IDEAS home Printed from https://ideas.repec.org/a/nat/natcom/v10y2019i1d10.1038_s41467-019-11407-2.html
   My bibliography  Save this article

Construction of stabilized bulk-nano interfaces for highly promoted inverse CeO2/Cu catalyst

Author

Listed:
  • Han Yan

    (Shandong University)

  • Chun Yang

    (Shandong University)

  • Wei-Peng Shao

    (Shandong University)

  • Li-Hua Cai

    (Shandong University)

  • Wei-Wei Wang

    (Shandong University)

  • Zhao Jin

    (Shandong University)

  • Chun-Jiang Jia

    (Shandong University)

Abstract

As the water-gas shift (WGS) reaction serves as a crucial industrial process, strategies for developing robust WGS catalysts are highly desiderated. Here we report the construction of stabilized bulk-nano interfaces to fabricate highly efficient copper-ceria catalyst for the WGS reaction. With an in-situ structural transformation, small CeO2 nanoparticles (2–3 nm) are stabilized on bulk Cu to form abundant CeO2-Cu interfaces, which maintain well-dispersed under reaction conditions. This inverse CeO2/Cu catalyst shows excellent WGS performances, of which the activity is 5 times higher than other reported Cu catalysts. Long-term stability is also very solid under harsh conditions. Mechanistic study illustrates that for the inverse CeO2/Cu catalyst, superb capability of H2O dissociation and CO oxidation facilitates WGS process via the combination of associative and redox mechanisms. This work paves a way to fabricate robust catalysts by combining the advantages of bulk and nano-sized catalysts. Catalysts with such inverse configurations show great potential in practical WGS applications.

Suggested Citation

  • Han Yan & Chun Yang & Wei-Peng Shao & Li-Hua Cai & Wei-Wei Wang & Zhao Jin & Chun-Jiang Jia, 2019. "Construction of stabilized bulk-nano interfaces for highly promoted inverse CeO2/Cu catalyst," Nature Communications, Nature, vol. 10(1), pages 1-10, December.
  • Handle: RePEc:nat:natcom:v:10:y:2019:i:1:d:10.1038_s41467-019-11407-2
    DOI: 10.1038/s41467-019-11407-2
    as

    Download full text from publisher

    File URL: https://www.nature.com/articles/s41467-019-11407-2
    File Function: Abstract
    Download Restriction: no

    File URL: https://libkey.io/10.1038/s41467-019-11407-2?utm_source=ideas
    LibKey link: if access is restricted and if your library uses this service, LibKey will redirect you to where you can use your library subscription to access this item
    ---><---

    Citations

    Citations are extracted by the CitEc Project, subscribe to its RSS feed for this item.
    as


    Cited by:

    1. Xin Tang & Chuqiao Song & Haibo Li & Wenyu Liu & Xinyu Hu & Qiaoli Chen & Hanfeng Lu & Siyu Yao & Xiao-nian Li & Lili Lin, 2024. "Thermally stable Ni foam-supported inverse CeAlOx/Ni ensemble as an active structured catalyst for CO2 hydrogenation to methane," Nature Communications, Nature, vol. 15(1), pages 1-12, December.
    2. Zelun Zhao & Guang Gao & Yongjie Xi & Jia Wang & Peng Sun & Qi Liu & Chengyang Li & Zhiwei Huang & Fuwei Li, 2024. "Inverse ceria-nickel catalyst for enhanced C–O bond hydrogenolysis of biomass and polyether," Nature Communications, Nature, vol. 15(1), pages 1-10, December.
    3. Kai Xu & Chao Ma & Han Yan & Hao Gu & Wei-Wei Wang & Shan-Qing Li & Qing-Lu Meng & Wei-Peng Shao & Guo-Heng Ding & Feng Ryan Wang & Chun-Jiang Jia, 2022. "Catalytically efficient Ni-NiOx-Y2O3 interface for medium temperature water-gas shift reaction," Nature Communications, Nature, vol. 13(1), pages 1-9, December.
    4. Hao-Xin Liu & Shan-Qing Li & Wei-Wei Wang & Wen-Zhu Yu & Wu-Jun Zhang & Chao Ma & Chun-Jiang Jia, 2022. "Partially sintered copper‒ceria as excellent catalyst for the high-temperature reverse water gas shift reaction," Nature Communications, Nature, vol. 13(1), pages 1-11, December.
    5. Xin-Pu Fu & Cui-Ping Wu & Wei-Wei Wang & Zhao Jin & Jin-Cheng Liu & Chao Ma & Chun-Jiang Jia, 2023. "Boosting reactivity of water-gas shift reaction by synergistic function over CeO2-x/CoO1-x/Co dual interfacial structures," Nature Communications, Nature, vol. 14(1), pages 1-11, December.

    More about this item

    Statistics

    Access and download statistics

    Corrections

    All material on this site has been provided by the respective publishers and authors. You can help correct errors and omissions. When requesting a correction, please mention this item's handle: RePEc:nat:natcom:v:10:y:2019:i:1:d:10.1038_s41467-019-11407-2. See general information about how to correct material in RePEc.

    If you have authored this item and are not yet registered with RePEc, we encourage you to do it here. This allows to link your profile to this item. It also allows you to accept potential citations to this item that we are uncertain about.

    We have no bibliographic references for this item. You can help adding them by using this form .

    If you know of missing items citing this one, you can help us creating those links by adding the relevant references in the same way as above, for each refering item. If you are a registered author of this item, you may also want to check the "citations" tab in your RePEc Author Service profile, as there may be some citations waiting for confirmation.

    For technical questions regarding this item, or to correct its authors, title, abstract, bibliographic or download information, contact: Sonal Shukla or Springer Nature Abstracting and Indexing (email available below). General contact details of provider: http://www.nature.com .

    Please note that corrections may take a couple of weeks to filter through the various RePEc services.

    IDEAS is a RePEc service. RePEc uses bibliographic data supplied by the respective publishers.