Resonant lifetime of core-excited organic adsorbates from first principles

arXiv:1404.5595v1We investigate by first-principles simulations the resonant electron-transfer lifetime from the excited state of an organic adsorbate to a semiconductor surface, namely, isonicotinic acid on rutile TiO2(110). The molecule-substrate interaction is described using density functional theory, while the effect of a truly semi-infinite substrate is taken into account by Green's function techniques. Excitonic effects due to the presence of core-excited atoms in the molecule are shown to be instrumental to understand the electron-transfer times measured using the so-called core-hole-clock technique. In particular, for the isonicotinic acid on TiO2(110), we find that the charge injection from the LUMO is quenched, since this state lies within the substrate band gap. We compute the resonant charge-transfer times from LUMO+1 and LUMO+2, and systematically investigate the dependence of the elastic lifetimes of these states on the alignment among adsorbate and substrate states. © 2014 American Chemical Society.We acknowledge support from the MIUR of Italy through PRIN project DSSCX (no. 20104XET32). C.M. thanks CARIPLO Foundation for its support within the PCAM European Doctoral Programme and Pirelli Corimav for his Ph.D. scholarship. D.S.-P. acknowledges support from the Basque Departamento de Educación, UPV/EHU (Grant No. IT-366-07), the Spanish Ministerio de Ciencia e Innovación (Grant No. FIS2010- 19609-C02-02), the ETORTEK program funded by the Basque Departamento de Industria and the Diputación Foral de Guipuzcoa, the EU through the FP7 PAMS project, and the German DFG through SFB 1083.Peer Reviewe

ultrafast electron injection into photo excited organic molecules

State-of-the-art X-ray spectroscopy allows femtosecond gating of energy levels of photo-excited molecules on a metal substrate enabling ultrafast and bi-directional charge transfer across the interface with controllable dependence on the molecular adsorption geometry

Optical properties of shortest-width zig-zag silicene nano-ribbons : effects of local fields

We have computed from first principles the structural, magnetic and optical properties of zig-zag oriented silicene nanoribbons. The minimal width for structurally stable planar structure having zig-zag edges corresponds to a 4-chains ribbon. Its ground state presents reconstructed and spin polarized edges, coupled antiferromagnetically. For this state, and for the corresponding excited state with ferromagnetically coupled edges, we computed the optical absorption spectra within the independent particle approximation, including local field effect corrections, for light polarized in the directions parallel and perpendicular to the ribbon axis. For the \u201cparallel\u201d light polarization the inclusion of local fields effects is limited to a slight reduction of the intensity of the main peak in the infrared region, as well as that of some minor peaks in the visible-ultraviolet structure. Conversely, the computed optical spectrum for light polarized perpendicularly to the ribbon axis shows that the short-width zig-zag nanoribbons are basically transparent in the infrared and visible region, because of the effect of electronic confinement combined with local fields

Electronic structure and magnetism of strained bcc phases across the fcc to bcc transition in ultrathin Fe films

We investigated the electronic structure of the bcc metastable phases involved in the fcc to bcc transition of Fe. Ultrathin Fe films were grown on a 2-monolayer (ML) Ni/W(110) substrate, where a fcc lattice is stabilized at low Fe coverages and the transition proceeds through the formation of bcc nuclei showing a specific "Kurdjumov-Sachs" orientation with the substrate. A comprehensive description of the electronic structure evolution is achieved by combining spin-resolved UV photoemission spectroscopy and ab initio calculations. According to our results, an exchange-split band structure is observed starting from 2 ML of Fe, concomitant with the formation of ferromagnetic bcc nuclei. Continuous modifications are observed in the spin-resolved photoemission spectra for increasing Fe coverage, especially for what concerns the minority states, possibly indicative of the progressive relaxation of the strained bcc phase starting from the bcc/fcc interface

Effects of the introduction of a chromium oxide monolayer at the C60/Fe(001) interface

The introduction of a two-dimensional oxide layer at the interface between an organic semiconductor and a ferromagnetic metal (spinterface) can help in tailoring the formation of spin-polarized hybridized interface states. Here, we consider the case of a Cr4O5 monolayer at the C-60/Fe(001) interface, which is already known to feature the occurrence of spin-polarized states in the fullerene molecules. In this work, we employ scanning tunneling microscopy/spectroscopy and photoemission spectroscopy to show that the C-60/Cr4O5/Fe(001) spinterface is characterized by the formation of a well-ordered fullerene monolayer and of strongly hybridized interface states. These experimental results are discussed in terms of state-of-the-art ab lingo calculations of the structural, electronic, and magnetic properties at the interface

Fingerprints of sp1 Hybridized C in the near-edge X-ray absorption spectra of surface-grown materials

Carbon structures comprising sp1 chains (e.g., polyynes or cumulenes) can be synthesized by exploiting on-surface chemistry and molecular self-assembly of organic precursors, opening to the use of the full experimental and theoretical surface-science toolbox for their characterization. In particular, polarized near-edge X-ray absorption fine structure (NEXAFS) can be used to determine molecular adsorption angles and is here also suggested as a probe to discriminate sp1/sp2 character in the structures. We present an ab initio study of the polarized NEXAFS spectrum of model and real sp1/sp2 materials. Calculations are performed within density functional theory with plane waves and pseudopotentials, and spectra are computed by core-excited C potentials. We evaluate the dichroism in the spectrum for ideal carbynes and highlight the main differences relative to typical sp2 systems. We then consider a mixed polymer alternating sp1 C4 units with sp2 biphenyl groups, recently synthesized on Au(111), as well as other linear structures and two-dimensional networks, pointing out a spectral line shape specifically due to the the presence of linear C chains. Our study suggests that the measurements of polarized NEXAFS spectra could be used to distinctly fingerprint the presence of sp1 hybridization in surface-grown C structures

Quantum ESPRESSO: a modular and open-source software project for quantum simulations of materials

Quantum ESPRESSO is an integrated suite of computer codes for electronic-structure calculations and materials modeling, based on density-functional theory, plane waves, and pseudopotentials (norm-conserving, ultrasoft, and projector-augmented wave). Quantum ESPRESSO stands for "opEn Source Package for Research in Electronic Structure, Simulation, and Optimization". It is freely available to researchers around the world under the terms of the GNU General Public License. Quantum ESPRESSO builds upon newly-restructured electronic-structure codes that have been developed and tested by some of the original authors of novel electronic-structure algorithms and applied in the last twenty years by some of the leading materials modeling groups worldwide. Innovation and efficiency are still its main focus, with special attention paid to massively-parallel architectures, and a great effort being devoted to user friendliness. Quantum ESPRESSO is evolving towards a distribution of independent and inter-operable codes in the spirit of an open-source project, where researchers active in the field of electronic-structure calculations are encouraged to participate in the project by contributing their own codes or by implementing their own ideas into existing codes.Comment: 36 pages, 5 figures, resubmitted to J.Phys.: Condens. Matte