Electronic structure of dipeptides in the gas-phase and as an adsorbed monolayer. Issue 10 (22nd February 2018)

• Record Type: Journal Article
• Authors: Guo, Cunlan; Sarkar, Soumyajit; Refaely-Abramson, Sivan; Egger, David A.; Bendikov, Tatyana; Yonezawa, Keiichirou; Suda, Yosuke; Yamaguchi, Takuma; Pecht, Israel; Kera, Satoshi; Ueno, Nobuo; Sheves, Mordechai; Kronik, Leeor; Cahen, David
• Is Part Of: Physical chemistry chemical physics. Volume 20:Issue 10(2018)
• Page Start: 6860
• Page End: 6867
• Publication Date: 2018-02-22
• Subjects: Chemistry, Physical and theoretical -- Periodicals; 541.3
• DOI: 10.1039/c7cp08043c
• Languages: English
• ISSNs: 1463-9076

Abstract

Abstract : UPS and DFT reveal how frontier energy levels and molecular orbitals of peptides are modified upon peptide binding to a gold substrate. Abstract : Peptide-based molecular electronic devices are promising due to the large diversity and unique electronic properties of biomolecules. These electronic properties can change considerably with peptide structure, allowing diverse design possibilities. In this work, we explore the effect of the side-chain of the peptide on its electronic properties, by using both experimental and computational tools to detect the electronic energy levels of two model peptides. The peptides include 2Ala and 2Trp as well as their 3-mercaptopropionic acid linker which is used to form monolayers on an Au surface. Specifically, we compare experimental ultraviolet photoemission spectroscopy measurements with density functional theory based computational results. By analyzing differences in frontier energy levels and molecular orbitals between peptides in gas-phase and in a monolayer on gold, we find that the electronic properties of the peptide side-chain are maintained during binding of the peptide to the gold substrate. This indicates that the energy barrier for the peptide electron transport can be tuned by the amino acid compositions, which suggests a route for structural design of peptide-based electronic devices.