arXiv subjects

Lukas Antoniuk

Publications and source records attributed to Lukas Antoniuk.

9 recordsLinked to original sources

arXiv2023

Controlling all Degrees of Freedom of the Optical Coupling in Hybrid Quantum Photonics

Nanophotonic quantum devices can significantly boost light-matter interaction which is important for applications such as quantum networks. Reaching a high interaction strength between an optical transition of a spin system and a single mode of light is an essential step which demands precise control over all degrees of freedom of the optical coupling. While current devices have reached a high accuracy of emitter positioning, the placement process remains overall statistically, reducing the device fabrication yield. Furthermore, not all degrees of freedom of the optical coupling can be controlled limiting the device performance. Here, we develop a hybrid approach based on negatively-charged silicon-vacancy center in nanodiamonds coupled to a mode of a Si$_3$N$_4$-photonic crystal cavity, where all terms of the coupling strength can be controlled individually. We use the frequency of coherent Rabi-oscillations and line-broadening as a measure of the device performance. This allows for iterative optimization of the position and the rotation of the dipole with respect to individual, preselected modes of light. Therefore, our work marks an important step for optimization of hybrid quantum photonics and enables to align device simulations with real device performance.

quant-ph↗

arXiv2023

All-Optical Spin Initialization via a Cavity Broadened Optical Transition in On-Chip Hybrid Quantum Photonics

Hybrid quantum photonic systems connect classical photonics to the quantum world and promise to deliver efficient light-matter quantum interfaces while leveraging the advantages of both, the classical and the quantum, subsystems. However, combining efficient, scalable photonics and solid state quantum systems with desirable optical and spin properties remains a formidable challenge. In particular the access to individual spin states and coherent mapping to photons remains unsolved for these systems. In this letter, we demonstrate all-optical initialization and readout of the electronic spin of a negatively-charged silicon-vacancy center in a nanodiamond coupled to a silicon nitride photonic crystal cavity. We characterize relevant parameters of the coupled emitter-cavity system and determine the silicon-vacancy center's spin-relaxation and spin-decoherence rate. Our results mark an important step towards the realization of a hybrid spin-photon interface based on silicon nitride photonics and the silicon-vacancy center's electron spin in nanodiamonds with potential use for quantum networks, quantum communication and distributed quantum computation.

quant-ph↗

arXiv2023

Room Temperature Fiber-Coupled single-photon devices based on Colloidal Quantum Dots and SiV centers in Back Excited Nanoantennas

We demonstrate an important step towards on chip integration of single photon sources operating at room temperature fiber coupling of a directional quantum emitter with back-excitation. Directionality is achieved with a hybrid metal-dielectric bullseye antenna, while back-excitation is permitted by placement of the emitter at or in a sub-wavelength hole positioned at the bullseye center. Overall, the unique design enables a direct laser excitation from the back of the on-chip device and very efficient coupling of the highly collimated photon emission to either low numerical aperture (NA) free space optics or directly to an optical fiber from the front. To show the versatility of the concept, we fabricate devices containing either a colloidal quantum dot or a silicon-vacancy center containing nanodiamond, which are accurately coupled to the nano-antenna using two different nano-positioning methods. Both back-excited devices display front collection efficiencies of about 70 % at NAs as low as 0.5. Moreover, the combination of back-excitation with forward low-NA directionality enables direct coupling of the emitted photons into a proximal optical fiber without the need of any coupling optics, thereby facilitating and greatly simplifying future integration.

physics.optics↗

arXiv2022

A Quantum Repeater Platform based on Single SiV$^-$ Centers in Diamond with Cavity-Assisted, All-Optical Spin Access and Fast Coherent Driving

Quantum key distribution enables secure communication based on the principles of quantum mechanics. The distance in fiber-based quantum communication is limited to about a hundred kilometers due to signal attenuation. Thus, quantum repeaters are required to establish large-scale quantum networks. Ideal quantum repeater nodes possess a quantum memory which is efficiently connected to photons, the carrier of quantum information. Color centers in diamond and, in particular, the negatively-charged silicon-vacancy centers are promising candidates to establish such nodes. The major obstacle is an inefficient connection between the color centers spin to the Gaussian optics of fiber networks. Here, we present an efficient spin-photon interface. Individual silicon-vacancy centers coupled to the mode of a hemispherical Fabry-Pérot microcavity show Purcell-factors larger than 1 when operated in a bath of liquid Helium. We demonstrate coherent optical driving with a Rabi frequency of $290\,\mathrm{MHz}$ and all-optical access to the electron spin in strong magnetic fields of up to $3.2\,\mathrm{T}$. Spin initialization within $67\,\mathrm{ns}$ with a fidelity of $80\,\%$ and a lifetime of $350\,\mathrm{ns}$ are reached inside the cavity. The spin-photon interface is passively stable, enabled by placing a color center containing nanodiamond in the hemispherical Fabry-Pérot mirror structure and by choosing short cavity lengths. Therefore, our demonstration opens the way to realize quantum repeater applications.

quant-ph↗

arXiv2022

Hybrid Quantum Nanophotonics: Interfacing Color Center in Nanodiamonds with Si3N4-Photonics

This chapter covers recent developments in the field of hybrid quantum photonics based on color centers in nanodiamonds and Si3N4-photonics towards a technology platform with applications in quantum information processing and quantum information distribution. The methodological approach can be divided in three main tasks. First, the fabrication and optimization of Si3N4-photonics. Second, the creation, characterization and control of color centers in nanodiamonds. Third, the assembly of hybrid quantum photonics by integrating the nanodiamonds into the photonic structures. One focus will be the efficient interfacing of the color centers done by optimizing the optical coupling. The chapter describes recent progress in all three steps and summarizes the established hybrid platform. We believe, that the hybrid approach provides a promising path to realize quantum photonic applications, such as quantum networks or quantum repeaters, in the near future.

