Low-loss nanostructured dielectric metasurfaces have emerged as a breakthrough platform for ultrathin optics and cutting-edge photonic applications, including beam shaping, focusing, and holography. However, the static nature of their constituent materials has traditionally limited them to fixed functionalities. Tunable all-dielectric infrared Huygens' metasurfaces consisting of multi-layer Ge disk meta-units with strategically incorporated non-volatile phase change material Ge 3 Sb 2 Te 6 are introduced. Switching the phase-change material between its amorphous and crystalline structural state enables nearly full dynamic light phase control with high transmittance in the mid-IR spectrum. The metasurface is realized experimentally, showing postfabrication tuning of the light phase within a range of 81% of the full 2π phase shift. Additionally, the versatility of the tunable Huygen's metasurfaces is demonstrated by optically programming the spatial light phase distribution of the metasurface with single meta-unit precision and retrieving high-resolution phase-encoded images using hyperspectral measurements. The programmable metasurface concept overcomes the static limitations of previous dielectric metasurfaces, paving the way for "universal" metasurfaces and highly efficient, ultracompact active optical elements like tunable lenses, dynamic holograms, and spatial light modulators.
The high dielectric optical contrast between the amorphous and crystalline structural phases of non-volatile phase-change materials (PCMs) provides a promising route towards tuneable nanophotonic devices. Here, we employ the next-generation PCM In3SbTe2 (IST) whose optical properties change from dielectric to metallic upon crystallization in the whole infrared spectral range. This distinguishes IST as a switchable infrared plasmonic PCM and enables a programmable nanophotonics material platform. We show how resonant metallic nanostructures can be directly written, modified and erased on and below the meta-atom level in an IST thin film by a pulsed switching laser, facilitating direct laser writing lithography without need for cumbersome multi-step nanofabrication. With this technology, we demonstrate large resonance shifts of nanoantennas of more than 4 µm, a tuneable mid-infrared absorber with nearly 90% absorptance as well as screening and nanoscale “soldering” of metallic nanoantennas. Our concepts can empower improved designs of programmable nanophotonic devices for telecommunications, (bio)sensing and infrared optics, e.g. programmable infrared detectors, emitters and reconfigurable holograms.
The chemical bond is one of the most powerful, yet much debated concepts in chemistry, explaining property trends in solids. Recently, a novel type of chemical bonding was identified in several higher chalcogenides, characterized by a unique property portfolio, unconventional bond breaking, and sharing of about one electron between adjacent atoms. This metavalent bond is a fundamental type of bonding in solids, besides covalent, ionic, and metallic bonding, raising the pertinent question as to whether there is a well‐defined transition between metavalent and covalent bonds. Here, three different pseudo‐binary lines, namely, GeTe1−xSex, Sb2Te3(1−x)Se3x, and Bi2−2xSb2xSe3, are studied, and a sudden change in several properties, including optical absorption ε2(ω), optical dielectric constant ε∞, Born effective charge Z*, electrical conductivity, as well as bond breaking behavior for a critical Se or Sb concentration, is evidenced. These findings provide a blueprint to experimentally explore the influence of metavalent bonding on attractive properties of phase‐change materials and thermoelectrics. Particularly important is its impact on optical properties, which can be tailored by the amount of electrons shared between adjacent atoms. This correlation can be used to design optoelectronic materials and to explore systematic changes in chemical bonding with stoichiometry and atomic arrangement.
An array of permanently electrically conducting lines with a width of 0.5 μm and a period of 0.9 μm has been produced in polyimide with a KrF laser using a holographic technique. The electrical resistivity of these submicron structures shows an ohmic characteristic and has a value of less than 0.5 Ω cm, while the resistivity perpendicular to the structures exceeds this value by more than a factor of 107. The temperature dependence of the conductivity in these wires is found to be similar to that found for macroscopic regions of polyimide which show laser induced conductivity.
scite is a Brooklyn-based organization that helps researchers better discover and understand research articles through Smart Citations–citations that display the context of the citation and describe whether the article provides supporting or contrasting evidence. scite is used by students and researchers from around the world and is funded in part by the National Science Foundation and the National Institute on Drug Abuse of the National Institutes of Health.
hi@scite.ai
10624 S. Eastern Ave., Ste. A-614
Henderson, NV 89052, USA
Copyright © 2024 scite LLC. All rights reserved.
Made with 💙 for researchers
Part of the Research Solutions Family.