• Haldar, Soumyajyoti
• Krueger, Anke
• Härtl, Patrick
• Christ, Andreas
• Heinze, Stefan
• Marder, Todd
• Leisegang, Markus
• Krebs, Johannes
• Toksabay, Sinem
• Bode, Matthias

Abstract

<jats:title>Abstract</jats:title><jats:p>The on‐surface self‐assembly of molecules to form holey nanographenes is a promising approach to control the properties of the resulting 2D lattice. Usually, planar molecules are utilized to prepare flat, structurally confined molecular layers, with only a few recent examples of warped precursors. However, control of the superstructures is limited thus far. Herein, we report the temperature‐controlled self‐assembly of a bowl‐shaped, acetylated <jats:italic>C</jats:italic><jats:sub>3</jats:sub>‐symmetric hexaphenyltribenzotriquinacene derivative on Cu(111). Combining scanning tunneling microscopy (STM) and density functional theory (DFT) confirms the formation of highly differing arrangements starting with π‐stacked bowl‐to‐bowl dimers at low coverage at room temperature via chiral honeycomb structures, an intermediate trigonal superstructure, followed by a fully carbon‐based, flattened hexagonal superstructure formed by on‐surface deacetylation, which is proposed as a precursor for holey graphene networks with unique defect structures.</jats:p>

Topics

• porous
• density
• impedance spectroscopy
• surface
• Carbon
• theory
• defect
• density functional theory
• defect structure
• scanning tunneling microscopy