Reflection absorption infrared spectroscopy of the surface chemistry of furfural on Pd(111)

The hydrolysis and subsequent acidic dehydration of biomass leads to the production of smaller oxygenates, including furfural, which can undergo subsequent reactions such as hydrogenation to produce value-added products. Palladium has been found to be an active catalyst for this process. As a result, the surface chemistry of furfural is investigated on a Pd(111) single-crystal surface using reflection-absorption infrared spectroscopy as a basis for understanding the catalytic conversion of furfural to value-added products. Following adsorption at 90 K, furfural adopts a flat-lying geometry at low coverages, but converts to a tilted species as the coverage approaches saturation. Heating to & SIM;175 K forms a tilted eta(1)(O) species that appears to deprotonate on heating to above 200 K to form an intermediate with a tilted furyl ring and a carbonyl group close to parallel to the surface. Further heating to & SIM;250 K and above caused this species to decarbonylate to form adsorbed carbon monoxide and an infrared invisible furyl intermediate. This can then undergo a ring-opening reaction to produce further CO and form a C3H3 intermediate that can hydrogenate to produce propylene. This reaction sequence is in good agreement with previous density functional theory calculations and with the products observed in temperature-programmed desorption.

Automated summary

The surface chemistry of furfural on a Pd(111) single-crystal surface was investigated to understand the catalytic conversion of furfural to value-added products. The adsorption and subsequent reactions of furfural were studied using reflection-absorption infrared spectroscopy, revealing the formation of intermediate species and the production of CO and propylene.