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N. Asger Mortensen

Publications and source records attributed to N. Asger Mortensen.

At least 55 records · Page 3Linked to original sources

Purifying single photon emission from giant shell CdSe/CdS quantum dots at room temperature

Giant shell CdSe/CdS quantum dots are bright and flexible emitters, with near-unity quantum yield and suppressed blinking, but their single photon purity is reduced by efficient multiexcitonic emission. We report the observation, at the single dot level, of a large blueshift of the photoluminescence biexciton spectrum ($24\pm5$ nm over a sample of 32 dots) for pure-phase wurtzite quantum dots. By spectral filtering, we demonstrate a 2.3 times reduction of the biexciton quantum yield relative to the exciton emission, while preserving as much as 60% of the exciton single photon emission, thus improving the purity from $g_2(0)=0.07\pm0.01$ to $g_2(0)=0.03\pm0.01$. At larger pump fluency the spectral purification is even more effective with up to a 6.6 times reduction in $g_2(0)$, which is due to the suppression of higher order excitons and shell states experiencing even larger blueshift. Our results indicate the potential for synthesis engineered giant shell quantum dots, with further increased biexciton blueshift, for quantum optical applications requiring both high purity and brightness.

cond-mat.mes-hall↗

Reconfigurable chirality with achiral excitonic materials in the strong-coupling regime

We introduce and theoretically analyze the concept of manipulating optical chirality via strong coupling of the optical modes of chiral nanostructures with excitonic transitions in molecular layers or semiconductors. With chirality being omnipresent in chemistry and biomedicine, and highly desirable for technological applications related to efficient light manipulation, the design of nanophotonic architectures that sense the handedness of molecules or generate the desired light polarization in an externally controllable manner is of major interdisciplinary importance. Here we propose that such capabilities can be provided by the mode splitting resulting from polaritonic hybridization. Starting with an object with well-known chiroptical response -- here, for a proof of concept, a chiral sphere -- we show that strong coupling with a nearby excitonic material generates two distinct frequency regions that retain the object's chirality density and handedness, which manifest most clearly through anticrossings in circular-dichroism or differential-scattering dispersion diagrams. These windows can be controlled by the intrinsic properties of the excitonic layer and the strength of the interaction, enabling thus the post-fabrication manipulation of optical chirality. Our findings are further verified via simulations of the circular dichroism of a realistic chiral architecture, namely a helical assembly of plasmonic nanospheres embedded in a resonant matrix.

physics.optics↗

Halevi's extension of the Euler-Drude model for plasmonic systems

The nonlocal response of plasmonic materials and nanostructures is usually described within a hydrodynamic approach which is based on the Euler-Drude equation. In this work, we reconsider this approach within linear response theory and employ Halevi's extension to this standard hydrodynamic model. After discussing the impact of this improved model, which we term the Halevi model, on the propagation of longitudinal volume modes, we accordingly extend the Mie-Ruppin theory. Specifically, we derive the dispersion relation of cylindrical surface plasmons. This reveals a nonlocal, collisional damping term which is related to earlier phenomenological considerations of limited-mean-free-path effects and influences both, peak width and amplitude of corresponding resonances in the extinction spectrum. In addition, we transfer the Halevi model into the time-domain thereby revealing a novel, diffusive contribution to the current which shares certain similarities with Cattaneo-type currents and analyze the resulting hybrid, diffusive-wave-like motion. Further, we discuss the relation of the Halevi model to other approaches commonly used in the literature. Finally, we demonstrate how to implement the Halevi model into the Discontinuous-Galerkin Time-Domain finite-element Maxwell solver and are able to identify an oscillatory contribution to the diffusive current. The Halevi model thus captures a number of relevant features beyond the standard hydrodynamic model. Contrary to other extensions of the standard hydrodynamic model, its use in time-domain Maxwell solvers is straightforward -- especially due its affinity to a class of descriptions that allow for a clear distinction between bulk and surface response. This is of particular importance for applications in nano-plasmonics where nano-gap structures and other nano-scale features have to be modeled efficiently and accurately.

