4.5 Article

Zirconium Oxycarbide: A Highly Stable Catalyst Material for Electrochemical Energy Conversion

Journal

CHEMPHYSCHEM
Volume 20, Issue 22, Pages 3067-3073

Publisher

WILEY-V C H VERLAG GMBH
DOI: 10.1002/cphc.201900539

Keywords

electrocatalysis; hydrogen evolution reaction; online DEMS; transition metal carbides; zirconium oxycarbide

Funding

  1. Austrian Science Fund (FWF) via DACH project [I4114-N37]
  2. University of Innsbruck
  3. DOE Office of Science User Facility [DE-AC02-05CH11231, ALS-08048]

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Metal carbides and oxycarbides have recently gained considerable interest due to their (electro)catalytic properties that differ from those of transition metals and that have potential to outperform them as well. The stability of zirconium oxycarbide nanopowders (ZrO0.31C0.69), synthesized via a hybrid solid-liquid route, is investigated in different gas atmospheres from room temperature to 800 degrees C by using in-situ X-ray diffraction and in-situ electrical impedance spectroscopy. To feature the properties of a structurally stable Zr oxycarbide with high oxygen content, a stoichiometry of ZrO0.31C0.69 has been selected. ZrO0.31C0.69 is stable in reducing gases with only minor amounts of tetragonal ZrO2 being formed at high temperatures, whereas it decomposes in CO2 and O-2 gas atmosphere. From online differential electrochemical mass spectrometry measurements, the hydrogen evolution reaction (HER) onset potential is determined at -0.4 V-RHE. CO2 formation is detected at potentials as positive as 1.9 V-RHE as ZrO0.31C0.69 decomposition product, and oxygen is anodically formed at 2.5 V-RHE, which shows the high electrochemical stability of this material in acidic electrolyte. This peopwery makes the material suited for electrocatalytic reactions at anodic potentials, such as CO and alcohol oxidation reactions, in general.

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