Chirality-Dependent Electron Spin Filtering by Molecular Monolayers of Helicenes

被引:187
作者
Kettner, Matthias [1 ,2 ]
Maslyuk, Volodymyr V. [3 ,4 ]
Nuerenberg, Daniel [1 ,2 ]
Seibel, Johannes [5 ]
Gutierrez, Rafael [3 ,4 ]
Cuniberti, Gianaurelio [3 ,4 ,6 ,7 ]
Ernst, Karl-Heinz [5 ,8 ]
Zacharias, Helmut [1 ,2 ]
机构
[1] Univ Munster, Ctr Soft Nanosci, D-48149 Munster, Germany
[2] Univ Munster, Phys Inst, D-48149 Munster, Germany
[3] Tech Univ Dresden, Inst Mat Sci, D-01062 Dresden, Germany
[4] Tech Univ Dresden, Max Bergmann Ctr Biomat, D-01062 Dresden, Germany
[5] Empa, Swiss Fed Labs Mat Sci & Technol, CH-8600 Dubendorf, Switzerland
[6] Tech Univ Dresden, Dresden Ctr Computat Mat Sci, D-01062 Dresden, Germany
[7] Tech Univ Dresden, Ctr Adv Elect Dresden, D-01062 Dresden, Germany
[8] Univ Zurich, Dept Chem, CH-8057 Zurich, Switzerland
基金
瑞士国家科学基金会;
关键词
SCATTERING;
D O I
10.1021/acs.jpclett.8b00208
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The interaction of low-energy photoelectrons with well-ordered mono layers 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 Pz = 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.
引用
收藏
页码:2025 / 2030
页数:11
相关论文
共 35 条
[1]   ENANTIOSELECTIVE SYNTHESIS USING CHIRAL HETEROGENEOUS CATALYSTS [J].
BLASER, HU .
TETRAHEDRON-ASYMMETRY, 1991, 2 (09) :843-866
[2]   Differential cross section for collisions between electrons and oriented chiral molecules [J].
Busalla, A ;
Blum, K ;
Thompson, DG .
PHYSICAL REVIEW LETTERS, 1999, 83 (08) :1562-1565
[3]   SPIN-DEPENDENT ELECTRON-SCATTERING FROM OPTICALLY-ACTIVE MOLECULES [J].
CAMPBELL, DM ;
FARAGO, PS .
NATURE, 1985, 318 (6041) :52-53
[4]   Anomalously Large Chiral Sensitivity in the Dissociative Electron Attachment of 10-Iodocamphor [J].
Dreiling, J. M. ;
Lewis, F. W. ;
Mills, J. D. ;
Gay, T. J. .
PHYSICAL REVIEW LETTERS, 2016, 116 (09)
[5]   Stereochemical Recognition of Helicenes on Metal Surfaces [J].
Ernst, Karl-Heinz .
ACCOUNTS OF CHEMICAL RESEARCH, 2016, 49 (06) :1182-1190
[6]   Two-dimensional separation of [7]helicene enantiomers on Cu(111) [J].
Ernst, KH ;
Kuster, Y ;
Fasel, R ;
Müller, M ;
Ellerbeck, U .
CHIRALITY, 2001, 13 (10) :675-678
[7]   ATTENUATION OF LONGITUDINALLY POLARIZED ELECTRON-BEAMS BY CHIRAL MOLECULES [J].
FANDREYER, R ;
THOMPSON, D ;
BLUM, K .
JOURNAL OF PHYSICS B-ATOMIC MOLECULAR AND OPTICAL PHYSICS, 1990, 23 (17) :3031-3040
[8]   Chirality transfer from single molecules into self-assembled monolayers [J].
Fasel, R ;
Parschau, M ;
Ernst, KH .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2003, 42 (42) :5178-5181
[9]   Orientation of chiral heptahelicene C30H18 on copper surfaces:: An x-ray photoelectron diffraction study [J].
Fasel, R ;
Cossy, A ;
Ernst, KH ;
Baumberger, F ;
Greber, T ;
Osterwalder, J .
JOURNAL OF CHEMICAL PHYSICS, 2001, 115 (02) :1020-1027
[10]   On-site approximation for spin-orbit coupling in linear combination of atomic orbitals density functional methods [J].
Fernandez-Seivane, L. ;
Oliveira, M. A. ;
Sanvito, S. ;
Ferrer, J. .
JOURNAL OF PHYSICS-CONDENSED MATTER, 2006, 18 (34) :7999-8013