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PSI4 1.1: An Open-Source Electronic Structure Program Emphasizing Automation, Advanced Libraries, and Interoperability
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DOI：10.1021/acs.jctc.7b00174.png)
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Abstract
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PSI4 is an ab initio electronic structure program providing methods such as Hartree Fock, density functional theory, configuration interaction, and coupled-cluster theory. The 1.1 release represents a major update meant to automate complex tasks, such as geometry optimization using complete basis-set extrapolation or focal-point methods. Conversion of the top-level code to a Python module means that PRI-can now be used in complex workflows alongside other Python tools. Several new features have been added with the aid of libraries providing easy access to techniques such as density fitting, Cholesky decomposition, and Laplace denominators. The build system has been completely rewritten to simplify interoperability with independent, reusable software components for quantum chemistry. Finally, a wide range of new theoretical methods and analyses have been added to the code base, including functional-group and open-shell symmetry adapted perturbation theory, density-fitted coupled cluster with frozen natural orbitals, orbital-optimized perturbation and coupled-cluster methods (e.g., OO-MP2 and OO-LCCD), density-fitted multiconfigurational self-consistent field, density cumulant functional theory, algebraic-diagrammatic construction excited states, improvements to the geometry optimizer, and the X2C approach to relativistic corrections, among many other improvements.
Keywords:
FRAGMENT POTENTIAL METHOD
ADAPTED PERTURBATION-THEORY
CUMULANT FUNCTIONAL THEORY
COUPLED-CLUSTER SINGLES
FROZEN NATURAL ORBITALS
BASIS-SET CONVERGENCE
CORRELATED CALCULATIONS
2-ELECTRON INTEGRALS
INTERACTION ENERGIES
SYMMETRY-BREAKING
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