• Damsgaard, Christian Danvad
• Kehres, Jan
• Carvalho, Hudson W. P.
• Chorkendorff, Ib
• Fiordaliso, Elisabetta Maria
• Grunwaldt, Jan-D.
• Sharafutdinov, Irek

Abstract

<p>The CO₂ hydrogenation to methanol is efficiently catalyzed at ambient pressure by nanodispersed intermetallic GaPd₂/SiO₂ catalysts prepared by incipient wetness impregnation. Here we optimize the catalyst in terms of metal content and reduction temperature in relation to its catalytic activity. We find that the intrinsic activity is higher for the GaPd₂/SiO₂ catalyst with a metal loading of 13 wt.% compared to catalysts with 23 wt.% and 7 wt.%, indicating that there is an optimum particle size for the reaction of around 8 nm. The highest catalytic activity is measured on catalysts reduced at 550 °C. To unravel the formation of the active phase, we studied calcined GaPd₂/SiO₂ catalysts with 23 wt.% and 13 wt.% using a combination of in situ techniques: X-ray diffraction (XRD), X-ray absorption near edge fine structure (XANES) and extended X-ray absorption fine structure (EXAFS). We find that the catalyst with higher metal content reduces to metallic Pd in a mixture of H₂/Ar at room temperature, while the catalyst with lower metal content retains a mixture of PdO and Pd up to 140 °C. Both catalysts form the GaPd₂ phase above 300 °C, albeit the fraction of crystalline intermediate Pd nanoparticles of the catalyst with higher metal loading reduces at higher temperature. In the final state, the catalyst with higher metal loading contains a fraction of unalloyed metallic Pd, while the catalyst with lower metal loading is phase pure. We discuss the alloying mechanism leading to the catalyst active phase formation selecting three temperatures: 25 °C, 320 °C and 550 °C.</p>

Topics

• nanoparticle
• impedance spectroscopy
• phase
• x-ray diffraction
• intermetallic
• extended X-ray absorption fine structure spectroscopy