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Objective: To evaluate the applicability of artificial intelligence-assisted compressed sensing (ACS) to anal fistula magnetic resonance imaging (MRI). Methods: 51 patients were included in this study and underwent T2-weighted sequence of MRI examinations both with ACS and without ACS technology in a 3.0 T MR scanner. Subjective image quality scores, and objective image quality-related metrics including scanning time, signal-to-noise ratio (SNR), and contrast-to-noise ratio (CNR), were evaluated and statistically compared between the images collected with and without ACS. Results: No significant difference in the subjective image quality of lesion conspicuity was observed between the two groups. However, ACS MRI decreased the acquisition time with regard to control group (74.00 s vs. 156.00 s). Besides, SNR of perianal and muscle in the ACS group was significantly higher than that of the control group (164.07 ± 33.35 vs 130.81 ± 29.10, p < 0.001; 109.87 ± 22.01 vs 87.61 ± 17.95, p < 0.001; respectively). The CNR was significantly higher in the ACS group than in the control group (54.02 ± 23.98 vs 43.20 ± 21.00; p < 0.001). Moreover, the accuracy rate of the ACS groups in evaluating the direction and internal opening of the fistula was 88.89 %, exactly the same as that of the control group. Conclusion: We demonstrated the applicability of using ACS to accelerate MR of anal fistulas with improved SNR and CNR. Meanwhile, the accuracy rates of the ACS group and the control were equivalent in evaluating the direction and internal opening of the fistula, based on the results of surgical exploration.
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All-inorganic halide perovskites (AIHPs) have emerged as highly promising optoelectronic materials owing to their remarkable properties, such as high-optical absorption coefficients, photoluminescence efficiencies, and dopant tolerance. Here, we investigate the AIHPs K4CdCl6:Sb3+,Mn2+ that demonstrate hue-tunable white-light emission with an exceptional photoluminescence quantum yield of up to 97%. Through a detailed investigation, we reveal that efficient energy transfer from Sb3+ to Mn2+ plays a dominant role in the photoluminescence of Mn2+, instead of the conventional 4T1g â 6A1g transition of Mn2+. Thermodynamic analysis highlights the crucial role of a Cl-rich environment in obtaining the K4CdCl6 phase, while transformation from K4CdCl6 to KCdCl3 can be achieved under Cl-poor and K-poor conditions. The theoretical analysis reveals that defect Cli is more readily formed compared to defect VK, corroborating experimental findings that the K4CdCl6:Sb3+ phase is exclusively obtained when the solution contains HCl concentrations higher than 4 mol L-1. Our work provides valuable insights into the photoluminescence mechanism of Sb3+, defect engineering through heterovalent doping, and efficient energy transfer between Sb3+ and Mn2+ in K-Cd-Cl-based perovskites, which offers a new perspective for the design and development of novel AIHPs with superior optoelectronic performance.
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High-temperature proton-exchange membrane fuel cells (HT-PEMFCs) with phosphoric-doped polybenzimidazole (PBI) membranes have a higher operating temperature compared to the PEMFCs operating below 373.15 K. The fuel cell is first heated from room temperature to the minimum operating temperature to avoid the generation of liquid water. The existence of liquid water can result in the loss of phosphoric acid and then affect the cell performance. In this study, the start-up process of HT-PEMFCs is numerically studied by establishing a three-dimensional non-isothermal mathematical model. Preheated gas is supplied into gas flow channels to heat the fuel cell, and then voltage load is applied to accelerate the start-up process. Effects of voltage (0.9 V, 0.7 V and 0.5 V) and flow arrangement (co-flow and counter flow) on temperature, current density, proton conductivity and stress distributions of fuel cells are examined. It is found that the maximum stress is increased when a lower voltage is adopted, and the counter-flow arrangement provides a more uniform stress distribution than that of co-flow arrangement.
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Single-component white light emitters based on the all-inorganic perovskites will act as outstanding candidates for applications in solid-state lighting thanks to their abundant energy states for self-trapped excitons (STE) with ultra-high photoluminescence (PL) efficiency. Here, a complementary white light is realized by dual STEs emissions with blue and yellow colors in a single-component perovskite Cs2 SnCl6 :La3+ microcrystal (MC). The dual emission bands centered at 450 and 560 nm are attributed to the intrinsic STE1 emission in host lattice Cs2 SnCl6 and the STE2 emission induced by the heterovalent La3+ doping, respectively. The hue of the white light can be tunable through energy transfer between the two STEs, the variation of excitation wavelength, and the Sn4+ /Cs+ ratios in starting materials. The effects of the doping heterovalent La3+ ions on the electronic structure and photophysical properties of the Cs2 SnCl6 crystals and the created impurity point defect states are investigated by the chemical potentials calculated using density functional theory (DFT) and confirmed by the experimental results. These results provide a facile approach to gaining novel single-component white light emitter and offer fundamental insights into the defect chemistry in the heterovalent ions doped perovskite luminescent crystals.
