Issue 10, 2011

Effect of the chemical composition on the work function of gold substrates modified by binary self-assembled monolayers

Abstract

This study demonstrated that the work function (Φ) of Au substrates can be fine-tuned by using series ratios of binary self-assembled monolayers (SAMs). By using pure amine- and carboxylic acid-bearing alkanethiol SAM on gold substrates, Φ of Au changed from 5.10 to 5.16 and 5.83, respectively, as determined by ultra-violet photoelectron spectrometry (UPS). The shift in Φ due to the use of different functional groups was rationalized by considering the dipole moments of the molecules anchored on the Au surface. A series of binary SAMs were fabricated by mixing carboxylic acid- and amine-terminated alkanethiols in the deposition solution. By mixing these functional groups in SAMs, a linear correlation between Φ with respect to chemical composition (hence the effective dipole moment on the Au surface) was observed. It was found that arbitrary Φ between extremes (5.16 and 5.83) controlled by respective functional groups can be obtained by changing the chemical composition of SAMs. The Scanning Kelvin Probe (SKP) was also used to measure the contact potential difference (CPD) between SAMs and referencing Au on a patterned substrate prepared by photo-lithography. It was found that the CPD of SAMs with different chemical compositions correlates to their Φ. However, the magnitude of the CPD was smaller than the difference in Φ measured by UPS that was possibly due to the adsorption of contaminants in air.

Graphical abstract: Effect of the chemical composition on the work function of gold substrates modified by binary self-assembled monolayers

Article information

Article type
Paper
Submitted
07 Nov 2010
Accepted
09 Dec 2010
First published
24 Jan 2011

Phys. Chem. Chem. Phys., 2011,13, 4335-4339

Effect of the chemical composition on the work function of gold substrates modified by binary self-assembled monolayers

S. Lee, W. Lin, C. Chang, C. Huang, C. Liu, C. Kuo, H. Chang, Y. You, W. Kao, G. Yen, D. Kuo, Y. Kuo, M. Tsai and J. Shyue, Phys. Chem. Chem. Phys., 2011, 13, 4335 DOI: 10.1039/C0CP02437F

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