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Nonequilibrium Charge-Density-Wave Melting in 1T-TaS2 Triggered by Electronic Excitation: A Real-Time Time-Dependent Density Functional Theory Study

Title
Nonequilibrium Charge-Density-Wave Melting in 1T-TaS2 Triggered by Electronic Excitation: A Real-Time Time-Dependent Density Functional Theory Study
Author(s)
Lee, JuhyungBang, JunhyeokKang, Joongoo
Issued Date
2022-06
Citation
Journal of Physical Chemistry Letters, v.13, no.25, pp.5711 - 5718
Type
Article
Keywords
PHASE-TRANSITIONSSTATEMICROSCOPYDYNAMICS
ISSN
1948-7185
Abstract
Ultrafast charge transfer in van der Waals (vdW) heterostructures enables efficient control of two-dimensional material properties through strong optical absorption and subsequent carrier transfer. Here, using real-time timedependent density functional theory coupled to molecular dynamics, we investigated the nonequilibrium dynamics of charge-density-wave (CDW) melting in 1T-TaS2 triggered by ultrafast charge transfer in 1T-TaS2/MoSe2 or WSe2 heterostructures. Despite the fast and sufficient charge transfer from the MoSe2 (or WSe2) "electrode" to the 1T-TaS2 layer, the electronic excitation of the vdW heterostructure does not lead to the nonthermal CDW transition of 1T-TaS2. Instead, the TaS2 lattice is heated by carrier-lattice scattering, leading to thermal CDW melting at high ionic temperatures. The lack of nonthermal melting follows from the fact that the time scale of carrier recombination in 1T-TaS2 is similar to or faster than that of charge transfer. These findings provide physical insights into understanding the CDW melting dynamics in vdW heterostructures under nonequilibrium conditions.
URI
http://hdl.handle.net/20.500.11750/17033
DOI
10.1021/acs.jpclett.2c01352
Publisher
American Chemical Society
Related Researcher
  • 강준구 Kang, Joongoo
  • Research Interests Computational Materials Science & Materials Design; Nanomaterials for Energy Applications; Theoretical Condensed Matter Physics
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Appears in Collections:
Department of Physics and Chemistry Computational Materials Theory Group 1. Journal Articles

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