Supported Ir oxide catalysts obtained from surfactant-free
colloidal Ir nanoparticles (NPs) synthesized in alkaline methanol (MeOH),
ethanol (EtOH), and ethylene glycol (EG) are investigated and compared. The
comparison of independent techniques such as transition electron microscopy
(TEM), small angle X-ray scattering (SAXS), and electrochemistry allows shedding
light on the parameters that affect the dispersion of the active phase as well
as the catalytic activity. The colloidal dispersions obtained are suitable to
develop supported catalysts with little NP agglomeration on a carbon support
leading to highly active catalysts with more than 400 A g<sup>-1</sup><sub>Ir</sub>
reached at 1.5 V<sub>RHE</sub> for the OER. While the more common
surfactant-free alkaline EG synthesis requires flocculation and re-dispersion
leading to Ir loss, the main difference between methanol and ethanol as solvent
is related to the dispersibility of the support material. The choice of the
suitable monoalcohol determines the maximum achieved Ir loading on the support
without detrimental particle agglomeration. This simple consideration on
catalyst design can readily lead to significantly improved catalysts.