We report recent results on the performance of FLASH (Free Electron Laser in Hamburg) operating at a wavelength of 13.7 nm where unprecedented peak and average powers for a coherent EUV radiation source have been measured. In the saturation regime the peak energy approached 170 µJ for individual pulses while the average energy per pulse reached 70 µJ. The pulse duration was in the region of 10 femtoseconds and peak

Femtosecond time-resolved photoelectron imaging is employed to investigate ultrafast electronic relaxation in aniline, a prototypical aromatic amine. The molecule is excited at wavelengths between 269 and 238 nm. We observe that the S2(pi3s/pi sigma*) state is populated directly during the excitation process at all wavelengths and that the population bifurcates to two decay pathways. One of these involves ultrafast relaxation from the Rydberg component of S2(pi3s/pi sigma*) to the S1(Pi Pi)* state, from which it relaxes back to the electronic ground state on a much longer timescale. The other appears to involve motion along the pi sigma* dissociative potential energy surface. At higher excitation energies, the dominant excitation is to the S3(pi pi*) state, which undergoes extremely efficient electronic relaxation back to the ground state. Our study supports some conclusions reached from H-atom photofragment translational spectroscopy measurements and pump-probe photoionization measurements and contradicts some others.

A photoexcited molecule undergoes multiple deactivation and reaction processes simultaneously or sequentially, which have been observed by combinations of various experimental methods. However, a single experimental method that enables complete observation of the photo-induced dynamics would be of great assistance for such studies. Here we report a full observation of cascaded electronic dephasing from S2(ππ(*)) in pyrazine (C4N2H4) by time-resolved photoelectron imaging (TRPEI) using 9.3-eV vacuum ultraviolet pulses with a sub-20 fs time duration. While we previously demonstrated a real-time observation of the ultrafast S2(ππ(*)) → S1(nπ(*)) internal conversion in pyrazine using TRPEI with UV pulses, this study presents a complete observation of the dynamics including radiationless transitions from S1 to S0 (internal conversion) and T1(nπ(*)) (intersystem crossing). Also discussed are the role of (1)Au(nπ(*)) in the internal conversion and the configuration interaction of the S2(ππ(*)) electronic wave function.

Efficient electronic relaxation following the absorption of ultraviolet light is crucial for the photostability of biological chromophores, so understanding the microscopic details of the decay pathways is of considerable interest. Here, we employ femtosecond time-resolved photoelectron imaging to investigate the ultrafast intramolecular dynamics of aniline, a prototypical aromatic amine, following excitation just below the second absorption maximum. We find that both the second ππ* state and the Rydberg state are populated during the excitation process. Surprisingly, the dominant non-radiative decay pathway is an ultrafast relaxation mechanism that transfers population straight back to the electronic ground-state. The vibrational energy resolution and photoelectron angular distributions obtained in our experiments reveal an interesting bifurcation of the Rydberg population to two non-radiative decay channels. The existence of these competing non-radiative relaxation channels in aniline illustrates how its photostability arises from a subtle balance between dynamics on different electronically excited states and importantly between Rydberg and valence states.

The accurate determination and control of the wavelength of light is fundamental to many fields of science. Speckle patterns resulting from the interference of multiple reflections in disordered media are well-known to scramble the information content of light by complex but linear processes. However, these patterns are, in fact, exceptionally rich in information about the illuminating source. We use a fibre-coupled integrating sphere to generate wavelength-dependent speckle patterns, in combination with algorithms based on the transmission matrix method and principal component analysis, to realize a broadband and sensitive wavemeter. We demonstrate sub-femtometre wavelength resolution at a centre wavelength of 780 nm, and a broad calibrated measurement range from 488 to 1,064 nm. This compares favourably to the performance of conventional wavemeters. Using this speckle wavemeter as part of a feedback loop, we stabilize a 780 nm diode laser to achieve a linewidth better than 1 MHz.