Covalent organic frameworks for design of ...
Type de document :
Article dans une revue scientifique: Article original
URL permanente :
Titre :
Covalent organic frameworks for design of ruthenium catalysts with high single-atom site density for CO 2 hydrogenation into formic acid
Auteur(s) :
Fellenberg, Ana [Auteur]
Unité de Catalyse et Chimie du Solide (UCCS) - UMR 8181
Addad, Ahmed [Auteur]
Unité Matériaux et Transformations (UMET) - UMR 8207
Chernyak, Sergei A. [Auteur]
Unité de Catalyse et Chimie du Solide - UMR 8181 [UCCS]
Yong, Zhou [Auteur]
Unité de Catalyse et Chimie du Solide (UCCS) - UMR 8181
Corda, Massimo [Auteur]
Unité de Catalyse et Chimie du Solide (UCCS) - UMR 8181
Oliveira De Souza, Danilo [Auteur]
Unité de Catalyse et Chimie du Solide (UCCS) - UMR 8181
Safonova, Olga V. [Auteur]
Paul Scherrer Institute [PSI]
Martin-Diaconescu, Vlad [Auteur]
ALBA Synchrotron light source [Barcelone]
Ordomsky, Vitaly [Auteur]
Unité de Catalyse et Chimie du Solide (UCCS) - UMR 8181
Ji, Gang [Auteur]
Unité Matériaux et Transformations (UMET) - UMR 8207
Khodakov, Andrei [Auteur]
Unité de Catalyse et Chimie du Solide (UCCS) - UMR 8181
Unité de Catalyse et Chimie du Solide (UCCS) - UMR 8181
Addad, Ahmed [Auteur]
Unité Matériaux et Transformations (UMET) - UMR 8207
Chernyak, Sergei A. [Auteur]
Unité de Catalyse et Chimie du Solide - UMR 8181 [UCCS]
Yong, Zhou [Auteur]
Unité de Catalyse et Chimie du Solide (UCCS) - UMR 8181
Corda, Massimo [Auteur]
Unité de Catalyse et Chimie du Solide (UCCS) - UMR 8181
Oliveira De Souza, Danilo [Auteur]
Unité de Catalyse et Chimie du Solide (UCCS) - UMR 8181
Safonova, Olga V. [Auteur]
Paul Scherrer Institute [PSI]
Martin-Diaconescu, Vlad [Auteur]
ALBA Synchrotron light source [Barcelone]
Ordomsky, Vitaly [Auteur]
Unité de Catalyse et Chimie du Solide (UCCS) - UMR 8181
Ji, Gang [Auteur]
Unité Matériaux et Transformations (UMET) - UMR 8207
Khodakov, Andrei [Auteur]
Unité de Catalyse et Chimie du Solide (UCCS) - UMR 8181
Titre de la revue :
Cell Rep. Phys. Sci.
Nom court de la revue :
Cell Rep. Phys. Sci.
Numéro :
5
Pagination :
-
Date de publication :
2024-06-08
ISSN :
2666-3864
Discipline(s) HAL :
Chimie/Catalyse
Chimie/Matériaux
Chimie/Matériaux
Résumé en anglais : [en]
Carbon dioxide is an abundant carbon resource for chemical and fuel synthesis. Formic acid, vital for hydrogen storage, has numerous applications. Covalent organic frameworks are a unique class of materials composed of ...
Lire la suite >Carbon dioxide is an abundant carbon resource for chemical and fuel synthesis. Formic acid, vital for hydrogen storage, has numerous applications. Covalent organic frameworks are a unique class of materials composed of interconnected organic building blocks through covalent bonds. They possess porosity and functional groups, making them suitable for creating supported metallic catalysts. In this study, we present a strategy that utilizes covalent organic frameworks with diverse structures and chemical compositions to enhance carbon dioxide hydrogenation to formic acid at low temperatures. This enhancement arises from both high density of single-atom ruthenium sites and their intrinsic activity. Operando X-ray absorption and catalytic tests demonstrate that the concentration of nitrogen functional groups affects the intrinsic single-site ruthenium activity, whereas the impact of oxygen-containing groups is minor. Catalyst stability is attributed to the ability of single atoms to resist reduction to metallic state. This strategy has broad applicability for various covalent organic framework-supported single-atom catalysts.Lire moins >
Lire la suite >Carbon dioxide is an abundant carbon resource for chemical and fuel synthesis. Formic acid, vital for hydrogen storage, has numerous applications. Covalent organic frameworks are a unique class of materials composed of interconnected organic building blocks through covalent bonds. They possess porosity and functional groups, making them suitable for creating supported metallic catalysts. In this study, we present a strategy that utilizes covalent organic frameworks with diverse structures and chemical compositions to enhance carbon dioxide hydrogenation to formic acid at low temperatures. This enhancement arises from both high density of single-atom ruthenium sites and their intrinsic activity. Operando X-ray absorption and catalytic tests demonstrate that the concentration of nitrogen functional groups affects the intrinsic single-site ruthenium activity, whereas the impact of oxygen-containing groups is minor. Catalyst stability is attributed to the ability of single atoms to resist reduction to metallic state. This strategy has broad applicability for various covalent organic framework-supported single-atom catalysts.Lire moins >
Langue :
Anglais
Audience :
Internationale
Vulgarisation :
Non
Établissement(s) :
Université de Lille
CNRS
Centrale Lille
ENSCL
Univ. Artois
CNRS
Centrale Lille
ENSCL
Univ. Artois
Collections :
Équipe(s) de recherche :
Catalyse pour l’énergie et la synthèse de molécules plateforme (CEMOP)
Métallurgie Physique et Génie des Matériaux
Métallurgie Physique et Génie des Matériaux
Date de dépôt :
2024-06-28T21:06:18Z
2024-07-10T07:45:20Z
2024-07-10T07:46:45Z
2024-07-10T07:45:20Z
2024-07-10T07:46:45Z
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