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We report the measurements of Λ hyperons’ global and local spin polarization from second phase of the RHIC Beam Energy Scan (BES-II) in Au+Au collisions at Λ and Λ¯ = 7.7−27 GeV. Global polarization measurements of Λ and Λ show no significant differences, offering insights into the late-stage evolution of the magnetic field. The new measurements of the local polarization of Λ perpendicular to the reaction plane (< P 2, y >) shows a monotonic increase with decreasing collision energy, while the component along the beam direction (< P 2, y >) for both Λ and Λ is small in magnitude with no strong energy dependence. The net local polarization observable, Λ and Λ¯ and 〈 P 2,y net > = 〈 P 2,y (Λ)〉 - 〈 P 2,y (Λ¯)〉 and 〈P 2,z net 〉 = 〈P 2,z (Λ)〉 - 〈P 2,z (Λ¯)〉 designed to probe baryonic spin Hall effect, is consistent with zero with large uncertainty.

The operation of traditional aqueous-electrolyte zinc-ion batteries is adversely affected by the uncontrollable growth of zinc dendrites and the occurrence of side reactions. These problems can be avoided by the development of functional hydrogel electrolytes as replacements for aqueous electrolytes. However, the mechanism by which most hydrogel electrolytes inhibit the growth of zinc dendrites on a zinc anode has not been investigated in detail, and there is a lack of a large-scale recovery method for mainstream hydrogel electrolytes. In this paper, we describe the development of a recyclable and biodegradable hydrogel electrolyte based on natural biomaterials, namely chitosan and polyaspartic acid. The distinctive adsorptivity and inducibility of chitosan and polyaspartic acid in the hydrogel electrolyte triggers a double coupling network and an associated synergistic inhibition mechanism, thereby effectively inhibiting the side reactions on the zinc anode. In addition, this hydrogel electrolyte played a crucial role in an aqueous acid-based Zinc/MnO 2 battery, by maintaining its interior two-electron redox reaction and inhibiting the formation of zinc dendrites. Furthermore, the sustainable biomass-based hydrogel electrolyte is biodegradable, and could be recovered from the Zinc/MnO 2 battery for subsequent recycling. Functional hydrogel electrolytes show promising potential for enhancing the sustainability of aqueous zinc-ion batteries. Here, the authors introduce a biomass-based hydrogel electrolyte that not only prevents side reactions on the zinc anode but also enables easy retrieval from the zinc batteries.

Dendrite growth of alkali metal anodes limited their lifetime for charge/discharge cycling. Here, we report near-perfect anodes of lithium, sodium, and potassium metals achieved by electrochemical polishing, which removes microscopic defects and creates ultra-smooth ultra-thin solid-electrolyte interphase layers at metal surfaces for providing a homogeneous environment. Precise characterizations by AFM force probing with corroborative in-depth XPS profile analysis reveal that the ultra-smooth ultra-thin solid-electrolyte interphase can be designed to have alternating inorganic-rich and organic-rich/mixed multi-layered structure, which offers mechanical property of coupled rigidity and elasticity. The polished metal anodes exhibit significantly enhanced cycling stability, specifically the lithium anodes can cycle for over 200 times at a real current density of 2 mA cm –2 with 100% depth of discharge. Our work illustrates that an ultra-smooth ultra-thin solid-electrolyte interphase may be robust enough to suppress dendrite growth and thus serve as an initial layer for further improved protection of alkali metal anodes. The dendrite growth of alkali metal anodes leads to charge/discharge cycling instability. Here, the authors show that electrochemical polishing can yield near-perfect anodes of three alkali metals by constructing smooth and thin solid-electrolyte interphase layers.

