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The rotational dynamics of a molecule is sensitive to neighboring atoms or molecules, which can be used to probe the intermolecular interactions in the gas phase. Here, we real-time track the laser-driven rotational dynamics of a single N2 molecule affected by neighboring Ar atoms using coincident Coulomb explosion imaging. We find that the alignment trace of N-N axis decays fast and only persists for a few picoseconds when an Ar atom is nearby. We show that the decay rate depends on the rotational geometry of whether the Ar atom stays in or out of the rotational plane of the N2 molecule. Additionally, the vibration of the van der Waals bond is found to be excited through coupling with the rotational N-N axis. The observations are well reproduced by solving the time-dependent Schrödinger equation after taking the interaction potential between the N2 and Ar into consideration. Our results demonstrate that environmental effects on a molecular level can be probed by directly visualizing the rotational dynamics.
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The formation of carbon-hydrogen (C-H) bonds via the reaction of small inorganic molecules is of great significance for understanding the fundamental transition from inorganic to organic matter, and thus the origin of life. Yet, the detailed mechanism of the C-H bond formation, particularly the time scale and molecular-level control of the dynamics, remain elusive. Here, we investigate the light-induced bimolecular reaction starting from a van der Waals molecular dimer composed of two small inorganic molecules, H2 and CO. Employing reaction microscopy driven by a tailored two-color light field, we identify the pathways leading to C-H photobonding thereby producing HCO+ ions, and achieve coherent control over the reaction dynamics. Using a femtosecond pump-probe scheme, we capture the ultrafast formation time, i.e., 198 ± 16 femtoseconds. The real-time visualization and coherent control of the dynamics contribute to a deeper understanding of the most fundamental bimolecular reactions responsible for C-H bond formation, thus contributing to elucidate the emergence of organic components in the universe.
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We explored the collision-induced vibrational decoherence of singly ionized D_{2} molecules inside a helium nanodroplet. By using the pump-probe reaction microscopy with few-cycle laser pulses, we captured in real time the collision-induced ultrafast dissipation of vibrational nuclear wave packet dynamics of D_{2}^{+} ion embedded in the droplet. Because of the strong coupling of excited molecular cations with the surrounding solvent, the vibrational coherence of D_{2}^{+} in the droplet interior only lasts for a few vibrational periods and completely collapses within 140 fs. The observed ultrafast coherence loss is distinct from that of isolated D_{2}^{+} in the gas phase, where the vibrational coherence persists for a long time with periodic quantum revivals. Our findings underscore the crucial role of ultrafast collisional dissipation in shaping the molecular decoherence and solvation dynamics during solution chemical reactions, particularly when the solute molecules are predominantly in ionic states.
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Aging negatively affects B cell production, resulting in a decrease in B-1 and B-2 cells and impaired antibody responses. Age-related B cell subsets contribute to inflammation. Investigating age-related alterations in the B-cell pool and developing targeted therapies are crucial for combating autoimmune diseases in the elderly. Additionally, optimal nutrition, including carbohydrates, amino acids, vitamins, and especially lipids, play a vital role in supporting immune function and mitigating the age-related decline in B cell activity. Research on the influence of lipids on B cells shows promise for improving autoimmune diseases. Understanding the aging B-cell pool and considering nutritional interventions can inform strategies for promoting healthy aging and reducing the age-related disease burden.
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Envejecimiento , Enfermedades Autoinmunes , Humanos , Anciano , Linfocitos B , Vitaminas , LípidosRESUMEN
Recent advances in laser technology have enabled tremendous progress in light-induced molecular reactions, at the heart of which the breaking and formation of chemical bonds are located. Such progress has been greatly facilitated by the development of an accurate quantum-mechanical simulation method, which, however, does not necessarily accompany clear dynamical scenarios and is rather computationally heavy. Here, we develop a wave-packet surface propagation (WASP) approach to describe the molecular bond-breaking dynamics from a hybrid quantum-classical perspective. Via the introduction of quantum elements including state transitions and phase accumulations to the Newtonian propagation of the nuclear wave packet, the WASP approach naturally comes with intuitive physical scenarios and accuracies. It is carefully benchmarked with the H_{2}^{+} molecule and is shown to be capable of precisely reproducing experimental observations. The WASP method is promising for the intuitive visualization of light-induced molecular dynamics and is straightforward extensible towards complex molecules.
