Spectroscopy and Structure of Diamondoid-Fullerene Hybrid Molecules at the Single-Molecule Level

ORAL

Abstract

Diamondoids---a nanometer-scale form of carbon sharing the \textit{sp}$^{3}$ bonding structure of bulk diamond---are promising new electronic and mechanical device elements and have recently become accessible to experiments. While new fields of research have also sprouted from carbon's \textit{sp}$^{2}$ forms (such as graphene, fullerenes, and carbon nanotubes), materials representing the intersection of \textit{sp}$^{2}$ and \textit{sp}$^{3}$ bonding structures are an exciting new arena for nanoscale science and technology. In this study, we investigate hybrid molecules fusing \textit{sp}$^{2}$ and \textit{sp}$^{3}$ allotropes of carbon (in the form of C$_{60}$ fullerenes and molecular diamondoids, respectively) into one well-defined system. We use low-temperature scanning tunneling microscopy to characterize monolayers and single molecules with sub-molecular resolution. We show the degree to which the electronic properties of the hybrid molecules differ from their single-allotrope components, and highlight the intriguing electronic features that emerge which have no analog in either of the separate molecular constituents.

*We thank S. Melinte for aiding measurements, and J. E. P. Dahl, R. M. Carlson, and P. R. Schreiner for materials and synthesis. We acknowledge support from DOE and the Chevron Corporation.

Authors

  • Jason C. Randel

  • Georges Ndabashimiye

  • Hari C. Manoharan

    • Stanford University