| Literature DB >> 32284598 |
Javier Taboada-Gutiérrez1,2, Gonzalo Álvarez-Pérez1,2, Jiahua Duan1,2, Weiliang Ma3, Kyle Crowley4, Iván Prieto5, Andrei Bylinkin6,7, Marta Autore7, Halyna Volkova8, Kenta Kimura9, Tsuyoshi Kimura9, M-H Berger8, Shaojuan Li10, Qiaoliang Bao3,10, Xuan P A Gao4, Ion Errea6,11,12, Alexey Y Nikitin6,13, Rainer Hillenbrand7,13, Javier Martín-Sánchez14,15, Pablo Alonso-González16,17.
Abstract
Phonon polaritons-light coupled to lattice vibrations-in polar van der Waals crystals are promising candidates for controlling the flow of energy on the nanoscale due to their strong field confinement, anisotropic propagation and ultra-long lifetime in the picosecond range1-5. However, the lack of tunability of their narrow and material-specific spectral range-the Reststrahlen band-severely limits their technological implementation. Here, we demonstrate that intercalation of Na atoms in the van der Waals semiconductor α-V2O5 enables a broad spectral shift of Reststrahlen bands, and that the phonon polaritons excited show ultra-low losses (lifetime of 4 ± 1 ps), similar to phonon polaritons in a non-intercalated crystal (lifetime of 6 ± 1 ps). We expect our intercalation method to be applicable to other van der Waals crystals, opening the door for the use of phonon polaritons in broad spectral bands in the mid-infrared domain.Year: 2020 PMID: 32284598 DOI: 10.1038/s41563-020-0665-0
Source DB: PubMed Journal: Nat Mater ISSN: 1476-1122 Impact factor: 43.841