No Arabic abstract
Nonlinear light sources are central to a myriad of applications, driving a quest for their miniaturisation down to the nanoscale. In this quest, nonlinear metasurfaces hold a great promise, as they enhance nonlinear effects through their resonant photonic environment and high refractive index, such as in high-index dielectric metasurfaces. However, despite the sub-diffractive operation of dielectric metasurfaces at the fundamental wave, this condition is not fulfilled for the nonlinearly generated harmonic waves, thereby all nonlinear metasurfaces to date emit multiple diffractive beams. Here, we demonstrate the enhanced single-beam second- and third-harmonic generation in a metasurface of crystalline transition-metal-dichalcogenide material, offering the highest refractive index. We show that the interplay between the resonances of the metasurface allows for tuning of the unidirectional second-harmonic radiation in forward or backward direction, not possible in any bulk nonlinear crystal. Our results open new opportunities for metasurface-based nonlinear light-sources, including nonlinear mirrors and entangled-photon generation.
We introduce the concept of nonlinear graphene metasurfaces employing the controllable interaction between a graphene layer and a planar metamaterial. Such hybrid metasurfaces support two types of subradiant resonant modes, asymmetric modes of structured metamaterial elements (metamolecules) and graphene plasmons exhibiting strong mutual coupling and avoided dispersion crossing. High tunability of graphene plasmons facilitates strong interaction between the subradiant modes, modifying the spectral position and lifetime of the associated Fano resonances. We demonstrate that strong resonant interaction, combined with the subwavelength localization of plasmons, leads to the enhanced nonlinear response and high efficiency of the second-harmonic generation.
Van der Waals epitaxy on the surface of two-dimensional (2D) layered crystals has gained significant research interest for the assembly of well-ordered nanostructures and fabrication of vertical heterostructures based on 2D crystals. Although van der Waals epitaxial assembly on the hexagonal phase of transition metal dichalcogenides (TMDCs) has been relatively well characterized, a comparable study on the distorted octahedral phase (1T or Td) of TMDCs is largely lacking. Here we investigate the assembly behavior of one-dimensional (1D) AgCN microwires on various distorted TMDC crystals, namely 1T-MoTe2, Td-WTe2, and 1T-ReS2. The unidirectional alignment of AgCN chains is observed on these crystals, reflecting the symmetry of underlying distorted TMDCs. Polarized Raman spectroscopy and transmission electron microscopy directly confirm that AgCN chains display the remarkable alignment behavior along the distorted chain directions of underlying TMDCs. The observed unidirectional assembly behavior can be attributed to the favorable adsorption configurations of 1D chains along the substrate distortion, which is supported by our theoretical calculations and observation of similar assembly behavior from different cyanide chains. The aligned AgCN microwires can be harnessed as facile markers to identify polymorphs and crystal orientations of TMDCs.
The interplay of symmetry and quenched disorder leads to some of the most fundamentally interesting and technologically important properties of correlated materials. It also poses the most vexing of theoretical challenges. Nowhere is this more apparent than in the study of spin glasses. A spin glass is characterized by an ergodic landscape of states - an innumerable number of possibilities that are only weakly distinguished energetically, if at all. We show in the material Fe$_x$NbS$_2$, this landscape of states can be biased by coexisitng antiferromagnetic order. This process leads to a phenomenon of broad technological importance: giant, tunable exchange bias. We observe exchange biases that exceed those of conventional materials by more than two orders of magnitude. This work illustrates a novel route to giant exchange bias by leveraging the interplay of frustration and disorder in exotic materials.
Second harmonic generation (SHG) is a coherent nonlinear phenomenon that plays an important role in laser color conversion. Lithium niobate (LN), which features both a large band gap and outstanding second-order nonlinearities, acts as an important optical material for nonlinear frequency conversion covering a wide spectral range from ultraviolet to mid-infrared. Here we experimentally demonstrate LN metasurfaces with controllable SHG properties. Distinct enhancements for the SHG efficiency are observed at Mie-resonances. And by changing the geometric parameters thus the resonances of the metasurfaces, we manage to selectively boost the SHG efficiency at different wavelengths. Our results would pave a way for developing with high flexibility the novel compact nonlinear light sources for applications, such as biosensing and optical communications.
We investigate proximity-induced superconductivity in monolayers of transition metal dichalcogenides (TMDs) in the presence of an externally generated exchange field. A variety of superconducting order parameters is found to emerge from the interplay of magnetism and superconductivity, covering the entire spectrum of possibilities to be symmetric or antisymmetric with respect to the valley and spin degrees of freedom, as well as even or odd in frequency. More specifically, when a conventional emph{s}-wave superconductor with singlet Copper pairs is tunnel-coupled to the TMD layer, both spin-singlet and triplet pairings between electrons from the same and opposite valleys arise due to the combined effects of intrinsic spin-orbit coupling and a magnetic-substrate-induced exchange field. As a key finding, we reveal the existence of an exotic even-frequency triplet pairing between equal-spin electrons from different valleys, which arises whenever the spin orientations in the two valleys are noncollinear. All types of superconducting order turn out to be highly tunable via straightforward manipulation of the external exchange field.