arXiv subjects

Jiahua Duan

Publications and source records attributed to Jiahua Duan.

14 recordsLinked to original sources

arXiv2026

Floquet polaritons in optically driven materials

Polaritons are coupled collective modes of light and matter in quantum materials. In modern pump-probe experiments, a pump light pulse may dramatically alter the properties of the polaritons, rendering them Floquet polaritons that can be detected by a probe pulse. We present a practical framework to describe Floquet polaritons in terms of the linear and nonlinear optical properties of the material. The central quantity that yields the spectra of Floquet polaritons is an effective linear optical susceptibility contributed by the pump through nonlinear optical susceptibilities. We apply this method to graphene and show that via its third-order optical nonlinearity, infrared pump leads to Floquet plasmon bands. Notably, near plasmonic band crossings, parametric instability leads to flat bands with unstable modes and exceptional points that closely resemble those of non-Hermitian systems. As a second example, we show that in hexagonal boron nitride pumped by mid-infrared laser, the pump induces Floquet phonon polariton bands via phononic nonlinearity, which can be detected with either far-field or near-field optical technique. Finally, in layered superconductors pumped by THz light polarized along the out-of-plane direction, the Josephson-type optical nonlinearity leads to Floquet Josephson plasmons, which manifest as new peaks in the THz reflectivity of a probe pulse.

cond-mat.mes-hall↗

arXiv2025

Directional strong coupling at the nanoscale between hyperbolic polaritons and organic molecules

Strong coupling (SC) is a fundamental concept in physics that describes extreme interactions between light and matter. Recent experiments have demonstrated SC at the nanometer scale, where strongly confined polaritons, rather than photons, couple to quantum emitters or molecular vibrations. Coupling with the latter is generally referred to as vibrational SC (VSC) and is of significant fundamental and technological interest, as it can be an effective tool for modifying molecular properties. However, the implementation of VSC, especially at the nanoscale, depends on the development of tuning mechanisms that allow control over the coupling strength and, eventually, its directionality, opening the door for the selective coupling of specific molecular vibrations. Here we report the observation of directional VSC. Specifically, we show nanoscale images of propagating hyperbolic phonon polaritons (PhPs) coupled to pentacene molecules revealing that the fingerprint of VSC for propagating polaritons -- a marked anti-crossing in their dispersion at the vibrational resonance -- can be modulated as a function of the direction of propagation. In addition, we show that VSC can exhibit an optimal condition for thin molecular layers, characterized by a maximum coupling strength along one single direction. This phenomenon is understood by analysing the overlap of the polariton field with molecular layers of varying thicknesses. Apart from their fundamental importance, our findings promise novel applications for directional sensing or local directional control of chemical properties at the nanoscale.

cond-mat.mtrl-sci↗

arXiv2025

Roadmap for Photonics with 2D Materials

Triggered by the development of exfoliation and the identification of a wide range of extraordinary physical properties in self-standing films consisting of one or few atomic layers, two-dimensional (2D) materials such as graphene, transition metal dichalcogenides (TMDs), and other van der Waals (vdW) crystals currently constitute a wide research field protruding in multiple directions in combination with layer stacking and twisting, nanofabrication, surface-science methods, and integration into nanostructured environments. Photonics encompasses a multidisciplinary collection of those directions, where 2D materials contribute with polaritons of unique characteristics such as strong spatial confinement, large optical-field enhancement, long lifetimes, high sensitivity to external stimuli (e.g., electric and magnetic fields, heating, and strain), a broad spectral range from the far infrared to the ultraviolet, and hybridization with spin and momentum textures of electronic band structures. The explosion of photonics with 2D materials as a vibrant research area is producing breakthroughs, including the discovery and design of new materials and metasurfaces with unprecedented properties as well as applications in integrated photonics, light emission, optical sensing, and exciting prospects for applications in quantum information, and nanoscale thermal transport. This Roadmap summarizes the state of the art in the field, identifies challenges and opportunities, and discusses future goals and how to meet them through a wide collection of topical sections prepared by leading practitioners.

