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Plasmonic high-entropy carbides

Author

Listed:
  • Arrigo Calzolari

    (CNR-NANO Research Center S3)

  • Corey Oses

    (Duke University
    Duke University)

  • Cormac Toher

    (Duke University
    University of Texas at Dallas)

  • Marco Esters

    (Duke University
    Duke University)

  • Xiomara Campilongo

    (Duke University)

  • Sergei P. Stepanoff

    (The Pennsylvania State University)

  • Douglas E. Wolfe

    (The Pennsylvania State University)

  • Stefano Curtarolo

    (Duke University
    Duke University)

Abstract

Discovering multifunctional materials with tunable plasmonic properties, capable of surviving harsh environments is critical for advanced optical and telecommunication applications. We chose high-entropy transition-metal carbides because of their exceptional thermal, chemical stability, and mechanical properties. By integrating computational thermodynamic disorder modeling and time-dependent density functional theory characterization, we discovered a crossover energy in the infrared and visible range, corresponding to a metal-to-dielectric transition, exploitable for plasmonics. It was also found that the optical response of high-entropy carbides can be largely tuned from the near-IR to visible when changing the transition metal components and their concentration. By monitoring the electronic structures, we suggest rules for optimizing optical properties and designing tailored high-entropy ceramics. Experiments performed on the archetype carbide HfTa4C5 yielded plasmonic properties from room temperature to 1500K. Here we propose plasmonic transition-metal high-entropy carbides as a class of multifunctional materials. Their combination of plasmonic activity, high-hardness, and extraordinary thermal stability will result in yet unexplored applications.

Suggested Citation

  • Arrigo Calzolari & Corey Oses & Cormac Toher & Marco Esters & Xiomara Campilongo & Sergei P. Stepanoff & Douglas E. Wolfe & Stefano Curtarolo, 2022. "Plasmonic high-entropy carbides," Nature Communications, Nature, vol. 13(1), pages 1-9, December.
  • Handle: RePEc:nat:natcom:v:13:y:2022:i:1:d:10.1038_s41467-022-33497-1
    DOI: 10.1038/s41467-022-33497-1
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    References listed on IDEAS

    as
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