4.8 Article

Economic Manganese-Oxide-Based Anodes for Efficient Water Oxidation: Rapid Synthesis and In Situ Transmission Electron Microscopy Monitoring

Journal

ACS CATALYSIS
Volume 11, Issue 5, Pages 2511-2523

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acscatal.0c03388

Keywords

in situ heating TEM; XAS; in situ heating STEM/EDX; water oxidation; manganese oxide; electrocatalysis; low-cost transition metals

Funding

  1. University of Zurich Research Priority Program (URPP) for Solar Light to Chemical Energy Conversion (LightChEC)
  2. Swiss National Science Foundation [CRSII2_160801/1]
  3. University of Zurich
  4. Forschungskredit grant [FK-18106]
  5. Scientific Centre for Optical and Electron Microscopy of ETH Zurich

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This study introduces an economical method for manufacturing stable and efficient manganese oxide anodes, and reveals the formation pathways and phase transformations by in situ monitoring.
Earth-abundant, environmentally friendly, and low-cost manganese oxide materials are promising resources for water oxidation catalysts in clean solar fuel applications. We here introduce a convenient and economic method for manufacturing stable and highly efficient manganese-oxide-based anodes for electrochemical water oxidation under neutral conditions. The electrodes were fabricated through thermal decomposition of acidic KMnO4 solution. The phase transitions of the manganese oxide film during calcination and thermal decomposition of KMnO4 were monitored with in situ heating transmission electron microscopy (TEM), in situ heating scanning transmission electron microscopy coupled with energy-dispersive X-ray spectroscopy (STEM/EDX), and in situ heating powder X-ray diffraction (PXRD). In-depth monitoring of formation pathways and phase transformations by in situ techniques under high temperatures shed light upon the fabrication of efficient manganese oxides for energy conversion applications. After parameter optimizations, the best-performing manganese oxide catalyst was applied for water electrolysis for 100 h with a stable current density of 1.0 mA/cm(2) at an overpotential of 490 mV in neutral pH. Post operando characterizations of key oxide film properties showed no significant changes. The readily commercially available precursor enables a simple and rapid fabrication method, and the promising stability and high performance of the herein developed electrodes render them quite promising for technological water splitting systems.

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