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A unique Co@CoO catalyst for hydrogenolysis of biomass-derived 5-hydroxymethylfurfural to 2,5-dimethylfuran

Author

Listed:
  • Shuang Xiang

    (East China University of Science and Technology)

  • Lin Dong

    (East China University of Science and Technology)

  • Zhi-Qiang Wang

    (East China University of Science and Technology)

  • Xue Han

    (University of Manchester)

  • Luke L. Daemen

    (Oak Ridge National Laboratory)

  • Jiong Li

    (Chinese Academy of Sciences)

  • Yongqiang Cheng

    (Oak Ridge National Laboratory)

  • Yong Guo

    (East China University of Science and Technology)

  • Xiaohui Liu

    (East China University of Science and Technology)

  • Yongfeng Hu

    (Sinopec Shanghai Research Institute of Petrochemical Technology)

  • Anibal J. Ramirez-Cuesta

    (Oak Ridge National Laboratory)

  • Sihai Yang

    (University of Manchester)

  • Xue-Qing Gong

    (East China University of Science and Technology)

  • Yanqin Wang

    (East China University of Science and Technology)

Abstract

The development of precious-metal-free catalysts to promote the sustainable production of fuels and chemicals from biomass remains an important and challenging target. Here, we report the efficient hydrogenolysis of biomass-derived 5-hydroxymethylfurfural to 2,5-dimethylfuran over a unique core-shell structured catalyst, Co@CoO that affords the highest productivity among all catalysts, including noble-metal-based catalysts, reported to date. Surprisingly, we find that the catalytically active sites reside on the shell of CoO with oxygen vacancies rather than the metallic Co. The combination of various spectroscopic experiments and computational modelling reveals that the CoO shell incorporating oxygen vacancies not only drives the heterolytic cleavage, but also the homolytic cleavage of H2 to yield more active Hδ− species, resulting in the exceptional catalytic activity. Co@CoO also exhibits excellent activity toward the direct hydrodeoxygenation of lignin model compounds. This study unlocks, for the first time, the potential of simple metal-oxide-based catalysts for the hydrodeoxygenation of renewable biomass to chemical feedstocks.

Suggested Citation

  • Shuang Xiang & Lin Dong & Zhi-Qiang Wang & Xue Han & Luke L. Daemen & Jiong Li & Yongqiang Cheng & Yong Guo & Xiaohui Liu & Yongfeng Hu & Anibal J. Ramirez-Cuesta & Sihai Yang & Xue-Qing Gong & Yanqin, 2022. "A unique Co@CoO catalyst for hydrogenolysis of biomass-derived 5-hydroxymethylfurfural to 2,5-dimethylfuran," Nature Communications, Nature, vol. 13(1), pages 1-9, December.
    • Handle: RePEc:nat:natcom:v:13:y:2022:i:1:d:10.1038_s41467-022-31362-9
    DOI: 10.1038/s41467-022-31362-9
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    References listed on IDEAS

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    1. Shaopeng Li & Minghua Dong & Junjuan Yang & Xiaomeng Cheng & Xiaojun Shen & Shulin Liu & Zhi-Qiang Wang & Xue-Qing Gong & Huizhen Liu & Buxing Han, 2021. "Selective hydrogenation of 5-(hydroxymethyl)furfural to 5-methylfurfural over single atomic metals anchored on Nb2O5," Nature Communications, Nature, vol. 12(1), pages 1-9, December.
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    Cited by:

    1. Hao Yan & Bowen Liu & Xin Zhou & Fanyu Meng & Mingyue Zhao & Yue Pan & Jie Li & Yining Wu & Hui Zhao & Yibin Liu & Xiaobo Chen & Lina Li & Xiang Feng & De Chen & Honghong Shan & Chaohe Yang & Ning Yan, 2023. "Enhancing polyol/sugar cascade oxidation to formic acid with defect rich MnO2 catalysts," Nature Communications, Nature, vol. 14(1), pages 1-11, December.
    2. Chengsheng Yang & Sicong Ma & Yongmei Liu & Lihua Wang & Desheng Yuan & Wei-Peng Shao & Lunjia Zhang & Fan Yang & Tiejun Lin & Hongxin Ding & Heyong He & Zhi-Pan Liu & Yong Cao & Yifeng Zhu & Xinhe Ba, 2024. "Homolytic H2 dissociation for enhanced hydrogenation catalysis on oxides," Nature Communications, Nature, vol. 15(1), pages 1-11, December.
    3. Zhongzhe Wei & Zijiang Zhao & Chenglong Qiu & Songtao Huang & Zihao Yao & Mingxuan Wang & Yi Chen & Yue Lin & Xing Zhong & Xiaonian Li & Jianguo Wang, 2023. "Tripodal Pd metallenes mediated by Nb2C MXenes for boosting alkynes semihydrogenation," Nature Communications, Nature, vol. 14(1), pages 1-11, December.

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