physics.optics↗

Disentangling cathodoluminescence spectra in nanophotonics: particle eigenmodes vs transition radiation

Cathodoluminescence spectroscopy performed in an electron microscope has proven a versatile tool for analysing the near- and far-field optical response of plasmonic and dielectric nanostructures. Nevertheless, the transition radiation produced by electron impact is often disregarded in the interpretation of the spectra recorded from resonant nanoparticles. Here we show, experimentally and theoretically, that transition radiation can by itself generate distinct resonances which, depending on the time of flight of the electron beam inside the particle, can result from constructive or destructive interference in time. Superimposed on the eigenmodes of the investigated structures, these resonances can distort the recorded spectrum and lead to potentially erroneous assignment of modal characters to the spectral features. We develop an intuitive analogy that helps distinguish between the two contributions. As an example, we focus on the case of silicon nanospheres, and show that our analysis facilitates the unambiguous interpretation of experimental measurements on Mie-resonant nanoparticles.

cond-mat.mes-hall↗

Fundamental issues with light propagation through $\mathcal{PT}$-symmetric systems

We analyse the emergence of unphysical superluminal group velocities in Su--Schrieffer--Heeger (SSH) parity-time ($\mathcal{PT}$) symmetric chains, and explore the origins of such a behaviour. By comparing the band structure of an infinite loss-gain SSH chain with that of a one-dimensional Bragg stack, we first exclude insufficient coupling consideration in the tight-binding description as the cause of group-velocity divergence. We then focus on material dispersion, and show that indeed, restoring causality in the description of both the lossy and the gain components resolves the problem and recovers finite group velocities, whose real part can only exceed the speed of light in vacuum when accompanied by a significant imaginary part. Our analysis introduces thus the required practical limits in the performance of common $\mathcal{PT}$-symmetric systems.

cond-mat.mes-hall↗

Near-field probing of image phonon-polaritons in hexagonal boron nitride on gold crystals

Near-field mapping has been widely used to study hyperbolic phonon-polaritons in van der Waals crystals. However, an accurate measurement of the polaritonic loss remains challenging because of the inherent complexity of the near-field signal and the substrate-mediated loss. Here we demonstrate that large-area monocrystalline gold flakes, an atomically-flat low-loss substrate for image polaritons, provide a platform for precise near-field measurement of the complex propagation constant of polaritons in van der Waals crystals. As a topical example, we measure propagation loss of the image phonon-polaritons in hexagonal boron nitride, revealing that their normalized propagation length exhibits a parabolic spectral dependency. Further, we show that image phonon-polaritons exhibit up to a twice lower normalized propagation loss, while being 2.4 times more compressed compared to the case of dielectric substrate. We conclude that the monocrystalline gold flakes provide a unique nanophotonic platform for probing and exploitation of the image modes in low-dimensional materials.

cond-mat.mtrl-sci↗

Extremely confined gap plasmon modes: when nonlocality matters

Historically, the field of plasmonics has been relying on the framework of classical electrodynamics, with the local-response approximation of material response being applied even when dealing with nanoscale metallic structures. However, when approaching the atomic-scale confinement of the electromagnetic radiation, mesoscopic effects are anticipated to become observable, e.g., those associated with the nonlocal electrodynamic surface response of the electron gas. We investigate nonlocal effects in propagating gap surface plasmon modes in ultrathin metal--dielectric--metal planar waveguides, exploiting monocrystalline gold flakes separated by atomic-layer-deposited aluminum oxide. We use scanning near-field optical microscopy to directly access the near-field of such confined gap plasmon modes and measure their dispersion relation (via their complex-valued propagation constants). We compare our experimental findings with the predictions of the generalized nonlocal optical response theory to unveil signatures of nonlocal damping, which becomes appreciable for smaller dielectric gaps.

