4.8 Article

Growth Mechanism of Transition Metal Dichalcogenide Monolayers: The Role of Self-Seeding Fullerene Nuclei

Journal

ACS NANO
Volume 10, Issue 5, Pages 5440-5445

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acsnano.6b01705

Keywords

two-dimensional materials; chalcogenides; transition metal dichalcogenides; chemical vapor deposition; growth; inorganic fullerene

Funding

  1. National Science Foundation [DMR-1507810]
  2. Soft and Hybrid Nanotechnology Experimental (SHyNE) Resource [NSF NNCI-1542205]
  3. MRSEC program at the Materials Research Center [NSF DMR-1121262]
  4. International Institute for Nanotechnology (IIN)
  5. Keck Foundation
  6. State of Illinois, through the IIN
  7. Department of Defense (DoD) through the National Defense Science and Engineering Fellowship (NDSEG) Program
  8. Ryan Fellowship
  9. Northwestern University International Institute for Nanotechnology

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Due to their unique optoelectronic properties and potential for next generation devices, monolayer transition metal dichalcogenides (TMDs) have attracted a great deal of interest since the first observation of monolayer MoS2 a few years ago. While initially isolated in monolayer form by mechanical exfoliation, the field has evolved to more sophisticated methods capable of direct growth of large-area monolayer TMDs. Chemical vapor deposition (CVD) is the technique used most prominently throughout the literature and is based on the sulfurization of transition metal oxide precursors. CVD-grown monolayers exhibit excellent quality, and this process is widely used in studies ranging from the fundamental to the applied. However, little is known about the specifics of the nucleation and growth mechanisms occurring during the CVD process. In this study, we have investigated the nucleation centers or seeds from which monolayer TMDs typically grow. This was accomplished using aberration-corrected scanning transmission electron microscopy to analyze the structure and composition of the nuclei present in CVD-grown MoS2-MoSe2 alloys. We find that monolayer growth proceeds from nominally oxi-chalcogenide nanoparticles which act as heterogeneous nucleation sites for monolayer growth. The oxi-chalcogenide nanoparticles are typically encased in a fullerene-like shell made of the TMD. Using this information, we propose a step-by-step nucleation and growth mechanism for monolayer TMDs. Understanding this mechanism may pave the way for precise control over the synthesis of 2D materials, heterostructures, and related complexes.

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