Please use this identifier to cite or link to this item: https://doi.org/10.1038/s41467-020-18793-y
Title: Suppressing material loss in the visible and near-infrared range for functional nanophotonics using bandgap engineering
Authors: Wang, M.
Krasnok, A.
Lepeshov, S.
Hu, G. 
Jiang, T.
Fang, J.
Korgel, B.A.
Alù, A.
Zheng, Y.
Issue Date: 2020
Publisher: Nature Research
Citation: Wang, M., Krasnok, A., Lepeshov, S., Hu, G., Jiang, T., Fang, J., Korgel, B.A., Alù, A., Zheng, Y. (2020). Suppressing material loss in the visible and near-infrared range for functional nanophotonics using bandgap engineering. Nature Communications 11 (1) : 5055. ScholarBank@NUS Repository. https://doi.org/10.1038/s41467-020-18793-y
Rights: Attribution 4.0 International
Abstract: All-dielectric nanostructures have recently opened exciting opportunities for functional nanophotonics, owing to their strong optical resonances along with low material loss in the near-infrared range. Pushing these concepts to the visible range is hindered by their larger absorption coefficient, thus encouraging the search for alternative dielectrics for nanophotonics. Here, we employ bandgap engineering to synthesize hydrogenated amorphous Si nanoparticles (a-Si:H NPs) offering ideal features for functional nanophotonics. We observe significant material loss suppression in a-Si:H NPs in the visible range caused by hydrogenation-induced bandgap renormalization, producing strong higher-order resonant modes in single NPs with Q factors up to ~100 in the visible and near-IR range. We also realize highly tunable all-dielectric meta-atoms by coupling a-Si:H NPs to photochromic spiropyran molecules. ~70% reversible all-optical tuning of light scattering at the higher-order resonant mode under a low incident light intensity is demonstrated. Our results promote the development of high-efficiency visible nanophotonic devices. © 2020, The Author(s).
Source Title: Nature Communications
URI: https://scholarbank.nus.edu.sg/handle/10635/198151
ISSN: 2041-1723
DOI: 10.1038/s41467-020-18793-y
Rights: Attribution 4.0 International
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