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Tzu-Yung Huang

Publications and source records attributed to Tzu-Yung Huang.

11 recordsLinked to original sources
arXiv2025

Quadrupolar resonance spectroscopy of individual nuclei using a room-temperature quantum sensor

Nuclear quadrupolar resonance (NQR) spectroscopy reveals chemical bonding patterns in materials and molecules through the unique coupling between nuclear spins and local fields. However, traditional NQR techniques require macroscopic ensembles of nuclei to yield a detectable signal, which precludes the study of individual molecules and obscures molecule-to-molecule variations due to local perturbations or deformations. Optically active electronic spin qubits, such as the nitrogen-vacancy (NV) center in diamond, facilitate the detection and control of individual nuclei through their local magnetic couplings. Here, we use NV centers to perform NQR spectroscopy on their associated nitrogen-14 ($^{14}$N) nuclei at room temperature. In mapping the nuclear quadrupolar Hamiltonian, we resolve minute variations between individual nuclei. The measurements further reveal correlations between the parameters in the NV center's electronic spin Hamiltonian and the $^{14}$N quadropolar Hamiltonian, as well as a previously unreported Hamiltonian term that results from symmetry breaking. We further design pulse sequences to initialize, readout, and control the quantum evolution of the $^{14}$N nuclear state using the nuclear quadrupolar Hamiltonian.

cond-mat.mes-hall↗
arXiv2024

Electronic Noise Considerations for Designing Integrated Solid-State Quantum Memories

As quantum networks expand and are deployed outside research laboratories, a need arises to design and integrate compact control electronics for each memory node. It is essential to understand the performance requirements for such systems, especially concerning tolerable levels of noise, since these specifications dramatically affect a system's design complexity and cost. Here, using an approach that can be easily generalized across quantum-hardware platforms, we present a case study based on nitrogen-vacancy (NV) centers in diamond. We model and experimentally verify the effects of phase noise and timing jitter in the control system in conjunction with the spin qubit's environmental noise. We further consider the impact of different phase noise characteristics on the fidelity of dynamical decoupling sequences. The results demonstrate a procedure to specify design requirements for integrated quantum control signal generators for solid-state spin qubits, depending on their coherence time, intrinsic noise spectrum, and required fidelity.

quant-ph↗
arXiv2023

Nanodiamond emulsions for enhanced quantum sensing and click-chemistry conjugation

Nanodiamonds containing nitrogen-vacancy (NV) centers can serve as colloidal quantum sensors of local fields in biological and chemical environments. However, nanodiamond surfaces are challenging to modify without degrading their colloidal stability or the NV center's optical and spin properties. Here, we report a simple and general method to coat nanodiamonds with a thin emulsion layer that preserves their quantum features, enhances their colloidal stability, and provides functional groups for subsequent crosslinking and click-chemistry conjugation reactions. To demonstrate this technique, we decorate the nanodiamonds with combinations of carboxyl- and azide-terminated amphiphiles that enable conjugation using two different strategies. We study the effect of the emulsion layer on the NV center's spin lifetime, and we quantify the nanodiamonds' chemical sensitivity to paramagnetic ions using $T_1$ relaxometry. This general approach to nanodiamond surface functionalization will enable advances in quantum nanomedicine and biological sensing.

cond-mat.mes-hall↗
arXiv2023

Room Temperature Dynamics of an Optically Addressable Single Spin in Hexagonal Boron Nitride

Hexagonal boron nitride (h-BN) hosts pure single-photon emitters that have shown evidence of optically detected electronic spin dynamics. However, the electrical and chemical structure of these optically addressable spins is unknown, and the nature of their spin-optical interactions remains mysterious. Here, we use time-domain optical and microwave experiments to characterize a single emitter in h-BN exhibiting room temperature optically detected magnetic resonance. Using dynamical simulations, we constrain and quantify transition rates in the model, and we design optical control protocols that optimize the signal-to-noise ratio for spin readout. This constitutes a necessary step towards quantum control of spin states in h-BN.

cond-mat.mes-hall↗
arXiv2022

Photon emission correlation spectroscopy as an analytical tool for quantum defects

Photon emission correlation spectroscopy is an indispensable tool for the study of atoms, molecules, and, more recently, solid-state quantum defects. In solid-state systems, its most common use is as an indicator of single-photon emission, a key property for quantum technology. Beyond an emitter's single-photon purity, however, photon correlation measurements can provide a wealth of information that can reveal details about its electronic structure and optical dynamics that are hidden by other spectroscopy techniques. This tutorial presents a standardized framework for using photon emission correlation spectroscopy to study quantum emitters, including discussion of theoretical background, considerations for data acquisition and statistical analysis, and interpretation. We highlight important nuances and best practices regarding the commonly-used $g^{(2)}(τ=0)<0.5$ test for single-photon emission. Finally, we illustrate how this experimental technique can be paired with optical dynamics simulations to formulate an electronic model for unknown quantum emitters, enabling the design of quantum control protocols and assessment of their suitability for quantum information science applications.

