Understanding the evolution of ternary alloyed nanoparticles during reversible exsolution from double perovskite oxides

Multicomponent nanoparticle exsolution has emerged as a promising process for obtaining highly active catalysts supported on perovskite oxides. For instance, FeCoNi alloys can be exsolved from Sr 2 FeCo 0.2 Ni 0.2 Mn 0.1 Mo 0.5 O 6− δ , boosting the electrocatalytic properties of these electrodes. H...

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Veröffentlicht in:Journal of materials chemistry. A, Materials for energy and sustainability Materials for energy and sustainability, 2024-08, Vol.12 (34), p.2269-22626
Hauptverfasser: López-García, Andrés, Carrillo, Alfonso J, Jiménez, Catalina Elena, Anzorena, Rosario Suarez, Garcia-Diez, Raul, Pérez-Dieste, Virginia, Villar-Garcia, Ignacio J, Hungría, Ana B, Bär, Marcus, Serra, José M
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container_issue 34
container_start_page 2269
container_title Journal of materials chemistry. A, Materials for energy and sustainability
container_volume 12
creator López-García, Andrés
Carrillo, Alfonso J
Jiménez, Catalina Elena
Anzorena, Rosario Suarez
Garcia-Diez, Raul
Pérez-Dieste, Virginia
Villar-Garcia, Ignacio J
Hungría, Ana B
Bär, Marcus
Serra, José M
description Multicomponent nanoparticle exsolution has emerged as a promising process for obtaining highly active catalysts supported on perovskite oxides. For instance, FeCoNi alloys can be exsolved from Sr 2 FeCo 0.2 Ni 0.2 Mn 0.1 Mo 0.5 O 6− δ , boosting the electrocatalytic properties of these electrodes. However, due to differences in cation diffusion properties, the composition of the nanoparticles is uneven and strongly affected by process conditions such as temperature. An additional key feature of exsolution is its reversibility, which could help in catalyst regeneration if poisoned. Nevertheless, there is little knowledge on the reversibility mechanisms of multicomponent exsolved alloys. For that purpose, a combination of synchrotron-based in situ X-ray Diffraction (XRD) and Near-Ambient Pressure X-ray Photoelectron Spectroscopy (NAP-XPS) was employed in this work to uncover these missing aspects of multicomponent alloyed exsolution. These techniques allowed determination of the crystallographic and surface-related phenomena occurring during reversible exsolution both to the nanoparticles and the perovskite oxide support. This enabled the identification of the exsolution onset temperature and the range at which the double perovskite to Ruddlesden-Popper transition occurred, a process that has notable implications for the electrocatalytic performance. Finally, in combination with microscopy analyses, it was possible to reveal the morphological and compositional changes that the exsolved nanoparticles experienced upon reduction-oxidation cycles. This resulted in a re-arrangement of the surface species and a variation in the composition (Fe enrichment) of the regenerated ternary alloyed exsolved nanoparticles. These results indicate that reversible exsolution might alter the catalytic properties of the exsolved nanoparticles, with profound implications in the performance of (electro)catalytic processes. This work unveils the mechanism of FeCoNi alloy reversible exsolution from double perovskites via in situ synchrotron-based NAP-XPS and time-resolved XRD.
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For instance, FeCoNi alloys can be exsolved from Sr 2 FeCo 0.2 Ni 0.2 Mn 0.1 Mo 0.5 O 6− δ , boosting the electrocatalytic properties of these electrodes. However, due to differences in cation diffusion properties, the composition of the nanoparticles is uneven and strongly affected by process conditions such as temperature. An additional key feature of exsolution is its reversibility, which could help in catalyst regeneration if poisoned. Nevertheless, there is little knowledge on the reversibility mechanisms of multicomponent exsolved alloys. For that purpose, a combination of synchrotron-based in situ X-ray Diffraction (XRD) and Near-Ambient Pressure X-ray Photoelectron Spectroscopy (NAP-XPS) was employed in this work to uncover these missing aspects of multicomponent alloyed exsolution. These techniques allowed determination of the crystallographic and surface-related phenomena occurring during reversible exsolution both to the nanoparticles and the perovskite oxide support. This enabled the identification of the exsolution onset temperature and the range at which the double perovskite to Ruddlesden-Popper transition occurred, a process that has notable implications for the electrocatalytic performance. Finally, in combination with microscopy analyses, it was possible to reveal the morphological and compositional changes that the exsolved nanoparticles experienced upon reduction-oxidation cycles. This resulted in a re-arrangement of the surface species and a variation in the composition (Fe enrichment) of the regenerated ternary alloyed exsolved nanoparticles. These results indicate that reversible exsolution might alter the catalytic properties of the exsolved nanoparticles, with profound implications in the performance of (electro)catalytic processes. 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For that purpose, a combination of synchrotron-based in situ X-ray Diffraction (XRD) and Near-Ambient Pressure X-ray Photoelectron Spectroscopy (NAP-XPS) was employed in this work to uncover these missing aspects of multicomponent alloyed exsolution. These techniques allowed determination of the crystallographic and surface-related phenomena occurring during reversible exsolution both to the nanoparticles and the perovskite oxide support. This enabled the identification of the exsolution onset temperature and the range at which the double perovskite to Ruddlesden-Popper transition occurred, a process that has notable implications for the electrocatalytic performance. Finally, in combination with microscopy analyses, it was possible to reveal the morphological and compositional changes that the exsolved nanoparticles experienced upon reduction-oxidation cycles. 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source Royal Society Of Chemistry Journals
subjects Alloys
Catalysts
Composition
Crystallography
Iron
Nanoalloys
Nanoparticles
Oxidation
Perovskites
Photoelectron spectroscopy
Photoelectrons
Pressure
X ray photoelectron spectroscopy
X-ray diffraction
title Understanding the evolution of ternary alloyed nanoparticles during reversible exsolution from double perovskite oxides
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