Journal Article FZJ-2018-06101

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Ultra-High Vacuum Deposition of Pyrene Molecules on Metal Surfaces

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2018
Wiley-VCH Weinheim

Physica status solidi / B 255(10), 1800235 () [10.1002/pssb.201800235]

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Abstract: Interfacial properties of organic adsorbates featuring aromatic π‐orbitals on metal surfaces play an important role for organic electronics and spintronics. Pyrene is a flat aromatic molecule with a size between ultimately small benzene and extended graphene segments. The deposition of pyrene molecules onto clean and reactive surfaces with a sub‐monolayer coverage under ultra‐high vacuum (UHV) conditions is challenging, since pyrene is a solid with a high vapor pressure. Here, a sublimation procedure under UHV and image pyrene adlayers on in situ prepared Au(111) and Fe/W(110) substrates by means of low‐temperature scanning tunneling microscopy is presented. For Au(111), the molecule–surface interaction is weak as indicated by the specific herringbone reconstruction of the Au(111) surface that is visible through the self‐assembled pyrene adlayer. Pyrene desorption due to weak intermolecular interaction self‐limits the growth to one monolayer (ML). On the more reactive 2–4 ML thick Fe films on W(110), the molecular order of the pyrene adlayer sensitively depends on the Fe thickness‐dependent dislocation pattern at the substrate surface. Irregular arrangements occur for 1 ML Fe and near substrate dislocations for 2–4 ML Fe. Self‐assembled ordered arrays form predominantly for 2 ML Fe, where the dislocation pattern leaves sufficiently large unperturbed areas between the dislocation lines.

Classification:

Contributing Institute(s):
  1. Elektronische Eigenschaften (PGI-6)
  2. JARA-FIT (JARA-FIT)
Research Program(s):
  1. 522 - Controlling Spin-Based Phenomena (POF3-522) (POF3-522)

Appears in the scientific report 2018
Database coverage:
Embargoed OpenAccess ; Current Contents - Physical, Chemical and Earth Sciences ; IF < 5 ; JCR ; SCOPUS ; Science Citation Index ; Science Citation Index Expanded ; Thomson Reuters Master Journal List ; Web of Science Core Collection
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Open Access

 Datensatz erzeugt am 2018-10-29, letzte Änderung am 2021-01-29


Published on 2018-09-09. Available in OpenAccess from 2019-09-09.:
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