Bayesian Analysis Reveals the Key to Extracting Pair Potentials from Neutron Scattering Data
arXiv:2407.04839 · doi:10.1021/acs.jpclett.4c02941
Abstract
The inverse problem of statistical mechanics is an unsolved, century-old challenge to learn classical pair potentials directly from experimental scattering data. This problem was extensively investigated in the 20th century but was eventually eclipsed by standard methods of benchmarking pair potentials to macroscopic thermodynamic data. However, it is becoming increasingly clear that existing force field models fail to reliably reproduce fluid structures even in simple liquids, which can result in reduced transferability and substantial misrepresentations of thermophysical behavior and self-assembly. In this study, we revisited the structure inverse problem for a classical Mie fluid to determine to what extent experimental uncertainty in neutron scattering data influences the ability to recover classical pair potentials. Bayesian uncertainty quantification was used to show that structure factors with random noise smaller than 0.005 to A are required to accurately recover pair potentials from neutron scattering. Notably, modern neutron instruments can achieve this precision to extract classical force models to within approximately 1.3 for the repulsive exponent, 0.068 A for atomic size, and 0.024 kcal/mol in the potential well-depth with 95\% confidence. Our results suggest the exciting possibility of improving molecular simulation accuracy through the incorporation of neutron scattering data, advancement in structural modeling, and extraction of model-independent measurements of local atomic forces in real fluids.
References in corpus (10)
- emcee: The MCMC Hammer
- Relation Between the Widom line and the Strong-Fragile Dynamic Crossover in Systems with a Liquid-Liquid Phase Transition
- freud: A Software Suite for High Throughput Analysis of Particle Simulation Data
- Derivation of coarse-grained potentials via multistate iterative Boltzmann inversion
- Emerging quantum computing algorithms for quantum chemistry
- Thermodynamic behavior of supercritical matter
- Parallel Gaussian Process Regression with Low-Rank Covariance Matrix Approximations
- Accelerated Bayesian Inference for Molecular Simulations using Local Gaussian Process Surrogate Models
- A framework for efficient ab initio electronic structure with Gaussian Process States
- Experimental data over quantum mechanics simulations for inferring the repulsive exponent of the Lennard-Jones potential in Molecular Dynamics