cond-mat.mtrl-sci↗

arXiv2025

Visualization of topological shear polaritons in gypsum thin films

Low symmetry crystals have recently emerged as a platform for exploring novel light-matter interactions in the form of hyperbolic shear polaritons. These excitations exhibit unique optical properties such as frequency-dispersive optical axes and asymmetric light propagation and energy dissipation, which arise from the presence of non-orthogonal resonances. However, only non-vdW materials have been demonstrated to support hyperbolic shear polaritons, limiting their exotic properties and potential applications. Here we introduce for the first time novel shear phenomena in low symmetry crystal thin films by demonstrating the existence of elliptical and canalized shear phonon polaritons in gypsum, an exfoliable monoclinic sulphate mineral. Our results unveil a topological transition from hyperbolic shear to elliptical shear polaritons, passing through a canalization regime with strong field confinement. Importantly, we observe a significant slowdown of group velocity, reaching values as low as 0.0005c, highlighting the potential of gypsum for "slow light" applications and extreme light-matter interaction control. These findings expand the application scope of low-symmetry crystals with the benefits that an exfoliable material provides, such as stronger field confinement, tunability, and versatility for its incorporation in complex photonic devices that might unlock new optical phenomena at the nanoscale.

physics.optics↗

arXiv2025

Broad Spectral Tuning of Ultra-Low Loss Polaritons in a van der Waals Crystal by Intercalation

Phonon polaritons (PhPs) -- light coupled to lattice vibrations -- in polar van der Waals (vdW) crystals are promising candidates for controlling the flow of energy at the nanoscale due to their strong field confinement, anisotropic propagation, and ultra-long lifetime in the picosecond range \cite{ref1,ref2,ref3,ref4,ref5}. However, the lack of tunability in their narrow and material-specific spectral range -- the Reststrahlen Band (RB) -- severely limits their technological implementation. Here, we demonstrate that the intercalation of Na atoms in the vdW semiconductor $α$-V$_2$O$_5$ enables a broad spectral shift of RBs, and that the PhPs excited exhibit ultra-low losses (lifetime of $4 \pm 1$~ps), similar to PhPs in the non-intercalated crystal (lifetime of $6 \pm 1$ ps). We expect our intercalation method to be applicable to other vdW crystals, opening the door for the use of PhPs in broad spectral bands in the mid-infrared domain.

physics.optics↗

arXiv2024

Unveiling the Mechanism of Phonon-Polariton Damping in α-MoO_3

Phonon polaritons (PhPs) (light coupled to lattice vibrations) in the highly anisotropic polar layered material molybdenum trioxide (α-MoO_3) are currently the focus of intense research efforts due to their extreme subwavelength field confinement, directional propagation and unprecedented low losses. Nevertheless, prior research has primarily concentrated on exploiting the squeezing and steering capabilities of α-MoO_3 PhPs, without inquiring much into the dominant microscopic mechanism that determines their long lifetimes, key for their implementation in nanophotonic applications. This study delves into the fundamental processes that govern PhP damping in α-MoO_3 by combining ab initio calculations with scattering-type scanning near-field optical microscopy (s-SNOM) and Fourier-transform infrared (FTIR) spectroscopy measurements across a broad temperature range (from 8 to 300 K). The remarkable agreement between our theoretical predictions and experimental observations allows us to identify third-order anharmonic phonon-phonon scattering as the main damping mechanism of α-MoO_3 PhPs. These findings shed light on the fundamental limits of low-loss PhPs, a crucial factor for assessing their implementation into nanophotonic devices.

cond-mat.mtrl-sci↗

arXiv2024

Canalization-based super-resolution imaging using a single van der Waals layer

Canalization is an optical phenomenon that enables unidirectional propagation of light in a natural way, i.e., without the need for predefined waveguiding designs. Predicted years ago, it was recently demonstrated using highly confined phonon polaritons (PhPs) in twisted layers of the van der Waals (vdW) crystal alpha-MoO3, offering unprecedented possibilities for controlling light-matter interactions at the nanoscale. However, despite this finding, applications based on polariton canalization have remained elusive so far, which can be explained by the complex sample fabrication of twisted stacks. In this work, we introduce a novel canalization phenomenon, arising in a single vdW thin layer (alpha-MoO3) when it is interfaced with a substrate exhibiting a given negative permittivity, that allows us to demonstrate a proof-of-concept application based on polariton canalization: super-resolution (up to ~λ0/220) nanoimaging. Importantly, we find that canalization-based imaging transcends conventional projection constraints, allowing the super-resolution images to be obtained at any desired location in the image plane. This versatility stems from the synergetic manipulation of three distinct parameters: incident frequency, rotation angle of the thin vdW layer, and thickness. These results provide valuable insights into the fundamental properties of canalization and constitute a seminal step towards multifaceted photonic applications, encompassing imaging, data transmission, and ultra-compact photonic integration.

