Localized coherent phonon generation in monolayer MoSe from ultrafast exciton trapping at shallow traps
We report spectroscopic evidence for the ultrafast trapping of band edge excitons at defects and the subsequent generation of defect-localized coherent phonons (CPs) in monolayer MoSe 2 . While the photoluminescence measurement provides signals of exciton recombination at both shallow and deep traps...
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Published in | Nanoscale horizons Vol. 8; no. 9; pp. 1282 - 1287 |
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Main Authors | , , , , |
Format | Journal Article |
Published |
21.08.2023
|
Online Access | Get full text |
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Abstract | We report spectroscopic evidence for the ultrafast trapping of band edge excitons at defects and the subsequent generation of defect-localized coherent phonons (CPs) in monolayer MoSe
2
. While the photoluminescence measurement provides signals of exciton recombination at both shallow and deep traps, our time-resolved pump-probe spectroscopy on the sub-picosecond time scale detects localized CPs only from the ultrafast exciton trapping at shallow traps. Based on occupation-constrained density functional calculations, we identify the Se vacancy and the oxygen molecule adsorbed on a Se vacancy as the atomistic origins of deep and shallow traps, respectively. Establishing the correlations between the defect-induced ultrafast exciton trapping and the generation of defect-localized CPs, our work could open up new avenues to engineer photoexcited carriers through lattice defects in two-dimensional materials.
Spectroscopic evidence for the conversion of defect-trapped excitons into localized coherent phonons in monolayer MoSe
2
is provided, and the V
Se
+ O
2
complex (an oxygen molecule adsorbed on a Se vacancy) is identified as the shallow trap center. |
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AbstractList | We report spectroscopic evidence for the ultrafast trapping of band edge excitons at defects and the subsequent generation of defect-localized coherent phonons (CPs) in monolayer MoSe
2
. While the photoluminescence measurement provides signals of exciton recombination at both shallow and deep traps, our time-resolved pump-probe spectroscopy on the sub-picosecond time scale detects localized CPs only from the ultrafast exciton trapping at shallow traps. Based on occupation-constrained density functional calculations, we identify the Se vacancy and the oxygen molecule adsorbed on a Se vacancy as the atomistic origins of deep and shallow traps, respectively. Establishing the correlations between the defect-induced ultrafast exciton trapping and the generation of defect-localized CPs, our work could open up new avenues to engineer photoexcited carriers through lattice defects in two-dimensional materials.
Spectroscopic evidence for the conversion of defect-trapped excitons into localized coherent phonons in monolayer MoSe
2
is provided, and the V
Se
+ O
2
complex (an oxygen molecule adsorbed on a Se vacancy) is identified as the shallow trap center. |
Author | Yee, Ki-Ju Bae, Soungmin Kim, Yong-Hoon Jeong, Tae Young Raebiger, Hannes |
AuthorAffiliation | Department of Electrical Engineering Yokohama National University Chungnam National University Korea Advanced Institute of Science and Technology (KAIST) Department of Physics |
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DOI | 10.1039/d3nh00194f |
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Title | Localized coherent phonon generation in monolayer MoSe from ultrafast exciton trapping at shallow traps |
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