AVS 59th Annual International Symposium and Exhibition
    Scanning Probe Microscopy Focus Topic Tuesday Sessions
       Session SP+AS+BI+ET+MI+NS-TuA

Paper SP+AS+BI+ET+MI+NS-TuA9
A Scanning Probe Microscopy Study of Trimesic Acid Self-Assembly on Highly Oriented Pyrolytic Graphite

Tuesday, October 30, 2012, 4:40 pm, Room 16

Session: Advances in Scanning Probe Imaging
Presenter: V. Korolkov, The University of Nottingham, UK
Authors: V. Korolkov, The University of Nottingham, UK
S. Allen, The University of Nottingham, UK
C.J. Roberts, The University of Nottingham, UK
S.J.B. Tendler, The University of Nottingham, UK
Correspondent: Click to Email

We have investigated trimesic acid (1,3,5-benzenetricarboxylic acid, TMA) adsorption on highly oriented pyrolytic graphite (HOPG) surfaces from aqueous medium at room temperature. Both atomic force (Peak Force Tapping mode) and scanning tunnelling microscopy were utilized to follow the adsorption dynamics and molecular arrangements. A chicken-wire arrangement for adsorbed molecules with an average pore size of 11 ± 1Å was established and observed using both scanning techniques. We found that this structure forms a monolayer within ~ 100 seconds of exposure of the HOPG surface to 50µM TMA solution in H2O. The monolayer structure was found to be stable for at least 48h under ambient conditions. STM was observed to lead to some desorption of TMA from a dynamically formed TMA film, and was only able to image the monolayer of TMA molecules in intimate contact with the HOPG. AFM revealed that TMA films formed using higher concentrations or longer adsorption times formed multilayers with similar molecular spacings and displayed an island growth morphology.
We have achieved an excellent resolution on an ambient running AFM. We have demonstrated that the combination of STM and AFM is essential, if not a must, to look at ultimate monolayers in the ambient conditions. Overall a facile green chemistry method for TMA monolayer fabrication from aqueous media on a HOPG surface has been established.