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Plasmon-induced selective carbon dioxide conversion on earth-abundant aluminum-cuprous oxide antenna-reactor nanoparticles

Author

Listed:
  • Hossein Robatjazi

    (Rice University
    Rice University)

  • Hangqi Zhao

    (Rice University
    Rice University)

  • Dayne F. Swearer

    (Rice University
    Rice University)

  • Nathaniel J. Hogan

    (Rice University
    Rice University)

  • Linan Zhou

    (Rice University
    Rice University)

  • Alessandro Alabastri

    (Rice University
    Rice University)

  • Michael J. McClain

    (Rice University
    Rice University)

  • Peter Nordlander

    (Rice University
    Rice University
    Rice University
    Rice University)

  • Naomi J. Halas

    (Rice University
    Rice University
    Rice University
    Rice University)

Abstract

The rational combination of plasmonic nanoantennas with active transition metal-based catalysts, known as ‘antenna-reactor’ nanostructures, holds promise to expand the scope of chemical reactions possible with plasmonic photocatalysis. Here, we report earth-abundant embedded aluminum in cuprous oxide antenna-reactor heterostructures that operate more effectively and selectively for the reverse water-gas shift reaction under milder illumination than in conventional thermal conditions. Through rigorous comparison of the spatial temperature profile, optical absorption, and integrated electric field enhancement of the catalyst, we have been able to distinguish between competing photothermal and hot-carrier driven mechanistic pathways. The antenna-reactor geometry efficiently harnesses the plasmon resonance of aluminum to supply energetic hot-carriers and increases optical absorption in cuprous oxide for selective carbon dioxide conversion to carbon monoxide with visible light. The transition from noble metals to aluminum based antenna-reactor heterostructures in plasmonic photocatalysis provides a sustainable route to high-value chemicals and reaffirms the practical potential of plasmon-mediated chemical transformations.

Suggested Citation

  • Hossein Robatjazi & Hangqi Zhao & Dayne F. Swearer & Nathaniel J. Hogan & Linan Zhou & Alessandro Alabastri & Michael J. McClain & Peter Nordlander & Naomi J. Halas, 2017. "Plasmon-induced selective carbon dioxide conversion on earth-abundant aluminum-cuprous oxide antenna-reactor nanoparticles," Nature Communications, Nature, vol. 8(1), pages 1-10, December.
  • Handle: RePEc:nat:natcom:v:8:y:2017:i:1:d:10.1038_s41467-017-00055-z
    DOI: 10.1038/s41467-017-00055-z
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    Cited by:

    1. Rishi Verma & Gunjan Sharma & Vivek Polshettiwar, 2024. "The paradox of thermal vs. non-thermal effects in plasmonic photocatalysis," Nature Communications, Nature, vol. 15(1), pages 1-45, December.
    2. Saideep Singh & Rishi Verma & Nidhi Kaul & Jacinto Sa & Ajinkya Punjal & Shriganesh Prabhu & Vivek Polshettiwar, 2023. "Surface plasmon-enhanced photo-driven CO2 hydrogenation by hydroxy-terminated nickel nitride nanosheets," Nature Communications, Nature, vol. 14(1), pages 1-18, December.
    3. Hidalgo, D. & Martín-Marroquín, J.M., 2020. "Power-to-methane, coupling CO2 capture with fuel production: An overview," Renewable and Sustainable Energy Reviews, Elsevier, vol. 132(C).
    4. Huai Chen & Yangyang Xiong & Jun Li & Jehad Abed & Da Wang & Adrián Pedrazo-Tardajos & Yueping Cao & Yiting Zhang & Ying Wang & Mohsen Shakouri & Qunfeng Xiao & Yongfeng Hu & Sara Bals & Edward H. Sar, 2023. "Epitaxially grown silicon-based single-atom catalyst for visible-light-driven syngas production," Nature Communications, Nature, vol. 14(1), pages 1-11, December.
    5. Daniel Lach & Jaroslaw Polanski & Maciej Kapkowski, 2022. "CO 2 —A Crisis or Novel Functionalization Opportunity?," Energies, MDPI, vol. 15(5), pages 1-20, February.
    6. Yajun Zheng & Hedan Yao & Ruinan Di & Zhicheng Xiang & Qiang Wang & Fangfang Lu & Yu Li & Guangxing Yang & Qiang Ma & Zhiping Zhang, 2022. "Water coordinated on Cu(I)-based catalysts is the oxygen source in CO2 reduction to CO," Nature Communications, Nature, vol. 13(1), pages 1-11, December.

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