Vibrational strong coupling between Tamm phonon polaritons and organic molecules

被引:0
|
作者
Xu, Chenran [1 ,2 ]
Cai, Han [1 ,2 ]
Wang, Da-Wei [1 ,2 ,3 ]
机构
[1] Zhejiang Univ, Interdisciplinary Ctr Quantum Informat, State Key Lab Modern Opt Instrumentat, Dept Phys, Hangzhou 310027, Zhejiang, Peoples R China
[2] Zhejiang Univ, Zhejiang Prov Key Lab Quantum Technol & Device, Dept Phys, Hangzhou 310027, Zhejiang, Peoples R China
[3] Univ Chinese Acad Sci, CAS Ctr Excellence Topol Quantum Computat, Beijing 100190, Peoples R China
基金
中国国家自然科学基金;
关键词
PLASMON EXCITON-POLARITONS; REACTIVITY;
D O I
10.1364/JOSAB.419042
中图分类号
O43 [光学];
学科分类号
070207 ; 0803 ;
摘要
Phonon polaritons (PhPs) have a long lifetime and high confinement of light fields compared with their plasmonic counterparts in the mid-infrared range. Thus, PhPs are promising candidates for realizing vibrational strong coupling (VSC) with molecules. However, VSCs of PhPs in nanoresonators and thin films require the near-field technique and are limited to the transverse magnetic mode. Here we propose a new configuration based on the Tamm structure, which supports PhPs excited by the free-space incident light in both transverse-electric and transverse-magnetic modes. The VSC of a 300 nm thick molecular layer can be achieved with 21 cm(-1) Rabi splitting, according to the numerically obtained angle resolved reflectivity spectra with the transfer matrix method. Our findings provide a promising platform for applications in free-space sensing of vibrational modes and control of chemical reactions in compact devices. (C) 2021 Optical Society of America
引用
收藏
页码:1505 / 1509
页数:5
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