Aromatic Chelating Layers Enable Advanced Zinc Ion Batteries
Aqueous zinc ion batteries (ZIBs) have gained prominence as promising contenders for grid-scale energy storage systems due to their inherent safety, cost-effectiveness, and high energy density; however, their practical implementation faces fundamental limitations stemming from uncontrolled dendritic formation caused by insufficient desolvation kinetics and sluggish Zn2+ diffusion mechanisms. Herein, the strategy for enhancing desolvation–diffusion kinetics is proposed by fabricating an aromatic chelating layer on the zinc anode via a unique bidentate chelation effect between o-phenylenediamine and a metallic zinc foil. The aromatic chelating layers effectively prevent interfacial corrosion from side reactions, and the conjugate electrostatic frameworks also promote Zn2+ transport with a lower barrier; these conclusions are confirmed by both experimental characterizations and theoretical studies. Consequently, the assembled cells exhibit a long-term lifespan with a low overpotential, and the Coulombic efficiency is prominently improved to 99.71%. Coupled with VO2 cathodes, both the constructions of the coin cell and pouch cell all possess high-capacity retentions after a long cycling process up to 2000 cycles, suggesting the bright application potential of aromatic chelating modification on the surface of zinc anodes.
Authors
- Li Min Lu
- Zhongting Wang
- Wanhui Wang
- Haotian Zhu
- Yang Zhou
- Yuezhan Feng
- Yumei Wang
- Ji Hu
Institutions
- Chongqing University (CN)
- National University of Singapore (SG)
- U.S. Energy Information Administration (US)
- Zhengzhou University (CN)
- Henan University of Engineering (CN)
- Advanced Processing Technology (United States) (US)
- Luoyang Institute of Science and Technology (CN)
Publication Details
- Journal
- ACS Sustainable Chemistry & Engineering
- Published
- 2026-01-29
- DOI
- https://doi.org/10.1021/acssuschemeng.5c11223
- Primary Topic
- Advanced battery technologies research
- Type
- article
- Field-Weighted Citation Impact
- 0.00