Pulsed Excitation Research Articles

Estimation of temperature field for blade battery based on frequency domain heat generation model

Sinusoidal pulse excitation is widely used in the pre-heating process of commercial lithium batteries due to its fast heating rate and almost no capacity degradation under long cycles. For the emerging blade cell, its temperature distribution gradient is significant under the Alternating Current (AC) pulse, and it isn't easy to realize the all-around monitoring of its temperature by the lumped parameter model. So this paper proposes a Joint Kalman Filter (JKF) based on a distributed heat source, and it can realize the joint estimation of tab temperature and the time-varying thermal coefficient. Firstly, the impedance at different temperatures is analyzed by Electrochemical Impedance Spectroscopy (EIS), and the distributed heat model in the frequency domain is constructed. Then, the thermal resistance grid is used to divide the nodes, and the heat transfer equation is formed by using the multi-point temperatures and time-varying heat coefficients to estimate the temperature field. Simulation results show that the method can track the temperature field of the blade cell and realize the temperature estimation with a maximum error of less than 1.5 ℃ in a wide domain range, which is expected to realize the online temperature management and has great application potential in the design of the thermal management system.

Spectrally selective and interleaved water imaging and fat imaging (siWIFI).

To develop a novel imaging sequence that independently acquires water and fat images while being inherently insensitive to motion. The new sequence, termed spectrally selective and interleaved water imaging and fat imaging (siWIFI), uses a narrow bandwidth RF pulse for selective excitation of water and fat separately. The interleaved acquisition method ensures that the obtained water and fat images are inherently coregistered. A radial sampling strategy further reduces motion-induced artifacts. Phantoms with lipid concentrations ranging from 0% to 50% were scanned to measure fat fraction. Moreover, healthy volunteers were scanned to assess the in vivo feasibility of fat fraction measurement at the hip, knee, and liver. In vivo fat fraction measurements were compared with those from vendor-provided iterative decomposition of water and fat with echo asymmetry and least-squares estimation (IDEAL) scans. Furthermore, a magnetization transfer (MT) preparation module was incorporated to demonstrate the feasibility of simultaneous measurement of fat fraction and MT ratio utilizing the siWIFI framework. The phantom fat fractions measured by siWIFI showed excellent correlation with lipid concentrations (R2 = 0.9995, p < 0.0001). In vivo studies demonstrated that the fat fractions obtained from siWIFI were comparable to those from IDEAL. Additionally, siWIFI demonstrates reduced motion artifacts from pulsatile flow in knee imaging compared to IDEAL scans and exhibits less sensitivity to respiratory motion in liver imaging compared to IDEAL scans without breath-hold. The knee imaging study demonstrated that MT-prepared siWIFI is capable of generating fat fraction and MT ratio maps simultaneously. The proposed siWIFI sequence allows selective water-fat imaging and quantification with reduced motion artifacts.

Atom Probe Tomography: a Local Probe for Chemical Bonds in Solids.

Atom probe tomography is frequently employed to characterize the elemental distribution in solids with atomic resolution. Here the potential of this technique to locally probe chemical bonds is reviewed and discussed. Two processes characterize the bond rupture in laser-assisted field emission, the probability of molecular ions (PMI), i.e., the probability that molecular ions are evaporated instead of single (atomic) ions, and the probability of multiple events (PME), i.e., the correlated field-evaporation of more than a single fragment upon laser- or voltage pulse excitation. Here it is demonstrated that one can clearly distinguish solids with metallic, covalent, and metavalent bonds based on their bond rupture, i.e., their PME and PMI values. These findings open new avenues in understanding and designing advanced materials, since they allow a quantification of bonds in solids on a nanometer scale, as will be shown for several examples. These possibilities would even justify calling the present approach bonding probe tomography (BPT).

Deep Ultraviolet Excitation Photoluminescence Characteristics and Correlative Investigation of Al-Rich AlGaN Films on Sapphire.

