Exact tunneling splittings of rotationally excited states from symmetrized path-integral molecular dynamics
Lea Zupan, Yu-Chen Wang, Jeremy O. Richardson

TL;DR
This paper introduces an exact symmetrized path-integral molecular dynamics method to compute tunneling splittings in rotationally excited molecular states, enabling efficient, simultaneous calculations across multiple angular momenta.
Contribution
The authors develop a formalism that projects onto specific rotational states and extracts tunneling splittings for various angular momenta from a single simulation set.
Findings
Validated the method on water's rotational levels beyond the rigid-rotor approximation.
Applied the approach to ammonia, achieving excellent agreement with variational benchmarks.
Captured the experimental trend of decreasing tunneling splitting with increasing angular momentum.
Abstract
We extend our previous symmetrized path-integral molecular dynamics approach to calculate tunneling splittings of molecules in rotationally excited states. In this new formalism, the system is rigorously projected onto selected rotational manifolds and states of a chosen symmetry through an Eckart spring, which connects the two end beads of the ring polymer via a permutation--inversion--rotation operation. This method is numerically exact within statistical uncertainty once convergence with respect to all simulation parameters has been achieved. Importantly, it enables the simultaneous extraction of tunneling splittings for multiple total angular-momentum quantum numbers from a single set of simulations, without additional computational cost relative to the original approach. After validating the formalism by computing the rotational levels of water (beyond the rigid-rotor…
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