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Joonhee Choi

Publications and source records attributed to Joonhee Choi.

30 records · Page 2Linked to original sources

Many-body cavity quantum electrodynamics with driven inhomogeneous emitters

Quantum emitters coupled to optical resonators are quintessential systems for exploring fundamental phenomena in cavity quantum electrodynamics (cQED) and are commonly used in quantum devices acting as qubits, memories and transducers. Many previous experimental cQED studies have focused on regimes in which a small number of identical emitters interact with a weak external drive, such that the system can be described with simple, effective models. However, the dynamics of a disordered, many-body quantum system subject to a strong drive have not been fully explored, despite its importance and potential in quantum applications. Here we study how a large, inhomogeneously broadened ensemble of solid-state emitters coupled with high cooperativity to a nanophotonic resonator behaves under strong excitation. We discover a sharp, collectively induced transparency (CIT) in the cavity reflection spectrum, resulting from quantum interference and collective response induced by the interplay between driven inhomogeneous emitters and cavity photons. Furthermore, coherent excitation within the CIT window leads to highly nonlinear optical emission, spanning from fast superradiance to slow subradiance. These phenomena in the many-body cQED regime enable new mechanisms for achieving slow light and frequency referencing, pave a way towards solid-state superradiant lasers and inform the development of ensemble-based quantum interconnects.

quant-ph↗

Nuclear spin-wave quantum register for a solid state qubit

Solid-state nuclear spins surrounding individual, optically addressable qubits provide a crucial resource for quantum networks, computation and simulation. While hosts with sparse nuclear spin baths are typically chosen to mitigate qubit decoherence, developing coherent quantum systems in nuclear spin-rich hosts enables exploration of a much broader range of materials for quantum information applications. The collective modes of these dense nuclear spin ensembles provide a natural basis for quantum storage, however, utilizing them as a resource for single spin qubits has thus far remained elusive. Here, by using a highly coherent, optically addressed 171Yb3+ qubit doped into a nuclear spin-rich yttrium orthovanadate crystal, we develop a robust quantum control protocol to manipulate the multi-level nuclear spin states of neighbouring 51V5+ lattice ions. Via a dynamically-engineered spin exchange interaction, we polarise this nuclear spin ensemble, generate collective spin excitations, and subsequently use them to implement a long-lived quantum memory. We additionally demonstrate preparation and measurement of maximally entangled 171Yb--51V Bell states. Unlike conventional, disordered nuclear spin based quantum memories, our platform is deterministic and reproducible, ensuring identical quantum registers for all 171Yb qubits. Our approach provides a framework for utilising the complex structure of dense nuclear spin baths, paving the way for building large-scale quantum networks using single rare-earth ion qubits.

quant-ph↗

Emergent quantum state designs from individual many-body wavefunctions

Quantum chaos in many-body systems provides a bridge between statistical and quantum physics with strong predictive power. This framework is valuable for analyzing properties of complex quantum systems such as energy spectra and the dynamics of thermalization. While contemporary methods in quantum chaos often rely on random ensembles of quantum states and Hamiltonians, this is not reflective of most real-world systems. In this paper, we introduce a new perspective: across a wide range of examples, a single non-random quantum state is shown to encode universal and highly random quantum state ensembles. We characterize these ensembles using the notion of quantum state $k$-designs from quantum information theory and investigate their universality using a combination of analytic and numerical techniques. In particular, we establish that $k$-designs arise naturally from generic states as well as individual states associated with strongly interacting, time-independent Hamiltonian dynamics. Our results offer a new approach for studying quantum chaos and provide a practical method for sampling approximately uniformly random states; the latter has wide-ranging applications in quantum information science from tomography to benchmarking.

