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Verfasst von:Settele, Simon [VerfasserIn]   i
 Berger, Felix J. [VerfasserIn]   i
 Lindenthal, Sebastian [VerfasserIn]   i
 Zhao, Shen [VerfasserIn]   i
 El Yumin, Abdurrahman Ali [VerfasserIn]   i
 Zorn, Nicolas [VerfasserIn]   i
 Asyuda, Andika [VerfasserIn]   i
 Zharnikov, Michael [VerfasserIn]   i
 Högele, Alexander [VerfasserIn]   i
 Zaumseil, Jana [VerfasserIn]   i
Titel:Synthetic control over the binding configuration of luminescent sp3-defects in single-walled carbon nanotubes
Verf.angabe:Simon Settele, Felix J. Berger, Sebastian Lindenthal, Shen Zhao, Abdurrahman Ali El Yumin, Nicolas F. Zorn, Andika Asyuda, Michael Zharnikov, Alexander Högele & Jana Zaumseil
E-Jahr:2021
Jahr:09 April 2021
Umfang:10 S.
Fussnoten:Im Titel erscheint die Ziffer 3 hochgestellt ; Gesehen am 20.04.2021
Titel Quelle:Enthalten in: Nature Communications
Ort Quelle:[London] : Nature Publishing Group UK, 2010
Jahr Quelle:2021
Band/Heft Quelle:12(2021), Artikel-ID 2119, Seite 1-10
ISSN Quelle:2041-1723
Abstract:The controlled functionalization of single-walled carbon nanotubes with luminescent sp3-defects has created the potential to employ them as quantum-light sources in the near-infrared. For that, it is crucial to control their spectral diversity. The emission wavelength is determined by the binding configuration of the defects rather than the molecular structure of the attached groups. However, current functionalization methods produce a variety of binding configurations and thus emission wavelengths. We introduce a simple reaction protocol for the creation of only one type of luminescent defect in polymer-sorted (6,5) nanotubes, which is more red-shifted and exhibits longer photoluminescence lifetimes than the commonly obtained binding configurations. We demonstrate single-photon emission at room temperature and expand this functionalization to other polymer-wrapped nanotubes with emission further in the near-infrared. As the selectivity of the reaction with various aniline derivatives depends on the presence of an organic base we propose nucleophilic addition as the reaction mechanism.
DOI:doi:10.1038/s41467-021-22307-9
URL:kostenfrei: Volltext: https://doi.org/10.1038/s41467-021-22307-9
 kostenfrei: Volltext: https://www.nature.com/articles/s41467-021-22307-9
 DOI: https://doi.org/10.1038/s41467-021-22307-9
Datenträger:Online-Ressource
Sprache:eng
K10plus-PPN:1755474954
Verknüpfungen:→ Zeitschrift
 
 
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