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Subnanometric Cu clusters on atomically Fe-doped MoO2 for furfural upgrading to aviation biofuels

Author

Listed:
  • Xin Zhao

    (South China University of Technology)

  • Fengliang Wang

    (South China University of Technology)

  • Xiangpeng Kong

    (Harbin Institute of Technology)

  • Ruiqi Fang

    (South China University of Technology)

  • Yingwei Li

    (South China University of Technology
    South China University of Technology−Zhuhai Institute of Modern Industrial Innovation)

Abstract

Single cluster catalysts (SCCs) are considered as versatile boosters in heterogeneous catalysis due to their modifiable single cluster sites and supports. In this work, we report subnanometric Cu clusters dispersed on Fe-doped MoO2 support for biomass-derived furfural upgrading. Systematical characterizations suggest uniform Cu clusters (composing four Cu atoms in average) are homogeneously immobilized on the atomically Fe-doped ultrafine MoO2 nanocrystals (Cu4/Fe0.3Mo0.7O2@C). The atomic doping of Fe into MoO2 leads to significantly modified electronic structure and consequently charge redistribution inside the supported Cu clusters. The as-prepared Cu4/Fe0.3Mo0.7O2@C shows superior catalytic performance in the oxidative coupling of furfural with C3~C10 primary/secondary alcohols to produce C8~C15 aldehydes/ketones (aviation biofuel intermediates), outperforming the conventionally prepared counterparts. DFT calculations and control experiments are further carried out to interpret the structural and compositional merits of Cu4/Fe0.3Mo0.7O2@C in the oxidative coupling reaction, and elucidate the reaction pathway and related intermediates.

Suggested Citation

  • Xin Zhao & Fengliang Wang & Xiangpeng Kong & Ruiqi Fang & Yingwei Li, 2022. "Subnanometric Cu clusters on atomically Fe-doped MoO2 for furfural upgrading to aviation biofuels," Nature Communications, Nature, vol. 13(1), pages 1-9, December.
    • Handle: RePEc:nat:natcom:v:13:y:2022:i:1:d:10.1038_s41467-022-30345-0
    DOI: 10.1038/s41467-022-30345-0
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    References listed on IDEAS

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