Titre :

Rethinking electronic and geometric structures of real hydrodesulfurization catalysts by in situ photon-in/photon-out spectroscopy

Auteur(s) :

Tougerti, Asma [Auteur]
Unité de Catalyse et Chimie du Solide (UCCS) - UMR 8181
Simon, Pardis [Auteur]
Unité de Catalyse et Chimie du Solide (UCCS) - UMR 8181
Desjacques, Charlotte [Auteur]
Unité de Catalyse et Chimie du Solide - UMR 8181 [UCCS]
Girardon, Jean-Sébastien [Auteur]
Unité de Catalyse et Chimie du Solide (UCCS) - UMR 8181
Mazzanti, Francesco [Auteur]
Unité de Catalyse et Chimie du Solide - UMR 8181 [UCCS]
Pipolo, Silvio [Auteur]
Unité de Catalyse et Chimie du Solide (UCCS) - UMR 8181
Trentesaux, Martine [Auteur]
Unité de Catalyse et Chimie du Solide (UCCS) - UMR 8181
Cristol, Sylvain [Auteur]
Unité de Catalyse et Chimie du Solide (UCCS) - UMR 8181

Titre de la revue :

Journal of Physical Chemistry C

Nom court de la revue :

J. Phys. Chem. C

Numéro :

124

Pagination :

17586-17598

Éditeur :

American Chemical Society (ACS)

Date de publication :

2020-08-03

ISSN :

1932-7447

Mot(s)-clé(s) en anglais :

Catalysts
Cobalt
Energy
Oxides
X-ray photoelectron spectroscopy

Discipline(s) HAL :

Chimie/Catalyse
Chimie/Chimie théorique et/ou physique

Résumé en anglais : [en]

Core level spectroscopy is a powerful tool to achieve a fine understanding of both the electronic and the geometric structure of heterogeneous catalysts. The present work shows use of photon-in/photon-out spectroscopy to ...
Lire la suite >Core level spectroscopy is a powerful tool to achieve a fine understanding of both the electronic and the geometric structure of heterogeneous catalysts. The present work shows use of photon-in/photon-out spectroscopy to investigate the structures of hydrodesulfurization catalysts actives sites. Despite countless studies carried out to understand the working phase of this class of catalyst, the exact localization of the promoter (cobalt) remains an open question for the “real hydrodesulfurization (HDS) catalyst”. The difficulty comes from the segregation of cobalt in different phases during the catalyst activation step. Consequently, most collected spectroscopic signal of cobalt involved in the catalyst, will corresponds to a weighted average of the contributions arising from all cobalt centers (active phase, nonactive sulfide phase, and the remaining cobalt oxide phase). To overcome this problem, for the first time in situ Co K-edge HERFD-XAS is used to discriminate between oxide (CoII–O) and sulfide (CoII–S) phases arising during HDS catalyst activation, allowing the localization of cobalt in the active phase of the catalysts. We find that Co is localized at S-edges of the MoS2 layers. Furthermore, in situ Co K-edge 1s2p RIXS of the sulfided catalyst shows excitations to bandlike unoccupied states revealing the metallic nature of cobalt in these structures. A new XPS fitting procedure, considering the exact electronic structure of the active phase is proposed bringing us to reconsider earlier Co-promotion rate published in the literature for a better correlation with the catalytic activity.Lire moins >

Langue :

Anglais

Audience :

Internationale

Vulgarisation :

Non

Établissement(s) :

CNRS
Centrale Lille
ENSCL
Univ. Artois
Université de Lille

Collections :

• Unité de Catalyse et Chimie du Solide (UCCS) - UMR 8181

Équipe(s) de recherche :

Matériaux pour la catalyse (MATCAT)
Modélisation et spectroscopies (MODSPEC)

Date de dépôt :

2022-03-02T07:13:24Z
2023-03-14T14:34:10Z
2024-04-04T12:54:38Z