Plasmonic Sensors for Aromatic Hydrocarbon Detection

Abstract

The development of innovative materials for sensitive and selective gas sensing is a very relevant field for the current nanotechnology research. A strong effort is dedicated to the fabrication of low-cost and efficient nanoscale devices capable of a fast detection. Resistive electrical devices are the most adopted solutions for in-situ and real-time detection, but their main drawbacks are the low selectivity, response drift, electromagnetic noise dependence and need of contact measurements. Optical gas sensors allow to overcome such limits, and could moreover exhibit thermal and mechanical stability, operate at room temperature, and be integrated on-chip. Within this framework, plasmon-based optical devices are knowing an increasing development and diffusion. Herein plasmonic sensors for aromatic hydrocarbon detection are presented. These systems are based on aryl-bridged polysilsesquioxanes (aryl-PSQs), obtained either $\textcircled{1}$ coupling such hybrid films with Au nanoparticles (NPs), aiming to the excitation of localized surface plasmon resonances (LSPRs), or $\textcircled{2}$ depositing them onto metallic waveguiding layers, to form gratings supporting the propagation of surface plasmon polaritons (SPPs). Aryl-PSQs are sol-gel materials characterized by a native controlled porosity and other functionalities (Loy and Shea, Chem Rev 95:1431–1442, 1995; Dabrowski et al., Appl Surf Sci 253:5747–5751, 2007; Brigo et al., Nanotechnology 23:325302, 2012). Temperature programmed desorption investigations of xylene on phenyl-bridged (ph-PSQ) and diphenyl-bridged (diph-PSQ) PSQ films indicate a specific π −π interaction between the organic component of the films and xylene molecules: the interaction energy is quantified in 38 ± 14 kJ/mol and 115 ± 13 kJ/mol, respectively (Brigo et al., J Mater Chem C 1:4252, 2013). For type $\textcircled{1}$ sensors, a thin film of aryl-PSQ was deposited on a submonolayer of Au NPs coating a fused silica substrate. These sensors were tested monitoring the variation of the LSPRs under cycles of exposure to N₂ and to 30 ppm xylene in N₂.