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Correction: Phosphate modification of Pd/Al2O3 enhances activity and stability in aromatic hydrogenation under CO-contaminated hydrogen
Adrian Seitza,
Yaoci Shengb,
Ian Backesa,
Phillip Nathratha,
Dennis Weberac,
Tanja Frankenac,
Roberto Félixd,
Angelo Rillerad,
Johannes Frischde,
Marcus Bärdefg,
Tanja Retzerb and
Patrick Schühle*a
aInstitute of Chemical Reaction Engineering, Friedrich-Alexander-Universität Erlangen-Nürnberg, Egerlandstraße 3, 91058 Erlangen, Germany. E-mail: patrick.schuehle@fau.de
bInterface Research and Catalysis, ECRC, Friedrich-Alexander-Universität Erlangen-Nürnberg, Egerlandstraße 3, 91058 Erlangen, Germany
cTechnical Chemistry I, Technische Universität Darmstadt, Peter-Grünberg-Straße 8, 64287 Darmstadt, Germany
dDepartment Interface Design, Helmholtz-Zentrum Berlin für Materialien und Energie GmbH (HZB), Albert-Einstein-Straße 15, 12489 Berlin, Germany
eEnergy Materials In Situ Laboratory Berlin (EMIL), Helmholtz-Zentrum Berlin für Materialien und Energie GmbH (HZB), Albert-Einstein-Straße 15, 12489 Berlin, Germany
fLehrstuhl für Physikalische Chemie II, Friedrich-Alexander-Universität Erlangen-Nürnberg, Egerlandstraße 3, 91058 Erlangen, Germany
gDepartment for X-ray Spectroscopy at Interfaces of Thin Films, Helmholtz-Institute Erlangen-Nürnberg for Renewable Energy, Albert-Einstein-Str. 15, 12489 Berlin, Germany
First published on 26th February 2026
Abstract
Correction for ‘Phosphate modification of Pd/Al2O3 enhances activity and stability in aromatic hydrogenation under CO-contaminated hydrogen’ by Adrian Seitz et al., EES Catal., 2026, 4, 118–133, https://doi.org/10.1039/D5EY00231A.
The authors regret the omission of acknowledgement of financial support from the FAU Competence Center Engineering of Advanced Materials (EAM), Friedrich-Alexander-Universität Erlangen-Nürnberg, in the original article. The correct acknowledgements section is as shown here.
The Royal Society of Chemistry apologises for these errors and any consequent inconvenience to authors and readers.
Acknowledgements
We gratefully acknowledge the Federal Ministry of Research, Technology and Space for funding of the BMFTR Junior Research Group FAIR-H2 (Grant number (FKZ): 03SF0730). We thank the Helmholtz-Zentrum Berlin für Materialien und Energie for the allocation of synchrotron radiation beamtime at the HiKE endstation located at the KMC-1 beamline and the Energy Materials In Situ Laboratory Berlin (EMIL) for providing access to facilities allowing for on-site sample mounting in inert (Ar) atmosphere. Y. S. and T. R. acknowledge funding by the Deutsche Forschungsgemeinschaft (DFG, German Research Foundation): Project-ID 431791331, SFB 1452 (CLINT Catalysis at Liquid Interfaces) and Project-ID 530732852. We thank the Center for Nanoanalysis and Electron Microscopy (CENEM) Erlangen for providing the HR-TEM facility. We thank Yousuf Raed Ramzi (HR-TEM), Abelina Ellert (ICP-OES), Ana de Oliveira (ICP-OES), Lukas Popp (N2 physisorption), Susanne Pachaly (XRD), Jiaqi Xiao and Felix Lott for experimental support. The authors gratefully acknowledge financial support from the FAU Competence Center Engineering of Advanced Materials (EAM), Friedrich-Alexander-Universität Erlangen-Nürnberg.| This journal is © The Royal Society of Chemistry 2026 |