Indications of field-directing and self-templating effects on the formation of organic lines on silicon.

It has previously been shown that multimolecular organic nanostructures form on H-Si(100)-2×1 via a radical mediated growth process. In this mechanism, growth begins through the addition of a molecule to a silicon surface dangling bond, followed by the abstraction of a neighboring H atom and generation of a new dangling bond on the neighboring site. Nanostructures formed by this mechanism grow along one edge of a dimer row.

Self-directed growth of contiguous perpendicular molecular lines on H-Si(100) surfaces.

Future nanoscale integrated circuits will require the realization of interconnections using molecular-scale nanostructures; a practical fabrication scheme would need to be largely self-assembling and operate on a large number of like structures in parallel. The self-directed growth of organic molecules on hydrogen-terminated silicon(100) [H-Si(100)] offers a simple method of realizing one-dimensional molecular lines. In this work, we introduce the ability to change the growth direction and form more complex, contiguous shapes.

Theoretical and spectroscopic study of the reaction of diethylhydroxylamine on silicon(100)-2 x 1.

Incorporating diversity into structures constructed from the organic modification of silicon surfaces requires the use of molecules that contain multiple substituents of different types. In this work we examine the possible dissociation pathways of diethylhydroxylamine (DEHA, (C(2)H(5))(2)NOH) on the surface of clean silicon(100)-2x1 using cluster and planewave computational methods and high resolution electron energy loss spectroscopy. Our computational results show that DEHA initially forms a strongly-bound complex with the surface via a dative N-Si bond.

Field regulation of single-molecule conductivity by a charged surface atom.

Electrical transport through molecules has been much studied since it was proposed that individual molecules might behave like basic electronic devices, and intriguing single-molecule electronic effects have been demonstrated. But because transport properties are sensitive to structural variations on the atomic scale, further progress calls for detailed knowledge of how the functional properties of molecules depend on structural features. The characterization of two-terminal structures has become increasingly robust and reproducible, and for some systems detailed structural characterization of molecules on electrodes or insulators is available.