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Time-resolved measurements of quantum dynamics are based on the availability of controlled events (e.g. pump and probe pulses) that are shorter in duration than the typical evolution time scale of the dynamical processes to be observed. Here we introduce the concept of noise-enhanced pump-probe spectroscopy, allowing the measurement of dynamics significantly shorter than the average pulse duration by exploiting randomly varying, partially coherent light fields consisting of bunched colored noise. It is shown that statistically fluctuating fields can be superior by more than a factor of 10 to frequency-stabilized fields, with important implications for time-resolved pump-probe experiments at x-ray free-electron lasers (FELs) and, in general, for measurements at the frontiers of temporal resolution (e.g. attosecond spectroscopy). As an example application, the concept is used to explain the recent experimental observation of vibrational wave packet motion in a deuterium molecular ion on time scales shorter than the average pulse duration.
We analyze the influence of classical Gaussian noise on Landau-Zener transitions during a two-level crossing in a time-dependent regular external field. Transition probabilities and coherence factors become random due to the noise. We calculate their
We investigate the valley related carrier dynamics in monolayer MoS2 using helicity resolved non-degenerate ultrafast pump-probe spectroscopy at the vicinity of the high-symmetry K point under the temperature down to 78 K. Monolayer MoS2 shows remark
Robust engineering of phonon squeezed states in optically excited solids has emerged as a promising tool to control and manipulate their properties. However, in contrast to quantum optical systems, detection of phonon squeezing is subtle and elusive,
We report here an experimental setup to perform three-pulse pump-probe measurements over a wide wavelength and temperature range. By combining two pump pulses in the visible (650-900 nm) and mid-IR (5-20 $mu$m) range, with a broadband supercontinuum
In high-resolution core-valence-valence (CVV) Auger electron spectroscopy from the surface of a solid at thermal equilibrium, the main correlation satellite, visible in the case of strong valence-electron correlations, corresponds to a bound state of