Álvaro Moreno, Lorenzo Cavicchi, Xia Wang, Mayra Peralta, Maia Vergniory, Kenji Watanabe, Takashi Taniguchi, Pablo Jarillo-Herrero, Claudia Felser, Marco Polini, Frank H. L. Koppens
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In this work, we propose a\nnovel approach using twisted bilayer graphene (TBG), a chiral 2D material with\na strong CD peak which energy is tunable through the twist angle. By matching\nthe CD resonance of TBG with the optical transition energy of the molecule, we\nachieve a decay rate enhancement mediated by resonant energy transfer that\ndepends on the electric-magnetic interaction, that is, on the chirality of both\nthe molecules and TBG. This leads to an enantioselective quenching of the\nmolecule fluorescence, allowing to retrieve the molecule chirality from\ntime-resolved photoluminescence measurements. 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引用次数: 0
摘要
手性分子的选择性传感是生物学、化学和药理学等领域的一个关键方面。然而,由于手性光与物质之间的相互作用较弱,圆二色性(CD)等传统光学方法受到了限制。为了增强CD或圆偏振发光(CPL),人们研究了多种策略,包括超手性光、等离子体纳米谐振器和介电纳米结构。然而,如何在空间均匀性和高灵敏度之间取得折衷,同时又不需要特定的分子功能化,仍然是一项挑战。在这项工作中,我们提出了一种使用扭曲双层石墨烯(TBG)的新方法,这种手性二维材料具有很强的 CD 峰,其能量可通过扭曲角度进行调节。通过将 TBG 的 CD 共振与分子的光学转变能相匹配,我们实现了由共振能量转移介导的衰变率增强,而这种能量转移取决于电-磁相互作用,即取决于分子和 TBG 的手性。这导致了分子荧光的对映选择性淬灭,从而可以从时间分辨光致发光测量中获取分子的手性。这种方法显示出低至单层分子的高灵敏度,有望实现单分子手性传感的最终目标,同时保持二维异质结构的空间均匀性和可集成性。
Twisted bilayer graphene for enantiomeric sensing of chiral molecules
Selective sensing of chiral molecules is a key aspect in fields spanning
biology, chemistry, and pharmacology. However, conventional optical methods,
such as circular dichroism (CD), encounter limitations owing to weak chiral
light-matter interactions. Several strategies have been investigated to enhance
CD or circularly polarised luminescence (CPL), including superchiral light,
plasmonic nanoresonators and dielectric nanostructures. However, a compromise
between spatial uniformity and high sensitivity, without requiring specific
molecular functionalization, remains a challenge. In this work, we propose a
novel approach using twisted bilayer graphene (TBG), a chiral 2D material with
a strong CD peak which energy is tunable through the twist angle. By matching
the CD resonance of TBG with the optical transition energy of the molecule, we
achieve a decay rate enhancement mediated by resonant energy transfer that
depends on the electric-magnetic interaction, that is, on the chirality of both
the molecules and TBG. This leads to an enantioselective quenching of the
molecule fluorescence, allowing to retrieve the molecule chirality from
time-resolved photoluminescence measurements. This method demonstrates high
sensitivity down to single layer of molecules, with the potential to achieve
the ultimate goal of single-molecule chirality sensing, while preserving the
spatial uniformity and integrability of 2D heterostructures.