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Vladislav Bushmakin

Publications and source records attributed to Vladislav Bushmakin.

7 recordsLinked to original sources

High-cooperativity coupling and spin-resolved extinction of tin-vacancy centers in a diamond-like microcavity

The tin-vacancy (SnV) center in diamond is a promising spin-photon interface for quantum networks, combining favorable optical properties with spin coherence above 1K. Unfolding the full potential requires cavity enhancement to increase photon-emitter coupling efficiency. Here, we demonstrate cavity-enhanced light-matter coupling of SnV centers in a fully tunable Fabry-P\'erot microcavity operating at temperatures down to 1K with in-situ magnetic field control. We access the diamond-like regime of hybrid cavity modes through integration of low-roughness diamond membranes, where the field is concentrated inside the diamond and Purcell enhancement is maximized. Diamond-like modes deliver a more than two-fold increase in the effective Purcell factor over air-like modes, reaching $C_0 = 4.1(1)$ compared to $C_0 = 1.85(5)$ in the air-like case, while simultaneously relaxing mechanical stability requirements. Resonant probing reveals coherent cavity-emitter coupling with 96% extinction contrast and a coherent cooperativity of $C = 4.0(14)$. By applying a magnetic field, we further achieve spin-resolved cavity extinction, observing spin-selective optical transitions with a contrast of ${\cal C}_{\rm spin} = 0.91$. These results establish SnV centers in diamond coupled to open Fabry-P\'erot microcavities as a promising platform for efficient spin-photon interfaces.

quant-ph

Electrically Reconfigurable Silicon Carbide Nanophotonic Cavities on Thin-Film Lithium Niobate

Interfacing integrated photonics with solid-state spin defects holds great promise for future quantum networks, but the scaling of spin-photon architectures is hindered by frequency mismatches arising from fabrication-induced variations in photonic cavity resonances and the inhomogeneous optical transition frequencies of individual spins. These challenges call for a photonic platform with deterministic and wide-range tunability. Here, we demonstrate a hybrid nanophotonic platform based on direct bonding of silicon carbide photonic crystal nanocavity arrays onto thin-film lithium niobate on insulator, enabling deterministic electrical tuning of multiple SiC nanocavities into mutual spectral resonance. By exploiting the strong electro-optic response of lithium niobate, we achieve continuous and wide-range cavity tuning of 380 GHz ($\sim$1.1 nm), sufficient to compensate both cavity disorder and spin inhomogeneity. The nanocavities balance strong optical confinement with electrical tunability, exhibiting a theoretical Purcell factor of approximately 400. This hybrid platform enables electrically reconfigurable spin-photon interfaces for large-scale integrated quantum photonics.

physics.optics

Color-Center-Compatible Freestanding Diamond Directional Couplers for Quantum Photonics

Freestanding all-diamond color-center photonics is a promising platform for optical integration of spin-based quantum defects. Within this geometry, we realize a key building block for quantum-network interconnects: a directional coupler that acts as an on-chip beam splitter. We design and simulate directional couplers with triangular cross sections using eigenmode and finite-difference time-domain simulations and target near-50:50 splitting at visible wavelengths. We fabricate the devices directly from bulk single-crystal diamond by angled oxygen reactive-ion-beam etching followed by a dry post-release hard-mask removal process. Room-temperature measurements at $\lambda_0\approx 637 \mathrm{nm}$ yield a mean coupling ratio of $C^\mathrm{meas}=46(16) \%$. Finally, we integrate SnV$^{-}$ centers into the nanophotonic structures and observe near-lifetime-limited optical linewidths and coherent optical Rabi oscillations without post-fabrication annealing, identifying the platform as a viable route towards integrated diamond quantum photonics.