physics.optics↗

arXiv2023

Thermal and electrostatic tuning of surface phonon-polaritons in LaAlO3/SrTiO3 heterostructures

Phonon polaritons are promising for infrared applications due to a strong light-matter coupling and subwavelength energy confinement they offer. Yet, the spectral narrowness of the phonon bands and difficulty to tune the phonon polariton properties hinder further progress in this field. SrTiO3 - a prototype perovskite oxide - has recently attracted attention due to two prominent far-infrared phonon polaritons bands, albeit without any tuning reported so far. Here we show, using cryogenic infrared near-field microscopy, that long-propagating surface phonon polaritons are present both in bare SrTiO3 and in LaAlO3/SrTiO3 heterostructures hosting a two-dimensional electron gas. The presence of the two-dimensional electron gas increases dramatically the thermal variation of the upper limit of the surface phonon polariton band due to temperature dependent polaronic screening of the surface charge carriers. Furthermore, we demonstrate a tunability of the upper surface phonon polariton frequency in LaAlO3/SrTiO3 via electrostatic gating. Our results suggest that oxide interfaces are a new platform bridging unconventional electronics and long-wavelength nanophotonics.

cond-mat.mtrl-sci↗

arXiv2022

Negative reflection of polaritons at the nanoscale in a low-loss natural medium

Negative reflection occurs when light is reflected towards the same side of the normal to the boundary from which it is incident. This exotic optical phenomenon, which provides a new avenue towards light manipulation, is not only yet to be visualized in real space but remains largely unexplored both at the nanoscale and in natural media. Here, we directly visualize nanoscale-confined polaritons negatively reflecting on subwavelength mirrors fabricated in a low-loss van der Waals crystal. Our near-field nanoimaging results unveil an unconventional and broad tunability of both the polaritonic wavelength and direction of propagation upon negative reflection. Based on these findings, we introduce a novel device in nano-optics: a hyperbolic nanoresonator, in which hyperbolic polaritons with different momenta reflect back to a common point source, enhancing its intensity. These results pave the way to realize nanophotonics in low-loss natural media, providing a novel and efficient route to confine and control the flow of light at the nanoscale, key for future optical on-chip nanotechnologies.

physics.optics↗

arXiv2021

Active tuning of highly anisotropic phonon polaritons in van der Waals crystal slabs by gated graphene

Phonon polaritons (PhPs) -- lattice vibrations coupled to electromagnetic fields -- in highly anisotropic media display a plethora of intriguing optical phenomena (including ray-like propagation, anomalous refraction, and topological transitions, among others), which have potential for unprecedented manipulation of the flow of light at the nanoscale. However, the propagation properties of these PhPs are intrinsically linked to the anisotropic crystal structure of the host material. Although in-plane anisotropic PhPs can be steered (and even canalized) by twisting individual crystal slabs in a van der Waals (vdW) stack, active control of their propagation via external stimuli presents a significant challenge. Here, we report on a technology in which anisotropic PhPs supported by biaxial vdW slabs are actively tunable by simply gating an integrated graphene layer. Excitingly, we predict active tuning of optical topological transitions, which enable controlling the canalization of PhPs along different in-plane directions in twisted heterostructures. Apart from their fundamental interest, our findings hold promises for the development of optoelectronic devices (sensors, photodetectors, etc.) based on PhPs with dynamically controllable properties.

physics.optics↗

arXiv2021

Focusing of in-plane hyperbolic polaritons in van der Waals crystals with tailored infrared nanoantennas

Phonon polaritons (PhPs),light coupled to lattice vibrations,with in-plane hyperbolic dispersion exhibit ray-like propagation with large wavevectors and enhanced density of optical states along certain directions on a surface. As such, they have raised a surge of interest as they promise unprecedented possibilities for the manipulation of infrared light with planar circuitry and at the nanoscale. Here, we demonstrate, for the first time, the focusing of in-plane hyperbolic PhPs propagating along thin slabs of MoO3. To that end, we developed metallic nanoantennas of convex geometries for both the efficient launching and focusing of the polaritons. Remarkably, the foci obtained exhibit enhanced near-field confinement and absorption compared to foci produced by in-plane isotropic PhPs. More intriguingly, foci sizes as small as lamdap/5 =lamda0/50 were achieved (lamdap is the polariton wavelength and lamda0 the photon wavelength). Focusing of in-plane hyperbolic polaritons introduces a first and most basic building block developing planar polariton optics utilizing in-plane anisotropic van der Waals materials and metasurfaces.

