| Literature DB >> 29618210 |
Matthias Kettner1, Volodymyr V Maslyuk2, Daniel Nürenberg1, Johannes Seibel3, Rafael Gutierrez2, Gianaurelio Cuniberti2,4, Karl-Heinz Ernst3,5, Helmut Zacharias1.
Abstract
The interaction of low-energy photoelectrons with well-ordered monolayers of enantiopure helical heptahelicene molecules adsorbed on metal surfaces leads to a preferential transmission of one longitudinally polarized spin component, which is strongly coupled to the helical sense of the molecules. Heptahelicene, composed of only carbon and hydrogen atoms, exhibits only a single helical turn but shows excess in longitudinal spin polarization of about P Z = 6 to 8% after transmission of initially balanced left- and right-handed spin polarized electrons. Insight into the electronic structure, that is, the projected density of states, and the spin-dependent electron scattering in the helicene molecule is gained by using spin-resolved density functional theory calculations and a model Hamiltonian approach, respectively. Our results support the semiclassical picture of electronic transport along a helical pathway under the influence of spin-orbit coupling induced by the electrostatic molecular potential.Entities:
Year: 2018 PMID: 29618210 DOI: 10.1021/acs.jpclett.8b00208
Source DB: PubMed Journal: J Phys Chem Lett ISSN: 1948-7185 Impact factor: 6.475