Chiral Second-Harmonic Generation from Monolayer WS2/Aluminum Plasmonic Vortex Metalens

Two-dimensional spiral plasmonic structures have emerged as a versatile approach to generate near-field vortex fields with tunable topological charges. We demonstrate here a far-field approach to observe the chiral second-harmonic generation (SHG) at designated visible wavelengths from a single plas...

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Veröffentlicht in:Nano letters 2020-04, Vol.20 (4), p.2857-2864
Hauptverfasser: Guo, Wan-Ping, Liang, Wei-Yun, Cheng, Chang-Wei, Wu, Wei-Lin, Wang, Yen-Ting, Sun, Quan, Zu, Shuai, Misawa, Hiroaki, Cheng, Pi-Ju, Chang, Shu-Wei, Ahn, Hyeyoung, Lin, Minn-Tsong, Gwo, Shangjr
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container_end_page 2864
container_issue 4
container_start_page 2857
container_title Nano letters
container_volume 20
creator Guo, Wan-Ping
Liang, Wei-Yun
Cheng, Chang-Wei
Wu, Wei-Lin
Wang, Yen-Ting
Sun, Quan
Zu, Shuai
Misawa, Hiroaki
Cheng, Pi-Ju
Chang, Shu-Wei
Ahn, Hyeyoung
Lin, Minn-Tsong
Gwo, Shangjr
description Two-dimensional spiral plasmonic structures have emerged as a versatile approach to generate near-field vortex fields with tunable topological charges. We demonstrate here a far-field approach to observe the chiral second-harmonic generation (SHG) at designated visible wavelengths from a single plasmonic vortex metalens. This metalens comprises an Archimedean spiral slit fabricated on atomically flat aluminum epitaxial film, which allows for precise tuning of plasmonic resonances and subsequent transfer of two-dimensional materials on top of the spiral slit. The nonlinear optical measurements show a giant SHG circular dichroism. Furthermore, we have achieved an enhanced chiral SHG conversion efficiency (about an order of magnitude greater than the bare aluminum lens) from monolayer tungsten disulfide (WS2)/aluminum metalens, which is designed at the C-exciton resonance of WS2. Since the C-exciton is not a valley exciton, the enhanced chiral SHG in this hybrid system originates from the plasmonic vortex field-enhanced SHG under the optical spin–orbit interaction.
doi_str_mv 10.1021/acs.nanolett.0c00645
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