Issue 32, 2024

Novel mixed self-assembled monolayers of l-cysteine and methanol on gold surfaces under ambient conditions

Abstract

In this work, we carried out an experimental and theoretical study on the formation of self-assembled monolayers of L-cysteine molecules on gold surfaces in the presence of methanol as a solvent. We report for the first time L-cysteine and methanol ordered structures forming a mixed self-assembled mono-layer on Au(100) surfaces under ambient conditions. Finger-like ordered structures with a relative height of 0.10–0.20 nm, average width of 2.0 nm and variable lengths were observed using scanning tunneling microscopy under room temperature and ambient pressure conditions. Using X-ray photoemission spectroscopy, it was determined that L-cysteine molecules bind to the gold surface through the sulfur atom of their thiol group in two molecular configurations: neutral and zwitterionic. We found that the finger-like structures are the result of complex interactions of L-cysteine molecules with gold surfaces and L-cysteine molecules with methanol molecules and among all three components of the system (L-cysteine + methanol + gold surfaces). These interactions were detected through attenuated total reflectance-Fourier transform infrared spectroscopy. Furthermore, adsorbate/substrate interactions were studied by employing ab initio calculations using density functional theory, resulting in molecular arrangements formed by chains of L-cysteine pairs surrounded by physisorbed methanol molecules.

Graphical abstract: Novel mixed self-assembled monolayers of l-cysteine and methanol on gold surfaces under ambient conditions

Supplementary files

Article information

Article type
Paper
Submitted
29 Apr 2024
Accepted
11 Jul 2024
First published
18 Jul 2024

Nanoscale, 2024,16, 15366-15380

Novel mixed self-assembled monolayers of L-cysteine and methanol on gold surfaces under ambient conditions

V. G. Franco, S. J. Rodríguez, F. C. Calaza, M. C. G. Passeggi and G. D. Ruano, Nanoscale, 2024, 16, 15366 DOI: 10.1039/D4NR01848F

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