Direct measurement of the local field within alkyl-ferrocenylalkanethiolate monolayers: Importance of the supramolecular and electronic structure on the voltammetric response and potential profile
posted on 2019-05-16, 11:33authored byThorin J. Duffin, Nisachol Nerngchamnong, Damien ThompsonDamien Thompson, Christian A. Nijhuis
This paper describes the electrochemical behaviour of self-assembled monolayers (SAMs) of n-alkanethiolates
with Fc groups inserted at 14 different positions along the alkyl chain (SCnFcC13-n, n ¼ 0e13)
studied by cyclic voltammetry. The electronic and supramolecular structures of the SAMs have been fully
characterised and all molecules are standing up, allowing for precise control over the position of the Fc
unit within the SAM as a function of n revealing the shape of the electrostatic potential profile across the
SAMs. The potential profile is highly non-linear due to electronic changes in the nature of the
Fcdelectrode interaction for small values of n < 5, and supramolecular changes for large values of n ¼ 11
e13. For intermediate values of n ¼ 5e11, the potential drop is linear and the data can be fitted to a model
developed by White and Smith. The electrochemical behaviour was dominated by a one-step reversible
redox-process, but the presence of a shoulder indicates that the Fc units are present in different microenvironments
resulting from the mismatch in size between the Fc units and the alkyl chains. Other
features, including peak splitting, peak broadening, and peak shifts, can be related to changes in the
electronic and supramolecular structure of the SAM revealed by molecular dynamics simulations and
spectroscopy. For small values of n < 5, electronic effects dominate and the peak oxidation waves are
shifted anodically (~150 mV) and broadened (full width at half maximum of up to 220 mV) because the
Fc units hybridise with the Au electrode (for n < 3) or interact with the Au electrode via van der Waals
interactions (n ¼ 4, 5). For intermediate values of n ¼ 5e11, supramolecular effects direct the packing
structure of the SAMs and clear odd-even effects are observed. For large values of n ¼ 11e13, the top alkyl
chains are liquid-like in character and do not block the Fc units from the electrolyte.
History
Publication
Electrochimica Acta;311,pp. 92-102
Publisher
Elsevier Ltd
Note
peer-reviewed
Other Funding information
SFI, National Research Foundation Prime Minister's Office of Singapore, HEA, Ministry of Education (MOE)