Journal
JOURNAL OF PHYSICAL CHEMISTRY C
Volume 119, Issue 33, Pages 19022-19029Publisher
AMER CHEMICAL SOC
DOI: 10.1021/acs.jpcc.5b05861
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Funding
- Office of Science of the U.S. Department of Energy [DE-SC0004993]
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Iron-doped nickel (oxy)hydroxide catalysts (FexNi1-xOOH) exhibit high electrocatalytic behavior for the oxygen evolution reaction in base. Recent findings suggest that the incorporation of Fe3+ into a NiOOH lattice leads to nearly optimal adsorption energies for OER intermediates on active Fe sites. Utilizing electrochemical impedance spectroscopy and activation energy measurements, we find that pure NiOOH and FeOOH catalysts exhibit exceedingly high Faradaic resistances and activation energies 40-50 kJ/mol(-1) higher than those of the most active FexNi1-xOOH catalysts. Furthermore, the most active FexNi1-xOOH catalysts in this study exhibit activation energies that approach those previously reported for IrO2 OER catalysts.
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