Search Results
Graphene-Like ZnO: A Mini Review
The isolation of a single layer of graphite, known today as graphene, not only demonstrated amazing new properties but also paved the way for a new class of materials often referred to as two-dimensional (2D) materials. Beyond graphene, other 2D materials include h-BN, transition metal dichalcogenides (TMDs), silicene, and germanene, to name a few. All tend to have exciting physical and chemical properties which appear due to dimensionality effects and modulation of their band structure. A more recent member of the 2D family is graphene-like zinc oxide (g-ZnO) which also holds great promise as a future functional material. This review examines current progress in the synthesis and characterization of g-ZnO. In addition, an overview of works dealing with the properties of g-ZnO both in its pristine form and modified forms (e.g., nano-ribbon, doped material, etc.) is presented. Finally, discussions/studies on the potential applications of g-ZnO are reviewed and discussed.
Crystal structure, synthesis and characterization of different chromium-based two-dimensional compounds
The field of two dimensional (2D) materials experienced a surge of discoveries after the isolation of graphene. Among these, the transition metal compounds of Molybdenum and tungsten have been the most extensively studied materials after graphene. More recently, their group member chromium has only recently come to the limelight after the discovery of its exciting magnetic properties. As such the body of work surrounding 2D chromium-based materials is growing. Here, we present an up-to-date summary of the chromium 2D materials showing the latest advances in their experimental synthesis, characterization and the applications of 2D Chromium-based compounds. Finally, we conclude with a perspective on the future of 2D chromium-based materials. We believe that this study will be helpful to understand the field of chromium-based 2D compounds.
Graphene transfer methods: A review
Graphene is a material with unique properties that can be exploited in electronics, catalysis, energy, and bio-related fields. Although, for maximal utilization of this material, high-quality graphene is required at both the growth process and after transfer of the graphene film to the application-compatible substrate. Chemical vapor deposition (CVD) is an important method for growing high-quality graphene on non-technological substrates (as, metal substrates, e.g., copper foil). Thus, there are also considerable efforts toward the efficient and non-damaging transfer of quality of graphene on to technologically relevant materials and systems. In this review article, a range of graphene current transfer techniques are reviewed from the standpoint of their impact on contamination control and structural integrity preservation of the as-produced graphene. In addition, their scalability, cost- and time-effectiveness are discussed. We summarize with a perspective on the transfer challenges, alternative options and future developments toward graphene technology.
Rapid synthesis of pristine graphene inside a transmission electron microscope using gold as catalyst
Multiple methods with distinctive strengths and drawbacks have been devised so far to produce graphene. However, they all need post-synthesis transfer steps to characterize the product. Here we report the synthesis of pristine graphene inside the transmission electron microscope using gold as catalyst and self-removing substrate without employing a specialized specimen holder. The process occurs at room temperature and takes place within milliseconds. The method offers the possibility of precise spatial control for graphene production and immediate characterization. Briefly, the irradiating electrons generate secondary electrons leading to surface charging if the gold particles reside on a poorly conducting support. At a critical charge density, the particle ejects ions mixed with secondary electrons (plasma) causing the particle to shrink. Simultaneously, hydrocarbon contamination within the electron microscope is cracked, thus providing carbon for the growth of graphene on the particle’s surface. The Technique is potentially attractive for the manufacture of in situ graphene-based devices. © 2019, The Author(s).
Flexible Piezoresistive Polystyrene Composite Sensors Filled with Hollow 3D Graphitic Shells
The objective of this research was to develop highly effective conductive polymer composite (CPC) materials for flexible piezoresistive sensors, utilizing hollow three-dimensional graphitic shells as a highly conductive particulate component. Polystyrene (PS), a cost-effective and robust polymer widely used in various applications such as household appliances, electronics, automotive parts, packaging, and thermal insulation materials, was chosen as the polymer matrix. The hollow spherical three-dimensional graphitic shells (GS) were synthesized through chemical vapor deposition (CVD) with magnesium oxide (MgO) nanoparticles serving as a support, which was removed post-synthesis and employed as the conductive filler. Commercial multi-walled carbon nanotubes (CNTs) were used as a reference one-dimensional graphene material. The main focus of this study was to investigate the impact of the GS on the piezoresistive response of carbon/polymer composite thin films. The distribution and arrangement of GS and CNTs in the polymer matrix were analyzed using techniques such as X-ray diffraction and scanning electron microscopy, while the electrical, thermal, and mechanical properties of the composites were also evaluated. The results revealed that the PS composite films filled with GS exhibited a more pronounced piezoresistive response as compared to the CNT-based composites, despite their lower mechanical and thermal performance.
Large-Area Single-Crystal Graphene via Self-Organization at the Macroscale
In 1665 Christiaan Huygens first noticed how two pendulums, regardless of their initial state, would synchronize. It is now known that the universe is full of complex self-organizing systems, from neural networks to correlated materials. Here, graphene flakes, nucleated over a polycrystalline graphene film, synchronize during growth so as to ultimately yield a common crystal orientation at the macroscale. Strain and diffusion gradients are argued as the probable causes for the long-range cross-talk between flakes and the formation of a single-grain graphene layer. The work demonstrates that graphene synthesis can be advanced to control the nucleated crystal shape, registry, and relative alignment between graphene crystals for large area, that is, a single-crystal bilayer, and (AB-stacked) few-layer graphene can been grown at the wafer scale. © 2020 The Authors. Published by Wiley-VCH GmbH