203 research outputs found
Harnessing nuclear spin polarization fluctuations in a semiconductor nanowire
Soon after the first measurements of nuclear magnetic resonance (NMR) in a
condensed matter system, Bloch predicted the presence of statistical
fluctuations proportional to in the polarization of an ensemble of
spins. First observed by Sleator et al., so-called "spin noise" has
recently emerged as a critical ingredient in nanometer-scale magnetic resonance
imaging (nanoMRI). This prominence is a direct result of MRI resolution
improving to better than 100 nm^3, a size-scale in which statistical spin
fluctuations begin to dominate the polarization dynamics. We demonstrate a
technique that creates spin order in nanometer-scale ensembles of nuclear spins
by harnessing these fluctuations to produce polarizations both larger and
narrower than the natural thermal distribution. We focus on ensembles
containing ~10^6 phosphorus and hydrogen spins associated with single InP and
GaP nanowires (NWs) and their hydrogen-containing adsorbate layers. We monitor,
control, and capture fluctuations in the ensemble's spin polarization in
real-time and store them for extended periods. This selective capture of large
polarization fluctuations may provide a route for enhancing the weak magnetic
signals produced by nanometer-scale volumes of nuclear spins. The scheme may
also prove useful for initializing the nuclear hyperfine field of electron spin
qubits in the solid-state.Comment: 18 pages, 5 figure
Investigation of Surface Magnetic Noise by Shallow Spins in Diamond
We present measurements of spin relaxation times (T1, T1ρ, T2) on very shallow (≲5 nm) nitrogen-vacancy centers in high-purity diamond single crystals. We find a reduction of spin relaxation times up to 30 times compared to bulk values, indicating the presence of ubiquitous magnetic impurities associated with the surface. Our measurements yield a density of 0.01–0.1μB/nm2 and a characteristic correlation time of 0.28(3) ns of surface states, with little variation between samples and chemical surface terminations. A low temperature measurement further confirms that fluctuations are thermally activated. The data support the atomistic picture where impurities are associated with the top carbon layers, and not with terminating surface atoms or adsorbate molecules. The low spin density implies that the presence of A single surface impurity is sufficient to cause spin relaxation of a shallow nitrogen-vacancy center
Quantum control of proximal spins using nanoscale magnetic resonance imaging
Quantum control of individual spins in condensed matter systems is an
emerging field with wide-ranging applications in spintronics, quantum
computation, and sensitive magnetometry. Recent experiments have demonstrated
the ability to address and manipulate single electron spins through either
optical or electrical techniques. However, it is a challenge to extend
individual spin control to nanoscale multi-electron systems, as individual
spins are often irresolvable with existing methods. Here we demonstrate that
coherent individual spin control can be achieved with few-nm resolution for
proximal electron spins by performing single-spin magnetic resonance imaging
(MRI), which is realized via a scanning magnetic field gradient that is both
strong enough to achieve nanometric spatial resolution and sufficiently stable
for coherent spin manipulations. We apply this scanning field-gradient MRI
technique to electronic spins in nitrogen-vacancy (NV) centers in diamond and
achieve nanometric resolution in imaging, characterization, and manipulation of
individual spins. For NV centers, our results in individual spin control
demonstrate an improvement of nearly two orders of magnitude in spatial
resolution compared to conventional optical diffraction-limited techniques.
This scanning-field-gradient microscope enables a wide range of applications
including materials characterization, spin entanglement, and nanoscale
magnetometry.Comment: 7 pages, 4 figure
On the Energy Transfer Performance of Mechanical Nanoresonators Coupled with Electromagnetic Fields
We study the energy transfer performance in electrically and magnetically
coupled mechanical nanoresonators. Using the resonant scattering theory, we
show that magnetically coupled resonators can achieve the same energy transfer
performance as for their electrically coupled counterparts, or even outperform
them within the scale of interest. Magnetic and electric coupling are compared
in the Nanotube Radio, a realistic example of a nano-scale mechanical
resonator. The energy transfer performance is also discussed for a newly
proposed bio-nanoresonator composed of a magnetosomes coated with a net of
protein fibers.Comment: 9 Pages, 3 Figure
Composite-pulse magnetometry with a solid-state quantum sensor
The sensitivity of quantum magnetometers is challenged by control errors and,
especially in the solid-state, by their short coherence times. Refocusing
techniques can overcome these limitations and improve the sensitivity to
periodic fields, but they come at the cost of reduced bandwidth and cannot be
applied to sense static (DC) or aperiodic fields. Here we experimentally
demonstrate that continuous driving of the sensor spin by a composite pulse
known as rotary-echo (RE) yields a flexible magnetometry scheme, mitigating
both driving power imperfections and decoherence. A suitable choice of RE
parameters compensates for different scenarios of noise strength and origin.
