MoS2 Monolayers on Au Nanodot Arrays: Surface Plasmon, Local Strain, and Interfacial Electronic Interaction

Metal and transition-metal dichalcogenide (TMD) hybrid systems have been attracting growing research attention because exciton–plasmon coupling is a desirable means of tuning the physical properties of TMD materials. Competing effects of metal nanostructures, such as the local electromagnetic field...

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Veröffentlicht in:The journal of physical chemistry letters 2020-04, Vol.11 (8), p.3039-3044
Hauptverfasser: Kim, Eunah, Lee, Chanwoo, Song, Jungeun, Kwon, Soyeong, Kim, Bora, Kim, Dae Hyun, Park, Tae Joo, Jeong, Mun Seok, Kim, Dong-Wook
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container_issue 8
container_start_page 3039
container_title The journal of physical chemistry letters
container_volume 11
creator Kim, Eunah
Lee, Chanwoo
Song, Jungeun
Kwon, Soyeong
Kim, Bora
Kim, Dae Hyun
Park, Tae Joo
Jeong, Mun Seok
Kim, Dong-Wook
description Metal and transition-metal dichalcogenide (TMD) hybrid systems have been attracting growing research attention because exciton–plasmon coupling is a desirable means of tuning the physical properties of TMD materials. Competing effects of metal nanostructures, such as the local electromagnetic field enhancement and luminescence quenching, affect the photoluminescence (PL) characteristics of metal/TMD nanostructures. In this study, we prepared TMD MoS2 monolayers on hexagonal arrays of Au nanodots and investigated their physical properties by micro-PL and surface photovoltage (SPV) measurements. MoS2 monolayers on bare Au nanodots exhibited higher PL intensities than those of MoS2 monolayers on 5-nm-thick Al2O3-coated Au nanodots. The Al2O3 spacer layer blocked charge transfer at the Au/MoS2 interface but allowed the transfer of mechanical strain to the MoS2 monolayers on the nanodots. The SPV mapping results revealed not only the electron-transfer behavior at the Au/MoS2 contacts but also the lateral drift of charge carriers at the MoS2 surface under light illumination, which corresponds to nonradiative relaxation processes of the photogenerated excitons.
doi_str_mv 10.1021/acs.jpclett.0c00691
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