quant-ph↗

arXiv2021

Hybrid quantum photonics based on artificial atoms placed inside one hole of a photonic crystal cavity

Spin-based quantum photonics promise to realize distributed quantum computing and quantum networks. The performance depends on efficient entanglement distribution, where the efficiency can be boosted by means of cavity quantum electrodynamics. The central challenge is the development of compact devices with large spin-photon coupling rates and high operation bandwidth. Photonic crystal cavities comprise strong field confinement but put high demands on accurate positioning of an atomic system in the mode field maximum. Color center in diamond, and in particular the negatively-charged Silicon-Vacancy center, emerged as a promising atom-like systems. Large spectral stability and access to long-lived, nuclear spin memories enabled elementary demonstrations of quantum network nodes including memory-enhanced quantum communication. In a hybrid approach, we deterministically place SiV$^-$-containing nanodiamonds inside one hole of a one-dimensional, free-standing, Si$_3$N$_4$-based photonic crystal cavity and coherently couple individual optical transitions to the cavity mode. We optimize the light-matter coupling by utilizing two-mode composition, waveguiding, Purcell-enhancement and cavity resonance tuning. The resulting photon flux is increased by more than a factor of 14 as compared to free-space. The corresponding lifetime shortening to below 460 ps puts the potential operation bandwidth beyond GHz rates. Our results mark an important step to realize quantum network nodes based on hybrid quantum photonics with SiV$^-$- center in nanodiamonds.

cond-mat.mtrl-sci↗

arXiv2020

Purcell-Enhanced Emission from Individual SiV$^-$ Center in Nanodiamonds Coupled to a Si$_3$N$_4$-Based, Photonic Crystal Cavity

Hybrid quantum photonics combines classical photonics with quantum emitters in a postprocessing step. It facilitates to link ideal quantum light sources to optimized photonic platforms. Optical cavities enable to harness the Purcell-effect boosting the device efficiency. Here, we postprocess a free-standing, crossed-waveguide photonic crystal cavity based on Si$_3$N$_4$ with SiV$^-$ center in nanodiamonds. We develop a routine that holds the capability to optimize all degrees of freedom of the evanescent coupling term utilizing AFM nanomanipulation. After a few optimization cycles we resolve the fine-structure of individual SiV$^-$ centers and achieve a Purcell enhancement of more than 4 on individual optical transitions, meaning that four out of five spontaneously emitted photons are channeled into the photonic device. Our work opens up new avenues to construct efficient quantum photonic devices.

cond-mat.mtrl-sci↗

arXiv2019

Preparing single SiV$^{-}$ center in nanodiamonds for external, optical coupling with access to all degrees of freedom

Optical coupling enables intermediate- and long-range interactions between distant quantum emitters. Such interaction may be the basic element in bottom-up approaches of coupled spin systems or for integrated quantum photonics and quantum plasmonics. Here, we prepare nanodiamonds carrying single, negatively-charged silicon-vacancy centers for evanescent optical coupling with access to all degrees of freedom by means of atomic force nanomanipulation. The color centers feature excellent optical properties, comparable to silicon-vacancy centers in bulk diamond, resulting in a resolvable fine structure splitting, a linewidth close to the Fourier-Transform limit under resonant excitation and a good polarization contrast. We determine the orbital relaxation time $T_{1}$ of the orbitally split ground states and show that all optical properties are conserved during translational nanomanipulation. Furthermore, we demonstrate the rotation of the nanodiamonds. In contrast to the translational operation, the rotation leads to a change in polarization contrast. We utilize the change in polarization contrast before and after nanomanipulation to determine the rotation angle. Finally, we evaluate the likelihood for indistinguishable, single photon emission of silicon-vacancy centers located in different nanodiamonds. Our work enables ideal evanescent, optical coupling of distant nanodiamonds containing silicon-vacancy centers with applications in the realization of quantum networks, quantum repeaters or complex quantum systems.

cond-mat.mtrl-sci↗

arXiv2018

Single SiV$^-$ centers in low-strain nanodiamonds with bulk-like spectral properties and nano-manipulation capabilities

We report on the isolation of single SiV$^-$ centers in nanodiamonds. We observe the fine-structure of single SiV$^-$ center with improved inhomogeneous ensemble linewidth below the excited state splitting, stable optical transitions, good polarization contrast and excellent spectral stability under resonant excitation. Based on our experimental results we elaborate an analytical strain model where we extract the ratio between strain coefficients of excited and ground states as well the intrinsic zero-strain spin-orbit splittings. The observed strain values are as low as best values in low-strain bulk diamond. We achieve our results by means of H-plasma treatment of the diamond surface and in combination with resonant and off-resonant excitation. Our work paves the way for indistinguishable, single photon emission. Furthermore, we demonstrate controlled nano-manipulation via atomic force microscope cantilever of 1D- and 2D-alignments with a so-far unreached accuracy of about 10nm, as well as new tools including dipole rotation and cluster decomposition. Combined, our results show the potential to utilize SiV$^-$ centers in nanodiamonds for the controlled interfacing via optical coupling of individually well-isolated atoms for bottom-up assemblies of complex quantum systems.

cond-mat.mes-hall↗