Atomic Resonance Research Articles

Novel Pseudo-Two-Dimensional 19F NMR Spectroscopy for Rapid Simultaneous Detection of Amines in Complex Mixture.

Rapid detection of amines in complex mixtures presents a significant challenge. Here, we introduce a novel nuclear magnetic resonance (NMR) method for amine detection utilizing a probe with two fluorine atoms in distinct chemical environments. Upon interaction with an amine, the probe generates two atomic resonance peaks, which are used to create coordinates, revealing fluorine chemical shifts on the 19F NMR spectroscopy. This innovative approach allows for the clear distinction of amine signals in a two-dimensional plane. This method has been effectively employed in analyzing amines in pharmaceuticals and amino acids in Ophiopogon japonicus and dry white wine, providing a robust and general approach for amine analysis.

The Duan-Kimble cavity-atom quantum memory loading scheme revisited

We reexamine the well-known Duan-Kimble entanglement scheme, wherein the state of a single-photon qubit is entangled with a quantum memory consisting of a single-atom qubit in a strongly coupled optical cavity, providing the capability to load the photon’s state into the memory. We correct a common error appearing in some subsequent papers regarding the validity of the single-photon reflectivity function that characterizes the essential phase shift at the heart of the protocol. Using the validated analytical solution, we introduce an improved scheme—the configuration—where the photon and cavity are tuned at the midpoint between atomic resonances and show that it can outperform the original configuration in which the photon and cavity are tuned exactly to one of the atomic resonances. The performance metric used is the final memory-state fidelity versus the heralding probability, which determines the memory-loading rate. The results should play a role in optimizing future quantum repeater schemes based on the Duan-Kimble protocol. Published by the American Physical Society 2024

Polarization measurement of vacuum ultraviolet light using visible fluorescence from neon atoms

The polarization state of the vacuum ultraviolet light has been studied with a fluorescence polarimeter based on the conversion of short wavelength light into visible fluorescence via atomic resonance. In addition to the previously established method using helium atoms, the results show that polarization state of vacuum ultraviolet light can be evaluated by observing the visible fluorescence emitted from neon atoms. This study demonstrates that a fluorescence polarimeter can be used in conjunction with a variety of atoms and molecules and thus extends the range of wavelengths to which this method can be applied.

Optical frequency filtering for Raman beams.

We present an optical filter that is appropriate for use with Raman beams in atomic interferometry. This is a filter that lets the light of the two frequencies of the Raman pair go through and rejects spurious frequencies that may be close to the atomic resonance and cause decoherence. We characterized the filter's performance optically and also by shining the light into atoms in a Ramsey sequence, to look for decoherence effects from photon scattering. We found that it is safe to use tapered amplifiers in single and double pass for light amplification in the Raman beams since the pedestal of emission has a negligible effect, which can be further reduced by the use of the filter we present.

Electromagnetically induced grating via amplitude and phase modulations in a three-level V-type atomic medium

Abstract A probe laser beam can be completely absorbed in an atomic resonance frequency region, however, if a coupling laser beam is further applied to the atom, the atomic medium can exhibit electromagnetically induced transparency (EIT), i.e, the probe beam can be completely transmitted through the atomic medium. Thus, if the coupling beam is a standing wave field with nodes and antinodes, it will cause in space a periodic modulation of the transmitted spectrum of the probe field. This means that the probe field propagates through the atomic medium just as it passes through a diffraction grating which is called electromagnetically induced grating (EIG). Based on amplitude or phase modulation of transmission function, the absorption grating or the phase grating can be formed, respectively. In this work, based on controllable absorption and dispersion properties of a three-level V-type atomic system, we study the control of the absorption grating and the phase grating with respect to the intensity and the frequency of the laser fields. The absorption diffraction pattern at the two-photon resonance is obtained, while the phase diffraction pattern appears when there is a frequency shift of either the coupling frequency or the probe frequency compared to the corresponding atomic resonance frequency. By adjusting the coupling or/and probe laser frequency, the absorption grating can be converted into the phase grating and the high-order diffraction efficiency can also be improved.

Synthesis of Novel Planar-Chiral Charge-Compensated nido-Carborane-Based Amino Acid.

