Synchrotron Radiation Source Research Articles

Study on Beam Orbit Shift due to Synchrotron Radiation

The beam orbit stability is the crucial indicator to evaluate the performance of the synchrotron radiation source. In order to obtain higher beam quality, higher stability requirements are placed on the beam orbit. The stability can be improved through accurate measurement of beam orbit by beam position monitors (BPMs) and appropriate feedback system. However, due to radiation of the synchrotron beams on the vacuum chamber, the thermal effect of synchrotron radiation causes the thermal deformation of the vacuum chamber. The thermal deformation drives the BPM fixed on the vacuum chamber to move, which will induce error to the beam orbit. We analyze the effect of beam current on the vacuum chamber movement and the effect of vacuum chamber movement on the beam orbit. We also built an online vacuum chamber displacement measurement system on Hefei Light Source II (HLS II), which is used to validate and correct our analysis. After analysis and verification, the vacuum chamber moves with the change of current. The larger the change of current, the larger the vacuum chamber displacement. The vacuum chamber displacement has a hysteresis compared to the current change.

Studies of radiation background at the synchrotron light source DELTA

The 1.5-GeV electron storage ring of the synchrotron radiation source DELTA at TU Dortmund University is surrounded by a 1 m thick concrete radiation shielding wall with a height varying between 3.0 and 4.3 m and with open top. The installation of a new 7-T superconducting wiggler and tentative plans for a new building in the vicinity motivated recent studies of background radiation either directly escaping the open-topped radiation shield or being scattered by air or the roof of the hall (the so-called radiation skyshine). Spectra of gamma radiation were recorded under different conditions using a high-purity germanium detector. Long-term measurements were made with photoluminescence dosimeters. The paper presents the results together with calculations of the spectral distribution of wiggler radiation as well as a model for the spatial distribution of radiation emitted by the whole storage ring.

Re-evaluating stoichiometric estimates of iron valence in magmatic clinopyroxene crystals

Clinopyroxene is a major rock forming mineral capable of incorporating diverse metal cations. As a consequence, clinopyroxene preserves valuable archives of magmatic processes. Understanding clinopyroxene is thus essential for understanding Earth’s wider chemical evolution. However, knowledge about the relative abundances of ferrous and ferric iron in magmatic clinopyroxene remains sparse because it is not currently possible to routinely measure the valence of iron in clinopyroxene crystals without either separating single crystals for bulk analysis or securing access to Mössbauer spectroscopy or a synchrotron radiation source to perform in-situ microanalysis. This is despite magmatic clinopyroxene crystals often containing appreciable quantities of ferric iron that affect its stability and behaviour in currently ill-constrained ways and limit our ability to exploit its chemistry to robustly reconstruct conditions of magma storage and evolution. Here we integrate optimised electron probe microanalysis and Mössbauer spectroscopy on endmember and single-crystal clinopyroxene samples to re-evaluate previously discredited approaches for estimating clinopyroxene ferric iron contents by stoichiometry. By ensuring that we measured all major and minor elements in clinopyroxene crystals with sufficient precision, we show that it is possible to readily obtain stoichiometric estimates of clinopyroxene ferric-to-total iron ratios with similar precisions to those derived from Mössbauer spectroscopy (1σ\\documentclass[12pt]{minimal} \\usepackage{amsmath} \\usepackage{wasysym} \\usepackage{amsfonts} \\usepackage{amssymb} \\usepackage{amsbsy} \\usepackage{mathrsfs} \\usepackage{upgreek} \\setlength{\\oddsidemargin}{-69pt} \\begin{document}$${\\sigma }$$\\end{document}∼\\documentclass[12pt]{minimal} \\usepackage{amsmath} \\usepackage{wasysym} \\usepackage{amsfonts} \\usepackage{amssymb} \\usepackage{amsbsy} \\usepackage{mathrsfs} \\usepackage{upgreek} \\setlength{\\oddsidemargin}{-69pt} \\begin{document}$$\\sim$$\\end{document} 3.5% absolute). Being able to robustly determine clinopyroxene ferric iron contents enables us to propose a new empirical scheme for assigning clinopyroxene components that explicitly accounts for ferric iron, which is primarily hosted within esseneite component (CaFe3+\\documentclass[12pt]{minimal} \\usepackage{amsmath} \\usepackage{wasysym} \\usepackage{amsfonts} \\usepackage{amssymb} \\usepackage{amsbsy} \\usepackage{mathrsfs} \\usepackage{upgreek} \\setlength{\\oddsidemargin}{-69pt} \\begin{document}$$^{3+}$$\\end{document}AlSiO6\\documentclass[12pt]{minimal} \\usepackage{amsmath} \\usepackage{wasysym} \\usepackage{amsfonts} \\usepackage{amssymb} \\usepackage{amsbsy} \\usepackage{mathrsfs} \\usepackage{upgreek} \\setlength{\\oddsidemargin}{-69pt} \\begin{document}$$_{6}$$\\end{document}) in clinopyroxenes dominated by quadrilateral components and aegirine component (NaFe3+\\documentclass[12pt]{minimal} \\usepackage{amsmath} \\usepackage{wasysym} \\usepackage{amsfonts} \\usepackage{amssymb} \\usepackage{amsbsy} \\usepackage{mathrsfs} \\usepackage{upgreek} \\setlength{\\oddsidemargin}{-69pt} \\begin{document}$$^{3+}$$\\end{document}Si2\\documentclass[12pt]{minimal} \\usepackage{amsmath} \\usepackage{wasysym} \\usepackage{amsfonts} \\usepackage{amssymb} \\usepackage{amsbsy} \\usepackage{mathrsfs} \\usepackage{upgreek} \\setlength{\\oddsidemargin}{-69pt} \\begin{document}$$_{2}$$\\end{document}O6\\documentclass[12pt]{minimal} \\usepackage{amsmath} \\usepackage{wasysym} \\usepackage{amsfonts} \\usepackage{amssymb} \\usepackage{amsbsy} \\usepackage{mathrsfs} \\usepackage{upgreek} \\setlength{\\oddsidemargin}{-69pt} \\begin{document}$$_{6}$$\\end{document}) in alkali clinopyroxenes. Our new scheme provides a framework for documenting the full spectrum of clinopyroxene compositions in both natural and experimental systems when analyses are performed with sufficient precision.

