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Ryeong Myeong Kim

Publications and source records attributed to Ryeong Myeong Kim.

6 recordsLinked to original sources

Helicity-Resolved Spatiotemporal Mapping of Chiral Plexcitons in Helicoids

Plasmon-exciton hybrids, or plexcitons, offer deeply subwavelength light-matter interactions with versatile pathways for energy redistribution. Incorporating chirality into such systems is particularly compelling, enabling spin-sensitive optical functionality that can operate on ultrafast timescales and within ultracompact volumes. Despite recent progress in chiral plexcitonic systems, how structural chirality and plasmon-exciton coupling determine chiroptical spectra and ultrafast energy flow remains elusive. Here we realize chiral plexcitons by functionalizing intrinsically chiral gold helicoid nanoparticles with molecular J-aggregates. Within a non-Hermitian framework, we trace the microscopic origin of the helicoid chiroptical response and its coupling to the excitonic transition, revealing how the helicity of light selectively addresses distinct hybrid responses. At the spatiotemporal extreme, we find that the gap-localized response not only enhances polarization-sensitive contrast but also strengthens the local hybrid interaction, leading to accelerated ultrafast relaxation. Together, these space-, time-, and polarization-resolved measurements provide a physically grounded and experimentally benchmarked picture of chiral plexcitonic coupling, identifying chirality as a practical control parameter for selectively steering nanoscale energy pathways and dynamics.

physics.optics↗

Broadband ultrafast self-heterodyned chiro-optical spectroscopy

Ultrafast chiro-optical spectroscopy provides unique access to the structural dynamics of molecules, spin-valley relaxation in semiconductors, and the non-equilibrium optical response of chiral nanophotonic systems. Yet, because chiral signals are intrinsically weak and time-resolved spectroscopy probes small photoinduced changes, transient chiro-optical responses are often difficult to isolate from parasitic achiral contributions. Here, we introduce a broadband ultrafast chiro-optical spectroscopy technique that integrates a birefringent common-path interferometer with an optical polarization bridge to sensitively detect photoinduced changes in the polarization state of light. Phase-sensitive self-heterodyned detection enables simultaneous measurement of transient circular dichroism and optical rotatory dispersion across a broad spectral range with ultrafast temporal resolution. Balanced detection suppresses excess laser noise, enabling exceptional sensitivity (<50 $μ$deg) close to shot-noise limit. We demonstrate this approach on an array of gold nano-helicoids, supported by a full-wave time-resolved model of the spatiotemporal dynamics of plasmonic non-equilibrium carriers and their associated optical nonlinearities. The model traces the system's transient chiro-optical response back to photoinduced modulations of the electric-magnetic dipole interaction in the nano-helicoid, elucidating the connection of near- and far-field dynamics in the non-equilibrium regime. We further investigate spin excitation, thermalization, and relaxation in a lead halide perovskite, establishing a novel approach to broadband time-resolved Faraday rotation. The simplicity, sensitivity, and wide applicability of this detection scheme provide a powerful platform for broadband ultrafast chiro-optical spectroscopy, opening new opportunities in biochemistry, solid-state physics, and nanophotonics.

physics.optics↗

On the Physical Layer Security of Visible Light Communications Empowered by Gold Nanoparticles

Visible light is a proper spectrum for secure wireless communications because of its high directivity and impermeability in indoor scenarios. However, if an eavesdropper is located very close to a legitimate receiver, secure communications become highly risky. In this paper, to further increase the level of security of visible light communication (VLC) and increase its resilience against to malicious attacks, we propose to capitalize on the recently synthesized gold nanoparticles (GNPs) with chiroptical properties for circularly polarized light resulting the phase retardation that interacts with the linear polarizer angle. GNP plates made by judiciously stacking many GNPs perform as physical secret keys. Transmitters send both the intended symbol and artificial noise to exploit the channel variation effect by the GNP plates, which is highly effective when an eavesdropper is closely located to the legitimate receiver. A new VLC channel model is first developed by representing the effect of GNP plates and linear polarizers in the circular polarization domain. Based on the new channel model, the angles of linear polarizers at the transmitters and legitimate receiver are optimized considering the effect of GNP plates to increase the secrecy rate in wiretapping scenarios. Simulations verify that when the transmitters are equipped with GNP plates, even if the eavesdropper is located right next to the legitimate receiver, insightful results on the physical layer security metrics are gained as follows: 1) the secrecy rate is significantly improved and 2) the symbol error rate gap between the legitimate receiver and eavesdropper becomes much larger due to the chiroptical properties of GNP plates.

cs.IT↗

Strain and Crystallographic Identification of the Helically Concaved Surfaces of Nanoparticles

Identifying the three-dimensional (3D) crystal-plane and strain-field distributions of nanocrystals is essential for optical, catalytic, and electronic applications. Here, we developed a methodology for visualizing the 3D information of chiral gold nanoparticles with concave gap structures by Bragg coherent X-ray diffraction imaging. The distribution of the high-Miller-index planes constituting the concave chiral gap was precisely determined. The highly strained region adjacent to the chiral gaps was resolved, which was correlated to the 432-symmetric morphology of the nanoparticles and its corresponding plasmonic properties were numerically predicted from the atomically defined structures. This approach can serve as a general characterization platform for visualizing the 3D crystallographic and strain distributions of nanoparticles, especially for applications where structural complexity and local heterogeneity are major determinants, as exemplified in plasmonics.

cond-mat.mtrl-sci↗

Second-harmonic optical circular dichroism of plasmonic chiral helicoid-III nanoparticles

While plasmonic particles can provide optical resonances in a wide spectral range from the lower visible up to the near-infrared, often symmetry effects are utilized to obtain particular optical responses. By breaking certain spatial symmetries, chiral structures arise and provide robust chiroptical responses to these plasmonic resonances. Here, we observe strong chiroptical responses in the linear and nonlinear optical regime for chiral L-handed helicoid III nanoparticles and quantify them by means of an asymmetric factor, the so-called g-factor. We calculate the linear-optical g-factors for two distinct chiroptical resonances to -0.12 and -0.43 and the nonlinear optical g-factors to -1.45 and -1.63. The results demonstrate that the chirality of the helicoid-III nanoparticles is strongly enhanced in the nonlinear regime.

physics.optics↗

Valley Polarization Enhancement Induced by a Single Chiral Nanoparticle

Valley polarization is amongst the most critical attributes of atomically thin materials. However, achieving a high contrast from monolayer transition metal dichalcogenides (TMDs) has so far been challenging. In this work, a giant valley polarization contrast up to 45% from a monolayer WS2 has been achieved at room temperature by using a single chiral plasmonic nanoparticle. The increased contrast is attributed to the selective enhancement of both the excitation and the emission rate having one particular handedness of the circular polarization. The experimental results were corroborated by the optical simulation using finite-difference time-domain (FDTD) method. Additionally, the single chiral nanoparticle enabled the observation of valley-polarized luminescence with a linear excitation. Our results provide a promising pathway to enhance valley contrast from monolayer TMDs and utilize them for nanophotonic devices.

physics.app-ph↗