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Substituent Effects in Iron Porphyrin Catalysts for the Hydrogen Evolution Reaction

datacite.relation.isSupplementTo https://doi.org/10.1002/chem.202202465
dc.contributor.author Heppe, Nils
dc.contributor.author Gallenkamp, Charlotte
dc.contributor.author Paul, Stephen
dc.contributor.author Segura-Salas, Nicole
dc.contributor.author von Rhein, Niklas
dc.contributor.author Kaiser, Bernhard
dc.contributor.author Jaegermann, Wolfram
dc.contributor.author Jafari, Atefeh
dc.contributor.author Sergueev, Ilya
dc.contributor.author Krewald, Vera
dc.contributor.author Kramm, Ulrike Ingrid
dc.date.accessioned 2022-12-09T17:44:53Z
dc.date.available 2022-12-09T17:44:53Z
dc.date.created 2022
dc.date.issued 2022-12-09
dc.description Data package used for the peer-reviewed publication: "Substituent Effects in Iron Porphyrin Catalysts for the Hydrogen Evolution Reaction" in Chemistry - A European Journal. DOI: 10.1002/chem.202202465 Abstract: For a future hydrogen economy, non-precious metal catalysts for the water splitting reactions are needed that can be implemented on a global scale. Metal-nitrogen-carbon (MNC) catalysts with active sites constituting a metal center with fourfold coordination of nitrogen (MN4) show promising performance, but an optimization rooted in structure-property relationships has been hampered by their low structural definition. Porphyrin model complexes are studied to transfer insights from well-defined molecules to MNC systems. This work combines experiment and theory to evaluate the influence of porphin substituents on the electronic and electrocatalytic properties of MN4 centers with respect to the hydrogen evolution reaction (HER) in aqueous electrolyte. We found that the choice of substituent affects their utilization on the carbon support and their electrocatalytic performance. We propose an HER mechanism for supported iron porphyrin complexes involving a [FeII(P▪)]- radical anion intermediate, in which a porphinic nitrogen atom acts as an internal base. While this work focuses on the HER, the limited influence of a simultaneous interaction with the support and an aqueous electrolyte will likely be transferrable to other catalytic applications. de_DE
dc.description.version DOI:10.1002/chem.202202465 de_DE
dc.identifier.uri https://tudatalib.ulb.tu-darmstadt.de/handle/tudatalib/3674
dc.language.iso en de_DE
dc.rights.licenseODC-BY-1.0 (https://opendatacommons.org/licenses/by/1.0/)
dc.subject Density functional theory;Electrochemistry;Heterogeneous catalysis;Hydrogen;Molecular electrochemistry;Renewable resources de_DE
dc.subject.classification 3.12-02
dc.subject.ddc 540
dc.title Substituent Effects in Iron Porphyrin Catalysts for the Hydrogen Evolution Reaction de_DE
dc.type Dataset de_DE
dcterms.accessRights restrictedAccess
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tuda.history.classification Version=2020-2024;322-02 Physikalische Chemie von Festkörpern und Oberflächen, Materialcharakterisierung
tuda.unit TUDa

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