论文标题
TAMM等离子体共振作为银/细菌相互作用的光学指纹
Tamm Plasmon Resonance as Optical Fingerprint of Silver/Bacteria Interaction
论文作者
论文摘要
将响应元素纳入光子晶体是建立活跃的光学组件的有效策略,将其用作传感器,执行器和调节器。在这些方面,TAMM等离子体(TP)模式最近是作为操纵轻度交互和建筑传感器/执行器的强大光学工具。这些出现在介电镜和等离子层之间的界面上,有趣的是,可以以相对较高的质量因子在正常入射角上激发。尽管它的磁场位于介电镜和金属之间的界面上,但最近的研究表明,纳米级的波纹允许从外部访问TP模式,从而为许多现实生活应用开辟了新的令人兴奋的视角。在这里,我们表明,通过用纳米结构的银层限制分布的bragg反射器获得的TP共振对细菌的存在敏感。我们观察到,纳米级波纹对于进入TP场是必不可少的,而银纳米结构的众所周知的生物反应性使这种局部模式与Escherichia Goli的存在明智。电培养实验证实了纳米结构化的关键作用,并加强了我们的假设,即暴露于细菌时TP模式的修饰与由于细菌驱动的Ag+离子从其晶格中的细菌驱动的去除而导致负电荷的积累有关。最后,我们设计了一项案例研究,在该案例研究中,我们将使用TP谐振作为读出的光学上脱离了增殖和非增生性细菌的存在,从而使这些设备成为有希望的简单的全光探针,用于细菌代谢活性,包括它们对药物和抗生素的反应。
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.