The method can be applied to nanoscale sensing in variable environments or to
realize noise spectroscopy. In a room-temperature implementation based on a
single electronic spin in diamond, composite-pulse magnetometry provides a
tunable trade-off between sensitivities in the microT/sqrt(Hz) range,
comparable to those obtained with Ramsey spectroscopy, and coherence times
approaching T1
Ultrasensitive force detection with a nanotube mechanical resonator
Since the advent of atomic force microscopy, mechanical resonators have been
used to study a wide variety of phenomena, such as the dynamics of individual
electron spins, persistent currents in normal metal rings, and the Casimir
force. Key to these experiments is the ability to measure weak forces. Here, we
report on force sensing experiments with a sensitivity of 12 zN Hz^(-1/2) at a
temperature of 1.2 K using a resonator made of a carbon nanotube. An
ultra-sensitive method based on cross-correlated electrical noise measurements,
in combination with parametric downconversion, is used to detect the
low-amplitude vibrations of the nanotube induced by weak forces. The force
sensitivity is quantified by applying a known capacitive force. This detection
method also allows us to measure the Brownian vibrations of the nanotube down
to cryogenic temperatures. Force sensing with nanotube resonators offers new
opportunities for detecting and manipulating individual nuclear spins as well
as for magnetometry measurements.Comment: Early version. To be published in Nature Nanotechnolog
Sensing remote nuclear spins
Sensing single nuclear spins is a central challenge in magnetic resonance
based imaging techniques. Although different methods and especially diamond
defect based sensing and imaging techniques in principle have shown sufficient
sensitivity, signals from single nuclear spins are usually too weak to be
distinguished from background noise. Here, we present the detection and
identification of remote single C-13 nuclear spins embedded in nuclear spin
baths surrounding a single electron spins of a nitrogen-vacancy centre in
diamond. With dynamical decoupling control of the centre electron spin, the
weak magnetic field ~10 nT from a single nuclear spin located ~3 nm from the
centre with hyperfine coupling as weak as ~500 Hz is amplified and detected.
The quantum nature of the coupling is confirmed and precise position and the
vector components of the nuclear field are determined. Given the distance over
which nuclear magnetic fields can be detected the technique marks a firm step
towards imaging, detecting and controlling nuclear spin species external to the
diamond sensor
A robust, scanning quantum system for nanoscale sensing and imaging
Controllable atomic-scale quantum systems hold great potential as sensitive
tools for nanoscale imaging and metrology. Possible applications range from
nanoscale electric and magnetic field sensing to single photon microscopy,
quantum information processing, and bioimaging. At the heart of such schemes is
the ability to scan and accurately position a robust sensor within a few
nanometers of a sample of interest, while preserving the sensor's quantum
coherence and readout fidelity. These combined requirements remain a challenge
for all existing approaches that rely on direct grafting of individual solid
state quantum systems or single molecules onto scanning-probe tips. Here, we
demonstrate the fabrication and room temperature operation of a robust and
isolated atomic-scale quantum sensor for scanning probe microscopy.
Specifically, we employ a high-purity, single-crystalline diamond nanopillar
probe containing a single Nitrogen-Vacancy (NV) color center. We illustrate the
versatility and performance of our scanning NV sensor by conducting
quantitative nanoscale magnetic field imaging and near-field single-photon
fluorescence quenching microscopy. In both cases, we obtain imaging resolution
in the range of 20 nm and sensitivity unprecedented in scanning quantum probe
microscopy
Hybrid Mechanical Systems
We discuss hybrid systems in which a mechanical oscillator is coupled to
another (microscopic) quantum system, such as trapped atoms or ions,
solid-state spin qubits, or superconducting devices. We summarize and compare
different coupling schemes and describe first experimental implementations.
Hybrid mechanical systems enable new approaches to quantum control of
mechanical objects, precision sensing, and quantum information processing.Comment: To cite this review, please refer to the published book chapter (see
Journal-ref and DOI). This v2 corresponds to the published versio
Universal Vectorial and Ultrasensitive Nanomechanical Force Field Sensor
Miniaturization of force probes into nanomechanical oscillators enables
ultrasensitive investigations of forces on dimensions smaller than their
characteristic length scale. Meanwhile it also unravels the force field
vectorial character and how its topology impacts the measurement. Here we
expose an ultrasensitive method to image 2D vectorial force fields by
optomechanically following the bidimensional Brownian motion of a singly
clamped nanowire. This novel approach relies on angular and spectral tomography
of its quasi frequency-degenerated transverse mechanical polarizations:
immersing the nanoresonator in a vectorial force field does not only shift its
eigenfrequencies but also rotate eigenmodes orientation as a nano-compass. This
universal method is employed to map a tunable electrostatic force field whose
spatial gradients can even take precedence over the intrinsic nanowire
properties. Enabling vectorial force fields imaging with demonstrated
sensitivities of attonewton variations over the nanoprobe Brownian trajectory
will have strong impact on scientific exploration at the nanoscale
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