Model Studies on the Ozone‐Mediated Synthesis of Cobalt Oxide Nanoparticles from Dicobalt Octacarbonyl in Ionic Liquids

Low‐temperature synthesis in ionic liquids (ILs) offers an efficient route for the preparation of metal oxide nanomaterials with tailor‐made properties in a water‐free environment. In this work, we investigated the role of 1‐butyl‐1‐methylpyrrolidinium bis(trifluoromethylsulfonyl)imide [C(4)C(1)Pyr][NTf(2)] in the synthesis of cobalt oxide nanoparticles from the molecular precursor Co(2)(CO)(8) with ozone. We performed a model study in ultra‐clean, ultrahigh vacuum (UHV) conditions by infrared reflection absorption spectroscopy (IRAS) using Au(111) as a substrate. Exposure of the pure precursor to ozone at low temperatures results in the oxidation of the first layers, leading to the formation of a disordered Co(x)O(y) passivation layer. Similar protection to ozone is also achieved by deposition of an IL layer onto a precursor film prior to ozone exposure. With increasing temperature, the IL gets permeable for ozone and a cobalt oxide film forms at the IL/precursor interface. We show that the interaction with the IL mediates the oxidation and leads to a more densely packed Co(x)O(y) film compared to a direct oxidation of the precursor.