NEXAFS Chemical State and Bond Lengths of p-Aminobenzoic Acid in Solution and Solid State

Solid-state and solution pH-dependent NEXAFS studies allow direct observation of the electronic state of para-aminobenzoic acid (PABA) as a function of its chemical environment, revealing the chemical state and bonding of the chemical species. Variations in the ionization potential (IP) and 1s→π* resonances unequivocally identify the chemical species (neutral, cationic, or anionic) present and the varying local environment. Shifts in σ* shape resonances relative to the IP in the NEXAFS spectra vary with C-N bond length, and the important effect of minor alterations in bond length is confirmed with nitrogen FEFF calculations, leading to the possibility of bond length determination in solution

The Structure of p-Aminobenzoic Acid in Water: Studies Combining UV-Vis, NEXAFS and RIXS Spectroscopies

NEXAFS-RIXS and home laboratory-based UV-Vis absorption spectroscopy are combined to examine the speciation and electronic structure of para-aminobenzoic acid (PABA) in aqueous solution as a function of pH. DFT and TD-DFT electronic structure calculations reproduce the experimental trends and provide a correlation between the experimental HOMO↔LUMO gap as well as the electronic transitions between molecular orbitals in the non-ionic, anionic and cationic forms of PABA

Studies Combining UV-Vis, NEXAFS and RIXS Spectroscopies

NEXAFS-RIXS and home laboratory-based UV-Vis absorption spectroscopy are combined to examine the speciation and electronic structure of para- aminobenzoic acid (PABA) in aqueous solution as a function of pH. DFT and TD- DFT electronic structure calculations reproduce the experimental trends and provide a correlation between the experimental HOMO↔LUMO gap as well as the electronic transitions between molecular orbitals in the non-ionic, anionic and cationic forms of PABA

Ultrafast electronic processes in an insulator The Be and O sites in BeO

The short time dynamics of amorphous beryllium oxide a BeO has been investigated for electronic excitation ionization by fast incident electrons, as well as by Ar7 , Ar15 , Xe15 , and Xe31 ions at velocities of 6 10 the speed of light. Site specific Auger electron spectra induced by fast heavy ions are the central point of this investigation. Electron induced Auger spectra serve as a reference and electron energy loss EELS spectroscopy as well as resonant inelastic X ray scattering RIXS are invoked for quantitative understanding. For the heavy ion case, we observe strong variations in the corresponding spectral distributions of Be K and O K Auger lines. These are related to local changes of the electron density, of the electron temperature and even of the electronic band structure of BeO on a femtosecond time scale after the passage of highly charged heavy ions

Local electronic structure of aqueous zinc acetate oxygen K edge X ray absorption and emission spectroscopy on micro jets

Oxygen K edge X ray absorption, emission, and resonant inelastic X ray scattering spectra were measured to site selectively gain insights into the electronic structure of aqueous zinc acetate solution. The character of the acetate ion and the influence of zinc and water on its local electronic structure are discusse

Resonant inelastic X ray scattering as a probe of molecular structure and electron dynamics in solutions

Resonant inelastic X ray scattering RIXS technique is applied to gain insight into the local electronic structure in liquid phase. The approach combines a liquid micro jet and an X ray emission spectrometer XES both installed in the recently developed LiXEdrom experimental station. Here we demonstrate how the combined approach enables investigation of the hydrogen bonding network in water and of chemical bonding in different solvents. In addition, the probe of energy transfer and electron dynamics at the metal solvent interface is achieved by comparing the integrated RIXS intensities of the different radiative decay channels of the 2p core hole of 3d transition metals. The integrated RIXS intensities build the partial and the inverse partial X ray fluorescence yields that allow for absorption measurements free from background signal of other elements or saturation effect