Chanda, V.; Rüdiger, O.; Cruz, D.; Mackert, V.; Sous, P.; Sonnenberg, M.; Solh, H.; Pielsticker, L.; Kucklick, L.; Hetaba, W.; Hirt, S. D.; Hoster, H. E.; Levin, N.: Cation–Anion Co-doping Enables Acid-Stable MnO2 Anodes for Proton Exchange Membrane Water Electrolysis. Small Science 6 (2026), p. e70388/1-11
10.1002/smsc.70388
Open Accesn Version
Abstract:
Developing acid-stable, earth-abundant oxygen evolution catalysts remains a central challenge for proton exchange membrane water electrolyzers (PEM-WE), due to catalyst degradation via overoxidation under strongly anodic conditions. Here, we introduce a cation–anion co-doping strategy that induces lattice-level electronic stabilization in manganese dioxide (MnO2) through incorporation of niobium (Nb5+) and fluoride (F−) into a γ/β-MnO2 framework. Structural and spectroscopic analyses, including operando X-ray absorption spectroscopy, show that co-doping stabilizes an electron-enriched Mn environment and suppresses oxidation to unstable high-valence states under OER conditions. This originates from charge redistribution across the Mn-O-Nb framework, enabling controlled Mn3+/Mn4+ dynamics and mitigating overoxidation-driven dissolution. As a result, MnO2-Nb-F catalyst demonstrates an overpotential of 410 mV at 10 mA cm−2 in 0.5 M H2SO4, a Tafel slope of 90 mV dec−1, and reduced charge transfer resistance compared to pristine MnO2. When integrated into a PEM electrolyzer (5 cm2, 60 °C), the catalyst achieves a cell voltage of 1.91 V at 1 A cm−2 and exhibits operational stability for 380 h at 0.4 A cm−2. These results demonstrate that synergistic cation–anion engineering decouples the activity-stability trade-off in MnO2, establishing a viable design strategy for noble-metal-free PEM-WE anodes.