Abstract
In this work, poly(vinylpyrrolidone)-stabilized 3–5 nm Rh@Co core–shell nanoparticles were synthesized by a sequential reduction method, which was further in situ transformed into Rh-Co2O3 heteroaggregate nanostructures on alumina supports. The studies of XRD, HAADF-STEM images with phase mappings, XPS, TPR, and DRIFT-IR with CO probes confirm that the as-synthesized Rh@Co nanoparticles were core–shell-like structures with Rh cores and Co-rich shells, and Rh-Co2O3 heteroaggregate nanostructures are obtained by calcination of Rh@Co nanoparticles and subsequent selective H2 reduction. The Rh-Co2O3/Al2O3 nanostructures demonstrated enhanced catalytic performance for hydrogenations of various substituted nitroaromatics relative to individual Rh/Al2O3 and illustrated a high catalytic stability during recycling experiments for o-nitrophenol hydrogenation reactions. The catalytic performance enhancement of Rh-Co2O3/Al2O3 nanocatalysts is ascribed to the Rh-Co2O3 interfaces where the Rh-Co2O3 interaction not only prevents the active Rh particles from agglomeration but also promotes the catalytic hydrogenation performance.
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