Hydrate-melt electrolyte design for aqueous aluminium-bromine batteries with enhanced energy-power merits

X Xingyuan Chu (Faculty of Chemistry and Food Chemistry & Center for Advancing Electronics Dresden (CFAED)) J Jingwei Du J Jiaxu Zhang (State Key Laboratory of Advanced Welding and Joining, MIIT Key Laboratory of Critical Materials Technology for New Energy Conversion and Storage, School of Chemistry and Chemical Engineering) X Xiaodong Li (Hefei National Research Center for Physical Sciences at the Microscale, State Key Laboratory of Precision and Intelligent Chemistry) X Xiaohui Liu (Hydrogen Energy Industry Institute of Jilin Province) Y Yongkang Wang J Johannes Hunger (Max-Planck Institute for Polymer Research 5 , Ackermannweg 10, 55128 Mainz,) A Ahiud Morag J Jinxin Liu (Department of Chemistry) Q Quanquan Guo (Faculty of Chemistry and Food Chemistry & Center for Advancing Electronics Dresden (cfaed)) D Dongqi Li (Faculty of Chemistry and Food Chemistry & Center for Advancing Electronics Dresden (cfaed)) Y Yu Han M Mischa Bonn X Xinliang Feng M Minghao Yu (Faculty of Chemistry and Food Chemistry & Center for Advancing Electronics Dresden (cfaed))

Abstract

Abstract Aluminium-based aqueous batteries hold promises for next-generation sustainable and large-scale energy storage due to the favorable metrics of Al and water-based electrolytes. However, the performance of current aluminium-based aqueous batteries falls significantly below theoretical expectations, with a critical bottleneck of realizing cathodes with high areal capacities. Herein, we present a hydrate-melt electrolyte design utilizing cost-effective AlCl3 and organic halide salts, which enables the demonstration of aqueous Al-Br batteries with enhanced energy-power characteristics. The optimal electrolyte features suppressed water activity and loosely bound halogen anions, attributed to its unique electrolyte structure, where the majority of water molecules engage in robust ion solvation (>98% as suggested by simulations) and halogen anions reside in the outer solvation sheath of cations. These distinctive features ensure good compatibility of the electrolyte with the reversible Br−/Br0/Br+ conversion, enabling cathodes with a high areal capacity of 5 mAh cm−2. Besides, the electrolyte allows for Zn-Al alloying/de-alloying with minimal polarization (around 100 mV at 5 mA cm−2) and a smooth alloy surface. The assembled Al-Br cell delivers an energy density (267 Wh L−1, based on the volume of anode, cathode and separator) comparable to commercial Li-ion batteries and a substantial power density (1069 W L−1) approaching electrochemical capacitors.

Article Details

Volume / Issue Vol. 16, Issue 1
Published July 09, 2025
ISSN 2041-1723
Publisher Nature Portfolio

Journal Info

Nature Communications

Nature Portfolio

ISSN: 2041-1723 Open Access Life Sciences

Authors (15)

X

Xingyuan Chu

Faculty of Chemistry and Food Chemistry & Center for Advancing Electronics Dresden (CFAED)

J

Jingwei Du

J

Jiaxu Zhang

State Key Laboratory of Advanced Welding and Joining, MIIT Key Laboratory of Critical Materials Technology for New Energy Conversion and Storage, School of Chemistry and Chemical Engineering

X

Xiaodong Li

Hefei National Research Center for Physical Sciences at the Microscale, State Key Laboratory of Precision and Intelligent Chemistry

X

Xiaohui Liu

Hydrogen Energy Industry Institute of Jilin Province

Y

Yongkang Wang

J

Johannes Hunger

Max-Planck Institute for Polymer Research 5 , Ackermannweg 10, 55128 Mainz,

A

Ahiud Morag

J

Jinxin Liu

Department of Chemistry

Q

Quanquan Guo

Faculty of Chemistry and Food Chemistry & Center for Advancing Electronics Dresden (cfaed)

D

Dongqi Li

Faculty of Chemistry and Food Chemistry & Center for Advancing Electronics Dresden (cfaed)

Y

Yu Han

M

Mischa Bonn

X

Xinliang Feng

M

Minghao Yu

Faculty of Chemistry and Food Chemistry & Center for Advancing Electronics Dresden (cfaed)