Hydrogen atom collisions with a semiconductor efficiently promote electrons to the conduction band.

The Born-Oppenheimer approximation is the keystone of modern computational chemistry and there is wide interest in understanding under what conditions it remains valid. Hydrogen atom scattering from insulator, semi-metal and metal surfaces has helped provide such information. The approximation is adequate for insulators and for metals it fails, but not severely. Here we present hydrogen atom scattering from a semiconductor surface: Ge(111)c(2 × 8). Experiments show bimodal energy-loss distributions revealing two channels. Molecular dynamics trajectories within the Born-Oppenheimer approximation reproduce one channel quantitatively. The second channel transfers much more energy and is absent in simulations. It grows with hydrogen atom incidence energy and exhibits an energy-loss onset equal to the Ge surface bandgap. This leads us to conclude that hydrogen atom collisions at the surface of a semiconductor are capable of promoting electrons from the valence to the conduction band with high efficiency. Our current understanding fails to explain these observations.

Real-time monitoring of aerosol particle formation from sulfuric acid vapor at elevated concentrations and temperatures.

In the present study, time-resolved aerosol particle formation from sulfuric acid vapor is examined with special attention to the stabilization of molecular clusters in the early phase of unary nucleation. An important factor governing this process is the amount of condensable acid vapor. Here it is produced from fast gas-phase reactions in a batch-type reaction cell for which we introduce modifications enabling real-time monitoring. The key component for size- and time-resolved detection of ultrafine particles is a new 1 nm-SMPS. With this new tool at hand, the effect of varying the precursor concentration over two orders of magnitude is investigated. We demonstrate the ability to tune between different growth scenarios as indicated by the size-resolved particle traces which exhibit a transition from sigmoidal over quasi-stationary to peak-like shape. The second key parameter relevant for nucleation studies is the temperature-dependent cluster evaporation. Due to a temperature rise during the mixing stage of the experiment, evaporation is strongly promoted in the early phase. Therefore, the present study extends the T-range used in, e.g., smog chambers. We investigate this temperature effect in a kinetic simulation and can successfully combine simulated and measured data for validating theoretical evaporation rates obtained from DLPNO-CCSD(T0)-calculations.