quant-ph↗
arXiv2022

Probing the Optical Dynamics of Quantum Emitters in Hexagonal Boron Nitride

Hexagonal boron nitride is a van der Waals material that hosts visible-wavelength quantum emitters at room temperature. However, experimental identification of the quantum emitters' electronic structure is lacking, and key details of their charge and spin properties remain unknown. Here, we probe the optical dynamics of quantum emitters in hexagonal boron nitride using photon emission correlation spectroscopy. Several quantum emitters exhibit ideal single-photon emission with noise-limited photon antibunching, $g^{(2)}(0)=0$. The photoluminescence emission lineshapes are consistent with individual vibronic transitions. However, polarization-resolved excitation and emission suggests the role of multiple optical transitions, and photon emission correlation spectroscopy reveals complicated optical dynamics associated with excitation and relaxation through multiple electronic excited states. We compare the experimental results to quantitative optical dynamics simulations, develop electronic structure models that are consistent with the observations, and discuss the results in the context of ab initio theoretical calculations.

cond-mat.mes-hall↗
arXiv2021

Template-Assisted Self Assembly of Fluorescent Nanodiamonds for Scalable Quantum Technologies

Milled nanodiamonds containing nitrogen-vacancy (NV) centers provide an excellent platform for sensing applications as they are optically robust, have nanoscale quantum sensitivity, and form colloidal dispersions which enable bottom-up assembly techniques for device integration. However, variations in their size, shape, and surface chemistry limit the ability to position individual nanodiamonds and statistically study properties that affect their optical and quantum characteristics. Here, we present a scalable strategy to form ordered arrays of nanodiamonds using capillary-driven, template-assisted self assembly. This method enables the precise spatial arrangement of isolated nanodiamonds with diameters below 50 nm across millimeter-scale areas. Measurements of over 200 assembled nanodiamonds yield a statistical understanding of their structural, optical, and quantum properties. The NV centers' spin and charge properties are uncorrelated with nanodiamond size, but rather are consistent with heterogeneity in their nanoscale environment. This flexible assembly method, together with improved understanding of the material, will enable the integration of nanodiamonds into future quantum photonic and electronic devices.

cond-mat.mes-hall↗
arXiv2019

Real-Time Charge Initialization of Diamond Nitrogen-Vacancy Centers for Enhanced Spin Readout

A common impediment to qubit performance is imperfect state initialization. In the case of the diamond nitrogen-vacancy (NV) center, the initialization fidelity is limited by fluctuations in the defect's charge state during optical pumping. Here, we use real-time control to deterministically initialize the NV center's charge state at room temperature. We demonstrate a maximum charge initialization fidelity of 99.4$\pm$0.1% and present a quantitative model of the initialization process that allows for systems-level optimization of the spin-readout signal-to-noise ratio. Even accounting for the overhead associated with the initialization sequence, increasing the charge initialization fidelity from the steady-state value of 75% near to unity allows for a factor-of-two speedup in experiments while maintaining the same signal-to-noise-ratio. In combination with high-fidelity readout based on spin-to-charge conversion, real-time initialization enables a factor-of-20 speedup over traditional methods, resulting in an ac magnetic sensitivity of 1.3 nT/Hz$^{1/2}$ for our single NV-center spin. The real-time control method is immediately beneficial for quantum sensing applications with NV centers as well as probing charge-dependent physics, and it will facilitate protocols for quantum feedback control over multi-qubit systems.

quant-ph↗
arXiv2017

Imaging a Nitrogen-Vacancy Center with a Diamond Immersion Metalens

Solid-state quantum emitters have emerged as robust single-photon sources and addressable spins: key components in rapidly developing quantum technologies for broadband magnetometry, biological sensing, and quantum information science. Performance in these applications, be it magnetometer sensitivity or quantum key generation rate, is limited by the number of photons detected. However, efficient collection of a quantum emitter's photoluminescence (PL) is challenging as its atomic scale necessitates diffraction-limited imaging with nanometer-precision alignment, oftentimes at cryogenic temperatures. In this letter, we image an individual quantum emitter, an isolated nitrogen-vacancy (NV) center in diamond, using a dielectric metalens composed of subwavelength pillars etched into the diamond's surface. The metalens eliminates the need for an objective by operating as a high-transmission-efficiency immersion lens with a numerical aperture (NA) greater than 1.0. This design provides a scalable approach for fiber coupling solid-state quantum emitters that will enable the development of deployable quantum devices.

physics.optics↗