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Organolead halide hybrids have many promising attributes for photocatalysis, e.g. tunable bandgaps and excellent carrier transport, but their instability constraints render them vulnerable to polar molecules and limit their photocatalysis in moisture. Herein, we report the construction of metal-organic frameworks based on [Pb2X]3+ (X = Br-/I-) chains as secondary building units and 2-amino-terephthalate as organic linkers, and extend their applications in photocatalytic CO2 reduction with water vapor as the reductant. Hall effect measurement and ultrafast transient absorption spectroscopy demonstrate the bromo/iodo-bridged frameworks have substantially enhanced photocarrier transport, which results in photocatalytic performances superior to conventional metal-oxo metal-organic frameworks. Moreover, in contrast to lead perovskites, the [Pb2X]3+-based frameworks have accessible porosity and high moisture stability for gas-phase photocatalytic reaction between CO2 and H2O. This work significantly advances the excellent carrier transport of lead perovskites into the field of metal-organic frameworks.
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OBJECT: To explore the feasibility and clinical application of AI -assisted compressed sensing (ACS) technology in kidney MR imaging. METHODS: 33 patients were enrolled in this study, affiliated to our hospital from September 2020 to April 2021. The patients underwent T2-weighed sequences of both the ACS scan and the conventional respiratory navigator (NAVI) scan. We evaluated the subjective image quality scores, including the sharpness of image edge, artifact and the overall image quality, and compared the objective image quality indicators such as scanning time, signal-to-noise ratio (SNR), and contrast signal-to-noise ratio (CNR). The Wilcoxon's rank sum test and the paired t test were used to compare the image quality between ACS and NAVI groups. The p-value less than 0.05 indicated a statistically significant difference. RESULTS: The edge sharpness of the ACS group was significant lower than that of the NAVI group (p < 0.01), however, there were no significant differences in the artifact and the overall rating of image quality between the two groups (p > 0.05). In terms of the objective image quality scores, the scanning time of the ACS group is significantly lower than that of control group. The SNR and CNR of ACS group were significantly higher than those of NAVI group (SNR:3.63 ± 0.76 vs 3.04 ± 0.44, p < 0.001; CNR: 14.44 ± 4.53 vs 12.05 ± 3.32, p < 0.001). In addition, the subjective and objective measurement results of the two radiologists were in good agreement (ICC = 0.61-0.88). CONCLUSION: ACS technology has obvious advantages when applied to kidney MR imaging, which can realize ultra-fast MR imaging. The images can be acquired with a single breath-hold (17 s), which greatly shortens the scanning time. Moreover, the image quality is equal to or better than the conventional technology, which can meet the diagnostic requirements. Thus, it has obvious advantages in diagnosis for kidney disease patients with different tolerance levels for the clinical promotion.
Subject(s)
Kidney , Magnetic Resonance Imaging , Artificial Intelligence , Feasibility Studies , Humans , Kidney/diagnostic imaging , TechnologyABSTRACT
Aerobic oxidation of benzylic C(sp3)-H bonds in a green and heterogeneous manner is a major target in organic catalysis. Herein, we report the synthesis of 3D coordination polymers containing [Co5(OH)6]4+ layers, affording reusable and efficient oxidation of ethylbenezene and tetralin by using O2 as the oxidant. Moreover, the cleavage of CoII-carboxylate bonding renders atomically thin cobaltate nanosheets and enhanced catalytic performance. This is one of the top catalytic performances for CoII-catalyzed benzylic C(sp3)-H oxidation (â¼0.02 mol% Co and 76% conversion for nanosheets), ascribed to the exposed, accessible and coordinatively unsaturated CoII species.