An interesting result that was recently reported for Mrk 421 is the detection of a significant excess at hard X-ray energies, which could provide useful information to investigate particle acceleration and emission mechanisms in the relativistic jet. Considering a two-injection scenario, we develop a self-consistent one-zone leptonic model to understand the origin of the hard X-ray excess in Mrk 421 during the period of extremely low X-ray and very high-energy flux in 2013 January. In the model, two populations of mono-energetic ultra-relativistic electrons are injected into the emission region, which is a magnetized plasmoid propagating along the blazar jet. We numerically calculate the emitting electron energy distribution by solving a kinetic equation that incorporates both shock acceleration and stochastic acceleration processes. Moreover, we infer analytic expressions relating the electrons’ acceleration, cooling, escape, and injection to the observed spectra and variability. In particular, for the injection luminosity, we derive a new approximate analytical expression for the case of continual injection with a mono-energetic distribution. Based on a comparison between the theoretical predictions and the observed SED, we conclude that the hard X-ray excess that was observed in Mrk 421 may be due to the synchrotron radiation emitted by an additional electron population, which is co-spatial with an electron population producing simultaneous optical/UV, soft X-ray, and γ-ray emissions. Therefore, stochastic acceleration may play a major role in producing the observed X-ray spectrum.

Chronic obstructive pulmonary disease (COPD) is characterized by persistent airflow limitation and chronic airway inflammation, traditionally managed with inhaled bronchodilators and corticosteroids. However, a significant subset of patients exhibits suboptimal response to these inhaled therapies, and disease progression remains challenging to control effectively. Recent advances in understanding the inflammatory pathways underlying COPD have led to the development of biologic agents targeting critical cytokines and their receptors, including IL-4 receptor (IL-4R), IL-5, IL-5 receptor (IL-5R), IL-33, ST2, and thymic stromal lymphopoietin (TSLP). Emerging drugs such as JKN2401, TQC2731, and tezepelumab demonstrate promising therapeutic potential by modulating these specific inflammatory mediators. This review comprehensively summarizes the pathophysiological roles of these cytokines in COPD, the current progress in biologic drug development targeting these molecules, and the outcomes of recent clinical trials. By elucidating these novel therapeutic avenues, the article aims to provide a theoretical foundation and clinical guidance for precision medicine approaches in COPD management beyond conventional inhaled treatments.

Compared with the popularity of various C-centred radicals, the N-centred radicals remain largely unexplored in catalytic radical cascade reactions because of a lack of convenient methods for their generation. Known methods for their generation typically require the use of N-functionalized precursors or various toxic, potentially explosive or unstable radical initiators. Recently, visible-light photocatalysis has emerged as an attractive tool for the catalytic formation of N-centred radicals, but the pre-incorporation of a photolabile groups at the nitrogen atom largely limited the reaction scope. Here, we present a visible-light photocatalytic oxidative deprotonation electron transfer/2,2,6,6-tetramethylpiperidine-1-oxyl (TEMPO)-mediation strategy for catalytic N-radical cascade reaction of unsaturated hydrazones. This mild protocol provides a broadly applicable synthesis of 1,6-dihydropyradazines with complete regioselectivity and good yields. The 1,6-dihydropyradazines can be easily transformed into diazinium salts that showed promising in vitro antifungal activities against fungal pathogens. DFT calculations are conducted to explain the mechanism. The use of N-centred radicals is limited by the difficulties in their preparation. Here, the authors report a photoredox method for the formation of N-centred radicals on hydrazones and their use for the synthesis of heterocyclic compounds through a radical cascade reaction.

