Post collision analyzer to study charge-exchange processes in ion-molecule collisions.

We have designed an electrostatic charge state analyzer for ion beams having energies in the range of 5-20 keV/q. It is primarily built to investigate the different ionization processes involved in the slow (v < 1 a.u.) impact of highly charged ions on molecules. The analyzer is a cylindrical deflector analyzer (CDA) based on a pair of concentric cylindrical sectors of radii 110.2 and 95 mm, subtending an angle of 127° at its center. Additionally, an Einzel lens and a quadrupole deflector are deployed to focus and steer the ion beam. The compact design of the analyzer permits easy integration with an ion momentum spectrometer used for studying the fragmentation of the target molecules. The characterization of the CDA including its calibration and its transmission function is carried out using an ion beam delivered from an electron beam ion source. To check the performance of the setup, we have carried out experiments comprising the impact of Ar16+ projectiles on CO2 target molecules at an energy of 18 keV/q. With the help of the CDA, different charge exchange ionization processes, such as single capture, double capture, and triple capture of electrons by the projectile ion have been separated efficiently. The possibility of a modification in the geometry of CDA is discussed to further improve its performance.

Hindered alignment in ultrashort, intense laser-induced fragmentation of O2.

Molecules ionized by intense (10-100 TW/cm2) and ultrashort (tens of femtoseconds) laser fields undergo rotation and alignment mediated through their polarizability. The expected alignment is indeed observed in the case of O2 molecules ionized by intense laser pulses of 800 nm wavelength and 25 fs duration, as observed through velocity imaging of the fragments. Strikingly, when 35 fs pulses of 400 nm wavelength of comparable intensity are employed, an anomalous hindering of this alignment is observed. In both cases, we propose dissociation pathways for the energetic ions consistent with the recorded kinetic energy distributions. Using a semiclassical model of induced rotation of the molecular ion that involves polarizabilities of the participating excited states, both behaviors are reproduced. The model suggests that the difference in the observations can be attributed to a transient negative polarizability in an intermediate state of the proposed pathway.