High-performance X-ray Research Articles

The concept for hard X-ray beamline optics atSLS2.0.

In the scope of the latest upgrade of the Swiss Light Source, five hard X-ray beamlines will be constructed or rebuilt. To use synergies between these beamline projects, a concept is developed here for hard X-ray beamlines that is tailored to the new storage ring. Herein, this concept is described from the source, via the front end, to the beamline optics. The latter will be outlined in detail, including a new and modular concept for hard X-ray monochromators, focusing optics and heat-load management. With a simple, easy-to-operate and robust beamline design, the new beamlines will greatly profit from the increased brilliance of the new storage ring. The performance increase is up to four orders of magnitude, while the beamline concept allows for the broad application of experimental techniques, from propagation-based methods, such as phase-contrast tomography, to imaging techniques with nanometre resolution. At the same time, spectroscopy experiments are possible as well as high-performance serial X-ray crystallography.

Confinement of methylammonium lead bromide nanocrystals in metal–organic frameworks as a stable scintillator for high-performance X-ray imaging

The development of perovskite nanocrystals (NCs) based composites with enhanced stability and exceptional photoelectric properties is of great significance for their application in scintillators for X-ray imaging, but it remains challenging. Herein, we demonstrate a novel and stable scintillator, achieved through a host–guest strategy involving the confinement of perovskite NCs, e.g., MAPbBr3 NCs, in metal–organic frameworks (MOFs). The host MOF, bio-MOF-100 (denoted as bMOF), facilitates the in-situ space-confined formation of MAPbBr3 NCs while providing quantum confinement, surface passivation, and protection to these guests. This host–guest strategy results in high exciton binding energy, bright and efficient luminescence, and significantly enhancing their stability against various factors such as air, heat, UV, solvents and X-ray irradiation. Consequently, this advancement prompts the transition of their application scenarios from the colloidal state to the solid state. The bMOF⊃MAPbBr3 scintillator exhibits a linear response to X-ray with a detection limit determined to be 170 nGyair s−1. Moreover, the bMOF⊃MAPbBr3–PMMA scintillator screen demonstrates high-quality X-ray imaging with an impressive spatial resolution of 14.7 lp mm−1. This work provides a new avenue for the development of perovskite NCs-based host–guest composites and paves the way for the broader implementation in solid-state optoelectronic applications.

Exploring mounting solutions for cryogenically cooled thin crystal optics in high power density x-ray free electron lasers.

This study investigates three mounting methods-clamping, soldering, and a hybrid clamping-soldering approach-for cryogenically cooled thin diamond crystals crucial to stable operation of X-ray Free Electron Laser (XFEL) systems. While clamping methods exhibit temperature resilience and flexibility, meticulous design is required to prevent stress-induced warping and reduce thermal contact area. Soldering methods offer reliable mechanical and thermal bonding but encounter challenges due to the coefficient of thermal expansion mismatch at cryogenic temperatures. The hybrid method, integrating clamping and soldering with strain relief cuts, effectively mitigates overall distortion caused by mounting and XFEL thermal loads. These findings offer a novel mounting solution for high-performance x-ray optics in XFEL research and applications, ensuring stability and optimal functionality in cryogenic conditions.

Through-Space Charge-Transfer Organogold(III) Complexes Enable High-Performance X-ray Scintillation and Imaging.

Organic scintillators have recently attracted growing attention for X-ray detection in industrial and medical applications. However, these materials still face critical obstacles of low attenuation efficiency and/or inefficient triplet exciton utilization. Here we developed a new category of organogold(III) complexes, Tp-Au-1 and Tp-Au-2, through adopting a through-space interaction motif to realize high X-ray attenuation efficiency and efficient harvesting of triplet excitons for emission. Thanks to the efficient through-space charge transfer process, this panel of complexes achieved higher photoluminescence quantum yield and shorter radiative lifetimes compared with the through-bond reference complexes. Inspiringly, these organogold(III) complexes exhibited polarity-dependent emission origins: thermally activated delayed fluorescence and/or phosphorescence. Under X-ray irradiation, Tp-Au-2 manifested intense radioluminescence together with a record-high scintillation light yield of 77,600 photons MeV-1 for organic scintillators. The resulting scintillator screens demonstrated high-quality X-ray imaging with >16.0 line pairs mm-1 spatial resolution, outstripping most organic and inorganic scintillators. This finding provides a feasible strategy for the design of superior organic X-ray scintillators.

