اشترك بالحزمة الذهبية واحصل على وصول غير محدود شمرا أكاديميا
تسجيل مستخدم جديدIntrinsically Honeycomb-patterned Hydrogenated Graphene with Spin Polarized Edge-states
144
0
0.0
(
0
)
اسأل ChatGPT حول البحث
ﻻ يوجد ملخص باللغة العربية
Since the advent of graphene ushered the era of two-dimensional materials, many forms of hydrogenated graphene have been reported, exhibiting diverse properties ranging from a tunable band gap to ferromagnetic ordering. Patterned hydrogenated graphene with micron-scale patterns has been fabricated by lithographic means. Here we report successful millimeter-scale synthesis of an intrinsically honeycomb patterned form of hydrogenated graphene on Ru(0001) by epitaxial growth followed by hydrogenation. Combining scanning tunneling microscopy observations with density-functional-theory (DFT) calculations, we reveal that an atomic-hydrogen layer intercalates between graphene and Ru(0001). The result is a hydrogen honeycomb structure that serves as a template for the final hydrogenation, which converts the graphene into graphane only over the template, yielding honeycomb-patterned hydrogenated graphene (HPHG). In effect, HPHG is a form of patterned graphane. DFT calculations find that the unhydrogenated graphene regions embedded in the patterned graphane exhibit spin-polarized edge states. This type of growth mechanism provides new pathways for the fabrication of intrinsically patterned graphene-based materials.
قيم البحث
اقرأ أيضاً
Graphene is an emerging class of two-dimensional (2D) material with unique electrical properties and a wide range of potential practical applications. In addition, graphene hybrid structures combined with other 2D materials, metal microstructures, si
licon photonic crystal cavities, and waveguides have more extensive applications in van der Waals heterostructures, hybrid graphene plasmonics, hybrid optoelectronic devices, and optical modulators. Based on well-developed transfer methods, graphene grown by chemical vapor deposition (CVD) is currently used in most of the graphene hybrid applications. Although mechanical exfoliation of highly oriented pyrolytic graphite provides the highest-quality graphene, the transfer of the desired microcleaving graphene (MG) to the structure at a specific position is a critical challenge, that limits the combination of MG with other structures. Herein, we report a new technique for the selective transfer of MG patterns and devices onto chosen targets using a bilayer-polymer structure and femtosecond laser microfabrication. This selective transfer technique, which exactly transfers the patterned graphene onto a chosen target, leaving the other flakes on the original substrate, provides an efficient route for the fabrication of MG-based microdevices. This method will facilitate the preparation of van der Waals heterostructures and enable the optimization of the performance of graphene hybrid devices.
The experimental study of edge states in atomically-thin layered materials remains a challenge due to the difficult control of the geometry of the sample terminations, the stability of dangling bonds and the need to measure local properties. In the c
ase of graphene, localised edge modes have been predicted in zig-zag and bearded edges, characterised by flat dispersions connecting the Dirac points. Polaritons in semiconductor microcavities have recently emerged as an extraordinary photonic platform to emulate 1D and 2D Hamiltonians, allowing the direct visualization of the wavefunctions in both real- and momentum-space as well as of the energy dispersion of eigenstates via photoluminescence experiments. Here we report on the observation of edge states in a honeycomb lattice of coupled micropillars. The lowest two bands of this structure arise from the coupling of the lowest energy modes of the micropillars, and emulate the {pi} and {pi}* bands of graphene. We show the momentum space dispersion of the edge states associated to the zig-zag and bearded edges, holding unidimensional quasi-flat bands. Additionally, we evaluate polarisation effects characteristic of polaritons on the properties of these states.
The intriguing properties, especially Dirac physics in graphene, have inspired the pursuit of two-dimensional materials in honeycomb structure. Here we achieved a monolayer transition metal monochalcogenide AgTe on Ag(111) by tellurization of the sub
strate. High-resolution scanning tunneling microscopy, combined with low-energy electron diffraction, angle-resolved photoemission spectroscopy, and density functional theory calculations, demonstrates the planar honeycomb structure of AgTe. The first principle calculations further reveal that, protected by the in-plane mirror reflection symmetry, two Dirac node-line Fermions exist in the electronic structures of free-standing AgTe when spin-orbit coupling (SOC) is ignored. While in fact the SOC leads to the gap opening, and resulting in the emergence of the topologically nontrivial quantum spin Hall edge state. Importantly, our experiments evidence the chemical stability of the monolayer AgTe in ambient conditions. It is possible to study AgTe by more ex-situ measurements and even to apply it in novel electronic devices.
The electronic properties of hydrogenated graphenes are investigated with the first-principles calculations. Geometric structures, energy bands, charge distributions, and density of states (DOS) strongly depend on the different configurations and con
centrations of hydrogen adatoms. Among three types of optimized periodical configurations, only in the zigzag systems the band gaps can be remarkably modulated by H-concentrations. There exist middle-gap semiconductors, narrow-gap semiconductors, and gapless systems. The band structures exhibit the rich features, including the destruction or recovery of the Dirac-cone structure, newly formed critical points, weakly dispersive bands, and (C,H)-related partially flat bands. The orbital-projected DOS are evidenced by the low-energy prominent peaks, delta-function-like peaks, discontinuous shoulders, and logarithmically divergent peaks. The DOS and spatial charge distributions clearly indicate that the critical bondings in C-C and C-H is responsible for the diversified properties.
An edge state is a time-harmonic solution of a conservative wave system, e.g. Schroedinger, Maxwell, which is propagating (plane-wave-like) parallel to, and localized transverse to, a line-defect or edge. Topologically protected edge states are edge
states which are stable against spatially localized (even strong) deformations of the edge. First studied in the context of the quantum Hall effect, protected edge states have attracted huge interest due to their role in the field of topological insulators. Theoretical understanding of topological protection has mainly come from discrete (tight-binding) models and direct numerical simulation. In this paper we consider a rich family of continuum PDE models for which we rigorously study regimes where topologically protected edge states exist. Our model is a class of Schroedinger operators on $mathbb{R}^2$ with a background 2D honeycomb potential perturbed by an edge-potential. The edge potential is a domain-wall interpolation, transverse to a prescribed rational edge, between two distinct periodic structures. General conditions are given for the bifurcation of a branch of topologically protected edge states from Dirac points of the background honeycomb structure. The bifurcation is seeded by the zero mode of a 1D effective Dirac operator. A key condition is a spectral no-fold condition for the prescribed edge. We then use this result to prove the existence of topologically protected edge states along zigzag edges of certain honeycomb structures. Our results are consistent with the physics literature and appear to be the first rigorous results on the existence of topologically protected edge states for continuum 2D PDE systems describing waves in a non-trivial periodic medium. We also show that the family of Hamiltonians we study contains cases where zigzag edge states exist, but which are not topologically protected.
سجل دخول لتتمكن من نشر تعليقات
التعليقات
جاري جلب التعليقات
سجل دخول لتتمكن من متابعة معايير البحث التي قمت باختيارها
