Abstract

We present a facile approach for the determination of the electromagnetic field enhancement of nanostructured TiN electrodes. As model system, TiN with partially collapsed nanotube structure obtained from nitridation of TiO2 nanotube arrays was used. Using surface-enhanced Raman scattering (SERS) spectroscopy, the electromagnetic field enhancement factors (EFs) of the substrate across the optical region were determined. The non-surface binding SERS reporter group azidobenzene was chosen, for which contributions from the chemical enhancement effect can be minimized. Derived EFs correlated with the electronic absorption profile and reached 3.9 at 786 nm excitation. Near-field enhancement and far-field absorption simulated with rigorous coupled wave analysis showed good agreement with the experimental observations. The major optical activity of TiN was concluded to originate from collective localized plasmonic modes at ca. 700 nm arising from the specific nanostructure.

Highlights

  • Academic Editor: Simone BorriTitanium nitride (TiN) is an emerging substrate material for optical and sensing applications [1,2]

  • Optical characterization was carried out using UV-Vis spectroscopy in reflection mode

  • We presented the fabrication of plasmonic TiN electrodes with partially collapsed nanotubular structure

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Summary

Introduction

Academic Editor: Simone BorriTitanium nitride (TiN) is an emerging substrate material for optical and sensing applications [1,2]. The surface plasmon resonance (LSPR) is typically located in the visible to near-IR region and can be tuned with respect to resonance frequency and magnitude by tailoring the material’s nanostructure [12,13]. In this respect, various TiN nanostructures have been investigated for their light modulation aptitude, including nanoparticle assemblies [14,15], nanocubes [16], nanotubes [17], nanorods [11,13], as well as thin films of TiN [18]. Each system has shown specific plasmonic activity that can be further fine-tuned by controlling structural parameters

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