Microscopic Theory of Externally Tunable Exciton Signatures of Two-Dimensional Materials
Doctoral thesis, 2021
The aim of this thesis is to use a microscopic many-particle theory to predict different strategies to externally control the optical fingerprint of TMDs.
We show that specific molecules can activate dark excitons leading to new pronounced resonances in optical spectra. We also find that these dark states are very sensitive to strain, leading to significant energy shifts and intensity changes. This renders 2D materials suitable for optical sensing of molecules and strain. Moreover, we investigate how local defects due to single molecules or local strain can trap excitons. We show direct signatures of localized bright excitonic states as well as indirect phonon-assisted side bands of localized momentum-dark excitons. We find that the visibility of these localized states is determined by the interplay between defect-induced exciton capture and intervalley exciton–phonon scattering. Finally, we investigate the formation dynamics and optical signatures of spatially separated interlayer excitons at interfaces of acene-based molecular crystals and 2D materials, which play a crucial role for conversion of light to electricity in photodetecting devices.
Overall, the work contributes to a better microscopic understanding of exciton optics and its control via strain, molecules, magnetic fields and impurities in atomically thin semiconductors.
localized states
density matrix formalism
magnetic field
transition metal dichalcogenides
Bloch equations
organic/inorganic heterostructures
dark excitons
strain
Author
Maja Feierabend
Chalmers, Physics, Condensed Matter and Materials Theory
Optical fingerprint of non-covalently functionalized transition metal dichalcogenides
Journal of Physics Condensed Matter,;Vol. 29(2017)p. Article no 384003 -
Journal article
Proposal for dark exciton based chemical sensors
Nature Communications,;Vol. 8(2017)
Journal article
Molecule signatures in photoluminescence spectra of transition metal dichalcogenides
Physical Review Materials,;Vol. 2(2018)
Journal article
Impact of strain on the optical fingerprint of monolayer transition-metal dichalcogenides
Physical Review B,;Vol. 96(2017)
Journal article
Dark exciton based strain sensing in tungsten-based transition metal dichalcogenides
Physical Review B,;Vol. 99(2019)
Journal article
Optical fingerprint of bright and dark localized excitonic states in atomically thin 2D materials
Physical Chemistry Chemical Physics,;Vol. 21(2019)p. 26077-26083
Journal article
Brightening of spin- and momentum-dark excitons in transition metal dichalcogenides
2D Materials,;Vol. 8(2021)
Journal article
Interlayer exciton landscape in WS<inf>2</inf>/tetracene heterostructures
Nanoscale,;Vol. In Press(2022)
Journal article
Following graphene's promising path, atomically thin materials have gained enormous attention. This can be traced back to their unique properties: they are ultrathin, strong, flexible, transparent and
conductive at the same time. These properties simply appear by changing the dimension of the material from 3D to 2D.
Transition metal dichalcogenides (TMDs)
belong to this class of atomically thin materials, and they are especially interesting since they show a strong signal when illuminated with light. They are also very sensitive to changes in their surroundings, which makes them perfect candidates for sensor applications.
In this thesis, we have developed a theoretical model
to describe and externally tune the optical fingerprint of TMDs. In particular, we show that optically inaccessible, so-called dark, states play a crucial role. We find that dark states can be activated by molecules attached to the material's surface, resulting in a significantly altered optical fingerprint. This presents a huge potential for sensing of molecules.
Furthermore, we show that the optical fingerprint of dark states undergoes large changes
when the material is mechanically deformed, offering potential for pressure sensing devices. Finally, following the vision of "atomic lego", we show that in combination with an organic layer, the optical response of TMDs can be further tuned to be used in a wide range of
optoelectronic applications.
Areas of Advance
Nanoscience and Nanotechnology
Infrastructure
C3SE (Chalmers Centre for Computational Science and Engineering)
Subject Categories
Atom and Molecular Physics and Optics
Condensed Matter Physics
ISBN
978-91-7905-471-7
Doktorsavhandlingar vid Chalmers tekniska högskola. Ny serie: 4938
Publisher
Chalmers
PJ salen, Kemigården 1, Chalmers
Opponent: Dr. Andres Castellanos-Gomez, Materials Science Institute of Madrid, Spain