Enhancing the performance of a novel CoRu/CeO2 bimetallic catalyst for the dry reforming of methane via a mechanochemical process
A mechanochemical synthesis method has been used to synthesize CoRu nanoparticles supported on CeO2 for methane dry reforming. In this work, we study the effect of Ru addition to Co/CeO2-based catalysts and of the synthesis method by screening their catalytic activity, using synchrotron X-ray diffra...
| Autores: | , , , , , , , , , , , , |
|---|---|
| Formato: | artículo |
| Fecha de publicación: | 2024 |
| País: | España |
| Recursos: | Universitat Politècnica de Catalunya (UPC) |
| Repositorio: | UPCommons. Portal del coneixement obert de la UPC |
| Idioma: | inglés |
| OAI Identifier: | oai:upcommons.upc.edu:2117/408129 |
| Acesso em linha: | https://hdl.handle.net/2117/408129 https://dx.doi.org/10.1016/j.apcatb.2023.123624 |
| Access Level: | acceso abierto |
| Palavra-chave: | Catalysis Mechanochemistry Methane dry reforming (DRM) Operando characterization Bimetallic catalyst Hydrogen production Catàlisi Àrees temàtiques de la UPC::Enginyeria química |
| Resumo: | A mechanochemical synthesis method has been used to synthesize CoRu nanoparticles supported on CeO2 for methane dry reforming. In this work, we study the effect of Ru addition to Co/CeO2-based catalysts and of the synthesis method by screening their catalytic activity, using synchrotron X-ray diffraction (XRD), and operando near-ambient pressure X-ray photoelectron spectroscopy (NAP-XPS). Ruthenium addition directly impacts the reducibility of cobalt species and results in smaller particle sizes, as demonstrated by H2-temperature programmed reduction and XRD. NAP-XPS shows that Ru modifies the metal-support interaction, as evidenced by the higher Ce3+/Ce ratios for the bimetallic samples and tuning the oxidation state of Ru. The synthesis method also influences the dispersion of Co and Ru on the surface. Mechanochemically-prepared samples (mono- and bimetallic) outperformed the conventionally-synthesized counterparts by reaching higher CH4 and CO2 conversions, resulting in a stable CoRu/CeO2 catalyst for 24 h at 700 °C and yielding an H2/CO ratio close to 1. |
|---|