Estimating complete basis set extrapolation error through random walk
arXiv:2503.09771 · doi:10.1021/acs.jpclett.5c00749
Abstract
We propose a method of estimating the uncertainty of a result obtained through extrapolation to the complete basis set limit. The method is based on an ensemble of random walks which simulate all possible extrapolation outcomes that could have been obtained if results from larger basis sets had been available. The results assembled from a large collection of random walks can be then analyzed statistically, providing a route for uncertainty prediction at a confidence level required in a particular application. The method is free of empirical parameters and compatible with any extrapolation scheme. The proposed technique is tested in a series of numerical trials by comparing the determined confidence intervals with reliable reference data. We demonstrate that the predicted error bounds are reliable, tight, yet conservative at the same time.
References in corpus (28)
- Search for New Physics with Atoms and Molecules
- Cold hybrid ion-atom systems
- Born-Oppenheimer potential for H
- Pair potential with submillikelvin uncertainties and nonadiabatic treatment of the halo state of helium dimer
- Complete basis set extrapolation of electronic correlation energies using the Riemann zeta function
- A Density-Based Basis-Set Correction For Wave Function Theory
- Systematic study of relativistic and chemical enhancements of -odd effects in polar diatomic radicals
- Ab initio potential energy curve for the ground state of beryllium dimer
- Highly polar molecules consisting of a copper or silver atom interacting with an alkali-metal or alkaline-earth-metal atom
- A Density-Based Basis-Set Incompleteness Correction for GW Methods
- Ab initio Calculation of Fluid Properties for Precision Metrology
- A basis-set error correction based on density-functional theory for strongly correlated molecular systems
- Fully numerical Hartree-Fock and density functional calculations. II. Diatomic molecules
- Ab initio properties of the NaLi molecule in the electronic state
- Prototypical pi-pi dimers re-examined by means of high-level CCSDT(Q) composite ab inito methods
- Theoretical determination of polarizability and magnetic susceptibility of neon
- First-principles calculation of the frequency-dependent dipole polarizability of argon
- Pinning down electron correlations in RaF via spectroscopy of excited states and high-accuracy relativistic quantum chemistry
- Chiral molecule candidates for trapped ion spectroscopy by ab initio calculations: from state preparation to parity violation
- Ultracold LiCr: a new pathway to quantum gases of paramagnetic polar molecules
- Interaction potentials, electric moments, polarizabilities, and chemical reactions of YbCu, YbAg, and YbAu molecules
- Potential energy curve for the state of lithium dimer with Slater-type orbitals
- Chemical reactions of ultracold alkaline-earth-metal diatomic molecules
- Ab initio potential energy curves, scattering lengths, and rovibrational levels of the He molecular ion in excited electronic states
- Collision-induced three-body polarizability of helium
- Relativistic coupled cluster calculations of the electron affinity and ionization potentials of lawrencium
- Correlation energies for many-electron atoms with explicitly correlated Slater functions
- Parity and time-reversal symmetry violation in diatomic molecules: LaO, LaS and LuO