One-Dimensional orthorhombic CsPbI3 polycrystalline thick film for efficient and highly stable direct X-ray detection and imaging

An ideal direct X-ray detector should convert a low dose of X-ray photons into large quantity of electrical signals, coupled with sustained long-term stability. Nevertheless, a notable conflict arises between X-ray absorption efficiency and carrier transport in thick polycrystalline perovskite films. Moreover, conventional perovskite materials exhibit inherent challenges regarding the stability of their crystal phase and the consistency of the photocurrent. To circumvent these limitations, a polycrystalline perovskite thick film is proposed using orthorhombic CsPbI3 (δ-CsPbI3) as a highly stable active material. Combined with the liquid epitaxy process, δ-CsPbI3 prefers one-dimensional growth along the carrier transportation direction, which suppresses the formation of grain boundaries, enabling high carrier mobility while maintaining X-ray absorption for a thick polycrystalline film. Consequently, the polycrystalline δ-CsPbI3 based detector exhibits a highest sensitivity of 1768.46 μC Gyair-1 cm−2 at an electric field of 432 V mm−1 which is 88.42-fold higher than α-Se based detectors and 190-fold higher than the single crystalline δ-CsPbI3 based detector, respectively. The sensitivity maintains 91.34 % of its initial state after 7 days exposure in the air. Combing with a thin-film transistor array, the detector achieves 8-bit imaging within a 64 × 64 matrix. This work provides a feasible method for commercialized production of high-performance direct X-ray detectors.

Stereo-Hindrance Engineering of A Cation toward -Oriented 2D Perovskite with Minimized Tilting and High-Performance X-Ray Detection.

2D <100>-oriented Dion-Jacobson or Ruddlesden-Popper perovskites are widely recognized as promising candidates for optoelectronic applications. However, the large interlayer spacing significantly hinders the carrier transport. <110>-oriented 2D perovskites naturally exhibit reduced interlayer spacings, but the tilting of metal halide octahedra is typically serious and leads to poor charge transport. Herein, a <110>-oriented 2D perovskite EPZPbBr4 (EPZ = 1-ethylpiperazine) with minimized tilting is designed through A-site stereo-hindrance engineering. The piperazine functional group enters the space enclosed by the three [PbBr6 ]4- octahedra, pushing Pb─Br─Pb closer to a straight line (maximum Pb─Br─Pb angle ≈180°), suppressing the tilting as well as electron-phonon coupling. Meanwhile, the ethyl group is located between layers and contributes an extremely reduced effective interlayer distance (2.22 Å), further facilitating the carrier transport. As a result, EPZPbBr4 simultaneously demonstrates high µτ product (1.8 × 10-3 cm2 V-1 ) and large resistivity (2.17 × 1010 Ω cm). The assembled X-ray detector achieves low dark current of 1.02 × 10-10 A cm-2 and high sensitivity of 1240 µC Gy-1 cm-2 under the same bias voltage. The realized specific detectivity (ratio of sensitivity to noise current density, 1.23 × 108 µC Gy-1 cm-1 A-1/2 ) is the highest among all reported perovskite X-ray detectors.

High-Performance Flat-Panel Perovskite X-ray Detectors Enabled by Defect Passivation in Ruddlesden-Popper Perovskites.

Halide perovskites have emerged as promising candidates in X-ray detection due to their strong X-ray absorption and excellent optoelectronic properties. The development of sensitive and stable flat-panel X-ray detectors with high resolution is crucial for practical applications. In this paper, we introduce a novel flat-panel X-ray detector that integrates quasi-two-dimensional (2D) Ruddlesden-Popper (RP) perovskite with a pixeled thin film transistor (TFT) backplane. We incorporate 2,5-dibromopyrimidine (DBPM) as an additive to passivate the Lewis acid defects in the quasi-2D RP perovskite. This modification results in suppressed ion migration, improved optoelectronic performance, and enhanced operational stability of the device. Impressively, the activation energy of the RP perovskite increases from 0.96 to 1.35 eV with the DBPM additive. As a result, X-ray detectors exhibit a high sensitivity of ∼13,600 μC Gyair-1 cm-2, a low detection limit of 6.56 nGyair s-1, and excellent operational stability. Moreover, the flat-panel detectors demonstrate a high spatial resolution of 3.7 line pairs per millimeter and excellent X-ray imaging properties under a remarkably low X-ray dose of ∼50 μGyair, which is just half of the X-ray dose typically used in commercial equipment. This study opens new avenues for the development of flat-panel perovskite X-ray detectors with significant potential for various applications.

