We report on a new, general-purpose particle detector consisting of a stretched foil of PVDF for use in pulsed supersonic jet experiments. The detector signal is analyzed in detail, allowing to exploit both the piezo- and the pyroelectric effects.

Experimental results for the hypersonic impact of singly charged, mass selected, water clusters at a hard surface demonstrate cooling of the heated cluster by sequential loss of a water molecule. The trends in the experiment are most simply summarized as an evaporation. This behavior is in contrast to the shattering phenomena observed for rare gas clusters. The same information theoretic approach that predicted the shattering transition is fully consistent with the results for the water clusters. It shows that the relatively high binding energy per water monomer is the key reason for the anomalous fragmentation. The tetra coordinated oxygen atom in a cluster does however imply that the fragmentation is not a pure evaporation but has residual elements of a shattering transition. For water clusters the transition is broadened to span the finite range in energy between the onset of boiling and the energy when the solvation of the hydronium ion is over and it is bare.

Pulsed, supersonic beams of propane have been investigated by mass-resolved time-of-flight measurements as a function of source pressure, covering sub- and supercritical expansion conditions. The experimental observation of a pronounced change in the terminal flow velocity is explained in terms of a thermodynamic model that is capable of describing the expansion of gases, liquids, and supercritical fluids; in particular, it allows the treatment of the vapor-liquid phase boundary and the critical point. Its major prediction is a distinct pressure dependence of the mean terminal flow velocity that is caused by condensation both in the stagnation reservoir and during the jet expansion. The agreement with experimental data is excellent.

We describe a generally applicable method for the experimental determination of stationary flow conditions in pulsed supersonic beams, utilizing time-resolved electron induced fluorescence measurements of high pressure jet expansions of helium. The detection of ultraviolet photons from electronically excited helium emitted very close to the nozzle exit images the valve opening behavior-with the decided advantage that a photon signal is not affected by beam-skimmer and beam-residual gas interactions; it thus allows to conclusively determine those operation parameters of a pulsed valve that yield complete opening. The studies reveal that a "flat-top" signal, indicating constant density and commonly considered as experimental criterion for continuous flow, is insufficient. Moreover, translational temperature and mean terminal flow velocity turn out to be significantly more sensitive in testing for the equivalent behavior of a continuous nozzle source. Based on the widely distributed Even-Lavie valve we demonstrate that, in principle, it is possible to achieve quasi-continuous flow conditions even with fast-acting valves; however, the two prerequisites are a minimum pulse duration that is much longer than standard practice and previous estimates, and a suitable tagging of the appropriate beam segment.

We describe an improved experimental method for the generation of cold, directed particle bunches, and the highly accurate determination of their velocities in a pulsed supersonic beam, allowing for high-resolution experiments of atoms, molecules, and clusters. It is characterized by a pulsed high pressure jet source with high brilliance and optimum repeatability, a flight distance of few metres that can be varied with a tolerance of setting of 50 μm, and a precision in the mean flight time of particles of better than 10(-4). The technique achieves unmatched accuracies in particle velocities and kinetic energies and also permits the reliable determination of enthalpy changes with very high precision.

The dissolution of the primary nucleobases in supercritical fluids has been investigated using pulsed molecular beam mass spectrometry. Due to the low critical temperatures of ethylene and carbon dioxide, their adiabatic jet expansion permits transferring thermally sensitive solutes into the gas phase. This feature is particularly attractive for pharmaceutical and biomedical applications. In this study, adenine, guanine, cytosine, thymine, and uracil have been dissolved in supercritical ethylene with a few percent of ethanol as cosolvent. At source temperatures of 313 K, these solutions have been expanded from supercritical pressures into high vacuum using a customized pulsed nozzle. A mass spectrometer was used to monitor the relative amounts of solute, solvent, and cosolvent in the supersonic beam. The results suggest a paramount influence of the cosolvent.

Argon gas at a high pressure (∼80 bar) has been expanded using a miniaturized pulsed valve at room temperature, producing a supersonic beam of cold, large argon droplets. Atoms of silver are subsequently embedded into the droplet using the pick-up technique. The resulting Ag(n)Ar(droplet) distribution was analyzed using multiphoton laser ionization time-of-flight mass spectrometry. Besides bare metal clusters, snowballs of silver monomers and dimers encapsulated in up to 50 argon atoms have been observed. The influence of the solvent on the optical absorption of the solute was studied for embedded Ag(8) using resonant two-photon ionization in the ultraviolet. A redshift and broadening of the Ag(8)Ar(droplet) optical spectrum compared to that measured in pure [Federmann et al., Eur. Phys. J. D 1999, 9, 11] and Ar-doped helium droplets [Diederich et al., J. Chem. Phys.2002, 116, 3263] was observed, which is attributed to the interaction with the larger Ar matrix environment.

