News & Scientific Highlights

The combination of in situ spectroscopy methods allowed to detect the evolution of a catalyst precursor to the catalytic material, and investigate a relevant reaction. The reduction of a mixture of perovskite, pyrochlore and nickel leads to the formation of active and selective catalytst, converting carbon dioxide and methane to syngas. 

_{Ammonium sulfate has been used as a probe for aerosol particles and investigated in situ by means of ambient pressure X-ray photoelectron spectroscopy. Unexpectedly, when the particles start to absorb water, a spontaneous redox reaction leading to nitrogen and elemental sulfur takes place.}

_{In situ and ex situ ambient pressure X-ray photoelectron spectroscopy have been used to investigate the solid-liquid interface of a LSCO water splitting catalyst. Experimental results, supported by theoretical simulations of the core-electron binding energy, detect the formation of cobalt oxyhydroxide under working conditions.} 

The evolution of atomically dispersed platinum species on ceria has been investigated by means of ambient pressure X-ray photoelectron spectroscopy and X-ray absorption near edge structure spectroscopy. Experimental results, supported by the theoretical simulation of the phase diagram, show that atomically dispersed species evolve towards nanoparticles during the activation of the catalysts. Such an evolution is influenced by the temperature and the reaction environment. 

The introduction of tin into ceria strongly influences its reducibility. In turn, the reaction mechanism towards the oxidation of carbon monoxide changes: the oxidation rate increases, the apparent activation energy decreases and the reaction order in oxygen increases.

Encapsulation of highly dispersed palladium oxide clusters in the microporous channels and voids of the nanosized silicalite-1 crystals has been achieved by using an amine-based ligand.

Platinum isolated atoms and clusters supported on molybdenum carbide have been extensively characterized. The presence of both species is essential to boost the stability, so that the catalysts displays high metal-normalized turnover number of 4,300,000 moles of hydrogen per mole of platinum

The strong metal support interaction has been investigated in situ by means of electron microscopy, XPS and XRD, to provide a complete overview about the interplay between the metal and the support. 

The temperature-dependent segregation of strontium-containing species on LSCO electrodes has been studied by means of XPS, SEM and XRD. Such surface species dissolve almost quantitatively upon immersion in water, leaving cobalt oxide, the active site of the reaction, free.