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Ultrafast electronic and nuclear dynamics in functional nano-materials and biosystems
Institute of Nanotechnology
Bldg. 640 Seminar room 0-167
Hermann-von-Helmholtz-Platz 1
76344 Eggenstein-Leopoldshafen
Talk given by
Prof. Stefan Haacke
Strasbourg University
CNRS-IPCMS
Strasbourg, France
Abstract:
The "Institut de Physique et Chimie des Matériaux de Strasbourg" (IPCMS, http://www.ipcms.unistra.fr/) is an interdisciplinary institute with a research profile combining fundamental physics and chemistry for new approaches in material science at the nanoscale. The talk will give a general overview of our research and outline more in detail a few emerging priority axes underscoring the interdisciplinary approach, and recent cutting-edge instrumental developments in the area of ultrafast spectroscopy and electron microscopy will be introduced.
In the second part, I will highlight two recent examples of topics under investigation in my research team. Using ultrafast UV-VIS spectroscopy we have made progress in understanding the molecular basis of the primary processes of vision and of primitive photo-synthesis at work in so-called retinal proteins [1]. It is well-known that these involve an ultrafast cis-trans photo-isomerization, but new information is now available as to how the protein environment steers this reaction in terms of speed and quantum efficiency [2]. A second example, is the development of new Fe(II) – N-heterocyclic carbene complexes with an enhanced ligand field splitting so as to avoid ultrafast spin crossover. As a result, these complexes display increased excited state lifetimes [3,4], which make them amenable to applications in solar cells and photo-catalysis.
References:
[1]"Ultrafast photo-induced reaction dynamics in bacteriorhodopsin and its Trp mutants", J. Briand, J. Léonard, and S. Haacke, J. Opt. 12 084004 (2010).
[2] "100 fs photo-isomerization with vibrational coherences but low quantum yield in Anabaena Sensory Rhodopsin", A. Cheminal, J. Léonard, S. Y. Kim, K.-H. Jung, H. Kandori, and S. Haacke, Phys. Chem. Chem. Phys., 17, 25429 – 25439 (2015).
[3] "An Iron-Based Photosensitizer with Extended Excited-State Lifetime: Photophysical and Photovoltaic Properties", T. Duchanois, T. Etienne, C. Cebrián, Li Liu, A. Monari, M. Beley, X. Assfeld, S. Haacke, P.C. Gros, Eur. J. Inorg. Chem. 14, 2469-2477 (2015).
[4] "A new record excited state 3MLCT lifetime for metalorganic Fe(II) complexes", L. Liu, T. Duchanois, T. Etienne, A. Monari, M. Beley, X. Assfeld, S. Haacke, P.C. Gros, Phys. Chem. Chem. Phys., 18, 12550-12556 (2016).
https://www.int.kit.edu/events.php
Prof. Stefan Haacke
Institut de Physique et de Chimie des Matériaux de Strasbourg
http://www.ipcms.unistra.fr/?page_id=7930
Prof. Mario Ruben
Institut für Nanotechnologie
KIT
Hermann-von-Helmholtz-Platz 1
76344 Eggenstein-Leopoldshafen
Mail: mario ruben ∂ kit edu
https://www.int.kit.edu/1938_mario.ruben.php
Interested / Everyone