KIP-Veröffentlichungen

Jahr 2020
Autor(en) Maria Caterina Giordano, Michael Tzschoppe, Matteo Barelli, Jochen Vogt, Christian Huck, Filippo Canepa, Annemarie Pucci, Francesco Buatier de Mongeot
Titel Self-Organized Nanorod Arrays for Large-Area Surface Enhanced Infrared Absorption
KIP-Nummer HD-KIP 20-09
KIP-Gruppe(n) F6
Dokumentart Paper
Quelle ACS Appl. Mater. Interfaces 2020, 12, 9, 11155-11162
doi 10.1021/acsami.9b19719
Abstract (en)

Highly sensitive Surface Enhanced Infrared Absorption (SEIRA) spectroscopy capabilities are demonstrated by exploiting large-area templates (cm2) based on self-organized (SO) nanorod antennas. We engineered highly dense arrays of gold nanorod antennas featuring polarization-sensitive localized plasmon resonances, tunable over a broadband near- and mid-infrared (IR) spectrum, in overlap with the so called ‘functional group’ window. We demonstrate polarization-sensitive SEIRA activity, homogenous over macroscopic areas and stable in time, by exploiting prototype self-assembled monolayers of IR-active octadecanthiol (ODT) molecules. The strong coupling between the plasmonic excitation and the molecular stretching modes give rise to characteristic Fano resonances in SEIRA. The SO engineering of the active hot-spots in the arrays allows to achieve signal amplitude improved up to the 5.7 \%. This figure is competitive to the response of lithographic nanoantennas and is stable when the optical excitation spot varies from the micro- to the macroscale, thus enabling highly sensitive SEIRA spectroscopy on cost-effective nanosensor devices

bibtex
@article{doi101021acsami9b19719,
  author   = {Giordano, Maria Caterina and Tzschoppe, Michael and Barelli, Matteo and Vogt, Jochen and Huck, Christian and Canepa, Filippo and Pucci, Annemarie and Buatier de Mongeot, Francesco},
  title    = {Self-Organized Nanorod Arrays for Large-Area Surface Enhanced Infrared Absorption},
  journal  = {ACS Applied Materials & Interfaces},
  year     = {2020},
  volume   = {12},
  number   = {9},
  pages    = {11155-11162},
  doi      = {10.1021/acsami.9b19719}
}
URL doi:10.1021/acsami.9b19719
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