Evaluation of the Interphase-Related Cycling Stability of Thin-Film Amino- and Hydroxy-Substituted Anthraquinone Electrodes for Sodium-Ion Batteries
Victoria Greussing, Daniel Werner, Dominik Wielend, Cristian Vlad Irimia, Elisabeth Leeb, Martin Ciganek, Jozef Krajčovič, Mihai Irimia-Vladu, Engelbert Portenkirchner

TL;DR
This paper evaluates organic cathode materials for sodium-ion batteries, identifying promising candidates with good cycle stability and environmental benefits.
Contribution
The study systematically tests 12 amino- and hydroxy-substituted anthraquinone derivatives for sodium-ion battery cathodes, many of which are untested in such systems.
Findings
1,8-dihydroxy-anthraquinone and 1,8-diamino-anthraquinone show high cycle stability with 72% and 73% capacity retention over 100 cycles.
Material solubility and structural properties strongly influence electrochemical performance.
Several naturally occurring anthraquinone derivatives demonstrate potential for sustainable battery cathodes.
Abstract
This study investigates sustainable approaches to designing organic cathode materials for sodium-ion batteries, aiming to replace traditional metal-based electrodes. Organic materials present a promising alternative due to their lower environmental impact, supply chain stability, and tunable electrochemical properties. In this work, the electrochemical performance of 12 commercially available amino- and hydroxy-substituted anthraquinone derivatives, including several naturally occurring compounds, was systematically evaluated in sodium-ion battery systems. By focusing on readily available commercial materials, this study identified the most stable and effective candidates for organic cathodes in sodium-ion batteries. Notably, the majority of these derivatives have never been tested in galvanostatic cycling in either lithium or other post-lithium battery systems. Through systematic…
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Taxonomy
TopicsAdvancements in Battery Materials · Advanced battery technologies research · Advanced Battery Technologies Research
