Abstract
Graphene nanoribbons (GNRs) of precise size and shape, critical for controlling electronic properties and future device applications, can be realized via precision synthesis on surfaces using rationally designed molecular precursors. Fluorine-bearing precursors have the potential to form GNRs on nonmetallic substrates suitable for device fabrication. Here, we investigate the deposition temperature-mediated growth of a new fluorine-bearing precursor, 6,11-diiodo-1,4-bis(2-fluorophenyl)-2,3-diphenyltriphenylene (C42H24F2I2), into helically shaped polymer intermediates and chevron-type GNRs on Au(111) by combining scanning tunneling microscopy, X-ray photoelectron spectroscopy, and density functional theory simulations. The fluorinated precursors do not adsorb on the Au(111) surface at lower temperatures, necessitating an optimum substrate temperature to achieve maximum polymer and GNR lengths. We compare the adsorption behavior with that of pristine chevron precursors and discuss the effects of C-H and C-F bonds. The results elucidate the growth mechanism of GNRs with fluorine-bearing precursors and establish a foundation for future synthesis of GNRs on nonmetallic substrates. (Figure presented.)
Original language | English |
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Article number | 193 |
Journal | Communications Chemistry |
Volume | 7 |
Issue number | 1 |
DOIs | |
State | Published - Dec 2024 |
Funding
This research was conducted at the Center for Nanophase Materials Sciences (CNMS), which is a DOE Office of Science User Facility. The electronic characterization was funded by ONR grants N00014-10-1-2302. The synthesis of the GNR precursors was supported by the ONR via N00014-19-1-2596. The supercomputer time was provided by DOE at the Oak Ridge Leadership Computing Facility and at the National Energy Research Scientific Computing Center (Contract No. DE-AC02-05CH11231 using NERSC award BES-ERCAP0027465).