroptical signature of the chirality of a system and is a prevalent way to characterize and distinguish systems on a fundamental level and for their technological applicability. Thus, engineering and maximizing the chiroptical response of a single chiral object or a metasurface composed of chiral entities is a formidable task. Current efforts strongly focus on individual metallic nanostructures and their periodic ensembles to harvest on (resonant) plasmonic properties and interactions. This route, however, waives the advantages of high‐refractive‐index nanoscale materials embracing low dissipative losses at optical wavelengths and electromagnetic fields penetrating and propagating in such materials. Herein, a strong circular dichroism is demonstrated in square lattices of nanohelices made of the high‐refractive‐index semiconductor germanium, with dissymmetry factors outperforming metal‐based ensembles. The observation of a much higher dissymmetry emerges for illumination with spatially coherent light, in comparison to spatially incoherent light. High dissymmetry is attributed to cooperative coupling between single helices, resulting from the combination of dielectric resonances of both the individual helical building blocks and the highly ordered lattice.
ISSN:2699-9293
2699-9293
DOI:10.1002/adpr.202300159