arXiv subjects

Cheng-I Ho

Publications and source records attributed to Cheng-I Ho.

6 recordsLinked to original sources

arXiv2026

Revealing and reducing growth-induced interfacial disorder in preferentially aligned nitrogen-vacancy centers in diamond

Nitrogen-vacancy (NV) centers in chemical-vapor-deposition (CVD) diamond can form preferentially oriented ensembles with high sensing performance and low densities of lattice defects. Thin films of this material are a cornerstone of various imaging modalities. However, nitrogen injection needed to produce such films can transiently drive growth out of equilibrium, generating interfacial strain and spin defects that degrade NV coherence. Here, we investigate this disorder in $^{12}\text{C}$-enriched, preferentially oriented NV layers grown on (111) diamond using two nitrogen-injection procedures, combined with nanometer-scale selective plasma etching and NV spin-coherence measurements. Pulsed nitrogen injection produces a pronounced nitrogen overshoot within a 60--80 nm interfacial region, generating excessive amounts of defects. By contrast, smooth nitrogen delivery through mass flow controllers substantially suppresses interfacial disorder, yielding coherence properties close to the theoretical limit imposed by spin-bath noise. A 50-nm NV layer is used to demonstrate proton nuclear magnetic resonance detection. This work reveals the role of interfacial disorder associated with the nitrogen-doping procedure and provides a route to growing high-quality, thin NV-doped layers for quantum-sensing applications.

quant-ph↗

arXiv2026

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↗

arXiv2025

Readout of a solid state spin ensemble at the projection noise limit

Spin ensembles are central to quantum science, from frequency standards and fundamental physics searches to magnetic resonance spectroscopy and quantum sensing. Their performance is ultimately constrained by spin projection noise, yet solid-state implementations have so far been limited by much larger photon shot noise. Here we demonstrate a direct, quantum non-demolition readout of a mesoscopic ensemble of nitrogen-vacancy (NV) centers in diamond that surpasses the photon shot-noise limit and approaches the intrinsic spin projection noise. By stabilizing the $^{14}$N nuclear spin bath at high magnetic fields and employing repetitive nuclear-assisted spin readout, we achieve a noise reduction of 3.8 dB below the thermal projection noise level. This enables direct access to the intrinsic fluctuations of the spin ensemble, allowing us to directly observe the signatures of correlated spin states. Our results establish projection noise-limited readout as a practical tool for solid-state quantum sensors, opening pathways to quantum-enhanced metrology, direct detection of many-body correlations, and the implementation of spin squeezing in mesoscopic solid-state ensembles.

quant-ph↗

arXiv2025

Deformation-Driven Enhancement of Spin Defect Emission in Hexagonal Boron Nitride

The negatively charged boron vacancy (VB-) in hexagonal boron nitride (hBN) has been extensively investigated as it offers a novel playground for two-dimensional quantum sensing, with ultimate proximity to target samples. However, its practical sensitivity is limited by the intrinsically weak photoluminescence of the spin ensemble. Here, we report a photoluminescence enhancement of up to 30 times from VB- centers in suspended regions of hBN compared to those in substrate-supported areas. The key spin properties, such as the optically detected magnetic resonance (ODMR) contrast and linewidth, as well as the spin lifetime, of the VB- centers in this region are well preserved. Detailed investigations, including measurements of zero-field ODMR, Raman spectroscopy, and Kelvin probe force microscopy, reveal a correlation between emission enhancement and local deformation in the sample. It is concluded that the suspended regions exhibit higher local deformation compared to the supported areas, breaking the local symmetry and thereby activating otherwise forbidden or weak optical transitions of the VB- centers.

quant-ph↗

arXiv2025

Optical levitation of fluorescent silicon carbide nanoparticles in vacuum

Levitated optomechanics is an emerging field in quantum science that explores the quantum motion of mesoscopic particles levitated in a vacuum. Expanding this approach to particles with intrinsic quantum defects opens new opportunities for quantum sensing and nontrivial quantum state generation. Here, we explore silicon carbide (SiC) nanoparticles as a promising platform that offers a range of controllable quantum defects and material tunability. We demonstrate stable optical levitation of 3C-polytype SiC nanoparticles containing single photon emitters in a vacuum. We observe stable fluorescence from the levitated particle, confirming the preservation of the emitters in the levitated state. We also investigate particle loss at low pressure and explore thermal annealing as a potential method to improve trapping stability. Our results establish SiC as a viable platform for levitated optomechanics, providing additional quantum degrees of freedom and material engineering capabilities.

physics.optics↗

arXiv2025

Efficient Detection of Statistical RF Fields at High Magnetic Field with a Quantum Sensor

Nuclear magnetic resonance (NMR) spectroscopy is widely used in fields ranging from chemistry, material science to neuroscience. Nanoscale NMR spectroscopy using Nitrogen-vacancy (NV) centers in diamond has emerged as a promising platform due to an unprecedented sensitivity down to the single spin level. At the nanoscale, high nuclear spin polarization through spin fluctuations (statistical polarization) far outweighs thermal polarization. However, until now efficient NMR detection using coherent averaging techniques could not be applied to the detection of statistical polarization, leading to long measurement times. Here we present two protocols to enable coherent averaging of statistical oscillating signals through rectification. We demonstrate these protocols on an artificial radiofrequency signal detected with a single NV center at 2.7 T. Through this, the signal-to-noise scaling with number of measurements $N$ is improved from $N^{0.5}$ to $N^1$, improving the measurement time significantly. The relevance of rectification for the detection of statistical polarization using NV ensembles is outlined, paving the way for efficient nanoscale NMR spectroscopy.

quant-ph↗