Selective detection of reaction intermediates using concentration-modulation excitation DRIFT spectroscopy

Concentration-modulation excitation spectroscopy (MES) experiments in combination with phase-sensitive detection (PSD) were used to monitor the gas–solid interface by means of in operando diffuse reflectance infrared spectroscopy (DRIFT). The MES methodology is a powerful technique because it allows sensitive and selective spectroscopic detection and monitoring of the dynamic behavior of species directly involved in a reaction.In this work, c-MES was employed to monitor the adsorption of hydrogen and carbon dioxide and their reaction (reverse water gas shift) on a model Pd(1 wt.%)/γ-Ga2O3 catalyst. Details of the reaction mechanism could be reached: (i) H2 is dissociatively chemisorbed on the gallium oxide surface giving Ga–H species; (ii) CO2 is adsorbed giving rise of carbonate groups; (iii) on the gallia surface, carbonates are hydrogenated by Ga–H to produce formate species with different coordination, e.g. monodentate, bidentate and bridged formates, which in turn are decomposed into CO(g); (iv) the metal phase increases the formate surface concentration onto the gallia because of an efficient supply of atomic hydrogen via a spillover. Results also indicated that monodentate formates are the most reactive intermediate.

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► Concentration-modulation excitation infrared spectroscopy was used to monitor surface intermediates.
► Reverse water gas shift reaction was investigated on a Pd(Ga)/Ga2O3 catalyst.
► Carbonates, formates and gallium hydride were selectively detected.
► Monodentate is the most reactive formate intermediate.