Scanning Tunneling Microscopy (STM) has been used to study the physisorption and chemisorption behaviour for three simple organic haloalkanes; 1,5 Dichloropentane (DCP), Bromomethane (CH3Br) and Chloromethane (CH3Cl)) on Si(100) 2x1, at temperatures ranging from 270 K to room temperature. The results were interpreted by Density Functional Theory (DFT) performed by collaborators at McGill University and the University of Liverpool. Physisorbed molecules of DCP were found to self assemble into stable lines aligned predominantly perpendicular to the Si dimer pair rows on the surface. A novel mechanism for line formation of Dichloropentane, termed, Dipole Directed Assembly (DDA), was elucidated by DFT calculations. For CH3Br three different patterns of dissociative attachment of reaction products (CH3 and Br/Cl) were observed, and assigned to three reaction pathways. These experimentally determined relative yields were used to obtain differences in reaction activation energy, Delta Ea, between the reaction pathways. These, in turn, were compared with computed differences in reaction barriers, Delta Eb, obtained ab initio for the same pathways by DFT. For CH3Cl, two single-molecule patterns of attachment were found, and a new reaction pathway for attaching CH3Cl in long chains of alternating CH3 and Cl was discovered. The mechanisms for chain growth were determined experimentally by examination of single molecular steps. This mechanism was explained ab initio by DFT to be the result of relative barrier heights for the possible chain-growth pathways.
| Identifer | oai:union.ndltd.org:TORONTO/oai:tspace.library.utoronto.ca:1807/26288 |
| Date | 18 February 2011 |
| Creators | Lim, Tingbin |
| Contributors | Polanyi, John |
| Source Sets | University of Toronto |
| Language | en_ca |
| Detected Language | English |
| Type | Thesis |
Page generated in 0.0019 seconds