材料科学
超导电性
剥脱关节
兴奋剂
离子
电荷密度
离子键合
相(物质)
插层(化学)
载流子
纳米尺度
纳米技术
凝聚态物理
化学物理
无机化学
光电子学
石墨烯
有机化学
物理
量子力学
化学
作者
José M. Pereira,Daniel Tezze,Iris Niehues,Yaiza Asensio,Haozhe Yang,Lars Mester,Shu Chen,Fèlix Casanova,Alexander M. Bittner,M. Ormaza,Frederik Schiller,Beatriz Martín‐García,Rainer Hillenbrand,Luis E. Hueso,Marco Gobbi
标识
DOI:10.1002/adfm.202208761
摘要
When doped into a certain range of charge carrier concentrations, MoS2 departs from its pristine semiconducting character to become a strongly correlated material characterized by exotic phenomena such as charge density waves or superconductivity. However, the required doping levels are typically achieved using ionic-liquid gating or air-sensitive alkali-ion intercalation, which are not compatible with standard device fabrication processes. Here, we report on the emergence of superconductivity and a charge density wave phase in air-stable organic cation intercalated MoS2 crystals. By selecting two different molecular guests, we show that these correlated electronic phases depend dramatically on the intercalated cation, demonstrating the potential of organic ion intercalation to finely tune the properties of 2D materials. Moreover, we find that a fully developed zero-resistance state is not reached in few-nm-thick flakes, indicating the presence of three-dimensional superconductive paths which are severed by the mechanical exfoliation. We ascribe this behavior to an inhomogeneous charge carrier distribution, which we probe at the nanoscale using scanning near-field optical microscopy. Our results establish organic-ion intercalated MoS2 as a platform to study the emergence and modulation of correlated electronic phases.
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