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All-inorganic halide perovskite crystals are considered excellent optical host lattices for various dopants to obtain wavelength-tunable emissions with ultra-broad bands even over a wide spectral range. Here, a series of Mn2+-doped bulk ligand-free CsCdCl3 (CCC) perovskite crystals with a hexagonal shape and size of about 1 millimeter (mm) have been prepared by a facile hydrothermal method. These CCC:Mn2+ (CCC:Mn) crystals emit the representative orange-red photoluminescence (PL) of Mn2+ (4T1(G)-6A1(S)) in the centers of hexagonal octahedrons coordinated with six Cl- ions. A fine-tuning of the Mn2+ concentration from 1 to 50 mol % Cd2+ induces a substantial red shift of emission spectra from 570 to 630 nm due to the shrinkage of the crystalline host lattice, and the maximum intensity of emission is achieved at 20 mol % Mn2+ doping. A further increase in the Mn2+ concentration causes a decrease of the PL intensity due to the phase transition from CCC to CsMnCl3·2H2O (CMCH). The strong excitation bands at 360, 370, 420, and 440 nm can make the excitation of the emissive CCC:Mn crystals possible with ultraviolet (UV) and blue chips for application in white light-emitting diodes (WLEDs). The similarity of the Mn2+-concentration-dependent emission spectra excited by various wavelengths indicates that there is only one type of site for Mn2+ occupation in CCC.
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A crucial challenge is to develop an in situ passivation treatment strategy for CsPbX3 (CPX, X=Cl, Br, and I) quantum dots (QDs) and simultaneously retain their luminous efficiency and wavelength. Here, a facile method to significantly improve the stability of the CPX QDs via in situ crystallization with the synergistic effect of 4-bromo-butyric acid (BBA) and oleylamine (OLA) in polar solvents including aqueous solution and a possible fundamental mechanism are proposed. Monodispersed CsPbBr3 (CPB) QDs obtained in water show high photoluminescence quantum yields (PLQYs) of 86.4 % and their PL features of CPB QDs have no significant change after being dispersed in aqueous solution for 96â h, which implies the structure of CPB QDs is unchanged. The results provide a viable design strategy to synthesize all-inorganic perovskite CPX QDs with strong stability against the attack of polar solvents and shed more light on their surface chemistry.
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@#Objective In tongue diagnosis, the location, color, and distribution of spots can be used to speculate on the viscera and severity of the heat evil. This work focuses on the image analysis method of artificial intelligence (AI) to study the spotted tongue recognition of traditional Chinese medicine (TCM). Methods A model of spotted tongue recognition and extraction is designed, which is based on the principle of image deep learning and instance segmentation. This model includes multiscale feature map generation, region proposal searching, and target region recognition. Firstly, deep convolution network is used to build multiscale low- and high-abstraction feature maps after which, target candidate box generation algorithm and selection strategy are used to select high-quality target candidate regions. Finally, classification network is used for classifying target regions and calculating target region pixels. As a result, the region segmentation of spotted tongue is obtained. Under non-standard illumination conditions, various tongue images were taken by mobile phones, and experiments were conducted. Results The spotted tongue recognition achieved an area under curve (AUC) of 92.40%, an accuracy of 84.30% with a sensitivity of 88.20%, a specificity of 94.19%, a recall of 88.20%, a regional pixel accuracy index pixel accuracy (PA) of 73.00%, a mean pixel accuracy (mPA) of 73.00%, an intersection over union (IoU) of 60.00%, and a mean intersection over union (mIoU) of 56.00%. Conclusion The results of the study verify that the model is suitable for the application of the TCM tongue diagnosis system. Spotted tongue recognition via multiscale convolutional neural network (CNN) would help to improve spot classification and the accurate extraction of pixels of spot area as well as provide a practical method for intelligent tongue diagnosis of TCM.
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In this work, a three-dimensional mathematical model including the fluid flow, heat transfer, mass transfer, and charge transfer incorporating electrochemical reactions was developed and applied to investigate the transport phenomena and performance in high-temperature proton exchange membrane fuel cells (HT-PEMFCs) with a membrane phosphoric acid doping level of 5, 7, 9, 11. The cell performance is evaluated and compared in terms of the polarization curve. The distributions of temperature, oxygen mass fraction, water mass fraction, proton conductivity, and local current density of four cases are given and compared in detail. Results show that the overall performance and local transport characteristics are significantly affected by the membrane phosphoric acid doping level.
