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Takayuki Iwasaki

Publications and source records attributed to Takayuki Iwasaki.

31 records · Page 2Linked to original sources

Low-Temperature Spectroscopic Investigation of Lead-Vacancy Centers in Diamond Fabricated by High-Pressure and High-Temperature Treatment

We report the optical observation of lead-vacancy (PbV) centers in diamond fabricated by Pb ion implantation and subsequent high-temperature annealing (2100 °C) under high pressure (7.7 GPa). Their optical properties were characterized by photoluminescence at varying temperatures down to 5.7 K. We observed intense emission peaks at 550 and 554 nm with a large splitting of approximately 3900 GHz. The two lines are thought to correspond to the zero phonon line (ZPL) of PbV centers with split ground and excited states. A cubic trend of the ZPL width was observed while varying temperature. We performed polarization measurements of the two lines in a single PbV center, showing nearly orthogonal dipole polarizations. These optical measurements strongly indicate that the PbV center possesses D3d symmetry in the diamond lattice. The observed large ground state splitting significantly suppresses the phonon-mediated transition, which causes decoherence of the electron spin state of the group IV color centers in diamond, expecting a long spin coherence time at a temperature of approximately 8 K.

quant-ph↗

Millimetre-scale magnetocardiography of living rats using a solid-state quantum sensor

A key challenge in cardiology is the non-invasive imaging of electric current propagation occurring in the cardiovascular system at an intra-cardiac scale. A promising approach for directly mapping the current dynamics is to monitor the associated stray magnetic field. However, in this magnetic field approach, the spatial resolution deteriorates significantly as the standoff distance between the target and the sensor increases. Existing sensors usually remain relatively far from the target and provide only centimetre-scale resolution because their operating temperature is not biocompatible. Here we demonstrate millimetre-scale magnetocardiography of living rats using a solid-state quantum sensor based on nitrogen-vacancy centres in diamond. The essence of the method is a millimetre proximity from the sensor to heart surface, which enhances the cardiac magnetic field to greater than nanoteslas and allows the mapping of these signals with intra-cardiac resolution. From the acquired magnetic images, we also estimate the source electric current vector, flowing from the right atria base via the Purkinje fibre bundle to the left ventricular apex. Our results establish the solid-state quantum sensor's capability to probe cardiac magnetic signals from mammalian animals and reveal their intra-cardiac electrodynamics. This technique will enable the study of the origin and progression of myriad cardiac arrhythmias including flutter, fibrillation, and tachycardia.

physics.med-ph↗

Label-free phase change detection of lipid bilayers using nanoscale diamond magnetometry

The NV center in a diamond is a quantum sensor with exceptional quality for highly sensitive nanoscale analysis of NMR spectra and thermometry. In this study, we investigate nanoscale phase change detection of lipid bilayers utilizing ensemble-averaged nuclear spin detection from small volume ~ (6 nm)$^{3}$, which was determined by the depth of the NV center. Analysis of nanoscale NMR signal confirm thickness of lipid bilayer to be 6.2 nm $\pm$ 3.4 nm with proton density of 65 proton/nm$^{3}$ verifying formation of lipid bilayer on top of diamond sample. Correlation spectroscopy from nanoscale volume reveals quantum oscillation at 3.06 MHz corresponding to the Larmor frequency of proton at an applied magnetic field of 71.8 mT. The result of the correlation spectroscopy was compared with the 2D molecular diffusion model constructed by Monte Carlo simulation combined with results from molecular dynamics simulation. There is a change in diffusion constant from 1.5 $\pm$ 0.25 nm$^{2}$/$μ$s to 3.0 $\pm$ 0.5 nm$^{2}$/$μ$s when the temperature changes from 26.5 $^\circ$C to 36.0 $^\circ$C. Our results demonstrate that simultaneous observation of changes in translational diffusion and temperature is possible in label-free measurements using nanoscale diamond magnetometry. Our method paves the way for label-free imaging of cell membranes for understanding its phase composition and dynamics.

physics.app-ph↗

Vector Electrometry in a Wide-Gap Semiconductor Device Using a Spin Ensemble Quantum Sensor

Nitrogen-vacancy (NV) centers in diamond work as a quantum electrometer. Using an ensemble state of NV centers, we propose vector electrometry and demonstrate measurements in a diamond electronic device. A transverse electric field applied to the N-V axis under a high voltage was measured while applying a transverse magnetic field. The response of the energy level shift against the electric field was significantly enhanced compared with that against an axial magnetic field. Repeating the measurement of the transverse electric field for multiple N-V axes, we obtained the components of the electric field generated in the device.

