We use femtosecond vibrational wavepacket techniques to time-resolve the coupled electronic and vibrational dynamics of exciton self-trapping in a series of materials in which the relative strength of the electron-phonon coupling can be compositionally tuned from the small to the large polaron limit. Transient absorption experiments are carried out in the quasi-one-dimensional halide-bridged mixed-valence transition metal linear chain complexes [Pt(en)2][Pt(en)2X2]⋅(ClO4)4 (en=ethylenediamine, C2H8N2) with X=Cl, Br and I. In each complex, we detect the formation of the self-trapped exciton through the appearance of its characteristic red-shifted optical absorption, and find that self-trapping occurs on a time scale of the order of a single vibrational period of the optical phonon mode that dominates the self-trapping dynamics. The associated optical phonon response, detected as wavepacket oscillations that modulate the exciton absorption, shows a significant softening of the optical phonon frequency compared to that of the unexcited system. The degree of softening is found to vary significantly with coupling strength, ranging from more than 40% in the strongly coupled chloride-bridged complex to less than 20% in the weakly coupled iodide-bridged complex. We relate these results to the extent of electronic delocalization by comparison with the electronic properties of the ground states of the materials and with the properties of their equilibrated self-trapped electronic states predicted by theoretical modeling.

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Picosecond-laser electronic-excitation tagging (PLEET), a seedless picosecond-laser-based velocimetry technique, is demonstrated in non-reactive flows at a repetition rate of 100 kHz with a 1064 nm, 100 ps burst-mode laser. The fluorescence lifetime of the PLEET signal was measured in nitrogen, and the laser heating effects were analyzed. PLEET experiments with a free jet of nitrogen show the ability to measure multi-point flow velocity fluctuations at a 100 kHz detection rate or higher. Both spectral and dynamic mode decomposition analyses of velocity on a Ma=0.8 free jet show two dominant Strouhal numbers around 0.24 and 0.48, respectively, well within the shear-layer flapping frequencies of the free jets. This technique increases the laser-tagging repetition rate for velocimetry to hundreds of kilohertz. PLEET is suitable for subsonic through supersonic laminar- and turbulent-flow velocity measurements.

Time-resolved particle image velocimetry (TR-PIV) has been achieved in a high-speed wind tunnel, providing velocity field movies of compressible turbulence events. The requirements of high-speed flows demand greater energy at faster pulse rates than possible with the TR-PIV systems developed for low-speed flows. This has been realized using a pulse-burst laser to obtain movies at up to 50 kHz, with higher speeds possible at the cost of spatial resolution. The constraints imposed by use of a pulse-burst laser are limited burst duration of 10.2 ms and a low duty cycle for data acquisition. Pulse-burst PIV has been demonstrated in a supersonic jet exhausting into a transonic crossflow and in transonic flow over a rectangular cavity. The velocity field sequences reveal the passage of turbulent structures and can be used to find velocity power spectra at every point in the field, providing spatial distributions of acoustic modes. The present work represents the first use of TR-PIV in a high-speed ground-test facility.

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