The design of molecular-based catalysts
for oxygen-evolution reaction
(OER) requires more investigations for the true catalyst to be found.
First-row transition metal complexes are extensively investigated
for OER, but the role of these metal complexes as a true catalyst
is doubtful. Some doubts have been expressed about the role of first-row
transition metal complexes for OER at high overpotentials (η
> 450). Generally, the detection of the true catalyst has so far
been
focused on high overpotentials (η > 450) because at low overpotentials
(η < 450), many methods are not sensitive enough to detect
small amounts of heterogeneous catalysts on the electrode surface
during the first seconds of the reaction. Ni(II) phthalocyanine-tetra
sulfonate tetrasodium (1) is in moderate conditions (at
20–50 °C and pH 5–13) in the absence of electrochemical
driving forces, which could make it noteworthy for OER. Herein, the
results of OER in the presence of 1 at low overpotentials
under alkaline conditions are presented. In addition, in the presence
of Ni complexes, using an Fe ion is introduced as a new method for
detecting Ni (hydr)oxide under OER. Our experiments indicate that
in the presence of a homogeneous OER (pre)catalyst, a deep investigation
is necessary to rule out the heterogeneous catalysts formed. Our approach
is a roadmap in the field of catalysis to understand the OER mechanism
in the presence of a molecular Ni-based catalyst design. Our results
shown in this study are likely to open up new perspectives and discussion
on many molecular catalysts in a considerable part of the chemistry
community.