Affiliation:
1. Chair in Hybrid Nanosystems Nanoinstitute Munich and Center for Nanoscience (CeNS) Faculty of Physics Ludwig Maximilian University of Munich 80539 Munich Germany
2. Centre for Nano Science and Technology Italian Institute of Technology Foundation Via Rubattino 81 Milan 20134 Italy
3. School of Physics and Astronomy Monash University Clayton Victoria 3800 Australia
4. Department of Physics Imperial College London London SW7 2AZ UK
Abstract
AbstractPhotonic metasurfaces offer exceptional control over light at the nanoscale, facilitating applications spanning from biosensing, and nonlinear optics to photocatalysis. Many metasurfaces, especially resonant ones, rely on periodicity for the collective mode to form, which makes them subject to the influences of finite size effects, defects, and edge effects, which have considerable negative impact at the application level. These aspects are especially important for quasi‐bound state in the continuum (BIC) metasurfaces, for which the collective mode is highly sensitive to perturbations due to high‐quality factors and strong near‐field enhancement. Here, the mode formation in quasi‐BIC metasurfaces on the individual resonator level using scattering scanning near‐field optical microscopy (s‐SNOM) in combination with a new image processing technique, is quantitatively investigated. It is found that the quasi‐BIC mode is formed at a minimum size of 10 × 10‐unit cells much smaller than expected from far‐field measurements. Furthermore, it is shown that the coupling direction of the resonators, defects and edge states have pronounced influence on the quasi‐BIC mode. This study serves as a link between the far‐field and near‐field responses of metasurfaces, offering crucial insights for optimizing spatial footprint and active area, holding promise for augmenting applications such as catalysis and biospectroscopy.
Funder
Deutsche Forschungsgemeinschaft
H2020 European Research Council
Center for NanoScience, Ludwig-Maximilians-Universität München
Cited by
2 articles.
订阅此论文施引文献
订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献