在可果美超导体的对称破缺表面形成和操纵二原子转子

Zihao Huang, Xianghe Han, Zhen Zhao, Haitao Yang, Hui Chen, Hong-Jun Gao
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引用次数: 0

摘要

人造分子转子和马达为功能纳米机器带来了巨大希望,但由于表面限制和有限的化学设计,构建对这些机器至关重要的二原子转子是一项挑战。在新发现的卡戈梅斯超导体 CsV3Sb5 的锑表面,一个铬原子或铁原子围绕一个铯原子旋转。旋转速率由转子和扫描隧道显微镜(STM)尖端之间的偏置电压控制。速率的空间分布呈现 C2 对称性,这可能与 CsV3Sb5 的对称破缺电荷序有关。我们已将转子结构扩展到不同的过渡金属(铬、铁、钒)和碱金属(铯、钾)。值得注意的是,转子的设计配置是通过 STM 操作实现的。我们的研究成果为在打破对称的量子材料上精确制造原子发动机建立了一个新平台,为先进的纳米级器件铺平了道路。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Formation and manipulation of diatomic rotors at the symmetry-breaking surfaces of kagome superconductors
Artificial molecular rotors and motors hold great promise for functional nanomachines, but constructing diatomic rotors, crucial for these machines, is challenging due to surface constraints and limited chemical design. Here we report the construction of diatomic Cr-Cs and Fe-Cs rotors where a Cr or Fe atom revolves around a Cs atom at the Sb surface of the newly-discovered kagome superconductor CsV3Sb5. The rotation rate is controlled by bias voltage between the rotor and scanning tunneling microscope (STM) tip. The spatial distribution of rates exhibits C2 symmetry, might linked to the symmetry-breaking charge orders of CsV3Sb5. We have expanded rotor construction to include different transition metals (Cr, Fe, V) and alkali metals (Cs, K). Remarkably, designed configurations of rotors are achieved through STM manipulation. Rotor orbits and quantum states are precisely controlled by tunning inter-rotor distance. Our findings establish a novel platform for the atomically precise fabrication of atomic motors on symmetry-breaking quantum materials, paving the way for advanced nanoscale devices.
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