Guorong Wu

A new crossed molecular beam apparatus using time-sliced ion velocity imaging technique

A new crossed molecular beam apparatus has been constructed for investigating polyatomic chemical reactions using the time-sliced ion velocity map imaging technique. A unique design is adopted for one of the two beam sources and allows us to set up the molecular beam source either horizontally or vertically. This can be conveniently used to produce versatile atomic or radical beams from photodissociation and as well as electric discharge. Intensive H-atom beam source with high speed ratio was produced by photodissociation of the HI molecule and was reacted with the CD(4) molecule. Vibrational-state resolved HD product distribution was measured by detecting the CD(3) product. Preliminary results were also reported on the F+SiH(4) reaction using the discharged F atom beam. These results demonstrate that this new instrument is a powerful tool for investigating chemical dynamics of polyatomic reactions.

Photodissociation dynamics of the methyl radical at 212.5 nm: Effect of parent internal excitation

Photodissociation dynamics of the CH3 radical at 212.5 nm has been investigated using the H atom Rydberg tagging time-of-flight method with a pure CH3 radical source generated by the photolysis of CH3I at 266 nm. Time-of-flight spectra of the H atom products from the photolysis of both cold and hot methyl radicals have been measured at different photolysis polarizations. Experimental results indicate that the photodissociation of the methyl radical in its ground vibrational state at 212.5 nm excitation occurs on a very fast time scale in comparison with its rotational period, indicating the CH3 dissociation at 212.5 nm occurs on the excited 3s Rydberg state surface. Experimental evidence also shows that the photodissociation of the methyl radical in the nu2 = 1 state of the umbrella mode at 212.5 nm excitation is characteristically different from that in the ground vibrational state.

Crossed molecular beam ion-imaging study of the Cl + SiH4 -> HCl + SiH3 reaction: product vibrational state-to-state correlation

The dynamics of the Cl + SiH(4) --> HCl + SiH(3) reaction has been studied using the crossed molecular beam technique with slice imaging. The ion images of the silyl radical (SiH(3)) product from the Cl + SiH(4) reaction were recorded at different collision energies, using the (2 + 1) resonance enhanced multi-photon ionization (REMPI) technique. The product velocity and angular distributions of this reaction were determined from the recorded images. The vibrational state-to-state correlation of the relative population between the two reaction products, SiH(3) and HCl, was also determined. Finally, the Cl + SiH(4) results are compared with that of the F + SiH(4) reaction.

Tunable VUV photochemistry using vacuum ultraviolet free electron laser combined with H-atom Rydberg tagging time-of-flight spectroscopy

In this article, we describe an experimental setup for studying tunable vacuum ultraviolet photochemistry using the H-atom Rydberg tagging time-of-flight technique. In this apparatus, two vacuum ultraviolet laser beams were used: one is generated by using a nonlinear four-wave mixing scheme in a Kr gas cell and fixed at 121.6 nm wavelength to probe the H-atom product through the Lyman α transition and the other beam, produced by a seeded free electron laser facility, can be continuously tunable for photodissociating molecules in the wavelength range of 50-150 nm with extremely high brightness. Preliminary results on the H2O photodissociation in the 4d (000) Rydberg state are reported here. These results suggest that the experimental setup is a powerful tool for investigating photodissociation dynamics in the vacuum ultraviolet region for molecules involving H-atom elimination processes.