اشترك بالحزمة الذهبية واحصل على وصول غير محدود شمرا أكاديميا
تسجيل مستخدم جديدMaterial design with the van der Waals stacking of bismuth-halide chains realizing a higher-order topological insulator
54
0
0.0
(
0
)
اسأل ChatGPT حول البحث
ﻻ يوجد ملخص باللغة العربية
The van der Waals (vdW) materials with low dimensions have been extensively studied as a platform to generate exotic quantum properties. Advancing this view, a great deal of attention is currently paid to topological quantum materials with vdW structures. Here, we provide a new concept of designing topological materials by the vdW stacking of quantum spin Hall insulators (QSHIs). Most interestingly, a slight shift of inversion center in the unit cell caused by a modification of stacking is found to induce the topological variation from a trivial insulator to a higher-order topological insulator (HOTI). Based on that, we present the first experimental realization of a HOTI by investigating a bismuth bromide Bi4Br4 with angle-resolved photoemission spectroscopy (ARPES). The unique feature in bismuth halides capable of selecting various topology only by differently stacking chains, combined with the great advantage of the vdW structure, offers a fascinating playground for engineering topologically non-trivial edge-states toward future spintronics applications.
قيم البحث
اقرأ أيضاً
Magnetic topological insulators (TI) provide an important material platform to explore quantum phenomena such as quantized anomalous Hall (QAH) effect and Majorana modes, etc. Their successful material realization is thus essential for our fundamenta
l understanding and potential technical revolutions. By realizing a bulk van der Waals material MnBi4Te7 with alternating septuple [MnBi2Te4] and quintuple [Bi2Te3] layers, we show that it is ferromagnetic in plane but antiferromagnetic along the c axis with an out-of-plane saturation field of ~ 0.22 T at 2 K. Our angle-resolved photoemission spectroscopy measurements and first-principles calculations further demonstrate that MnBi4Te7 is a Z2 antiferromagnetic TI with two types of surface states associated with the [MnBi2Te4] or [Bi2Te3] termination, respectively. Additionally, its superlattice nature may make various heterostructures of [MnBi2Te4] and [Bi2Te3] layers possible by exfoliation. Therefore, the low saturation field and the superlattice nature of MnBi4Te7 make it an ideal system to investigate rich emergent phenomena.
We propose a second version of the van der Waals density functional (vdW-DF2) of Dion et al. [Phys. Rev. Lett. 92, 246401 (2004)], employing a more accurate semilocal exchange functional and the use of a large-N asymptote gradient correction in deter
mining the vdW kernel. The predicted binding energy, equilibrium separation, and potential-energy curve shape are close to those of accurate quantum chemical calculations on 22 duplexes. We anticipate the enabling of chemically accurate calculations in sparse materials of importance for condensed-matter, surface, chemical, and biological physics.
Three-dimensional epitaxial heterostructures are based on covalently-bonded interfaces, whereas those from 2-dimensional (2D) materials exhibit van der Waals interactions. Under the right conditions, however, material structures with mixed interfacia
l van der Waals and covalent bonding may be realized. Atomically thin layers formed at the epitaxial graphene (EG)/silicon carbide (SiC) interface indicate that EG/SiC interfaces provide this unique environment and enable synthesis of a rich palette of 2D materials not accessible with traditional techniques. Here, we demonstrate a method termed confinement heteroepitaxy (CHet), to realize air-stable, structurally unique, crystalline 2D-Ga, In, and Sn at the EG/SiC interface. The first intercalant layer is covalently-bonded to the SiC, and is accompanied by a vertical bonding gradient that ends with van der Waals interactions. Such structures break out of plane centrosymmetry, thereby introducing atomically thin, non-centrosymmetric 2D allotropes of 3D materials as a foundation for tunable superconductivity, topological states, and plasmonic properties.
We demonstrate a new method of designing 2D functional magnetic topological heterostructure (HS) by exploiting the vdw heterostructure (vdw-HS) through combining 2D magnet CrI$_3$ and 2D materials (Ge/Sb) to realize new 2D topological system with non
zero Chern number (C=1) and chiral edge state. The nontrivial topology originates primarily from the CrI$_3$ layer while the non-magnetic element induces the charge transfer process and proximity enhanced spin-orbit coupling. Due to these unique properties, our topological magnetic vdw-HS overcomes the weak magnetization via proximity effect in previous designs since the magnetization and topology coexist in the same magnetic layer. Specifically, our systems of bilayer CrI$_3$/Sb and trilayer CrI$_3$/Sb/CrI$_3$ exhibit different topological ground state ranging from antiferromagnetic topological crystalline insulator (C$_M$= 2) to a QAHE. These nontrivial topological transition is shown to be switchable in a trilayer configuration due to the magnetic switching from antiferromagnetism to ferromangetism in the presence an external perpendicular electric field with value as small as 0.05 eV/A. Thus our study proposes a realistic system to design switchable magnetic topological device with electric field.
Exotic properties in single or few layers of van der Waals materials carry great promise for applications in nanoscaled electronics, optoelectronics and flexible devices. The established, distinct examples include extremely high mobility and superior
thermal conductivity in graphene, a large direct band gap in monolayer MoS2 and quantum spin Hall effect in WTe2 monolayer, etc. All these exotic properties arise from the electron quantum confinement effect in the two-dimensional limit. Here we report a novel phenomenon due to one-dimensional (1D) confinement of carriers in a layered van der Waals material NbSi0.45Te2 revealed by angle-resolved photoemission spectroscopy, i.e. directional massless Dirac fermions. The 1D behavior of the carriers is directly related to a stripe-like structural modulation with the long-range translational symmetry only along the stripe direction, as perceived by scanning tunneling microscopy experiment. The four-fold degenerated node of 1D Dirac dispersion is essential and independent on band inversion, because of the protection by nonsymmorphic symmetry of the stripe structure. Our study not only provides a playground for investigating the striking properties of the essential directional massless Dirac fermions, but also introduces a unique monomer with 1D long-range order for engineering nano-electronic devices based on heterostructures of layered van der Waals materials.
سجل دخول لتتمكن من نشر تعليقات
التعليقات
جاري جلب التعليقات
سجل دخول لتتمكن من متابعة معايير البحث التي قمت باختيارها
