• Spennati, Elena
• Riani, Paola
• Atakoohi, Sina Ebrahim
• Garbarino, Gabriella
• Maron, Jacopo De
• Vattuone, Luca
• Savio, Letiza

Abstract

<jats:p>Laboratory‐prepared GnP using molten salt, commercial Gnp and reduced graphene oxide (rGO) have been characterized and utilized as support for CO2 hydrogenation catalysts. Ni‐ and Ru‐ catalysts supported over Gnp, commercial Gnp and rGO have been deeply characterized at different stages using Raman, IR, XRD, FE‐SEM‐EDXS, SEM‐EDXS, XPS, and TEM, also addressing carbon loss before reaction and evolved species, thus allowing a better comprehension of the produced materials. Ni and Ru/rGO were inactive while Gnp‐supported ones were active. Ru has been found almost completely selective toward reverse Water Gas Shift to CO, approaching the forecasted thermodynamic equilibrium at 723 K, in the tested conditions (YCO~55%), with an apparent activation energy in the range of 70‐90 kJ/mol. Exhaust catalysts pointed out the presence of sulfur partially linked to the carbon matrix and partially producing the corresponding metal sulfide with the detection of surface oxidized species in the cationic form and adsorbed species as well. The metal‐based nanoparticles displayed a quite narrow size distribution, confirming the promising behavior of these catalytic systems for CO2 utilization.</jats:p>

Topics

• nanoparticle
• surface
• Carbon
• scanning electron microscopy
• x-ray diffraction
• x-ray photoelectron spectroscopy
• transmission electron microscopy
• activation
• Energy-dispersive X-ray spectroscopy