| Résumé | We introduce a new method, called CNNAS (convolutional neural networks for atomistic systems), for calculating the total energy of atomic systems which rivals the computational cost of empirical potentials while maintaining the accuracy of ab initio calculations. This method uses deep convolutional neural networks (CNNs), where the input to these networks are simple representations of the atomic structure. We use this approach to predict energies obtained using density functional theory (DFT) for 2D hexagonal lattices of various types. Using a dataset consisting of graphene, hexagonal boron nitride (hBN), and graphene-hBN heterostructures, with and without defects, we trained a deep CNN that is capable of predicting DFT energies to an extremely high accuracy, with a mean absolute error (MAE) of 0.198 meV/atom (maximum absolute error of 16.1 meV/atom). To explore our new methodology, we investigate the ability of a deep neural network (DNN) in predicting a Lennard-Jones energy and separation distance for a dataset of dimer molecules in both two and three dimensions. In addition, we systematically investigate the flexibility of the deep learning models by performing interpolation and extrapolation tests. |
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