High-Entropy Electrolyte for Scalable Zinc–Iodine Flow Batteries
Zinc metal anodes offer high capacity and intrinsic safety for aqueous batteries but are limited by sluggish interfacial desolvation and dendrite-induced instability under high utilization. Here, we design a high-entropy aqueous electrolyte by introducing multiple water-affine, low-molecular-weight alcohols at a fixed additive content, enabling solvent diversity to be tuned independently of concentration. Temperature-dependent transport analysis and electrochemical characterizations reveal entropy-assisted Zn2+ desolvation with a reduced activation barrier and a cleaner electrode–electrolyte interface, as evidenced by minimal solvent retention during deposition. This entropy-enabled interfacial regulation promotes preferential Zn (002) growth, suppresses parasitic reactions, and improves plating/stripping reversibility. When applied in a Zn–I2 flow battery, the electrolyte delivers a volumetric anodic capacity of 1905 mAh cm–3 in a 100 cm2 cell, together with high Coulombic and energy efficiencies. This work demonstrates entropy engineering of solvent environments as a strategy for stabilizing zinc metal anodes in scalable aqueous energy storage systems.
Authors
- Jianxiong Gao
- Xinyu Zhao (ORCID: https://orcid.org/0000-0002-5128-4424)
- Yanyun Song
- Mingfei Shao
- Shimeng Zhang
- Yu Wu
- Bowen Jin
- Ju Xiao
- Zhilong Wang
Institutions
- Institute for Learning Innovation (US)
- Qinghai New Energy (China) (CN)
- State Key Laboratory of Chemical Engineering (CN)
- Beijing University of Chemical Technology (CN)
Publication Details
- Journal
- ACS Energy Letters
- Published
- 2026-01-05
- DOI
- https://doi.org/10.1021/acsenergylett.5c04158
- Citations
- 2
- Primary Topic
- Advanced battery technologies research
- Type
- article
- Field-Weighted Citation Impact
- 43.86