Charge-symmetric and -asymmetric fragmentation dynamics of argon dimers in slow Ar8+-Ar2 collisions.

We present an experimental study of multiple-electron capture-induced fragmentation dynamics of Ar2m+ (4 ≤m≤ 7) dimer ions in 4 keV/u Ar8+-Ar2 collisions. The fragment recoil ion pairs and the charge-changing projectiles are coincidentally measured using a double coincidence technique. The branching ratios between the different charge-sharing fragmentation channels show an inherent enhancement of the asymmetric channels. The kinetic energy release (KER) distributions for the associated electron capture process show a shift in the mean KER values toward the higher side with increasing capture stabilization. The interplay between the different projectile autoionization processes sheds light on the energy depositions to the system during collisions. The Coulomb potential energy curves give a physical insight into the role of the projectile final states in the dimer fragmentation dynamics. The dimer-axis orientation-dependent cross sections for the asymmetric fragmentation channels reveal a forward-backward asymmetry that arises from the geometry of the collision system. Our findings thus give insight into the impact parameter-controlled fragmentation dynamics of multiply charged Ar2m+ dimer ions in highly charged ion-dimer slow collisions.

Development of a cold target recoil ion momentum spectrometer and a projectile charge state analyzer setup to study electron transfer processes in highly charged ion-atom/molecule collisions.

We report the development and performance of a cold target recoil ion momentum spectrometer (COLTRIMS) setup at TIFR, which is built to study various atomic and molecular processes involving the interaction of slow, highly charged ions from an electron cyclotron resonance based ion accelerator. We give a detailed description of the experimental setup, as well as report some initial results on the electron-capture process in collisions of Ar8+ ions with helium and carbon monoxide targets. Here, we present the longitudinal momentum transfer and the sub-shell resolved Q-value spectrum in the case of 2, 4, and 6 keV/u Ar8+ beams in collision with helium. A longitudinal momentum resolution of 0.27 a.u. is achieved in the present system. We also report the state-selective scattering angle distributions for all the collision systems under investigation. We further discuss the fragmentation of the CO2+ molecular ions for different electron capture channels for the 5 keV/u Ar8+ beam. The combination of the COLTRIMS, along with the beam cleaner, the electrostatic deflectors, and the charge state analyzer, is shown to have certain advantages.

A recoil ion momentum spectrometer for probing ionization, e-capture, and capture-ionization induced molecular fragmentation dynamics.

The development of a recoil ion momentum spectrometer (RIMS) along with a post-collision projectile charge state analyzer (CSA) and its performance for carrying out studies of molecular fragmentation following direct ionization, electron-capture, and capture-ionization have been demonstrated here. This is a two-stage Wiley-McLaren type spectrometer with slight modification introduced by adding a lens to achieve higher momentum resolution as well as larger angular acceptance. Along with the time and position sensitive detector, it can measure all the three momentum components of singly charged recoil ions of energy up to 10 eV emitted in all directions. The CSA assembly is designed for separating out any neutral or singly or doubly charged post-collision projectiles typically of keV energy. The RIMS with initial trigger ("start") from CSA or an ionized electron can uniquely determine the dynamics of molecular fragmentation following different electron-capture or direct ionization events, respectively. To check the performance of the setup, we carried out an experimental study of the fragmentation of N2 molecules under the impact of 250 keV protons. Apart from the single-electron-capture channel, we could clearly identify three more capture-ionization channels, which lead to fragmentation. The essential features of the momentum distributions and the kinetic energy release distributions of all three fragmentation channels are discussed in detail. These results are compared with the findings from the ionization induced fragmentation experiments and with the available results from theoretical calculations as well as high resolution experiments. The branching ratios of these fragmentation channels are determined.

Author Correction: Differential electron emission from polycyclic aromatic hydrocarbon molecules under fast ion impact.

A correction to this article has been published and is linked from the HTML version of this paper. The error has been fixed in the paper.

Differential electron emission from polycyclic aromatic hydrocarbon molecules under fast ion impact.

Interaction between polycyclic aromatic hydrocarbon (PAH) molecule and energetic ion is a subject of interest in different areas of modern physics. Here, we present measurements of energy and angular distributions of absolute double differential electron emission cross section for coronene (C24H12) and fluorene (C13H10) molecules under fast bare oxygen ion impact. For coronene, the angular distributions of the low energy electrons are quite different from that of simpler targets like Ne or CH4, which is not the case for fluorene. The behaviour of the higher electron energy distributions for both the targets are similar to that for simple targets. In case of coronene, a clear signature of plasmon resonance is observed in the analysis of forward-backward angular asymmetry of low energy electron emission. For fluorene, such signature is not identified probably due to lower oscillator strength of plasmon compared to the coronene. The theoretical calculation based on the first-order Born approximation with correct boundary conditions (CB1), in general, reproduced the experimental observations qualitatively, for both the molecules, except in the low energy region for coronene, which again indicates the role of collective excitation. Single differential and total cross sections are also deduced. An overall comparative study is presented.

