从“魔角”石墨烯到摩尔超晶格量子模拟器

自从魔角石墨烯在实验上被证实以来,转角摩尔超晶格体系中存在的关联绝缘态和超导态吸引了大批科学家的目光,并发展出了一门新的科学分支—转角电子学.本文主要综述了最近转角摩尔超晶格体系在实验上的发展,包括转角双层石墨烯(TBG)、转角双层-双层石墨烯(TDBG)以及其他二维摩尔超晶格体系,并简单介绍了摩尔超晶格量子模拟器的概念.其中实验里浮现的关联绝缘态、超导态、以及铁磁态几乎囊括了近代凝聚态物理的几大热门话题,同时,逐步发展的二维摩尔超晶格量子模拟器研究也似乎有可能为强关联量子多体体系寻找一个突破口.     

超冷~(87)Rb原子在二维光晶格中Mott绝缘态的实验实现

超冷原子气体的量子相变是研究量子关联多体物理的核心内容之一.本文采用单一激光光束通过折叠反射产生二维光晶格,通过控制激光偏振产生两种不同的二维光晶格结构,一种是两个独立的一维光晶格构成,另一种是两个方向的一维光晶格互相干涉形成.将超冷~(87)Rb原子装载到二维光晶格中,通过改变光晶格激光功率调控原子在光晶格中的隧穿强度和相互作用强度,观察到~(87)Rb原子从超流态到Mott绝缘态之间的量子相变,并且分析了两种光晶格对量子相变的影响,为今后开展光晶格中强关联物理研究奠定基础.     

一维有限超晶格的电子态与透射问题的转移矩阵方法研究

采用转移矩阵方法,研究了一维有限超晶格的电子态与透射问题.计算了一维有限超晶格含单个缺陷层或少量缺陷层的透射谱和波函数,以及当电子被束缚在一维有限超晶格中电子的本征值和相应的定态本征函数.给出的方法对于研究电子通过任意排列的一维有限超晶格的输运具有普适性.     

二维范德瓦耳斯半导体莫尔超晶格实验研究进展

在二维范德瓦耳斯材料中,可以通过转角及晶格失配构造周期性的莫尔超晶格.自从实验上在“魔角”石墨烯系统中观察到关联绝缘体态和超导电性以来,利用各种二维范德瓦耳斯材料构造莫尔超晶格并研究其中的新奇量子物态成为了凝聚态物理研究的热点和前沿问题.本文主要综述了最近几年在二维半导体过渡金属硫族化合物莫尔超晶格系统中的相关实验进展.在该系统中实现电子“平带”不依赖于特定魔角,实验上,一系列的关联电子物态和拓扑电子物态被相继发现和证实.进一步的理论和实验研究有望在该系统中揭示更多的受电子关联作用和拓扑物理共同支配的新奇量子物态.     

石墨烯纳米网电导特性的能带机理：第一原理计算

通过第一原理电子结构计算来研究有序多孔纳米网的电导特性变化的能带机理.能带结构分析结果表明:石墨烯纳米网超晶格(3m,3n)(m和n为整数)的电子本征态在布里渊区中心点发生四重简并;碳空位孔洞规则排列形成的石墨烯纳米网具有由简并态分裂形成的宽度可调带隙,无论石墨烯的两个子晶格是否对等.在具有磁性网孔阵列的石墨烯纳米网中,反铁磁耦合使对称子晶格的反演对称性增加了一项量子限制条件,导致能带结构在K点的二重简并态分裂成带隙.通过控制网孔密度能够有效调节石墨烯纳米网的带隙宽度,为实现新一代石墨烯纳米电子器件提供了理论依据.     

首次实现莫尔量子点阵列与微腔光子的强耦合

正"魔角"石墨烯在电子能态调控上不断给人们带来惊喜,开辟了凝聚态物理研究的新篇章。类似的,将两种单层过渡金属硫族化合物(TMDCs)叠加起来,也可以在面内形成纳米尺度的半导体超晶格结构,称为莫尔超晶格。莫尔超晶格可以调控激子的能级,并且晶格周期可由转角连续调控,提供了在纳米尺度内调控实物粒子量子态的平台。     

石墨烯莫尔超晶格

石墨烯莫尔超晶格来源于六方氮化硼衬底对石墨烯的二维周期势调控. 由于这种外加的周期势对石墨烯能带具有显著的调制作用, 近年来引发了人们广泛的关注. 利用氮化硼衬底上外延的单晶石墨烯薄膜, 我们系统研究了基底调制下的莫尔超晶格以及相关的物理特性. 首先, 我们在电子端和空穴端都观测到了超晶格狄拉克点, 并且超晶格狄拉克点同本征狄拉克点类似, 都表现出绝缘体的特性. 在低温强磁场下, 可以观测到到单层石墨烯和双层石墨烯的量子霍尔效应. 并且, 从朗道扇形图中, 可以清晰的看到磁场下形成的超晶格朗道能级. 此外, 利用红外光谱的方法研究了强磁场下石墨烯超晶格体系不同朗道能级之间的跃迁, 发现这种跃迁满足有质量狄拉克费米子的行为, 对应38 meV的本征能隙. 在此基础上, 我们在380 meV位置发现一个同超晶格能量对应的光电导峰. 通过利用旋量势中三个不同的势分量对光电导峰进行拟合, 发现赝自旋杂化势起主导作用. 进一步研究表明赝自旋杂化势强度随载流子浓度的增大显著降低, 表明电子-电子相互作用引起的旋量势的重构.     

