Highly active screen-printed electrocatalysts for water oxidation based on beta-manganese oxide

Fekete, Monika, Hocking, Rosalie K., Chang, Shery L.Y., Italiano, Cristina, Patti, Antonio F., Arena, Francesco, and Spicci, Leone (2013) Highly active screen-printed electrocatalysts for water oxidation based on beta-manganese oxide. Energy & Environmental Science, 6 (7). pp. 2222-2232.

[img] PDF (Published Version) - Published Version
Restricted to Repository staff only

View at Publisher Website: http://dx.doi.org/10.1039/c3ee40429c
 
104
4


Abstract

A versatile screen-printing method is applied for the preparation of efficient water oxidation catalysts based on a nanostructured β-MnO₂ material prepared by a redox-precipitation method, and commercial β-MnO₂. The catalyst films were tested for activity in water oxidation over a range of neutral to alkaline pH. The onset of water oxidation in case of the nanostructured MnO₂ films is found at an overpotential (η) of 300 mV at pH 13.6 (1.0 M NaOH), with current densities reaching 10 mA cm⁻² at η= 500 mV. The screen-printed MnO₂ (nano) is one of the most active manganese oxide-based catalysts reported to date, despite consisting mostly of the common pyrolusite (β-MnO₂) phase, so far generally found inactive in water oxidation. The films prepared from commercial β-MnO2 were found to be moderately active, with an onset of water oxidation at η= 500 mV (pH 13.6), and currents up to 5 mA cm⁻² at η= 800 mV. At pH 6, the two samples exhibit similar activity and also match or surpass the performance of recent benchmark manganese oxides. X-ray absorption spectroscopy (XAS) studies suggest that the crystal phase is unchanged after prolonged electrochemical cycling. Scanning electron microscopy (SEM) analysis indicates very little corrosion of the surface morphology after prolonged catalyst operation at alkaline pH. However, high-resolution transmission electron microscopy (HRTEM) analysis shows the formation of a small amount of an amorphous phase on the surface of the nanorods after oxygen evolution over 12 hours in alkaline media.

Item ID: 29074
Item Type: Article (Research - C1)
ISSN: 1754-5706
Funders: Australian Research Council (ARC)
Date Deposited: 28 Aug 2013 05:33
FoR Codes: 03 CHEMICAL SCIENCES > 0302 Inorganic Chemistry > 030207 Transition Metal Chemistry @ 100%
SEO Codes: 85 ENERGY > 8504 Energy Transformation > 850402 Hydrogen-based Energy Systems (incl. Internal Hydrogen Combustion Engines) @ 50%
97 EXPANDING KNOWLEDGE > 970103 Expanding Knowledge in the Chemical Sciences @ 50%
Downloads: Total: 4
More Statistics

Actions (Repository Staff Only)

Item Control Page Item Control Page