Comparative Investigation of the Microstructure of MgCl2 Aqueous Solutions Using Different X-ray Scattering Sources, Raman Spectroscopy, and Atomistic Simulations.

Aqueous solutions of magnesium chloride (MgCl2(aq)) are often used to test advances in the theory of electrolyte solutions because they are considered an ideal strong 2:1 electrolyte. However, there is evidence that some ion association occurs in these solutions, even at low concentrations. Even a small ion-pairing constant can have a significant impact on the chemical speciation of ions, so it is important to determine whether ion pairing actually occurs. In this study, MgCl2(aq) with concentrations ranging from 1 to 35% was studied using three methods: X-ray scattering (XRS) with the Shanghai Synchrotron Radiation Facility (SSRF) and silver-anode laboratory sources, Raman spectroscopy, and molecular dynamics (MD) simulations with the COMPASS-II and Madrid force fields. XRS results were analyzed in the framework of PDF theory to obtain the reduced structure function F(Q) and the reduced pair distribution function G(r). The F(Q) values from synchrotron radiation and laboratory sources both showed that the tetrahedral hydrogen bonds in bulk water were destroyed with the increased MgCl2 concentration. The results of G(r) indicated that the main peaks centered at 2.05 and 2.80 Å can be ascribed to the interactions of Mg-O and O-O, respectively. The peak at 3.10 Å is attributed to the combined effect of O-O and Cl-O. By comparing the structural information on MgCl2 solution obtained from the two light sources, it was found that both SSRF and silver-anode laboratory sources can reflect the above-mentioned structural information on MgCl2 solution. The radial distribution function (RDF) obtained from MD simulations of MgCl2 solutions assigned the peaks at 2.0, 2.8, and 3.2 Å to the Mg-O, O-O, and Cl-O interatomic pairs, respectively. The decrease in the O-O coordination number confirms that the hydrogen-bonding network of water is disrupted by increasing MgCl2 observed by X-ray scattering. The proportion of Mg-Cl contact ion pairs gradually increases with MgCl2 concentration as does the coordination number. Raman spectroscopy results show that the bond type changes from double donor double acceptor (DDAA) to single donor-single acceptor (DA) with increasing concentration, providing explicit details of the hydrogen-bond evolution in the aqueous solution.

