In processes when particles such as nanodroplets, clusters, or molecules move through a dilute background gas and undergo capture collisions, it is often important to know how much translational kinetic energy is deposited into the particles by these pick-up events. For sticking collisions with a Maxwell-Boltzmann gas, an exact expression is derived which is valid for arbitrary relative magnitudes of the particle and thermal gas speeds.
We propose and demonstrate a momentum filter for atomic gas based on a designed Talbot-Lau interferometer. It consists in two identical optical standing wave pulses separated by a delay equal to odd multiples of the half Talbot time. The one dimensional momentum width along the long direction of a cigar shape condensate is rapidly and greatly purified to a minimum, which corresponds to the ground state energy of the confining trap in our experiment. We find good agreement between theoretical analysis and experimental results. The filter is also effective for non-condensed cold atoms and could be applied widely.
We study the process of absorption or emission of a bosonic collective excitation by a fermionic quasiparticle in a superfluid of paired fermions. From the RPA equation of motion of the bosonic excitation annihilation operator, we obtain an expression of the coupling amplitude of this process which is limited neither to resonant processes nor to the long wavelength limit. We confirm our result by independently deriving it in the functional integral approach using the gaussian fluctuation approximation, and by comparing it in the long wavelength limit to the quantum hydrodynamic result. Last, we give a straightforward application of the coupling amplitude we obtain by calculating the lifetime of the bosonic excitations of arbitrary wave number. We find a mode quality factor that decreases from its maximum at low wave numbers and vanishes when the bosonic branch hits the pair-breaking continuum.
We investigate the peptide AcPheAla5LysH+, a model system for studying helix formation in the gas phase, in order to fully understand the forces that stabilize the helical structure. In particular, we address the question of whether the local fixation of the positive charge at the peptides C-terminus is a prerequisite for forming helices by replacing the protonated C-terminal Lys residue by Ala and a sodium cation. The combination of gas-phase vibrational spectroscopy of cryogenically cooled ions with molecular simulations based on density-functional theory (DFT) allows for detailed structure elucidation. For sodiated AcPheAla6, we find globular rather than helical structures, as the mobile positive charge strongly interacts with the peptide backbone and disrupts secondary structure formation. Interestingly, the global minimum structure from simulation is not present in the experiment. We interpret that this is due to high barriers involved in re-arranging the peptide-cation interaction that ultimately result in kinetically trapped structures being observed in the experiment.
Charge transfer in collisions of Na_n^+ cluster ions with Cs atoms is investigated theoretically in the microscopic framework of non-adiabatic quantum molecular dynamics. The competing reaction channels and related processes affecting the charge transfer (electronic excitations, fragmentation, temperature) are described. Absolute charge transfer cross sections for Na_n^+(2.7 keV) + Cs --> Na_n + Cs^+ have been calculated in the size range 4 <= n <= 11 reproducing the size dependence of the experimental cross sections. The energy dependence of the cross section is predicted for n=4,7,9. An exotic charge transfer channel producing Cs^- is found to have a finite probability.
Electronic and vibrational degrees of freedom in atom-cluster collisions are treated simultaneously and self-consistently by combining time-dependent density functional theory with classical molecular dynamics. The gradual change of the excitation mechanisms (electronic and vibrational) as well as the related relaxation phenomena (phase transitions and fragmentation) are studied in a common framework as a function of the impact energy (eV...MeV). Cluster transparency characterized by practically undisturbed atom-cluster penetration is predicted to be an important reaction mechanism within a particular window of impact energies.
Jiahao Liang
,Vitaly V. Kresin
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(2020)
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"Kinetic energy deposited into a nanodroplet, cluster, or molecule in a sticking collision with background gas"
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Vitaly Kresin
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