Electrodeposition of gold templated by patterned thiol monolayers
Date
15/06/2016Grant ID
EP/E061303/1
EP/I004602/1
EP/K031252/1
EP/K039210/1
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Abstract
The electrochemical deposition of Au onto Au substrates modified by self-assembled monolayers (SAMs) was studied by linear sweep voltammetry (LSV), atomic force microscopy (AFM) and scanning electron microscopy (SEM). Patterned SAMs exhibiting electrochemical contrast were prepared by two different methods. One used microcontact printing (μCP) to generate a binary SAM of ω-(4'-methyl-biphenyl-4-yl)-propane thiol (CH3-C6H4-C6H4-(CH2)3-SH, MBP3) and octadecane thiol (CH3(CH2)17SH, ODT). Templated by the SAM, a gold microelectrode structure was electrodeposited featuring a line 15 μm wide and 3 mm long. After transfer to an epoxy substrate the structure proved to be electrically conductive across the full length. The other patterning method applied electron beam lithography (EBL) where electrochemical contrast was achieved by crosslinking molecules in a single component SAM of MBP3. An electron dose above 250 mC/cm2 results in a high deposition contrast. The choice of parameters for the deposition/lift-off process is found to be more critical for Au compared to Cu studied previously. The origin of the differences and implications for nanoscale patterning are discussed.
Citation
She , Z , Di Falco , A , Hähner , G & Buck , M 2016 , ' Electrodeposition of gold templated by patterned thiol monolayers ' , Applied Surface Science , vol. 373 , pp. 51-60 . https://doi.org/10.1016/j.apsusc.2015.12.054
Publication
Applied Surface Science
Status
Peer reviewed
ISSN
0169-4332Type
Journal article
Rights
Copyright © 2015 Elsevier B.V. All rights reserved. This work is made available online in accordance with the publisher’s policies. This is the author created, accepted version manuscript following peer review and may differ slightly from the final published version. The final published version of this work is available at: https://dx.doi.org/10.1016/j.apsusc.2015.12.054
Description
The work was supported by EPSRC (EP/E061303/1 and EP/L017008/1). ADF acknowledges support from EPSRC (EP/I004602/1).Collections
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