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Based on the vector diffraction theory, this paper investigated the energy flow evolution of focusing an azimuthally polarized Lorentz-Gaussian beam modulated by concentric vortex phase mask. Three concentric zones make up the concentric vortex phase mask: the center zone, middle circular zone, and outer circular zone. Each zone has an adjusted phase. The findings demonstrate that flexible transverse energy flow rings can be obtained in the focal plane and that transverse energy flows with various polygonal forms can be produced by varying the middle circular radius or phase distribution. By adjusting the phase of the center zone and outer circular zone, the normalized transverse energy flow distribution can be rotated or changed. Findings demonstrate that this technique offers a potent means of controlling the distribution and orientation of Poynting vectors and electromagnetic fields. Moreover, a series of energy flow rings are generated to facilitate the transportation of absorptive particles to predetermined positions. These phenomena may provide a new approach for particle capture and optical particle manipulation.
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We report the stereodynamic control of D3+ formation from the laser-induced bimolecular reaction in a weakly bound D2-D2 dimer via impulsive molecular alignment. Using a linearly polarized moderately intense femtosecond pump pulse, the D2 molecules in the dimer were prealigned prior to the bimolecular reaction triggered by a delayed probe pulse. The rotationally excited D2 in the dimer was observed to rotate freely as if it were a monomer. It was demonstrated that the yield of photoreaction product D3+ is increased or decreased when the molecular axis of D2 is parallel or perpendicular to the probe laser polarization, respectively. The underlying physics of this steric effect is the alignment-dependent bond cleavage of D2+ in the dimer induced by a photon-coupled parallel transition.
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This paper explored the optically induced magnetization properties of radially polarized Bessel-Gaussian vortex beams with radial phase modulation in a 4π high numerical aperture (NA) focusing system, which is based on the vector diffraction theory and the inverse Faraday effect. The results show that in the case of radial modulation parameter L=0, one longitudinal magnetization chain with adjustable length can be obtained by modulating the truncation parameter ß. When the radial modulation parameter L=1.3, two magnetization chains can be obtained by modulating the truncation parameter ß. By modulating the radial modulation parameter L, two magnetization chains along the optical axis can be generated, each with four dark magnetic traps; meanwhile, the spacing between two magnetization chains can be adjusted. These results may be helpful in high-density all-optical magnetic recording, atom capture, and magnetic resonance microscopy.
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This work presents a thorough investigation of the focusing characteristic of chirped phase modulated Lorentz-Gaussian (LG) vortex beams based on the vector diffraction theory. The results show that changing the first-order chirp parameter c 1 can effectively adjust the size of the focusing spot, and the distance between focusing spots can also be controlled. The second-order chirp parameter c 2 can control the up-and-down movement of the optical chain in the focusing region. Simultaneously, the length of the focusing spots can be accurately changed by modulating the waist width ω. In addition, the influence of integer topological charge number m on controlling the size of an optical dark trap is discussed in detail. And fractional topological charge number m can control the rotation of focus peak and the number of optical dark traps. Potential applications of these findings include optical shape and capture, optical particle transmission, and contemporary medical care.
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Talaromyces albobiverticillius, a prominent pathogen responsible for pomegranate pulp rot disease, inflicts significant damage on Punica granatum L. Besides its pathogenicity, this fungus possesses the potential to produce substantial amounts of red pigments, making it promising for industrial applications. This study presents the genome annotation of T. albobiverticillius field strain Tp-2, isolated from pomegranates. The genome assembly, generated through a combination of Oxford Nanopore and Illumina sequencing reads, yielded a high-quality assembly with 14 contigs, featuring an N50 length of 4,594,200 bp. The complete genome of strain Tp-2 spans 38,354,882 bp, with a GC content of 45.78%. Importantly, the assembly exhibits remarkable integrity, with 98.3% of complete Benchmarking Universal Single-Copy Orthologs validating genome completeness. Genome prediction analysis reveals the presence of 10,380 protein-coding genes. To our knowledge, this study is the first report on the genome sequence of T. albobiverticillius, offering valuable insights into its genetic variation and molecular mechanisms of pigment production.
