Photoemission, resonant photoemission, and x-ray absorption of a Ru(II) complex adsorbed on rutile TiO2 (110) prepared by in situ electrospray deposition
Mayor, Louise C. ; Ben Taylor, J. ; Magnano, Graziano ; Rienzo, Anna ; Satterley, Christopher J. ; O'Shea, James N. and Schnadt, Joachim LU
(2008)
In Journal of Chemical Physics
129(11).
- Abstract
- An experimental study of the bonding geometry and electronic coupling of cis-bis(isothiocyanato)bis(2,2'-bipyridyl-4,4'-dicarboxylato)-ruthenium( II) (N3) adsorbed on rutile TiO2(110) is presented, along with supporting theoretical calculations of the bonding geometry. Samples were prepared in situ using ultrahigh vacuum electrospray deposition. Core-level photoemission spectroscopy was used to characterize the system and to deduce the nature of the molecule-surface bonding. Valence band photoemission and N 1s x-ray absorption spectra were aligned in a common binding energy scale to enable a quantitative analysis of the bandgap region. A consideration of the energetics in relation to optical absorption is used to identify the... (More)
- An experimental study of the bonding geometry and electronic coupling of cis-bis(isothiocyanato)bis(2,2'-bipyridyl-4,4'-dicarboxylato)-ruthenium( II) (N3) adsorbed on rutile TiO2(110) is presented, along with supporting theoretical calculations of the bonding geometry. Samples were prepared in situ using ultrahigh vacuum electrospray deposition. Core-level photoemission spectroscopy was used to characterize the system and to deduce the nature of the molecule-surface bonding. Valence band photoemission and N 1s x-ray absorption spectra were aligned in a common binding energy scale to enable a quantitative analysis of the bandgap region. A consideration of the energetics in relation to optical absorption is used to identify the photoexcitation channel between the highest occupied and lowest unoccupied molecular orbitals in this system, and also to quantify the relative binding energies of core and valence excitons. The core-hole clock implementation of resonant photoemission spectroscopy is used to reveal that electron delocalization from N3 occurs within 16 fs. (c) 2008 American Institute of Physics. [DOI: 10.1063/1.2975339] (Less)
Please use this url to cite or link to this publication:
https://lup.lub.lu.se/record/1285760
- author
- Mayor, Louise C.
; Ben Taylor, J.
; Magnano, Graziano
; Rienzo, Anna
; Satterley, Christopher J.
; O'Shea, James N.
and Schnadt, Joachim
LU
- organization
- publishing date
- 2008
- type
- Contribution to journal
- publication status
- published
- subject
- in
- Journal of Chemical Physics
- volume
- 129
- issue
- 11
- publisher
- American Institute of Physics (AIP)
- external identifiers
-
- wos:000259883900032
- scopus:52349093764
- pmid:19044974
- ISSN
- 0021-9606
- DOI
- 10.1063/1.2975339
- language
- English
- LU publication?
- yes
- id
- 844a145d-43ac-4992-84e2-89615a9d8aee (old id 1285760)
- date added to LUP
- 2016-04-01 12:17:22
- date last changed
- 2022-02-23 02:16:56
@article{844a145d-43ac-4992-84e2-89615a9d8aee,
abstract = {{An experimental study of the bonding geometry and electronic coupling of cis-bis(isothiocyanato)bis(2,2'-bipyridyl-4,4'-dicarboxylato)-ruthenium( II) (N3) adsorbed on rutile TiO2(110) is presented, along with supporting theoretical calculations of the bonding geometry. Samples were prepared in situ using ultrahigh vacuum electrospray deposition. Core-level photoemission spectroscopy was used to characterize the system and to deduce the nature of the molecule-surface bonding. Valence band photoemission and N 1s x-ray absorption spectra were aligned in a common binding energy scale to enable a quantitative analysis of the bandgap region. A consideration of the energetics in relation to optical absorption is used to identify the photoexcitation channel between the highest occupied and lowest unoccupied molecular orbitals in this system, and also to quantify the relative binding energies of core and valence excitons. The core-hole clock implementation of resonant photoemission spectroscopy is used to reveal that electron delocalization from N3 occurs within 16 fs. (c) 2008 American Institute of Physics. [DOI: 10.1063/1.2975339]}},
author = {{Mayor, Louise C. and Ben Taylor, J. and Magnano, Graziano and Rienzo, Anna and Satterley, Christopher J. and O'Shea, James N. and Schnadt, Joachim}},
issn = {{0021-9606}},
language = {{eng}},
number = {{11}},
publisher = {{American Institute of Physics (AIP)}},
series = {{Journal of Chemical Physics}},
title = {{Photoemission, resonant photoemission, and x-ray absorption of a Ru(II) complex adsorbed on rutile TiO2 (110) prepared by in situ electrospray deposition}},
url = {{http://dx.doi.org/10.1063/1.2975339}},
doi = {{10.1063/1.2975339}},
volume = {{129}},
year = {{2008}},
}