Time-resolved observations of water oxidation intermediates on a cobalt oxide nanoparticle catalyst.

Nat Chem

Physical Biosciences Division, Lawrence Berkeley National Laboratory, University of California, Berkeley, California 94720.

Published: April 2014

AI Article Synopsis

  • Understanding the process of water oxidation is crucial for creating better catalysts from affordable, Earth-abundant materials like transition-metal oxides.
  • Researchers used advanced spectroscopy to identify two key intermediates involved in this oxidation process when using cobalt oxide (Co3O4) as a catalyst.
  • The findings show different catalytic sites for these intermediates, which will help inform the design of more efficient materials for water oxidation in artificial photosynthesis.

Article Abstract

In any artificial photosynthetic system, the oxidation of water to molecular oxygen provides the electrons needed for the reduction of protons or carbon dioxide to a fuel. Understanding how this four-electron reaction works in detail is important for the development of improved robust catalysts made of Earth-abundant materials, like first-row transition-metal oxides. Here, using time-resolved Fourier-transform infrared spectroscopy and under reaction conditions, we identify intermediates of water oxidation catalysed by an abundant metal-oxide catalyst, cobalt oxide (Co3O4). One intermediate is a surface superoxide (three-electron oxidation intermediate absorbing at 1,013 cm(-1)), whereas a second observed intermediate is attributed to an oxo Co(IV) site (one-electron oxidation intermediate absorbing at 840 cm(-1)). The temporal behaviour of the intermediates reveals that they belong to different catalytic sites. Knowledge of the structure and kinetics of surface intermediates will enable the design of improved metal-oxide materials for more efficient water oxidation catalysis.

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http://dx.doi.org/10.1038/nchem.1874DOI Listing

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