Bifunctional hexagonal Ni/NiO nanostructures: Influence of the core-shell phase on magnetism, electrochemical sensing of serotonin, and catalytic reduction of 4-nitrophenol
Abstract
© 2019 The Royal Society of Chemistry.Ni0/NiO (nickel/nickel oxide) core-shell nanostructures were synthesized through a facile combustible redox reaction. Remarkably, the hetero-phase boundary with different crystalline orientations offered dual properties, which helped in bifunctional catalysis. Presence of a metallic Ni phase changed physicochemical properties and some emerging applications (magnetic properties, optical conductivity, electrochemical sensitivity, catalytic behaviour) could be foreseen. Moreover, formation of a NiO layer on metal surface prevented magnetism-induced aggregation, arrested further oxidation by hindering oxygen diffusion, and acted as a good sorbent to enhance the surface adsorption of the analyte. Hexagonal Ni/NiO nanostructures manifested well-defined ferromagnetic behavior and the catalyst could be collected easily at the end of the catalytic reduction. Ni/NiO core-shell catalysts at the nanoscale had outstanding catalytic performance (reduction of 4-nitrophenol to 4-aminophenol) compared with pure NiO catalysts beyond a reaction time of ∼9 min. The estimated sensitivity, limit of detection and limit of quantification towards the electrochemical sensing of serotonin were 0.185, 0.43 and 1.47 μM μA-1, respectively. These results suggest that a bifunctional Ni/NiO nanostructure could be a suitable catalyst for electrochemical detection of serotonin and reduction of 4-nitrophenol.
Más información
Título según SCOPUS: | Bifunctional hexagonal Ni/NiO nanostructures: Influence of the core-shell phase on magnetism, electrochemical sensing of serotonin, and catalytic reduction of 4-nitrophenol |
Título de la Revista: | NANOSCALE ADVANCES |
Volumen: | 1 |
Número: | 4 |
Editorial: | ROYAL SOC CHEMISTRY |
Fecha de publicación: | 2019 |
Página de inicio: | 1531 |
Página final: | 1540 |
Idioma: | English |
DOI: |
10.1039/C8NA00342D |
Notas: | WOS-ESCI, SCOPUS |