AlGaN is attractive for fabricating deep ultraviolet (DUV) optoelectronic and electronic devices of light-emitting diodes (LEDs), photodetectors, high-electron-mobility field-effect transistors (HEMTs), etc. We investigated the quality and optical properties of AlxGa1-xN films with high Al fractions (60-87%) grown on sapphire substrates, including AlN nucleation and buffer layers, by metal-organic chemical vapor deposition (MOCVD). They were initially investigated by high-resolution X-ray diffraction (HR-XRD) and Raman scattering (RS). A set of formulas was deduced to precisely determine x(Al) from HR-XRD data. Screw dislocation densities in AlGaN and AlN layers were deduced. DUV (266 nm) excitation RS clearly exhibits AlGaN Raman features far superior to visible RS. The simulation on the AlGaN longitudinal optical (LO) phonon modes determined the carrier concentrations in the AlGaN layers. The spatial correlation model (SCM) analyses on E2(high) modes examined the AlGaN and AlN layer properties. These high-x(Al) AlxGa1-xN films possess large energy gaps Eg in the range of 5.0-5.6 eV and are excited by a DUV 213 nm (5.8 eV) laser for room temperature (RT) photoluminescence (PL) and temperature-dependent photoluminescence (TDPL) studies. The obtained RTPL bands were deconvoluted with two Gaussian bands, indicating cross-bandgap emission, phonon replicas, and variation with x(Al). TDPL spectra at 20-300 K of Al0.87Ga0.13N exhibit the T-dependences of the band-edge luminescence near 5.6 eV and the phonon replicas. According to the Arrhenius fitting diagram of the TDPL spectra, the activation energy (19.6 meV) associated with the luminescence process is acquired. In addition, the combined PL and time-resolved photoluminescence (TRPL) spectroscopic system with DUV 213 nm pulse excitation was applied to measure a typical AlGaN multiple-quantum well (MQW). The RT TRPL decay spectra were obtained at four wavelengths and fitted by two exponentials with fast and slow decay times of ~0.2 ns and 1-2 ns, respectively. Comprehensive studies on these Al-rich AlGaN epi-films and a typical AlGaN MQW are achieved with unique and significant results, which are useful to researchers in the field.

Coherent dynamics in an optical quantum dot with phonons and photons

Genuine quantum-mechanical effects are readily observable in modern optomechanical systems comprising “classical” (bosonic) optical resonators. Unique features and advantages of optical two-level systems (qubits) for optomechanics, however, have not been so thoroughly explored. We experimentally demonstrate these advantages using charge-controlled InAs quantum dots (QDs) in surface-acoustic-wave resonators. We coherently control QD population dynamics using engineered optical pulses and mechanical motion, i.e., using both phonons and photons. As a first example, at moderate acoustic drive strengths, we demonstrate the potential of this technique to maximize fidelity in quantum microwave-to-optical transduction. Specifically, the scheme is tailored to enhance mechanically assisted photon scattering over the direct detuned photon scattering from the QD. Spectral analysis reveals distinct scattering channels related to Rayleigh scattering and luminescence in our pulsed excitation measurements, which lead to time-dependent scattering spectra. Quantum-mechanical calculations show good agreement with our experimental results, together providing a comprehensive description of excitation, scattering, and emission in a coupled QD-phonon system. These results highlight unique opportunities to expand the functionality of quantum optomechanical systems.

Design of calibration-free RF pulses for T -weighted single-slab 3D turbo-spin-echo sequences at 7T utilizing parallel transmission.

