TY - JOUR
T1 - Photoluminescence enhancement and structure repairing of monolayer MoSe2 by hydrohalic acid treatment
AU - Han, Hau-Vei
AU - Lu, Ang-Yu
AU - Lu, Li-Syuan
AU - Huang, Jing-Kai
AU - Li, Henan
AU - Hsu, Chang-Lung
AU - Lin, Yung-Chang
AU - Chiu, Ming-Hui
AU - Suenaga, Kazu
AU - Chu, Chih-Wei
AU - Kuo, Hao-Chung
AU - Chang, Wen-Hao
AU - Li, Lain-Jong
AU - Shi, Yumeng
N1 - Publication details (e.g. title, author(s), publication statuses and dates) are captured on an “AS IS” and “AS AVAILABLE” basis at the time of record harvesting from the data source. Suggestions for further amendments or supplementary information can be sent to [email protected].
PY - 2016/1/26
Y1 - 2016/1/26
N2 - Atomically thin two-dimensional transitionmetal dichalcogenides (TMDCs) have attracted much attention recently due to their unique electronic and optical properties for future optoelectronic devices. The chemical vapor deposition (CVD) method is able to generate TMDCs layers with a scalable size and a controllable thickness. However, the TMDC monolayers grown by CVD may incorporate structural defects, and it is fundamentally important to understand the relation between photoluminescence and structural defects. In this report, point defects (Se vacancies) and oxidized Se defects in CVD-grown MoSe2 monolayers are identified by transmission electron microscopy and X-ray photoelectron spectroscopy. These defects can significantly trap free charge carriers and localize excitons, leading to the smearing of free band-To-band exciton emission. Here, we report that the simple hydrohalic acid treatment (such as HBr) is able to efficiently suppress the trapstate emission and promote the neutral exciton and trion emission in defective MoSe2 monolayers through the p-doping process, where the overall photoluminescence intensity at room temperature can be enhanced by a factor of 30. We show that HBr treatment is able to activate distinctive trion and free exciton emissions even from highly defective MoSe2 layers. Our results suggest that the HBr treatment not only reduces the n-doping in MoSe2 but also reduces the structural defects. The results provide further insights of the control and tailoring the exciton emission from CVD-grown monolayer TMDCs. © 2015 American Chemical Society.
AB - Atomically thin two-dimensional transitionmetal dichalcogenides (TMDCs) have attracted much attention recently due to their unique electronic and optical properties for future optoelectronic devices. The chemical vapor deposition (CVD) method is able to generate TMDCs layers with a scalable size and a controllable thickness. However, the TMDC monolayers grown by CVD may incorporate structural defects, and it is fundamentally important to understand the relation between photoluminescence and structural defects. In this report, point defects (Se vacancies) and oxidized Se defects in CVD-grown MoSe2 monolayers are identified by transmission electron microscopy and X-ray photoelectron spectroscopy. These defects can significantly trap free charge carriers and localize excitons, leading to the smearing of free band-To-band exciton emission. Here, we report that the simple hydrohalic acid treatment (such as HBr) is able to efficiently suppress the trapstate emission and promote the neutral exciton and trion emission in defective MoSe2 monolayers through the p-doping process, where the overall photoluminescence intensity at room temperature can be enhanced by a factor of 30. We show that HBr treatment is able to activate distinctive trion and free exciton emissions even from highly defective MoSe2 layers. Our results suggest that the HBr treatment not only reduces the n-doping in MoSe2 but also reduces the structural defects. The results provide further insights of the control and tailoring the exciton emission from CVD-grown monolayer TMDCs. © 2015 American Chemical Society.
KW - Layered materials
KW - Molybdenum diselenide
KW - Photoluminescence
KW - Transition-metal dichalcogenides
KW - Two-dimensional materials
UR - https://www.scopus.com/pages/publications/84989908671
UR - https://www.scopus.com/record/pubmetrics.uri?eid=2-s2.0-84989908671&origin=recordpage
U2 - 10.1021/acsnano.5b06960
DO - 10.1021/acsnano.5b06960
M3 - RGC 21 - Publication in refereed journal
SN - 1936-0851
VL - 10
SP - 1454
EP - 1461
JO - ACS Nano
JF - ACS Nano
IS - 1
ER -