cond-mat.mes-hall↗

Image polaritons in van der Waals crystals

Polaritonic modes in low-dimensional materials enable strong light-matter interactions and provide a platform for light manipulation at nanoscale. Very recently, a new class of polaritons has attracted considerable interest in nanophotonics: image polaritons in van der Waals crystals, manifesting when a polaritonic material is in close proximity to a highly conductive metal, so that the polaritonic mode couples with its mirror image. Image modes constitute an appealing nanophotonic platform, providing an unparalleled degree of optical field compression into nanometric volumes while exhibiting lower normalized propagation loss compared to conventional polariton modes in van der Waals crystals on non-metallic substrates. Moreover, the ultra-compressed image modes provide access to the nonlocal regime of light-matter interaction. In this Review, we systematically overview the young yet rapidly growing field of image polaritons. We discuss their dispersion properties, showcase the diversity of image modes in various van der Waals materials, and highlight the experimental breakthroughs owing to the unique properties of image polaritons.

physics.optics↗

Polaritons in two-dimensional parabolic waveguides

The suite of highly confined polaritons supported by two-dimensional (2D) materials constitutes a versatile platform for nano-optics, offering the means to channel light on deep-subwavelength scales. Graphene, in particular, has attracted considerable interest due to its ability to support long-lived plasmons that can be actively tuned via electrical gating. While the excellent optoelectronic properties of graphene are widely exploited in plasmonics, its mechanical flexibility remains relatively underexplored in the same context. Here, we present a semi-analytical formalism to describe plasmons and other polaritons supported in waveguides formed by bending a 2D material into a parabolic shape. Specifically, for graphene parabolas, our theory reveals that the already large field confinement associated with graphene plasmons can be substantially increased by bending an otherwise flat graphene sheet into a parabola shape, thereby forming a plasmonic waveguide without introducing potentially lossy edge terminations via patterning. Further, we show that the high field confinement associated with such channel polaritons in 2D parabolic waveguides can enhance the spontaneous emission rate of a quantum emitter near the parabola vertex. Our findings apply generally to 2D polaritons in atomically thin materials deposited onto grooves or wedges prepared on a substrate or freely suspended in a quasi-parabolic (catenary) shape. We envision that both the optoelectronic and mechanical flexibility of 2D materials can be harnessed in tandem to produce 2D channel polaritons with versatile properties that can be applied to a wide range of nano-optics functionalities, including subwavelength polaritonic circuitry and bright single-photon sources.

cond-mat.mes-hall↗

Quantum Nanophotonics in Two-Dimensional Materials

The field of 2D materials-based nanophotonics has been growing at a rapid pace, triggered by the ability to design nanophotonic systems with in situ control, unprecedented degrees of freedom, and to build material heterostructures from bottom up with atomic precision. A wide palette of polaritonic classes have been identified, comprising ultra confined optical fields, even approaching characteristic length scales of a single atom. These advances have been a real boost for the emerging field of quantum nanophotonics, where the quantum mechanical nature of the electrons and-or polaritons and their interactions become relevant. Examples include, quantum nonlocal effects, ultrastrong light matter interactions, Cherenkov radiation, access to forbidden transitions, hydrodynamic effects, single plasmon nonlinearities, polaritonic quantization, topological effects etc. In addition to these intrinsic quantum nanophotonic phenomena, the 2D material system can also be used as a sensitive probe for the quantum properties of the material that carries the nanophotonics modes, or quantum materials in its vicinity. Here, polaritons act as a probe for otherwise invisible excitations, e.g. in superconductors, or as a new tool to monitor the existence of Berry curvature in topological materials and superlattice effects in twisted 2D materials.

physics.optics↗

Quantum Surface-Response of Metals Revealed by Acoustic Graphene Plasmons

A quantitative understanding of the electromagnetic response of materials is essential for the precise engineering of maximal, versatile, and controllable light--matter interactions. Material surfaces, in particular, are prominent platforms for enhancing electromagnetic interactions and for tailoring chemical processes. However, at the deep nanoscale, the electromagnetic response of electron systems is significantly impacted by quantum surface-response at material interfaces, which is challenging to probe using standard optical techniques. Here, we show how ultra-confined acoustic graphene plasmons (AGPs) in graphene--dielectric--metal structures can be used to probe the quantum surface-response functions of nearby metals, here encoded through the so-called Feibelman $d$-parameters. Based on our theoretical formalism, we introduce a concrete proposal for experimentally inferring the low-frequency quantum response of metals from quantum shifts of the AGPs' dispersion, and demonstrate that the high field confinement of AGPs can resolve intrinsically quantum mechanical electronic length-scales with subnanometer resolution. Our findings reveal a promising scheme to probe the quantum response of metals, and further suggest the utilization of AGPs as plasmon rulers with ångström-scale accuracy.

