Abstract
The oxygen-evolution reaction (OER) through water oxidation is an inevitable reaction for water splitting toward storing energy. However, OER is a four-electron and slow reaction, which is also a bottleneck for water splitting. To find the role of Pt and PtO2 on the OER in the presence of Fe, the electrochemistry of Pt foil and PtO2 is investigated in the absence/presence of K2FeO4 as a soluble Fe salt at pH ≈ 13. After the addition of K2FeO4, a remarkable increase in the OER is recorded in the presence of Pt or PtO2. The obtained catalysts were characterized by operando visible spectroscopy, high-resolution transmission electron microscopy, scanning electron microscopy, electron-spin resonance spectroscopy, X-ray photoelectron spectroscopy, X-ray diffraction, and electrochemical methods. KOH solutions usually contain Fe and/or Ni impurities. It is found that neither Pt nor PtO2 is an OER catalyst in a Ni/Fe-free KOH, and even at an overpotential of 570 mV in purified KOH (pH ≈ 13), no clear OER was observed.
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