cond-mat.mes-hall↗

Spectroscopic Investigations of Negatively Charged Tin-Vacancy Centres in Diamond

The recently discovered negatively charged tin-vacancy centre in diamond is a promising candidate for applications in quantum information processing (QIP). We here present a detailed spectroscopic study encompassing single photon emission and polarisation properties, the temperature dependence of emission spectra as well as a detailed analysis of the phonon sideband and Debye-Waller factor. Using photoluminescence excitation spectroscopy (PLE) we probe an energetically higher lying excited state and prove fully lifetime limited linewidths of single emitters at cryogenic temperatures. For these emitters we also investigate the stability of the charge state under resonant excitation. These results provide a detailed insight into the spectroscopic properties of the $\text{SnV}^-$ centre and lay the foundation for further studies regarding its suitability in QIP.

quant-ph↗

Simultaneous Wide-field Imaging of Phase and Magnitude of AC Magnetic Signal Using Diamond Quantum Magnetometry

Spectroscopic analysis of AC magnetic signal using diamond quantum magnetometry is a promising technique for inductive imaging. Conventional dynamic decoupling like XY8 provides a high sensitivity of an oscillating magnetic signal with intricate dependence on magnitude and phase, complicating high throughput detection of each parameter. In this study, a simple measurement scheme for independent and simultaneous detection of magnitude and phase is demonstrated by a sequential measurement protocol. Wide-field imaging experiment was performed for an oscillating magnetic field with approximately 100$μ$m-squared observation area. Single pixel phase precision was $2.1^\circ$ for 0.76$μ$T AC magnetic signal. Our method enables potential applications including inductive inspection and impedance imaging.

cond-mat.mes-hall↗

Wide-field diamond magnetometry with millihertz frequency resolution and nanotesla sensitivity

The nitrogen-vacancy (NV) center in diamond allows room-temperature wide-field quantum magnetometry and metrology for a small volume, which is an important technology for applications in biology. Although coherence of the NV center has a limited frequency resolution of diamond magnetometry to 10-100 kHz, recent studies have shown that a phase sensitive protocol can beat the coherence limit on a confocal setup. Here, we report a new measurement protocol, "iQdyne," for improving the frequency resolution of wide-field imaging beyond the coherence limit of the NV center. We demonstrate wide-field magnetometry with a frequency resolution of 238 mHz and a magnetic sensitivity of 65 nT/sqrtHz, which are superior to the conventional XY8-based technique, which paves the way to in vivo microscale nuclear magnetic resonance imaging. We find that the experimental performance of iQdyne agrees well with that of an analytical model.

quant-ph↗

Highly sensitive macro-scale diamond magnetometer operated by dynamical decoupling sequence with coplanar waveguide resonator

Ultimate sensitivity for quantum magnetometry using nitrogen-vacancy (NV) centers in diamond is limited by number of NV centers and coherence time. Microwave irradiation with a high and homogeneous power density for a large detection volume is necessary to achieve highly sensitive magnetometer. Here, we demonstrate a microwave resonator to enhance the power density of the microwave field and an optical system with a detection volume of 1.4e-3 mm$^3$. The strong microwave field enables us to achieve 48 ns Rabi oscillation which is sufficiently faster than the phase relaxation time of NV centers. This system combined with a decoupling pulse sequence, XY16, extends the spin coherence time (T2) up to 27 times longer than that with a spin echo method. Consequently, we obtained an AC magnetic field sensitivity of 10.8 pT/Hz$^{1/2}$ using the dynamical decoupling pulse sequence.

quant-ph↗

Perfectly Aligned Shallow Ensemble Nitrogen-Vacancy Centers in (111) Diamond

We report the formation of perfectly aligned, high-density, shallow nitrogen vacancy (NV) centers on the ($111$) surface of a diamond. The study involved step-flow growth with a high flux of nitrogen during chemical vapor deposition (CVD) growth, which resulted in the formation of a highly concentrated (>$10^{19}$ cm$^{-3}$) nitrogen layer approximately $10$ nm away from the substrate surface. Photon counts obtained from the NV centers indicated the presence of $6.1$x$10^{15}$-$3.1$x$10^{16}$ cm$^{-3}$ NV centers, which suggested the formation of an ensemble of NV centers. The optically detected magnetic resonance (ODMR) spectrum confirmed perfect alignment (more than $99$ %) for all the samples fabricated by step-flow growth via CVD. Perfectly aligned shallow ensemble NV centers indicated a high Rabi contrast of approximately $30$ % which is comparable to the values reported for a single NV center. Nanoscale NMR demonstrated surface-sensitive nuclear spin detection and provided a confirmation of the NV centers depth. Single NV center approximation indicated that the depth of the NV centers was approximately $9$-$10.7$ nm from the surface with error of less than $\pm$$0.8$ nm. Thus, a route for material control of shallow NV centers has been developed by step-flow growth using a CVD system. Our finding pioneers on the atomic level control of NV center alignment for large area quantum magnetometry.

