An alloy chemistry strategy to tailoring the d-band center of Ni by Cu for efficient and selective catalytic hydrogenation of furfural

[Display omitted] •Ni-Cu alloy (NiCux/C) were prepared by pyrolyzing NiCux-BTC precursors.•Alloying Ni with Cu can downshift the d-band center of Ni, promoting the desorption of H* from Ni.•Once alloyed by Cu, the orientation of FA on Ni changes from flat mode to tilted one.•NiCu0.33/C can hydrogena...

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Veröffentlicht in:Journal of catalysis 2020-03, Vol.383, p.172-180
Hauptverfasser: Tang, Feiying, Wang, Liqiang, Dessie Walle, Maru, Mustapha, Abdulhadi, Liu, You-Nian
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Sprache:eng
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Zusammenfassung:[Display omitted] •Ni-Cu alloy (NiCux/C) were prepared by pyrolyzing NiCux-BTC precursors.•Alloying Ni with Cu can downshift the d-band center of Ni, promoting the desorption of H* from Ni.•Once alloyed by Cu, the orientation of FA on Ni changes from flat mode to tilted one.•NiCu0.33/C can hydrogenate FA into FOL or TFOL on demand with high efficiency and selectivity. Nickel is a promising catalyst for the hydrogenation of furfural (FA) into furfuryl alcohol (FOL) and tetrahydrofurfuryl alcohol (TFOL). However, slow H* desorption and low catalytic selectivity limit its practical application. Herein, we employed an alloying strategy to tailoring the d-band center of Ni by Cu for efficient and selective catalytic hydrogenation of furfural. A series of Ni-Cu alloy catalysts (NiCux/C) were prepared by pyrolyzing NiCux-BTC (a MOF containing Cu and Ni) precursors. Theoretical calculation demonstrates that Ni exhibits a downshifted d-band center once alloyed by Cu. This change can not only promote the desorption of H from Ni surface to improve the catalytic activity but also thermodynamically favor the transformation of adsorption orientation of FA (from a flat orientation on Ni to a tilted one on Ni-Cu alloy) to enable the selective conversion of FA into FOL or TFOL on demand. NiCu0.33/C catalyst exhibits enhanced activity and selectivity for FA hydrogenation compared to pure Ni and Cu.
ISSN:0021-9517
1090-2694
DOI:10.1016/j.jcat.2020.01.019