High-Performance and Stable Perovskite X-ray Detection and Imaging Based on a Ti Cathode.

High-energy radiation detectors with a good imaging resolution, fast response, and high sensitivity are desired to operate at a high electric field. However, strong ion migration triggered by electrochemical reactions at the interface between a high-potential electrode and an organic-inorganic hybrid perovskite limits the stability of radiation detectors under a high electric field. Herein, we demonstrate that such ion migration could be effectively suppressed in devices with a Ti cathode, even at a high electric field of 50 V mm-1, through time-of-flight secondary-ion mass spectrometry. X-ray photoelectron spectroscopy illustrates that Ti-N bonds formed at the interface of MAPbBr3 perovskite single crystals/Ti electrode effectively inhibit the electrochemical reaction in organic-inorganic hybrid perovskite devices and ultimately improve the operating stability under a high electric field. The device with a Ti electrode reaches a high sensitivity of 96 ± 1 mC Gyair-1 cm-2 and a low detection limit of 2.8 ± 0.3 nGy s-1 under hard X-ray energy.

Experimental and Analytical Investigation of Performance of Liquid Metal Herringbone Grooved Bearings with Cylindricity Errors

Liquid metal herringbone grooved bearings (LM-HGBs) are customarily used in high-performance x-ray tubes to support the high-speed rotating anode and facilitate heat transfer from the anode to the coolant. This article investigates the impact of cylindricity errors on LM-HGBs performance through simulations and experiments. The analysis considers both the Reynolds equation modified by turbulence and the film equation incorporating cylindricity errors to construct the prediction model of LM-HGBs. An experiment rig was constructed to measure the friction torque of LM-HGBs. The predictions were validated by comparing to experimental results. The pressure distribution was predicted under different cylindricity errors. The test and experimental results demonstrate that cylindricity error impacts the uniformity of groove depth and has a significant effect on the friction torque of the bearings. Theoretical results reveal that concavity and convexity errors alter the pressure distribution and have opposing effects on bearing static and dynamic parameters. Decreasing the ratio of error amplitude to groove depth and the ratio of error amplitude to radius clearance can reduce the effect of cylindricity errors.

Dynamic X-ray imaging with screen-printed perovskite CMOS array.

High performance X-ray detector with ultra-high spatial and temporal resolution are crucial for biomedical imaging. This study reports a dynamic direct-conversion CMOS X-ray detector assembled with screen-printed CsPbBr3, whose mobility-lifetime product is 5.2 × 10-4 cm2 V-1 and X-ray sensitivity is 1.6 × 104 µC Gyair-1 cm-2. Samples larger than 5 cm[Formula: see text]10 cm can be rapidly imaged by scanning this detector at a speed of 300 frames per second along the vertical and horizontal directions. In comparison to traditional indirect-conversion CMOS X-ray detector, this perovskite CMOS detector offers high spatial resolution (5.0 lp mm-1) X-ray radiographic imaging capability at low radiation dose (260 nGy). Moreover, 3D tomographic images of a biological specimen are also successfully reconstructed. These results highlight the perovskite CMOS detector's potential in high-resolution, large-area, low-dose dynamic biomedical X-ray and CT imaging, as well as in non-destructive X-ray testing and security scanning.

Toward Low-Voltage and High-Sensitivity Direct X-ray Detectors Based on Thick Bulk Heterojunction Organic Device.