Amino acids with unusual types of chirality and their derivatives have recently attracted attention as precursors in the synthesis of chiral catalysts and peptide analogues with unique properties. In this study, we have synthesized a new nido-carborane-based planar-chiral amino acid, in the molecule of which the amino group is directly bonded to the B(3) atom, and the carboxyl group is attached to the B(9) atom through the CH2S+(Me) fragment. 3-Amino-9-dimethylsulfonio-nido-carborane, prepared in three steps from 3-amino-closo-carborane in a high yield, was a key intermediate in the synthesis of the target planar-chiral amino acid. The carboxymethyl group at the sulfur atom was introduced by the demethylation reaction of the dimethylsulfonio derivative, followed by S-alkylation. The structure of new 3,9-disubstituted nido-carboranes was studied for the first time using NMR spectroscopy. The resonances of all boron atoms in the 11B NMR spectrum of 3-amino-9-dimethylsulfonio-nido-carborane were assigned based on the 2D NMR correlation experiments. The nido-carborane-based planar-chiral amino acid and related compounds are of interest as a basis for peptide-like compounds and chiral ligands.

In-situ suppression of high-frequency magnetic field generated by the electric heater for atomic magnetometers

In this study, an in-situ suppression for the high-frequency magnetic field (HFMF) generated by the electric heater based on the detection of the atomic magnetometer signal is proposed. Specifically, by modeling the response of atomic spin precession signals from an optically pumped atomic magnetometer to the HFMF, the in-situ suppression is achieved by the radio frequency fields produced by coils to compensate the HFMF. The suppression of the HFMF generated by the electric heater is judged based on the amplitude response of the spin precession signal detected at the atomic resonance. Our proposed method is validated through both simulation and experimental results. Before and after in-situ suppression of the HFMF generated by the electric heater, the sensitivity of 13000 nT and 15000 nT static magnetic field within the heating frequency band is measured, resulting in approximately 50% and 60% increases in sensitivity after suppression, respectively.

Area theorem for surface plasmons interacting with resonant atoms

Area theorem for surface plasmons interacting with resonant atoms

Development of an Earth-Field Nuclear Magnetic Resonance Spectrometer: Paving the Way for AI-Enhanced Low-Field Nuclear Magnetic Resonance Technology.

Today, it is difficult to have a high-field nuclear magnetic resonance (NMR) device due to the high cost of its acquisition and maintenance. These high-end machines require significant space and specialist personnel for operation and offer exceptional quality in the acquisition, processing, and other advanced functions associated with detected signals. However, alternative devices are low-field nuclear magnetic resonance devices. They benefit from the elimination of high-tech components that generate static magnetic fields and advanced instruments. Instead, they used magnetic fields induced by ordinary conductors. Another category of spectrometers uses the Earth's magnetic field, which is simple and economical but limited in use. These devices are called Earth-Field Nuclear Magnetic Resonance (EFNMR) devices. This device is ideal for educational purposes, especially for engineers and those who study nuclear magnetic resonance, such as chemistry or other experimental sciences. Students can observe their internal workings and conduct experiments that complement their education without worrying about damaging equipment. This article provides a detailed explanation of the design and construction of electrical technology devices for the excitation of atomic spin resonance using Earth's magnetic fields. It covers all necessary stages, from research to analysis, including simulation, assembly, construction of each component, and the development of comprehensive software for spectrometer control.

Topological photonic band gaps in honeycomb atomic arrays

lattice of two-level atoms coupled by the in-plane electromagnetic field may exhibit band gaps that can be opened either by applying an external magnetic field or by breaking the symmetry between the two triangular sublattices of which the honeycomb one is a superposition. We establish the conditions of band gap opening, compute the width of the gap, and characterize its topological property by a topological index (Chern number). The topological nature of the band gap leads to inversion of the population imbalance between the two triangular sublattices for modes with frequencies near band edges. It also prohibits a transition to the trivial limit of infinitely spaced, noninteracting atoms without closing the spectral gap. Surrounding the lattice by a Fabry-Pérot cavity with small intermirror spacing d < \pi/k_0d<π/k0, where k_0k0 is the free-space wave number at the atomic resonance frequency, renders the system Hermitian by suppressing the leakage of energy out of the atomic plane without modifying its topological properties. In contrast, a larger dd allows for propagating optical modes that are built up due to reflections at the cavity mirrors and have frequencies inside the band gap of the free-standing lattice, thus closing the latter.