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This paper focuses on the focusing pattern of the Laguerre-Gaussian (LG) beam with polarization mixing helical-conical phase modulation, which is based on the vector diffraction theory. The results show that the topological charge number l can sensitively control the intensity of the intensity peaks. The focal spot will split along the optical axis under different polarization parameters P. When l=1, the spot position and the peak intensity can be modulated by changing the polarization parameter P. The truncation parameter ß makes the focusing spot form an optical trap. By adjusting the eccentricity parameter K, the opening direction of the optical trap can be well controlled. These results may be helpful in optical applications such as optical manipulation, optical focusing, and optical information transmission.
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Spatial localization ability is crucial for free-living animals to fit the environment. As shown by previous studies, planarians can be conditioned to discriminate directions. However, due to their simplicity and primitiveness, they had never been considered to have true spatial localization ability to retrieve locations of objects and places in the environment. Here, we introduce a light maze training paradigm to demonstrate that a planarian worm can navigate to a former recognized place from the start point, even if the worm is transferred into a newly produced maze. This finding identifies the spatial localization ability of planarians for the first time, which provides clues for the evolution of spatial learning. Since the planarians have a primitive brain with simple structures, this paradigm can also provide a simplified model for a detailed investigation of spatial learning.
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Planarias , Animales , Encéfalo , CabezaRESUMEN
We demonstrate that dissociative ionization of H_{2} can be fully manipulated in an angle-time-resolved fashion, employing a polarization-skewed (PS) laser pulse in which the polarization vector rotates. The leading and falling edges of the PS laser pulse, characterized by unfolded field polarization, trigger, sequentially, parallel and perpendicular transitions of stretching H_{2} molecules, respectively. These transitions result in counterintuitive proton ejections that deviate significantly from the laser polarization directions. Our findings demonstrate that the reaction pathways can be controlled through fine-tuning the time-dependent polarization of the PS laser pulse. The experimental results are well reproduced using an intuitive wave-packet surface propagation simulation method. This research highlights the potential of PS laser pulses as powerful tweezers to resolve and manipulate complex laser-molecule interactions.
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We experimentally studied the three-body fragmentation dynamics of a noble gas cluster (ArKr2) upon its multiple ionization by an intense femtosecond laser pulse. The three-dimensional momentum vectors of correlated fragmental ions were measured in coincidence for each fragmentation event. A novel comet-like structure was observed in the Newton diagram of the quadruple-ionization-induced breakup channel of ArKr2 4+â Ar+ + Kr+ + Kr2+. The concentrated head part of the structure mainly originates from the direct Coulomb explosion process, while the broader tail part of the structure stems from a three-body fragmentation process involving electron transfer between the distant Kr+ and Kr2+ ion fragments. Due to the field-driven electron transfer, the Coulomb repulsive force of the Kr2+ and Kr+ ions with respect to the Ar+ ion undergoes exchange, leading to changes in the ion emission geometry in the Newton plot. An energy sharing among the separating Kr2+ and Kr+ entities was observed. Our study indicates a promising approach for investigating the strong-field-driven intersystem electron transfer dynamics by using the Coulomb explosion imaging of an isosceles triangle van der Waals cluster system.
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We investigate the above-threshold multiphoton ionization of H_{2} embedded in superfluid He nanodroplets driven by ultraviolet femtosecond laser pulses. We find that the surrounding He atoms enhance the dissociation of in-droplet H_{2}^{+} from lower vibrational states as compared to that of isolated gas-phase molecules. As a result, the discrete peaks in the photoelectron energy spectrum correlated with the HHe^{+} from the dissociative in-droplet molecule shift to higher energies. Based on the electron-nuclear correlation, the photoelectrons with higher energies are correlated to the nuclei of the low-vibrationally excited molecular ion as the nuclei share less photon energy. Our time-dependent nuclear wave packet quantum simulation using a simplified He-H_{2}^{+} system confirms the joint contribution of the driving laser field and the neighboring He atoms to the dissociation dynamics of the solute molecular ion. The results strengthen our understanding of the role of the environment on light-induced ultrafast dynamics of molecules.
