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Levitated diamond particles in high vacuum with internal spin qubits have been proposed for exploring macroscopic quantum mechanics, quantum gravity, and precision measurements. The coupling between spins and particle rotation can be utilized to study quantum geometric phase, create gyroscopes and rotational matter-wave interferometers. However, previous efforts in levitated diamonds struggled with vacuum level or spin state readouts. To address these gaps, we fabricate an integrated surface ion trap with multiple stabilization electrodes. This facilitates on-chip levitation and, for the first time, optically detected magnetic resonance measurements of a nanodiamond levitated in high vacuum. The internal temperature of our levitated nanodiamond remains moderate at pressures below 10-5 Torr. We have driven a nanodiamond to rotate up to 20 MHz (1.2 × 109 rpm), surpassing typical nitrogen-vacancy (NV) center electron spin dephasing rates. Using these NV spins, we observe the effect of the Berry phase arising from particle rotation. In addition, we demonstrate quantum control of spins in a rotating nanodiamond. These results mark an important development in interfacing mechanical rotation with spin qubits, expanding our capacity to study quantum phenomena.
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Spin defects in van der Waals materials offer a promising platform for advancing quantum technologies. Here, we propose and demonstrate a powerful technique based on isotope engineering of host materials to significantly enhance the coherence properties of embedded spin defects. Focusing on the recently-discovered negatively charged boron vacancy center ([Formula: see text]) in hexagonal boron nitride (hBN), we grow isotopically purified h10B15N crystals. Compared to [Formula: see text] in hBN with the natural distribution of isotopes, we observe substantially narrower and less crowded [Formula: see text] spin transitions as well as extended coherence time T2 and relaxation time T1. For quantum sensing, [Formula: see text] centers in our h10B15N samples exhibit a factor of 4 (2) enhancement in DC (AC) magnetic field sensitivity. For additional quantum resources, the individual addressability of the [Formula: see text] hyperfine levels enables the dynamical polarization and coherent control of the three nearest-neighbor 15N nuclear spins. Our results demonstrate the power of isotope engineering for enhancing the properties of quantum spin defects in hBN, and can be readily extended to improving spin qubits in a broad family of van der Waals materials.
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A levitated nonspherical nanoparticle in a vacuum is ideal for studying quantum rotations and is an ultrasensitive torque detector for probing fundamental particle-surface interactions. Here, we optically levitate a silica nanodumbbell in a vacuum at 430 nm away from a sapphire surface and drive it to rotate at GHz frequencies. The relative linear speed between the tip of the nanodumbbell and the surface reaches 1.4 km s-1 at a submicrometer separation. The rotating nanodumbbell near the surface demonstrates a torque sensitivity of (5.0 ± 1.1) × 10-26 N m Hz-1/2 at room temperature. Moreover, we probed the near-field laser intensity distribution beyond the optical diffraction limit with a nanodumbbell levitated near a nanograting. Our numerical simulations show that the system can measure the Casimir torque and will improve the detection limit of non-Newtonian gravity by several orders of magnitude.
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Optically active spin defects in van der Waals materials are promising platforms for modern quantum technologies. Here we investigate the coherent dynamics of strongly interacting ensembles of negatively charged boron-vacancy ([Formula: see text]) centers in hexagonal boron nitride (hBN) with varying defect density. By employing advanced dynamical decoupling sequences to selectively isolate different dephasing sources, we observe more than 5-fold improvement in the measured coherence times across all hBN samples. Crucially, we identify that the many-body interaction within the [Formula: see text] ensemble plays a substantial role in the coherent dynamics, which is then used to directly estimate the concentration of [Formula: see text]. We find that at high ion implantation dosage, only a small portion of the created boron vacancy defects are in the desired negatively charged state. Finally, we investigate the spin response of [Formula: see text] to the local charged defects induced electric field signals, and estimate its ground state transverse electric field susceptibility. Our results provide new insights on the spin and charge properties of [Formula: see text], which are important for future use of defects in hBN as quantum sensors and simulators.
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The negatively charged boron vacancy (VB-) defect in hexagonal boron nitride (hBN) with optically addressable spin states has emerged due to its potential use in quantum sensing. Remarkably, VB- preserves its spin coherence when it is implanted at nanometer-scale distances from the hBN surface, potentially enabling ultrathin quantum sensors. However, its low quantum efficiency hinders its practical applications. Studies have reported improving the overall quantum efficiency of VB- defects with plasmonics; however, the overall enhancements of up to 17 times reported to date are relatively modest. Here, we demonstrate much higher emission enhancements of VB- with low-loss nanopatch antennas (NPAs). An overall intensity enhancement of up to 250 times is observed, corresponding to an actual emission enhancement of â¼1685 times by the NPA, along with preserved optically detected magnetic resonance contrast. Our results establish NPA-coupled VB- defects as high-resolution magnetic field sensors and provide a promising approach to obtaining single VB- defects.