The effect of constant electric field on the crack growth process of aluminum nanosheet using molecular dynamics simulation

Aluminum nanosheets are a form of Al nanoparticle that have been recently manufactured on an industrial scale and have a variety of uses. Al nanoparticles are extensively used in a variety of sectors, including aerospace, construction, medical, chemistry, and marine industries. Crack propagation in various constructions must be investigated thoroughly for structural design purposes. Cracks in nanoparticles may occur during the production of nanosheets (NSs) or when different mechanical or thermal pressures were applied. In this work, the effect of a continuous electric field on the fracture formation process of aluminum nanosheets was investigated. For this study, molecular dynamics simulation and LAMMPS software were used. The effects of various electric fields on several parameters, including as stress, velocity (Velo), and fracture length, were explored, and numerical data were retrieved using software. The results show that the amplitude of the electric field parameter affected the atomic development of modeled Al nanosheets throughout the fracture operation. This effect resulted in atomic resonance (amplitude) fluctuations, which affected the mean interatomic forces and led the temporal evolution of atoms to converge to certain specified initial conditions. The crack length in our modeled samples ranged from 22.88 to 32.63 Å, depending on the electric field parameter (0.1–1 V/Å). Finally, it was determined that the crack growth of modeled Al nanosheets may be controlled using CEF parameters in real-world situations.

Spin-flip-induced quadrupole resonance in odd- A exotic atoms

We examine the possible existence of quadrupole resonances in exotic atoms containing odd-A nuclei. We find that the spin flip of the deexciting exotic particle can induce a resonance, altering the orbital angular momentum of the nucleus by one quantum. This process results in an excited nucleus with a suppression in x-ray photon emissions during the exotic atom cascade. We provide specific cases of antiprotonic atoms of stable elements where this resonance effect is expected to occur. The study of this phenomena may provide insight into the strong interaction of deeply bound antiprotonic states in the proximity of the unpaired nucleon, and serve as a tool for probing short-lived excited nuclear states. Published by the American Physical Society 2024

How Resilient is Wood Xylan to Enzymatic Degradation in a Matrix with Kraft Lignin?

Despite the potential of lignocellulose in manufacturing value-added chemicals and biofuels, its efficient biotechnological conversion by enzymatic hydrolysis still poses major challenges. The complex interplay between xylan, cellulose, and lignin in fibrous materials makes it difficult to assess underlying physico- and biochemical mechanisms. Here, we reduce the complexity of the system by creating matrices of cellulose, xylan, and lignin, which consists of a cellulose base layer and xylan/lignin domains. We follow enzymatic degradation using an endoxylanase by high-speed atomic force microscopy and surface plasmon resonance spectroscopy to obtain morphological and kinetic data. Fastest reaction kinetics were observed at low lignin contents, which were related to the different swelling capacities of xylan. We demonstrate that the complex processes taking place at the interfaces of lignin and xylan in the presence of enzymes can be monitored in real time, providing a future platform for observing phenomena relevant to fiber-based systems.

Localized surface plasmon resonance and atomic force microscopy study of model lipid membranes and their interactions with amyloid and melatonin

Alzheimer's disease (AD) is a progressive neurodegenerative disorder characterized by the accumulation of amyloid plaques in the brain. The toxicity of amyloid to neuronal cell surfaces arises from interactions between small intermediate aggregates, namely amyloid oligomers, and the cell membrane. The nature of these interactions changes with age and disease progression. In our previous work, we demonstrated that both membrane composition and nanoscale structure play crucial roles in amyloid toxicity, and that membrane models mimicking healthy neuron were less affected by amyloid than model membranes mimicking AD neuronal membranes. This understanding introduces the possibility of modifying membrane properties with membrane-active molecules, such as melatonin, to protect them from amyloid-induced damage. In this study, we employed atomic force microscopy and localized surface plasmon resonance to investigate the protective effects of melatonin. We utilized synthetic lipid membranes that mimic the neuronal cellular membrane at various stages of AD and explored their interactions with amyloid-β (1–42) in the presence of melatonin. Our findings reveal that the early diseased membrane model is particularly vulnerable to amyloid binding and subsequent damage. However, melatonin exerts its most potent protective effect on this early-stage membrane. These results suggest that melatonin could act at the membrane level to alleviate amyloid toxicity, offering the most protection during the initial stages of AD.

Precipitation of oxide dispersion strength steels after long-term annealing at temperature of 475 °C

Oxide dispersion strengthened steels are key alloys used in nuclear installations. Steels with chromium content of up to 10 wt % are suitable due to their advantageous properties and these alloys are used for the construction of technological devices in the primary circuit of nuclear power plants. From other studies, it can be concluded that chromium has anti-corrosive properties due to the formation of a passivation layer, which results in reduced activation of the material by thermal neutrons. Macroscopic properties are determined by their microstructure, and therefore, the description of the microstructure is important. Transmission Mössbauer spectroscopy and atom probe tomography were used to characterise the material. This provides information about the physical and/or chemical environment of the resonant atoms can be obtained. Obtained spectral parameters reach saturation values from which the solubility limit of chromium in iron can be determined. In Cr-rich phase, the solubility limit can be estimated from the value of spectral parameters of the single-line in the spectrum annealed for the longest time. The suggested procedures are subsequently applied to the case studies of stainless steels suitable for the construction of various components of the III+/IVth generation of nuclear reactors (including fast and fusion reactors).

