Role of Pt and PtO2 in the Oxygen-Evolution Reaction in the Presence of Iron under Alkaline Conditions.

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.

Homogeneous or heterogeneous electrocatalysis: reinvestigation of a cobalt coordination compound for water oxidation.

A cobalt coordination compound with azo-ligand linkers combined with linked bisulfonate moieties has been argued to be an efficient catalyst for the oxygen-evolution reaction (OER) (H.-T. Shi, X.-X. Li, F.-H. Wu and W.-B. Yu, Dalton Trans., 2017, 46, 16321.). In the previously published report, this cobalt compound (compound 1) was believed to display a high turnover frequency (5 s-1) at η = 720 mV at pH 9. Herein, the OER in the presence of compound 1 is reinvestigated. The nanosized oxide-based particles formed after the OER in the presence of compound 1 were tracked by electrochemical methods, scanning electron microscopy (SEM), energy dispersive spectrometry (EDX), X-ray diffraction studies (XRD), (High-resolution) transmission electron microscopy ((HR)TEM), Raman spectroscopy, X-ray absorption spectroscopy (XAS), and X-ray photoelectron spectroscopy (XPS). Based on these experiments, it is proposed that a candidate for the true catalyst of the OER in the presence of compound 1 is cobalt oxide. During the OER and using chronoamperometry, the oxidation state of Co ions for the formed Co oxide is (III), but after consecutive CVs the oxidation states of Co ions for the formed Co oxide are (II) and (III). The results shed new light on the role of Co oxide nanoparticles formed in the presence of this Co coordination compound during the OER. Our experimental data also show that for the OER in the presence of a homogeneous (pre)catalyst, careful analyses to find the role of metal oxides are necessary for informed progress. The present findings also might help to find the mechanism of the OER in the presence of coordination compounds.