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Metal-organic frameworks (MOFs) with low-dimensional, deformable haloplumbate secondary building units (SBUs) are an emerging class of intrinsic white-light emitters combining advantageous properties of both MOFs and lead perovskites. Herein, we have successfully synthesized two MOFs with haloplumbate SBUs occupying an extremely high degree of structural strain with local zigzag Pb-X-Pb-X (X = Cl/Br) connectivity located in single-stranded helices. Thus, the electron-phonon coupling in the deformable SBUs affords intrinsic white-light emission and moderately high external photoluminescence quantum efficiencies of 12-15%, superior to our previously reported MOFs. Moreover, the excellent photocarrier diffusion properties of lead perovskites have been successfully incorporated into the MOFs with high chemical robustness in moisture (up to 90% relative humidity, RH).
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The outbreak of Coronavirus Disease 2019 (COVID-19) is a huge threat to global public health security. In the absence of specific antiviral medicines to prevent or treat COVID-19, it is essential to detect the infected patients at an early stage and immediately isolate them from the healthy population. In view of the advantages of sensitivity and high spatial resolution, CT imaging has played an important role in screening and diagnosing of COVID-19 in China. The radiologic technologists performing CT scans for the infected patients become high-risk medical care personnel. It is critical for the radiology department to ensure the personal safety of radiologic technologists and avoid cross-infection. In this review article, we describe the systematic strategies to combat COVID-19 from the radiology department in Tongji hospital in Wuhan, P.R. China, including personnel arrangements, environmental modification, protection levels and configurations, radiological imaging (CT and radiography), and disinfection methods. It can provide guidance to other radiology departments faced with COVID-19 to reduce infection risk for radiologic technologists.
Subject(s)
Coronavirus Infections/epidemiology , Personnel, Hospital , Pneumonia, Viral/epidemiology , Radiology Department, Hospital , Betacoronavirus , COVID-19 , China/epidemiology , Coronavirus Infections/diagnostic imaging , Disease Outbreaks , Disinfection , Humans , Occupational Health , Pandemics , Personal Protective Equipment , Pneumonia, Viral/diagnostic imaging , Radiography, Thoracic , Radiologists , SARS-CoV-2 , Tomography, X-Ray ComputedABSTRACT
The secondary building units in metal-organic frameworks (MOFs) are commonly well-defined metal-oxo clusters or chains with very limited structural strain. Herein, the structurally deformable haloplumbate units that are often observed in organolead halide perovskites have been successfully incorporated into MOFs. The resultant materials are a rare class of isoreticular MOFs exhibiting large Stokes-shifted broadband white-light emission, which is probably induced by self-trapped excitons from electron-phonon coupling in the deformable, zigzag [Pb2 X3 ]+ (X=Cl, Br, or I) chains. In contrast, MOFs with highly symmetric, robust haloplumbate chains only exhibit narrow UV-blue photoemission. The designed MOF-based intrinsic white-light photoemitters have a number of advantages over hybrid inorganic-organic perovskites in terms of stability and tunability, including moisture resistance, facile functionalization of photoactive moieties onto the organic linkers, introduction of luminescent guests.
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We discover a rare bluish white-light-emitting Sb3+-based coordination polymer with an unusually large Stokes shift of 230 nm (2.3 eV), ascribed to the assymetric-symmetric coordination shift of the Sb3+ centers. The photoemission renders both a high photoluminescence quantum yield exceeding 30% and a large full width at half maximum of 116 nm. Moreover, the strongly light-emissive material exhibits a linear relationship between the correlated color temperature and the absolute temperature in a wide range (157-457 K), thus presenting the first solid-state luminescent thermometer based on photoemission energy.
