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Surfactant-Free Colloidal Strategies for Highly Dispersed and Active Supported IrO2 Catalysts: Synthesis and Performance Evaluation for the Oxygen Evolution Reaction

preprint
submitted on 26.01.2021, 17:02 and posted on 28.01.2021, 07:32 by Francesco Bizzotto, Jonathan Quinson, Johanna Schröder, Alessandro Zana, Matthias Arenz
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-1Ir reached at 1.5 VRHE 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.

Funding

SNF project No. 200021_184742

Marie Skłodowska-Curie grant agreement No. 840523 (CoSolCat)

History

Email Address of Submitting Author

matthias.arenz@dcb.unibe.ch

Institution

University of Bern

Country

Switzerland

ORCID For Submitting Author

0000-0001-9765-4315

Declaration of Conflict of Interest

No conflict of interest.

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