Lifshitz Transition and Band Structure Evolution in Alkali Metal Intercalated 1T′-MoTe2

IF 3.3 3区 化学 Q2 CHEMISTRY, PHYSICAL The Journal of Physical Chemistry C Pub Date : 2025-02-26 DOI:10.1021/acs.jpcc.4c07689
Joohyung Park, Ayan N. Batyrkhanov, Jonas Brandhoff, Felix Otto, Marco Gruenewald, Maximilian Schaal, Saban Hus, Torsten Fritz, Florian Göltl, An-Ping Li, Oliver L. A. Monti
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Abstract

In van der Waals materials, coupling between adjacent layers is weak, and consequently interlayer interactions are weakly screened. This opens the possibility to profoundly modify the electronic structure, e.g., by applying electric fields or with adsorbates. Here, we show for the case of the topologically trivial semimetal 1T′-MoTe2 that potassium dosing at room temperature significantly transforms its band structure. With a combination of angle-resolved photoemission spectroscopy, scanning tunneling microscopy, X-ray photoemission spectroscopy, and density functional theory we show that (i) for small concentrations of K, 1T′-MoTe2 undergoes a Lifshitz transition with the electronic structure shifting rigidly, and (ii) for larger K concentrations 1T′-MoTe2 undergoes significant band structure transformation. Our results demonstrate that the origin of this electronic structure change stems from alkali metal intercalation.

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在范德华材料中,相邻层之间的耦合很弱,因此层间相互作用的屏蔽也很弱。这就为通过施加电场或使用吸附剂等方法深刻改变电子结构提供了可能。在这里,我们以拓扑上微不足道的半金属 1T′-MoTe2 为例,说明在室温下掺入钾能显著改变其带状结构。结合角度分辨光发射光谱、扫描隧道显微镜、X 射线光发射光谱和密度泛函理论,我们证明:(i) 在钾浓度较小的情况下,1T′-MoTe2 发生了李夫希茨转变,电子结构发生了刚性移动;(ii) 在钾浓度较大的情况下,1T′-MoTe2 发生了明显的带状结构转变。我们的研究结果表明,这种电子结构变化源于碱金属插层。
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来源期刊
The Journal of Physical Chemistry C
The Journal of Physical Chemistry C 化学-材料科学:综合
CiteScore
6.50
自引率
8.10%
发文量
2047
审稿时长
1.8 months
期刊介绍: The Journal of Physical Chemistry A/B/C is devoted to reporting new and original experimental and theoretical basic research of interest to physical chemists, biophysical chemists, and chemical physicists.
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