Journal
JOURNAL OF PHYSICAL CHEMISTRY C
Volume 119, Issue 5, Pages 2804-2812Publisher
AMER CHEMICAL SOC
DOI: 10.1021/jp510015v
Keywords
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Funding
- Danish National Research Foundation [DNRF54]
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The oxidation and reduction of CuZn nanoparticles was studied using X-ray photoelectron spectroscopy (XPS) and in situ transmission electron microscopy (TEM). CuZn nanoparticles with a narrow size distribution were produced with a gas-aggregation cluster source in conjunction with mass-filtration. A direct comparison between the spatially averaged XPS information and the local TEM observations was thus made possible. Upon oxidation in O-2, the as-deposited metal clusters transform into a polycrystalline cluster consisting of separate CuO and ZnO nanocrystals. Specifically, the CuO is observed to segregate to the cluster surface and partially cover the ZnO nanocrystals. Upon subsequent reduction in H-2 the CuO converts into metallic Cu with ZnO nanocrystal covering their surface. In addition, a small amount of metallic Zn is detected suggesting that ZnO is reduced. It is likely that Zn species can migrate to the Cu surface forming a Cu-Zn surface alloy. The oxidation and reduction dynamics of the CuZn nanoparticles is of great importance to industrial methanol synthesis for which the direct interaction of Cu and ZnO nanocrystals synergistically boosts the catalytic activity. Thus, the present results demonstrate a new model approach that should be generally applicable to address metal-support interactions in coprecipitated catalysts and multicomponent nanomaterials.
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