All-optical materials design of chiral edge modes in transition-metal dichalcogenides
Abstract
Monolayer transition-metal dichalcogenides are novel materials which at low energies constitute a condensed-matter realization of massive relativistic fermions in two dimensions. Here, we show that this picture breaks for optical pumping—instead, the added complexity of a realistic materials description leads to a new mechanism to optically induce topologically protected chiral edge modes, facilitating optically switchable conduction channels that are insensitive to disorder. In contrast to graphene and previously discussed toy models, the underlying mechanism relies on the intrinsic three-band nature of transition-metal dichalcogenide monolayers near the band edges. Photo-induced band inversions scale linearly in applied pump field and exhibit transitions from one to two chiral edge modes on sweeping from red to blue detuning. As a result, we develop an ab initio strategy to understand non-equilibrium Floquet–Bloch bands and topological transitions, and illustrate for WS2 that control of chiral edge modes can be dictated solely from symmetry principles and is not qualitatively sensitive to microscopic materials details.
- Authors:
-
- SLAC National Accelerator Lab. and Stanford Univ., Stanford, CA (United States)
- SLAC National Accelerator Lab. and Stanford Univ., Stanford, CA (United States); Univ. of North Dakota, Grand Forks, ND (United States)
- Publication Date:
- Research Org.:
- SLAC National Accelerator Laboratory (SLAC), Menlo Park, CA (United States)
- Sponsoring Org.:
- USDOE
- OSTI Identifier:
- 1348405
- Grant/Contract Number:
- AC02-76SF00515
- Resource Type:
- Accepted Manuscript
- Journal Name:
- Nature Communications
- Additional Journal Information:
- Journal Volume: 7; Journal ID: ISSN 2041-1723
- Publisher:
- Nature Publishing Group
- Country of Publication:
- United States
- Language:
- English
- Subject:
- 36 MATERIALS SCIENCE; electronic properties and materials; theory and computation
Citation Formats
Claassen, Martin, Jia, Chunjing, Moritz, Brian, and Devereaux, Thomas P. All-optical materials design of chiral edge modes in transition-metal dichalcogenides. United States: N. p., 2016.
Web. doi:10.1038/ncomms13074.
Claassen, Martin, Jia, Chunjing, Moritz, Brian, & Devereaux, Thomas P. All-optical materials design of chiral edge modes in transition-metal dichalcogenides. United States. https://doi.org/10.1038/ncomms13074
Claassen, Martin, Jia, Chunjing, Moritz, Brian, and Devereaux, Thomas P. Mon .
"All-optical materials design of chiral edge modes in transition-metal dichalcogenides". United States. https://doi.org/10.1038/ncomms13074. https://www.osti.gov/servlets/purl/1348405.
@article{osti_1348405,
title = {All-optical materials design of chiral edge modes in transition-metal dichalcogenides},
author = {Claassen, Martin and Jia, Chunjing and Moritz, Brian and Devereaux, Thomas P.},
abstractNote = {Monolayer transition-metal dichalcogenides are novel materials which at low energies constitute a condensed-matter realization of massive relativistic fermions in two dimensions. Here, we show that this picture breaks for optical pumping—instead, the added complexity of a realistic materials description leads to a new mechanism to optically induce topologically protected chiral edge modes, facilitating optically switchable conduction channels that are insensitive to disorder. In contrast to graphene and previously discussed toy models, the underlying mechanism relies on the intrinsic three-band nature of transition-metal dichalcogenide monolayers near the band edges. Photo-induced band inversions scale linearly in applied pump field and exhibit transitions from one to two chiral edge modes on sweeping from red to blue detuning. As a result, we develop an ab initio strategy to understand non-equilibrium Floquet–Bloch bands and topological transitions, and illustrate for WS2 that control of chiral edge modes can be dictated solely from symmetry principles and is not qualitatively sensitive to microscopic materials details.},
doi = {10.1038/ncomms13074},
journal = {Nature Communications},
number = ,
volume = 7,
place = {United States},
year = {Mon Oct 10 00:00:00 EDT 2016},
month = {Mon Oct 10 00:00:00 EDT 2016}
}
Web of Science
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