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Rajput, Jyoti

Publications and source records attributed to Rajput, Jyoti.

Native frames: An approach for separating sequential and concerted three-body fragmentation

Disentangling sequential and concerted three-body fragmentation has been a longstanding endeavor in studies of molecular dynamics. To accomplish this goal, we recently introduced a novel method to separate sequential from concerted breakup, where the sequential events are analyzed in their native frames [J. Rajput et al., Phys. Rev. Lett. 120, 103001 (2018)]. The essence of this method is the use of the Jacobi coordinates' conjugate momenta to reduce the dimensionality of the multibody fragmentation in combination with a clear signature for sequential breakup. To demonstrate this method, we employ coincidence momentum imaging to study the strong-field dissociative ionization of OCS into O + +C + + S + , which typically undergoes concerted fragmentation or sequential breakup involving either a metastable CO 2+ or CS 2+ molecule. We identify sequential breakup using a uniform distribution as a function of the angle between the conjugate momenta, associated with the first and second fragmentation steps, which is due to the rotation of the intermediate molecule in the fragmentation plane. Furthermore, by exploiting this uniform distribution, we separate the sequential and concerted distributions in any plot created from the measured momenta.

Atomic & molecular processes in external fields↗

Strong-field-induced bond rearrangement in triatomic molecules

A comparative study of bond rearrangement is reported for the double ionization of three triatomic molecules: carbon dioxide, carbonyl sulfide, and water (D 2 O). Specifically, we study the formation of the molecular cation AC + from the edge atoms of a triatomic molecular dication ABC 2+ following double ionization by intense, short (23 fs, 790 nm) laser pulses. The comparison is made using the double ionization branching ratio of each molecule, thereby minimizing differences due to differing ionization rates. The rearrangement branching ratio is highest for water, which has a bent initial geometry, while CO 2 and OCS are linear molecules. The angular distribution of O 2 + fragments arising from CO 2 is essentially isotropic, while SO + from OCS and $D$ $^{+}_{2}$ from D 2 O are aligned with the laser polarization. In the CO 2 and D 2 O cases, the angular distributions of the bond rearrangement channels are different from the angular distributions of the dominant dissociative double ionization channels CO + + O + and OD + + D + . Only the angular distribution of SO+ from OCS is both aligned with the laser polarization and similar to the angular distribution of the largest dissociative channel, CO + + S + . As a result, the mixed behavior observed from the angular distributions of the different molecules stands in contrast to the relative consistency of the magnitude of the bond rearrangement branching ratio.

74 ATOMIC AND MOLECULAR PHYSICS↗

Orientation and alignment effects in ion-induced fragmentation of water: A triple coincidence study

The technique of recoil ion momentum spectroscopy is employed to determine the complete momentum vectors for three fragment dissociation channels, [D{sub 2}O]{sup (q+2)} → (D{sup +} + D{sup +} + O{sup q+}) with q = 1, 2, or 3 formed in collisions of isolated water molecules with 450 keV Xe{sup 9+} ions. The kinetic energy released in each of these dissociation channels is measured and angular correlations between the fragment momenta are determined. From the angular correlations of the three fragment ions with the direction of the incoming beam, a strong anisotropy in the emission of recoil fragments is reported. It is inferred that the molecular plane prefers to lie orthogonal to the incoming beam direction with certain orientations being more preferred than others and a clear signature of non-coplanar dissociation is also observed.

37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CH↗

Fragmentation of water by ion impact: Kinetic energy release spectra

The fragmentation of isolated water molecules on collision with 450-keV Ar{sup 9+} has been studied using time-of-flight mass spectrometry employing multihit detection. The kinetic energy release spectrum for the dissociation of [H{sub 2}O]{sup 2+ White-Star} into (H{sup White-Star },H{sup +},O{sup +}) fragments has been measured where H{sup White-Star} is a neutral Rydberg hydrogen atom. Ab initio calculations are carried out for the lowest states of [H{sub 2}O]{sup q+} with q=2 and 3 to help interpret the kinetic energy release spectra.

74 ATOMIC AND MOLECULAR PHYSICS↗