Organic semiconducting materials are promising for the fabrication of flexible ionizing radiation detectors for imaging because of their tissue equivalence, simple large-scale processing, and mass production. However, it is challenging to achieve high-sensitivity detection for organic direct detectors prepared by low-cost solution processing because of the compromise between thickness and carrier transport. In this study, high-performance organic direct X-ray detectors were fabricated by building a micrometer-thick bulk heterojunction (BHJ) using poly(3-hexylthiophene-2,5-diyl) (P3HT):(6,6)-phenyl c71 butyric acid methyl ester. A 5 μm BHJ film was fabricated by drop-casting and enhanced crystallization of P3HT using binary solvents and high-boiling-point additives to improve the charge carrier mobility. Furthermore, this organic direct X-ray detector has a sensitivity of >654.26 μC Gyair s-1 and a self-powered response. Because of the architecture of the thick active layer and the energy cascade in this diode detector, it has a very low dark current of 46.26 pA at -2 V. A fast and efficient approach was developed for fabricating thick, highly mobile organic BHJ films for high-performance direct X-ray detectors. It has great potential for application in a new generation of flexible and portable large-area flat-panel detectors.

Polycrystalline Lead-Free Perovskite Direct X-Ray Detectors with High Durability and Low Limit of Detection via Low-Temperature Coating.

Direct X-ray detectors represent a transformative technology in the realm of radiography and imaging. The double halide-based perovskite cesium silver bismuth bromide (Cs2AgBiBr6) has emerged as a promising material for use in direct X-ray imaging, owing to its nontoxic composition, strong X-ray absorption, decent charge mobility lifetime product (μτ), and low-cost preparation. However, formidable issues related to scalability and ion migration, stemming from intrinsic factors such as halogen vacancies and grain boundaries, have presented significant impediments. These issues have been associated with substantial noise, baseline instability, and a curtailment of detection performance. In response to these multifaceted challenges, we propose a slurry-based in situ treatment technique for fabricating robust Cs2AgBiBr6 thick films. This novel approach adeptly mitigates halogen vacancies, actively passivates grain boundaries, and concurrently elevates the ion migration activation energy, thus effectively suppressing ion migration. Consequently, the obtained X-ray detector exhibits excellent operating stability with minimal signal drift of 8.5 × 10-9 nA cm-1 s-1 V-1 and achieves a remarkable 385% increase in sensitivity with a limit of detection as low as 7.8 nGyair s-1. These results mark a significant step toward the development of high-performance and long-lasting lead-free perovskite direct X-ray detectors.

Transparent and Planar Cs3Cu2Cl5 Crystals for Micrometer-Resolution X-ray Imaging Screen.

Copper-based (I) halide perovskites have emerged as a promising candidate for scintillation screens in X-ray inspection and imaging areas due to their solution processability and high light yield. Here, a centimeter-sized Cs3Cu2Cl5 single crystal was grown by a slow-cooling method. The planar orientation was controlled in a space-confined chamber, generating a planar crystal which is readily used for a scintillation screen without any further shaping. The crystal exhibited a unity photoluminescence quantum yield and superior scintillation performance. The Cs3Cu2Cl5 single crystal exhibited a high light yield up to 95,000 photons/MeV, which enabled an X-ray detector of a detection limit down to 2.7 μGyair/s. The homemade imager demonstrated a spatial resolution of 105 lp/mm, representing an unprecedented micrometer resolution in laboratory. Importantly, the stability of Cs3Cu2Cl5 was significantly improved by a new surface passivation procedure, whereby the passivated crystal reserved its phase after 6 months' storage in a vial. This work introduced a new solution-based synthetic method for two-dimensional scintillating crystals, opening many avenues to high-performance X-ray imaging applications.

Cation-π interactions enabled water-stable perovskite X-ray flat mini-panel imager

Sensitive and stable perovskite X-ray detectors are attractive in low-dosage medical examinations. The high sensitivity, tunable chemical compositions, electronic dimensions, and low-cost raw materials make perovskites promising next-generation semiconductors. However, their ionic nature brings serious concerns about their chemical and water stability, limiting their applications in well-established technologies like crystal polishing, micro-processing, photolithography, etc. Herein we report a one-dimensional tryptamine lead iodide perovskite, which is stable in water for several months as the strong cation-π interactions between organic cations. The one-dimensional and two-dimensional tryptamine lead iodide perovskite tablets are switchable through thermal-annealing or water-soaking treatments to relax microstrains. The water-stable and microstrain-free one-dimensional perovskite tablets yield a large sensitivity of 2.5 × 106 μC Gyair−1 cm−2 with the lowest detectable dose rate of 5 nGyair s−1. Microelectrode arrays are realized by surface photolithography to construct high-performance X-ray flat mini-panels with good X-ray imaging capability, and a record spatial resolution of 17.2 lp mm−1 is demonstrated.