Tiresia: A code for molecular electronic continuum states and photoionization

The Tiresia program [1] provides access to numerically accurate solutions of the one-particle Schrödinger equation for highly excited states of complex polyatomic molecules, both bound and continuum, that cannot be described by conventional Quantum Chemistry approaches. It is based on an expansion of the required solution in a local multicentric basis set, with primitive functions built as products of a radial B-spline times a real spherical harmonic. In conjunction with Density Functional Theory (DFT), it has been extensively employed in a large variety of photoionization studies, also for rather large systems. Highly excited bound states as well as wavepacket propagation can also be accurately described. In fact, the flexibility of the basis essentially allows accurate solutions of linear operator equations, like Poisson or inhomogeneous perturbative equations, which are employed in the code. The program is parallelized with standard MPI-I instructions and makes extensive use of the Scalapack linear algebra library. Ancillary programs are available for the evaluation of photoionization cross sections and angular distributions from randomly to fully oriented molecules. Program summaryProgram Title: TiresiaCPC Library link to program files:https://doi.org/10.17632/fcrjxwgjxh.1Licensing provisions: GPLv3Programming language: Fortran77, Fortran90, MPISupplementary material: Program manual documentNature of problem: Accurate solutions for highly excited and continuum electronic states in complex polyatomic molecules. Molecular photoionization cross sections and angular distributions under high energy, high-intensity radiation pulses from Synchrotron radiation and laser sources, photoelectron imaging in pump-probe experiments, basis for electronic wavepackets under ultrafast or nonperturbative excitation.Solution method: Solution of the Schrödinger and similar linear operator equations in a finite domain is obtained via basis set expansion. Flexible basis set, that may approach practical completeness within the domain, is obtained as a multicenter set of B-spline radial functions times spherical harmonics. Accurate numerical integration is employed for the evaluation of matrix elements, and conventional diagonalization for bound states, or Galerkin approach for the full multichannel solution in the continuum. Full hamiltonian and dipole matrices in the spectral basis are available for time propagation. DFT many-body description is available, and strong correlations in the bound states may be incorporated via Dyson orbitals.Additional comments including restrictions and unusual features: The code is noted for computational efficiency, which allows fast yet reasonably accurate photoionization calculations for medium-sized molecules, allowing, e.g., calculations at many molecular geometries as required to describe time-resolved photoelectron spectra in pump-probe experiments.

Characterization of iLGADs using soft X-rays

Experiments at synchrotron radiation sources and X-ray Free-Electron Lasers in the soft X-ray energy range (250 eV–2 keV) stand to benefit from the adaptation of the hybrid silicon detector technology for low energy photons. Inverse Low Gain Avalanche Diode (iLGAD) sensors provide an internal gain, enhancing the signal-to-noise ratio and allowing single photon detection below 1 keV using hybrid detectors. In addition, an optimization of the entrance window of these sensors enhances their quantum efficiency (QE).In this work, the QE and the gain of a batch of different iLGAD diodes with optimized entrance windows were characterized using soft X-rays at the Surface/Interface:Microscopy beamline of the Swiss Light Source synchrotron. Above 250 eV, the QE is larger than 55% for all sensor variations, while the charge collection efficiency is close to 100%. The average gain depends on the gain layer design of the iLGADs and increases with photon energy. A fitting procedure is introduced to extract the multiplication factor as a function of the absorption depth of X-ray photons inside the sensors. In particular, the multiplication factors for electron- and hole-triggered avalanches are estimated, corresponding to photon absorption beyond or before the gain layer, respectively.

A low-frequency normal conducting cavity with higher-order mode damping for fourth-generation synchrotron radiation sources.

The utilization of a low-frequency (<200MHz) RF system in storage facilitates the attainment of ultra-low emittances in synchrotron light sources through on-axis injection. This paper focuses on the development of a low-frequency normal conducting (NC) cavity with higher-order mode (HOM) damping for fourth-generation synchrotron light sources. We propose a novel approach to achieve efficient HOM damping in a NC cavity by optimizing the lowest frequency HOM and implementing a beam-line absorber. Notably, unlike conventional NC cavities, the presence of a large beam tube for the beam-line absorber does not compromise the accelerating performance in a coaxial resonant cavity, enabling effective HOM damping while maintaining a high shunt impedance. Through simulations, the prototype design of a 166.6MHz HOM-damped cavity demonstrates a fundamental mode impedance of ∼8 MΩ, with longitudinal and transverse HOM impedances below 2.0 and 50 kΩ/m, respectively.