quant-ph↗

High-Fidelity Entanglement and Detection of Alkaline-Earth Rydberg Atoms

Trapped neutral atoms have become a prominent platform for quantum science, where entanglement fidelity records have been set using highly-excited Rydberg states. However, controlled two-qubit entanglement generation has so far been limited to alkali species, leaving the exploitation of more complex electronic structures as an open frontier that could lead to improved fidelities and fundamentally different applications such as quantum-enhanced optical clocks. Here we demonstrate a novel approach utilizing the two-valence electron structure of individual alkaline-earth Rydberg atoms. We find fidelities for Rydberg state detection, single-atom Rabi operations, and two-atom entanglement surpassing previously published values. Our results pave the way for novel applications, including programmable quantum metrology and hybrid atom-ion systems, and set the stage for alkaline-earth based quantum computing architectures.

physics.atom-ph↗

Probing and manipulating embryogenesis via nanoscale thermometry and temperature control

Understanding the coordination of cell division timing is one of the outstanding questions in the field of developmental biology. One active control parameter of the cell cycle duration is temperature, as it can accelerate or decelerate the rate of biochemical reactions. However, controlled experiments at the cellular-scale are challenging due to the limited availability of biocompatible temperature sensors as well as the lack of practical methods to systematically control local temperatures and cellular dynamics. Here, we demonstrate a method to probe and control the cell division timing in Caenorhabditis elegans embryos using a combination of local laser heating and nanoscale thermometry. Local infrared laser illumination produces a temperature gradient across the embryo, which is precisely measured by in-vivo nanoscale thermometry using quantum defects in nanodiamonds. These techniques enable selective, controlled acceleration of the cell divisions, even enabling an inversion of division order at the two cell stage. Our data suggest that the cell cycle timing asynchrony of the early embryonic development in C. elegans is determined independently by individual cells rather than via cell-to-cell communication. Our method can be used to control the development of multicellular organisms and to provide insights into the regulation of cell division timings as a consequence of local perturbations.

physics.bio-ph↗

Robust Dynamic Hamiltonian Engineering of Many-Body Spin Systems

We introduce a new approach for the robust control of quantum dynamics of strongly interacting many-body systems. Our approach involves the design of periodic global control pulse sequences to engineer desired target Hamiltonians that are robust against disorder, unwanted interactions and pulse imperfections. It utilizes a matrix representation of the Hamiltonian engineering protocol based on time-domain transformations of the Pauli spin operator along the quantization axis. This representation allows us to derive a concise set of algebraic conditions on the sequence matrix to engineer robust target Hamiltonians, enabling the simple yet systematic design of pulse sequences. We show that this approach provides an efficient framework to (i) treat any secular many-body Hamiltonian and engineer it into a desired form, (ii) target dominant disorder and interaction characteristics of a given system, (iii) achieve robustness against imperfections, (iv) provide optimal sequence length within given constraints, and (v) substantially accelerate numerical searches of pulse sequences. Using this systematic approach, we develop novel sets of pulse sequences for the protection of quantum coherence, optimal quantum sensing and quantum simulation. Finally, we experimentally demonstrate the robust operation of these sequences in a system with the most general interaction form.

quant-ph↗

Quantum Metrology with Strongly Interacting Spin Systems

Quantum metrology makes use of coherent superpositions to detect weak signals. While in principle the sensitivity can be improved by increasing the density of sensing particles, in practice this improvement is severely hindered by interactions between them. Using a dense ensemble of interacting electronic spins in diamond, we demonstrate a novel approach to quantum metrology. It is based on a new method of robust quantum control, which allows us to simultaneously eliminate the undesired effects associated with spin-spin interactions, disorder and control imperfections, enabling a five-fold enhancement in coherence time compared to conventional control sequences. Combined with optimal initialization and readout protocols, this allows us to break the limit for AC magnetic field sensing imposed by interactions, opening a promising avenue for the development of solid-state ensemble magnetometers with unprecedented sensitivity.

quant-ph↗

Probing quantum thermalization of a disordered dipolar spin ensemble with discrete time-crystalline order

We investigate thermalization dynamics of a driven dipolar many-body quantum system through the stability of discrete time crystalline order. Using periodic driving of electronic spin impurities in diamond, we realize different types of interactions between spins and demonstrate experimentally that the interplay of disorder, driving and interactions leads to several qualitatively distinct regimes of thermalization. For short driving periods, the observed dynamics are well described by an effective Hamiltonian which sensitively depends on interaction details. For long driving periods, the system becomes susceptible to energy exchange with the driving field and eventually enters a universal thermalizing regime, where the dynamics can be described by interaction-induced dephasing of individual spins. Our analysis reveals important differences between thermalization of long-range Ising and other dipolar spin models.