T -weighted turbo-spin-echo (TSE) sequences are a fundamental technique in brain imaging but suffer from field inhomogeneities at ultra-high fields. Several methods have been proposed to mitigate the problem, but were limited so far to nonselective three-dimensional (3D) measurements, making short acquisitions difficult to achieve when targeting very high resolution images, or needed additional calibration procedures, thus complicating their application. Slab-selective excitation pulses were designed for flexible placement utilizing the concept of k -spokes. Phase-coherent refocusing universal pulses were subsequently optimized with the Gradient Ascent Pulse Engineering algorithm and tested in vivo for improved signal homogeneity. Implemented within a 3D variable flip angle TSE sequence, these pulses led to a signal-to-noise ratio (SNR) improvement ranging from 10%to 30% compared to a two-dimensional (2D) T2w TSE sequence employing -shimmed pulses. field inhomogeneities could be mitigated and artifacts from deviations reduced. The concept of universal pulses was successfully applied. We present a pulse design method which provides a set of calibration-free universal pulses (UPs) for slab-selective excitation and phase-coherent refocusing in slab-selective TSE sequences.

Plasma response to pulsed ion acoustic wave excitation

Plasma response to pulsed ion acoustic wave excitation

Optical Quantum Control of the Electron Transfer Reactions in Protein Flavodoxin.

The optical quantum control has been successfully applied in modulating biological processes such as energy transfer and bond isomerization. Among the reactions in realizing biological functions, the electron transfer (ET) process is fundamental; hence, the quantum control over such an ET reaction is of far-reaching significance. Here, we realized optical quantum control over ultrafast ET processes in a protein, flavodoxin, by applying various chirped excitation pulses. We observed the wavepacket dynamics within a dephasing time of less than 1 ps. Within this time window, we found that the ultrafast photoinduced ET reaction can be controlled by different chirped excitations with a rate change by a factor of about 2. Furthermore, the control effect is propagated into the subsequent ultrafast back ET reaction, showing a variation of the BET dynamics with different excitation chirps. The underlying mechanism is the initial wavepacket dynamics; the differently prepared wavepackets with chirped excitation evolve along various pathways, resulting in the changes of ET rates. The successful demonstration of optical quantum control of ultrafast biological ET is significant and opens a new avenue to explore the quantum control of real biological ET reactions.

The substituent effect on pulsed laser beam self-action manifestation in azo-azomethine PMMA composites thin films in visible and near IR ranges

Efficiency of nonlinear optical response was studied for a set of azo-azomethines dyes with substituted electron-withdrawing/donating groups, being embedded in poly(methyl methacrylate) (PMMA) matrix, via self-action effects manifestation of mode-locked Nd:YAG laser single pulses in visible at 532 nm, and in near IR at 1064 nm ranges. Photoinduced variations of refractive index and optical absorption/bleaching are crucially dependent on electron-donating/accepting substituents' properties with |Re(χ(3))| ∼ 10−7 esu and |Im(χ(3))| ∼ 10−9 esu efficiencies correspondingly at moderate laser excitation up to 10 MW/cm2. Incorporation of the azomethine group has provided tendency for fractional self-focusing effect manifestation in visible range against reference Azo dye, while at 1064 nm – self-defocusing one. For some dyes magnitudes of |Re(χ(3))| in near IR range are comparable and even higher than for the corresponding ones at 532 nm due to resonant cascaded three photon excitation into the peak vicinity of π→π∗ transitions of the dyes. It was established linear relationship between second-order hyperpolarizabilities under pulsed and CW laser excitation in visible range, being preliminary irradiated within full spectra of UV lamp for CW laser diagnostics mode. It proofs a suggestion that picosecond range single pulses transfer dyes into the same excited state as full spectrum of a mercury lamp irradiation – conventional tool for the smart molecules’ isomerization. Analysis of the experimental data has shown a high potential for the azo-azomethines dyes doped polymer composites in nonlinear optical applications.

Mechanisms of separation of the elastic step and the thermal step

The elastic interaction causes a two‐step conversion from the low‐spin (LS) to the high‐spin state (HS) following a femtosecond laser pulse excitation. These steps occur on different timescales: a spin conversion (elastic step) in a short time due to pressure propagation and a late spin conversion (thermal step) resulting from heat diffusion. In this paper, we provide a brief review of models for spin crossover phenomena, emphasizing the role of the difference of degeneracy of the HS state and LS state and elastic interaction due to changes in local structures. We also review theoretical approaches to these effects. Additionally, to analyze the dynamical process of spin conversion after photo‐irradiation, it is necessary to consider mechanisms of heat transfer among spins. Recently, we proposed a two‐temperature model that incorporates both lattice and spin temperatures, which enables us to reproduce the two steps under an early uniformization of the lattice temperature, highlighting the importance of the timescales of these processes. Furthermore, we explore possible mechanisms to separate the two steps by examining the different timescales of processes of spin conversions by mechanical and entropic forces, and also by considering changes of local temperature due to spin conversion.