Structure of four vat dyes and of violanthrene

The structures of four industrially valuable vat dyes are solved for the first time: 1,1′-diethyl-[3,3′-bidibenzo[cd,g]indazole]-6,6′(1H,1′H)-dione (Vat Red 13, Cibanone Red 6B, Carbanthrene Red G 2B, Ahcovat Rubine R), 16,17-dimethoxyviolanthrone (Vat Green 1, Caledon Jade Green, Jade Green Base, Indanthren Brilliant Green B), pyranthrone (Vat Orange 9, Ahcovat Golden Orange G, Benzadone Gold Orange G, Pigment Orange 40), 2,8-diphenylanthra(2,1-d:6,5-d')bisthiazole-6,12-dione (Vat Yellow 2, Anthra Yellow, Tyrian Yellow A-GC) and violanthrene. Violanthrene was obtained by reduction of 16,17-dimethoxyviolanthrone with sodium metal in ethanol. The single crystals were grown by vacuum sublimation and examined with a synchrotron radiation source. The structures of all the four vat dyes represent a stacking motif, whereas violanthrene molecules form sandwiches of two molecules. The interplanar distance between the molecules in the stacks (sandwiches) is 3.35–3.48 Å which is typical of polycyclic aromatic compounds.

Laboratory-Based Correlative Soft X-ray and Fluorescence Microscopy in an Integrated Setup.

Correlative microscopy is a powerful technique that combines the advantages of multiple imaging modalities to achieve a comprehensive understanding of investigated samples. For example, fluorescence microscopy provides unique functional contrast by imaging only specifically labeled components, especially in biological samples. However, the achievable structural information on the sample in its full complexity is limited. Here, the intrinsic label-free carbon contrast of water window soft X-ray microscopy can complement fluorescence images in a correlative approach ultimately combining nanoscale structural resolution with functional contrast. However, soft X-ray microscopes are complex and elaborate, and are usually installed on large-scale synchrotron radiation sources due to the demanding photon flux requirements. Yet, with modern high-power lasers it has become possible to generate sufficient photon flux from laser-produced plasmas, thus enabling laboratory-based setups. Here, we present a compact table-top soft X-ray microscope with an integrated epifluorescence modality for "in situ" correlative imaging. Samples remain in place when switching between modalities, ensuring identical measurement conditions and avoiding sample alteration or destruction. We demonstrate our new method by multimodal images of several exemplary samples ranging from nanoparticles to various multicolor labeled cell types. A structural resolution of down to 50 nm was reached.

Hard and corrosion-resistant pig iron-based (Fe62Cr8Nb4Mo4(C,B)22) steel glass

In this article, the Fe62Cr8Nb4Mo4(C,B)22 steel glass was produced using inexpensive pig iron as the main master alloy, with minor addition of commercially available ferrous alloys. The fully vitreous nature of the steel produced by melt-spinning was confirmed through X-ray diffraction, from conventional and synchrotron radiation sources, and transmission electron microscopy. Differential scanning calorimetry confirmed the glass transition temperature of approximately 553 °C, and the onset of the crystallization at 574 °C, with supercooled liquid temperature interval of 21 °C. The Fe62Cr8Nb4Mo4(C,B)22 steel glass proved to be harder than the pig iron (1070 vs. 666 HV0.1, respectively) and more stable in chloride-rich medium than the 444 stainless steel, as assessed by the passivation window prior to pit corrosion (1253 vs. 738 mV, respectively) and the ease reprotection upon the reverse scan. The results contribute to the strategies for production of affordable hard and corrosion-resistant steel glasses for demanding applications.

Preparation and Crystallographic Analysis of a Complex of SARS-CoV-2 S-Protein Receptor-Binding Domain with a Virus-Neutralizing Nanoantibody

Coronavirus SARS-CoV-2 was the cause of global pandemic COVID-19 that has claimed millions of lives around the world. One of the approaches to the therapy of severe forms of COVID-19 is based on the use of virus-neutralizing antibodies against the receptor-binding domain (RBD) of the virus spike glycoprotein (S). Detailed structural data on particular epitopes recognized by these virus-neutralizing antibodies is an important aspect of the improvement of available antibodies in order to extend the range of recognized virus strains. A stoichiometric complex of the virus-neutralizing single-domain antibody P2C5 and the glycosylated form of SARS-CoV-2 S protein RBD was obtained. Despite numerous conditions in which the crystal growth of the complex was observed, these crystals showed poor diffraction, apparently because of heterogeneity associated with the glycosylation of RBD. With the aim of improving the crystal quality, deglycosylase PNGase F was produced in a bacterial expression system and deglycosylation of RBD was performed. Despite low solubility of the deglycosylated form of RBD, it retains the ability to bind to the nanoantibody P2C5, resulting in the formation of a stable heterodimeric complex during gel filtration. The crystals of this complex were obtained. They showed diffraction to a similar resolution of ~4 Å on a laboratory X-ray diffractometer and at a synchrotron radiation source. The symmetry space group, the unit cell parameters of the crystal, and its protein composition were determined.

