arXiv subjects

Jan Renger

Publications and source records attributed to Jan Renger.

13 recordsLinked to original sources

arXiv2026

Designing metallo-dielectric antennas for cryogenic applications

We present the design of cryogenic metallo-dielectric antennas tailored to single organic emitters, where the choice of host material imposes specific constraints on the antenna geometry. Using dibenzoterrylene (DBT) in para-dichlorobenzene (p-DCB}) as a model system, we show that photon collection efficiencies exceeding 90% can be achieved for arbitrary dipole orientations of the fluorescent molecule. The antenna design is intrinsically broadband and tolerant to emitter positioning within the structure. We further provide concrete fabrication guidelines for the full antenna architecture, and experimentally demonstrate its operating principle by recording a back-focal-plane image (BFP) of a single molecule inside a fabricated antenna.

physics.optics↗

arXiv2026

Design of monolithic microcavities for enhancing organic quantum emitters

Single organic molecules are a well-established platform for high-quality single-photon generation: they can emit lifetime-limited photons with high purity and indistinguishability. However, their emission is accompanied by a pronounced red-shifted phonon sideband and higher-order vibrational peaks, which reduce the fraction of photons emitted into the desired narrowband zero-phonon line. The standard approach to suppressing this unwanted emission is to integrate the emitter into a monolithic photonic nanostructure that provides Purcell enhancement. However, incorporating organic materials using clean-room techniques has proven challenging, and has in fact so far prevented their integration into monolithic microcavities altogether. As a result, efficient, narrowband organic single-photon sources for applications in quantum information processing have remained elusive despite their considerable promise. Here, we propose three monolithic microcavity designs tailored to provide sufficient Purcell enhancement for organic quantum emitters. The Purcell effect induced by these cavities preferentially enhances emission into the 0-0 zero-phonon line, increasing spectral purity, photon extraction, and shortening the excited-state lifetime, which in turn relaxes the requirements for generating indistinguishable photons. The cavities have been optimized using Bayesian optimization and the adaptive Antoulas-Anderson (AAA) algorithm for rational approximation, which offer global optimization and the efficient reconstruction of spectra from scattering simulations, respectively. These structures are compatible with both standard clean-room processing and single-molecule preparation techniques. Therefore, they offer a clear route to realize high-quality, practically monochromatic organic single-photon light sources.

quant-ph↗

arXiv2024

Cavity-mediated hybridization of several molecules in the strong coupling regime

Molecular complexes are held together via a variety of bonds, but they all share the common feature that their individual entities are in contact. In this work, we introduce and demonstrate the concept of a \textit{molecular optical bond}, resulting from the far-field electromagnetic coupling of several molecules via a shared mode of an optical microcavity. We discuss a collective enhancement of the vacuum Rabi splitting and study super- and sub-radiant states that arise from the cavity-mediated coupling both in the resonant and dispersive regimes. Moreover, we demonstrate a two-photon transition that emerges between the ground and excited states of the new optical compound. Our experimental data are in excellent agreement with the predictions of the Tavis-Cummings Hamiltonian and open the door to the realization of hybrid light-matter materials.

cond-mat.mes-hall↗

arXiv2024

High-resolution Cryogenic Spectroscopy of Single Molecules in Nanoprinted Crystals

We perform laser spectroscopy at liquid helium temperatures (T=2 K) to investigate single dibenzoterrylene (DBT) molecules doped in anthracene crystals of nanoscopic height fabricated by electrohydrodynamic dripping. Using high-resolution fluorescence excitation spectroscopy, we show that zero-phonon lines of single molecules in printed nanocrystals are nearly as narrow as the Fourier-limited transitions observed for the same guest-host system in the bulk. Moreover, the spectral instabilities are comparable to or less than one linewidth. By recording super-resolution images of DBT molecules and varying the polarization of the excitation beam, we determine the dimensions of the printed crystals and the orientation of the crystals' axes. Electrohydrodynamic printing of organic nano and microcrystals paves the way for a series of applications, where controlled positioning of quantum emitters with narrow optical transitions is desirable.

quant-ph↗

arXiv2023

Quantum Efficiency of Single Dibenzoterrylene Molecules in para-Dichlorobenzene at Cryogenic Temperatures

We measure the quantum efficiency (QE) of individual dibenzoterrylene (DBT) molecules embedded in para-dichlorobenzene at cryogenic temperatures. To achieve this, we apply two distinct methods based on the maximal photon emission and on the power required to saturate the zero-phonon line. We find that the outcome of the two approaches are in good agreement, reporting a large fraction of molecules with QE values above 50%, with some exceeding 70%. Furthermore, we observe no correlation between the observed lower bound on the QE and the lifetime of the molecule, suggesting that most of the molecules have a QE exceeding the established lower bound. This confirms the suitability of DBT for quantum optics experiments. In light of previous reports of low QE values at ambient conditions, our results hint at the possibility of a strong temperature dependence of the QE.

quant-ph↗

arXiv2023

On-chip interference of scattering from two individual molecules in plastic

Integrated photonic circuits offer a promising route for studying coherent cooperative effects of a controlled collection of quantum emitters. However, spectral inhomogeneities, decoherence and material incompatibilities in the solid state make this a nontrivial task. Here, we demonstrate efficient coupling of a pair of organic molecules embedded in a plastic film to a TiO$_2$ microdisc resonator on a glass chip. Moreover, we tune the resonance frequencies of the molecules with respect to that of the microresonator by employing nanofabricated electrodes. For two molecules separated by a distance of about 8$\,\mu$m and an optical phase difference of about $\pi/2$, we report on a large collective extinction of the incident light in the forward direction and the destructive interference of its scattering in the backward direction. Our work sets the ground for the coherent coupling of several molecules via a common mode and the realization of polymer-based hybrid quantum photonic circuits.

