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  <channel rdf:about="https://scholar.dgist.ac.kr/handle/20.500.11750/73">
    <title>Repository Community: null</title>
    <link>https://scholar.dgist.ac.kr/handle/20.500.11750/73</link>
    <description />
    <items>
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        <rdf:li rdf:resource="https://scholar.dgist.ac.kr/handle/20.500.11750/60677" />
        <rdf:li rdf:resource="https://scholar.dgist.ac.kr/handle/20.500.11750/60542" />
        <rdf:li rdf:resource="https://scholar.dgist.ac.kr/handle/20.500.11750/60357" />
        <rdf:li rdf:resource="https://scholar.dgist.ac.kr/handle/20.500.11750/58574" />
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    <dc:date>2026-09-13T07:13:46Z</dc:date>
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  <item rdf:about="https://scholar.dgist.ac.kr/handle/20.500.11750/60677">
    <title>Superradiance and Broadband Emission Driving Fast Electron Dephasing in Open Quantum Systems</title>
    <link>https://scholar.dgist.ac.kr/handle/20.500.11750/60677</link>
    <description>Title: Superradiance and Broadband Emission Driving Fast Electron Dephasing in Open Quantum Systems
Author(s): Bae, Gimin; Kim, Youngjae; Lee, Jae Dong
Abstract: The physical origin of the ultrashort dephasing time T 2 (approximate to O(1) fs), persistently addressed in the solid-state high-harmonic generation (HHG), remains an unresolved and challenging issue because the electron scattering at such a short timescale within solids is hardly identified. Here we investigate HHG of the 1D Hubbard model in the dissipative quantum environment within a frame of the Lindblad equation. In the study, in the limit of a small interatomic distance, we make the first verification of the solid-state Dicke superradiance, the coherent stimulated emission triggered by the spontaneous emission, as well as the broadband emission mimicking the blackbody radiation due to the electron scattering in each harmonic multiple. Further, we find a strong destructive interference between the Dicke superradiance and the broadband emission, which makes a scale down of the effective electron scattering time and leads to just few-femtosecond dephasing time T 2. This finding explains a long-standing problem of the ultrafast femtosecond electron dephasing in HHG. The present study could also serve as a pertinent platform for understanding the nonequilibrium dissipative dynamics of correlated electron systems.</description>
    <dc:date>2026-04-30T15:00:00Z</dc:date>
  </item>
  <item rdf:about="https://scholar.dgist.ac.kr/handle/20.500.11750/60542">
    <title>Manipulating nonlinear dephasing dynamics of Dirac fermions in nearly degenerate four-wave mixing</title>
    <link>https://scholar.dgist.ac.kr/handle/20.500.11750/60542</link>
    <description>Title: Manipulating nonlinear dephasing dynamics of Dirac fermions in nearly degenerate four-wave mixing
Author(s): Ha, Seongju; Choi, Youngchan; Park, Nam Hun; Choi, Jungseok; Park, Jaedeok; Ahn, Kwang Jun; Park, Hee-Su; Lee, JaeDong; Lee, Sang Min; Yeom, Dong-Il
Abstract: Graphene has led the exploration of nonlinear optical responses in two-dimensional materials with exceptionally strong third-order nonlinearity and its electrical controllability. Nonlinear wave mixing with difference-frequency is particularly interesting in graphene because of the divergent nature of third-order susceptibility as the frequency difference approaches zero, but the study on nearly degenerated four-wave mixing (NDFWM) process in graphene is largely unexplored. In this work, we report the giant third-order susceptibility of monolayer graphene, reaching the order of 10-13 m2 V-2 at the optical telecom C-band via the NDFWM process, and its electrical tunability with a high on-off contrast of 23 dB. Moreover, we observed that the NDFWM response under electrical doping exhibits a resonance feature at low pump intensity in ambient conditions, which is substantially altered by varying the pump power. Through non-perturbative quantum master equation calculations, we revealed that our observation is closely related to the dephasing nature of the Dirac fermion of graphene. The decoherence time of photoexcited carriers is estimated up to 70 fs at low pump intensity, which regime is not accessible by other nonlinear means such as high harmonic generation requiring high intensity light. Our findings not only pave an unprecedented route for probing nonlinear dynamics of photoexcited carriers across a wide range but also have a significant impact on ultrafast nonlinear information processing in graphene.</description>
    <dc:date>2026-05-31T15:00:00Z</dc:date>
  </item>
  <item rdf:about="https://scholar.dgist.ac.kr/handle/20.500.11750/60357">
    <title>Pseudospin-selective polarimetric singularities in high-harmonic generation of black phosphorus</title>
    <link>https://scholar.dgist.ac.kr/handle/20.500.11750/60357</link>
    <description>Title: Pseudospin-selective polarimetric singularities in high-harmonic generation of black phosphorus
Author(s): Choi, Youngchan; Bae, Gimin; Lee, J. D.
Abstract: Black phosphorus (BP) exhibits net opposite pseudospin polarizations for the electron and hole states. The pseudospin structure of BP causes a selectivity in the optical excitation engaging the symmetry between the optical pump polarization and the pseudospin state, which is confirmed in a simulation of the time-resolved angle-resolved photoemission spectroscopy (tr-ARPES). Further, the pseudospin selectivity is found to drive a unique polarimetric singularity in the high-harmonic generation (HHG). Given the nth-order high-harmonic signal, we reveal that the singularity arises predominantly through the multiphoton interband pathway and thereby becomes markedly substantial at n omega pump &gt;= Eg. omega pump is the pump photon energy and Eg the energy gap of BP. This permits a coherent understanding of the pseudospin selectivity from tr-ARPES to HHG. In particular, the pseudospin-selective polarimetric singularity suggests a potential for the pseudospintronics to be integrated into the intrinsic dynamics due to the light-matter interaction in two-dimensional materials.</description>
    <dc:date>2026-02-28T15:00:00Z</dc:date>
  </item>
  <item rdf:about="https://scholar.dgist.ac.kr/handle/20.500.11750/58574">
    <title>Floquet engineering of excitons in monolayer MoS2</title>
    <link>https://scholar.dgist.ac.kr/handle/20.500.11750/58574</link>
    <description>Title: Floquet engineering of excitons in monolayer MoS2
Author(s): Park, Hyosub; Lee, JaeDong
Abstract: Floquet dynamics temporally deforms the band structure of the system, called Floquet engineering, under a strong optical field. Although a single resonant pulse simultaneously drives both exciton and Floquet dynamics, the Floquet engineering during exciton generation remains unexplored. We examine the Floquet engineering of excitons by a theoretical simulation of the time-resolved and angle-resolved photoemission spectroscopy in monolayer MoS2. Our finding reveals that the exciton experiences nontrivial engineering inducing a distinct asymmetry in the development of spectral splitting with the time delay and pump intensity, which are underlain by the electron-hole interaction inherent in the exciton binding. © 2025 American Physical Society.</description>
    <dc:date>2025-04-30T15:00:00Z</dc:date>
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