In Situ Spectroscopic Investigation into the Active Sites for Crotonaldehyde Hydrogenation at the Pt Nanoparticle–Co3O4 Interface

• Published in: ACS catalysis 2016-10, Vol.6 (10), p.7140-7147
• Main Authors: Kennedy, Griffin, Melaet, Gérôme, Han, Hui-Ling, Ralston, Walter T, Somorjai, Gabor A
• Format: Article
• Language: English
• Subjects: ambient-pressure XPS; cobalt oxide; hydrogenation; in situ characterization; INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CHEMISTRY; sum frequency generation; support effects
• ISSN: 2155-5435; 2155-5435
• DOI: 10.1021/acscatal.6b01640

The hydrogenation of crotonaldehyde by platinum nanoparticles supported on cobalt oxide was used as a reaction to probe the effect of the interface between the two materials on the activity and selectivity of the catalyst. Four potential products can be formed by this reaction: propylene, butyraldehyde, crotyl alcohol, and butanol. When Pt nanoparticles are supported on SiO2, an inert support, only propylene and butyraldehyde are formed. However, when Pt is supported on cobalt oxide, the alcohols make up roughly 40% of the total activity, indicating that cobalt oxide plays a pivotal role in the reaction, much like other active supports such as TiO2. To elucidate the mechanism of alcohol formation, in situ sum frequency generation vibrational spectroscopy (SFG) and ambient-pressure X-ray photoelectron spectroscopy (AP-XPS) were utilized to probe the reactant adsorption and intermediate formation and the chemical state of the materials under working catalytic conditions. The SFG data indicate that crotonaldehyde adsorbs on the oxide surface, likely through the aldehyde oxygen as well as on the Pt surface through the alkene group. AP-XPS results show that the surface of the Co3O4 support becomes partially reduced under the reaction conditions and Pt exists in its metallic state. Taking these results together, we propose that the crotonaldehyde adsorbs at reduced oxide surface sites and that this adsorption mode is responsible for the production of alcohol products. A platinum nanoparticle density dependence study was also undertaken to change the abundance of interface sites and study their effect on the reaction. The selectivity between the two alcohol products was altered as a function of the Pt nanoparticle density: higher selectivity toward butanol and lower selectivity toward crotyl alcohol was obtained with increasing density, while propylene and butyraldehyde selectivities were constant with respect to density. On the basis of the data presented, we propose that butanol is preferentially formed at the metal–oxide interface, while crotyl alcohol is formed at oxide surface sites by reaction with spillover hydrogen.