One-Pot Synthesis of Ni<sub>0.05</sub>Ce<sub>0.95</sub>O<sub>2−δ</sub> Catalysts with Nanocubes and Nanorods Morphology for CO<sub>2</sub> Methanation Reaction and in Operando DRIFT Analysis of Intermediate Species

The valorization of CO<sub>2</sub> via renewable energy sources allows one to obtain carbon-neutral fuels through its hydrogenation, like methane. In this study, Ni<sub>0.05</sub>Ce<sub>0.95</sub>O<sub>2−δ</sub> catalysts were prepared using a simple o...

Descripción completa

Guardado en:
Detalles Bibliográficos
Autores principales: Igor Luisetto, Stefano Stendardo, Sakkarapalayam Murugesan Senthil Kumar, Karuppiah Selvakumar, Jagadesh Kopula Kesavan, Giovanna Iucci, Umberto Pasqual Laverdura, Simonetta Tuti
Formato: article
Lenguaje:EN
Publicado: MDPI AG 2021
Materias:
Acceso en línea:https://doaj.org/article/838a0134d4dd48ef8b62fafa97b9f5fd
Etiquetas: Agregar Etiqueta
Sin Etiquetas, Sea el primero en etiquetar este registro!
Descripción
Sumario:The valorization of CO<sub>2</sub> via renewable energy sources allows one to obtain carbon-neutral fuels through its hydrogenation, like methane. In this study, Ni<sub>0.05</sub>Ce<sub>0.95</sub>O<sub>2−δ</sub> catalysts were prepared using a simple one-pot hydrothermal method yielding nanorod and nanocube particles to be used for the methanation reaction. Samples were characterized by XRD, BET, TEM, H<sub>2</sub>-TPR, and H<sub>2</sub>-TPD experiments. The catalytic activity tests revealed that the best performing catalyst was Ni<sub>0.05</sub>Ce<sub>0.95</sub>O<sub>2−δ</sub>, with nanorod morphology, which gave a CO<sub>2</sub> conversion of 40% with a selectivity of CH<sub>4</sub> as high as 93%, operating at 325 °C and a GHSV of 240,000 cm<sup>3</sup> h<sup>−1</sup> g<sup>−1</sup>. However, the lower activation energy was found for Ni<sub>0.05</sub>Ce<sub>0.95</sub>O<sub>2−δ</sub> catalysts with nanocube morphology. Furthermore, an in operando diffuse reflectance infrared Fourier transform spectroscopy (DRIFTS) analysis was performed flowing CO<sub>2</sub>:H<sub>2</sub> or CO:H<sub>2</sub> mixture, showing that the main reaction pathway, for the CO<sub>2</sub> methanation, is the direct hydrogenation of formate intermediate.