Spectroscopic Studies of Nanoparticulate Thin Films
of a Cobalt-Based Oxygen Evolution Catalyst
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Abstract
Nanoparticle (NP) cobalt–phosphate
(Co-P<sub>i</sub>) water
oxidation catalysts are prepared as thin films by anodic electrodeposition
from solutions of Co<sup>2+</sup> dissolved in proton-accepting electrolytes.
Compositional and structural insight into the nature of the catalyst
film is provided from advanced spectroscopy. Infrared spectra demonstrate
that counteranions incorporate into the Co-P<sub>i</sub> thin films
and that the phosphate ion, among various anion electrolytes, exhibits
the highest binding affinity to the cobalt centers. Atomic force microscopy
images show a highly porous morphology of the thin film that is composed
of Co-P<sub>i</sub> NPs. Whereas conventional X-ray powder diffraction
technique shows catalyst films to be amorphous, synchrotron-based
X-ray grazing incidence diffraction reveals well-defined diffraction
patterns that are indicative of long-range ordering within the film.
Azimuthal scans imply that as-prepared films possess a highly preferred
orientation and texture on the electrode surface