4.8 Article

Reversible Al Metal Anodes Enabled by Amorphization for Aqueous Aluminum Batteries

Journal

JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
Volume 144, Issue 25, Pages 11444-11455

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/jacs.2c04820

Keywords

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Funding

  1. National Natural Science Foundation of China [52101246]
  2. Fundamental Research Funds for the Central Universities [5710010721]
  3. Singapore MOE AcRF Tier 1 grant [2020-T1-001- 031]
  4. Singapore A * ST A R project [A19D9a0096]
  5. Camille Dreyfus Teacher-Scholar Award
  6. Welch Foundation [F- 1861]

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This study demonstrates that amorphization is an effective strategy to address critical issues in aqueous aluminum metal batteries (AMBs). By shifting the reduction potential for aluminum deposition, the amorphous aluminum (a-Al) interfacial layer facilitates stable aluminum plating and stripping, while mitigating passivation and enhancing interfacial ion transfer kinetics. The use of a noncorrosive, low-cost, and fluorine-free electrolyte further contributes to the excellent electrochemical performance of the AMBs.
Aqueous aluminum metal batteries (AMBs) are regarded as one of the most sustainable energy storage systems among post-lithium-ion candidates, which is attributable to their highest theoretical volumetric capacity, inherent safe operation, and low cost. Yet, the development of aqueous AMBs is plagued by the incapable aluminum plating in an aqueous solution and severe parasitic reactions, which results in the limited discharge voltage, thus making the development of aqueous AMBs unsuccessful so far. Here, we demonstrate that amorphization is an effective strategy to tackle these critical issues of a metallic Al anode by shifting the reduction potential for Al deposition. The amorphous aluminum (a-Al) interfacial layer is triggered by an in situ lithium-ion alloying/dealloying process on a metallic Al substrate with low strength. Unveiled by experimental and theoretical investigations, the amorphous structure greatly lowers the Al nucleation energy barrier, which forces the Al deposition competitive to the electron-stealing hydrogen evolution reaction (HER). Simultaneously, the inhibited HER mitigates the passivation, promoting interfacial ion transfer kinetics and enabling steady aluminum plating/stripping for 800 h in the symmetric cell. The resultant multiple full cells using Al@a-Al anodes deliver approximately a 0.6 V increase in the discharge voltage plateau compared to that of bare Al-based cells, which far outperform all reported aqueous AMBs. In both symmetric cells and full cells, the excellent electrochemical performances are achieved in a noncorrosive, low-cost, and fluorine-free Al-2(SO4)(3) electrolyte, which is ecofriendly and can be easily adapted for sustainable large-scale applications. This work brings an intriguing picture of the design of metallic anodes for reversible and high-voltage AMBs.

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