We probe the dynamics of valence electrons in photoexcited [Fe(terpy)2]2+ in solution to gain deeper insight into the Fe–ligand bond changes. We use hard X-ray emission spectroscopy (XES), which combines element specificity and high penetration with sensitivity to orbital structure, making it a powerful technique for molecular studies in a wide variety of environments. A picosecond-time-resolved measurement of the complete 1s X-ray emission spectrum captures the transient photoinduced changes and includes the weak valence-to-core (vtc) emission lines that correspond to transitions from occupied valence orbitals to the nascent core-hole. Vtc-XES offers particular insight into the molecular orbitals directly involved in the light-driven dynamics; a change in the metal–ligand orbital overlap results in an intensity reduction and a blue energy shift in agreement with our theoretical calculations and more subtle features at the highest energies reflect changes in the frontier orbital populations.

X-ray parametric down-conversion is a fundamental nonlinear effect that promises a wide range of possible applications. Nevertheless, it has been scarcely investigated and unequivocal evidence of the effect is still missing for certain spectral regions. In particular, this is the case for down-conversion into pairs of x-ray and optical photons, which would open pathways to characterise and image valence electron-density fluctuations. In this work, we present a systematic approach to scan the parameter space, wherein we expect to identify the effect based on its characteristic signature. Within the resolution of the experimental setup we cannot establish any evidence for the nonlinear effect. Instead, we trace the measured signals back to elastic scattering contributions, thereby challenging the interpretation of previous studies on the effect of x-ray parametric down conversion producing photons in the visible spectral range. As a benchmark for future investigations of x-ray parametric down-conversion -both experimental and theoretical -we extract an upper bound for the effect's conversion efficiency of 10 −11 within the resolution of our setup.

We present a novel, highly versatile, and self-referenced arrival time monitor for measuring the femtosecond time delay between a hard X-ray pulse from a free-electron laser and an optical laser pulse, measured directly on the same sample used for pump-probe experiments. Two chirped and picosecond long optical supercontinuum pulses traverse the sample with a mutually fixed time delay of 970 fs, while a femtosecond X-ray pulse arrives at an instant in between both pulses. Behind the sample the supercontinuum pulses are temporally overlapped to yield near-perfect destructive interference in the absence of the X-ray pulse. Stimulation of the sample with an X-ray pulse delivers non-zero contributions at certain optical wavelengths, which serve as a measure of the relative arrival time of the X-ray pulse with an accuracy of better than 25 fs. We find an excellent agreement of our monitor with the existing timing diagnostics at the SACLA XFEL with a Pearson correlation value of 0.98. We demonstrate a high sensitivity to measure X-ray pulses with pulse energies as low as 30 $$\upmu $$ μ J. Using a free-flowing liquid jet as interaction sample ensures the full replacement of the sample volume for each X-ray/optical event, thus enabling its utility even at MHz repetition rate XFEL sources.