Synergistic Effects of Bimetallic AuPd and La2O3 in the Catalytic Reduction of NO with CO

Bimetallic AuPd nanoparticles supported on TiO2 are known to catalyze the reduction of NO with CO. Here, we investigated the effects of the addition of lanthanum oxide to a AuPd/TiO2 catalyst with a AuPd particle size of 2.1–2.2 nm. The addition of La2O3 enhanced the catalytic activity; for example, at 250 °C, there was 40.9% NO conversion and 49.3% N2-selectivity for AuPd/TiO2, and 100% NO conversion and 100% N2-selectivity for AuPd-La (1:1)/TiO2. The temperature requiring 100% NO conversion dropped from 400 °C to 200 °C by the simple post-impregnation of La2O3 onto AuPd/TiO2. In situ diffuse reflectance infrared Fourier transform spectroscopy (DRIFTS) combined with modulation excitation spectroscopy (MES) demonstrated that CO adsorption occurs first on Au atoms and then, within 80 s, moves onto Pd atoms. This transformation between two adsorption sites was facilitated by the addition of La2O3.

CO2 Methanation over Rh/CeO2 Studied with Infrared Modulation Excitation Spectroscopy and Phase Sensitive Detection

Methane is a well-established fuel molecule whose production from CO 2 through methanation garners increasing interest as an energy storage solution. While often produced with Ni based catalysts, other metals are of interest thanks to higher robustness and activity-selectivity numbers. The Rh/CeO 2 catalyst has shown appreciable properties for CO 2 methanation and its structural dynamics has been studied in situ. However, the reaction pathway is unknown. Here, we present infrared modulation excitation spectroscopy measurements with phase sensitive detection of a Rh/CeO 2 catalyst adsorbate composition during H 2 pulsing (0–2 vol.%) to a constant CO 2 (0.5 vol.%) feed. Various carbonyl (CO) and carbonate (b-CO 3 /p-CO 3 ) ad-species clearly respond to the hydrogen stimulus, making them potential reaction intermediates. The different CO ad-species are likely intermediates for product CO and CH 4 but their individual contributions to the respective formations are not unambiguously ascertained. As for the carbonate dynamics, it might be linked to the reduction/oxidation of the CeO 2 surface upon H 2 pulsing. Formate (HCOO) ad-species are clearly visible but appear to be, if not spectators, linked to slow side reactions possibly also affected by CeO 2 redox processes.

Detection of key transient Cu intermediates in SSZ-13 during NH3-SCR deNOx by modulation excitation IR spectroscopy

Protagonists in the standard SCR reaction have been caught in the act by modulation excitation IR & XAFS spectroscopy.