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Portably parallel construction of a CI wave function from a matrix-product state using the Charm++ framework
Ting Wang, Yingjin Ma, Lian Zhao, Jinrong Jiang
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The constructions of configuration interaction (CI) expansions from a matrix-product state (MPS) involves numerous matrix operations and the skillful sampling of important configurations when in a huge Hilbert space. In this work, we present an efficient procedure for constructing CI expansions from MPS using the Charm++ parallel programming framework, upon which automatic load balancing and object migration facilities can be employed. This procedure was employed in the MPS-to-CI utility (Moritz et al., J. Chem. Phys. 2007, 126, 224109), sampling-reconstructed complete active space algorithm (SR-CAS, Boguslawski et al., J. Chem. Phys. 2011, 134, 224101) and entanglement-driven genetic algorithm (EDGA, Luo et al., J. Chem. Theory Comput. 2017, 13, 4699-4710). It enhances productivity and allows the sampling programs evolve to their population-expansion versions (e.g., EDGA with population expansion [PE-EDGA]). Examples of 1,2-dioxetanone and firefly dioxetanone anion (FDO-) molecules demonstrated that 1) the procedure could be flexibly employed among various multi-core architectures; 2) the parallel efficiencies could be persistently improved simply by increasing the proportion of asynchronous executions; 3) PE-EDGA could construct a CAS-type CI wave function from a huge Hilbert space, with 0.9952 CI completeness and 96.7% correlation energy via ~1.66x10^6 configurations (only 0.0000028% of the total configurations) of a bi-radical state of FDO- molecule using the full valence active space within a few hours.
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