4.8 Article

Surface Properties of Laser-Treated Molybdenum Disulfide Nanosheets for Optoelectronic Applications

期刊

ACS APPLIED MATERIALS & INTERFACES
卷 10, 期 21, 页码 18104-18112

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acsami.8b04717

关键词

molybdenum disulfide; X-ray photoelectron spectroscopy; confocal Raman spectroscopy; atomic force microscopy; nanoparticles; laser irradiation

资金

  1. Arab-American Frontiers fellowship from the National Academies of Sciences, Engineering, and Medicine
  2. National Science Foundation (NSF) [1542224]
  3. King Abdulaziz City for Science and Technology (KACST) through the Center of Excellence for Green Nanotechnologies (CEGN) part of the joint centers of excellence program
  4. National Research Foundation of Korea (NRF)
  5. Ministry of Science, ICT, and Future Planning [NRF-2017R1A2B4009651]
  6. National Institute of Standards and Technology

向作者/读者索取更多资源

Transition metal dichalcogenide two-dimensional materials have attracted significant attention due to their unique optical, mechanical, and electronic properties. For example, molybdenum disulfide (MoS2) exhibits a tunable band gap that strongly depends on the numbers of layers, which makes it an attractive material for optoelectronic applications. In addition, recent reports have shown that laser thinning can be used to engineer an MoS2 monolayer with specific shapes and dimensions. Here, we study laser thinned MoS2 in both ambient and vacuum conditions via confocal mu-Raman spectroscopy, imaging X-ray photoelectron spectroscopy (i-XPS), and atomic force microscopy (AFM). For low laser powers in ambient environments, there is insufficient energy to oxidize MoS, which leads to etching and redeposition of amorphous MoS2 on the nanosheet as confirmed by AFM. At high powers in ambient, the laser energy and oxygen environment enable both MoS2 nanoparticle formation and nanosheet oxidation as revealed in AFM and i-XPS. At comparable laser power densities in vacuum, MoS2 oxidation is suppressed and the particle density is reduced as compared to ambient. The extent of nanoparticle formation and nanosheet oxidation in each of these regimes is found to be dependent on the number of layers and laser treatment time. Our results can shed some light on the underlying mechanism of which atomically thin MoS2 nanosheets exhibit under high incident laser power for future optoelectronic applications.

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