Excited state reaction dynamics of Ti(a5FJ) + O2 → TiO(A3Φ, B3Π, C3Δ) + O studied by a crossed-beam velocity map imaging technique

2015 ◽  
Vol 142 (15) ◽  
pp. 154307
Author(s):  
Kenji Honma ◽  
Yuhki Tanaka
Nanophotonics ◽  
2021 ◽  
Vol 0 (0) ◽  
Author(s):  
Fenghao Sun ◽  
Hui Li ◽  
Shanshan Song ◽  
Fei Chen ◽  
Jiawei Wang ◽  
...  

Abstract Using single-shot velocity map imaging technique, explosion imaging of different ion species ejected from 50 nm SiO2 nanoparticles are obtained excitedly by strong near-infrared and ultraviolet femtosecond laser fields. Characteristic momentum distributions showing forward emission of the ions at low excitation intensities and shock wave behaviors at high intensities are observed. When the excitation intensity is close to the dissociative ionization threshold of the surface molecules, the resulting ion products can be used to image the instant near-field distributions. The underlying dynamics of shock formation are simulated by using a Coulomb explosion model. Our results allow one to distinguish the ultrafast strong-field response of various molecular species in nanosystems and will open a new way for further exploration of the underlying dynamics of laser-and-nanoparticle interactions.


Author(s):  
Valérie Blanchet ◽  
Dominique Descamps ◽  
stephane Petit ◽  
Yann Mairesse ◽  
bernard Pons ◽  
...  

We study isomeric effects using time resolved photoelectron circular dichroism (PECD). By a (1+1’)pump-probe ionisation with photoelectron collected by velocity map imaging technique, we compare relaxation dynamics from the 3s-Rydberg...


1999 ◽  
Vol 19 (1-4) ◽  
pp. 305-309
Author(s):  
Anthony P. Esposito ◽  
Catherine E. Foster ◽  
Philip J. Reid

The condensed-phase excited-state reaction dynamics of chlorine dioxide are investigated using resonance Raman intensity analysis. Absolute Raman intensities are measured on resonance with the 2B2–2A2 electronic transition and used to establish the excited-state structural evolution which occurs on the 2A2 surface following photoexcitation. Analysis of the intensities demonstrates that excited-state relaxation occurs along all three normal coordinates; however, only modest evolution is observed along the asymmetric stretch. This limited relaxation stands in contrast to the extensive motion along this coordinate in the gas phase. It is proposed that the initial excited-state structural relaxation serves to define the symmetry of the reaction coordinate and thus the mechanism of Cl production following photolysis of OClO.


1986 ◽  
Vol 25 (27) ◽  
pp. 4893-4897 ◽  
Author(s):  
S. Wieland ◽  
J. DiBenedetto ◽  
R. Van Eldik ◽  
P. C. Ford

Author(s):  
D. H. Parker ◽  
B. L. G. Bakker ◽  
R. Delmdahl ◽  
T. Berg ◽  
A. T. J. B. Eppink

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