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Water Solvation of Charged and Neutral Gold Nanoparticles

MPG-Autoren
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Roldan Cuenya,  Beatriz
Department of Physics, Ruhr University Bochum;
Interface Science, Fritz Haber Institute, Max Planck Society;

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Zitation

Novelli, F., Lopez, M. B., Schwaab, G., Roldan Cuenya, B., & Havenith, M. (2019). Water Solvation of Charged and Neutral Gold Nanoparticles. The Journal of Physical Chemistry B, 123(30), 6521-6528. doi:10.1021/acs.jpcb.9b02358.


Zitierlink: https://hdl.handle.net/21.11116/0000-0003-F53E-4
Zusammenfassung
Gold nanoparticles are unique electrocatalysts for oxygen reduction, carbon dioxide reduction, and alcohol
oxidation. Electrocatalytic processes are influenced by the interaction with the solvent, yet the direct investigation of the solvation of nanoparticles is scarce. Here we select gold nanoparticles as
~10 nm sized solutes of which we can control the charge. We perform mid‐infr
ared and terahertz spectroscopy to
compare the behavior of the water in solution with micelles loaded with neutral and positive gold nanoparticles. We find indications that the hydration water aro
und the gold‐loaded micelles is characterized by weaker hydrogen bonds than bulk water. A positive nanoparticle charge is observed to result in a larger blue shift of the OH stretch, quenches the intensity of the collective translational mode, and increases the absorption by librating water molecules. Water at the interface of a positive gold
nanoparticle could experience a stiffer potential energy surface which, in turn, might unveil local thermodynamic properties.