Tamm Plasmon Resonance as Optical Fingerprint of Silver/Bacteria Interaction

TL;DR

This paper demonstrates that Tamm Plasmon resonance, when combined with nanostructured silver layers on dielectric mirrors, can serve as an optical fingerprint for detecting and differentiating bacteria, offering a new approach for bacterial sensing.

Contribution

It introduces a novel bacterial sensing method based on Tamm Plasmon resonance sensitive to bacterial presence and activity, utilizing nanostructured silver layers on photonic crystals.

Findings

TP resonance is sensitive to bacteria presence.

Nanostructuring is essential for accessing TP mode.

The method can distinguish proliferative from non-proliferative bacteria.

Abstract

Incorporation of responsive elements into photonic crystals is an effective strategy for building up active optical components to be used as sensors, actuators and modulators. In these regards, Tamm Plasmon (TP) modes have arisen recently as powerful optical tools for the manipulation of light-matter interaction and for building sensors/actuators. These emerge at the interface between a dielectric mirror and a plasmonic layer and, interestingly, can be excited at normal incidence angle with relatively high quality factors. Although its field is located at the interface between the dielectric mirror and the metal, recent studies have demonstrated that corrugation at the nanoscale permits to access the TP mode from the outside, opening new exciting perspectives for many real-life applications. Here, we show that the TP resonance obtained by capping a distributed Bragg reflector with a nanostructured layer of silver is sensitive to the presence of bacteria. We observed that nanoscale corrugation is essential for accessing the TP field, while the well-known bio-responsivity of silver nanostructures renders such a localised mode sensible to the presence of Escherichia Coli. Electrodoping experiments confirm the pivotal role of nanostructuration, as well as strengthening our hypothesis that the modifications of the TP mode upon exposure to bacteria are related to the accumulation of negative charge due to the bacterial-driven removal of Ag+ ions from its lattice. Finally, we devised a case study in which we disentangled optically the presence of proliferative and non-proliferative bacteria using the TP resonance as a read-out, thus making these devices as promising simple all-optical probes for bacterial metabolic activity, including their response against drugs and antibiotics.