Dense Arrays of Nanohelices: Raman Scattering from Achiral Molecules Reveals the Near-Field Enhancements at Chiral Metasurfaces

Robin R. Jones, Cornelia Miksch, Hyunah Kwon, Coosje Pothoven, Kristina R. Rusimova, Maarten Kamp, Kedong Gong, Liwu Zhang, Tim Batten, Brian Smith, Alejandro V. Silhanek, Peer Fischer, Daniel Wolverson, Ventsislav K. Valev

Research output: Contribution to journalArticlepeer-review

13 Citations (Scopus)

Abstract

Against the background of the current healthcare and climate emergencies, surface enhanced Raman scattering (SERS) is becoming a highly topical technique for identifying and fingerprinting molecules, e.g., within viruses, bacteria, drugs, and atmospheric aerosols. Crucial for SERS is the need for substrates with strong and reproducible enhancements of the Raman signal over large areas and with a low fabrication cost. Here, dense arrays of plasmonic nanohelices (≈100 nm in length), which are of interest for many advanced nanophotonics applications, are investigated, and they are shown to present excellent SERS properties. As an illustration, two new ways to probe near-field enhancement generated with circular polarization at chiral metasurfaces are presented, first using the Raman spectra of achiral molecules (crystal violet) and second using a single, element-specific, achiral molecular vibrational mode (i.e., a single Raman peak). The nanohelices can be fabricated over large areas at a low cost and they provide strong, robust and uniform Raman enhancement. It is anticipated that these advanced materials will find broad applications in surface enhanced Raman spectroscopies and material science.

Original languageEnglish
Article number2209282
JournalAdvanced Materials
Volume35
Issue number34
DOIs
Publication statusPublished - 2023 Aug 24

Bibliographical note

Publisher Copyright:
© 2023 The Authors. Advanced Materials published by Wiley-VCH GmbH.

All Science Journal Classification (ASJC) codes

  • General Materials Science
  • Mechanics of Materials
  • Mechanical Engineering

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