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Designing 2D carbon dot nanoreactors for alcohol oxidation coupled with hydrogen evolution

Author

Listed:
  • Qitao Chen

    (Jiangsu University)

  • Baodong Mao

    (Jiangsu University)

  • Yanhong Liu

    (Jiangsu University)

  • Yunjie Zhou

    (Soochow University)

  • Hui Huang

    (Soochow University)

  • Song Wang

    (Hubei University of Arts and Science)

  • Longhua Li

    (Jiangsu University)

  • Wei-Cheng Yan

    (Jiangsu University)

  • Weidong Shi

    (Jiangsu University)

  • Zhenhui Kang

    (Soochow University
    Taipa)

Abstract

The coupled green energy and chemical production by photocatalysis represents a promising sustainable pathway, which poses great challenges for the multifunction integration of catalytic systems. Here we show a promising green photocatalyst design using Cu-ZnIn2S4 nanosheets and carbon dots as building units, which enables the integration of reaction, mass transfer, and separation functions in the nano-space, mimicking a nanoreactor. This function integration results in great activity promotion for benzyl alcohol oxidation coupled H2 production, with H2/benzaldehyde production rates of 45.95/46.47 mmol g−1 h−1, 36.87 and 36.73 times to pure ZnIn2S4, respectively, owning to the enhanced charge accumulation and mass transfer according to in-situ spectroscopies and computational simulations of the built-in electrical field. Near-unity selectivity of benzaldehyde is achieved via the effective separation enabled by the Cu(II)-mediated conformation flipping of the intermediates and subsequent π-π conjugation. This work demonstrates an inspiring proof-of-concept nanoreactor design of photocatalysts for coupled sustainable systems.

Suggested Citation

  • Qitao Chen & Baodong Mao & Yanhong Liu & Yunjie Zhou & Hui Huang & Song Wang & Longhua Li & Wei-Cheng Yan & Weidong Shi & Zhenhui Kang, 2024. "Designing 2D carbon dot nanoreactors for alcohol oxidation coupled with hydrogen evolution," Nature Communications, Nature, vol. 15(1), pages 1-14, December.
  • Handle: RePEc:nat:natcom:v:15:y:2024:i:1:d:10.1038_s41467-024-52406-2
    DOI: 10.1038/s41467-024-52406-2
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