Amin Azizi

Dislocation motion and grain boundary migration in two-dimensional tungsten disulphide

Dislocations have a significant effect on mechanical, electronic, magnetic and optical properties of crystals. For a dislocation to migrate in bulk crystals, collective and simultaneous movement of several atoms is needed. In two-dimensional crystals, in contrast, dislocations occur on the surface and can exhibit unique migration dynamics. Dislocation migration has recently been studied in graphene, but no studies have been reported on dislocation dynamics for two-dimensional transition metal dichalcogenides with unique metal-ligand bonding and a three-atom thickness. This study presents dislocation motion, glide and climb, leading to grain boundary migration in a tungsten disulphide monolayer. Direct atomic-scale imaging coupled with atomistic simulations reveals a strikingly low-energy barrier for glide, leading to significant grain boundary reconstruction in tungsten disulphide. The observed dynamics are unique and different from those reported for graphene. Through strain field mapping, we also demonstrate how dislocations introduce considerable strain along the grain boundaries and at the dislocation cores.

Freestanding van der Waals Heterostructures of Graphene and Transition Metal Dichalcogenides

Vertical stacking of two-dimensional (2D) crystals has recently attracted substantial interest due to unique properties and potential applications they can introduce. However, little is known about their microstructure because fabrication of the 2D heterostructures on a rigid substrate limits ones ability to directly study their atomic and chemical structures using electron microscopy. This study demonstrates a unique approach to create atomically thin freestanding van der Waals heterostructures-WSe2/graphene and MoS2/graphene-as ideal model systems to investigate the nucleation and growth mechanisms in heterostructures. In this study, we use transmission electron microscopy (TEM) imaging and diffraction to show epitaxial growth of the freestanding WSe2/graphene heterostructure, while no epitaxy is maintained in the MoS2/graphene heterostructure. Ultra-high-resolution aberration-corrected scanning transmission electron microscopy (STEM) shows growth of monolayer WSe2 and MoS2 triangles on graphene membranes and reveals their edge morphology and crystallinity. Photoluminescence measurements indicate a significant quenching of the photoluminescence response for the transition metal dichalcogenides on freestanding graphene, compared to those on a rigid substrate, such as sapphire and epitaxial graphene. Using a combination of (S)TEM imaging and electron diffraction analysis, this study also reveals the significant role of defects on the heterostructure growth. The direct growth technique applied here enables us to investigate the heterostructure nucleation and growth mechanisms at the atomic level without sample handling and transfer. Importantly, this approach can be utilized to study a wide spectrum of van der Waals heterostructures.

High‐Performance Polymers Sandwiched with Chemical Vapor Deposited Hexagonal Boron Nitrides as Scalable High‐Temperature Dielectric Materials

Polymer dielectrics are the preferred materials of choice for power electronics and pulsed power applications. However, their relatively low operating temperatures significantly limit their uses in harsh-environment energy storage devices, e.g., automobile and aerospace power systems. Herein, hexagonal boron nitride (h-BN) films are prepared from chemical vapor deposition (CVD) and readily transferred onto polyetherimide (PEI) films. Greatly improved performance in terms of discharged energy density and charge-discharge efficiency is achieved in the PEI sandwiched with CVD-grown h-BN films at elevated temperatures when compared to neat PEI films and other high-temperature polymer and nanocomposite dielectrics. Notably, the h-BN-coated PEI films are capable of operating with >90% charge-discharge efficiencies and delivering high energy densities, i.e., 1.2 J cm-3 , even at a temperature close to the glass transition temperature of polymer (i.e., 217 °C) where pristine PEI almost fails. Outstanding cyclability and dielectric stability over a straight 55 000 charge-discharge cycles are demonstrated in the h-BN-coated PEI at high temperatures. The work demonstrates a general and scalable pathway to enable the high-temperature capacitive energy applications of a wide range of engineering polymers and also offers an efficient method for the synthesis and transfer of 2D nanomaterials at the scale demanded for applications.

Individual Mo Dopant Atoms in WS2 Monolayers: Atomic Structure and Induced Strain

1. Department of Materials Science and Engineering, Materials Research Institute, and Center for Two Dimensional and Layered Materials, The Pennsylvania State University, University Park, USA 2. FEI Company, 5350 NE Dawson Creek Drive, Hillsboro, Oregon 97124, United States 3. Department of Physics, and Center for Two Dimensional and Layered Materials, The Pennsylvania State University, University Park, USA

Atomic-scale Observation of Grains and Grain Boundaries in Monolayers of WS 2

1 Department of Materials Science and Engineering, Materials Research Institute, and Center for Two Dimensional and Layered Materials, The Pennsylvania State University, University Park, USA 2 Department of Mechanical Engineering and Materials Science, Rice University, Houston, USA 3 National Center for Electron Microscopy, Lawrence Berkeley National Laboratory, Berkeley, USA 4 Department of Physics, Department of Chemistry, and Center for Two Dimensional and Layered Materials, The Pennsylvania State University, University Park, USA

Observation of a Quasi-ordered Structure in Monolayer W x Mo (1-x) S 2 Alloys

1. Department of Materials Science and Engineering, and Materials Research Institute, The Pennsylvania State University, University Park, USA 2. Center for Two Dimensional and Layered Materials, The Pennsylvania State University, University Park, USA 3. Department of Physics, The Pennsylvania State University, University Park, USA 4. Materials Characterization Lab, Materials Research Institute, The Pennsylvania State University, University Park, USA 5. Department of Chemistry, The Pennsylvania State University, University Park, USA