Abstract
Reduction potentials of redox-active molecules and materials are essential descriptors of their performance as catalysts, antioxidants, electrode materials, etc. For a given species, its practical applications often span a range of solvent environments, which profoundly impact its redox properties. In this work, we present a message passing graph neural network architecture with a set transformer readout trained on ca. 20,000 reduction potentials of chemically diverse closed- and open-shell organic redox-active molecules (the “ReSolved” dataset), computed using a rigorously benchmarked density functional theory procedure. The predictor model affords high accuracy with mean absolute errors of ca. 0.2 eV and is uniquely able to generalise to previously unseen solvents. We couple this architecture with an evolutionary algorithm to inverse-design synthetically accessible candidate molecules with target reduction potentials for several battery-related practical applications.
Supplementary materials
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Supporting Information
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Further computational details, methods benchmarks, and full list of candidate molecules produced by the inverse design framework (PDF)
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Supplementary weblinks
Title
ReSolved Database
Description
ReSolved dataset, including SMILES, DFT-optimised geometries and DFT-computed electron affinities and one-electron reduction potentials in five solvents for 19,785 molecules
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