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Augmented Quantum Yield of a 2D Monolayer Photodetector by Surface Plasmon Coupling

Monolayer (1L) transition metal dichalcogenides (TMDCs) are promising materials for nanoscale optoelectronic devices because of their direct band gap and wide absorption range (ultraviolet to infrared). However, 1L-TMDCs cannot be easily utilized for practical optoelectronic device applications (e.g...

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Bibliographic Details
Published in:Nano letters 2018-04, Vol.18 (4), p.2316-2323
Main Authors: Bang, Seungho, Duong, Ngoc Thanh, Lee, Jubok, Cho, Yoo Hyun, Oh, Hye Min, Kim, Hyun, Yun, Seok Joon, Park, Chulho, Kwon, Min-Ki, Kim, Ja-Yeon, Kim, Jeongyong, Jeong, Mun Seok
Format: Article
Language:English
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Summary:Monolayer (1L) transition metal dichalcogenides (TMDCs) are promising materials for nanoscale optoelectronic devices because of their direct band gap and wide absorption range (ultraviolet to infrared). However, 1L-TMDCs cannot be easily utilized for practical optoelectronic device applications (e.g., photodetectors, solar cells, and light-emitting diodes) because of their extremely low optical quantum yields (QYs). In this investigation, a high-gain 1L-MoS2 photodetector was successfully realized, based on the surface plasmon (SP) of the Ag nanowire (NW) network. Through systematic optical characterization of the hybrid structure consisting of a 1L-MoS2 and the Ag NW network, it was determined that a strong SP and strain relaxation effect influenced a greatly enhanced optical QY. The photoluminescence (PL) emission was drastically increased by a factor of 560, and the main peak was shifted to the neutral exciton of 1L-MoS2. Consequently, the overall photocurrent of the hybrid 1L-MoS2 photodetector was observed to be 250 times better than that of the pristine 1L-MoS2 photodetector. In addition, the photoresponsivity and photodetectivity of the hybrid photodetector were effectively improved by a factor of ∼1000. This study provides a new approach for realizing highly efficient optoelectronic devices based on TMDCs.
ISSN:1530-6984
1530-6992
DOI:10.1021/acs.nanolett.7b05060