cond-mat.mes-hall↗

Surface-response functions obtained from equilibrium electron-density profiles

Surface-response functions are one of the most promising routes for bridging the gap between fully quantum-mechanical calculations and phenomenological models in quantum nanoplasmonics. Within all the currently available recipes for obtaining such response functions, \emph{ab initio} calculations remain one of the most predominant, wherein the surface-response function are retrieved via the metal's non-equilibrium response to an external perturbation. Here, we present a complementary approach where one of the most appealing surface-response functions, namely the Feibelman $d$-parameters, yield a finite contribution even in the case where they are calculated directly from the equilibrium properties described under the local-response approximation (LRA), but with a spatially varying equilibrium electron density. Using model calculations that mimic both spill-in and spill-out of the equilibrium electron density, we show that the obtained $d$-parameters are in qualitative agreement with more elaborate, but also more computationally demanding, \emph{ab initio} methods. The analytical work presented here illustrates how microscopic surface-response functions can emerge out of entirely local electrodynamic considerations.

cond-mat.mes-hall↗

Harnessing Ultraconfined Graphene Plasmons to Probe the Electrodynamics of Superconductors

We show that the Higgs mode of a superconductor, which is usually challenging to observe by far-field optics, can be made clearly visible using near-field optics by harnessing ultraconfined graphene plasmons. As near-field sources we investigate two examples: graphene plasmons and quantum emitters. In both cases the coupling to the Higgs mode is clearly visible. In the case of the graphene plasmons, the coupling is signaled by a clear anticrossing stemming from the interaction of graphene plasmons with the Higgs mode of the superconductor. In the case of the quantum emitters, the Higgs mode is observable through the Purcell effect. When combining the superconductor, graphene, and the quantum emitters, a number of experimental knobs become available for unveiling and studying the electrodynamics of superconductors.

cond-mat.mes-hall↗

Manipulating the photonic Hall effect with hybrid Mie-exciton resonances

We examine the far-field optical response, under-plane wave excitation in the presence of a static magnetic field, of core-shell nanoparticles involving a gyroelectric component, either as the inner or the outer layer, through analytic calculations based on appropriately extended Mie theory. We focus on absorption and scattering of light by bismuth-substituted yttrium iron garnet (Bi:YIG) nanospheres and nanoshells, combined with excitonic materials such as organic-molecule aggregates or two-dimensional transition-metal dichalcogenides, and discuss the hybrid character of the modes emerging from the coupling of the two constituents. We observe the excitation of strong magneto-optic phenomena and explore, in particular, the response and tunability of a magneto-transverse light current, indicative of the photonic Hall effect. We show how interaction between the Bi:YIG and excitonic layers leads to a pair of narrow bands of highly directional scattering, emerging from the aforementioned hybridization, which can be tuned at will by adjusting the geometrical or optical parameters of the system. Our theoretical study introduces optically anisotropic media as promising templates for strong coupling in nanophotonics, offering a means to combine tunable magnetic and optical properties, with potential implications both in the design of all-dielectric photonic devices but also in novel clinical applications.

cond-mat.mes-hall↗

Anisotropic Second Harmonic Generation From Monocrystalline Gold Flakes

Noble metals with well-defined crystallographic orientation constitute an appealing class of materials for controlling light-matter interactions on the nanoscale. Nonlinear optical processes, being particularly sensitive to anisotropy, are a natural and versatile probe of crystallinity in nano-optical devices. Here we study the nonlinear optical response of monocrystalline gold flakes, revealing a polarization dependence in second-harmonic generation from the {111} surface that is markedly absent in polycrystalline films. Apart from suggesting an approach for directional enhancement of nonlinear response in plasmonic systems, we anticipate that our findings can be used as a rapid and non-destructive method for characterization of crystal quality and orientation that may be of significant importance in future applications.