Preliminary X-ray Diffraction Analysis of Purine Nucleoside Phosphorylase from the Haloalkaliphilic Bacterium Halomonas chromatireducens

Crystals of the enzyme purine nucleoside phosphorylase from the extremophilic bacterium Halomonas Chromatireducens AGD 8-3, suitable for X-ray diffraction, were grown by the vapor-diffusion method. The X-ray diffraction data were collected from these crystals at the Belok beamline of the Kurchatov synchrotron radiation source (National Research Centre “Kurchatov Institute”) at 100 K to 1.80 Å resolution. The X-ray diffraction data were processed in the space groups P1, P2, P21, and P622. The structure was solved by the molecular replacement method taking into account the twinning in the space groups P21 and P1 with one and two hexamers of the enzyme per asymmetric unit, respectively.

A dedicated application of evolutionary algorithms: synchrotron X-ray radiation optimization based on an in-vacuum undulator

Following the rapid growth in accelerator-based light sources research since the mid of 20th century, miscellaneous third generation synchrotron radiation (SR) facilities such as SSRL, APS, ESRF, PETRA-III, and SPring-8 have come into existence. These SR source facilities provide 1020–1025 photons/s/mrad2/mm2/0.1%BW peak brightness within the photon energy range of 10–105 eV. Since different measurement techniques are utilized at X-ray beamlines of SR facilities, many kinds of insertion devices (i.e., undulators and wigglers) and optical components (e.g., high-resolution monochromators, double-crystal monochromators, lenses, mirrors, etc.) are employed for each experimental setup as a matter of course. Under the circumstances, optimization of a synchrotron beamline is a big concern for many scientists to ensure required radiation characteristics (i.e., photon flux, spot size, photon energy, etc.) for dedicated user experiments. In this respect, an in-vacuum hybrid undulator driven by a 6 GeV synchrotron electron beam is optimized using evolutionary algorithms (EA). Finally, it is shown that EA results are well consistent with both the literature and the analytical calculations, resulting in a promising design estimation for beamline scientists.

Two-dimensional spatial coherence measurement of X-ray sources using aperture array mask.

Fourth-generation synchrotron radiation delivers x-ray sources with unprecedented coherence and brilliance, which enables the development of many advanced coherent techniques taking advantage of the inherent high coherence of the x-ray beams. Simple and accurate measurement of two-dimensional (2D) coherence is of utmost importance for the applications of these coherent experimental techniques. Here, we propose a novel approach based on diffraction of aperture array mask (AAM) to obtain accurate 2D spatial coherence with a single-shot measurement. We utilize a coherent mode decomposition algorithm to simulate the diffraction of AAM illuminated by Gaussian-Schell model beam and demonstrate that spatial coherence function of the incident light beam can be accurately and robustly retrieved. We expect that this new approach will be applied into transverse coherence measurements for the new-generation synchrotron radiation source and relevant coherent experimental techniques.

At-wavelength characterization of X-ray wavefronts in Bragg diffraction from crystals.

The advent of next-generation synchrotron radiation sources and X-ray free-electron lasers calls for high-quality Bragg-diffraction crystal optics to preserve the X-ray beam coherence and wavefront. This requirement brings new challenges in characterizing crystals in Bragg diffraction in terms of Bragg-plane height errors and wavefront phase distortions. Here, a quantitative methodology to characterize crystal optics using a state-of-the-art at-wavelength wavefront sensing technique and statistical analysis is proposed. The method was tested at the 1-BM-B optics testing beamline at the Advanced Photon Source for measuring silicon and diamond crystals in a self-referencing single-crystal mode and an absolute double-crystal mode. The phase error sensitivity of the technique is demonstrated to be at the λ/100 level required by most applications, such as the characterization of diamond crystals for cavity-based X-ray free-electron lasers.

