Tailoring α-MnO2 gas diffusion electrodes for enhanced oxygen reduction in aluminum-air batteries

An optimization strategy for gas diffusion electrodes is presented by tuning the α-MnO 2 -to-Vulcan ratio, significantly enhancing oxygen reduction reaction (ORR) performance and demonstrating improved efficiency in a prototype Al-O 2 cell. α-MnO 2 is a promising, inexpensive, and readily producible catalyst for the oxygen reduction reaction (ORR) in alkaline media, but its application is limited by low electronic conductivity. In this study, we enhance the performance of α-MnO 2 electrodes by systematically varying the α-MnO 2 -to-Vulcan ratio within the catalyst layer. Electrodes are evaluated in a gas diffusion electrode (GDE) half-cell, where an optimized catalyst layer composition leads to significantly improved ORR performance. By fine-tuning both the α-MnO 2 -Vulcan ratio and the α-MnO 2 loading, the electrode outperforms a commercial MnO 2 -based electrode and approaches the performance of the Pt/C benchmark. The improvement is attributed to the presence of a three-dimensional (3D) Vulcan network electronically connecting catalytically active α-MnO 2 sites with the substrate. Additionally, the optimized electrodes are employed in a prototype Al-O 2 flow cell. Under constant oxygen flow, power densities exceed 250 mW cm −2 , which is significantly higher than that of conventional Al-air batteries. Electrochemical impedance spectroscopy combined with distribution of relaxation times (DRT) analysis enables the separation of anode and cathode charge transfer impedances without the need for an additional reference electrode. The analysis reveals that the anode contributes more than twice as much impedance as the cathode, highlighting the need for further anode optimization. This work demonstrates a transferable approach for catalyst layer screening under technically relevant conditions in the GDE half-cell. Subsequent measurements in an Al-O 2 flow cell validate the approach. The methodology is widely applicable to the development of advanced electrodes for a variety of metal-air battery technologies.

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Journal
Journal of Energy Chemistry
Published
2025-10-28
DOI
https://doi.org/10.1016/j.jechem.2025.10.028
Citations
1
Primary Topic
Electrocatalysts for Energy Conversion
Type
article
Field-Weighted Citation Impact
0.36
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article

Tailoring α-MnO2 gas diffusion electrodes for enhanced oxygen reduction in aluminum-air batteries

Robert Leiter, Roswitha Zeis, Simon Fleischmann, Alexander Rampf et al.
1 citations
Journal of Energy Chemistry
Electrocatalysts for Energy Conversion
0.36
article

Tailoring α-MnO2 gas diffusion electrodes for enhanced oxygen reduction in aluminum-air batteries

Robert Leiter, Roswitha Zeis, Simon Fleischmann, Alexander Rampf, Giuseppe Antonio Elia
article en
1 citations

Abstract

An optimization strategy for gas diffusion electrodes is presented by tuning the α-MnO 2 -to-Vulcan ratio, significantly enhancing oxygen reduction reaction (ORR) performance and demonstrating improved efficiency in a prototype Al-O 2 cell. α-MnO 2 is a promising, inexpensive, and readily producible catalyst for the oxygen reduction reaction (ORR) in alkaline media, but its application is limited by low electronic conductivity. In this study, we enhance the performance of α-MnO 2 electrodes by systematically varying the α-MnO 2 -to-Vulcan ratio within the catalyst layer. Electrodes are evaluated in a gas diffusion electrode (GDE) half-cell, where an optimized catalyst layer composition leads to significantly improved ORR performance. By fine-tuning both the α-MnO 2 -Vulcan ratio and the α-MnO 2 loading, the electrode outperforms a commercial MnO 2 -based electrode and approaches the performance of the Pt/C benchmark. The improvement is attributed to the presence of a three-dimensional (3D) Vulcan network electronically connecting catalytically active α-MnO 2 sites with the substrate. Additionally, the optimized electrodes are employed in a prototype Al-O 2 flow cell. Under constant oxygen flow, power densities exceed 250 mW cm −2 , which is significantly higher than that of conventional Al-air batteries. Electrochemical impedance spectroscopy combined with distribution of relaxation times (DRT) analysis enables the separation of anode and cathode charge transfer impedances without the need for an additional reference electrode. The analysis reveals that the anode contributes more than twice as much impedance as the cathode, highlighting the need for further anode optimization. This work demonstrates a transferable approach for catalyst layer screening under technically relevant conditions in the GDE half-cell. Subsequent measurements in an Al-O 2 flow cell validate the approach. The methodology is widely applicable to the development of advanced electrodes for a variety of metal-air battery technologies.

Journal of Energy ChemistryVol. 114
Karlsruhe Institute of Technology (DE), Politecnico di Torino (IT), Friedrich-Alexander-Universität Erlangen-Nürnberg (DE), University of Toronto (CA), Helmholtz-Institute Ulm (DE)
Openalex Percentile: Top 37%
Electrocatalysts for Energy Conversion
0.36
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