TY - GEN A1 - Jay, Raphael J. A1 - Norell, Jesper A1 - Kunnus, Kristjan A1 - Lundberg, Marcus A1 - Gaffney, Kelly A1 - Wernet, Philippe A1 - Odelius, Michael A1 - Föhlisch, Alexander T1 - Dynamcis of local charge densities and metal-ligand covalency in iron complexes from femtosecond resonant inelastic soft X-ray scattering T2 - Abstracts of Papers of the American Chemical Society Y1 - 2018 U6 - http://nbn-resolving.de/urn/resolver.pl?urn:nbn:se:uu:diva-370051 SN - 0065-7727 VL - 256 PB - American Chemical Society CY - Washington ER - TY - JOUR A1 - Jay, Raphael M. A1 - Norell, Jesper A1 - Eckert, Sebastian A1 - Hantschmann, Markus A1 - Beye, Martin A1 - Kennedy, Brian A1 - Quevedo, Wilson A1 - Schlotter, William F. A1 - Dakovski, Georgi L. A1 - Minitti, Michael P. A1 - Hoffmann, Matthias C. A1 - Mitra, Ankush A1 - Moeller, Stefan P. A1 - Nordlund, Dennis A1 - Zhang, Wenkai A1 - Liang, Huiyang W. A1 - Kunnus, Kristian A1 - Kubicek, Katharina A1 - Techert, Simone A. A1 - Lundberg, Marcus A1 - Wernet, Philippe A1 - Gaffney, Kelly A1 - Odelius, Michael A1 - Föhlisch, Alexander T1 - Disentangling Transient Charge Density and Metal-Ligand Covalency in Photoexcited Ferricyanide with Femtosecond Resonant Inelastic Soft X-ray Scattering JF - The journal of physical chemistry letters N2 - Soft X-ray spectroscopies are ideal probes of the local valence electronic structure of photocatalytically active metal sites. Here, we apply the selectivity of time resolved resonant inelastic X-ray scattering at the iron L-edge to the transient charge distribution of an optically excited charge-transfer state in aqueous ferricyanide. Through comparison to steady-state spectra and quantum chemical calculations, the coupled effects of valence-shell closing and ligand-hole creation are experimentally and theoretically disentangled and described in terms of orbital occupancy, metal-ligand covalency, and ligand field splitting, thereby extending established steady-state concepts to the excited-state domain. pi-Back-donation is found to be mainly determined by the metal site occupation, whereas the ligand hole instead influences sigma-donation. Our results demonstrate how ultrafast resonant inelastic X-ray scattering can help characterize local charge distributions around catalytic metal centers in short-lived charge-transfer excited states, as a step toward future rationalization and tailoring of photocatalytic capabilities of transition-metal complexes. Y1 - 2018 U6 - https://doi.org/10.1021/acs.jpclett.8b01429 SN - 1948-7185 VL - 9 IS - 12 SP - 3538 EP - 3543 PB - American Chemical Society CY - Washington ER - TY - JOUR A1 - Vaz da Cruz, Vinicius A1 - Eckert, Sebastian A1 - Iannuzzi, Marcella A1 - Ertan, Emelie A1 - Pietzsch, Annette A1 - Couto, Rafael C. A1 - Niskanen, Johannes A1 - Fondell, Mattis A1 - Dantz, Marcus A1 - Schmitt, Thorsten A1 - Lu, Xingye A1 - McNally, Daniel A1 - Jay, Raphael Martin A1 - Kimberg, Victor A1 - Föhlisch, Alexander A1 - Odelius, Michael T1 - Probing hydrogen bond strength in liquid water by resonant inelastic X-ray scattering JF - Nature Communications N2 - Local probes of the electronic ground state are essential for understanding hydrogen bonding in aqueous environments. When tuned to the dissociative core-excited state at the O1s pre-edge of water, resonant inelastic X-ray scattering back to the electronic ground state exhibits a long vibrational progression due to ultrafast nuclear dynamics. We show how the coherent evolution of the OH bonds around the core-excited oxygen provides access to high vibrational levels in liquid water. The OH bonds stretch into the long-range part of the potential energy curve, which makes the X-ray probe more sensitive than infra-red spectroscopy to the local environment. We exploit this property to effectively probe hydrogen bond strength via the distribution of intramolecular OH potentials