Understanding Anomalous Gas-Phase Peak Shifts in Dip-and-Pull Ambient Pressure XPS Experiments
(2024) In Journal of Physical Chemistry C- Abstract
Dip-and-pull ambient pressure X-ray photoelectron spectroscopy (AP-XPS) holds promise to uncover elementary processes of (photo)electrochemistry. We show, however, that the sample for such experiments should preferably be nonporous and the potential on the surface homogeneous. We carried out dip-and-pull AP-XPS experiments on a hematite thin film sample under the photoelectrochemical oxygen evolution reaction (OER) and find unexpected O 1s core level shifts. Upon electrochemical biasing under simulated solar light illumination, the gas-phase water peak shifted more than the electrolyte peak. To uncover the origin of the unexpected larger shift of the gas-phase peak, we performed electrostatic simulations using COMSOL, to map the... (More)
Dip-and-pull ambient pressure X-ray photoelectron spectroscopy (AP-XPS) holds promise to uncover elementary processes of (photo)electrochemistry. We show, however, that the sample for such experiments should preferably be nonporous and the potential on the surface homogeneous. We carried out dip-and-pull AP-XPS experiments on a hematite thin film sample under the photoelectrochemical oxygen evolution reaction (OER) and find unexpected O 1s core level shifts. Upon electrochemical biasing under simulated solar light illumination, the gas-phase water peak shifted more than the electrolyte peak. To uncover the origin of the unexpected larger shift of the gas-phase peak, we performed electrostatic simulations using COMSOL, to map the potential field in the relevant volume between the sample and the first aperture of the XPS spectrometer. A number of geometric models were considered. We find that when the potential on the sample surface is inhomogeneous, e.g., with ionically isolated electrolyte patches, the gas-phase peak of the spectrum can shift more than the peak due to the electrolyte film. This suggests that at the measured sample position, the local potential was not as set by the potentiostat. Despite this, we find reversible consumption and replenishment of hydroxide in the spectra, which, due to OH- being the reactant of the OER in alkaline electrolyte, makes sense chemically. We propose that this is linked to OH- diffusion across the measured sample position, driven by the potential dependent consumption and replenishment of OH- at the nearby well-connected surface regions.
(Less)
- author
- Teschner, Detre ; Plescher, Julius ; Piccinin, Simone ; Jones, Travis E. ; Hammud, Adnan ; Schmidt, Franz ; Knop-Gericke, Axel ; Bluhm, Hendrik and Shavorskiy, Andrey LU
- organization
- publishing date
- 2024
- type
- Contribution to journal
- publication status
- epub
- subject
- in
- Journal of Physical Chemistry C
- publisher
- The American Chemical Society (ACS)
- external identifiers
-
- scopus:85191150816
- ISSN
- 1932-7447
- DOI
- 10.1021/acs.jpcc.4c00113
- language
- English
- LU publication?
- yes
- id
- 9a472d47-d55a-4cd7-b6cb-fa8a80560e02
- date added to LUP
- 2024-05-07 16:52:32
- date last changed
- 2024-05-07 16:53:30
@article{9a472d47-d55a-4cd7-b6cb-fa8a80560e02,
abstract = {{<p>Dip-and-pull ambient pressure X-ray photoelectron spectroscopy (AP-XPS) holds promise to uncover elementary processes of (photo)electrochemistry. We show, however, that the sample for such experiments should preferably be nonporous and the potential on the surface homogeneous. We carried out dip-and-pull AP-XPS experiments on a hematite thin film sample under the photoelectrochemical oxygen evolution reaction (OER) and find unexpected O 1s core level shifts. Upon electrochemical biasing under simulated solar light illumination, the gas-phase water peak shifted more than the electrolyte peak. To uncover the origin of the unexpected larger shift of the gas-phase peak, we performed electrostatic simulations using COMSOL, to map the potential field in the relevant volume between the sample and the first aperture of the XPS spectrometer. A number of geometric models were considered. We find that when the potential on the sample surface is inhomogeneous, e.g., with ionically isolated electrolyte patches, the gas-phase peak of the spectrum can shift more than the peak due to the electrolyte film. This suggests that at the measured sample position, the local potential was not as set by the potentiostat. Despite this, we find reversible consumption and replenishment of hydroxide in the spectra, which, due to OH<sup>-</sup> being the reactant of the OER in alkaline electrolyte, makes sense chemically. We propose that this is linked to OH<sup>-</sup> diffusion across the measured sample position, driven by the potential dependent consumption and replenishment of OH<sup>-</sup> at the nearby well-connected surface regions.</p>}},
author = {{Teschner, Detre and Plescher, Julius and Piccinin, Simone and Jones, Travis E. and Hammud, Adnan and Schmidt, Franz and Knop-Gericke, Axel and Bluhm, Hendrik and Shavorskiy, Andrey}},
issn = {{1932-7447}},
language = {{eng}},
publisher = {{The American Chemical Society (ACS)}},
series = {{Journal of Physical Chemistry C}},
title = {{Understanding Anomalous Gas-Phase Peak Shifts in Dip-and-Pull Ambient Pressure XPS Experiments}},
url = {{http://dx.doi.org/10.1021/acs.jpcc.4c00113}},
doi = {{10.1021/acs.jpcc.4c00113}},
year = {{2024}},
}