New Dimension in Ab Initio Electronic Structure Theory: Temperature, Pressure, and Chemical Potential

Abstract

Ab initio electronic structure theory has transformed gas-phase molecular science with its predictive ability. In the attempt to bring such predictive ability to macroscopic systems and condensed matter, the theory must integrate quantum mechanics with statistical thermodynamics so that thermodynamic functions such as free energy, internal energy, entropy, and chemical potentials are computed as functions of temperature in a systematically converging series of approximations. A general, versatile strategy of elevating any ab initio electronic structure theory to nonzero temperatures is introduced and discussed.