论文标题

通过局部对称性触发石墨烯中的全球密度波不稳定性

Triggering a global density wave instability in graphene via local symmetry-breaking

论文作者

Qu, Amy C., Nigge, Pascal, Link, Stefan, Levy, Giorgio, Michiardi, Matteo, Spandar, Parsa L., Matthé, Tiffany, Schneider, Michael, Zhdanovich, Sergey, Starke, Ulrich, Gutiérrez, Christopher, Damascelli, Andrea

论文摘要

二维量子材料提供了一个强大的平台,用于研究由于其电子性质的高可调性,因此研究对称性破裂的有序相。例如,能够通过堆叠和扭曲结构通过Moiré超级晶格在石墨烯中创建新的电子带结构的能力,从而发现了几个相关和拓扑阶段。在这里,我们报告了一种替代方法,可以在毫米尺度上诱导石墨烯中的初期对称性相位。我们表明,表面充分原子的极稀释浓度($ <\!0.3 \%$)可以自组装并触发石墨烯原子晶格的崩溃成一个独特的kekulé键键密度波相,从而使碳c-c-c-c-bond对称性在全球范围内损坏。使用互补的动量分辨技术,例如角度分辨光发射光谱(ARPES)和低能电子衍射(LEED),我们直接探测了该密度波相的存在,并确认了在DIRAC点上的能量差距的打开。我们进一步表明,这种kekulé密度波相发生在各种费米表面的大小和形状上,这表明这种晶格不稳定性是由强的电子晶格相互作用驱动的。我们的结果表明,稀释的自组装吸附原子浓度为设计新型量子相的途径提供了一种有吸引力的替代途径。

Two-dimensional quantum materials offer a robust platform for investigating the emergence of symmetry-broken ordered phases owing to the high tuneability of their electronic properties. For instance, the ability to create new electronic band structures in graphene through moiré superlattices from stacked and twisted structures has led to the discovery of several correlated and topological phases. Here we report an alternative method to induce an incipient symmetry-broken phase in graphene at the millimetre scale. We show that an extremely dilute concentration ($<\!0.3\% $) of surface adatoms can self-assemble and trigger the collapse of the graphene atomic lattice into a distinct Kekulé bond density wave phase, whereby the carbon C-C bond symmetry is broken globally. Using complementary momentum-resolved techniques such as angle-resolved photoemission spectroscopy (ARPES) and low-energy electron diffraction (LEED), we directly probe the presence of this density wave phase and confirm the opening of an energy gap at the Dirac point. We further show that this Kekulé density wave phase occurs for various Fermi surface sizes and shapes, suggesting that this lattice instability is driven by strong electron-lattice interactions. Our results demonstrate that dilute concentrations of self-assembled adsorbed atoms offer an attractive alternative route towards designing novel quantum phases in two-dimensional materials.

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