TY - JOUR
T1 - Machine Learning Density Functionals from the Random-Phase Approximation
AU - Riemelmoser, Stefan
AU - Verdi, Carla
AU - Kaltak, Merzuk
AU - Kresse, Georg
N1 - Publisher Copyright:
© 2023 The Authors. Published by American Chemical Society.
PY - 2023/10/24
Y1 - 2023/10/24
N2 - Kohn-Sham density functional theory (DFT) is the standard method for first-principles calculations in computational chemistry and materials science. More accurate theories such as the random-phase approximation (RPA) are limited in application due to their large computational cost. Here, we use machine learning to map the RPA to a pure Kohn-Sham density functional. The machine learned RPA model (ML-RPA) is a nonlocal extension of the standard gradient approximation. The density descriptors used as ingredients for the enhancement factor are nonlocal counterparts of the local density and its gradient. Rather than fitting only RPA exchange-correlation energies, we also include derivative information in the form of RPA optimized effective potentials. We train a single ML-RPA functional for diamond, its surfaces, and liquid water. The accuracy of ML-RPA for the formation energies of 28 diamond surfaces reaches that of state-of-the-art van der Waals functionals. For liquid water, however, ML-RPA cannot yet improve upon the standard gradient approximation. Overall, our work demonstrates how machine learning can extend the applicability of the RPA to larger system sizes, time scales, and chemical spaces.
AB - Kohn-Sham density functional theory (DFT) is the standard method for first-principles calculations in computational chemistry and materials science. More accurate theories such as the random-phase approximation (RPA) are limited in application due to their large computational cost. Here, we use machine learning to map the RPA to a pure Kohn-Sham density functional. The machine learned RPA model (ML-RPA) is a nonlocal extension of the standard gradient approximation. The density descriptors used as ingredients for the enhancement factor are nonlocal counterparts of the local density and its gradient. Rather than fitting only RPA exchange-correlation energies, we also include derivative information in the form of RPA optimized effective potentials. We train a single ML-RPA functional for diamond, its surfaces, and liquid water. The accuracy of ML-RPA for the formation energies of 28 diamond surfaces reaches that of state-of-the-art van der Waals functionals. For liquid water, however, ML-RPA cannot yet improve upon the standard gradient approximation. Overall, our work demonstrates how machine learning can extend the applicability of the RPA to larger system sizes, time scales, and chemical spaces.
UR - http://www.scopus.com/inward/record.url?scp=85175356566&partnerID=8YFLogxK
U2 - 10.48550/arXiv.2308.00665
DO - 10.48550/arXiv.2308.00665
M3 - Article
C2 - 37800677
AN - SCOPUS:85175356566
SN - 1549-9618
VL - 19
SP - 7287
EP - 7299
JO - Journal of Chemical Theory and Computation
JF - Journal of Chemical Theory and Computation
IS - 20
ER -