石墨烯形核初期Cu(111)面上CxHy团簇生成的理论研究

采用基于密度泛函理论的第一原理计算方法,我们研究了Cu(111)表面上石墨烯成核生长过程中CxHy小团簇的吸附和生成行为. 计算结果表明：随着氢原子饱和度、氢原子个数的增大,CxHy团簇的形成能减小,碳原子与铜表面的平均距离增加,C-C键的平均键长呈增大趋势. 然而,当生成的CxHy团簇具有空间对称结构时,在一定程度上打破了上述规律性. 令人惊奇的是,形成的C3H4和C3H5对称团簇具有类似石墨烯的空间结构,这类结构可能在石墨烯的形成过程中起着重要的作用.     

石墨烯形核初期Cu(111)面上C_xH_y团簇生成的理论研究

采用基于密度泛函理论的第一原理计算方法,我们研究了Cu(111)表面上石墨烯成核生长过程中CxHy小团簇的吸附和生成行为.计算结果表明:随着氢原子饱和度、氢原子个数的增大,CxHy团簇的形成能减小,碳原子与铜表面的平均距离增加,C-C键的平均键长呈增大趋势.然而,当生成的CxHy团簇具有空间对称结构时,在一定程度上打破了上述规律性.令人惊奇的是,形成的C3H4和C3H5对称团簇具有类似石墨烯的空间结构,这类结构可能在石墨烯的形成过程中起着重要的作用.     

超晶格和层状结构传热特性的连续模型及其在能源材料设计中的应用

层状材料和超晶格结构为提高热电材料和隔热涂层提供了新的设计思路, 并成为最近的研究热点. 应用连续波动方程和线性阻尼理论, 本文研究了此类材料中的声子输运特性. 给出了在整个相空间里的界面调制和声子局域化效应, 得出了超晶格材料热导率的上极限和下极限; 同时, 分析表明界面锐化加强了声子带隙, 使得部分模态的声子局域化加强. 最后, 通过对石墨烯/氮化硼超晶格(G/hBN)和硅/锗超晶格的分子模拟(Si/Ge), 验证了该理论模型. 该方法适用于所有的层状材料和超晶格结构, 对此类新能源材料的设计提供了普适的设计思路.     

Charge-transfer-induced cesium superlattices on graphene

We investigate cesium (Cs) adsorption on graphene formed on a 6H-SiC(0001) substrate by a combined scanning tunneling microscopy and density functional theory study. Individual Cs atoms adsorb preferentially at the rim region of the well-defined 6×6 substrate superstructure and on multilayer graphene. By finely controlling the graphene thickness and Cs coverages (1/3 ML and 1?ML), we here demonstrate two intriguing and well-ordered Cs superlattices on bilayer and multilayer graphene (<6 layers). Statistical analysis of the Cs-Cs interatomic distance reveals a hitherto unobserved Cs-Cs long-range electrostatic potential caused by charge transfer from Cs to graphene, which couples with the inhomogeneous substrate potential to stabilize the observed Cs superlattices. The present study provides a new avenue to fabricate atomic and molecular superlattices for applications in high-density recording and data storage.     

Mode selective control of flow turbulence

We study spin transport in normal/ferromagnetic/normal/ferromagnetic.../normal graphene superlattices, which can be realized by putting a series of magnetic insulator bars on top of a graphene sheet. Owing to magnetic proximity effect, local exchange splittings will be induced in the graphene sheet, effectively forming a magnetic graphene superlattice. The spin polarization of tunneling conductance and the magneto resistance (MR) exhibit oscillatory behavior with the gate voltage. The superlattice structure leads to an enhanced spin polarization and MR ratio, making the magnetic graphene superlattice become very promising in spintronics applications.     

On the correction of errors in quantum cryptography systems

The Raman and photoluminescence spectra of short-period C/SiC superlattices produced by RF magnetron sputtering are investigated. The Raman data indicate that, in 35-period Sitall/Ni/[C/SiC] superlattices with the C and SiC effective thicknesses of 3.5 and 3 Å, respectively, subjected to postgrowth avalanche annealing, the carbon layers assume the structure of multilayer graphene with 3–5 graphene sheets per superlattice period. A method for the fabrication of graphene-like carbon structures on the basis of short-period superlattices grown by RF sputtering is suggested and implemented.     

