4.6 Article

Ultra-low power threshold for laser induced changes in optical properties of 2D molybdenum dichalcogenides

期刊

2D MATERIALS
卷 3, 期 4, 页码 -

出版社

IOP PUBLISHING LTD
DOI: 10.1088/2053-1583/3/4/045008

关键词

MoS2; MoSe2; photoluminescence; optical properties; doping

资金

  1. ANR MoS2ValleyControl
  2. ERC [306719]
  3. ITN SpinNANO
  4. grant NEXT [ANR-10-LABX-0037]
  5. Elemental Strategy Initiative
  6. JSPS
  7. National Science Foundation [DMR-1552220]
  8. INSA Toulouse
  9. European Research Council (ERC) [306719] Funding Source: European Research Council (ERC)
  10. Direct For Mathematical & Physical Scien
  11. Division Of Materials Research [1552220] Funding Source: National Science Foundation

向作者/读者索取更多资源

The optical response of traditional semiconductors depends on the laser excitation power used in experiments. For two-dimensional (2D) semiconductors, laser excitation effects are anticipated to be vastly different due to complexity added by their ultimate thinness, high surface to volume ratio, and laser-membrane interaction effects. Weshow in this article that under laser excitation the optical properties of 2D materials undergo irreversible changes in vacuum. Most surprisingly these effects take place even at low steady state excitation, which is commonly thought to be non-intrusive. In low temperature photoluminescence (PL) we show for monolayer (ML) MoSe2 samples grown by different techniques that laser treatment increases significantly the trion (i.e. charged exciton) contribution to the emission compared to the neutral exciton emission. Comparison between samples exfoliated onto different substrates shows that laser induced doping is more efficient for ML MoSe2 on SiO2/Si compared to h-BN and gold. For ML MoS2 we show that exposure to laser radiation with an average power in the mu W mu m(-2) range does not just increase the trion-to-exciton PL emission ratio, but may result in the irreversible disappearance of the neutral exciton PL emission and a shift of the main PL peak to lower energy.

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