Abstract The experimental realization of accurately defined source conditions, combined with an undisturbed flight path of precisely known length, permits the generation of supersonic molecular beams with an extremely well characterized axial velocity distribution. This achievement can be used for a quantitative assessment of theoretical models of condensation during the jet expansion, based on high accuracy equations of state. For helium-4, which is commonly put on a level with the ideal gas, we contrast two empirical equations of state with respect to enthalpy changes. These can be validated through a comparison with experimentally determined mean terminal flow velocities. At cryogenic temperatures, strong deviations from the ideal gas behavior are observed. Most notably, even the differences between the predictions of the two fundamental equations are large enough to be distinguished by high-resolution time-of-flight measurements.

A systematic crystal morphology study on the pharmaceutical model compound caffeine has been conducted on different surfaces: silicon, silver, soda lime glass, and silver subsurface ion-exchanged soda-lime silicate (SIMO) glasses. The morphology of the solid caffeine deposits has been investigated using environmental scanning electron microscopy (ESEM), atomic force microscopy (AFM), and X-ray diffraction (XRD). Needle-shaped caffeine crystals have been observed by drop-casting and also by applying the rapid expansion of supercritical solutions (RESS) technique using supercritical carbon dioxide. The aspect ratio of the crystalline needles typically vary between 10 and 100, but have been observed as large as SOO. The XRD data of the RESS products indicate unambiguously the presence of the thermodynamically most stable polymorph of caffeine known as the, beta-form. Under defined conditions we observe a unique, surfacemediated morphology for caffeine crystals with nearly perfect hexagonal shape. The relative fraction of the hexagons was seen to strongly increase especially when SIMO glasses were used. These hexagons have a distinct upper size limit depending on the solvent and substrate being used. The size distribution analysis of the hexagons yielded an average perimeter of typically 10 mu m. The mechanism of the formation process of this new hexagonal motif is explained in terms of the spinodal dewetting of the thin film of caffeine solution on the surface.

Computer simulations and experiments have been performed to quantify the effects of nozzle shape and skimmer placement on high-density supersonic jets. It is shown that the on axis beam intensity achieved is much higher than intensity achieved using standard sonic nozzles. Changes in skimmer design and positioning are required to allow this intense jet to propagate in a typical supersonic beam setup.

We introduce a straightforward experimental approach for determining the mean flow velocity of a supersonic jet with very high precision. While time measurements easily can achieve accuracies of Δt/t ≤ 10(-4), typically the absolute flight distances are much less well-defined. This causes significantly increased errors in calculations of the mean flow velocity and mean kinetic energy. The basic concept to improve on this situation is changing the flight distance in vacuo by precisely defined increments employing a linear translation stage. We demonstrate the performance of this method with a flight path that can be varied by approximately 15% with a tolerance of setting of 50 μm. In doing so, an unprecedented accurate value for the mean flow velocity of Δv/ < 3 × 10(-4) has been obtained without prior knowledge of the total distance. This very high precision in source pressure, temperature, and particle speed facilitates an improved energetic analysis of condensation processes in supersonic jet expansions. The technique is also of broad interest to other fields employing the strong adiabatic cooling of supersonic beams, in particular, molecular spectroscopy. In the presented case study, a thorough analysis of arrival time spectra of neutral helium implies cluster formation even at elevated temperatures.

Supersonic molecular beams constitute a very powerful technique in modern chemical physics. They offer several unique features such as a directed, collision-free flow of particles, very high luminosity, and an unsurpassed strong adiabatic cooling during the jet expansion. While it is generally recognized that their maximum flow velocity depends on the molecular weight and the temperature of the working fluid in the stagnation reservoir, not a lot is known on the effects of elevated particle densities. Frequently, the characteristics of supersonic beams are treated in diverse approximations of an ideal gas expansion. In these simplified model descriptions, the real gas character of fluid systems is ignored, although particle associations are responsible for fundamental processes such as the formation of clusters, both in the reservoir at increased densities and during the jet expansion. In this contribution, the various assumptions of ideal gas treatments of supersonic beams and their shortcomings are reviewed. It is shown in detail that a straightforward thermodynamic approach considering the initial and final enthalpy is capable of characterizing the terminal mean beam velocity, even at the liquid-vapor phase boundary and the critical point. Fluid properties are obtained using the most accurate equations of state available at present. This procedure provides the opportunity to naturally include the dramatic effects of nonideal gas behavior for a large variety of fluid systems. Besides the prediction of the terminal flow velocity, thermodynamic models of isentropic jet expansions permit an estimate of the upper limit of the beam temperature and the amount of condensation in the beam. These descriptions can even be extended to include spinodal decomposition processes, thus providing a generally applicable tool for investigating the two-phase region of high supersaturations not easily accessible otherwise.

We report on the concept, progress and status of the new project Distributed Open Access Reference Citations Services, DOARC . The emphasis is to exploit especially the Open Access documents on Institutional Repositories: analyzing their reference lists for citations, analyzing the full text for research field specific two-word shingles, and use this for powerful author and user tools, one of which can be tested in a demonstrator: plotting the content affinity of scientific papers in dynamically generated graphs. Author-identification is realized by AuthorClaim .

We report on the concept, progress and status of the new project Distributed Open Access Reference Citations Services, DOARC . The emphasis is to exploit especially the Open Access documents on Institutional Repositories: analyzing their reference lists for citations, analyzing the full text for research field specific two-word shingles, and use this for powerful author and user tools, one of which can be tested in a demonstrator: plotting the content affinity of scientific papers in dynamically generated graphs. Author-identification is realized by AuthorClaim .