Objective: Deregulation of long noncoding RNAs (lncRNAs) is involved in the initiation and progression of cancer. LncRNA DLX6-AS1 is regarded as an oncogene in many cancer types. However, the clinical role of serum exosomal lncRNA DLX6-AS1 in cervical cancer (CC) is poorly known. This study aimed to analyze the diagnostic and prognostic value of serum exosomal lncRNA DLX6-AS1 in CC. Methods: A total of 114 patients with CC, 60 patients with CIN (cervical intraepithelial neoplasia), and 110 healthy women were enrolled in this study. Real-time quantitative reverse transcription-polymerase chain reaction (qRT-PCR) was performed to measure the serum exosomal lncRNA DLX6-AS1 levels in all participants. Results: Serum exosomal lncRNA DLX6-AS1 level was significantly elevated in CC patients compared with CIN patients and normal controls. In addition, high serum exosomal lncRNA DLX6-AS1 expression was positively associated with lymph node metastasis, differentiation, FIGO stage, and shortened survival. Patients with high serum exosomal lncRNA DLX6-AS1 expression were more prone to have a relapse. Furthermore, univariate and multivariate analyses suggested that serum exosomal lncRNA DLX6-AS1 was a potential prognostic indicator for overall survival of CC patients. Conclusions: These findings demonstrated that serum lncRNA DLX6-AS1 might serve as a promising marker for the diagnosis and prognosis prediction of CC.

This mini-review aims to examine how molecular PET and immuno-PET may complement tissue-based biomarkers in gastric cancer immunotherapy by enabling whole-body assessment of target expression, stromal biology, immune effector activity, and treatment-related inflammatory changes. Gastric cancer remains a major global health burden, while immunotherapy is expanding from advanced disease into perioperative and conversion settings. However, clinical benefit remains heterogeneous, and conventional biomarkers such as PD-L1, HER2, and MSI/dMMR do not fully capture spatial and temporal variation across lesions. Molecular PET broadly encompasses tracers targeting metabolism, receptors, stromal components, and immune biology, whereas immuno-PET uses radiolabeled antibodies or related scaffold proteins to visualize target distribution and, in some settings, pharmacodynamic changes in vivo . Current evidence in gastric cancer suggests potential roles for HER2-targeted PET, FAPI PET, and granzyme B PET in lesion characterization, stromal phenotyping, early response assessment, and prognostic stratification. However, PD-L1 imaging in gastric cancer remains supported mainly by preclinical data, and much of the checkpoint-imaging literature is extrapolated from non-gastric malignancies. Major barriers include limited gastric-cancer-specific prospective cohorts, heterogeneous tracer formats and imaging time points, lack of standardized quantitative thresholds, and a shortage of outcome-driven studies. Overall, molecular PET and immuno-PET should currently be viewed as promising translational tools rather than routine clinical biomarkers, with their greatest near-term value likely lying in multimodal patient stratification and early pharmacodynamic assessment.

Benzosultams represent one category of multi-heteroatom heterocyclic scaffolds, which have been frequently found in pharmaceuticals, agricultural agents, and chiral catalysts. Given the diversely significant functions of these compounds in organic and medicinal chemistry, great efforts have been made to develop novel catalytic systems for the efficient construction of benzosultam motifs over the past decades. Herein, in this review, we mainly summarize the recent advances in the field of catalytic synthesis of benzosultams from 2017 to August of 2020, with an emphasis on the scopes and mechanisms of representative reactions.

Solar eruptions are well-recognized as major drivers of space weather but what causes them remains an open question. Here we show how an eruption is initiated in a non-potential magnetic flux-emerging region using magnetohydrodynamic modelling driven directly by solar magnetograms. Our model simulates the coronal magnetic field following a long-duration quasi-static evolution to its fast eruption. The field morphology resembles a set of extreme ultraviolet images for the whole process. Study of the magnetic field suggests that in this event, the key transition from the pre-eruptive to eruptive state is due to the establishment of a positive feedback between the upward expansion of internal stressed magnetic arcades of new emergence and an external magnetic reconnection which triggers the eruption. Such a nearly realistic simulation of a solar eruption from origin to onset can provide important insight into its cause, and also has the potential for improving space weather modelling. Solar eruptions heavily influence space weather, but what are their causes remains an open question. Here the authors present a magnetohydrodynamic model of a solar eruption directly driven by solar magnetograms, following the transition from pre-eruptive to eruptive state.