Band structures of bilayer graphene superlattices

We formulate a low energy effective Hamiltonian to study superlattices in bilayer graphene (BLG) using a minimal model which supports quadratic band touching points. We show that a one dimensional (1D) periodic modulation of the chemical potential or the electric field perpendicular to the layers leads to the generation of zero-energy anisotropic massless Dirac fermions and finite energy Dirac points with tunable velocities. The electric field superlattice maps onto a coupled chain model comprised of "topological" edge modes. 2D superlattice modulations are shown to lead to gaps on the mini-Brillouin zone boundary but do not, for certain symmetries, gap out the quadratic band touching point. Such potential variations, induced by impurities and rippling in biased BLG, could lead to subgap modes which are argued to be relevant to understanding transport measurements.     

Engineering the electronic structure of graphene superlattices via Fermi velocity modulation

Graphene superlattices have attracted much research interest in the last years, since it is possible to manipulate the electronic properties of graphene in these structures. It has been verified that extra Dirac points appear in the electronic structure of the system. The electronic structure in the vicinity of these points has been studied for a gapless and gapped graphene superlattice and for a graphene superlattice with a spatially modulated energy gap. In each case a different behavior was obtained. In this work we show that via Fermi velocity engineering it is possible to tune the electronic properties of a graphene superlattice to match all the previous cases studied. We also obtained new features of the system never observed before, reveling that the electronic structure of graphene is very sensitive to the modulation of the Fermi velocity. The results obtained here are relevant for the development of novel graphene-based electronic devices.     

磁性硅烯超晶格中电场调制的谷极化和自旋极化

研究了基于硅烯的静电势超晶格、铁磁超晶格、反铁磁超晶格中谷极化、自旋极化以及赝自旋极化的输运性质,分析了铁磁交换场、反铁磁交换场以及化学势对输运性质的影响,讨论了电场对谷极化、自旋极化以及赝自旋极化的调控作用.结果表明:当3种超晶格的晶格数达到10以上时,在硅烯超晶格中很容易实现100%的谷极化、自旋极化和赝自旋极化,而且通过调节超晶格上的外加电场可以使极化方向发生翻转,从而在硅烯超晶格中实现外电场对谷自由度、自旋自由度以及赝自旋自由度的操控.     

Formation of graphene on Ru（0001） surface

We report on the formation of a graphene monolayer on a Ru(0001) surface by annealing the Ru(0001) crystal. The samples are characterized by scanning tunnelling microscopy (STM) and Auger electron spectroscopy (AES). STM images show that the Moir\'{e} pattern is caused by the graphene layer mismatched with the underlying Ru(0001) surface and has an $N\times N$ superlattice. It is further found that the graphene monolayer on a Ru(0001) surface is very stable at high temperatures. Our results provide a simple and convenient method to produce a graphene monolayer on the Ru(0001) surface, which is used as a template for fabricating functional nanostructures needed in future nano devices and catalysis.     

Superlattices consisting of “lines” of adsorbed hydrogen atom pairs on graphene

The structures and electron properties of new superlattices formed on graphene by adsorbed hydrogen molecules are theoretically described. It has been shown that superlattices of the (n, 0) zigzag type with linearly arranged pairs of H atoms have band structures similar to the spectra of (n, 0) carbon nanotubes. At the same time, superlattices of the (n, n) type with a “staircase” of adsorbed pairs of H atoms are substantially metallic with a high density of electronic states at the Fermi level and this property distinguishes their spectra from the spectra of the corresponding (n, n) nanotubes. The features of the spectra have the Van Hove form, which is characteristic of each individual superlattice. The possibility of using such planar structures with nanometer thickness is discussed.     

Delocalization of phonon-plasmon modes in GaAs/AlAs superlattices with tunnel-thin AlAs barriers

The technique of Raman spectroscopy has been used to investigate doped (n-type) and undoped GaAs/AlAs superlattices with AlAs barrier thicknesses from 17 to 1 monolayers. The peak corresponding to the scattering by a two-dimensional plasmon was found in the Raman spectrum of a doped superlattice with relatively thick barriers. The position of the experimental peak corresponded to the value calculated in the model of plasma oscillations in periodic planes of a two-dimensional electron gas. The electron tunneling effects played an increasingly prominent role as the AlAs barrier thickness decreased. The peaks corresponding to the scattering by coupled phonons with three-dimensional plasmons were found in the Raman spectra for a superlattice with an AlAs thickness of 2 monolayers; i.e., the delocalization of coupled modes was observed. In this case, the folding of acoustic phonons was observed in the superlattice under consideration, indicative of its good periodicity, while the localization of optical phonons in GaAs layers was observed in undoped superlattices with an AlAs thickness of 2 monolayers.     

Highly anisotropic Dirac cones in epitaxial graphene modulated by an island superlattice

We present a new method to engineer the charge carrier mobility and its directional asymmetry in epitaxial graphene by using metal cluster superlattices self-assembled onto the moiré pattern formed by graphene on Ir(111). Angle-resolved photoemission spectroscopy reveals threefold symmetry in the band structure associated with strong renormalization of the electron group velocity close to the Dirac point giving rise to highly anisotropic Dirac cones. We further find that the cluster superlattice also affects the spectral-weight distribution of the carbon bands as well as the electronic gaps between graphene states.