Highly efficient and ultra-stable CsPbBr3 composites for LCD devices and X-ray imaging

Highly luminescent CsPbBr3-DPSI/MS composites with excellent overall stabilities are synthesized using a solid-state reaction method. These composites exhibit a promising foreground in high-performance LCD and X-ray imaging.

Development of high-performance direct X-ray detector materials: from hybrid halide perovskites to all-inorganic lead-free perovskites

X-rays Detection plays a vital role in medical imaging, industrial defect detection, security screening and scientific research. Direct X-ray detectors are of greater interest to researchers because they offer the...

A 0D hybrid lead-free halide with near-unity photoluminescence quantum yield toward multifunctional optoelectronic applications.

Zero-dimensional (0D) hybrid metal halides have emerged as highly efficient luminescent materials, but integrated multifunction in a structural platform remains a significant challenge. Herein, a new hybrid 0D indium halide of (Im-BDMPA)InCl6·H2O was designed as a highly efficient luminescent emitter and X-ray scintillator toward multiple optoelectronic applications. Specifically, it displays strong broadband yellow light emission with near-unity photoluminescence quantum yield (PLQY) through Sb3+ doping, acting as a down-conversion phosphor to fabricate high-performance white light emitting diodes (WLEDs). Benefiting from the high PLQY and negligible self-absorption characteristics, this halide exhibits extraordinary X-ray scintillation performance with a high light yield of 55 320 photons per MeV, which represents a new scintillator in 0D hybrid indium halides. Further combined merits of a low detection limit (0.0853 μGyair s-1), ultra-high spatial resolution of 17.25 lp per mm and negligible afterglow time (0.48 ms) demonstrate its excellent application prospects in X-ray imaging. In addition, this 0D halide also exhibits reversible luminescence off-on switching toward tribromomethane (TBM) but fails in any other organic solvents with an ultra-low detection limit of 0.1 ppm, acting as a perfect real-time fluorescent probe to detect TBM with ultrahigh sensitivity, selectivity and repeatability. Therefore, this work highlights the multiple optoelectronic applications of 0D hybrid lead-free halides in white LEDs, X-ray scintillation, fluorescence sensors, etc.

1D Pb halide perovskite-like materials for high performance X-ray detection.

The strategy of bandgap regulation is important for X-ray detection, but has not been reported for 1D Pb halide perovskite materials. In this work, three such materials, 1, 2 and 3, with a tunable bandgap, were fabricated for application in X-ray detection. 3 shows high sensitivity, far superior to commercial X-ray detectors.

A two-dimensional lead-free double perovskite for self-powered and high performance X-ray detection

Two-dimensional Dion–Jacobson (DJ) phase hybrid perovskites are gradually coming to the stage of optoelectronic devices because of their excellent photoelectric properties.

A Multilayer Nested Space Ray Telescope Assembly and Adjustment System Based on Online Monitoring Feedback

In order to adapt to the rapid development of deep space exploration, pulsar navigation and space astronomical observation technology, the development of high-efficiency and high-performance X-ray space telescopes has become one of the hotspots for research in the fields of autonomous spacecraft navigation and astronomical observation. Since the X-ray multilayer nested mirror shells are thin-walled and deformable cylindrical structures with high requirements for surface shape accuracy, a slight change in the position or surface shape will lead to a reduction in the focusing imaging quality, so it is necessary to develop a high-precision assembly and adjustment system based on closed-loop real-time monitoring. In this paper, a multi-layer nested space ray telescope assembly and adjustment system with online monitoring feedback is developed, and a method for precision assembly and adjustment of multi-layer nested mirror shells based on online real-time detection and feedback is proposed, which specifically includes key innovative assembly technologies such as three-dimensional face shape measurement, flexible vacuum adsorption, precision adjustment that have been broken through in the process, and the imaging quality of the focused spot of the mirror shells is evaluated and analyzed in the end. The results of the experiment indicate that the assembly and adjustment of the multilayer nested mirror shells can effectively complete the high-precision assembly, and the relevant results can provide a certain reference significance for the further enhancement of the assembly and adjustment performance of the multilayer nested mirror shells.