Nanoplasmonic sensing to study CO and oxygen adsorption and CO oxidation on size-selected Pt clusters.

The adsorption of CO and oxygen and CO oxidation on size-selected Pt clusters were studied by indirect nanoplasmonic sensing (INPS) in the pressure range of 1-100 Pa at = 418 K. CO adsorption was reversible, inducing a blue-shift in the localised surface plasmon resonance (LSPR) response, regardless of the initial CO pressure. We observe a plateau at approximately Δ = -0.

Low-Temperature Selective Oxidative Dehydrogenation of Cyclohexene by Titania-Supported Nanostructured Pd, Pt, and Pt-Pd Catalytic Films.

Films of titania-supported monometallic Pd, Pt, and bimetallic Pt-Pd catalysts made of metallic nanoparticles were prepared by magnetron sputtering and studied in the oxidative dehydrogenation (ODH) of cyclohexene. Pd/TiO and Pt-Pd/TiO were found active at as low temperature as 150 °C and showed high catalytic activity with high conversion (up to 81%) and benzene selectivity exceeding 97% above 200 °C. In turn, the Pt/TiO catalyst performed poorly with the onset of benzene production at 200 °C only and conversions not exceeding 5%.

Cyclohexane Oxidative Dehydrogenation on Graphene-Oxide-Supported Cobalt Ferrite Nanohybrids: Effect of Dynamic Nature of Active Sites on Reaction Selectivity.

In this work, we investigated cyclohexane oxidative dehydrogenation (ODH) catalyzed by cobalt ferrite nanoparticles supported on reduced graphene oxide (RGO). We aim to identify the active sites that are specifically responsible for full and partial dehydrogenation using advanced spectroscopic techniques such as X-ray photoelectron emission microscopy (XPEEM) and X-ray photoelectron spectroscopy (XPS) along with kinetic analysis. Spectroscopically, we propose that Fe/T sites could exclusively produce benzene through full cyclohexane dehydrogenation, while kinetic analysis shows that oxygen-derived species (O*) are responsible for partial dehydrogenation to form cyclohexene in a single catalytic sojourn.

Oxidative dehydrogenation of cyclohexene on atomically precise subnanometer CuPd (0 ≤ ≤ 4) tetramer clusters: the effect of cluster composition and support on performance.

The pronounced effects of the composition of four-atom monometallic Cu and Pd and bimetallic CuPd clusters and the support on the catalytic activity and selectivity in the oxidative dehydrogenation of cyclohexene are reported. The ultra-nanocrystalline diamond supported clusters are highly active and dominantly produce benzene; some of the mixed clusters also produce cyclohexadiene, which are all clusters with a much suppressed combustion channel. The also highly active TiO-supported tetramers solely produce benzene, without any combustion to CO.

Atom by atom built subnanometer copper cluster catalyst for the highly selective oxidative dehydrogenation of cyclohexene.

The effect of particle size and support on the catalytic performance of supported subnanometer copper clusters was investigated in the oxidative dehydrogenation of cyclohexene. From among the investigated seven size-selected subnanometer copper particles between a single atom and clusters containing 2-7 atoms, the highest activity was observed for the titania-supported copper tetramer with 100% selectivity toward benzene production and being about an order of magnitude more active than not only all the other investigated cluster sizes on the same support but also the same tetramer on the other supports, AlO, SiO, and SnO. In addition to the profound effect of cluster size on activity and with Cu outstanding from the studied series, Cu clusters supported on SiO provide an example of tuning selectivity through support effects when this particular catalyst also produces cyclohexadiene with about 30% selectivity.