Abstract

Facile synthesis of uniform supported metal catalysts is of great significance yet remains challenging for sustainable catalysis. Herein, a nanopore confinement strategy is developed to efficiently anchor metal ions in suitably sized polymer nanopores via strong coordinate bonds and ensure successful fabrication of uniform carbon-supported metal nanoparticles. Specifically, Ni2+-coordinated polydopamine (PDA) mesoporous layer was coated on GO nanosheets for the confinement of the nickel atoms (GO@PDA-Ni-x, x means pore size of PDA layer), resulting Ni@C-x nanosheets catalysts with uniformly dispersed Ni nanoparticles after pyrolysis in H2/Ar atmosphere. Characterization methods including SEM, TEM, and XPS reveal the intrinsic formation mechanism and physicochemical details. In the catalytic reaction of NaBH4-mediated hydrogenation of 4-nitrophenol (4-NP), the obtained Ni/C-10 exhibits exceptional catalytic performance with a rapid rate constant (0.686 min−1), outperforming many previously reported metal catalysts. Moreover, the catalytic activity remains almost unchanged after being recycled five times, proving the prominent stability. This work opens up an innovative avenue for rational design and synthesis of supported catalysts with controllable size for broad catalytic applications.

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