Issue 34, 2022

A stable and high-energy aqueous aluminum based battery

Abstract

Aqueous aluminum ion batteries (AAIBs) have received growing attention because of their low cost, safe operation, eco-friendliness, and high theoretical capacity. However, one of the biggest challenges for AAIBs is the poor reversibility due to the presence of an oxide layer and the accompanying hydrogen evolution reaction. Herein, we develop a strongly hydrolyzed/polymerized aluminum–iron hybrid electrolyte to improve the electrochemical behavior of AAIBs. On the one hand, the designed electrolyte enables aluminum ion intercalation/deintercalation on the cathode while stable deposition/stripping of aluminium occurs on the anode. On the other hand, the electrolyte contributes to the electrochemical energy storage through an iron redox reaction. These two reactions are parallel and coupled through an Fe–Al alloy on the anode, thus enhancing the reversibility and energy density of AAIBs. As a result, this hybrid-ion battery delivers a specific volumetric capacity of 35 A h L−1 at the current density of 1.0 mA cm−2, and remarkable stability with a capacity retention of 90% over 500 cycles. Furthermore, the hybrid-ion battery achieves a high energy density of approximately 42 W h L−1 with an average operating voltage of 1.1 V. This green electrolyte for high-energy AAIBs holds promises for large-scale energy storage applications.

Graphical abstract: A stable and high-energy aqueous aluminum based battery

Supplementary files

Article information

Article type
Edge Article
Submitted
20 Jun 2022
Accepted
28 Jul 2022
First published
28 Jul 2022
This article is Open Access

All publication charges for this article have been paid for by the Royal Society of Chemistry
Creative Commons BY license

Chem. Sci., 2022,13, 10066-10073

A stable and high-energy aqueous aluminum based battery

R. Tao, C. Gao, E. Xie, B. Wang and B. Lu, Chem. Sci., 2022, 13, 10066 DOI: 10.1039/D2SC03455G

This article is licensed under a Creative Commons Attribution 3.0 Unported Licence. You can use material from this article in other publications without requesting further permissions from the RSC, provided that the correct acknowledgement is given.

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