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Get Free AccessGraphene is a privileged 2D platform for hosting confined light-matter excitations known as surface plasmon-polaritons (SPPs), as it possesses low intrinsic losses with a high degree of optical confinement. However, the inherently isotropic optical properties of graphene limit its ability to guide and focus SPPs, making it less suitable than anisotropic elliptical and hyperbolic materials as a platform for polaritonic lensing and canalization. Here, we present the graphene/CrSBr heterostructure as an engineered 2D interface that hosts highly anisotropic SPP propagation over a wide range of frequencies in the mid-infrared and terahertz. Using a combination of scanning tunneling microscopy (STM), scattering-type scanning near-field optical microscopy (s-SNOM), and first-principles calculations, we demonstrate mutual doping in excess of 10$^{13}$ cm$^{-2}$ holes/electrons between the interfacial layers of graphene/CrSBr heterostructures. SPPs in graphene activated by charge transfer interact with charge-induced anisotropic intra- and interband transitions in the interfacial doped CrSBr, leading to preferential SPP propagation along the quasi-1D chains that compose each CrSBr layer. This multifaceted proximity effect both creates SPPs and endows them with anisotropic transport and propagation lengths that differ by an order-of-magnitude between the two in-plane crystallographic axes of CrSBr.
Daniel J. Rizzo, Eric Seewald, Fangzhou Zhao, Jordan M. Cox, Kaichen Xie, Rocco A. Vitalone, Francesco L. Ruta, Daniel G. Chica, Yinming Shao, Sara Shabani, Evan J. Telford, Matthew Strasbourg, Thomas P. Darlington, Suheng Xu, Siyuan Qiu, Aravind Devarakonda, Takashi Taniguchi, Kenji Watanabe, Xiaoyang Zhu, P. James Schuck, Cory R. Dean, Xavier Roy, Andrew J. Millis, Ting Cao, Ángel Rubio, Abhay N. Pasupathy, D. N. Basov (2024). Uniaxial plasmon polaritons $\textit{via}$ charge transfer at the graphene/CrSBr interface. , DOI: https://doi.org/10.48550/arxiv.2407.07178.
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Type
Preprint
Year
2024
Authors
27
Datasets
0
Total Files
0
Language
en
DOI
https://doi.org/10.48550/arxiv.2407.07178
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