Spatial Effect on the Performance of Carboxylate Anode Materials in Na‐Ion Batteries

Developing low‐voltage carboxylate anode materials is critical for achieving low‐cost, high‐performance, and sustainable Na‐ion batteries (NIBs). However, the structure design rationale and structure‐performance correlation for organic carboxylates in NIBs remains elusive. Herein, the spatial effect on the performance of carboxylate anode materials is studied by introducing heteroatoms in the conjugation structure and manipulating the positions of carboxylate groups in the aromatic rings. Planar and twisted organic carboxylates are designed and synthesized to gain insight into the impact of geometric structures to the electrochemical performance of carboxylate anodes in NIBs. Among the carboxylates, disodium 2,2’‐bipyridine‐5,5’‐dicarboxylate (2255‐Na) with a planar structure outperforms the others in terms of highest specific capacity (210 mAh g−1), longest cycle life (2000 cycles), and best rate capability (up to 5 A g−1). The cyclic stability and redox mechanism of 2255‐Na in NIBs are exploited by various characterization techniques. Moreover, high‐temperature (up to 100 °C) and all‐organic batteries based on a 2255‐Na anode, a polyaniline (PANI) cathode, and an ether‐based electrolyte are achieved and exhibited exceptional electrochemical performance. Therefore, this work demonstrates that designing organic carboxylates with extended planar conjugation structures is an effective strategy to achieve high‐performance and sustainable NIBs. Planar and twisted organic carboxylates are designed and synthesized to gain insight into the impact of geometric structures to the electrochemical performance of carboxylate anodes in Na‐ion batteries. The planar carboxylate compound outperforms the twisted carboxylate compounds in terms of specific capacity, cycle life, and rate capability due to improved structure stability and aromaticity of the planar conjugation structure.