Predicting Structure and Electrochemistry of Dilithium Thiophene-2,5-Dicarboxylate Electrodes by Density Functional Theory and Evolutionary Algorithms

Authors: Cleber F. N. Marchiori, Daniel Brandell, and C. Moyses Araujo

Organic electroactive materials are promising candidates to be used as lithium insertion electrodes in the next generation of environmentally friendly battery technologies. In this work, evolutionary algorithms at interplay with density functional theory calculations have been employed to predict the crystal structure for both delithiated and lithiated phases of dilithium thiophene dicarboxylate (Li2TDC). On the basis of the resulting crystals, electronic structure modifications and voltage profiles for the lithiation process have been calculated. The obtained structure for the delithiated phase showed a well-defined salt layer intercalating the organic components, forming a so-called lithium organic framework (LOF). Upon lithiation, new structures appear which deviate from the LOF as a consequence of the reduction of the S atoms, which coordinate with the additional Li ions. The calculated average potential of ∼1.00 V vs Li/Li+ is found to be in good agreement with experimental findings. An additional study at the molecular level has also been conducted aiming at gaining insight into the importance of the crystallographic environment on the structural and thermodynamics properties. This strategy is suitable for an initial assessment of the electrochemical process that underlies the lithiation mechanism of electrode materials. Moreover, the employed evolutionary algorithm emerges as a promising tool to predict crystal structures during lithiation, which are otherwise difficult to resolve experimentally.

https://doi.org/10.1021/acs.jpcc.8b11341

J. Phys. Chem. C, 2019 123, 8, p. 4691-4700

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