Adhesive hydrophobicity of Cu2O nano-columnar arrays induced by nitrogen ion irradiation.

Low energy nitrogen ions are used in this work to manipulate wetting properties of the surface of the array of Cu2O nano-columns, which yields remarkable results. The nano-columnar thin films were grown on a highly conductive silicon surface by a sputter deposition technique. The films were irradiated at two different fluences of 5 × 10(15) and 1 × 10(16) ions per cm(2), respectively. With increasing fluence the shape of column tip changes, columns are bent and porous channels between columns are clogged up. While the surface of the pristine sample is hydrophilic, the irradiated surface turns into hydrophobic but having adhesion properties. We have analysed the structural and chemical properties of the surface in detail to understand the initial and modified wetting properties. Furthermore, the temporal evolutions of different droplet parameters are investigated to realize the interactions between the water droplet, the sample surface and the atmosphere. We envisage that such modified surfaces can be beneficial for transport of a small volume of liquids with minimum loss and spectroscopic studies, where a small amount of water droplet is available for measurements.

A recoil ion momentum spectrometer for molecular and atomic fragmentation studies.

We report the development and performance studies of a newly built recoil ion momentum spectrometer for the study of atomic and molecular fragmentation dynamics in gas phase upon the impact of charged particles and photons. The present design is a two-stage Wiley-McLaren type spectrometer which satisfies both time and velocity focusing conditions and is capable of measuring singly charged ionic fragments up-to 13 eV in all directions. An electrostatic lens has been introduced in order to achieve velocity imaging. Effects of the lens on time-of-flight as well as on the position have been investigated in detail, both, by simulation and in experiment. We have used 120 keV proton beam on molecular nitrogen gas target. Complete momentum distributions and kinetic energy release distributions have been derived from the measured position and time-of-flight spectra. Along with this, the kinetic energy release spectra of fragmentation of doubly ionized nitrogen molecule upon various projectile impacts are presented.

Nano-welding and junction formation in hydrogen titanate nanowires by low-energy nitrogen ion irradiation.

Crystalline hydrogen titanate (H2Ti3O7) nanowires were irradiated with N(+) ions of different energies and fluences. Scanning electron microscopy reveals that at relatively lower fluence the nanowires are bent and start to adhere strongly to one another as well as to the silicon substrate. At higher fluence, the nanowires show large-scale welding and form a network of mainly 'X' and 'Y' junctions. Transmission electron microscopy and Raman scattering studies confirm a high degree of amorphization of the nanowire surface after irradiation. We suggest that while ion-irradiation induced defect formation and dangling bonds may lead to chemical bonding between nanowires, the large scale nano-welding and junction network formation can be ascribed to localized surface melting due to heat spike. Our results demonstrate that low energy ion irradiation with suitable choice of fluence may provide an attractive route to the formation and manipulation of large-area nanowire-based devices.

On the photoabsorption by permanganate ions in vacuo and the role of a single water molecule. New experimental benchmarks for electronic structure theory.

We report electronic spectra of mass-selected MnO4(-) and MnO4(-)⋅H2O using electronic photodissociation spectroscopy. Bare MnO4(-) fragments by formation of MnO3(-) and MnO2(-), while the hydrated complex predominantly decays by loss of the water molecule. The band in the visible spectral region shows a well-resolved vibrational progression consistent with the excitation of a Mn-O stretching mode. The presence of a single water molecule does not significantly perturb the spectrum of MnO4(-). Comparison with the UV/Vis absorption spectrum of permanganate in aqueous solution shows that complete hydration causes a small blueshift, while theoretical models including a dielectric medium have predicted a redshift. The experimental data can be used as benchmarks for electronic structure theory methods, which usually predict electronic spectra in the absence of a chemical environment.

Effect of collective response on electron capture and excitation in collisions of highly charged ions with fullerenes.

Projectile deexcitation Lyman x-ray emission following electron capture and K excitation has been studied in collisions of bare and Li-like sulphur ions (of energy 110 MeV) with fullerenes (C(60)/C(70)) and different gaseous targets. The intensity ratios of different Lyman x-ray lines in collisions with fullerenes are found to be substantially lower than those for the gas targets, both for capture and excitation. This has been explained in terms of a model based on "solidlike" effect, namely, wakefield induced stark mixing of the excited states populated via electron capture or K excitation: a collective phenomenon of plasmon excitation in the fullerenes under the influence of heavy, highly charged ions.