By combining modulated excitation and Raman spectroscopy, we obtained mechanistic insights that go beyond what is currently achievable with Raman experiments under steady-state conditions.
Exploitation of the self-regenerative property of perovskite-type oxides allowed to demonstrate recovery of La0.3Sr0.55Ti0.95Ni0.05O3 from sulfur poisoning by reversible segregation-incorporation of Ni at SOFC temperatures.
Using targeted synthesis and in situ characterization a palladium catalyst with improved stability against sintering during methane oxidation was prepared.
Through the combination of time-resolved X-ray absorption spectroscopy and transient experimentation, we were able to capture an ammonia inhibition effect on the rate-limiting copper re-oxidation at low temperature.
Kinetic studies of the Pt carbonate-mediated, room-temperature oxidation of carbon monoxide by oxygen
The kinetics involved in ambient-temperature catalytic oxidation of carbon monoxide by oxygen over a Pt/Al2O3 catalyst is evaluated under periodic redox operation using combined mass spectrometry, diffuse reflectance infrared spectroscopy and time-resolved Pt L3-edge X-ray absorption spectroscopy.
Supported gold as catalyst for the decomposition of ammonia precursors in the selective catalytic reduction of NOx
Titanium dioxide-supported gold was found to catalyze the hydrolysis of formate-based ammonia precursor compounds which are proposed for the selective catalytic reduction of nitrogen oxides (NOx) in combustion exhaust gas. In contrast to other noble metals, the supported gold does not oxidize the released NH3, while it maintains decomposition of intermediate formic acid.
The hydrolysis of isocyanic acid was studied experimentally and theoretically and a reaction mechanism on different catalysts was established. The decreasing NOx emission limits for diesel vehicles impel the further development of the existing NOx deactivation technologies, particularly the selective catalytic reduction (SCR) of nitrogen oxides with urea. In the urea-SCR process, urea is injected into the hot exhaust gas, where it thermally decomposes into isocyanic acid (HNCO) and ammonia.