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R. Ramprasad

Publications and source records attributed to R. Ramprasad.

4 recordsLinked to original sources

Physically-informed artificial neural networks for atomistic modeling of materials

Large-scale atomistic computer simulations of materials heavily rely on interatomic potentials predicting the potential energy and Newtonian forces on atoms. Traditional interatomic potentials are based on physical intuition but contain few adjustable parameters and are usually not accurate. The emerging machine-learning (ML) potentials achieve highly accurate interpolation between the energies in a large DFT database but, being purely mathematical constructions, suffer from poor transferability to unknown structures. We propose a new approach that can drastically improve the transferability of ML potentials by informing them of the physical nature of interatomic bonding. This is achieved by combining a rather general physics-based model (analytical bond-order potential) with a neural-network regression. The network adjusts the parameters of the physics-based model on the fly during the simulations according to the local environments of individual atoms. This approach, called the physically-informed neural network (PINN) potential, is demonstrated by developing a general-purpose PINN potential for Al. The potential provides a DFT-level accuracy of energy predictions and excellent agreement with experimental and DFT data for a wide range of physical properties. We suggest that the development of physics-based ML potentials is the most effective way forward in the field of atomistic simulations.

cond-mat.mtrl-sci

Strength of Cu-TiN and Al-TiN interfaces from first-principles

Using density functional theory (DFT) based first principles calculations, we show that the preferred interfacial plane orientation relationship is determined by the strength of bonding at the interface. The thermodynamic stability, and the ideal tensile and shear strengths of Cu/TiN and Al/TiN interfaces are calculated. While there is a strong orientation relation (OR) preference for Al/TiN interface, there is no OR preference for Cu/TiN interface. Both the ideal tensile and shear strengths of Cu/TiN interfaces are lower than those of bulk Cu and TiN, suggesting such interfaces are weaker than their bulk components. By comparison, the ideal strengths of Al/TiN interface are comparable to the constituents in the bulk form. Such contrasting interfaces can be a test-bed for studying the role of interfaces in determining the mechanical behavior of the nanolayered structures.

cond-mat.mtrl-sci

Dopant-mediated structural and magnetic properties of TbMnO3

Structural and magnetic properties of the doped terbium manganites (Tb,A)MnO3 (A = Gd, Dy and Ho) have been investigated using first-principles calculations and further confirmed by subse- quent experimental studies. Both computational and experimental studies suggest that compared to the parent material, namely, TbMnO3 (with a magnetic moment of 9.7 /muB for Tb3+) Dy- and Ho- ion substituted TbMnO3 results in an increase in the magnetic moment (< 10.6/muB for Dy3+ and Ho3+). The observed spiral-spin AFM order in TbMnO3 is stable with respect to the dopant substitutions, which modify the Mn-O-Mn bond angles and lead to stronger the ferromagnetic component of the magnetic moment. Given the fact that magnetic ordering in TbMnO3 causes the ferroelectricity, this is an important step in the field of the magnetically driven ferroelectricity in the class of magnetoelectric multiferroics, which traditionally have low magnetic moments due to the predominantly antiferromagnetic order. In addition, the present study reveals important insights on the phenomenological coupling mechanism in detail, which is essential in order to design new materials with enhanced magneto-electric effects at higher temperatures.

cond-mat.mtrl-sci

Efficient method to calculate total energies of large nanoclusters

We present an approach to calculate total energies of nanoclusters based on first principles estimates. For very large clusters the total energy can be separated into surface, edge and corner energies, in addition to bulk contributions. Using this separation and estimating these with direct, first principles calculations, together with the relevant chemical potentials, we have calculated the total energies of Cu and CdSe tetrahedrons containing a large number of atoms. In our work we consider polyhedral clusters so that in addition our work provides direct information on relaxation. For Cu the effects are very small and the clusters vary uniformly from very small to very large sizes. For CdSe there are important variations in surface and edge structures for specific sizes; nevertheless, the approach can be used to extrapolate to large non-stoichiometric clusters with polar surfaces.

cond-mat.mtrl-sci