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Tribocatalysis is a method that converts mechanical energy into chemical energy. In this study, we synthesized tungsten bronze structured Ba0.75Sr0.25Nb1.9Ta0.1O6 ferroelectric ceramic submicron powder using a traditional solid-state route, and the powder exhibited excellent performance in tribocatalytic water splitting for hydrogen production. Under the friction stirring of three polytetrafluoroethylene (PTFE) magnetic stirring bars in pure water, the rate of hydrogen generation by the Ba0.75Sr0.25Nb1.9Ta0.1O6 ferroelectric submicron powder is 200 µmol h-1 g-1, and after 72 hours, the accumulated hydrogen production reaches 15 892.8 µmol g-1. Additionally, this ferroelectric tungsten bronze ferroelectric material also exhibits excellent tribocatalytic degradation ability toward RhB dyes, with degradation efficiency reaching 96% in 2 hours. The study of tribocatalysis based on tungsten bronze ferroelectric materials represents a significant step forward in versatile energy utilization for clean energy and environmental wastewater degradation.
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Chemical design of lead-free relaxors with simultaneously high energy density (Wrec) and high efficiency (η) for capacitive energy-storage has been a big challenge for advanced electronic systems. The current situation indicates that realizing such superior energy-storage properties requires highly complex chemical components. Herein, we demonstrate that, via local structure design, an ultrahigh Wrec of 10.1 J/cm3, concurrent with a high η of 90%, as well as excellent thermal and frequency stabilities can be achieved in a relaxor with a very simple chemical composition. By introducing 6s2 lone pair stereochemical active Bi into the classical BaTiO3 ferroelectric to generate a mismatch between A- and B-site polar displacements, a relaxor state with strong local polar fluctuations can be formed. Through advanced atomic-resolution displacement mapping and 3D reconstructing the nanoscale structure from neutron/X-ray total scattering, it is revealed that the localized Bi enhances the polar length largely at several perovskite unit cells and disrupts the long-range coherent Ti polar displacements, resulting in a slush-like structure with extremely small size polar clusters and strong local polar fluctuations. This favorable relaxor state exhibits substantially enhanced polarization, and minimized hysteresis at a high breakdown strength. This work offers a feasible avenue to chemically design new relaxors with a simple composition for high-performance capacitive energy-storage.
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BACKGROUND: At present, skeletal tuberculosis (TB) diagnosis is mostly by histopathology, but the positivity rate is low. There is a need to develop new methods for the molecular identification of this disorder. Therefore, we aimed to investigate the clinical utility of quantitative PCR (qPCR)-based diagnosis of skeletal TB from formalin-fixed paraffin-embedded (FFPE) tissues and its comparative evaluation with acid-fast bacillus staining (AFS). METHODS: We detected Mycobacterium tuberculosis (M. tuberculosis/MTB) DNA using qPCR and AFS in FFPE tissue samples from 129 patients suspected of having skeletal TB. The sensitivity, specificity as well as area under the curve (AUC) of qPCR and AFS were calculated. Meanwhile, some factors potentially affecting qPCR and AFS results were investigated. RESULTS: Overall, qPCR outperformed AFS in detecting M. tuberculosis. The AUC of qPCR was higher than that of AFS (0.744 vs.0.561, p < 0.001). Furthermore, decalcification of bone tissues did not affect the sensitivity and specificity of qPCR tests. Whereas it impacted the performance of AFS, decalcification increased AFS's specificity and decreased its sensitivity (p < 0.05). Moreover, qPCR had a significantly larger AUC than AFS in decalcified and non-decalcified groups (0.735/0.756 vs. 0.582/0.534, p < 0.001) respectively. Similarly, the AUC of PCR was more extensive than that of AFS regardless of skeletal TB patients with concomitant pulmonary TB or not (0.929 vs. 0.762; 0.688 vs. 0.524, p < 0.01). CONCLUSIONS: Our data demonstrate that qPCR offers superior accuracy for the detection of mycobacteria in FFPE tissues compared to traditional AFS, indicating its clinical value in osteoarticular TB diagnosis.
