No abstract

A general and rigorous quantum method is proposed for studying capture dynamics between two diatomic molecules in full dimensionality. By solving the time-independent Schrödinger equation with proper boundary conditions, this method is ideally suited for studying quantum dynamics of cold and ultracold reactions. To illustrate its applicability, the capture dynamics between ultracold KRb molecules is characterized in full six dimensions for the first time using a first-principles based long-range interaction potential. The calculated capture rates for collisions involving distinguishable and indistinguishable 40K87Rb molecules are in good agreement with the experiment and exhibit clear Wigner threshold behaviors. Predictions for ultracold collisions between internally excited 40K87Rb suggest minor changes in the loss rate, consistent with experimental observations in similar systems.

A full-dimensional time-independent quantum mechanical theory for ro-vibrationally inelastic scattering of triatomic molecules with atoms is formulated. The Jacobi−Radau coordinate system used in the calculation allows not only a near perfect description of the vibrational problem but also the adaptation of the exchange symmetry for A 2 B type triatoms. The S-matrix elements are obtained by solving the close-coupling equations with contracted basis using the log-derivative method. This method is applied to the inelastic scattering of the water molecule by a chlorine atom, which sheds light on the energy gap law in energy transfer in atom−triatom collisions.

We present a new full-dimensional ab initio potential energy surface (PES) of a hydrogen fluoride dimer [(HF)2] using the supermolecular approach. The calculations were performed at the coupled-cluster single double triple level, with an augmented correlation-consistent polarized valence quadruple-zeta basis set plus bond functions. The basis set superposition error was corrected by a full counterpoise procedure. With the exchange symmetry of the two HF molecules, the permutation invariant polynomial neural network approach was used to fit the hypersurface with a root-mean-square-error of 0.465 cm−1 for about 110 000 points. The ab initio noise of intermolecular potential in the long range was smoothed by the long-range coefficients method. The equilibrium configuration of the complex was found to be a Cs structure located at two equivalent minima with the well depth of 1573.495 cm−1. The eigenstates were calculated by employing a symmetry-adapted Lanczos propagation algorithm in the mixed radical discrete variable representation/angular finite basis representation. The tunneling splitting for the ground state of (HF)2 is 0.665 cm−1, agreeing well with experimental value of 0.65869 cm−1. Vibrational fundamentals are also very close to the observed values. The results of vibrational states calculations demonstrate the high accuracy of our new PES.

A full-dimensional global potential energy surface for the KRb + KRb → K 2 + Rb 2 reaction is developed from 20 759 ab initio points calculated using a coupled cluster singles, doubles, and perturbative triples (CCSD(T)) method with effective core potentials, extrapolated to the complete basis set limit. The ab initio points are represented with high fidelity (root-mean-square error of 1.86 cm −1 ) using the permutationinvariant polynomial−neural network method, which enforces the permutation invariance of the potential with respect to exchange of identical nuclei. The potential energy surface features two D 2h minima and one C s minimum connected by the isomerization saddle points. The Rice− Ramsperger−Kassel−Marcus lifetime of the K 2 Rb 2 reaction intermediate estimated using the potential energy surface is 227 ns, in reasonable agreement with the latest experimental measurement.