Measurements of the electronic circular dichroism (CD) are highly sensitive to the absolute configuration and conformation of chiral molecules and supramolecular assemblies and have therefore found widespread application in the chemical and biological sciences. Here, we demonstrate an approach to simultaneously follow changes in the CD and absorption response of photoexcited systems over the ultraviolet−visible spectral range with 100 fs time resolution. We apply the concept to chiral polyfluorene copolymer thin films and track their electronic relaxation in detail. The transient CD signal stems from the supramolecular response of the system and provides information regarding the recovery of the electronic ground state. This allows for a quantification of singlet−singlet annihilation and charge-pair formation processes. Spatial mapping of chiral domains on femtosecond time scales with a resolution of 50 μm and diffraction-limited steady-state imaging of the circular dichroism and the circularly polarised luminescence (CPL) of the films is demonstrated.

The ultrafast charge carrier dynamics of the metaldeficient lead-free perovskite derivative methylammonium antimony iodide ((CH 3 NH 3 ) 3 Sb 2 I 9 , MASbI) is studied using femtosecond UV−vis−NIR transient absorption spectroscopy. The transient and steady-state absorption spectra show strong excitonic features. This is confirmed by an analysis of the near-band-gap absorption using Elliott's theory and its reformulation by Tanguy with subsequent modeling of the free-carrier and exciton contributions using the Saha equation. Time scales of the different carrier scattering processes are identified. The kinetics in the UV−vis range is largely independent of pump laser fluence suggesting that the dynamics involves localized excitons, with recombination time constants of 190 ps and >5 ns. Damped oscillations in the kinetics indicate coherent phonon dynamics and strong electron-phonon coupling. Fourier transformation of the time-domain data provides the steady-state Raman spectrum of MASbI which is dominated by vibrations of the [Sb 2 I 9 ] 3− anion. Exciton dissociation at the interfaces with mesoporous TiO 2 and a triarylamine-based hole transport material is found to be negligible. Our experiments suggest that it will be challenging to fabricate efficient photovoltaic devices from such lead-free antimony-and also bismuth-based zero-dimensional perovskite derivatives, because nonradiative exciton recombination largely governs their carrier dynamics.

Low-dimensional copper halides, such as CsCu 2 I 3 , have emerged as promising LED materials featuring strongly Stokes-shifted photoluminescence with high quantum yield. Previous calculations suggest an exciton self-trapping mechanism; however, direct experimental evidence for this process is still lacking. Here, we present femtosecond UV−vis transient absorption experiments of CsCu 2 I 3 thin films. The films were analyzed by SEM, XRD, and 133 Cs/ 63 Cu NMR for crystallinity and defects. Unique spectral dynamics is observed. The band gap absorption exhibits a characteristic double-peak structure arising from the 130 meV spin− orbit splitting of the copper d electrons. Emission at the direct band gap disappears because of the formation of the lowest-energy self-trapped exciton state. We determined the time constant of 12 ps for the trapping process of thermally relaxed free excitons, with an energy barrier of at least 60 meV. The data are successfully modeled by global kinetic analysis, providing also accurate time constants for charge carrier cooling processes.

We observed efficient induction of chirality in polyfluorene copolymer thin films by mixing with helicene-type chiral additives based on the dibenzo-[c,h]acridine motif. Images obtained from circular dichroism (CD) and circularly polarized luminescence (CPL) microscopy provide information about the chiral arrangements in the thin films with diffraction-limited resolution. The CD signal shows a characteristic dependence on the film thickness, which supports a supramolecular origin of the strong chiral response of the copolymer. In particular, we demonstrate the discrimination between films of opposite chirality based on their ultrafast transient chiral response through the use of femtosecond broadband CD spectroscopy and a newly developed setup for transient CPL spectroscopy with 28 ps time resolution. A systematic variation of the enantiomeric excess of the chiral additive shows that the "Sergeants and Soldiers" concept and "Majority Rules" are not obeyed.