A General Concept for the Electronic and Steric Modification of 1-Metallacyclobuta-2,3-dienes: A Case Study of Group 4 Metallocene Complexes.

The synthesis of group 4 metal 1-metallacyclobuta-2,3-dienes as organometallic analogues of elusive 1,2-cyclobutadiene has so far been limited to SiMe3 substituted examples. We present the synthesis of two Ph substituted dilithiated ligand precursors for the preparation of four new 1-metallacyclobuta-2,3-dienes [rac-(ebthi)M] (M=Ti, Zr; ebthi=1,2-ethylene-1,10-bis(η5-tetrahydroindenyl)). The organolithium compounds [Li2(RC3Ph)] (1 b: R=Ph, 1 c: R=SiMe3) as well as the metallacycles of the general formula [rac-(ebthi)M(R1C3R2)] (2 b: M=Ti, R1=R2=Ph, 2 c: M=Ti, R1=Ph, R2=SiMe3; 3 b: M=Zr, R1=R2=Ph; 3 c: M=Zr, R1=Ph, R2=SiMe3) were fully characterised. Single crystal X-ray diffraction and quantum chemical bond analysis of the Ti and Zr complexes reveal ligand influence on the biradicaloid character of the titanocene complexes. X-band EPR spectroscopy of structurally similar Ti complexes [rac-(ebthi)Ti(Me3SiC3SiMe3)] (2 a), 2 b, and 2 c was carried out to evaluate the accessibility of an EPR active triplet state. Cyclic voltammetry shows that introduction of Ph groups renders the complexes easier to reduce. 13C CPMAS NMR analysis provides insights into the cause of the low field shift of the resonances of metal-bonded carbon atoms and provides evidence of the absence of the β-C-Ti interaction.

Collisional shifts of hyperfine resonances of ground-state atoms calculated with modified pseudopotential and orthogonalization

Collisional shifts of hyperfine resonances of ground-state atoms calculated with modified pseudopotential and orthogonalization

Sub-Doppler spectroscopy of the Cs atom 6S1/2-7P1/2 transition at 459 nm in a microfabricated vapor cell.

We report on the characterization of sub-Doppler resonances detected by probing the 6S1/2 - 7P1/2 transition of the Cs atom at 459 nm in a microfabricated vapor cell. The dependence of the sub-Doppler resonance (linewidth, amplitude) on some key experimental parameters, including the laser intensity and the cell temperature, is investigated. These narrow atomic resonances are of interest for high-resolution spectroscopy and instrumentation and may constitute the basis of a high-stability microcell optical standard.

Quasi-integrability and nonlinear resonances in cold atoms under modulation.

Quantum dynamics of a collection of atoms subjected to phase modulation has been carefully revisited. We present an exact analysis of the evolution of a two-level system (represented by a spinor) under the action of a time-dependent matrix Hamiltonian. The dynamics is shown to evolve on two coupled potential energy surfaces (PESs): one of them is binding, while the other one is scattering type. The dynamics is shown to be quasi-integrable with nonlinear resonances. The bounded dynamics with intermittent scattering at random moments presents a scenario reminiscent of Anderson and dynamical localization. We believe that a careful analytical investigation of a multi-component system that is classically non-integrable is relevant to many other fields, including quantum computation with multi-qubit systems.

Loading atoms from a large magnetic trap to a small intra-cavity optical lattice

We show that an optimized loading of a cold ensemble of rubidium-87 atoms from a magnetic trap into an optical lattice sustained by a single, far-red-detuned mode of a high-Q optical cavity can be efficient despite the large volume mismatch of the traps. The magnetically trapped atoms are magnetically transported to the vicinity of the cavity mode and released from the magnetic trap in a controlled way meanwhile undergoing an evaporation period. Large number of atoms get trapped in the dipole potential of the cavity mode for several hundreds of milliseconds. We monitor the number of atoms in the mode volume by a second tone of the cavity close to the atomic resonance. While this probe tone can pump atoms to another ground state uncoupled to the probe, we demonstrate state-independent trapping by applying a repumper laser.