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  4. Revealing formic acid adsorption geometries on magnetite (001) and (111) surfaces by IRRAS line shape analysis
 
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Revealing formic acid adsorption geometries on magnetite (001) and (111) surfaces by IRRAS line shape analysis

Citation Link: https://doi.org/10.15480/882.17214
Publikationstyp
Journal Article
Date Issued
2026-05-05
Sprache
English
Author(s)
Noei, Heshmat  
Deutsches Elektronen-Synchrotron DESY  
Creutzburg, Marcus  
Deutsches Elektronen-Synchrotron DESY  
Vonbun-Feldbauer, Gregor  orcid-logo
Grenzflächenphysik und -technologie M-29  
Stierle, Andreas  
Deutsches Elektronen-Synchrotron DESY  
TORE-DOI
10.15480/882.17214
TORE-URI
https://hdl.handle.net/11420/63270
Journal
Physical chemistry, chemical physics  
Volume
28
Issue
22
Start Page
13380
End Page
13393
Citation
Physical Chemistry Chemical Physics 28 (22): 13380-13393 (2026)
Publisher DOI
10.1039/d5cp00848d
Scopus ID
2-s2.0-105038619019
Publisher
RSC Publ
The sign and intensity of infrared (IR) bands on oxide surfaces strongly depend on light polarization and the adsorption geometry of surface species. In this study, we investigate formic acid adsorption on single crystalline magnetite Fe<inf>3</inf>O<inf>4</inf>(001) and Fe<inf>3</inf>O<inf>4</inf>(111) surfaces, which being neither perfect metals nor insulators exhibit characteristic Fano shaped IR line profiles. Using both s- and p-polarized infrared reflection absorption spectroscopy (IRRAS), we identify distinct spectral features and reveal vibrational bands that were previously unobserved in experiments employing unpolarized or solely p-polarized light. Complementary density functional theory (DFT) calculations provide structural and vibrational insights into the adsorbed species. On Fe<inf>3</inf>O<inf>4</inf>(001), a new band at 1555 cm<sup>−1</sup> observed with p-polarized light is attributed to the asymmetric OCO stretching vibration of formate bound to octahedral Fe sites with tetrahedral Fe<inf>tet1</inf> underneath. On Fe<inf>3</inf>O<inf>4</inf>(111), a band at 1730 cm<sup>−1</sup> detected in both unpolarized and s-polarized light corresponds to the CO stretch of a monodentate species. These results highlight the crucial role of light polarization in IRRAS for elucidating adsorption geometries and electronic properties of oxide surfaces.
DDC Class
541.3: Physical Chemistry
530: Physics
Lizenz
https://creativecommons.org/licenses/by/3.0/
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