Efficient force field and energy emulation through partition of permutationally equivalent atoms

Gaussian process (GP) emulator has been used as a surrogate model for predicting force field and molecular potential, to overcome the computational bottleneck of ab initio molecular dynamics simulation. Integrating both atomic force and energy in predictions was found to be more accurate than using energy alone, yet it requires O((NM)(3)) computational operations for computing the likelihood function and making predictions, where N is the number of atoms and M is the number of simulated configurations in the training sample due to the inversion of a large covariance matrix. The high computational cost limits its applications to the simulation of small molecules. The computational challenge of using both gradient information and function values in GPs was recently noticed in machine learning communities, whereas conventional approximation methods may not work well. Here, we introduce a new approach, the atomized force field model, that integrates both force and energy in the emulator with many fewer computational operations. The drastic reduction in computation is achieved by utilizing the naturally sparse covariance structure that satisfies the constraints of the energy conservation and permutation symmetry of atoms. The efficient machine learning algorithm extends the limits of its applications on larger molecules under the same computational budget, with nearly no loss of predictive accuracy. Furthermore, our approach contains an uncertainty assessment of predictions of atomic forces and energies, useful for developing a sequential design over the chemical input space. Published under an exclusive license by AIP Publishing.

Automated summary

Gaussian process emulator is used to predict force field and molecular potential, overcoming the computational bottleneck of ab initio molecular dynamics simulation. Integrating both atomic force and energy in predictions provides more accurate results, but requires a large number of computational operations. A new approach is introduced, which drastically reduces computation by utilizing a sparse covariance structure. This efficient algorithm extends the method's applications to larger molecules with nearly no loss of predictive accuracy.