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3D atomic-scale imaging of mixed Co-Fe spinel oxide nanoparticles during oxygen evolution reaction

The three-dimensional (3D) distribution of individual atoms on the surface of catalyst nanoparticles plays a vital role in their activity and stability. Optimising the performance of electrocatalysts requires atomic-scale information, but it is difficult to obtain. Here, we use atom probe tomography...

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Detalles Bibliográficos
Autores principales: Xiang, Weikai, Yang, Nating, Li, Xiaopeng, Linnemann, Julia, Hagemann, Ulrich, Ruediger, Olaf, Heidelmann, Markus, Falk, Tobias, Aramini, Matteo, DeBeer, Serena, Muhler, Martin, Tschulik, Kristina, Li, Tong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8748757/
https://www.ncbi.nlm.nih.gov/pubmed/35013310
http://dx.doi.org/10.1038/s41467-021-27788-2
Descripción
Sumario:The three-dimensional (3D) distribution of individual atoms on the surface of catalyst nanoparticles plays a vital role in their activity and stability. Optimising the performance of electrocatalysts requires atomic-scale information, but it is difficult to obtain. Here, we use atom probe tomography to elucidate the 3D structure of 10 nm sized Co(2)FeO(4) and CoFe(2)O(4) nanoparticles during oxygen evolution reaction (OER). We reveal nanoscale spinodal decomposition in pristine Co(2)FeO(4). The interfaces of Co-rich and Fe-rich nanodomains of Co(2)FeO(4) become trapping sites for hydroxyl groups, contributing to a higher OER activity compared to that of CoFe(2)O(4). However, the activity of Co(2)FeO(4) drops considerably due to concurrent irreversible transformation towards Co(IV)O(2) and pronounced Fe dissolution. In contrast, there is negligible elemental redistribution for CoFe(2)O(4) after OER, except for surface structural transformation towards (Fe(III), Co(III))(2)O(3). Overall, our study provides a unique 3D compositional distribution of mixed Co-Fe spinel oxides, which gives atomic-scale insights into active sites and the deactivation of electrocatalysts during OER.