AVS 54th International Symposium
    Tribology Thursday Sessions
       Session TR2+BI+NS+MN-ThM

Paper TR2+BI+NS+MN-ThM2
Correlation between XPS Data and Liquid Phase Self-Assembly of Alkanethiols

Thursday, October 18, 2007, 8:20 am, Room 617

Session: Biolubrication, Sensing and Adhesion
Presenter: H.M. Meyer III, Oak Ridge National Laboratory
Authors: H.M. Meyer III, Oak Ridge National Laboratory
T.G. Thundat, Oak Ridge National Laboratory
R. Desikan, Oak Ridge National Laboratory
R.G. White, Thermo Fisher Scientific, UK
Correspondent: Click to Email

The relative ease in which self-assembled monolayers (SAM) can be applied have made them part of the standard tool set used for functionalizing and patterning surfaces at the nanoscale. Recently, alkanethiol-based SAMs have been used for immobilizing selective chemical receptors on the gold-coated side of a microcantilever. In this configuration, adsorption on the funtionalized side of the microcantilever generates nanomechanical motion (i.e. bending) which can be accurately sensed and used for detecting a variety of chemical and biological molecules. Achieving reliable selectivity and sensitivity depends primarily on the reproducible formation of the functional layer on one side of the microcantilever. We have recently investigated the effect of chain length on the packing density of the alkanethiols and, in turn, how this affects the sensitivity of the sensor. We present XPS characterization of microfabricated cantilevers functionalized with alkanethiol-based SAMs. The results are correlated with similar cantilevers that have been monitored during adsorption/immobilization of the same alkanethiols in the liquid phase. Previous liquid phase results indicated an unusual change in packing density of the thiol molecules as the chain length was increased and were difficult to correlate with preliminary XPS data, indicating major difference between how these films form in liquid phase vs. post-formation analysis in-vacuuo. These new results attempt to illuminate those differences. Research sponsored in part by grant NSF Award ID 0330410 in collaboration with Drs. V.P. Dravid, G. Shekhawat, and A. Majumdar and in part by the Assistant Secretary for Energy Efficiency and Renewable Energy, Office of FreedomCAR and Vehicle Technologies, as part of the High Temperature Materials Laboratory User Program, Oak Ridge National Laboratory, managed by UT-Battelle, LLC, for the U.S. Department of Energy under contract number DE-AC05-00OR22725.