4.8 Article

Mechanistic insight into the chemical treatments of monolayer transition metal disulfides for photoluminescence enhancement

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NATURE COMMUNICATIONS
卷 12, 期 1, 页码 -

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NATURE PORTFOLIO
DOI: 10.1038/s41467-021-26340-6

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资金

  1. European Research Council (ERC) under the European Union [758826, 756962]
  2. Swedish research council, Vetenskapsradet [2018-06610]
  3. Royal Society and Tata Group [UF150033]
  4. Newton International Fellowship
  5. EPSRC
  6. Winton Programme for the Physics of Sustainability
  7. European Research Council (ERC) [758826] Funding Source: European Research Council (ERC)
  8. Swedish Research Council [2018-06610] Funding Source: Swedish Research Council

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The use of cation donors has been demonstrated to significantly enhance the photoluminescence of monolayer transition metal disulfides, which is more effective than commonly used p-dopants. In addition, the ionic salts used in the treatments are environmentally friendly and easier to handle, providing the possibility of treatments during device fabrication.
There is a growing interest in obtaining high quality monolayer transition metal disulfides for optoelectronic applications. Surface treatments using a range of chemicals have proven effective to improve the photoluminescence yield of these materials. However, the underlying mechanism for the photoluminescence enhancement is not clear, which prevents a rational design of passivation strategies. Here, a simple and effective approach to significantly enhance the photoluminescence is demonstrated by using a family of cation donors, which we show to be much more effective than commonly used p-dopants. We develop a detailed mechanistic picture for the action of these cation donors and demonstrate that one of them, bis(trifluoromethane)sulfonimide lithium salt (Li-TFSI), enhances the photoluminescence of both MoS2 and WS2 to a level double that of the currently best performing super-acid trifluoromethanesulfonimide (H-TFSI) treatment. In addition, the ionic salts used in our treatments are compatible with greener solvents and are easier to handle than super-acids, providing the possibility of performing treatments during device fabrication. This work sets up rational selection rules for ionic chemicals to passivate transition metal disulfides and increases their potential in practical optoelectronic applications. The low photoluminescence of monolayer transition metal disulfides remains a challenge for their optoelectronic application. Here the authors present an effective and green method to enhance the photoluminescence of monolayer MoS2 and WS2, and a detailed mechanistic picture of the treatments.

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