Laboratory for Synchrotron Radiation and Femtochemistry (LSF)
Mission
We are at the forefront of method and instrumentation development for X-ray and VUV spectroscopy in the temporal and spatial domains to gain novel insights into the elemental composition, the chemical state, and reaction dynamics. In collaborations with Swiss and international scientists, we build upon these strengths to pursue state-of-the-art multidisciplinary research projects. We are competent partners for academic and industrial users.
Scientific Highlights
Operando X-ray diffraction during laser 3D printing
Ultra-fast operando X-ray diffraction experiments reveal the temporal evolution of low and high temperature phases and the formation of residual stresses during laser 3D printing of a Ti-6Al-4V alloy. The profound influence of the length of the laser-scanning vector on the evolving microstructure is revealed and elucidated.
Taking a snapshot of the triplet excited state of an OLED organometallic luminophore using X-rays
In this work, the complementarity of pump-probe experiments at SwissFEL (ALVRA endstation) and at synchrotrons (SuperXAS beamline of SLS and ID09 of ESRF) is used to investigate the triplet excited state of Cu OLED materials. Details about the charge transfer and structural rearrangements in the excited state of this material are revealed and obtained data can be used to verify computational methods for rational development of new OLED materials.
Elucidating the Oxygen Activation Mechanism on Ceria-Supported Copper-Oxo Species Using Time-Resolved X-ray Absorption Spectroscopy
We monitored the dynamic structure of the active sites in a catalyst containing highly dispersed copper-oxo species on ceria during low-temperature CO oxidation using time-resolved X-ray absorption spectroscopy. We quantitatively demonstrate that the CO oxidation mechanism below 90 °C involves an oxygen intermediate strongly bound to the active sites as well as the redox activity of Cu2+/Cu+ and Ce4+/Ce3+ couples.
Elucidating the mechanism of heterogeneous Wacker oxidation over Pd-Cu/zeolite Y by transient XAS
Unlike the homogeneous Wacker process, the understanding of the mechanism of the heterogeneous system has long remained to be superficial. Here the authors investigated the mechanism of heterogeneous Wacker oxidation over Pd-Cu/zeolite Y through transient XAS coupled with kinetic studies and chemometric analysis.
Spectroscopic disentanglement of the quantum states of highly excited dicopper molecules
Transition metals, characterized by their partially filled d-orbitals, provide the basis for many of the most relevant processes in chemistry, biology, and physics. Embedded as single atoms or in small clusters, they give rise to exceptional optical, chemical, and magnetic properties. So far, it has proven impossible to disentangle the complex network of excited quantum states, which greatly hinders predicting and controlling of material properties. We employed double-resonant four-wave mixing spectroscopy to quantitatively resolve the bright and perturbing dark quantum states of the neutral copper dimer.
Christoph Bostedt named APS Fellow
Christoph Bostedt, Head of the Laboratory for Femtochemistry, was named APS Felllow. He received his fellowship certificate at at the 50th Annual Meeting of the APS Division of Atomic, Molecular and Optical Physics (DAMOP) APS Meeting in Milwaukee.
HERCULES school 2019 at SLS
In the week of April 1-5 PSI welcomes 20 PhD students and postdocs taking part in the European HERCULES 2019 school on Neutron and Synchrotron Radiation. They will attend lectures and perform two days of practical courses at several beam lines of the Swiss Light Source.
Selective Alkane Functionalization to Olefins
Light alkanes are abundantly available and cheap resources that are often burned at oil wells because of the missing infrastructure for valorization. Novel technologies are needed for their selective functionalization to use natural gas as an energy vector in the transition between the oil and the renewables era. Catalytic oxyhalogenation may unlock the transformation of cheap and abundant alkanes into commodities. When chlorine-based reactions are compared with bromine, improved selectivities above an iron catalyst arise from surface-confinement of the reaction mechanism in the case of chlorine as halogen.
Investigation of anionic redox activities in organic-based electrode for Li-ion batteries
To date the electrochemical activity of battery materials was always relying in the oxidation/reduction of cationic redox (change of oxidation state of transition metals generally). However, recently, it was established in new cathode materials (so call Li-rich cathode) that the oxygen from the crystal lattice might also play the role of anionic redox center leading to enhance then the specific charge of battery materials.