Please use this identifier to cite or link to this item: https://doi.org/10.1021/acs.nanolett.1c00281
Title: Hybridized Hyperbolic Surface Phonon Polaritons at α-MoO3 and Polar Dielectric Interfaces
Authors: Qing Zhang 
Qingdong Ou
Guangwei Hu 
Jingying Liu
Zhigao Dai
Michael S. Fuhrer
Qiaoliang Bao
Cheng-Wei Qiu 
Keywords: 2D materials
Issue Date: 25-Mar-2021
Citation: Qing Zhang, Qingdong Ou, Guangwei Hu, Jingying Liu, Zhigao Dai, Michael S. Fuhrer, Qiaoliang Bao, Cheng-Wei Qiu (2021-03-25). Hybridized Hyperbolic Surface Phonon Polaritons at α-MoO3 and Polar Dielectric Interfaces. Nano Letters. ScholarBank@NUS Repository. https://doi.org/10.1021/acs.nanolett.1c00281
Rights: Attribution-NonCommercial-ShareAlike 4.0 International
Abstract: Surface phonon polaritons (SPhPs) in polar dielectrics offer new opportunities for infrared nanophotonics. However, bulk SPhPs inherently propagate isotropically with limited photon confinement, and how to collectively realize ultralarge confinement, in-plane hyperbolicity, and unidirectional propagation remains elusive. Here, we report an approach to solve the aforementioned issues of bulk SPhPs in one go by constructing a heterostructural interface between biaxial van der Waals material (e.g., α-MoO3) and bulk polar dielectric (e.g., SiC, AlN, and GaN). Because of anisotropy-oriented mode couplings, the hybridized SPhPs with a large confinement factor (>100) show in-plane hyperbolicity that has been switched to the orthogonal direction as compared to that in natural α-MoO3. More interestingly, this proof of concept allows steerable and unidirectional polariton excitation by suspending α-MoO3 on patterned SiC air cavities. Our finding exemplifies a generalizable framework to manipulate the flow of nanolight in many other hybrid systems consisting of anisotropic materials and polar dielectrics.
Source Title: Nano Letters
URI: https://scholarbank.nus.edu.sg/handle/10635/191568
ISSN: 15306984
15306992
DOI: 10.1021/acs.nanolett.1c00281
Rights: Attribution-NonCommercial-ShareAlike 4.0 International
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