Equations of state

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Thermodynamic equations of state (EOS) for crystalline solids describe material behaviors under changes in pressure, volume, entropy and temperature. Despite over a century of theoretical development and experimental testing of energy-volume (E-V) EOS for solids, there is still a lack of consensus with regard to which equation is indeed optimal, as well as to what metric is most appropriate for making this judgment.

The calculation of EOS is automated using self-documenting workflows compiled in the atomate code base that couples pymatgen for materials analysis, custodian for just-in-time debugging of DFT codes, and Fireworks for workflow management. The EOS workflow begins with a structure optimization and subsequently calculates the energy of isotropic deformations including ionic relaxation with volumetric strain ranging from from -15.7% to 15.7% (-5% to 5% linear strain) of the optimized structure. Density-functional-theory (DFT) calculations were performed as necessary using the projector augmented wave (PAW) method as implemented in the Vienna Ab Initio Simulation Package (VASP) within the Perdew-Burke-Enzerhof (PBE) Generalized Gradient Approximation (GGA) formulation of the exchange-correlation functional. A cut-off for the plane waves of 520 eV is used and a uniform k-point density of approximately 1,000 per reciprocal atom is employed. In addition, standard Materials Project Hubbard U corrections are used for a number of transition metal oxides, as documented and implemented in the pymatgen VASP input sets. We note that the computational and convergence parameters were chosen consistently with the settings used in the Materials Project to enable direct comparisons with the large set of available MP data.

Fitted Equation Forms

EOS eqtable.png


  1. Katherine Latimer
  2. Shyam Dwaraknath
  3. Donny Winston