Clusters in molecular beam experiments can mimic aerosol nanoclusters and provide molecular-level details for various processes relevant to atmospheric aerosol research. Aerosol nanoclusters, particles of sizes below 10 nm, are difficult to investigate in ambient atmosphere and thus represent a gap in our understanding of the new particle formation process. Recent field measurements and laboratory experiments are closing this gap; however, experiments with clusters in molecular beams are rarely involved. Yet, they can offer an unprecedented detailed insight into the processes including particles in this size range. In this Perspective, we discuss several up-to-date molecular beam experiments with clusters and demonstrate that the investigated clusters approach aerosol nanoclusters in terms of their complexity and chemistry. We examine remaining gaps between atmospheric aerosols and clusters in molecular beams and speculate about future experiments bridging these gaps.

• Publikační typ
• časopisecké články MeSH
• přehledy MeSH

The uptake of molecules on nanometer-size clusters of polyaromatic hydrocarbons (PAHs) is important for the condensation of water on PAH aerosols in the atmosphere and for ice mantle growth on nanoparticles in the interstellar medium. We generate benzene clusters BzN of mean size N̅ ≈ 300 (radius R̅ ≈ 2.2 Å) as a model system for the PAH nanoparticles. Using molecular beams and mass spectrometry detection, we investigate the uptake of water, methanol, and ethanol by these clusters. All picked up molecules are highly mobile on BzN and generate clusters within <3 ms. The relative uptakes for the different investigated molecules can be directly compared and quantified. Water molecules exhibit the lowest relative pickup probability that is ∼30% lower than those for methanol and ethanol, which are approximately the same.

• Publikační typ
• časopisecké články MeSH

The dominant pathway of radiation damage begins with the ionization of water. Thus far, however, the underlying primary processes could not be conclusively elucidated. Here, we directly study the earliest steps of extreme ultraviolet (XUV)-induced water radiolysis through one-photon excitation of large water clusters using time-resolved photoelectron imaging. Results are presented for H2O and D2O clusters using femtosecond pump pulses centered at 133 or 80 nm. In both excitation schemes, hydrogen or proton transfer is observed to yield a prehydrated electron within 30 to 60 fs, followed by its solvation in 0.3 to 1.0 ps and its decay through geminate recombination on a ∼10-ps time scale. These results are interpreted by comparison with detailed multiconfigurational non-adiabatic ab-initio molecular dynamics calculations. Our results provide the first comprehensive picture of the primary steps of radiation chemistry and radiation damage and demonstrate new approaches for their study with unprecedented time resolution.

• Publikační typ
• časopisecké články MeSH
• práce podpořená grantem MeSH