Chalcogenide-gold dual-layers coupled to gold nanoparticles for reconfigurable perfect absorption

被引:14
作者
Cao, Tun [1 ]
Liu, Kuan [1 ]
Lu, Li [2 ]
Chui, Hsiang-Chen [1 ]
Simpson, Robert E. [2 ]
机构
[1] Dalian Univ Technol, Sch Optoelect Engn & Instrumentat Sci, Dalian 116024, Peoples R China
[2] Singapore Univ Technol & Design, 8 Somapah Rd, Singapore 487372, Singapore
基金
对外科技合作项目(国际科技项目);
关键词
PHASE-CHANGE MATERIALS; ABSORBER; NONVOLATILE; COMPOSITE; PLASMONS;
D O I
10.1039/c9nr04759j
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Recently, tunable high absorptance from various nanophotonic structures has been demonstrated. However, most of these structures require nano-lithography, which is expensive and slow. Lithography-free tuneable absorbers are rarely explored for tuneable visible and near-infrared photonics. Herein, we demonstrate a gold (Au)/chalcogenide dual-layer that is resonantly coupled to Au nanoparticles (NPs). The structure exhibits angle and polarisation-independent high absorptance. At resonance, waveguide cavity-like modes are excited between the film and NPs whilst gap plasmon modes are excited between the NPs. Coalescence of the waveguide cavity-like modes, the gap plasmon modes, and the highly absorbing chalcogenide semiconductor not only leads to perfect absorptance but also a reconfigurable response via reversible structural phase transitions in the chalcogenide film. In the amorphous state, the design provides nearly perfect absorptance for both p- and s-polarisation states at an incident angle of 20 degrees. However, after switching to the crystalline state, the peak absorptance spectrally broadens and red-shifts from 980 to 1520 nm. This experimental observation was theoretically validated by the finite element method. Thermal-electric modeling was performed to show that the structural transition from crystalline to amorphous states is possible in just 5 ns, thus allowing high-speed reconfigurable perfect absorbers.
引用
收藏
页码:20546 / 20553
页数:8
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