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Dual-interface strategy unlocks high-performance Ah-level aqueous zinc-iodine pouch cells

08.11.26 | Dalian Institute of Chemical Physics, Chinese Academy Sciences
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In a new study published in the Journal of the American Chemical Society , researchers have developed a dual-interface coordination orchestration strategy to enable high-energy aqueous zinc-iodine batteries, providing a new pathway toward safe, durable, and Ah-level aqueous Zn||I 2 pouch cells.

Aqueous Zn||I 2 batteries are promising for large-scale energy storage because of their high safety and high theoretical capacity. However, the four-electron I - /I 0 /I + conversion chemistry faces challenges from the unstable high-valence iodine species, polyiodide shuttling, and parasitic side reactions at the Zn anode, which severely limit the practical applications of these batteries.

To address these challenges, a research team led by Prof. CHEN Zhongwei and Prof. WANG Dongdong from the Dalian Institute of Chemical Physics (DICP) of the Chinese Academy of Sciences (CAS) identified N-methylimidazolium chloride (MImCl) as a multifunctional electrolyte additive through systematic screening of nitrogen-containing cationic ligands. The MIm + cations dynamically migrate between the cathode and anode interfaces, enabling simultaneous regulation of iodine chemistry and Zn deposition.

At the cathode interface, MIm + coordinates with iodine intermediates, stabilizing high-valence iodine species and suppressing polyiodide migration. At the Zn anode, it regulates Zn 2+ deposition and promotes uniform Zn plating and stripping. According to the researchers, this dual-interface coordination improves the reversibility of the four-electron iodine chemistry while stabilizing the Zn electrode.

Based on this strategy, the researchers constructed high-loading Zn||I 2 batteries and further demonstrated an Ah-level pouch cell with a capacity of 1.4 Ah. The pouch cell delivered stable cycling over 800 cycles and achieved an energy density of 455 Wh kg -1 based on the mass of the active cathode material.

"Our study provides new insights into electrolyte-mediated interface regulation and offers a promising pathway toward high-energy and durable aqueous Zn metal batteries," said Prof. CHEN.

Journal of the American Chemical Society

10.1021/jacs.6c11308

Commentary/editorial

Not applicable

Unveiling Dual-Interface Coordination Orchestration for Durable Aqueous Zinc–Iodine Pouch Cells with Four-Electron Chemistry

4-Aug-2026

Keywords

Article Information

Contact Information

Jean Wang
Dalian Institute of Chemical Physics, Chinese Academy Sciences
wangyj@dicp.ac.cn

How to Cite This Article

APA:
Dalian Institute of Chemical Physics, Chinese Academy Sciences. (2026, August 11). Dual-interface strategy unlocks high-performance Ah-level aqueous zinc-iodine pouch cells. Brightsurf News. https://www.brightsurf.com/news/LRD042O8/dual-interface-strategy-unlocks-high-performance-ah-level-aqueous-zinc-iodine-pouch-cells.html
MLA:
"Dual-interface strategy unlocks high-performance Ah-level aqueous zinc-iodine pouch cells." Brightsurf News, Aug. 11 2026, https://www.brightsurf.com/news/LRD042O8/dual-interface-strategy-unlocks-high-performance-ah-level-aqueous-zinc-iodine-pouch-cells.html.