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@ARTICLE{Thuermer:630677,
author = {Thuermer, Stephan and Stemer, Dominik and Trinter, Florian
and Kiyan, Igor Yu and Winter, Bernd and Wilkinson, Iain},
title = {{L}ow-{E}nergy {P}hotoelectron {S}pectroscopy and
{S}cattering from {A}queous {S}olutions and the {R}ole of
{S}olute {S}urface {A}ctivity},
journal = {Journal of the American Chemical Society},
volume = {147},
number = {23},
issn = {0002-7863},
address = {Washington, DC},
publisher = {ACS Publications},
reportid = {PUBDB-2025-01897},
pages = {19868 - 19877},
year = {2025},
note = {Open Access},
abstract = {Experimental insights into low-kinetic-energy electron
scattering in aqueous solutions are essential for an
improved understanding of electron-driven chemistry and
radiobiology, and the development and informed application
of aqueous-phase electron-based spectroscopy and dichroism
methods. Generally, in aqueous environments and for electron
kinetic energies below 12–15 eV, significant and, thus
far, incompletely understood low-energy-transfer inelastic
electron scattering with solvent molecules preponderates.
This leads to cascades of tens-of-meV kinetic-energy losses
that distort nascent photoelectron spectra, prevent direct
and accurate electron-binding-energy measurements, and limit
possibilities to determine electron-scattering cross
sections at especially low electron kinetic energies. Here,
we quantify aqueous-phase inelastic-scattering-based energy
losses using 1–30 eV kinetic energy photoelectrons and
liquid-jet photoemission spectroscopy, specifically by
photoionizing an exemplary surface-active solute and
comparing the results with those from the homogeneously
distributed aqueous solvent. Thereby, we identify a general
≳17 eV electron-kinetic-energy requirement for the direct
and accurate measurement of aqueous-phase electron binding
energies, irrespective of interfacial concentration
profiles. Further, at electron kinetic energies from 10 eV
down to a few-eV above the ionization threshold, we observe
and quantify lower degrees of scattering for photoelectrons
generated from surface-active solutes, allowing moderately
distorted surface-active-solute photoemission peaks to be
resolved down to just few-eV electron kinetic energies.
These results demonstrate that liquid-jet photoemission
spectroscopy can be used to probe interfacial
surface-active-solute dynamics and dichroism effects close
to ionization thresholds, in stark contrast to similar
experiments on homogeneously distributed solution
components. Furthermore, they offer novel insights into
low-electron-kinetic-energy scattering in aqueous
environments, thereby addressing the current lack of
reliable experimental data in this critical energy range.},
cin = {DOOR ; HAS-User},
ddc = {540},
cid = {I:(DE-H253)HAS-User-20120731},
pnm = {6G3 - PETRA III (DESY) (POF4-6G3) / FS-Proposal:
II-20210015 (II-20210015) / FS-Proposal: II-20230689
(II-20230689) / AQUACHIRAL - Chiral aqueous-phase chemistry
(883759)},
pid = {G:(DE-HGF)POF4-6G3 / G:(DE-H253)II-20210015 /
G:(DE-H253)II-20230689 / G:(EU-Grant)883759},
experiment = {EXP:(DE-H253)P-P04-20150101},
typ = {PUB:(DE-HGF)16},
pubmed = {pmid:40454638},
doi = {10.1021/jacs.5c04263},
url = {https://bib-pubdb1.desy.de/record/630677},
}