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Enabling direct-growth route for highly efficient ethanol upgrading to long-chain alcohols in aqueous phase

Author

Listed:
  • Juwen Gu

    (Guangdong University of Technology)

  • Wanbing Gong

    (University of Science and Technology of China)

  • Qian Zhang

    (Guangdong University of Technology
    Guangdong Provincial Key Laboratory of Plant Resources Biorefinery
    Guangzhou Key Laboratory of Clean Transportation Energy and Chemistry)

  • Ran Long

    (University of Science and Technology of China)

  • Jun Ma

    (University of Science and Technology of China)

  • Xinyu Wang

    (University of Science and Technology of China)

  • Jiawei Li

    (University of Science and Technology of China)

  • Jiayi Li

    (University of Science and Technology of China)

  • Yujian Fan

    (Guangdong University of Technology)

  • Xinqi Zheng

    (Guangdong University of Technology)

  • Songbai Qiu

    (Guangdong University of Technology
    Guangdong Provincial Key Laboratory of Plant Resources Biorefinery
    Guangzhou Key Laboratory of Clean Transportation Energy and Chemistry)

  • Tiejun Wang

    (Guangdong University of Technology
    Guangdong Provincial Key Laboratory of Plant Resources Biorefinery
    Guangzhou Key Laboratory of Clean Transportation Energy and Chemistry)

  • Yujie Xiong

    (University of Science and Technology of China
    University of Science and Technology of China)

Abstract

Upgrading ethanol to long-chain alcohols (LAS, C6+OH) offers an attractive and sustainable approach to carbon neutrality. Yet it remains a grand challenge to achieve efficient carbon chain propagation, particularly with noble metal-free catalysts in aqueous phase, toward LAS production. Here we report an unconventional but effective strategy for designing highly efficient catalysts for ethanol upgrading to LAS, in which Ni catalytic sites are controllably exposed on surface through sulfur modification. The optimal catalyst exhibits the performance well exceeding previous reports, achieving ultrahigh LAS selectivity (15.2% C6OH and 59.0% C8+OH) at nearly complete ethanol conversion (99.1%). Our in situ characterizations, together with theoretical simulation, reveal that the selectively exposed Ni sites which offer strong adsorption for aldehydes but are inert for side reactions can effectively stabilize and enrich aldehyde intermediates, dramatically improving direct-growth probability toward LAS production. This work opens a new paradigm for designing high-performance non-noble metal catalysts for upgrading aqueous EtOH to LAS.

Suggested Citation

  • Juwen Gu & Wanbing Gong & Qian Zhang & Ran Long & Jun Ma & Xinyu Wang & Jiawei Li & Jiayi Li & Yujian Fan & Xinqi Zheng & Songbai Qiu & Tiejun Wang & Yujie Xiong, 2023. "Enabling direct-growth route for highly efficient ethanol upgrading to long-chain alcohols in aqueous phase," Nature Communications, Nature, vol. 14(1), pages 1-10, December.
  • Handle: RePEc:nat:natcom:v:14:y:2023:i:1:d:10.1038_s41467-023-43773-3
    DOI: 10.1038/s41467-023-43773-3
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    References listed on IDEAS

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    3. Yongmeng Wu & Cuibo Liu & Changhong Wang & Yifu Yu & Yanmei Shi & Bin Zhang, 2021. "Converting copper sulfide to copper with surface sulfur for electrocatalytic alkyne semi-hydrogenation with water," Nature Communications, Nature, vol. 12(1), pages 1-11, December.
    4. Kamran Dastafkan & Xiangjian Shen & Rosalie K. Hocking & Quentin Meyer & Chuan Zhao, 2023. "Monometallic interphasic synergy via nano-hetero-interfacing for hydrogen evolution in alkaline electrolytes," Nature Communications, Nature, vol. 14(1), pages 1-10, December.
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