quant-ph↗

Controlling the coherence of a diamond spin qubit through strain engineering

The uncontrolled interaction of a quantum system with its environment is detrimental for quantum coherence. In the context of solid-state qubits, techniques to mitigate the impact of fluctuating electric and magnetic fields from the environment are well-developed. In contrast, suppression of decoherence from thermal lattice vibrations is typically achieved only by lowering the temperature of operation. Here, we use a nano-electro-mechanical system (NEMS) to mitigate the effect of thermal phonons on a solid-state quantum emitter without changing the system temperature. We study the silicon-vacancy (SiV) colour centre in diamond which has optical and spin transitions that are highly sensitive to phonons. First, we show that its electronic orbitals are highly susceptible to local strain, leading to its high sensitivity to phonons. By controlling the strain environment, we manipulate the electronic levels of the emitter to probe, control, and eventually, suppress its interaction with the thermal phonon bath. Strain control allows for both an impressive range of optical tunability and significantly improved spin coherence. Finally, our findings indicate that it may be possible to achieve strong coupling between the SiV spin and single phonons, which can lead to the realisation of phonon-mediated quantum gates and nonlinear quantum phononics.

quant-ph↗

Critical thermalization of a disordered dipolar spin system in diamond

Statistical mechanics underlies our understanding of macroscopic quantum systems. It is based on the assumption that out-of-equilibrium systems rapidly approach their equilibrium states, forgetting any information about their microscopic initial conditions. This fundamental paradigm is challenged by disordered systems, in which a slowdown or even absence of thermalization is expected. We report the observation of critical thermalization in a three dimensional ensemble of $\sim 10^6$ electronic spins coupled via dipolar interactions. By controlling the spin states of nitrogen vacancy color centers in diamond, we observe slow, sub-exponential relaxation dynamics and identify a regime of power-law decay with disorder-dependent exponents; this behavior is modified at late times owing to many-body interactions. These observations are quantitatively explained by a resonance counting theory that incorporates the effects of both disorder and interactions.

cond-mat.mes-hall↗

Observation of discrete time-crystalline order in a disordered dipolar many-body system

Understanding quantum dynamics away from equilibrium is an outstanding challenge in the modern physical sciences. It is well known that out-of-equilibrium systems can display a rich array of phenomena, ranging from self-organized synchronization to dynamical phase transitions. More recently, advances in the controlled manipulation of isolated many-body systems have enabled detailed studies of non-equilibrium phases in strongly interacting quantum matter. As a particularly striking example, the interplay of periodic driving, disorder, and strong interactions has recently been predicted to result in exotic "time-crystalline" phases, which spontaneously break the discrete time-translation symmetry of the underlying drive. Here, we report the experimental observation of such discrete time-crystalline order in a driven, disordered ensemble of $\sim 10^6$ dipolar spin impurities in diamond at room-temperature. We observe long-lived temporal correlations at integer multiples of the fundamental driving period, experimentally identify the phase boundary and find that the temporal order is protected by strong interactions; this order is remarkably stable against perturbations, even in the presence of slow thermalization. Our work opens the door to exploring dynamical phases of matter and controlling interacting, disordered many-body systems.

quant-ph↗

Depolarization dynamics in a strongly interacting solid-state spin ensemble

We study the depolarization dynamics of a dense ensemble of dipolar interacting spins, associated with nitrogen-vacancy centers in diamond. We observe anomalously fast, density-dependent, and non-exponential spin relaxation. To explain these observations, we propose a microscopic model where an interplay of long-range interactions, disorder, and dissipation leads to predictions that are in quantitative agreement with both current and prior experimental results. Our results pave the way for controlled many-body experiments with long-lived and strongly interacting ensembles of solid-state spins.

quant-ph↗