physics.optics↗

Optical response of noble metal nanostructures: Quantum surface effects in crystallographic facets

Noble metal nanostructures are ubiquitous elements in nano-optics, supporting plasmon modes that can focus light down to length scales commensurate with nonlocal effects associated with quantum confinement and spatial dispersion in the underlying electron gas. Nonlocal effects are naturally more prominent for crystalline noble metals, which potentially offer lower intrinsic loss than their amorphous counterparts, and with particular crystal facets giving rise to distinct electronic surface states. Here, we employ a quantum-mechanical model to describe nonclassical effects impacting the optical response of crystalline noble-metal films and demonstrate that these can be well-captured using a set of surface-response functions known as Feibelman $d$-parameters. In particular, we characterize the $d$-parameters associated with the (111) and (100) crystal facets of gold, silver, and copper, emphasizing the importance of surface effects arising due to electron wave function spill-out and the surface-projected band gap emerging from atomic-layer corrugation. We then show that the extracted $d$-parameters can be straightforwardly applied to describe the optical response of various nanoscale metal morphologies of interest, including metallic ultra-thin films, graphene-metal heterostructures hosting extremely confined acoustic graphene plasmons, and crystallographic faceted metallic nanoparticles supporting localized surface plasmons. The tabulated $d$-parameters reported here can circumvent computationally expensive first-principles atomistic simulations to describe microscopic nonlocal effects in the optical response of mesoscopic crystalline metal surfaces, which are becoming widely available with increasing control over morphology down to atomic length scales for state-of-the-art experiments in nano-optics.

cond-mat.mes-hall↗

Stimulated plasmon polariton scattering

The plasmon and phonon polaritons of two-dimensional (2d) and van-der-Waals materials have recently gained substantial interest. Unfortunately, they are notoriously hard to observe in linear response because of their strong confinement, low frequency and longitudinal mode symmetry. Here, we propose a fundamentally new approach of harnessing nonlinear resonant scattering that we call stimulated plasmon polariton scattering (SPPS) in analogy to the opto-acoustic stimulated Brillouin scattering (SBS). We show that SPS allows to excite, amplify and detect 2d plasmon and phonon polaritons all across the THz-range while requiring only optical components in the near-IR or visible range. We present a coupled-mode theory framework for SPS and based on this find that SPS power gains exceed the very top gains observed in on-chip SBS by at least an order of magnitude. This opens exciting new possibilities to fundamental studies of 2d materials and will help closing the THz gap in spectrocopy and information technology.

cond-mat.mes-hall↗

Role of diffusive surface scattering in nonlocal plasmonics

The recent generalised nonlocal optical response (GNOR) theory for plasmonics is analysed, and its main input parameter, namely the complex hydrodynamic convection-diffusion constant, is quantified in terms of enhanced Landau damping due to diffusive surface scattering of electrons at the surface of the metal. GNOR has been successful in describing plasmon damping effects, in addition to the frequency shifts originating from induced-charge screening, through a phenomenological electron diffusion term implemented into the traditional hydrodynamic Drude model of nonlocal plasmonics. Nevertheless, its microscopic derivation and justification is still missing. Here we discuss how the inclusion of a diffusion-like term in standard hydrodynamics can serve as an efficient vehicle to describe Landau damping without resorting to computationally demanding quantum-mechanical calculations, and establish a direct link between this term and the Feibelman $d$ parameter for the centroid of charge. Our approach provides a recipe to connect the phenomenological fundamental GNOR parameter to a frequency-dependent microscopic surface-response function. We therefore tackle one of the principal limitations of the model, and further elucidate its range of validity and limitations, thus facilitating its proper application in the framework of nonclassical plasmonics.

cond-mat.mes-hall↗