PreprintCC BY 4.0arXiv
Role of Local Structural Variation in X-ray Photoelectron Spectrum of Silicon Oxide Interfaces
Abstract
We show that the broad X-ray photoelectron lines of silicon oxide on silicon arise from a continuous statistical distribution of core-level binding energies. Statistical simulations spanning compositions from Si to SiO2 reproduce the full extent of this broadening, reaching 5 eV for SiO1.0 , in quantitative agreement with 0.23 nm layer-resolved spectra reconstructed from Ar+ sputtering data. This continuous distribution blurs distinct spectral fingerprints of local structural motifs, thereby challenging conventional chemical state assignment in oxide X-ray photoelectron spectra.
Versions
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BibTeX
@misc{santonen2026role,
title = {{Role of Local Structural Variation in X-ray Photoelectron Spectrum of Silicon Oxide Interfaces}},
author = {Mikael Santonen and Sari Granroth and Johanna Laaksonen and Pekka Laukkanen and Johannes Niskanen},
howpublished = {arXiv},
year = {2026},
month = oct,
doi = {10.48550/arxiv.2606.18769},
eprint = {2606.18769},
archivePrefix = {arXiv},
url = {https://arxiv.org/abs/2606.18769},
note = {CC BY 4.0},
}
RIS
TY - UNPB
TI - Role of Local Structural Variation in X-ray Photoelectron Spectrum of Silicon Oxide Interfaces
AU - Mikael Santonen
AU - Sari Granroth
AU - Johanna Laaksonen
AU - Pekka Laukkanen
AU - Johannes Niskanen
PY - 2026
DA - 2026/10/16
PB - arXiv
DO - 10.48550/arxiv.2606.18769
UR - https://arxiv.org/abs/2606.18769
AB - We show that the broad X-ray photoelectron lines of silicon oxide on silicon arise from a continuous statistical distribution of core-level binding energies. Statistical simulations spanning compositions from Si to SiO_2 reproduce the full extent of this broadening, reaching 5 eV for SiO_1.0 , in quantitative agreement with 0.23 nm layer-resolved spectra reconstructed from Ar^+ sputtering data. This continuous distribution blurs distinct spectral fingerprints of local structural motifs, thereby challenging conventional chemical state assignment in oxide X-ray photoelectron spectra.
ER -