4.8 Article

Enhancing Multifunctionalities of Transition-Metal Dichalcogenide Monolayers via Cation Intercalation

Journal

ACS NANO
Volume 11, Issue 9, Pages 9390-9396

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acsnano.7b04880

Keywords

hydrogen ion; lithium ion; intercalation; molybdenum sulfide; tungsten sulfide; molybdenum selenide; tungsten selenide

Funding

  1. CAREER from the National Science Foundation [DMR-1352028]
  2. National Science Foundation [ECCS-1508856]
  3. Agency for Science, Technology and Research (A*STAR)
  4. State of North Carolina
  5. National Science Foundation
  6. Direct For Mathematical & Physical Scien
  7. Division Of Materials Research [1352028] Funding Source: National Science Foundation
  8. Directorate For Engineering
  9. Div Of Electrical, Commun & Cyber Sys [1508856] Funding Source: National Science Foundation

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We have demonstrated that multiple functionalities of transition-metal dichalcogenide (TMDC) monolayers may be substantially improved by the intercalation of small cations (H+ or Li+) between the monolayers and underlying substrates. The functionalities include photoluminescence (PL) efficiency and catalytic activity. The improvement in PL efficiency may be up to orders of magnitude and can be mainly ascribed to two effects of the intercalated cations: p-doping to the monolayers and reducing, the influence of substrates, but more studies are necessary to better understand the mechanism for the improvement in the catalytic functionality. The cation intercalation may be achieved by simply immersing substrate-supported monolayers into the solution of certain acids or salts. It is more difficult to intercalate under the monolayers interacting with substrates stronger, such as as-grown monolayers or the monolayers on 2D material substrates. This result presents a versatile strategy to simultaneously optimize multiple functionalities of TMDC monolayers.

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