Spray characteristics and combustion mechanism influence on combustion stability of UDMH/NTO pre-combustor under external excitation

To study the combustion stability of liquid rocket engines with hypergolic propellant more comprehensively, external pressure pulse excitation was applied to the UDMH (unsymmetrical dimethylhydrazine)/NTO (methylhydrazine) pre-combustor. The effects of pressure pulse intensity, spray characteristics (droplet diameter and spray cone angle), and combustion mechanism on combustion stability characteristic frequencies and attenuation characteristics after excitation were investigated. The simulation results show that all operation conditions capture the first three longitudinal frequencies of the pre-combustor, and all factors have a greater impact on frequencies with higher orders. Increasing the pulse intensity and reducing the droplet diameter are not conducive to combustion stability. The influence of the spray cone angle on the combustion stability is not monotonous. The pre-combustor has good stability when the spray cone angle is 70°. Different combustion mechanisms have a significant effect on the results before and after pressure pulses, and considering a more complete combustion process may increase the attenuation time in the pre-combustor. The obtained rules can provide a reference for the design and simulation of hypergolic liquid rocket engines, which is beneficial for predicting and evaluating the combustion stability of liquid rocket engines.

Heteroepitaxy of ε‐Ga2O3 thin film for artificial synaptic device

AbstractEmerging‐wide bandgap semiconductor Ga2O3 shows distinct characteristics for optoelectronic applications and a stable crystal phase of Ga2O3 is highly desired. Herein, we have first reported a metal‐semiconductor‐metal structure photonic synaptic device based on the ε‐Ga2O3 thin film. The ε‐Ga2O3 epilayer is grown on the c‐sapphire with a low temperature nucleation layer, which presents a crystal orientation relationship with the c‐sapphire (ε‐Ga2O3 &lt;010&gt; // c‐sapphire &lt;1–100&gt; and ε‐Ga2O3 &lt;001&gt; // c‐sapphire &lt;0001&gt;). The ε‐Ga2O3 photonic device was stimulated by UV pulses at different pulse widths, pulse intervals, and reading voltages. Under the UV pulse excitation, the photonic device exhibits primary synaptic functions including excitatory postsynaptic current, short term memory, pair pulse facilitation, long term memory, and STM‐to‐LTM conversion. In addition, stronger and repeated stimuli can naturally contribute to the higher learning capability, thus prolonging the memory time.

Evaluation of static bending caused damage of glass-fiber composite structure using terahertz inspection

Abstract Composite materials find increasing applications in modern industry and transport. However, they may lose desirable mechanical properties due to external mechanical excitations, ultraviolet radiation, moisture penetration, or other factors. Therefore, an effective way to assess the condition of materials is necessary. In this article, a nondestructive evaluation of glass fiber-reinforced composite subjected to five-stage static bending is presented. For this reason, pulsed excitation terahertz imaging was utilized, and a data processing/exploration scheme was proposed. The proposed, novel approach consists of an efficient data registration algorithm based on surface approximation (for surface roughness and unevenness elimination) and a parametrization scheme applied for the signals gained from the time response of the glass fiber-reinforced polymer layer. Obtained parameters enable the global description of the evaluated material state and prediction of failure effectively, even in the early stages of destruction.