Assuntos
Mycobacterium tuberculosis , Tuberculose dos Linfonodos , Formaldeído , Humanos , Mycobacterium tuberculosis/genética , Inclusão em Parafina , Reação em Cadeia da Polimerase em Tempo Real/métodos , Sensibilidade e EspecificidadeRESUMO
As an efficient and economical way of dealing with organic pollutants, piezo-photocatalysis has attracted great interest. In this work, we demonstrated that ferroelectricity and Schottky heterojunction engineering could significantly enhance the piezo-photocatalytic activity of AgNbO3. The poled 20 mol % K+ doped AgNbO3 disclosed its superior piezo-photocatalytic activity of 0.131 min-1 for 10 mg·L-1 RhB, which is 7.8 times of the pristine one under the condition of illumination only. The designed piezo-photocatalyst also exhibited good piezo-photocatalytic stability after four cycles. These merits are attributed to the built-in electric field associated with the large spontaneous polarization and low coercive field originated from the stable ferroelectric state after ferroelectricity engineering, plus with the electron trapper effect of the in situ precipitated metal Ag particles. Our work not only provides a promising piezo-photocatalyst for degrading organic contaminants but also paves a good way for developing high piezo-photocatalytic activity catalysts.
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The immune responses and the function of immune cells among asymptomatic severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection cases, especially in immuno-compromised individuals, remain largely unknown. Here we present a case of asymptomatic SARS-CoV-2 infection that lasted for at least 67 days. The patient has administrated Thymalfasin as 1.6 mg per dose every other day from Day 45 to 70, plus 200 mg per dose Arbidol antiviral therapy three doses per day from Day 48 to 57. Throughout the infection, no anti-SARS-CoV-2 specific IgM or IgG antibodies were detected. Instead, the patient showed either a low percentage or an absolute number of non-classical monocytes, dendritic cells (DCs), CD4+ T cells, and regulatory T cells (Tregs), which may account for the clinical feature and absence of antibody response. This case may shed new light on the outbreak management related to control/prevention, treatment, and vaccination of SARS-CoV-2 and other virus infections in immunocompromised individuals.
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Searching for a new approach in environmental remediation in terms of dye degradation is important in industrialized society. In this work, ferroelectric Ba2.5Sr2.5Nb8Ta2O30 (BSNT) submicron powders prepared by the high-temperature solid-phase method are used for dye degradation under magnetic stirring. The dye in solution can be quickly degraded by magnetically stirring BSNT submicron particles in the dark in ambient temperature conditions. More importantly, the degradation efficiency can be greatly improved through simple modification of the stirring materials from glass to polypropylene, with a degradation efficiency of rhodamine B as high as 99% in 1.5 h at a gentle stirring speed of 300 rpm. Control experiments reveal that the degradation of the dye is mainly contributed by the friction between BSNT submicron particles and PTFE stirring rods. It is proposed that the friction between ferroelectric polar BSNT particles and PTFE causes charge transfer and induces a non-zero internal electric field to drive the separation of electron-hole pairs in BSNT particles, resulting in a novel tribocatalytic degradation of the dye, which is proven by the detection of ËOH and ËO2 - intermediate products during stirring. This work demonstrates that the friction energy of ferroelectric materials with strong polarization is an alternative approach for highly efficient dye degradation.
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Narrow band-gap (NBG) Ag2S nanocrystals (NCs) attaching on the surface of wide band-gap (WBG) Ag8W4O16 nanorods were prepared by employing a facile in situ anion exchange method with the reaction between S(2)(-) and WO4(2-), and the photocatalytic activity was evaluated by the photocatalytic decolorization of methyl orange solution under visible-light irradiation. It was found that in situ anion exchange could uniformly deposit Ag2S NCs on the surface of Ag8W4O16 nanorods, controllably adjust the size, distribution and amount of Ag2S NCs, and solidly connect Ag2S NCs to the Ag8W4O16 nanorods via the replacement of S(2)(-) in the solution with lattice WO4(2-) on the Ag8W4O16 surface. The photocatalytic results indicated that the as-prepared Ag2S/Ag8W4O16 composite photocatalysts exhibited obviously higher activity compared with the pure Ag8W4O16 and N-TiO2 photocatalysts. On the basis of band structures of Ag2S and Ag8W4O16 semiconductors and the quantum size effect of Ag2S NCs, a possible photocatalytic mechanism about the Ag2S nanocrystal-sensitized Ag8W4O16 nanorods was proposed to account for the effective visible-light photocatalytic activities. This present work may provide some insight into the design of novel and high-efficiency NBG semiconductor NCs coupled with WBG semiconductor composite photocatalysts.