Active metals decorated NiCoO yolk-shell nanospheres as nanoreactors for catalytic reduction of nitroarenes and azo dyes.

Chemosphere

School of Chemistry and Environmental Engineering, Key Laboratory of Green Chemical Engineering Process of Ministry of Education, Engineering Research Center of Phosphorus Resources Development and Utilization of Ministry of Education, Hubei Key Laboratory of Novel Reactor and Green Chemical Technology, Key Laboratory of Novel Biomass-Based Environmental and Energy Materials in Petroleum and Chemical Industry, Wuhan Institute of Technology, Wuhan, 430073, PR China. Electronic address:

Published: February 2024

Transition-metal oxides (TMOs) have received a great deal of research attention and have been widely used in a variety of fields. However, conventional TMOs do not possess high specific surface area, sufficient active site on their surfaces, and limited their applications in catalysis. This study presents a two-step method for synthesizing active metal (M) decorated NiCoO (M/NiCoO, M = Pd or Cu) nanospheres with yolk-shell nanostructures. Taking advantage of the unique morphology and the combination of dual active components (i.e., active NiCoO substrate and decorated active metal), the as-prepared M/NiCoO yolk-shell nanospheres can be employed as nanoreactors in the organic reactions. In catalyzing the reduction of a representative nitroarene (i.e., 4-NP) by NaBH, the Pd/NiCoO nanoreactors exhibit a superior catalytic efficiency to their counterparts (Cu/NiCoO and NiCoO). The turnover frequency is much higher than that of various TMOs supported nanocatalysts have been reported over the past five years. Furthermore, the Pd/NiCoO nanoreactors show excellent stability and common applicability of the reduction of various substituted nitrobenzenes and azo dyes. This work provides new rational design concept and preparation strategy for efficient nanoreactors with dual active components and sheds light on the practical application of chemical reactions.

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http://dx.doi.org/10.1016/j.chemosphere.2023.141102DOI Listing

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