quant-ph↗

arXiv2020

Nanoscopic charge fluctuations in a gallium phosphide waveguide measured by single molecules

We present efficient coupling of single organic molecules to a gallium phosphide subwavelength waveguide (nanoguide). By examining and correlating the temporal dynamics of various single-molecule resonances at different locations along the nanoguide, we reveal light-induced fluctuations of their Stark shifts. Our observations are consistent with the predictions of a simple model based on the optical activation of a small number of charges in the GaP nanostructure.

quant-ph↗

arXiv2020

The Truncated Metallo-dielectric Omnidirectional Reflector: Collecting Single Photons in the Fundamental Gaussian Mode with 95% Efficiency

We propose a novel antenna structure which funnels single photons from a single emitter with unprecedented efficiency into a low-divergence fundamental Gaussian mode. Our device relies on the concept of creating an omnidirectional photonic bandgap to inhibit unwanted large-angle emission and to enhance small-angle defect-guided-mode emission. The new photon collection strategy is intuitively illustrated, rigorously verified and optimized by implementing an efficient body-of-revolution finite-difference time-domain method for in-plane dipole emitters. We investigate a few antenna designs to cover various boundary conditions posed by fabrication processes or material restrictions and theoretically demonstrate that collection efficiencies into the fundamental Gaussian mode exceeding 95% are achievable. Our antennas are broadband, insensitive to fabrication imperfections and compatible with a variety of solid-state emitters such as organic molecules, quantum dots and defect centers in diamond. Unidirectional and low-divergence Gaussian-mode emission from a single emitter may enable the realization of a variety of photonic quantum computer architectures as well as highly efficient light-matter interfaces.

physics.optics↗

arXiv2020

Partial cloaking of a gold particle by a single molecule

Extinction of light by material particles stems from losses incurred by absorption or scattering. The extinction cross section is usually treated as an additive quantity, leading to the exponential laws that govern the macroscopic attenuation of light. In this work, we demonstrate that the extinction cross section of a large gold nanoparticle can be substantially reduced, i.e., the particle becomes more transparent, if a single molecule is placed in its near field. This partial cloaking effect results from a coherent plasmonic interaction between the molecule and the nanoparticle, whereby each of them acts as a nano-antenna to modify the radiative properties of the other.

quant-ph↗

arXiv2019

Coherent coupling of single molecules to on-chip ring resonators

We report on cryogenic coupling of organic molecules to ring microresonators obtained by looping sub-wavelength waveguides (nanoguides). We discuss fabrication and characterization of the chip-based nanophotonic elements which yield resonator finesse in the order of 20 when covered by molecular crystals. Our observed extinction dips from single molecules reach 22%, consistent with the expected Purcell enhancements up to 11 folds. Future efforts will aim at efficient coupling of a handful of molecules via their interaction with a ring microresonator mode, setting the ground for the realization of quantum optical cooperative effects.

physics.app-ph↗

arXiv2017

On-chip linear and nonlinear control of single molecules coupled to a nanoguide

While experiments with one or two quantum emitters have become routine in various laboratories, scalable platforms for efficient optical coupling of many quantum systems remain elusive. To address this issue, we report on chip-based systems made of one-dimensional subwavelength dielectric waveguides (nanoguides) and polycyclic aromatic hydrocarbon molecules. After discussing the design and fabrication requirements, we present data on coherent linear and nonlinear spectroscopy of single molecules coupled to a nanoguide mode. Our results show that external microelectrodes as well as optical beams can be used to switch the propagation of light in a nanoguide via the Stark effect and a nonlinear optical process, respectively. The presented nanoguide architecture paves the way for the investigation of many-body phenomena and polaritonic states and can be readily extended to more complex geometries for the realization of quantum integrated photonic circuits.

quant-ph↗

arXiv2012

3D optical manipulation of a single electron spin

Nitrogen vacancy (NV) centers in diamond are promising elemental blocks for quantum optics [1, 2], spin-based quantum information processing [3, 4], and high-resolution sensing [5-13]. Yet, fully exploiting these capabilities of single NV centers requires strategies to accurately manipulate them. Here, we use optical tweezers as a tool to achieve deterministic trapping and 3D spatial manipulation of individual nano-diamonds hosting a single NV spin. Remarkably, we find the NV axis is nearly fixed inside the trap and can be controlled in-situ, by adjusting the polarization of the trapping light. By combining this unique spatial and angular control with coherent manipulation of the NV spin and fluorescent lifetime measurements near an integrated photonic system, we prove optically trapped NV center as a novel route for both 3D vectorial magnetometry and sensing of the local density of optical states.

physics.optics↗

arXiv2010

Hidden progress: broadband plasmonic invisibility

The key challenge in current research into electromagnetic cloaking is to achieve invisibility over an extended bandwidth. There has been significant progress towards this using the idea of cloaking by sweeping under the carpet of Li and Pendry, with dielectric structures superposed on a mirror. Here, we show that we can harness surface plasmon polaritons at a metal surface structured with a dielectric material to obtain a unique control of their propagation. We exploit this to control plasmonic coupling and demonstrate both theoretically and experimentally cloaking over an unprecedented bandwidth (650-900 nm). Our non-resonant plasmonic metamaterial allows a curved reflector to mimic a flat mirror. Our theoretical predictions are validated by experiments mapping the surface light intensity at the wavelength 800 nm.

physics.optics↗