Electron and ion spectroscopy of azobenzene in the valence and core shells.

Azobenzene is a prototype and a building block of a class of molecules of extreme technological interest as molecular photo-switches. We present a joint experimental and theoretical study of its response to irradiation with light across the UV to x-ray spectrum. The study of valence and inner shell photo-ionization and excitation processes combined with measurement of valence photoelectron-photoion coincidence and mass spectra across the core thresholds provides a detailed insight into the site- and state-selected photo-induced processes. Photo-ionization and excitation measurements are interpreted via the multi-configurational restricted active space self-consistent field method corrected by second order perturbation theory. Using static modeling, we demonstrate that the carbon and nitrogen K edges of azobenzene are suitable candidates for exploring its photoinduced dynamics thanks to the transient signals appearing in background-free regions of the NEXAFS and XPS.

Oscillatory Failure Case detection in flight control systems via wavelets decomposition.

A fault detection design is proposed for addressing the Oscillatory Failure Case (OFC) detection problem, introduced in the joint Airbus-Stellenbosch university aerospace industrial-benchmark competition called at the IFAC 2020 World Congress1. The detection scheme is comprised of an output estimator, a wavelet decomposition and an energy-based denoising method, and the residual evaluation unit. The detection problem of wide frequency range OFCs is also addressed. According to the achieved simulation results, the proposed fault detection method is able to satisfy the competition prescriptions in the frequency range [1 10] Hz for those OFC's having an amplitude greater than 2.3 mm for OFCs at rod position sensor, or 1.4 mA for OFCs at servo input current, regardless of disturbances level, uncertainties and load factor control input. In other cases, faults are detected slightly after the prescribed detection limit, with some interesting exceptions.

Insights into 2- and 4(5)-Nitroimidazole Decomposition into Relevant Ions and Molecules Induced by VUV Ionization.

Nitromidazoles are relevant compounds of multidisciplinary interest, and knowledge of their physical-chemical parameters as well as their decomposition under photon irradiation is needed. Here we report an experimental and theoretical study of the mechanisms of VUV photofragmentation of 2- and 4(5)-nitromidazoles, compounds used as radiosensitizers in conjunction with radiotherapy as well as high-energy density materials. Photoelectron-photoion coincidence experiments, measurements of the appearance energies of the most important ionic fragments, density functional theory, and single-point coupled cluster calculations have been used to provide an overall insight into the energetics and structure of the different ionic/neutral products of the fragmentation processes. The results show that these compounds can be an efficient source of relevant CO, HCN, NO, and NO2 molecules and produce ions of particular astrophysical interest, like the isomers of azirinyl cation ( m/ z 40), predicted to exist in the interstellar medium, and protonated hydrogen cyanide ( m/ z 28).

Communication: "Position" does matter: The photofragmentation of the nitroimidazole isomers.

A combined experimental and theoretical approach has been used to disentangle the fundamental mechanisms of the fragmentation of the three isomers of nitroimidazole induced by vacuum ultra-violet (VUV) radiation, namely, 4-, 5-, and 2-nitroimidazole. The results of mass spectrometry as well as photoelectron-photoion coincidence spectroscopy display striking differences in the radiation-induced decomposition of the different nitroimidazole radical cations. Based on density functional theory (DFT) calculations, a model is proposed which fully explains such differences, and reveals the subtle fragmentation mechanisms leading to the release of neutral species like NO, CO, and HCN. Such species have a profound impact in biological media and may play a fundamental role in radiosensitising mechanisms during radiotherapy.

Elemental chemical analysis of submerged targets by double-pulse laser-induced breakdown spectroscopy.

Double-pulse laser-induced plasma spectroscopy (DP-LIPS) is applied to submerged targets to investigate its feasibility for elemental analysis. The role of experimental parameters, such as inter-pulse delay and detection time, has been discussed in terms of the dynamics of the laser-induced bubble produced by the first pulse and its confinement effect on the plasma produced by the second laser pulse. The analytical performance of this technique applied to targets in a water environment are discussed. The elemental analysis of submerged copper alloys by DP-LIPS has been compared with conventional (single-pulse) LIBS in air. Theoretical investigation of the plasma dynamics in water bubbles and open air has been performed.