Sergei Manzhos 교수

We review progress in neural network (NN)-based methods for the construction of interatomic potentials from discrete samples (such as ab initio energies) for applications in classical and quantum dynamics including reaction dynamics and computational spectroscopy. The main focus is on methods for building molecular potential energy surfaces (PES) in internal coordinates that explicitly include all many-body contributions, even though some of the methods we review limit the degree of coupling, du

We combine the high dimensional model representation (HDMR) idea of Rabitz and co-workers [J. Phys. Chem. 110, 2474 (2006)] with neural network (NN) fits to obtain an effective means of building multidimensional potentials. We verify that it is possible to determine an accurate many-dimensional potential by doing low dimensional fits. The final potential is a sum of terms each of which depends on a subset of the coordinates. This form facilitates quantum dynamics calculations. We use NNs to repr

Development and applications of neural network (NN)‐based approaches for representing potential energy surfaces (PES) of bound and reactive molecular systems are reviewed. Specifically, it is shown that when the density of ab initio points is low, NNs‐based potentials with multibody or multimode structure are advantageous for representing high‐dimensional PESs. Importantly, with an appropriate choice of the neuron activation function, PESs in the sum‐of‐products form are naturally obtained, thus

It is shown that neural networks (NNs) are efficient and effective tools for fitting potential energy surfaces. For H2O, a simple NN approach works very well. To fit surfaces for HOOH and H2CO, we develop a nested neural network technique in which we first fit an approximate NN potential and then use another NN to fit the difference of the true potential and the approximate potential. The root-mean-square error (RMSE) of the H2O surface is 1 cm(-1). For the 6-D HOOH and H2CO surfaces, the nested

By using exponential activation functions with a neural network (NN) method we show that it is possible to fit potentials to a sum-of-products form. The sum-of-products form is desirable because it reduces the cost of doing the quadratures required for quantum dynamics calculations. It also greatly facilitates the use of the multiconfiguration time dependent Hartree method. Unlike potfit product representation algorithm, the new NN approach does not require using a grid of points. It also produc

Abstract In recent years, we have been witnessing a paradigm shift in computational materials science. In fact, traditional methods, mostly developed in the second half of the XXth century, are being complemented, extended, and sometimes even completely replaced by faster, simpler, and often more accurate approaches. The new approaches, that we collectively label by machine learning, have their origins in the fields of informatics and artificial intelligence, but are making rapid inroads in all

We demonstrate that it is possible to obtain good potentials using high-dimensional model representations (HDMRs) fitted with neural networks (NNs) from data in 12 dimensions and 15 dimensions. The HDMR represents the potential as a sum of lower-dimensional functions and our NN-based approach makes it possible to obtain all of these functions from one set of fitting points. To reduce the number of terms in the HDMR, we use optimized redundant coordinates. By using exponential neurons, one obtain

We propose a method for fitting potential energy surfaces with a sum of component functions of lower dimensionality. This form facilitates quantum dynamics calculations. We show that it is possible to reduce the dimensionality of the component functions by introducing new and redundant coordinates obtained with linear transformations. The transformations are obtained from a neural network. Different coordinates are used for different component functions and the new coordinates are determined as

Abstract Machine learning (ML) methods have recently been increasingly widely used in quantum chemistry. While ML methods are now accepted as high accuracy approaches to construct interatomic potentials for applications, the use of ML to solve the Schrödinger equation, either vibrational or electronic, while not new, is only now making significant headway towards applications. We survey recent uses of ML techniques to solve the Schrödinger equation, including the vibrational Schrödinger equation

By means of density functional theory, we systematically investigate the insertion and diffusion of Na and Li in layered Si materials (polysilane and H-passivated silicene), in comparison with bulk Si. It is found that Na binding and mobility can be significantly facilitated in layered Si structures. In contrast to the Si bulk, where Na insertion is energetically unfavorable, Na storage can be achieved in polysilane and silicene. The energy barrier for Na diffusion is reduced from 1.06 eV in the