Raymond F. Boyce, Donald D. Chamberlin, et al.
CACM
Metal-organic frameworks (MOFs) are porous materials composed of metal ions and organic linkers. Due to their chemical diversity, MOFs can support a broad range of applications in chemical separations. However, the vast amount of structural compositions encoded in crystallographic information files complicates application-oriented computational screening and design. The existing crystallographic data, therefore, requires augmentation by simulated data so that suitable descriptors for machine-learning tasks become available. Here, we provide extensive simulation data augmentation for MOFs within the QMOF dataset. We have applied a tight-binding, lattice Hamiltonian and density functional theory to MOFs for performing electronic structure calculations. Specifically, we provide a tight-binding representation of 10,000 MOFs, and an Extended Hubbard model representation for a sub-set of 240 MOFs containing transition metals, where intra-site U and inter-site V parameters are computed self-consistently. In addition to computational workflows for identifying structure-property correlations, the data supports quantum computing tasks that rely on tight-binding Hamiltonian and self-consistent computed Hubbard parameters. For validation and reuse, we have made the data publicly available.
Raymond F. Boyce, Donald D. Chamberlin, et al.
CACM
Heinz Koeppl, Marc Hafner, et al.
BMC Bioinformatics
Anupam Gupta, Viswanath Nagarajan, et al.
Operations Research
Victor Valls, Panagiotis Promponas, et al.
IEEE Communications Magazine