Additive-Driven Interfacial Engineering of Aluminum Metal Anode for Ultralong Cycling Life

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Additive-Driven Interfacial Engineering of Aluminum Metal Anode for Ultralong Cycling Life
Title:
Additive-Driven Interfacial Engineering of Aluminum Metal Anode for Ultralong Cycling Life
Journal Title:
Nano-Micro Letters
Publication Date:
29 December 2022
Citation:
Kumar, S., Rama, P., Yang, G., Lieu, W. Y., Chinnadurai, D., & Seh, Z. W. (2022). Additive-Driven Interfacial Engineering of Aluminum Metal Anode for Ultralong Cycling Life. Nano-Micro Letters, 15(1). https://doi.org/10.1007/s40820-022-01000-6
Abstract:
AbstractRechargeable Al batteries (RAB) are promising candidates for safe and environmentally sustainable battery systems with low-cost investments. However, the currently used aluminum chloride-based electrolytes present a significant challenge to commercialization due to their corrosive nature. Here, we report for the first time, a novel electrolyte combination for RAB based on aluminum trifluoromethanesulfonate (Al(OTf)3) with tetrabutylammonium chloride (TBAC) additive in diglyme. The presence of a mere 0.1 M of TBAC in the Al(OTf)3 electrolyte generates the charge carrying electrochemical species, which forms the basis of reaction at the electrodes. TBAC reduces the charge transfer resistance and the surface activation energy at the anode surface and also augments the dissociation of Al(OTf)3 to generate the solid electrolyte interphase components. Our electrolyte's superiority directly translates into reduced anodic overpotential for cells that ran for 1300 cycles in Al plating/stripping tests, the longest cycling life reported to date. This unique combination of salt and additive is non-corrosive, exhibits a high flash point and is cheaper than traditionally reported RAB electrolyte combinations, which makes it commercially promising. Through this report, we address a major roadblock in the commercialization of RAB and inspire equivalent electrolyte fabrication approaches for other metal anode batteries.
License type:
Attribution 4.0 International (CC BY 4.0)
Funding Info:
This research is supported by core funding from: SERC
Grant Reference no. : NA
Description:
ISSN:
2150-5551
2311-6706
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