Optical material anisotropy in high-index transition metal dichalcogenide Mie nanoresonators

被引:41
|
作者
Green, Thomas D. [1 ]
Baranov, Denis G. [1 ]
Munkhbat, Battulga [1 ]
Verre, Ruggero [1 ]
Shegai, Timur [1 ]
Kall, Mikael [1 ]
机构
[1] Chalmers Univ Technol, Dept Phys, S-41296 Gothenburg, Sweden
来源
OPTICA | 2020年 / 7卷 / 06期
关键词
LIGHT; GENERATION; METASURFACES; SCATTERING; MATTER;
D O I
10.1364/OPTICA.389192
中图分类号
O43 [光学];
学科分类号
070207 ; 0803 ;
摘要
Resonant optical antennas provide unprecedented opportunities to control light on length scales far below the diffraction limit. Recent studies have demonstrated that nanostructures made of multilayer transition metal dichalcogenides (TMDCs) can exhibit well-defined and intense Mie resonances in the visible to the near-infrared spectral range. These resonances are realizable because the TMDC materials exhibit very high in-plane refractive indices, in fact higher than what is found in typical high-index dielectric materials like Si orGaAs. However, their out-of-plane refractive indices are comparatively low. Here we experimentally and theoretically investigate how this unusually large material anisotropy influences the optical response of individual TMDC nanoresonators made of MoS2. We find that anisotropy strongly affects the far-field optical response of the resonators, as well as complex interference effects, such as anapole and resonant Kerker conditions. Moreover, we show that it is possible to utilize the material anisotropy to probe the vectorial nature of the nanoresonator internal near fields. Specifically, we show that Raman spectra originating from individual MoS2 nanoresonators exhibit mode-specific anisotropic enhancement factors that vary with the nanoresonator size and correlate with specific modes supported at resonance. Our study indicates that exploring material anisotropy in novel high-index dielectrics may lead to new nanophotonic effects and applications. (C) 2020 Optical Society of America under the terms of the OSA Open Access Publishing Agreement
引用
收藏
页码:680 / 686
页数:7
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