Potential- and Buffer-Dependent Catalyst Decomposition during Nickel-Based Water Oxidation Catalysis.

ABSTRACT

The production of hydrogen by water electrolysis benefits from the development of water oxidation catalysts. This development process can be aided by the postulation of design rules for catalytic systems. The analysis of the reactivity of molecular complexes can be complicated by their decomposition under catalytic conditions into nanoparticles that may also be active. Such a misinterpretation can lead to incorrect design rules. In this study, the nickel-based water oxidation catalyst [NiII (meso-L)](ClO4 )2 , which was previously thought to operate as a molecular catalyst, is found to decompose to form a NiOx layer in a pH 7.0 phosphate buffer under prolonged catalytic conditions, as indicated by controlled potential electrolysis, electrochemical quartz crystal microbalance, and X-ray photoelectron spectroscopy measurements. Interestingly, the formed NiOx layer desorbs from the surface of the electrode under less anodic potentials. Therefore, no nickel species can be detected on the electrode after electrolysis. Catalyst decomposition is strongly dependent on the pH and buffer, as there is no indication of NiOx layer formation at pH 6.5 in phosphate buffer nor in a pH 7.0 acetate buffer. Under these conditions, the activity stems from a molecular species, but currents are much lower. This study demonstrates the importance of in situ characterization methods for catalyst decomposition and metal oxide layer formation, and previously proposed design elements for nickel-based catalysts need to be revised.