Colloidal platinum nanoparticles are obtained via a surfactant-free polyol process in alkaline ethylene glycol. In this popular synthesis, ethylene glycol functions as solvent and reducing agent. The preparation procedure is known for its reproducibility to obtain 1-2 nm nanoparticles, but at the same time the controlled preparation of larger nanoparticles is challenging. A reliable size control without the use of surfactants is a fundamental yet missing achievement for systematic investigations. In this work it is demonstrated how the molar ratio between NaOH and the platinum precursor determines the final particle size and how this knowledge can be used to prepare and study in a systematic way supported catalysts with defined size and Pt to carbon ratio. Using small-angle X-ray scattering, transmission electron microscopy, infrared spectroscopy, X-ray absorption spectroscopy, pair distribution function and electrochemical analysis it is shown that changing the NaOH/Pt molar ratio from 25 to 3, the Pt nanoparticle size is tuned from 1 to 5 nm. This size range is of interest for various catalytic applications, such as the oxygen reduction reaction (ORR). Supporting the nanoparticles onto a high surface area carbon, we demonstrate how the particle size effect can be studied keeping the Pt to carbon ratio constant, an important aspect that in previous studies could not be accomplished.

The preparation of colloidal nanoparticles in alkaline ethylene glycol is a powerful approach for the preparation of model catalysts and ligand-functionalized nanoparticles. For these systems the term "unprotected" nanoparticles has been established because no strongly binding stabilizers are required to achieve stable colloids. Irrespective of this fact, the particles must be considered as being covered by adsorbates, as otherwise the particles would coalesce and precipitate. The identification of these protecting adsorbate species is however still under debate and is the scope of the present study. "Unprotected" Pt and Ru nanoparticles were characterized by NMR spectroscopy, which does not evidence the presence of any C−H containing species bound to the particle surface. Instead, the colloids were found to be covered by CO, as demonstrated by IR spectroscopy. However, analysis of the stretching mode reveals the presence of a second species. On the basis of the spectroscopic characterization this species is concluded to be OH − , and it is demonstrated that the applied synthesis route results only in stable colloids if OH − is present within the reaction mixture. IR spectroscopy reveals that the CO coverage increases as the NaOH concentration used in the precursor solution is decreased. However, even at the lowest for the synthesis suitable OH − concentration the surface was found to be covered by both species. Finally, the effect of the OH − concentration on the particle size distribution was studied. The maximum was found to shift to larger particle diameters as the OH − concentration is lowered which is accompanied by broadening of the size distribution.

A unique approach is presented to isolate surfactant-free nanoparticles as solid powders and their subsequent use for heterogeneous catalytic processes without loss of performance.

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