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Naji, M. |
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Motta, Antonella |
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Aletan, Dirar |
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Mohamed, Tarek |
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Ertürk, Emre |
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Taccardi, Nicola |
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Kononenko, Denys |
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Petrov, R. H. | Madrid |
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Alshaaer, Mazen | Brussels |
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Bih, L. |
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Casati, R. |
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Muller, Hermance |
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Kočí, Jan | Prague |
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Šuljagić, Marija |
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Kalteremidou, Kalliopi-Artemi | Brussels |
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Azam, Siraj |
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Ospanova, Alyiya |
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Blanpain, Bart |
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Ali, M. A. |
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Popa, V. |
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Rančić, M. |
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Ollier, Nadège |
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Azevedo, Nuno Monteiro |
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Landes, Michael |
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Rignanese, Gian-Marco |
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Fabbri, Emiliana
in Cooperation with on an Cooperation-Score of 37%
Topics
Publications (16/16 displayed)
- 2024Designing bifunctional perovskite catalysts for the oxygen reduction and evolution reactionscitations
- 2024Cobalt-free layered perovskites RBaCuFeO 5+ δ (R = 4f lanthanide) as electrocatalysts for the oxygen evolution reactioncitations
- 2023Operando Investigations of Reversible and Irreversible Transformations of Metal Organic Framework Based Catalysts during the Oxygen Evolution Reaction
- 2023Influence of carbon on the dynamic changes in <scp>C</scp>o oxidation state of Ba0.<scp>5Sr0</scp>.<scp>5Co0</scp>.<scp>8Fe0</scp>.<scp>2O3</scp>‐δ perovskite catalyst during the oxygen reduction and evolution reactionscitations
- 2023Influence of carbon on the dynamic changes in Co oxidation state of Ba0.5Sr0.5Co0.8Fe0.2O3-δ perovskite catalyst during the oxygen reduction and evolution reactionscitations
- 2022Investigating Perovskite Oxide Catalysts As Bifunctional Oxygen Electrodes Using Operando XAS
- 2021Correlation between Oxygen Vacancies and Oxygen Evolution Reaction Activity for a Model Electrode: PrBaCo2O5+δ
- 2021Correlation between Oxygen Vacancies and Oxygen Evolution Reaction Activity for a Model Electrode: PrBaCo<sub>2</sub>O<sub>5+<i>δ</i></sub>citations
- 2020Tuning the Co oxidation state in Ba 0.5 Sr 0.5 Co 0.8 Fe 0.2 O 3-δ by flame spray synthesis towards high oxygen evolution reaction activitycitations
- 2019Fe-doping in double perovskite PrBaCo 2(1-x) Fe 2x O 6-δ : insights into structural and electronic efects to enhance oxygen evolution catalyst stabilitycitations
- 2019Fe-Doping in Double Perovskite PrBaCo2(1-x)Fe2xO6-δ: Insights into Structural and Electronic Effects to Enhance Oxygen Evolution Catalyst Stabilitycitations
- 2018Highly Active Nanoperovskite Catalysts for Oxygen Evolution Reaction: Insights into Activity and Stability of Ba0.5Sr0.5Co0.8Fe0.2O2+δ and PrBaCo2O5+δcitations
- 2017Unraveling thermodynamics, stability, and oxygen evolution activity of strontium ruthenium perovskite oxidecitations
- 2017Dynamic surface self-reconstruction is the key of highly active perovskite nano-electrocatalysts for water splittingcitations
- 2015Probing the bulk ionic conductivity by thin film hetero-epitaxial engineeringcitations
- 2014Catalyzed SnO2 thin films: theoretical and experimental insights into fabrication and electrocatalytic propertiescitations
Places of action
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article
Operando Investigations of Reversible and Irreversible Transformations of Metal Organic Framework Based Catalysts during the Oxygen Evolution Reaction
Abstract
<jats:p>Intermittency issues due to the growth of renewable energy usage lead to an increasing interest in energy storage systems. Thereby, one can use the excess energy for the production of hydrogen from water by anion exchange membrane (AEM) water electrolysis using earth-abundant, non-noble metal catalysts. However, the kinetics of the oxygen evolution reaction (OER) limit the activity of the catalyst and hence, the development of performance stable and active OER catalysts is of great importance for the commercialization of AEM water electrolyzers. In metal organic frameworks (MOFs), a porous structure is created by linking metal atoms/clusters with other metal centres using organic ligands. The resulting structure with a high surface area and dispersed metal centres is a promising catalyst for OER.</jats:p><jats:p>MOF catalysts with Ni and Co metal centres show impressive OER activity. Both, Co-MOF-74 and Ni-MOF-74 exhibit higher OER activity than their oxide counterparts produced by flame spray synthesis in form of nanoparticles (Fabbri (2017) and Abbott (2018)).<jats:sup>1,2</jats:sup> Thereby, an increasing OER activity of Ni-MOF-74 during rotating disk electrode stability tests, indicates that the catalytic species undergoes favorable electronic and structural transformations.</jats:p><jats:p>Using an in-house-developed spectro-electrochemical flow cell, these transformations were studied by <jats:italic>operando</jats:italic> X-ray absorption spectroscopy (XAS) and X-ray diffraction (XRD). <jats:italic>Operando</jats:italic> XAS enabled us to monitor the changes occurring in the Ni metal centers while performing cyclic voltammetry (CV) from 1 V<jats:sub>RHE</jats:sub> up to potentials above the OER onset potential with a time resolution of 5 sec. The operando XAS measurements show that Ni-MOF-74 develops into a highly OER active and stable catalytic species. However, <jats:italic>operando</jats:italic> XRD measurements prove that the crystalline MOF structure changes into an amorphous structure during OER. Monitoring the electronic and structural transformations due to potential cycling, three different structures were extracted: an initial state, which disappeared within the first eight CV cycles, and two novel electronic/local structures appearing at low and high potential, respectively. The transformations in the electronic and local structure of the Ni metal centers occurring between low and high potential appear to be reversible, as the Ni metal centers return to their initial state during long-term storage in air. However, XRD measurements indicate that this further transformation does not affect the structure of the catalyst: Even though the Ni centers return to their original local structure and oxidation state after long-term storage in air, the long-range structure stays amorphous.</jats:p><jats:p>The study focuses on elucidating the structure-performance relations of Ni-MOF-74 based OER catalysts providing the key structural parameters that lead to the formation of the highly OER active species. The mechanism of reversible and irreversible transformations occurring in Ni-MOF-74 catalysts allows the extraction of activity descriptors for the development of highly OER active and stable non-noble metal catalysts for AEM water electrolysis.</jats:p><jats:p>References: <jats:list list-type="roman-lower"><jats:list-item><jats:p> Fabbri, E., Nachtegaal, M., Binninger, T. <jats:italic>et al.</jats:italic> Dynamic surface self-reconstruction is the key of highly active perovskite nano-electrocatalysts for water splitting. <jats:italic>Nature Mater</jats:italic><jats:bold>16</jats:bold>, 925-931 (2017).</jats:p></jats:list-item><jats:list-item><jats:p>Abbott, D. F., Fabbri, E., Borlaf, M. et al. Operando X-ray absorption investigations into the role of Fe in the electrochemical stability and oxygen evolution activity of Ni<jats:sub>1−x</jats:sub>Fe<jats:sub>x</jats:sub>O<jats:sub>y</jats:sub><jats:italic>J Mater Chem A</jats:italic><jats:bold>6</jats:bold>, 24534-24549 (2018).</jats:p></jats:list-item></jats:list></jats:p>