cond-mat.mes-hall↗

Tin-Vacancy Quantum Emitters in Diamond

Tin-vacancy (SnV) color centers were created in diamond by ion implantation and subsequent high temperature annealing up to 2100 °C at 7.7 GPa. The first-principles calculation suggests that the large atom of tin can be incorporated into the diamond lattice with a split-vacancy configuration, in which a tin atom sits on an interstitial site with two neighboring vacancies. The SnV center shows a sharp zero phonon line at 619 nm at room temperature. This line splits into four peaks at cryogenic temperatures with a larger ground state splitting of ~850 GHz than those of color centers based on other IV group elements, silicon-vacancy (SiV) and germanium vacancy (GeV) centers. The excited state lifetime was estimated to be ~5 ns by Hanbury Brown-Twiss interferometry measurements on single SnV quantum emitters. The order of the experimentally obtained optical transition energies comparing with the SiV and GeV centers is good agreement with the theoretical calculations.

quant-ph↗

Photoluminescence excitation spectroscopy of SiV$^{-}$ and GeV$^{-}$ color center in diamond

Color centers in diamond are important quantum emitters for a broad range of applications ranging from quantum sensing to quantum optics. Understanding the internal energy level structure is of fundamental importance for future applications. We experimentally investigate the level structure of an ensemble of few negatively charged silicon-vacancy (SiV$^{-}$) and germanium-vacancy (GeV$^{-}$) centers in bulk diamond at room temperature by photoluminescence (PL) and excitation (PLE) spectroscopy over a broad wavelength range from 460 nm to 650 nm and perform power-dependent saturation measurements. For SiV$^{-}$ our experimental results confirm the presence of a higher energy transition at ~ 2.31 eV. By comparison with detailed theoretical simulations of the imaginary dielectric function we interpret the transition as a dipole-allowed transition from $^{2}E_{g}$-state to $^{2}A_{2u}$-state where the corresponding $a_{2u}$-level lies deeply inside the diamond valence band. Therefore, the transition is broadened by the diamond band. At higher excitation power of 10 mW we indicate signs of a parity-conserving transition at ~2.03 eV supported by saturation measurements. For GeV$^{-}$ we demonstrate that the PLE spectrum is in good agreement with the mirror image of the PL spectrum of the zero-phonon line (ZPL). Experimentally we do not observe a higher lying energy level up to a transition wavelength of 460 nm. The observed PL spectra are identical, independent of excitation wavelength, suggesting a rapid decay to $^{2}E_{u}$ excited state and followed by optical transition to $^{2}E_{g}$ ground state. Our investigations convey important insights for future quantum optics and quantum sensing experiments based on SiV$^{-}$ center and GeV$^{-}$ center in diamond.

cond-mat.mtrl-sci↗

A Germanium-Vacancy Single Photon Source in Diamond

Color centers in diamond are widely recognized as a promising solid state platform for quantum cryptography and quantum information processing. For these applications, single photon sources with a high intensity and reproducible fabrication methods are required. Here, we report a novel color center in diamond, composed of a germanium (Ge) and a vacancy (V) and named the GeV center, which has a sharp and strong photoluminescence band with a zero-phonon line at 602 nm at room temperature. We demonstrate this new color center works as a single photon source. Both ion implantation and chemical vapor deposition techniques enabled fabrication of GeV centers in diamond. A first-principles calculation revealed the atomic crystal structure and energy levels of the GeV center.

cond-mat.mtrl-sci↗

Charged defects in graphene and the ionicity of hexagonal boron nitride in direct images

We report on the detection and charge distribution analysis for nitrogen substitutional dopants in single layer graphene membranes by aberration-corrected high-resolution transmission electron microscopy (HRTEM). Further, we show that the ionicity of single-layer hexagonal boron nitride can be confirmed from direct images. For the first time, we demonstrate by a combination of HRTEM experiments and first-principles electronic structure calculations that adjustments to the atomic potentials due to chemical bonding can be discerned in HRTEM images. Our experiments open a way to discern electronic configurations in point defects or other non-periodic arrangements or nanoscale objects that can not be analyzed in an electron or x-ray diffraction experiment.

cond-mat.mtrl-sci↗