范德瓦尔斯力
各向异性
光电发射光谱学
凝聚态物理
电子结构
点反射
单层
材料科学
角分辨光电子能谱
超晶格
光谱学
密度泛函理论
过渡金属
化学
分子物理学
X射线光电子能谱
物理
计算化学
核磁共振
纳米技术
光学
分子
量子力学
催化作用
有机化学
生物化学
作者
Lewis S. Hart,James L. Webb,Sara E. C. Dale,S. J. Bending,Marcin Mucha-Kruczyński,D. Wolverson,Chaoyu Chen,J. Ávila,M. C. Asensio
标识
DOI:10.1038/s41598-017-05361-6
摘要
ReSe2 and ReS2 are unusual compounds amongst the layered transition metal dichalcogenides as a result of their low symmetry, with a characteristic in-plane anisotropy due to in-plane rhenium chains. They preserve inversion symmetry independent of the number of layers and, in contrast to more well-known transition metal dichalcogenides, bulk and few-monolayer Re-TMD compounds have been proposed to behave as electronically and vibrational decoupled layers. Here, we probe for the first time the electronic band structure of bulk ReSe2 by direct nanoscale angle-resolved photoemission spectroscopy. We find a highly anisotropic in- and out-of-plane electronic structure, with the valence band maxima located away from any particular high-symmetry direction. The effective mass doubles its value perpendicular to the Re chains and the interlayer van der Waals coupling generates significant electronic dispersion normal to the layers. Our density functional theory calculations, including spin-orbit effects, are in excellent agreement with these experimental findings.
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