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Scalable, Highly Uniform, and Robust Colloidal Mie Resonators for All‐Dielectric Soft Meta‐Optics

YongDeok ChoSKKU Advanced Institute of Nanotechnology (SAINT) Sungkyunkwan University (SKKU) Suwon 16419 Republic of KoreaJi‐Hyeok HuhKU‐KIST Graduate School of Converging Science and Technology Korea University Seoul 02841 Republic of KoreaKwang‐Jin KimSKKU Advanced Institute of Nanotechnology (SAINT) Sungkyunkwan University (SKKU) Suwon 16419 Republic of KoreaSeungwoo LeeKU‐KIST Graduate School of Converging Science and Technology Korea University Seoul 02841 Republic of Korea
2018en
ABI

Аннотация

Abstract All‐dielectric nanoparticles (NPs) with high (>3.0) or moderate (1.7–3.0) refractive indices have become fundamental to meta‐optics, as they enable low‐loss, low‐heating, and quenching‐free magnetodielectric Mie resonances, which are difficult to achieve by use of plasmonic counterparts. However, a scalable and versatile synthetic route for such magnetodielectric NPs retaining high uniformity, roundness, and robustness has remained elusive. Thus, soft self‐assembly still represents an underutilized method in the optical engineer's toolset, which in turn limits the accessible range of meta‐optics. Herein, a gram‐scale and versatile synthesis of dielectric colloidal Mie resonators is presented, in which selenous acid precursors are converted into highly uniform, crystalline colloids by a low demand reaction. These crystalline selenium (c‐Se) colloids enable strong electric and magnetic resonances due to their moderate refractive index (2.8–3.2 at optical frequencies), while simultaneously satisfying the requirements of high uniformity, roundness, and robustness. Even with these exotic properties, c‐Se colloids are successfully self‐assembled into various all‐dielectric meta‐optics systems including (i) metafluids exhibiting directional scattering, (ii) metamolecules with nanogap‐dielectric resonances, and (iii) metacrystals with magnetodielectric bandgaps. The design space of all‐dielectric meta‐optics will be greatly expanded by utilizing soft self‐assembly of c‐Se colloids.

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