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 inNanoscale horizons Vol. 8; no. 9; pp. 1282 - 1287
Main Authors Bae, Soungmin, Jeong, Tae Young, Raebiger, Hannes, Yee, Ki-Ju, Kim, Yong-Hoon
Format Journal Article
Published 21.08.2023
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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.
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
AuthorAffiliation_xml – name: Korea Advanced Institute of Science and Technology (KAIST)
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  givenname: Ki-Ju
  surname: Yee
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– sequence: 5
  givenname: Yong-Hoon
  surname: Kim
  fullname: Kim, Yong-Hoon
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Snippet We report spectroscopic evidence for the ultrafast trapping of band edge excitons at defects and the subsequent generation of defect-localized coherent phonons...
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