Materials Map

Discover the materials research landscape. Find experts, partners, networks.

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The Materials Map is an open tool for improving networking and interdisciplinary exchange within materials research. It enables cross-database search for cooperation and network partners and discovering of the research landscape.

The dashboard provides detailed information about the selected scientist, e.g. publications. The dashboard can be filtered and shows the relationship to co-authors in different diagrams. In addition, a link is provided to find contact information.

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The Materials Map is still under development. In its current state, it is only based on one single data source and, thus, incomplete and contains duplicates. We are working on incorporating new open data sources like ORCID to improve the quality and the timeliness of our data. We will update Materials Map as soon as possible and kindly ask for your patience.

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Wigner Research Centre for Physics

in Cooperation with on an Cooperation-Score of 37%

Topics

Publications (5/5 displayed)

  • 2024Nonadiabatic Charge Transfer within Photoexcited Nickel Porphyrinscitations
  • 2024Nonadiabatic Charge Transfer within Photoexcited Nickel Porphyrins4citations
  • 2020Vibrational wavepacket dynamics in Fe carbene photosensitizer determined with femtosecond X-ray emission and scattering102citations
  • 2019Simulation of ultrafast excited-state dynamics and elastic x-ray scattering by quantum wavepacket dynamics19citations
  • 2017Probing Transient Valence Orbital Changes with Picosecond Valence-to-Core X-ray Emission Spectroscopy28citations

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Co-Authors (by relevance)

  • Canton, Sophie E.
  • Meng, Jie
  • Abdellah, Mohamed
  • Pan, Qinying
  • Qingyu, Kong
  • Bressler, Christian
  • Paveliuc, Gheorghe
  • Zheng, Kaibo
  • Khakhulin, Dmitry
  • Kubicek, Katharina
  • Akter, Marufa
  • Lima, Frederico Alves
  • Zalden, Peter
  • Gawelda, Wojciech
  • Kalinko, Aleksandr
  • Lawson Daku, Latévi Max
  • Retegan, Marius
  • Biednov, Mykola
  • Rahaman, Ahibur
  • Naumova, Maria
  • Geng, Huifang
  • Lin, Weihua
  • Németh, Zoltán
  • Vankó, György
  • Nielsen, Martin Meedom
  • Penfold, Thomas J.
  • Rozgonyi, Tamás
  • Møller, Klaus Braagaard
  • Doumy, Gilles
  • March, Anne Marie
  • Harder, Manuel
  • Diez, Michael
  • Assefa, Tadesse A.
  • Britz, Alexander
  • Yavas, Hasan
  • Southworth, Stephen H.
  • Schulz, Sebastian
  • Young, Linda
  • Galler, Andreas
  • Boemer, Christina
OrganizationsLocationPeople

article

Simulation of ultrafast excited-state dynamics and elastic x-ray scattering by quantum wavepacket dynamics

  • Pápai, Mátyás Imre
  • Penfold, Thomas J.
  • Rozgonyi, Tamás
  • Møller, Klaus Braagaard
  • Nielsen, Martin Meedom
Abstract

Simulation of the ultrafast excited-state dynamics and elastic X-ray scattering of the [Fe(bmip)<sub>2</sub>]<sup>2+</sup> [bmip = 2,6-bis(3-methyl-imidazole-1-ylidine)-4-pyridine] complex is presented and analyzed. We employ quantum wavepacket dynamics simulations on a 5-dimensional potential energy surface (PES) calculated by time-dependent density functional theory with 26 coupled diabatic states. The simulations are initiated by explicit inclusion of a time-dependent electromagnetic field. In the case of resonant excitation into singlet metal-to-ligand charge transfer (<sup>1</sup>MLCT) states, kinetic (exponential) population dynamics are observed with small nuclear motion. In agreement with transient optical absorption spectroscopy experiments, we observe a subpicosecond <sup>1</sup>MLCT → <sup>3</sup>MLCT intersystem crossing and a subsequent decay into triplet metal-centered (<sup>3</sup>MC) states on a picosecond time scale. The simulated time-resolved difference scattering signal is dominated by the <sup>3</sup>MC component, for which the structural distortions are significant. On the other hand, excitation into <sup>1</sup>MC states leads to ballistic (nonexponential) population dynamics with strong nuclear motion. The reason for these ballistic dynamics is that in this case, the excitation occurs into a nonequilibrium region, i.e., far from the minimum of the <sup>1</sup>MC PES. This results in wavepacket dynamics along the principal breathing mode, which is clearly visible in both the population dynamics and difference scattering. Finally, the importance of decomposing the difference scattering into components by electronic states is highlighted, information which is not accessible from elastic X-ray scattering experiments.

Topics
  • density
  • impedance spectroscopy
  • surface
  • inclusion
  • theory
  • experiment
  • simulation
  • density functional theory
  • photoelectron spectroscopy
  • X-ray scattering