Synchrotron radiation of a single electron application for optical spectroradiometry

Objectives. The investigations of optical radiation sources and metrological detector characteristics in the infrared (IR), visible, and air ultraviolet (UV) spectral regions are partially based on the unique metrological properties of synchrotron radiation. The aim of this work is to develop a high-precision method for determining the storage ring accelerated electron number with synchrotron radiation of a single electron to establish spectroradiometry and photometry units.Methods. By determining the number of accelerated electrons, any storage ring can be used to calculate the synchrotron radiation characteristics at wavelengths of many large then the critical wavelength in the visible, air UV, and IR regions of the spectrum. This makes it possible to determine the main metrological characteristics normalized to the number of electrons, such as luminous intensity, luminance, illuminance, radiant power, radiance, irradiance, etc., regardless of the energy of the electrons.Results. When applying the method for determining the number of accelerated electrons at low currents of the electronic storage ring, a total standard deviation of the number of accelerated electrons is less than 0.01% for an exposure range of the CCD matrix from 10−2 to 3 · 103 s in a wide dynamic range of 1−1010 electrons per orbit.Conclusions. The use of a CCD-based radiometer-comparator calibrated by responsivity on a synchrotron radiation source is particularly relevant in monitoring luminance contrast thresholds and spatial distribution of object and background brightness, as well as determining metrological characteristics of optoelectronic measuring instruments, including CCD cameras, radiometers, spectroradiometers and photometers.

Developing an Interferometric Method for Measuring the Transverse Dimensions of a Particle Beam in Cyclic Accelerators

This work is devoted to the development of a method for measuring beam sizes in cyclic charged particle accelerators using an interferometer based on the Young scheme with a double-slit diaphragm. We have carried out an experimental verification of the original spectral method for scanning the interference pattern. The results of measurements of the spectrum of low-frequency oscillations of the beam of the storage ring of the Kurchatov Synchrotron Radiation Source (KSRS) obtained by means of the Optical Observation Station (OOS) of the storage ring are presented.

SARS-CoV-2 proteins structural studies using synchrotron radiation.

In the process of the development of structural biology, both the size and the complexity of the determined macromolecular structures have grown significantly. As a result, the range of application areas for the results of structural studies of biological macromolecules has expanded. Significant progress in the development of structural biology methods has been largely achieved through the use of synchrotron radiation. Modern sources of synchrotron radiation allow to conduct high-performance structural studies with high temporal and spatial resolution. Thus, modern techniques make it possible to obtain not only static structures, but also to study dynamic processes, which play a key role in understanding biological mechanisms. One of the key directions in the development of structural research is the drug design based on the structures of biomolecules. Synchrotron radiation offers insights into the three-dimensional time-resolved structure of individual viral proteins and their complexes at atomic resolution. The rapid and accurate determination of protein structures is crucial for understanding viral pathogenicity and designing targeted therapeutics. Through the application of experimental techniques, including X-ray crystallography and small-angle X-ray scattering (SAXS), it is possible to elucidate the structural details of SARS-CoV-2 virion containing 4 structural, 16 nonstructural proteins (nsp), and several accessory proteins. The most studied potential targets for vaccines and drugs are the structural spike (S) protein, which is responsible for entering the host cell, as well as nonstructural proteins essential for replication and transcription, such as main protease (Mpro), papain-like protease (PLpro), and RNA-dependent RNA polymerase (RdRp). This article provides a brief overview of structural analysis techniques, with focus on synchrotron radiation-based methods applied to the analysis of SARS-CoV-2 proteins.

Measurement of the Parameters of the RF Gun of the Linear Accelerator of the Siberian Ring Source of Photons

The paper analyzes the results of the first experiments to obtain the design parameters of the RF cannon beam of the linear accelerator of the Siberian Ring Synchrotron Radiation Source (SKIF) and describes the diagnostic methods used in this case. The studied parameters include the transverse and longitudinal profiles of the beam, its emittance, energy and energy spread, current, charge and particle losses. The obtained values are compared with the numerical simulation data.

Exploring beam size measurement based on the Talbot effect at BEPCII.

Vertical beam size measurements were carried out at Beijing Electron-Positron Collider II (BEPCII) using a phase grating and an absorption grating based on the Talbot effect. The transverse coherence of synchrotron radiation is closely related to beam size. Due to the partial coherence of the synchrotron radiation source, the coherence length can be calculated by measuring the visibility decay of interferograms recorded at different distances behind the gratings. A vertical beam size of 68.19 ± 2 µm was obtained based on the relationship between the coherence length and beam size at the 3W1 beamline of BEPCII. A comparison of the vertical emittance derived from the grating Talbot method and the synchrotron radiation visible light interferometer method was presented. The vertical emittances from the two methods are 1.41 nm rad and 1.40 nm rad, respectively. The 0.1% difference indicates that the grating Talbot method for beam size measurement is reliable. This technique has great potential for small beam size measurement of fourth-generation synchrotron radiation light sources, considering its small diffraction limitation and simple experimental setups.