Poly(1,4-anthraquinone) as an Organic Cathode Material: Simulation of Observable Bonding Properties to Li, Na, Mg, and Ca

Laura Femmer; Lukas Köbbing; Juliane Heitkämper; Sibylle Riedel; Devran Cay; Florin Adler; Birgit Esser; Alexander J. C. Kuehne; Zhirong Zhao-Karger; Piotr de Silva; Juan Maria García-Lastra; Birger Horstmann

arXiv · 2608.14185

Poly(1,4-anthraquinone) as an Organic Cathode Material: Simulation of Observable Bonding Properties to Li, Na, Mg, and Ca

Laura Femmer·Lukas Köbbing·Juliane Heitkämper·Sibylle Riedel·Devran Cay·Florin Adler·Birgit Esser·Alexander J. C. Kuehne·Zhirong Zhao-Karger·Piotr de Silva·Juan Maria García-Lastra·Birger Horstmann

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Abstract

Poly(1,4-anthraquinone) (P14AQ) has emerged as a promising cathode material, offering high capacity and good cycling stability, yet the atomic-scale mechanisms governing metal-ion binding and electrochemical behavior remain poorly understood. To address this, we investigate the binding mechanisms of Li, Na, Mg, and Ca to P14AQ using quantum mechanical methods, particularly DFT and DFTB. A key challenge lies in the material's structural complexity: multiple conformers of P14AQ are energetically similar but kinetically isolated due to significant energy barriers. To account for this, we develop an automated method to generate all unique P14AQ conformers for a periodic polymer chain without rotational duplicates through an orientation labeling scheme. For each conformer, we systematically place a metal atom adjacent to every oxygen site, enabling a complete exploration of binding configurations. We observe two structural motifs: a single metal-oxygen bond and coordination to two opposite oxygen atoms. While Li and Na exhibit continuous energy distributions, Mg and Ca show an energy gap between the two motifs, with a strong preference for the two-oxygen binding configuration. Galvanostatic measurements support these findings by showing lower gravimetric capacities for Ca and Mg than for Li and Na. For Na, the different numbers of metal-oxygen bonds are reflected in the two voltage plateaus observed experimentally. Overall, the combined computational and experimental results explain the higher capacity of monovalent ions in P14AQ: divalent ions cannot bind efficiently to a single oxygen site due to unfavorable energetics, and the conformational distribution of the polymer chain prevents optimal coordination.

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Laura Femmer, Lukas Köbbing, Juliane Heitkämper, Sibylle Riedel, Devran Cay, Florin Adler, Birgit Esser, Alexander J. C. Kuehne, Zhirong Zhao-Karger, Piotr de Silva, Juan Maria García-Lastra, Birger Horstmann. 2026-08-14. Poly(1,4-anthraquinone) as an Organic Cathode Material: Simulation of Observable Bonding Properties to Li, Na, Mg, and Ca. https://arxiv.org/abs/2608.14185

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