RESUMEN
Bimetallic nanoparticle (NP) catalysts are widely used in many heterogeneous gas-based reactions because they often outperform their monometallic counterparts. During these reactions, NPs often undergo structural changes, which impact their catalytic activity. Despite the important role of the structure in the catalytic activity, many aspects of how a reactive gaseous environment affects the structure of bimetallic nanocatalysts are still lacking. Here, using gas-cell transmission electron microscopy (TEM), it is shown that during a CO oxidation reaction over PdCu alloy NPs, the selective oxidation of Cu causes the segregation of Cu and transforms the NPs into Pd-CuO NPs. The segregated NPs are very stable and have high activity for the conversion of CO into CO2 . Based on the observations, the segregation of Cu from Cu-based alloys during a redox reaction is likely to be general and may have a positive impact on the catalytic activity. Hence, it is believed that similar insights based on direct observation of the reactions under relevant reactive conditions are critical both for understanding and designing high-performance catalysts.
RESUMEN
Cerium(IV) oxide (CeO2), or ceria, is one of the most abundant rare-earth materials that has been extensively investigated for its catalytic properties over the past two decades. However, due to the global scarcity and increasing cost of rare-earth materials, efficient utilization of this class of materials poses a challenging issue for the materials research community. Thus, this work is directed toward an exploration of making ultrathin hollow ceria or other rare-earth metal oxides and mixed rare-earth oxides in general. Such a hollow morphology appears to be attractive, especially when the thickness is trimmed to its limit, so that it can be viewed as a two-dimensional sheet of organized nanoscale crystallites, while remaining three-dimensional spatially. This ensures that both inner and outer shell surfaces can be better utilized in catalytic reactions if the polycrystalline sphere is further endowed with mesoporosity. Herein, we have devised our novel synthetic protocol for making ultrathin mesoporous hollow spheres of ceria or other desired rare-earth oxides with a tunable shell thickness in the region of 10 to 40 nm. Our ceria ultrathin hollow spheres are catalytically active and outperform other reported similar nanostructured ceria for the oxidation reaction of carbon monoxide in terms of fuller utilization of cerium. The versatility of this approach has also been extended to fabricating singular or multicomponent rare-earth metal oxides with the same ultrathin hollow morphology and structural uniformity. Therefore, this approach holds good promise for better utilization of rare-earth metal elements across their various technological applications, not ignoring nano-safety considerations.