Attempting to improve the comprehension of supersonic molecular beams at elevated pressures we present a comparative study of thermodynamic descriptions of the terminal flow velocity in free jet expansions. As model system we choose carbon dioxide due to its widespread utilization in supercritical fluid technology. Numerical results for the thermodynamic quantities are obtained using a high accuracy equation of state explicit in the Helmholtz free energy. The influence of pressure and temperature on the beam velocity is investigated for a broad range of stagnation conditions. A consistent physical picture is obtained for calculations employing the initial and final molar enthalpies, while enormous discrepancies are found for descriptions based on the molar isobaric heat capacity or the heat capacity ratio. The deviations are particularly pronounced at the gas–liquid phase transition and in the vicinity of the critical point and can be related to the diverse assumptions of ideal gas behavior. It is shown that computations using real fluid enthalpies permit to assess the fraction of condensation in supersonic jets.

The mathematical term for the mean flow velocity in supersonic beams of ideal gases is extended to include real gas properties. This procedure yields an explicit dependence of the flow velocity on pressure, as observed in recent experiments of free jet expansions. Applied to stagnation conditions slightly above the critical point, the model suggests that seeded high-pressure jet expansions might be suitable for slowing down virtually any molecule with maximum efficiency. Moreover, we discuss the consequence of a pressure-dependent flow velocity v(0) for the speed ratio S=v(0)/Delta v(parallel to) with respect to collisional cooling and suggest to use the velocity spread Delta v(parallel to) as a more nonambiguous measure of translational temperature in high-pressure jet expansions.

Crystallization processes under different conditions are of fundamental interest in chemistry, pharmacy, and medicine. Therefore, we have studied the formation of micro- and nanosized crystals using water-caffeine (1,3,7-trimethyl-1 H-purine-2,6(3 H,7 H)-dione) solutions under ambient conditions as a relevant model system. When droplets of an aqueous caffeine solution evaporate and eventually dry on surfaces (glass, polystyrene, and polyester), stable "coffee tabletop" rings with a perimeter of typically 3 mm are formed after 20 to 50 min. Using a micro focus X-ray beam available at the BESSY muSpot-beamline, the fine structure of different caffeine needles can be distinguished. Unexpectedly, both crystal modifications (alpha- and beta-caffeine) are present, but locally separated in these rings. Furthermore, AFM studies reveal the presence of even smaller particles on a nanometer length scale. To eliminate influences of surface irregularities from the crystallization process, acoustic levitation of liquid samples was employed. Such levitated droplets are trapped in a stable position and only surrounded by air. The solvent in an ultrasonically levitated drop evaporates completely, and the resulting crystallization of caffeine was followed in situ by synchrotron X-ray diffraction. In this case, the diffraction pattern is in accordance with pure alpha-caffeine and does not indicate the formation of the room temperature polymorph beta-caffeine. Hence, our investigations open new vistas that may lead to a controlled formation of cocrystals and novel polymorphs of micro- and nanocrystalline materials, which are of relevance for fundamental studies as well as for pharmaceutical and medical applications.

The dissolution of molecules of biological interest in supercritical carbon dioxide is investigated using pulsed molecular beam mass spectrometry. Due to the mild processing temperatures of most supercritical fluids, their adiabatic expansion into vacuum permits to transfer even thermally very sensitive substances into the gas phase, which is particularly attractive for pharmaceutical and biomedical applications. In addition, supercritical CO2constitutes a chemically inert solvent that is compatible with hydrocarbon-free ultrahigh vacuum conditions. Here, we report on the dissolution and pulsed supersonic jet expansion of caffeine (C8H10N4O2), the provitamin menadione (C11H8O2), and the amino acid derivative l-phenylalanine tert-butyl ester hydrochloride (C6H5CH2CH(NH2)COOC(CH3)3⋅HCl), into vacuum. An on-axis residual gas analyzer is used to monitor the relative amounts of solute and solvent in the molecular beam as a function of solvent density. The excellent selectivity and sensitivity provided by mass spectrometry permits to probe even trace amounts of solutes. The strong density variation of CO2 close to the critical point results in a pronounced pressure dependence of the relative ion currents of solute and solvent molecules, reflecting a substantial change in solubility.

We describe an experimental setup for supersonic jet expansions of supercritical fluids. It is characterized by well-defined thermodynamic values to allow systematic investigations of pressure and temperature effects on molecular beam parameters. The design permits stagnation temperatures T(0)=225-425 K with a thermal stability DeltaT(0)<30 mK and stagnation pressures p(0)=0.2-12 MPa that are measured with 0.05% precision. For optimum stability, gas reservoir, pressure transducer, and gauge amplifier are temperature-controlled, and a feedback loop permits active pressure stabilization using a pulseless syringe pump. With this approach stagnation pressures can be reproduced and kept constant to Deltap(0)<2.9 kPa. As a result, flow velocity and kinetic energy of molecular beams can be controlled with maximum accuracy.