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Verfasst von:Asyuda, Andika [VerfasserIn]   i
 Das, Saunak [VerfasserIn]   i
 Zharnikov, Michael [VerfasserIn]   i
Titel:Thermal stability of alkanethiolate and aromatic thiolate self-assembled monolayers on Au(111)
Titelzusatz:an X-ray photoelectron spectroscopy study
Verf.angabe:Andika Asyuda, Saunak Das, and Michael Zharnikov
E-Jahr:2021
Jahr:September 28, 2021
Umfang:10 S.
Fussnoten:Gesehen am 18.11.2021
Titel Quelle:Enthalten in: The journal of physical chemistry <Washington, DC> / C
Ort Quelle:Washington, DC : Soc., 2007
Jahr Quelle:2021
Band/Heft Quelle:125(2021), 39, Seite 21754-21763
ISSN Quelle:1932-7455
Abstract:Applications of functional self-assembled monolayers (SAMs) rely to a large extent on their stability, with the thermal stability being of particular importance. In this context, thermal stability of archetypical, non-substituted alkanethiolate (AT) and aromatic thiolate (ArT) SAMs on gold was studied by synchrotron-based high-resolution X-ray photoelectron spectroscopy, taking several monolayers with different lengths of the molecular backbones as representative examples and heating them in UHV. Evaporated, grain-structured Au(111) was used as the support, in view of broad practical relevance of this substrate type. AT and ArT SAMs were found to be stable up to temperatures of ∼373 and ∼383-393 K, respectively, followed by extensive molecular desorption and decomposition upon further heating. The decomposition was mediated by the cleavage of C-S bonds, which represented the so-called “weak or weakest link” in the systems. This process contributed minorly to the temperature-induced degradation of AT SAMs but was the dominant degradation channel for the ArT case. The residual films exhibited ∼10% (AT) or ∼ 35% (ArT) of the initial packing density and represented a superposition of the laying-down phase and atomically adsorbed sulfur, with a possible coexistence of a restructured, standing-up phase in the ArT case.
DOI:doi:10.1021/acs.jpcc.1c06984
URL:Bitte beachten Sie: Dies ist ein Bibliographieeintrag. Ein Volltextzugriff für Mitglieder der Universität besteht hier nur, falls für die entsprechende Zeitschrift/den entsprechenden Sammelband ein Abonnement besteht oder es sich um einen OpenAccess-Titel handelt.

Volltext: https://doi.org/10.1021/acs.jpcc.1c06984
 DOI: https://doi.org/10.1021/acs.jpcc.1c06984
Datenträger:Online-Ressource
Sprache:eng
K10plus-PPN:1777930553
Verknüpfungen:→ Zeitschrift

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