Colloidal 2D Mo1−xWxS2 nanosheets
an atomic- to ensemble-level spectroscopic study
- verfasst von
- Markus Fröhlich, Marco Kögel, Jonas Hiller, Leo Kahlmeyer, Alfred J. Meixner, Marcus Scheele, Jannika Lauth, Jannik C. Meyer
- Abstract
Composition dependent tuning of electronic and optical properties in semiconducting two-dimensional (2D) transition metal dichalcogenide (TMDC) alloys is promising for tailoring the materials for optoelectronics. Here, we report a solution-based synthesis suitable to obtain predominantly monolayered 2D semiconducting Mo1−xWxS2 nanosheets (NSs) with controlled composition as substrate-free colloidal inks. Atomic-level structural analysis by high-angle annular dark-field (HAADF) scanning transmission electron microscopy (STEM) coupled with energy dispersive X-ray spectroscopy (EDXS) depicts the distribution of individual atoms within the Mo1−xWxS2 NSs and reveals the tendency for domain formation, especially at low molar tungsten fractions. These domains cause a broadening in the associated ensemble-level Raman spectra, confirming the extrapolation of the structural information from the microscopic scale to the properties of the entire sample. A characterization of the Mo1−xWxS2 NSs by steady-state optical spectroscopy shows that a band gap tuning in the range of 1.89-2.02 eV (614-655 nm) and a spin-orbit coupling-related exciton splitting of 0.16-0.38 eV can be achieved, which renders colloidal methods viable for upscaling low cost synthetic approaches toward application-taylored colloidal TMDCs.
- Organisationseinheit(en)
-
PhoenixD: Simulation, Fabrikation und Anwendung optischer Systeme
- Externe Organisation(en)
-
Eberhard Karls Universität Tübingen
- Typ
- Artikel
- Journal
- Physical Chemistry Chemical Physics
- Band
- 26
- Seiten
- 13271-13278
- Anzahl der Seiten
- 8
- ISSN
- 1463-9076
- Publikationsdatum
- 2024
- Publikationsstatus
- Veröffentlicht
- Peer-reviewed
- Ja
- ASJC Scopus Sachgebiete
- Physik und Astronomie (insg.), Physikalische und Theoretische Chemie
- Elektronische Version(en)
-
https://doi.org/10.1039/d4cp00530a (Zugang:
Offen)