derived from measurements. In contrast, the dynamical splitting in the spectral feature of the lowest valence-excited state arises from the short-range part of the OH potential curve and is rather insensitive to hydrogen bonding. Y1 - 2019 U6 - https://doi.org/10.1038/s41467-019-08979-4 SN - 2041-1723 VL - 10 PB - Nature Publ. Group CY - London ER - TY - JOUR A1 - Eckert, Sebastian A1 - Norell, Jesper A1 - Jay, Raphael Martin A1 - Fondell, Mattis A1 - Mitzner, Rolf A1 - Odelius, Michael A1 - Föhlisch, Alexander T1 - T-1 Population as the Driver of Excited-State Proton-Transfer in 2-Thiopyridone JF - Chemistry - a European journal N2 - Excited-state proton transfer (ESPT) is a fundamental process in biomolecular photochemistry, but its underlying mediators often evade direct observation. We identify a distinct pathway for ESPT in aqueous 2-thiopyridone, by employing transient N1s X-ray absorption spectroscopy and multi-configurational spectrum simulations. Photoexcitations to the singlet S-2 and S-4 states both relax promptly through intersystem crossing to the triplet T-1 state. The T-1 state, through its rapid population and near nanosecond lifetime, mediates nitrogen site deprotonation by ESPT in a secondary intersystem crossing to the S-0 potential energy surface. This conclusively establishes a dominant ESPT pathway for the system in aqueous solution, which is also compatible with previous measurements in acetonitrile. Thereby, the hitherto open questions of the pathway for ESPT in the compound, including its possible dependence on excitation wavelength and choice of solvent, are resolved. KW - excited-state proton-transfer KW - intersystem crossing KW - nitrogen KW - photochemistry KW - X-ray absorption Y1 - 2019 U6 - https://doi.org/10.1002/chem.201804166 SN - 0947-6539 SN - 1521-3765 VL - 25 IS - 7 SP - 1733 EP - 1739 PB - Wiley-VCH CY - Weinheim ER - TY - GEN A1 - Norell, Jesper A1 - Jay, Raphael A1 - Hantschmann, Markus A1 - Eckert, Sebastian A1 - Guo, Meiyuan A1 - Gaffney, Kelly A1 - Wernet, Philippe A1 - Lundberg, Marcus A1 - Föhlisch, Alexander A1 - Odelius, Michael T1 - Fingerprints of electronic, spin and structural dynamics from resonant inelastic soft x-ray scattering in transient photo-chemical species T2 - Physical chemistry, chemical physics N2 - We describe how inversion symmetry separation of electronic state manifolds in resonant inelastic soft X-ray scattering (RIXS) can be applied to probe excited-state dynamics with compelling selectivity. In a case study of Fe L3-edge RIXS in the ferricyanide complex Fe(CN)63−, we demonstrate with multi-configurational restricted active space spectrum simulations how the information content of RIXS spectral fingerprints can be used to unambiguously separate species of different electronic configurations, spin multiplicities, and structures, with possible involvement in the decay dynamics of photo-excited ligand-to-metal charge-transfer. Specifically, we propose that this could be applied to confirm or reject the presence of a hitherto elusive transient Quartet species. Thus, RIXS offers a particular possibility to settle a recent controversy regarding the decay pathway, and we expect the technique to be similarly applicable in other model systems of photo-induced dynamics. Y1 - 2018 U6 - https://doi.org/10.1039/c7cp08326b SN - 1463-9084 IS - 20 SP - 7243 EP - 7253 PB - RSC Publ. CY - Cambridge ER - TY - JOUR A1 - Vaz da Cruz, Vinícius A1 - Ignatova, Nina A1 - Couto, Rafael A1 - Fedotov, Daniil A1 - Rehn, Dirk R. A1 - Savchenko, Viktoriia A1 - Norman, Patrick A1 - Ågren, Hans A1 - Polyutov, Sergey A1 - Niskanen, Johannes A1 - Eckert, Sebastian A1 - Jay, Raphael Martin A1 - Fondell, Mattis A1 - Schmitt, Thorsten A1 - Pietzsch, Annette A1 - Föhlisch, Alexander A1 - Odelius, Michael A1 - Kimberg, Victor A1 - Gel’mukhanov, Faris T1 - Nuclear dynamics in resonant inelastic