تقرير
Achieving Optical Refractive Index of 10-Plus by Colloidal Self-Assembly
العنوان: | Achieving Optical Refractive Index of 10-Plus by Colloidal Self-Assembly |
---|---|
المؤلفون: | Kim, NaYeoun, Huh, Ji-Hyeok, Cho, YongDeok, Park, Sung Hun, Kim, Hyeon Ho, Rho, Kyung Hun, Lee, Jaewon, Lee, Seungwoo |
سنة النشر: | 2024 |
المجموعة: | Condensed Matter Physics (Other) |
مصطلحات موضوعية: | Physics - Optics, Condensed Matter - Materials Science |
الوصف: | This study demonstrates the developments of self-assembled optical metasurfaces to overcome inherent limitations in polarization density (P) within natural materials, which hinder achieving high refractive indices (n) at optical frequencies. The Maxwellian macroscopic description establishes a link between P and n, revealing a static limit in natural materials, restricting n to approximately 4.0 at optical frequencies. Optical metasurfaces, utilizing metallic colloids on a deep-subwavelength scale, offer a solution by unnaturally enhancing n through electric dipolar (ED) resonances. Self-assembly enables the creation of nanometer-scale metallic gaps between metallic nanoparticles (NPs), paving the way for achieving exceptionally high n at optical frequencies. This study focuses on assembling polyhedral gold (Au) NPs into a closely packed monolayer by rationally designing the polymeric ligand to balance attractive and repulsive forces, in that polymeric brush-mediated self-assembly of the close-packed Au NP monolayer is robustly achieved over a large-area. The resulting monolayer of Au nanospheres (NSs), nanooctahedras (NOs), and nanocubes (NCs) exhibits high macroscopic integrity and crystallinity, sufficiently enough for pushing n to record-high regimes. The study underlies the significance of capacitive coupling in achieving an unnaturally high n and explores fine-tuning Au NC size to optimize this coupling. The achieved n of 10.12 at optical frequencies stands as a benchmark, highlighting the potential of polyhedral Au NPs in advancing optical metasurfaces. |
نوع الوثيقة: | Working Paper |
URL الوصول: | http://arxiv.org/abs/2403.16911 |
رقم الأكسشن: | edsarx.2403.16911 |
قاعدة البيانات: | arXiv |
الوصف غير متاح. |