Out-of-focus spatial map imaging of magnetically deflected sodium ammonia clusters.

This paper introduces out-of-focus spatial map imaging (SMI) as a detection method for magnetic deflection of molecular/cluster beams, using Nam(NH3)n to illustrate its capabilities. This method enables imaging of the complete spatial distribution, simplifying measurements and allowing for cluster-size-resolved analysis by shifting away from traditional in-focus SMI conditions. Incorporating out-of-focus SMI with TOF-MS and velocity map imaging into a single setup allows for direct assessment of clusters' magnetic moments without needing to pre-select velocities. Key findings include a slower relaxation for Na(NH3)4 compared to Na(NH3)3 and Na(NH3)5, unexpectedly high deflection for larger clusters up to Na(NH3)9, hinting at changes in cluster dynamics as the first solvation shell closes. The study also covers the first measurements of Na2(NH3)1 and Na3(NH3)n, showing distinct deflection behaviors and underscoring the improved capabilities of the new detection method.

Magnetic deflection of neutral sodium-doped ammonia clusters.

We describe the setup and the performance of a new pulsed Stern-Gerlach deflector and present results for small sodium-doped ammonia clusters Na(NH3)n (n = 1-4) in a molecular beam. NaNH3 shows the expected deflection of a spin ½ system, while all lager clusters show much smaller deflections. Experimental deflection ratios are compared with the values calculated from molecular dynamics simulations. The comparison reveals that intracluster spin relaxation in NaNH3 takes place on a time scale significantly longer than 200 µs. Assuming that intracluster relaxation is the cause of the reduced deflection, relaxation times seem to be on the order of 200 µs for all larger clusters Na(NH3)n (n = 2-4). Our work is a first attempt to understand the magnetic properties of isolated, weakly-bound clusters with relevance to the variety of diamagnetic and paramagnetic species expected in solvated electron systems.

Low-Energy Electron Escape from Liquid Interfaces: Charge and Quantum Effects.

The high surface sensitivity and controlled surface charge state of submicron sized droplets is exploited to study low-energy electron transport through liquid interfaces using photoelectron imaging. Already a few charges on a droplet are found to modify the photoelectron images significantly. For narrow escape barriers, the comparison with an electron scattering model reveals pronounced quantum effects in the form of above-barrier reflections at electron kinetic energies below about 1 eV. The observed susceptibility to the characteristics of the electron escape barrier might provide access to these properties for liquid interfaces, which are generally difficult to investigate.

PFI-ZEKE photoelectron spectra of the methane cation and the dynamic Jahn-Teller effect

High resolution pulsed-field-ionization (PFI) zero-kinetic-energy (ZEKE) photoelectron spectroscopy has been used to record the photoelectron spectra of CH4, CDH3, CD2H2 and CD4. The observed extensive progression of rotationally resolved transitions between 100,800 cm-1 and 104,100 cm-1 reveals for the first time the complex energy level structure of the methane cation. The high resolution enabled the determination of accurate values for the adiabatic ionization potentials of the different isotopomers. Based on a simple one-dimensional model for the pseudorotation in the different isotopomers, progress has been made towards the understanding of the Jahn-Teller effect at low energies. The static Jahn-Teller distortion in the ion could be determined directly from the vibrationless photoelectron transition in CD2H2. The analysis of the rotational structure in this spectrum with a rigid rotor model leads to an approximate experimental C2v structure. The dynamics of the other methane isotopomers near the adiabatic ionization potentials is dominated by large amplitude vibrational motions between equivalent structures. The corresponding ground state tunneling motions takes place on a picosecond time scale.

Spectroscopic characterization of N(2)O aggregates: from clusters to the particulate state.

Collisional cooling is used to generate N(2)O particles with radii ranging from the subnanometer to the submicrometer region. The vibrational dynamics of the aggregates is studied by Fourier transform infrared spectroscopy. In the region of the stretching fundamentals and combination bands, the infrared spectra of the particles exhibit characteristic size-dependent features. For the very small particles, the results obtained from collisional cooling are compared for the first time with corresponding results from supersonic jet expansions. It turns out that with both methods very similar clusters are generated. A pronounced temperature dependence of a combination band maximum in the collisional cooling cell spectra is found. This correlation is exploited to estimate cluster temperatures in supersonic jet spectra.

Phase behavior of methane haze.

Methane aerosols play a fundamental role in the atmospheres of Neptune, Uranus, and Saturn's moon Titan as borne out by the recent Cassini-Huygens mission. Here we present the first study of the phase behavior of free methane aerosol particles combining collisional cooling with rapid-scan infrared spectroscopy in situ. We find fast (within minutes) phase transitions to crystalline states directly after particle formation and characteristic surface effects for nanometer-sized particles. From our results, we conclude that in atmospheric clouds solid methane particles are crystalline.