X-ray scattering and X-ray absorption of methanol JF - The journal of chemical physics : bridges a gap between journals of physics and journals of chemistr N2 - We report on a combined theoretical and experimental study of core-excitation spectra of gas and liquid phase methanol as obtained with the use of X-ray absorption spectroscopy (XAS) and resonant inelastic X-ray scattering (RIXS). The electronic transitions are studied with computational methods that include strict and extended second-order algebraic diagrammatic construction [ADC(2) and ADC(2)-x], restricted active space second-order perturbation theory, and time-dependent density functional theory-providing a complete assignment of the near oxygen K-edge XAS. We show that multimode nuclear dynamics is of crucial importance for explaining the available experimental XAS and RIXS spectra. The multimode nuclear motion was considered in a recently developed "mixed representation" where dissociative states and highly excited vibrational modes are accurately treated with a time-dependent wave packet technique, while the remaining active vibrational modes are described using Franck-Condon amplitudes. Particular attention is paid to the polarization dependence of RIXS and the effects of the isotopic substitution on the RIXS profile in the case of dissociative core-excited states. Our approach predicts the splitting of the 2a RIXS peak to be due to an interplay between molecular and pseudo-atomic features arising in the course of transitions between dissociative core- and valence-excited states. The dynamical nature of the splitting of the 2a peak in RIXS of liquid methanol near pre-edge core excitation is shown. The theoretical results are in good agreement with our liquid phase measurements and gas phase experimental data available from the literature. (C) 2019 Author(s). Y1 - 2019 U6 - https://doi.org/10.1063/1.5092174 SN - 0021-9606 SN - 1089-7690 VL - 150 IS - 23 PB - American Institute of Physics CY - Melville ER - TY - GEN A1 - Norell, Jesper A1 - Jay, Raphael Martin A1 - Hantschmann, Markus A1 - Eckert, Sebastian A1 - Guo, Meiyuan A1 - Gaffney, Kelly J. A1 - Wernet, Philippe A1 - Lundberg, Marcus A1 - Föhlisch, Alexander A1 - Odelius, Michael T1 - Fingerprints of electronic, spin and structural dynamics from resonant inelastic soft X-ray scattering in transient photo-chemical species T2 - Postprints der Universität Potsdam Mathematisch-Naturwissenschaftliche Reihe N2 - We describe how inversion symmetry separation of electronic state manifolds in resonant inelastic soft X-ray scattering (RIXS) can be applied to probe excited-state dynamics with compelling selectivity. In a case study of Fe L-3-edge RIXS in the ferricyanide complex Fe(CN)(6)(3-), we demonstrate with multi-configurational restricted active space spectrum simulations how the information content of RIXS spectral fingerprints can be used to unambiguously separate species of different electronic configurations, spin multiplicities, and structures, with possible involvement in the decay dynamics of photo-excited ligand-to-metal charge-transfer. Specifically, we propose that this could be applied to confirm or reject the presence of a hitherto elusive transient Quartet species. Thus, RIXS offers a particular possibility to settle a recent controversy regarding the decay pathway, and we expect the technique to be similarly applicable in other model systems of photo-induced dynamics. T3 - Zweitveröffentlichungen der Universität Potsdam : Mathematisch-Naturwissenschaftliche Reihe - 779 KW - charge-transfer KW - relaxation dynamics KW - absorption-spectra KW - energy-conversion KW - basis-sets KW - ab-initio KW - complexes KW - photoelectron KW - spectroscopy KW - simulations Y1 - 2019 U6 - http://nbn-resolving.de/urn/resolver.pl?urn:nbn:de:kobv:517-opus4-437493 SN - 1866-8372 IS - 779 SP - 7243 EP - 7253 ER -