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A remarkable prediction of quantum field theory is that there are quantum electromagnetic fluctuations (virtual photons) everywhere, which leads to the intriguing Casimir effect. While the Casimir force between two objects has been studied extensively for several decades, the Casimir force between three objects has not been measured yet. Here, we report the experimental demonstration of an object under the Casimir force exerted by two other objects simultaneously. Our Casimir system consists of a micrometer-thick cantilever placed in between two microspheres, forming a unique sphere-plate-sphere geometry. We also propose and demonstrate a three-terminal switchable architecture exploiting opto-mechanical Casimir interactions that can lay the foundations of a Casimir transistor. Beyond the paradigm of Casimir forces between two objects in different geometries, our Casimir transistor represents an important development for controlling three-body virtual photon interactions and will have potential applications in sensing and information processing.
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Spin defects like the negatively charged boron vacancy color center (VB-) in hexagonal boron nitride (hBN) may enable new forms of quantum sensing with near-surface defects in layered van der Waals heterostructures. Here, the effect of strain on VB- color centers in hBN is revealed with correlative cathodoluminescence and photoluminescence microscopies. Strong localized enhancement and redshifting of the VB- luminescence is observed at creases, consistent with density functional theory calculations showing VB- migration toward regions with moderate uniaxial compressive strain. The ability to manipulate spin defects with highly localized strain is critical to the development of practical 2D quantum devices and quantum sensors.
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Electron spins in van der Waals materials are playing a crucial role in recent advances in condensed-matter physics and spintronics. However, nuclear spins in van der Waals materials remain an unexplored quantum resource. Here we report optical polarization and coherent control of nuclear spins in a van der Waals material at room temperature. We use negatively charged boron vacancy ([Formula: see text]) spin defects in hexagonal boron nitride to polarize nearby nitrogen nuclear spins. We observe the Rabi frequency of nuclear spins at the excited-state level anti-crossing of [Formula: see text] defects to be 350 times larger than that of an isolated nucleus, and demonstrate fast coherent control of nuclear spins. Further, we detect strong electron-mediated nuclear-nuclear spin coupling that is five orders of magnitude larger than the direct nuclear-spin dipolar coupling, enabling multi-qubit operations. Our work opens new avenues for the manipulation of nuclear spins in van der Waals materials for quantum information science and technology.
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The recently discovered spin-active boron vacancy (V[Formula: see text]) defect center in hexagonal boron nitride (hBN) has high contrast optically-detected magnetic resonance (ODMR) at room-temperature, with a spin-triplet ground-state that shows promise as a quantum sensor. Here we report temperature-dependent ODMR spectroscopy to probe spin within the orbital excited-state. Our experiments determine the excited-state spin Hamiltonian, including a room-temperature zero-field splitting of 2.1 GHz and a g-factor similar to that of the ground-state. We confirm that the resonance is associated with spin rotation in the excited-state using pulsed ODMR measurements, and we observe Zeeman-mediated level anti-crossings in both the orbital ground- and excited-state. Our observation of a single set of excited-state spin-triplet resonance from 10 to 300 K is suggestive of symmetry-lowering of the defect system from D3h to C2v. Additionally, the excited-state ODMR has strong temperature dependence of both contrast and transverse anisotropy splitting, enabling promising avenues for quantum sensing.
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One of the fundamental predictions of quantum mechanics is the occurrence of random fluctuations in a vacuum caused by the zero-point energy. Remarkably, quantum electromagnetic fluctuations can induce a measurable force between neutral objects, known as the Casimir effect1, and it has been studied both theoretically2,3 and experimentally4-9. The Casimir effect can dominate the interaction between microstructures at small separations and is essential for micro- and nanotechnologies10,11. It has been utilized to realize nonlinear oscillation12, quantum trapping13, phonon transfer14,15 and dissipation dilution16. However, a non-reciprocal device based on quantum vacuum fluctuations remains an unexplored frontier. Here we report quantum-vacuum-mediated non-reciprocal energy transfer between two micromechanical oscillators. We parametrically modulate the Casimir interaction to realize a strong coupling between the two oscillators with different resonant frequencies. We engineer the system's spectrum such that it possesses an exceptional point17-20 in the parameter space and explore the asymmetric topological structure in its vicinity. By dynamically changing the parameters near the exceptional point and utilizing the non-adiabaticity of the process, we achieve non-reciprocal energy transfer between the two oscillators with high contrast. Our work demonstrates a scheme that employs quantum vacuum fluctuations to regulate energy transfer at the nanoscale and may enable functional Casimir devices in the future.
