Supported Rh nanoparticles (NPs) exhibit excellent activity
for
the chemoselective hydrogenation of halonitrobenzenes (HNBs), but
their selectivity to aromatic amines is not satisfactory due to the
side reaction on the carbon–halogen bonds, and their recycling
stability is limited due to the aggregation and the leaching of active
component during the long-term usage. Herein, we design a yolk–shell-structured
catalyst that consists of RhCu alloy cores and hollow/microporous
carbon shells (HCS) to overcome these problems. The obtained RhCu@HCS
catalyst with a Rh/Cu ratio of 1:1 showed good activity, selectivity,
and stability in the hydrogenation of p-CNB (p-chloronitrobenzene) to produce p-CAN
(p-chloroaniline) due to the synergistic effect between
Rh and Cu. The protective carbon shells not only prevented the aggregation
of metal NPs but also allowed the reactants to diffuse freely across
the shells. Therefore, our research provides a general strategy to
design highly efficient and stable hydrogenation catalysts.