How Contacting Electrodes Affect Single π-Conjugated Molecular Electronic States: Local Density of States of Phthalocyanine Nanomolecules on MgO(001), Cu(111), Ag(001), Fe(001), and Mn(001)

Abstract

Single molecules have attracted much interest as new materials for future spin electronic devices; however, many open questions still remain. One of them is how the electronic local density of states (LDOS) of single molecules is affected when they are in contact with electrodes. We show a systematic study of the LDOS of π-conjugated phthalocyanine (H2Pc) nanomolecules adsorbed on various electrodes, namely, (1) MgO(001) thin films grown on Ag(001), (2) noble metals of Cu(111) and Ag(001), and (3) 3d magnetic metals of Fe(001) and Mn(001), adupting scanning tunneling spectroscopy techniques with an ultrahigh-vacuum scanning tunneling microscopy setup at room temperature. Since MgO thin films cut the electronic coupling from the substrate Ag(001), we could observe H2Pc molecular states at -1.5 and +1.0 eV. H2Pc molecules on the noble metal substrates form a pattern with a square unit cell of about 1.5×1.5 nm2 and have similar LDOS peaks near the Fermi energy. Strong hybridizations between the substrate 3d spin-polarized states and the molecular π orbitals produce new molecular states of H2Pc molecules adsorbed on Fe(001) and Mn(001) near the energy positions of the Fe(001) minority spin state and the Mn(001) majority spin state, respectively.