A large aperture magnification lens for velocity map imaging.

We have designed and implemented a large aperture electrostatic Einzel lens that magnifies the images of low energy ions or electrons in a standard velocity map imaging apparatus by up to a factor of 5 while allowing the normal use of the apparatus (without blocking any part of the detector). The field strength in the interaction region remains reasonably constant with or without magnification, and the lens can be used in the normal "crush" mode or with any of the different variants of the "slicing" mode. We have characterized the performance of the lens by imaging ion recoil due to two-photon resonant three-photon ionization [(2+1) REMPI] of O((3)P(2)) atoms and by imaging slow NO molecules from the near-threshold photodissociation of the NO-Ar van der Waals complex.

Control and imaging of O(1D2) precession.

Larmor precession of a quantum mechanical angular momentum vector about an applied magnetic field forms the basis for a range of magnetic resonance techniques, including nuclear magnetic resonance spectroscopy and magnetic resonance imaging. We have used a polarized laser pump-probe scheme with velocity-map imaging detection to visualize, for the first time, the precessional motion of a quantum mechanical angular momentum vector. Photodissociation of O(2) at 157 nm provides a clean source of fast-moving O((1)D(2)) atoms, with their electronic angular momentum vector strongly aligned perpendicular to the recoil direction.

Predissociation of the A2Sigma+ (v' = 3) state of the OH radical.

Predissociation of electronically excited OH A(2)Sigma(+) (v' = 3) is studied using velocity-map imaging of the atomic oxygen photofragments. Fine structure yields, angular distributions and alignment parameters are obtained for the O((3)P(J)), J = 2,1,0 products. Angular distributions for the O(3)P(0) (J = 0) fragment, which has no angular momentum polarization, agree well with predictions from the angular distribution simulation computer routine by Kim et al.

Photodissociation of vibrationally excited SH and SD radicals at 288 and 291 nm: the S(1D2) channel.

Ultraviolet photodissociation of SH (X 2Pi, upsilon"=2-7) and SD (X 2Pi, upsilon"=3-7) has been studied at 288 and 291 nm, using the velocity map imaging technique to probe the angular and speed distributions of the S(1D2) products. Photodissociation cross sections for the A 2Sigma+<--X 2Pi(upsilon") and 2Delta<--X 2Pi(upsilon") transitions have been obtained by ab initio calculations at the CASSCF-MRSDCI/aug-cc-pV5Z level of theory. Both the experimental and theoretical results show that SH/SD photodissociation from X 2Pi (upsilon" View Article and Find Full Text PDF

Imaging the dynamics of gas phase reactions.

Ion imaging methods are making ever greater impact on studies of gas phase molecular reaction dynamics. This article traces the evolution of the technique, highlights some of the more important breakthroughs with regards to improving image resolution and in image processing and analysis methods, and then proceeds to illustrate some of the many applications to which the technique is now being applied--most notably in studies of molecular photodissociation and of bimolecular reaction dynamics.