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铯嵌入/脱嵌诱导的单层TaS在Au(111)上的超结构、适配及旋转

Superstructures, Commensurations, and Rotation of Single-Layer TaS on Au(111) Induced by Cs Intercalation/Deintercalation.

作者信息

Weng Xiaorong, David Philippe, Guisset Valérie, Martinelli Lucio, Geaymond Olivier, Coraux Johann, Renaud Gilles

机构信息

Université Grenoble Alpes, CEA, IRIG/MEM/NRS, 38000 Grenoble, France.

Université Grenoble Alpes, CNRS, Institut NEEL, 38000 Grenoble, France.

出版信息

ACS Nano. 2023 Mar 28;17(6):5459-5471. doi: 10.1021/acsnano.2c10655. Epub 2023 Mar 13.

DOI:10.1021/acsnano.2c10655
PMID:36912862
Abstract

We use synchrotron grazing incidence X-ray diffraction and X-ray reflectivity to investigate with high resolution the structure of a two-dimensional single layer of tantalum sulfide grown on a Au(111) surface and its evolution during intercalation by Cs atoms and deintercalation, which decouples and recouples the two materials, respectively. The grown single layer consists of a mixture of TaS and its S-depleted version, TaS, both aligned with gold, and forming moirés where 7 (respectively 13) lattice constants of the 2D layer almost perfectly match 8 (respectively 15) substrate lattice constants. Intercalation fully decouples the system by lifting the single layer by ∼370 pm and induces an increase of its lattice parameter by 1-2 picometers. The system gradually evolves, during cycles of intercalation/deintercalation assisted by an HS atmosphere, toward a final coupled state consisting of the fully stoichiometric TaS dichalcogenide whose moiré is found very close to the 7/8 commensurability. The reactive HS atmosphere appears necessary to achieve full deintercalation, presumably by preventing S depletion and the concomitant strong bonding with the intercalant. The structural quality of the layer improves during the cyclic treatment. In parallel, because they are decoupled from the substrate by the intercalation of cesium, some of the TaS flakes rotate by 30°. These produce two additional superlattices with characteristic diffraction patterns of different origins. The first is aligned with gold's high symmetry crystallographic directions and is a commensurate moiré ((6 × 6)-Au(111) coinciding with (3√3 × 3√3)R30°-TaS). The second is incommensurate and corresponds to a near coincidence of (6 × 6) unit cells of 30°-rotated TaS with (4√3 × 4√3)Au(111) surface ones. This structure, which is less coupled to gold, might be related to the ∼(3× 3) charge density wave previously reported even at room temperature in TaS grown on noninteracting substrates. A (3 × 3) superstructure of 30°-rotated TaS islands is indeed revealed by complementary scanning tunneling microscopy.

摘要

我们使用同步辐射掠入射X射线衍射和X射线反射率,以高分辨率研究生长在Au(111)表面的二维单层硫化钽的结构,以及其在铯原子嵌入和脱嵌过程中的演变,这两个过程分别使两种材料解耦和重新耦合。生长的单层由TaS及其硫贫化版本TaS的混合物组成,两者都与金对齐,并形成莫尔条纹,其中二维层的7个(分别为13个)晶格常数几乎完美匹配8个(分别为15个)衬底晶格常数。嵌入通过将单层提升约370皮米使系统完全解耦,并使其晶格参数增加1 - 2皮米。在由HS气氛辅助的嵌入/脱嵌循环过程中,系统逐渐演变为最终的耦合状态,即由完全化学计量的TaS二硫属化物组成,其莫尔条纹非常接近7/8的可公度性。反应性HS气氛似乎是实现完全脱嵌所必需的,大概是通过防止硫耗尽以及与嵌入剂的伴随强键合。在循环处理过程中,层的结构质量得到改善。同时,由于通过铯的嵌入它们与衬底解耦,一些TaS薄片旋转了30°。这些产生了另外两个具有不同起源特征衍射图案的超晶格。第一个与金的高对称晶体学方向对齐,是一个可公度的莫尔条纹((6×6)-Au(111)与(3√3×3√3)R30°-TaS重合)。第二个是不可公度的,对应于30°旋转的TaS的(6×6)晶胞与(4√3×4√3)Au(111)表面晶胞的近乎重合。这种与金耦合较弱的结构,可能与先前报道的即使在室温下生长在非相互作用衬底上的TaS中约(3×3)电荷密度波有关。互补的扫描隧道显微镜确实揭示了30°旋转的TaS岛的(3×3)超结构。

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