4.7 Article

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

期刊

APPLIED SURFACE SCIENCE
卷 397, 期 -, 页码 1-12

出版社

ELSEVIER
DOI: 10.1016/j.apsusc.2016.11.016

关键词

Passivation; Self-assembled monolayer; Liquid phase; Alkanethiol; GaAs(100)

资金

  1. Intel Corporation

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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 (CnH2n+1-SH where n=3, 6, 12, 18, 20) and one alkanedithiol (HS-(CH2)(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 +/- 0.06 angstrom for each C atom in the chain and the surface density by 0.13 +/- 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 (CH2) 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 angstrom(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 2-4x for n =18 and 20 based on the C l s 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. (C) 2016 Elsevier B.V. All rights reserved.

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