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The recently discovered spin defects in hexagonal boron nitride (hBN), a layered van der Waals material, have great potential in quantum sensing. However, the photoluminescence and the contrast of the optically detected magnetic resonance (ODMR) of hBN spin defects are relatively low so far, which limits their sensitivity. Here we report a record-high ODMR contrast of 46% at room temperature and simultaneous enhancement of the photoluminescence of hBN spin defects by up to 17-fold by the surface plasmon of a gold film microwave waveguide. Our results are obtained with shallow boron vacancy spin defects in hBN nanosheets created by low-energy He+ ion implantation and a gold film microwave waveguide fabricated by photolithography. We also explore the effects of microwave and laser powers on the ODMR and improve the sensitivity of hBN spin defects for magnetic field detection. Our results support the promising potential of hBN spin defects for nanoscale quantum sensing.
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Fluorescence nanoscopy has become an indispensable tool for studying organelle structures, protein dynamics, and interactions in biological sciences. Single-molecule localization microscopy can now routinely achieve 10-50 nm resolution through fluorescently labeled specimens in lateral optical sections. However, visualizing structures organized along the axial direction demands scanning and imaging each of the lateral imaging planes with fine intervals throughout the whole cell. This iterative process suffers from photobleaching of tagged probes, is susceptible to alignment artifacts and also limits the imaging speed. Here, we focused on the axial plane super-resolution imaging which integrated the single-objective light-sheet illumination and axial plane optical imaging with single-molecule localization technique to resolve nanoscale cellular architectures along the axial (or depth) dimension without scanning. We demonstrated that this method is compatible with DNA points accumulation for imaging in nanoscale topography (DNA-PAINT) and exchange-PAINT by virtue of its light-sheet illumination, allowing multiplexed super-resolution imaging throughout the depth of whole cells. We further demonstrated this proposed system by resolving the axial distributions of intracellular organelles such as microtubules, mitochondria, and nuclear pore complexes in both COS-7 cells and glioblastoma patient-derived tumor cells.
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Torque sensors such as the torsion balance enabled the first determination of the gravitational constant by Henri Cavendish1 and the discovery of Coulomb's law. Torque sensors are also widely used in studying small-scale magnetism2,3, the Casimir effect4 and other applications5. Great effort has been made to improve the torque detection sensitivity by nanofabrication and cryogenic cooling. Until now, the most sensitive torque sensor has achieved a remarkable sensitivity of 2.9 × 10-24 N m Hz-1/2 at millikelvin temperatures in a dilution refrigerator6. Here, we show a torque sensor reaching sensitivity of (4.2 ± 1.2) × 10-27 N m Hz-1/2 at room temperature. It is created by an optically levitated nanoparticle in vacuum. Our system does not require complex nanofabrication. Moreover, we drive a nanoparticle to rotate at a record high speed beyond 5 GHz (300 billion r.p.m.). Our calculations show that this system will be able to detect the long sought after vacuum friction7-10 near a surface under realistic conditions. The optically levitated nanorotor will also have applications in studying nanoscale magnetism2,3 and the quantum geometric phase11.
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High-temperature thermal photonics presents unique challenges for engineers as the database of materials that can withstand extreme environments are limited. In particular, ceramics with high temperature stability that can support coupled light-matter excitations, that is, polaritons, open new avenues for engineering radiative heat transfer. Hexagonal boron nitride (hBN) is an emerging ceramic 2D material that possesses low-loss polaritons in two spectrally distinct mid-infrared frequency bands. The hyperbolic nature of these frequency bands leads to a large local density of states (LDOS). In 2D form, these polaritonic states are dark modes, bound to the material. In cylindrical form, boron nitride nanotubes (BNNTs) create subwavelength particles capable of coupling these dark modes to radiative ones. In this study, we leverage the high-frequency optical phonons present in BNNTs to create strong mid-IR thermal antenna emitters at high temperatures (938 K). Through direct measurement of thermal emission of a disordered system of BNNTs, we confirm their radiative polaritonic modes and show that the antenna behavior can be observed even in a disordered system. These are among the highest-frequency optical phonon polaritons that exist and could be used as high-temperature mid-IR thermal nanoantenna sources.
