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    Self-assembly of alkanethiolates directs sulfur bonding with GaAs(100)

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    Author
    Mancheno-Posse, Pablo
    Muscat, Anthony J. cc
    Affiliation
    Department of Chemical and Environmental Engineering, University of Arizona
    Issue Date
    2017-04-06
    Keywords
    Passivation
    Self-assembled monolayer
    Liquid phase
    Alkanethiol
    GaAs(100)
    
    Metadata
    Show full item record
    Publisher
    Elsevier
    Citation
    Mancheno-Posso, P., & Muscat, A. J. (2017). Self-assembly of alkanethiolates directs sulfur bonding with GaAs (100). Applied Surface Science, 397, 1-12.
    Journal
    Applied Surface Science
    Rights
    © 2016 Elsevier B.V. All rights reserved.
    Collection Information
    This item from the UA Faculty Publications collection is made available by the University of Arizona with support from the University of Arizona Libraries. If you have questions, please contact us at repository@u.library.arizona.edu.
    Abstract
    Molecules that contain linear alkane chains self-assemble on a variety of surfaces changing the degree of wetting, lubricity, and reactivity. We report on the reoxidation of GaAs(100) in air after adsorbing five alkanethiols (C$_n$H$_{2n+1}$-SH where $n=$ 3, 6, 12, 18, 20) and one alkanedithiol (HS-(CH$_2$)$_8$-SH) deposited from the liquid phase. The alignment of the alkane chains forms a self-assembled layer, however, air diffuses readily through the carbon layer and reaches the surface. The impact of alignment is to improve the bonding of sulfur with the surface atoms which reduces the oxidation rate based on fitting the data to a reaction-diffusion model. The layer thickness and molecular density scale linearly with the number of carbon atoms in the alkane chain. The thickness of the alkanethiolate (RS$^{-}$) layer grows by $0.87 \pm 0.06$ {\AA} for each C atom in the chain and the surface density by $0.13 \pm 0.03$ molecule per nm$^2$ per C atom up to a coverage of 5.0 molecules/nm$^2$ for $n=20$ or 0.8 monolayer. The surface coverage increases with length because interactions between methylene (CH$_2$) groups in neighboring chains reduce the tilt angle of the molecules with the surface normal. The tight packing yields areas per alkanethiolate as low as 20 \AA$^2$ for $n=20$. The amount of C in the layer divided by the chain length is approximately constant up to $n=12$ but increases sharply by a factor of 2-4$\times$ for $n=18$ and 20 based on the C 1s x-ray photoelectron spectroscopy (XPS) peak. Fourier transform infrared (FTIR) spectroscopy shows that the asymmetric methylene stretch shifts continuously to lower wavenumber and the relative peak area increases sharply with the length of the alkane chain. Fitting the data to a reaction-diffusion model shows that for times less than 30 min the surface oxide coverage does not depend on the thickness of the self-assembled layer nor the diffusivity of oxygen through the layer. Instead increasing the layer thickness makes more S available for bonding with the predominately As termination and reduces the rate coefficient for reaction of oxygen with the GaAs surface.
    Note
    24 month Embargo; Available online 9 November 2016
    DOI
    10.1016/j.apsusc.2016.11.016
    Version
    Final accepted manuscript
    Sponsors
    Intel Corporation
    Additional Links
    http://dx.doi.org/10.1016/j.apsusc.2016.11.016
    ae974a485f413a2113503eed53cd6c53
    10.1016/j.apsusc.2016.11.016
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