physics.optics

Optically Addressable Molecular Spins at 2D Surfaces

Optically addressable spins at material surfaces have represented a long-standing ambition in quantum sensing, providing atomic resolution and quantum-limited sensitivity. However, they are constrained by a finite depth at which the quantum spins can be stabilized. Here, we demonstrate a hybrid molecular-2D architecture that realizes quantum spin sensors directly on top of the surface. By anchoring spin-active molecules onto hexagonal boron nitride (hBN), we eliminate the depth of the quantum sensor while also exhibiting robust spin properties from 4~K to room temperature (RT). The Hahn-echo spin coherence time exceeds \(T_2 = 3.4~\upmu\text{s}\) at 4~K, outperforming values in bulk organic crystals and overturning the prevailing expectation that spin inevitably deteriorates upon approaching the surface. By chemically tuning the molecule through deuteration, \(T_2\) improves by more than 10-fold, and under dynamic decoupling, coherence is prolonged to the intrinsic lifetime limit, exceeding 300~\(\upmu\text{s}\). Proximal proton spins and the magnetic response of two-dimensional magnets beneath the hBN layer have been detected at RT. These molecular spins form surface quantum sensors with long coherence, optical addressability, and interfacial versatility, enabling a scalable, adaptable architecture beyond what conventional solid-state platforms offer.

quant-ph

Two-Photon Interference of Photons from Remote Tin-Vacancy Centers in Diamond

Scalable quantum networks rely on optical connections between long-lived qubits to distribute entanglement. Tin vacancies in diamond have emerged as promising long-lived qubits, offering extended spin coherence times at liquid helium temperatures and spin-dependent, highly coherent optical transitions for effective photon-based communication. Connecting remote nodes requires quantum interference of indistinguishable photons, which is challenging in an inhomogeneous solid-state environment. Here, we demonstrate a two-node experiment with tin vacancies in diamond, which exhibit a resonant frequency distribution spanning approximately 8 GHz. To overcome the frequency mismatch, we tune the resonant frequencies of one node using the Stark effect. We achieve tunability up to 4 GHz while maintaining optical coherence. As a demonstration, we achieve detuning-dependent remote two-photon interference between separate nodes, obtaining 80(6)% interference visibility without postprocessing when the defects' optical transitions are tuned into resonance, and 63(8)% with detuning up to 20 times their natural linewidths. These results highlight the potential of tin-vacancy centres in diamond for establishing robust optical links between remote quantum registers.

quant-ph

The silicon vacancy centers in SiC: determination of intrinsic spin dynamics for integrated quantum photonics

The negatively-charged silicon vacancy center ($\rm V_{Si}^-$) in silicon carbide (SiC) is an emerging color center for quantum technology covering quantum sensing, communication, and computing. Yet, limited information currently available on the internal spin-optical dynamics of these color centers prevents us achieving the optimal operation conditions and reaching the maximum performance especially when integrated within quantum photonics. Here, we establish all the relevant intrinsic spin dynamics of negatively charged $\rm V_{Si}^-$ center in 4H-SiC by an in-depth electronic fine structure modeling including intersystem-crossing and deshelving mechanisms. With carefully designed spin-dependent measurements, we obtain all previously unknown spin-selective radiative and non-radiative decay rates. To showcase the relevance of our work for integrated quantum photonics, we use the obtained rates to propose a realistic implementation of time-bin entangled multi-photon GHZ and cluster state generation. We find that up to 3-photon GHZ/cluster states are readily within reach using the existing nanophotonic cavity technology.

quant-ph

A narrow-band sodium-resonant fiber-coupled single photon source

Quantum technology requires the creation and control over single photons as an important resource. We present a single photon source based on a single molecule which is attached to the end-facet of an optical fiber. To realize a narrow linewidth, the system is cooled down to liquid-helium temperatures. The molecule is optically excited and its fluorescence is collected through the fiber. We have recorded an excitation spectrum, a saturation curve and analyzed the contributions of Raman background fluorescence. This presents to date the crucial limit for the introduced device. The single photon nature is proven by an anti-bunched auto-correlation recording, which also shows coherent Rabi oscillations.

quant-ph