Aqueous zinc batteries have attracted attention as next-generation energy storage devices due to their low cost, safety, and high capacity. However, zinc–organic batteries, which promise abundant raw materials and recyclability, face critical limitations such as low working voltage, poor cycling stability, and rapid capacity fading. Small molecules often dissolve, while one- and two-dimensional polymers suffer from restacking, leading to sluggish charge transfer. The introduction of three-dimensional (3D) polymer frameworks has shown success in lithium batteries but has rarely been applied to zinc–organic systems. Due to these issues, new strategies are urgently required to develop high-voltage, long-lifespan organic cathodes for aqueous zinc batteries.
A research team from Nanjing University of Posts and Telecommunications, the National University of Singapore, the Suzhou Institute of Nano-Tech and Nano-Bionics, and A*STAR (Singapore) has unveiled a hexaazatriphenylene-based polymer with a 3D architecture that sets new records for aqueous zinc–organic batteries. Published (DOI: 10.1016/j.esci.2025.100379) online on July, 2025, in eScience, the study demonstrates a cathode capable of delivering an initial discharge voltage of 1.32 V and maintaining 93.4% capacity after 40,000 cycles. This marks a significant step forward in designing durable, high-energy organic batteries.
The study introduces HAT-TP, a novel polymer formed by coupling hexaazatrinaphtylene (HAT-CN) and hexaaminotriptycene (THA-NH2) into a 3D framework. This architecture enhances stability by suppressing solubility and exposing abundant electroactive C=N sites for ion coordination. Characterizations, including XRD, FT-IR, NMR, and electron microscopy, confirmed the successful synthesis and porous 3D morphology. Electrochemical testing revealed a record initial discharge voltage of 1.32 V with a midpoint of 1.17 V, far surpassing conventional organic cathodes. The HAT-TP battery achieved ultralong cycling stability, retaining 93.4% of capacity after 40,000 cycles at 5 A g⁻¹, while maintaining nearly 100% Coulombic efficiency. Ex situ analyses and density functional theory simulations demonstrated a reversible Zn²⁺/H⁺ co-insertion mechanism, with five-electron transfer pathways driving high redox activity. Theoretical calculations showed stronger Gibbs free energy gains for Zn²⁺/H⁺ binding in HAT-TP compared with HAT-CN, explaining the higher discharge potential. Together, these features enable superior rate capability and energy densities up to 192.8 Wh kg⁻¹, highlighting the power of 3D molecular engineering in zinc–organic battery design.
“Our work demonstrates that 3D molecular polymerization is a powerful strategy to overcome long-standing barriers in zinc–organic batteries,” said corresponding authors Prof. Chaobin He, Prof. Wenyong Lai and Prof. Qichong Zhang. “By coupling hexaazatriphenylene with triptycene units, we created a stable, conductive, and highly active cathode material that combines high voltage with ultralong cycling life. The ability to retain more than 90% capacity over 40,000 cycles is unprecedented in this field, and it opens new possibilities for designing organic materials that are not only recyclable but also competitive with inorganic systems.”
The successful design of HAT-TP cathodes offers practical implications for advancing safe, sustainable, and high-performance energy storage. With its long lifespan and competitive energy density, this technology could support large-scale grid storage, where reliability and safety are critical, as well as flexible and wearable electronics requiring lightweight and environmentally friendly power sources. Beyond zinc–organic batteries, the principles of 3D polymer engineering demonstrated here can be extended to other electrochemical systems, including lithium-sulfur and sodium batteries. This research thus represents an important step toward next-generation organic batteries that merge sustainability with industrial practicality.
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References
DOI
10.1016/j.esci.2025.100379
Original Source URL
https://doi.org/10.1016/j.esci.2025.100379
Funding Information
This work was supported by the National Natural Science Foundation of China (52203215), and the Natural Science Research Start-up Foundation of Recruiting Talents of Nanjing University of Posts and Telecommunications (Grant No. NY225035).
About eScience
eScience – a Diamond Open Access journal cooperated with KeAi and published online at ScienceDirect. eScience is founded by Nankai University (China) in 2021 and aims to publish high quality academic papers on the latest and finest scientific and technological research in interdisciplinary fields related to energy, electrochemistry, electronics, and environment. eScience provides insights, innovation and imagination for these fields by built consecutive discovery and invention. Now eScience has been indexed by SCIE, CAS, Scopus and DOAJ. Its first impact factor is 36.6, which is ranked first in the field of electrochemistry.