Tailoring Nanohole Plasmonic Resonance with Light-Responsive Azobenzene Compound

ACS Appl Mater Interfaces. 2019 Jan 16;11(2):2254-2263. doi: 10.1021/acsami.8b17258. Epub 2019 Jan 3.

Abstract

Metal-based nanohole structures, featuring a continuous matrix and discrete voids, have seen a wide spectrum of practical applications, ranging from plasmonic sensing to extraordinary optical transmission. It would not be uncommon to pursue further enhancement of their optical tunability, and incorporation with other functional materials offers an intriguing lead. In this study, the first step involves colloidal lithography fabrication of gold-based, short-range ordered nanohole structures on a glass substrate with varying geometrical parameters. Plasmonic resonance in optical waveband is readily achieved from the coupling between bonding surface plasmons and nanohole lattices. Resonant features observed in transmission measurements could also be well reproduced both from numerical simulations as well as theoretical calculations based on the grating coupling mechanism. With the introduction of a thin layer of azobenzene compound by spin-coating comes the critical transformation that not only alters optical performances by impacting the surface environment but also bestows the structures with light responsiveness. After 488 nm of laser irradiation, it is observed that the structures underwent cross polarization conversion, which could be attributed to the photoalignment behavior from trans-cis isomerization within the azobenzene layer, yielding further optical tunability with the linearly polarized probe light compared to that in the preirradiated state. The tuning of plasmonic resonances through light stimuli paves a noncontacting path for achieving desired optical responses with potentially high spatial and temporal resolution. This work may serve as a fountainhead for future efforts on optically tailorable photonic devices associated with nanohole plasmonics.

Keywords: azobenzene compound; light-responsive; nanoholes; plasmonic resonance; trans−cis isomerization.