Hierarchical Self-Assembly and Conformation of Tb Double-Decker Molecular Magnets: Experiment and Molecular Dynamics

Nanostructures, fabricated by locating molecular building blocks in well-defined positions, for example, on a lattice, are ideal platforms for studying atomic-scale quantum effects. In this context, STM data obtained from self-assembled Bis(phthalocyaninato) Terbium (III) (TbPc2) single-molecule magnets on various substrates have raised questions about the conformation of the TbPc2 molecules within the lattice. In order to address this issue, molecular dynamics simulations were carried out on a 2D assembly of TbPc2 molecules. The calculations are in excellent agreement with the experiment, and thus improve our understanding of the self-assembly process. In particular, the calculated electron density of the molecular assembly compares well with STM contrast of self-assembled TbPc2 on Au(111), simultaneously providing the conformation of the two Pc ligands of the individual double-decker molecule. This approach proves valuable in the identification of the STM contrast of LnPc(2) layers and could be used in similar cases where it is difficult to interpret the STM images of an assembly of molecular complexes.

Automated summary

Nanostructures, created by precisely positioning molecular building blocks, are perfect for studying quantum effects at the atomic scale. The conformation of TbPc2 molecules within a lattice has been questioned based on STM data from self-assembled TbPc2 single-molecule magnets on different substrates. Molecular dynamics simulations of a 2D assembly of TbPc2 molecules were conducted to address this issue. The simulations agree well with experimental results, improving our understanding of the self-assembly process and providing valuable insights for interpreting STM images of molecular complexes.