physics.optics↗

arXiv2021

Enabling propagation of anisotropic polaritons along forbidden directions via a topological transition

Recent discoveries of polaritons in van der Waals (vdW) crystals with directional in-plane propagation, ultra-low losses, and broad spectral tunability have opened the door for unprecedented manipulation of the flow of light at the nanoscale. However, despite their extraordinary potential for nano-optics, these unique polaritons also present an important limitation: their directional propagation is intrinsically determined by the crystal structure of the host material, which imposes forbidden directions of propagation and hinders its control. Here, we theoretically predict and experimentally demonstrate that directional polaritons (in-plane hyperbolic phonon polaritons) in a vdW biaxial slab (alpha-phase molybdenum trioxide) can be steered along previously forbidden directions by inducing an optical topological transition, which naturally emerges when placing the slab on a substrate with a given negative permittivity (4H-SiC). Importantly, due to the low-loss nature of this topological transition, we are able to visualize in real space exotic intermediate polaritonic states between mutually orthogonal hyperbolic regimes, which permit to unveil the unique topological origin of the transition. This work provides new insights into the emergence of low-loss optical topological transitions in vdW crystals, offering a novel route to efficiently steer the flow of energy at the nanoscale.

physics.optics↗

arXiv2020

Twisted Nano-optics: Manipulating Light at the Nanoscale with Twisted Phonon Polaritonic Slabs

Recent discoveries have shown that when two layers of van der Waals (vdW) materials are superimposed with a relative twist angle between their respective in-plane principal axes, the electronic properties of the coupled system can be dramatically altered. Here, we demonstrate that a similar concept can be extended to the optics realm, particularly to propagating polaritons, hybrid light-matter interactions. To do this, we fabricate stacks composed of two twisted slabs of a polar vdW crystal (MoO3) supporting low-loss anisotropic phonon polaritons (PhPs), and image the propagation of the latter when launched by localized sources (metal antennas). Our images reveal that under a critical angle the PhPs isofrequency curve (determining the PhPs momentum at a fixed frequency) undergoes a topological transition. Remarkably, at this angle, the propagation of PhPs is strongly guided along predetermined directions (canalization regime) with no geometrical spreading (diffraction-less). These results demonstrate a new degree of freedom (twist angle) for controlling the propagation of polaritons at the nanoscale with potential for nano-imaging, (bio)-sensing, quantum applications and heat management.

physics.optics↗

arXiv2020

Infrared permittivity of the biaxial van der Waals semiconductor $α$-MoO$_3$ from near- and far-field correlative studies

The biaxial van der Waals semiconductor $α$-phase molybdenum trioxide ($α$-MoO$_3$) has recently received significant attention due to its ability to support highly anisotropic phonon polaritons (PhPs) -infrared (IR) light coupled to lattice vibrations in polar materials-, offering an unprecedented platform for controlling the flow of energy at the nanoscale. However, to fully exploit the extraordinary IR response of this material, an accurate dielectric function is required. Here, we report the accurate IR dielectric function of $α$-MoO$_3$ by modelling far-field, polarized IR reflectance spectra acquired on a single thick flake of this material. Unique to our work, the far-field model is refined by contrasting the experimental dispersion and damping of PhPs, revealed by polariton interferometry using scattering-type scanning near-field optical microscopy (s-SNOM) on thin flakes of $α$-MoO$_3$, with analytical and transfer-matrix calculations, as well as full-wave simulations. Through these correlative efforts, exceptional quantitative agreement is attained to both far- and near-field properties for multiple flakes, thus providing strong verification of the accuracy of our model, while offering a novel approach to extracting dielectric functions of nanomaterials, usually too small or inhomogeneous for establishing accurate models only from standard far-field methods. In addition, by employing density functional theory (DFT), we provide insights into the various vibrational states dictating our dielectric function model and the intriguing optical properties of $α$-MoO$_3$.

physics.app-ph↗