Dilation framing camera with the dual-pulse excitation technique

In an inertial confinement fusion (ICF) ultrafast diagnostic system that is based on electron beam time-dilation, an ultrafast electrical pulse is used to excite a microstrip photocathode (PC), which generates a varying PC voltage to obtain a photoelectron velocity that varies with emission time. The photoelectron beam achieves time-dilation through the drift process and is then detected by a time-resolved sensor, thereby increasing the temporal resolution of the diagnostic system. A pulse time-dilation diagnostic system is simulated, while the sensor is a gated microchannel plate (MCP) detector with a temporal resolution of 100 ps and an excitation pulse on a PC with a slope of 3 V/ps; the diagnostic system achieves a temporal resolution of 11.12 ps. However, the excitation pulse creates a voltage difference across the PC. A voltage difference of 900 V can be acquired for a PC length of 60 mm, which yields a nonuniform spatial resolution ranging from 30.4 µm to approximately 3000 µm. Furthermore, the voltage difference across the PC also limits the frame size to 2.2 mm along the pulse propagation direction according to the simulation results. To achieve a uniform spatial resolution and a larger frame size, a dual-pulse excitation technique on a PC is presented, which is the technique to symmetrically apply voltage pulses at both ends of the PC microstrip. The theoretical results show that this technique will improve the uniformity of the PC voltage spatial distribution. When the PC pulse slope is 3 V/ps and the dual-pulse excitation technique is employed, the diagnostic system has a temporal resolution of 5.91 ps and a uniform spatial resolution of 30.4 µm. Furthermore, the frame size along the pulse propagation direction is improved to the effective length of the microstrip PC.

High quality factor, monodisperse micron-sized random lasers based on porous PLGA spheres.

Miniature random lasers with high quality factor are crucial for applications in barcoding, bioimaging, and on-chip technologies. However, achieving monodisperse and size-tunable biocompatible random lasers has been a significant challenge. In this study, we employed poly(lactic-co-glycolic) acid (PLGA), a biocompatible material approved for medical use, as the base material for random lasers. By integrating a dye-doped PLGA solution with a microfluidic system, we successfully fabricated monodisperse and miniature dye-doped PLGA spheres with tunable sizes ranging from 25 to 52 µm. Upon optical pulse excitation, these spheres exhibited strong random lasing emission at 610-640 nm with a threshold of approximately 22 µJ·mm-2. The lasing modes demonstrated a spectral linewidth of 0.2 nm, corresponding to a quality factor of 3100. Fourier transform analysis of the lasing emission revealed fundamental cavity lengths, providing insights into the properties of the random lasers.

Development of differential hall sensors for Pulsed Eddy Current Testing using Gaussian pulse excitation

This study presents the use of differential Hall sensors in Pulsed Eddy Current Testing with Gaussian pulse excitation. This method was selected for its ability to effectively distribute energy across the frequency spectrum, thereby enhancing inspection depth and precision compared to the conventional rectangular pulses. The design of the differential Hall sensors, which includes two Hall sensors, greatly minimizes interference from the primary magnetic field, resulting in improved accuracy in detecting defects, particularly corrosion, across varying lift-off distances. 3D-FEM simulations and experimental results demonstrate that differential Hall sensors outperform traditional single Hall sensors in reducing noise and maintaining corrosion signal. Compared to traditional single Hall sensors, the differential Hall sensors exhibit a significantly improved signal-to-noise ratio, particularly at larger lift-off distances. Additionally, the study employs the Full Width at Half Maximum method to accurately estimate the size of corrosion, offering a precise and non-invasive approach to assessing structural integrity.

Near-petahertz fieldoscopy of liquid

AbstractMeasuring transient optical fields is pivotal not only for understanding ultrafast phenomena but also for the quantitative detection of various molecular species in a sample. Here we demonstrate near-petahertz electric field detection of a few femtosecond pulses with 200 attosecond temporal resolution and subfemtojoule detection sensitivity. By field-resolved detection of the impulsively excited molecules in the liquid phase, termed femtosecond fieldoscopy, we demonstrate temporal isolation of the response of the target molecules from those of the environment and the excitation pulse. In a proof-of-concept analysis of aqueous and liquid samples, we demonstrate field-sensitive detection of combination bands of 4.13 μmol ethanol for the first time. This method expands the scope of aqueous sample analysis to higher detection sensitivity and dynamic range, while the simultaneous direct measurements of phase and intensity information pave the path towards high-resolution biological spectro-microscopy.

