Publications by authors named "T Brixner"

Article Synopsis
  • - This text discusses methods to suppress unwanted background signals in coherent multidimensional spectroscopy, highlighting the use of phase-cycling techniques borrowed from NMR spectroscopy.
  • - It presents an overview of cogwheel phase cycling, which varies all pulse phases simultaneously in defined increments, and how it can improve the extraction of complex nonlinear signals compared to traditional nested phase cycling.
  • - The authors derive selection rules for detecting fourth-order signals and suggest numerical methods to optimize phase-cycling schemes, showing through experiments that cogwheel phase cycling often captures nonlinear signals more efficiently than nested methods.
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2,5-Bis(phenylethynyl) rhodacyclopentadienes (RCPDs), as a type of Rh(iii) complex, exhibit unusually intense fluorescence and slow intersystem crossing (ISC) due to weak metal-ligand interactions. However, details on their ultrafast photophysics and ISC dynamics are limited. In this work, electronic relaxation upon photoexcitation of two substituted RCPDs with two -COMe (A-RC-A) or -NMe/-COMe (D-RC-A) end groups are comprehensively investigated using femtosecond transient absorption spectroscopy and theoretical analysis.

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Charged molecules play essential roles in many natural and artificial functional processes, ranging from photosynthesis to photovoltaics to chemical reactions and more. It is often difficult to identify the optical dynamic properties of relevant redox species because they cannot be easily prepared, their spectra overlap, or they evolve on a femtosecond timescale. Here, we address these challenges by combining spectroelectrochemistry, ultrafast transient absorption spectroscopy, and suitable data analysis.

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Experimental and theoretical foundations for femtosecond time-resolved circular dichroism (TRCD) spectroscopy of excitonic systems are presented. In this method, the system is pumped with linearly polarized light and the signal is defined as the difference between the transient absorption spectrum probed with left and with right circularly polarized light. We present a new experimental setup with a polarization grating as key element to generate circularly polarized pulses.

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Transient absorption and coherent two-dimensional spectroscopy are widely established methods for the investigation of ultrafast dynamics in quantum systems. Conventionally, they are interpreted in the framework of perturbation theory at the third order of interaction. Here, we discuss the potential of higher-(than-third-)order pump-probe and multidimensional spectroscopy to provide insight into excited multiparticle states and their dynamics.

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