scholarly journals Assessing many-body contributions to intermolecular interactions of the AMOEBA force field using energy decomposition analysis of electronic structure calculations

2017 ◽  
Vol 147 (16) ◽  
pp. 161721 ◽  
Author(s):  
Omar Demerdash ◽  
Yuezhi Mao ◽  
Tianyi Liu ◽  
Martin Head-Gordon ◽  
Teresa Head-Gordon
Keyword(s):  
Electronic Structure ◽  
Force Field ◽  
Intermolecular Interactions ◽  
Decomposition Analysis ◽  
Electronic Structure Calculations ◽  
Energy Decomposition Analysis ◽  
Energy Decomposition ◽  
Many Body ◽  
Amoeba Force Field ◽  
Structure Calculations

Active Learning of Many-Body Configuration Space: Application to the Cs+–water MB-nrg Potential Energy Function as a Case Study

2020 ◽  
Author(s):  
Yaoguang Zhai ◽  
Alessandro Caruso ◽  
Sicun Gao ◽  
Francesco Paesani
Keyword(s):  
Electronic Structure ◽  
Active Learning ◽  
Potential Energy ◽  
Molecular Simulations ◽  
Electronic Structure Calculations ◽  
Many Body ◽  
High Level ◽  
Structure Calculations ◽  
Training Sets

<div> <div> <div> <p>The efficient selection of representative configurations that are used in high-level electronic structure calculations needed for the development of many-body molecular models poses a challenge to current data-driven approaches to molecular simulations. Here, we introduce an active learning (AL) framework for generating training sets corresponding to individual many-body contributions to the energy of a N-body system, which are required for the development of MB-nrg potential energy functions (PEFs). Our AL framework is based on uncertainty and error estimation, and uses Gaussian process regression (GPR) to identify the most relevant configurations that are needed for an accurate representation of the energy landscape of the molecular system under exam. Taking the Cs<sup>+</sup>–water system as a case study, we demonstrate that the application of our AL framework results in significantly smaller training sets than previously used in the development of the original MB-nrg PEF, without loss of accuracy. Considering the computational cost associated with high-level electronic structure calculations for training set configurations, our AL framework is particularly well-suited to the development of many-body PEFs, with chemical and spectroscopic accuracy, for molecular simulations from the gas to condensed phase. </p> </div> </div> </div>

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