Résumé
The classical capture model for chemical reactions assumes that all trajectories with enough energyto cross the (centrifugal) barrier in the effective potential actually do so, and then proceed to formthe products. However, wave effects (not accounted for in a classical approach, by definition)become increasingly important with decreasing temperature and may dominate the collisionalbehavior at ultra-low temperatures.In this contribution we propose a new approach that describes the capture process by evolvingquantum trajectories [1,2] in the reactant channel up to a given limit, the capture distance, on theinside of the centrifugal barrier. The quantum trajectories take full account of quantum effects alongthe reaction path direction in the entrance channel. In particular, tunneling and quantum reflection,which can change the reaction rate by orders of magnitude, are accurately computed. In addition,quantum trajectories give valuable physical insight into the quantum capture process all along theapproach of the reactants. They also provide a technical means to determine the optimum capturedistance.Moreover, quantum trajectories along the reactant approach can easily be coupled with classicaltrajectories that drive the rest of the degrees of freedom of the system [3]. Apart from the captureprocess, which is guided by a quantum trajectory, all other coordinates are treated classically [3].This mixed quantum-classical capture approach is thus highly “classical-like” [3] and is aimed atlarge system reactions with quantum effects, still out of reach for current quantum scattering codes.Preliminary results will be presented at the conference.The authors are very grateful to Bill Poirier for his ongoing encouragement.[1] B. Poirier, “Bohmian mechanics without pilot waves”, Chem. Phys. 370, 4 (2010)[2] J. Schiff and B. Poirier, “Quantum mechanics without wavefunctions”, J. Chem. Phys. 136,