The reaction D + H2 + HD + H has been investigated in two molecular beam scattering experiments. Angular and time-of-flight distributions have been measured for the initial vibrational ground state ( u = 0) at a most probable collision energy of E,, = 1.5 eV and for the first vibrational excited sta
Determination of the absolute scattering cross section for the reaction D + H2(v=1) → HD+H at 0.33 eV
✍ Scribed by R. Götting; V. Herrero; J.P. Toennies; M. Vodegel
- Publisher
- Elsevier Science
- Year
- 1987
- Tongue
- English
- Weight
- 749 KB
- Volume
- 137
- Category
- Article
- ISSN
- 0009-2614
No coin nor oath required. For personal study only.
✦ Synopsis
The reaction D+ H2( v= I ) has been investigated in a crossed molecular beam experiment at the most probable collision energy of&=0.33 eV. Angular and time-of-flight distributions have been measured and the total absolute cross section has been determined to be a&, = 0, v= 1, EC ,,,. = 0.33 eV) = 1.14 + 0.50 A2. This value, as well as the distributions, are in good agreement with the results of quasiclassical trajectory calculations ( QCT) and the reactive infinite-order sudden approximation (RIOSA) .
📜 SIMILAR VOLUMES
Differentialandtotal state-to-state~sssectionsfoortheD+H,(u=O,j=O-3)~HD(u',j')+Hreactioninthe0.35-1.10eV collision energy range, have been calculated on the UTH surface using the QCT method. The results are commented on and compared to recent quantum mechanical calculations and to experimental measu
Integral and differential state-resolved cross sections have been calculated by the method of quasiclassical trajectories for the H t D,+HD+D reaction in the range of initial conditions of interest to recent experiments. When possible, the results are compared to exact quantum-mechanical calculation
Using translationally hot H atoms generated via the photolysis of HBr at 193 nm, we have investigated the dynamics of the reaction H + D20--,OD + H D at a center-of-mass energy of Ec.m. = 2.53 eV. The nascent OD (v= 0) rotational distribution was probed by laser-induced fluorescence. We found that o
## Static-static distorted wave and vibrationally adiabatic distorted wave calculations have been performed for the product rotational distributions of the H.+ Dz + HD + D reaction using an accurate ab initio potential energy surface. Comparison is made with coupled states and quasiclassical traje