dc.contributor.author
Guerrero-Felipe, Juan Pablo
dc.contributor.author
Valencia, Ana M.
dc.contributor.author
Cocchi, Caterina
dc.date.accessioned
2024-01-16T12:40:34Z
dc.date.available
2024-01-16T12:40:34Z
dc.identifier.uri
https://refubium.fu-berlin.de/handle/fub188/42051
dc.identifier.uri
http://dx.doi.org/10.17169/refubium-41776
dc.description.abstract
The adsorption of carbon-conjugated molecules represents an established route to tuning the electronic and optical properties of transition-metal dichalcogenide (TMDC) monolayers. Here, we demonstrate from first principles that such a functionalization with prototypical compounds pyrene and tetracene can also enhance the magnitude of selected plasmon resonances in a MoS2 single sheet without significantly altering their energy and dispersion. Our proof-of-principle results indicate that such a magnification can be achieved by the proper alignment of the molecules with respect to the direction of the transferred momentum. The distinct signatures in the loss function of the interface compared to those of its constituents suggest not only the presence of non-negligible interactions between them but also the possibility of using electron energy loss spectroscopy to detect the presence and the orientation of molecular adsorbates on TMDCs.
en
dc.format.extent
9 Seiten
dc.rights.uri
https://creativecommons.org/licenses/by/4.0/
dc.subject
Aromatic compounds
en
dc.subject
Electron energy loss spectroscopy
en
dc.subject
Hydrocarbons
en
dc.subject.ddc
500 Naturwissenschaften und Mathematik::530 Physik::530 Physik
dc.title
Magnification of Plasmon Resonances in Monolayer MoS2 via Conjugated Molecular Adsorbates
dc.type
Wissenschaftlicher Artikel
dcterms.bibliographicCitation.doi
10.1021/acs.jpcc.3c05923
dcterms.bibliographicCitation.journaltitle
The Journal of Physical Chemistry C
dcterms.bibliographicCitation.number
49
dcterms.bibliographicCitation.pagestart
23926
dcterms.bibliographicCitation.pageend
23934
dcterms.bibliographicCitation.volume
127
dcterms.bibliographicCitation.url
https://doi.org/10.1021/acs.jpcc.3c05923
refubium.affiliation
Physik
refubium.resourceType.isindependentpub
no
dcterms.accessRights.openaire
open access
dcterms.isPartOf.eissn
1932-7455
refubium.resourceType.provider
WoS-Alert