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Rabi oscillation is an elementary laser-driven physical process in atoms and artificial atoms from solid-state systems, while it is rarely demonstrated in molecules. Here, we investigate the bond-length-dependent Rabi oscillations with varying Rabi frequencies in strong-laser-field dissociation of H2+. The coupling of the bond stretching and Rabi oscillations makes the nuclei gain different kinetic energies while the electron is alternatively absorbing and emitting photons. The resulting proton kinetic energy spectra show rich structures beyond the prediction of the Floquet theorem and the well-accepted resonant one-photon dissociation pathway. Our study shows that the laser-driven Rabi oscillations accompanied by nuclear motions are essential to understanding the bond-breaking mechanism and provide a time-resolved perspective to manipulate rich dynamics of the strong-laser-field dissociation of molecules.
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An integrated interferometric fiber optic velocimetry sensor has been proposed and demonstrated at the central wavelength of 638 nm. The sensor is based on the principle of two laser-beams' interference. The light signal scattered from the particles or vapor is demodulated to measure the water surface velocity and water vapor velocity. Three velocity measurement experiments are carried out to measure the velocity, and the experimental data shows that the velocity increases linearly in the range of 4 mm·s-1 to 100 mm·s-1, with a slope of linear fitting curve of 0.99777 and the R-Square of 1.00000. The velocity calculated from frequency shift fits well with the reference velocity. The maximum average relative error in the three velocity measurements is less than 2.5%. In addition, the maximum speed of 4.398 m·s-1 is confirmed in the rotating disk calibration experiment, which expands the sensor's velocity measurement range. To solve the problem that it is difficult to directly measure the velocity of small-scale water surface flow velocity, especially from the aspect of the low velocity of air-water surface, the interferometric fiber optic sensor can be applied to the measurement of water surface velocity and wind velocity on the water surface.
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Multiple object tracking (MOT) plays an important role in intelligent video-processing tasks, which aims to detect and track all moving objects in a scene. Joint-detection-and-tracking (JDT) methods are thriving in MOT tasks, because they accomplish the detection and data association in a single stage. However, the slow training convergence and insufficient data association limit the performance of JDT methods. In this paper, the anchor-based query (ABQ) is proposed to improve the design of the JDT methods for faster training convergence. By augmenting the coordinates of the anchor boxes into the learnable queries of the decoder, the ABQ introduces explicit prior spatial knowledge into the queries to focus the query-to-feature learning of the JDT methods on the local region, which leads to faster training speed and better performance. Moreover, a new template matching (TM) module is designed for the JDT methods, which enables the JDT methods to associate the detection results and trajectories with historical features. Finally, a new transformer-based MOT method, ABQ-Track, is proposed. Extensive experiments verify the effectiveness of the two modules, and the ABQ-Track surpasses the performance of the baseline JDT methods, TransTrack. Specifically, the ABQ-Track only needs to train for 50 epochs to achieve convergence, while that for TransTrack is 150 epochs.
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Rotational dynamics of D_{2} molecules inside helium nanodroplets is induced by a moderately intense femtosecond pump pulse and measured as a function of time by recording the yield of HeD^{+} ions, created through strong-field dissociative ionization with a delayed femtosecond probe pulse. The yield oscillates with a period of 185 fs, reflecting field-free rotational wave packet dynamics, and the oscillation persists for more than 500 periods. Within the experimental uncertainty, the rotational constant B_{He} of the in-droplet D_{2} molecule, determined by Fourier analysis, is the same as B_{gas} for an isolated D_{2} molecule. Our observations show that the D_{2} molecules inside helium nanodroplets essentially rotate as free D_{2} molecules.
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Probing transient charge localization in the innershell orbital of atoms and molecules has been made possible by the recent progress of advanced light sources. Here, we demonstrate that the ultrafast electron tunneling ionization by an intense femtosecond laser pulse could induce an asymmetric transient charge localization in the valence shell of the HCl molecule during the dissociative ionization process. The transient charge localization is encoded in the laser impulse acquired by the outgoing ionic fragments, and the asymmetry is revealed by carefully examining the electron tunneling-site distinguished momentum angular distribution of the ejected H^{+} fragments. Our work proposes a way to visualize the transient valence charge motion and will stimulate further investigations of the tunneling-site-sensitive ultrafast dynamics of molecules in strong laser fields.