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OBJECTIVE:: To evaluate the image quality of magnetic resonance dacryocystography (MRD) using three-dimesional fast spin-echo -Cube (3D-FSE-Cube) and 3D-FSE-Cube-Flex sequences to examine the lacrimal drainage system (LDS). METHODS:: 21 healthy volunteers underwent 3D-FSE-Cube and 3D-FSE-Cube-Flex MRD after topical administration of compound sodium chloride eye drops. Two radiologists assessed LDS images in a blinded fashion. The signal-to-noise ratio of fluid-filling and the contrast-to-noise ratio of fluid-turbinate were compared between the two sequences. Overall image quality, sharpness, artefacts, visualization of anatomical structures, and visibility of LDS segments were also compared. RESULTS:: Overall image quality, visualization of anatomic structures, and artefact were significantly better on 3D-FSE-Cube-Flex MRD (p < 0.001, respectively). when compared to 3D-FSE-Cube. 3D-FSE-Cube showed lower fluid-filling signal-to-noise ratio and fluid-inferior turbinate CNR (all p < 0.001). In comparison with 3D-FSE-Cube-Flex, 3D-FSE-Cube produced superior visibility of the upper drainage segments (superior canaliculi, p = 0.003; common canaliculus, p = 0.033; inferior canaliculi, p < 0.001), but inferior in lower-LDS visibility (lacrimal sac, p = 0.001; nasolacrimal duct, p < 0.001). There was no difference in the total number of segments visualized per LDS between the two sequences (p = 0.068). CONCLUSIONS:: 3D-FSE-Cube-Flex demonstrated superior image quality and visibility of the lower LDS segments. 3D-FSE-Cube showed an advantage in visualizing the upper LDS segments. The combination of these sequences can improve LDS visibility. ADVANCES IN KNOWLEDGE:: 3D-FSE-Cube-Flex provides robust water & fat separation and mitigates lower LDS-associated inhomogeneity artefacts. 3D-FSE-Cube shows optimal upper LDS visualization. The combined application of these sequences is a non-invasive and effective method for assessing LDS disease.
Subject(s)
Image Enhancement/methods , Imaging, Three-Dimensional/methods , Lacrimal Apparatus/diagnostic imaging , Magnetic Resonance Imaging/methods , Healthy Volunteers , Humans , Magnetic Resonance Imaging/instrumentation , Sodium Chloride/administration & dosageABSTRACT
Herein, we report the unusual broadband white-light emission as an intrinsic property from two cationic lead bromide frameworks. This is the first time that the metal halide materials adopting a purely inorganic positively-charged three-dimensional (3D) topology have been synthesized, thus affording highly distorted PbII centers. The single-component white-light emitters achieve an external quantum efficiency of up to 5.6% and a correlated color temperature of 5727 K, producing typical white-light close to that of fluorescent light sources. Unlike the air/moisture-sensitive 3D organolead halide perovskites, our cationic materials are chemically "inert" over a wide range of pH as well as aqueous boiling condition. Importantly, these long-sought ultrastable lead halide materials exhibit undiminished photoluminescence upon continuous UV-irradiation for 30 days under atmospheric condition (â¼60% relative humidity, 1 bar). Our mechanistic studies indicate the broadband emission have contributions from the self-trapped excited states through electron-vibrational coupling in the highly deformable and anharmonic lattice, as demonstrated by variable-temperature photoluminescence/absorption spectra as well as X-ray crystallography studies. The chemical robustness and structural tunability of the 3D cationic bromoplumbates open new paths for the rational design of hybrid bulk emitters with high photostability.
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We report a family of cationic lead halide layered materials, formulated as [Pb2 X2 ]2+ [- O2 C(CH)2 CO2- ] (X=F, Cl, Br), exhibiting pronounced broadband white-light emission in bulk form. These well-defined PbX-based structures achieve an external quantum efficiency as high as 11.8 %, which is comparable to the highest reported value (ca.9 %) for broadband phosphors based on layered organolead halide perovskites. More importantly, our cationic materials are ultrastable lead halide materials, which overcome the air/moisture-sensitivity problems of lead perovskites. In contrast to the perovskites and other bulk emitters, the white-light emission intensity of our materials remains undiminished after continuous UV irradiation for 30â days under atmospheric conditions (ca.60 % relative humidity). Our mechanistic studies confirm that the broadband emission is ascribed to short-range electron-phonon coupling in the strongly deformable lattice and generated self-trapped carriers.
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The aim of this study is to evaluate the application of magnetic resonance imaging (MRI) to assess ovarian maturation in live female Rhinogobio ventralis (Sauvage & Dabry de Thiersant, 1874). The fish were randomly collected from the Jiangjin area of the Yangtze River between January and April 2014. Magnetic resonance imaging was performed using a 3.0 T clinical MRI scanner with a brain coil and two pulse sequences (IDEAL and 3D CUBE) were employed. Magnetic resonance and histologic images at different stages of ovarian maturation (I-IV) were acquired. An empirical equation (y = -0.1 + 1.56 × x) was derived by traditional method to describe the relationship between the gonadosomatic index (y) and the percentage volume of the ovary (x). A significant correlation (R(2) = 0.977, P < 0.01, N = 53) was found between measurements of the percentage volume of the ovary by MRI and traditional methods. The research findings suggested that MRI was a reliable, rapid, and noninvasive method to assess stages of ovarian maturity in female R. ventralis.