Please use this identifier to cite or link to this item: https://scholarbank.nus.edu.sg/handle/10635/193451
Title: APPLICATIONS OF MULTI-MODAL ATOMIC FORCE MICROSCOPE IN 2D TRANSITION METAL DICHALCOGENIDES
Authors: WANG XINYUN
Keywords: 2D materials, multi-modal AFM, photoluminescence
Issue Date: 16-Mar-2021
Citation: WANG XINYUN (2021-03-16). APPLICATIONS OF MULTI-MODAL ATOMIC FORCE MICROSCOPE IN 2D TRANSITION METAL DICHALCOGENIDES. ScholarBank@NUS Repository.
Abstract: The multi-mode AFM has been proved to be a powerful characterization tool. The heterogenous distribution of intrinsic defects in the as-grown TMDs can be unambiguously unveiled using the Kelvin probe force microscopy (KPFM), with the findings further being corroborated by scanning transmission electron microscopy (STEM) and density functional theory (DFT) calculations. Moreover, a defect-related conductivity map of the sample is also revealed by the PeakForce tunneling atomic force microscopy (PF-TUNA). In addition to defects, the evolution of interlayer coupling strength in twisted TMDs can also be revealed by its work function variation using the KPFM, while the moiré superlattices in these twisted TMDs can be visualized with Piezoresponse force microscopy (PFM), through the flexoelectric effect from the polarized domain walls. Beyond its characterization capabilities, AFM is also demonstrated as a sophisticated manipulation tool to 2D materials. Utilizing the force between tip and sample surfaces, we can either exert a dynamic control of the orientation between the layers, or tune the interlayer coupling strength in a vdW bilayer structure. Finally, careful studies of the exciton behaviors in response to defect, strain, twisting angle and interlayer coupling, will also be illustrated in this dissertation.
URI: https://scholarbank.nus.edu.sg/handle/10635/193451
Appears in Collections:Ph.D Theses (Open)

Show full item record
Files in This Item:
File Description SizeFormatAccess SettingsVersion 
XINYUN_2021_PHD_THESIS.pdf8.49 MBAdobe PDF

OPEN

NoneView/Download

Google ScholarTM

Check


Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.