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The spin in a rotating frame has attracted a lot of attentions recently, as it deeply relates to both fundamental physics such as pseudo-magnetic field and geometric phase, and applications such as gyroscopic sensors. However, previous studies only focused on adiabatic limit, where the rotating frequency is much smaller than the spin frequency. Here we propose to use a levitated nano-diamond with a built-in nitrogen-vacancy (NV) center to study the dynamics and the geometric phase of a rotating electron spin without adiabatic approximation. We find that the transition between the spin levels appears when the rotating frequency is comparable to the spin frequency at zero magnetic field. Then we use Floquet theory to numerically solve the spin energy spectrum, study the spin dynamics and calculate the geometric phase under a finite magnetic field, where the rotating frequency to induce resonant transition could be greatly reduced.
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Levitated optomechanics has great potential in precision measurements, thermodynamics, macroscopic quantum mechanics, and quantum sensing. Here we synthesize and optically levitate silica nanodumbbells in high vacuum. With a linearly polarized laser, we observe the torsional vibration of an optically levitated nanodumbbell. This levitated nanodumbbell torsion balance is a novel analog of the Cavendish torsion balance, and provides rare opportunities to observe the Casimir torque and probe the quantum nature of gravity as proposed recently. With a circularly polarized laser, we drive a 170-nm-diameter nanodumbbell to rotate beyond 1 GHz, which is the fastest nanomechanical rotor realized to date. Smaller silica nanodumbbells can sustain higher rotation frequencies. Such ultrafast rotation may be used to study material properties and probe vacuum friction.
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Atom-like defects in two-dimensional (2D) hexagonal boron nitride (hBN) have recently emerged as a promising platform for quantum information science. Here, we investigate single-photon emissions from atomic defects in boron nitride nanotubes (BNNTs). We demonstrate the first, to the best of our knowledge, optical modulation of the quantum emission from BNNTs with a near-infrared laser. This one-dimensional system displays a bright single-photon emission, as well as high stability at room temperature, and is an excellent candidate for optomechanics. The fast optical modulation of a single-photon emission shows multiple electronic levels of the system and has potential applications in optical signal processing.
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Nonequilibrium processes of small systems such as molecular machines are ubiquitous in biology, chemistry, and physics but are often challenging to comprehend. In the past two decades, several exact thermodynamic relations of nonequilibrium processes, collectively known as fluctuation theorems, have been discovered and provided critical insights. These fluctuation theorems are generalizations of the second law and can be unified by a differential fluctuation theorem. Here we perform the first experimental test of the differential fluctuation theorem using an optically levitated nanosphere in both underdamped and overdamped regimes and in both spatial and velocity spaces. We also test several theorems that can be obtained from it directly, including a generalized Jarzynski equality that is valid for arbitrary initial states, and the Hummer-Szabo relation. Our study experimentally verifies these fundamental theorems and initiates the experimental study of stochastic energetics with the instantaneous velocity measurement.
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Photonic graphene, a honeycomb lattice of evanescently coupled waveguides, has provided a superior platform for investigating a host of fundamental phenomena such as unconventional edge states, synthetic magnetic fields, photonic Landau levels, Floquet topological insulators, and pseudospin effects. Here, we demonstrate both experimentally and numerically, topological vortex degeneracy lifting and Aharonov-Bohm-like interference from local deformation in a photonic honeycomb lattice. When a single valley is excited, lattice deformation leads to the generation of a vortex pair due to the lifting of degeneracy associated with pseudospin states. In the case of double-valley excitation, we observe the Aharonov-Bohm-like interference merely due to the deformation of the graphene lattice, which gives rise to an artificial gauge field. Our results may provide insight into the understanding of similar phenomena in other graphene-like materials and structures.
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We crystallize up to 15 ^{40}Ca^{+} ions in a ring with a microfabricated silicon surface Paul trap. Delocalization of the Doppler laser-cooled ions shows that the translational symmetry of the ion ring is preserved at millikelvin temperatures. By characterizing the collective motion of the ion crystals, we identify homogeneous electric fields as the dominant symmetry-breaking mechanism at this energy scale. With increasing ion numbers, such detrimental effects are reduced. We predict that, with only a ten-ion ring, uncompensated homogeneous fields will not break the translational symmetry of the rotational ground state. This experiment opens a door towards studying quantum many-body physics with translational symmetry at the single-particle level.