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Updated: Feb 5, 2026

Gyroid Nickel Nanostructures from Diblock Copolymer Supramolecules
Published on: April 28, 2014
A robust core-shell nanostructured nickel-iron alloy@nitrogen-containing carbon catalyst for the highly efficient
Yaowen Zhang1, Chunling Liu, Guoli Fan
1State Key Laboratory of Chemical Resources Engineering, Beijing Advanced Innovation Center for Soft Matter Science and Engineering, Beijing University of Chemical Technology, Beijing, 100029, China. lifeng@mail.buct.edu.cn.
Abstract:
Currently, the catalytic selective hydrogenation of nitroarenes to produce aromatic amines is one of the most important key reactions in many fine chemical processes. In particular, non-noble-metal-catalyzed hydrogenation of nitroarenes represents more sustainable chemical processes. Here, we report a new robust and recyclable core-shell nanostructured nickel-iron alloy@nitrogen-containing carbon (NiFe@NC) catalyst and the beneficial effect of alloying Ni with Fe for the above reaction. The key to this synthetic strategy was thermally transforming the Ni-Fe layered double hydroxide (NiFe-LDH)/melamine mixture to form a fixed NiFe@NC nanostructure. A series of characterization results revealed the formation of NiFe alloy nanoparticles (NPs) coated with the NC overlayer. The as-fabricated NiFe@NC catalyst with a Ni/Fe atomic ratio of 3.0 exhibited superior activity for the reduction of the nitro group in o-chloronitrobenzene, with a 99.5% yield of o-chloroaniline under mild reaction conditions. The initial reaction rate over the catalyst was nearly three times that over the monometallic Ni@NC counterpart, and even one-order magnitude higher than that over pristine NiFe-LDH-derived NiFe alloy NPs. The extraordinary activity of NiFe@NC was reasonably attributed to the unique core-shell nanostructure, where both the NiFe alloy core and the NC overlayer shell could construct a significant promotional effect, being beneficial for the selective cleavage of the N-O bond. Recycling experiments indicated that the catalyst could be easily separated and recovered under an external magnetic field and experienced excellent recyclability during seventeen cycles without an obvious loss of catalytic activity. Furthermore, the present catalyst was also highly active for the chemoselective hydrogenation of other substituted nitroarenes bearing different functional groups to the corresponding anilines.
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