2023
DOI: 10.1039/d3sc01674a
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Time-resolved circular dichroism of excitonic systems: theory and experiment on an exemplary squaraine polymer

Abstract: 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...

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Cited by 6 publications
(5 citation statements)
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“…Such pump-induced LD can couple with stray LB of the optics before the sample, and transient contributions arising from this effect may overlap with the TrCD signal 42 . Indeed, this could be the reason why some of our previously recorded TrCD spectra employing a pump beam with linear polarisation for thin-film samples of opposite chirality did not resemble a perfect mirror symmetry 24 , despite the fact that they were carried out at the “magic angle” condition for TrCD spectroscopy 43 45 .…”
Section: Resultsmentioning
confidence: 98%
“…Such pump-induced LD can couple with stray LB of the optics before the sample, and transient contributions arising from this effect may overlap with the TrCD signal 42 . Indeed, this could be the reason why some of our previously recorded TrCD spectra employing a pump beam with linear polarisation for thin-film samples of opposite chirality did not resemble a perfect mirror symmetry 24 , despite the fact that they were carried out at the “magic angle” condition for TrCD spectroscopy 43 45 .…”
Section: Resultsmentioning
confidence: 98%
“…An exact treatment of the response of the system requires consideration of contributions from all elements of the density matrix. However, for delay times longer than vibrational relaxation, it is reasonable to ignore the response contributions of coherences and compute only the sequential contribution to the signal, as customarily done. …”
Section: Methods and Computational Detailsmentioning
confidence: 99%
“…47 Furthermore, we neglect the coherent term of the response, and compute only the sequential term, which is related to population evolution during the waiting time t 2 . 47 This approximation has been commonly used for TA simulations of multichromophoric systems, 9,11,13,46,48 and corresponds to assuming that vibrational relaxation is much faster than the delay time t 2 between the pump and the probe. 46 The third-order transient absorption signal at a probe frequency ω can be expressed as a sum of ground-state bleaching (GSB), stimulated emission (SE), and excited-state absorption (ESA):…”
Section: Transient Absorption Spectramentioning
confidence: 99%
“…The window response functions for each exciton can be written directly in the frequency domain, where we ignore the pulse shape for the probe pulse. The doorway population of exciton a created by the pump pulse is determined by the overlap between the pump and the absorption spectrum of exciton a 48,49 :…”
Section: Transient Absorption Spectramentioning
confidence: 99%