Feasibility of Surface Nuclear Magnetic Resonance With Absurdly Long Excitation Pulses

AbstractThe common understanding in surface nuclear magnetic resonance (NMR) is that the excitation pulse should be kept much shorter than the NMR relaxation times for an effective excitation. We present analytic, numerical, and experimental evidence demonstrating that this need not be so, and surface NMR signals can be retrieved even for absurdly long excitation pulses. We solve the Bloch equations in the limit of infinitely long excitation and use this result to demonstrate that a measurable magnetization can be obtained with long excitation pulses. We perform numerical simulations of the Bloch equations incorporating effects of relaxation‐during‐pulse, and our results suggest that long excitation pulses can be used to increase the depth of investigation, but that the spatial resolution of long pulse excitation is low. Data collected in Kompedal, Denmark using up to 3 s long excitation pulses provide experimental proof for the feasibility of long pulse surface NMR.

Charge Carrier Dynamics at the Perovskite Interface with Self-Assembled Monolayers.

Self-assembled monolayers (SAMs) deposited on the hole-collecting electrodes of p-i-n perovskite solar cells effectively replace bulky hole transporting layers. However, the mechanism by which monolayers control the electronic processes and how they depend on the properties of the monolayer molecules remain poorly understood. In this study, we developed a simplified perovskite solar cell imitator with blocked electron extraction to investigate the photocurrent dynamics between the perovskite and the hole-collecting ITO electrode. We investigated the photoluminescence and photovoltage dynamics under short laser pulse excitation and addressed the influence of bulky and monomolecular hole transport layers. Our findings reveal that the photovoltage dynamics is significantly affected by the properties of the transport and perovskite layers, which in turn depend on the methods of sample preparation and exploration. Photocurrent dynamics is determined by several processes, including charge carrier displacement in the local electric field, hole transport to ITO, trapping of holes in interface trap states, and electron-hole recombination at the interface. We propose a model that takes into account molecular dipole moments and their ionization potentials to partially explain the different influences of different monolayers on the hole extraction and interfacial recombination rates. Additionally, the photovoltage dynamics also strongly depends on the illumination of the sample and shows memory effects that persist over minutes and hours and are attributed to the redistribution of ions.

Novel Approach for Lifetime-Proportional Luminescence Imaging Using Frame Straddling.

Optode-based chemical imaging is a rapidly evolving field that has substantially enhanced our understanding of the role of microenvironments and chemical gradients in biogeochemistry, microbial ecology, and biomedical sciences. Progress in sensor chemistry has resulted in a broadened spectrum of analytes, alongside enhancements in sensor performance (e.g., sensitivity, brightness, and photostability). However, existing imaging techniques are often costly, challenging to implement, and limited in their recording speed. Here we use the "frame-straddling" technique, originally developed for particle image velocimetry for imaging the O2-dependent, integrated luminescence decay of optical O2 sensor materials. The method synchronizes short excitation pulses and camera exposures to capture two frames at varying brightness, where the first excitation pulse occurs at the end of the exposure of the first frame and the second excitation pulse at the beginning of the second frame. Here the first frame truncates the luminescence decay, whereas the second frame fully captures it. The difference between the frames quantifies the integral of the luminescence decay curve, which is proportional to the luminescence lifetime, at time scales below one millisecond. Short excitation pulses avoid depopulation of the ground state of luminophores, resulting in a linear Stern-Volmer response with increasing concentrations of the quencher (O2), which can be predicted through a simple model. This methodology is compatible with a wide range of camera systems, making it a versatile tool for various optode based chemical imaging applications. We showcase the utility of frame straddling in measuring O2 dynamics around algae and by observing O2 scavenging sodium dithionite particles sinking through oxygenated water.