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Low-energy constraints on photoelectron spectra measured from liquid water and aqueous solutions
- Source :
- Physical Chemistry Chemical Physics, Physical chemistry, chemical physics 23(14), 8246-8260 (2021). doi:10.1039/D1CP00430A, Physical chemistry chemical physics : PCCP, vol 23, iss 14
- Publication Year :
- 2021
-
Abstract
- Physical chemistry, chemical physics 23(14), 8246 - 8260 (2021). doi:10.1039/D1CP00430A<br />We report on the effects of electron collision and indirect ionization processes, occurring at photoexcitation and electron kinetic energies well below 30 eV, on the photoemission spectra of liquid water. We show that the nascent photoelectron spectrum and, hence, the inferred electron binding energy can only be accurately determined if electron energies are large enough that cross sections for quasi-elastic scattering processes, such as vibrational excitation, are negligible. Otherwise, quasi-elastic scattering leads to strong, down-to-few-meV kinetic energy scattering losses from the direct photoelectron features, which manifest in severely distorted intrinsic photoelectron peak shapes. The associated cross-over point from predominant (known) electronically inelastic to quasi-elastic scattering seems to arise at surprisingly large electron kinetic energies, of approximately 10–14 eV. Concomitantly, we present evidence for the onset of indirect, autoionization phenomena (occurring via superexcited states) within a few eV of the primary and secondary ionization thresholds. These processes are inferred to compete with the direct ionization channels and primarily produce low-energy photoelectrons at photon and electron impact excitation energies below ∼15 eV. Our results highlight that vibrational inelastic electron scattering processes and neutral photoexcitation and autoionization channels become increasingly important when photon and electron kinetic energies are decreased towards the ionization threshold. Correspondingly, we show that for neat water and aqueous solutions, great care must be taken when quantitatively analyzing photoelectron spectra measured too close to the ionization threshold. Such care is essential for the accurate determination of solvent and solute ionization energies as well as photoelectron branching ratios and peak magnitudes.<br />Published by RSC Publ., Cambridge
- Subjects :
- Materials science
Photoemission spectroscopy
Atom and Molecular Physics and Optics
Binding energy
physics.chem-ph
General Physics and Astronomy
FOS: Physical sciences
02 engineering and technology
01 natural sciences
Molecular physics
Physical Chemistry
Matter Dynamics Mechanisms and Control
Engineering
Autoionization
Ionization
Physics - Chemical Physics
0103 physical sciences
Physics::Atomic and Molecular Clusters
Physics::Atomic Physics
Physical and Theoretical Chemistry
Electron ionization
Fysikalisk kemi
Chemical Physics (physics.chem-ph)
Chemical Physics
010304 chemical physics
Scattering
021001 nanoscience & nanotechnology
Photoexcitation
Condensed Matter::Soft Condensed Matter
Physical Sciences
Chemical Sciences
ddc:540
Atom- och molekylfysik och optik
Ionization energy
0210 nano-technology
Subjects
Details
- Language :
- English
- Database :
- OpenAIRE
- Journal :
- Physical Chemistry Chemical Physics, Physical chemistry, chemical physics 23(14), 8246-8260 (2021). doi:10.1039/D1CP00430A, Physical chemistry chemical physics : PCCP, vol 23, iss 14
- Accession number :
- edsair.doi.dedup.....5c348a5f6dfb3057d626e6cf1294574e
- Full Text :
- https://doi.org/10.1039/D1CP00430A