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Immunotherapy based on immune checkpoint genes (ICGs) has recently made significant progress in the treatment of bladder cancer patients, but many patients still cannot benefit from it. In the present study, we aimed to perform a comprehensive analysis of ICGs in bladder cancer tissues with the aim of evaluating patient responsiveness to immunotherapy and prognosis. We scored ICGs in each BLCA patient from TCGA and GEO databases by using ssGSEA and selected genes that were significantly associated with ICGs scores by using the WCGNA algorithm. NMF clustering analysis was performed to identify different bladder cancer molecular subtypes based on the expression of ICGs-related genes. Based on the immune related genes differentially expressed among subgroups, we further constructed a novel stratified model containing nine genes by uni-COX regression, LASSO regression, SVM algorithm and multi-COX regression. The model and the nomogram constructed based on the model can accurately predict the prognosis of bladder cancer patients. Besides, the patients classified based on this model have large differences in sensitivity to immunotherapy and chemotherapy, which can provide a reference for individualized treatment of bladder cancer. [ABSTRACT FROM AUTHOR]

With the rapid growth of energy storage capacitors in advanced power systems, the pursuit of lightweight devices is gradually gaining importance despite the urgent need for device miniaturization. To reduce the mass of dielectric energy storage materials, certain light metal elements, such as potassium (K) and sodium (Na), offer promising prospects for achieving low material density. However, the intrinsic formation of point defects, including alkali metal vacancies and oxygen vacancies (Schottky defects), is inevitable during high-temperature sintering because of the volatilization of alkali metal oxides. These defects can lead to high conductivity under high electric fields, thereby deteriorating energy storage performance (ESP). In this work, we focus on a potassium-rich composition, K2La0.75Gd0.25Nb5O15, which is characterized by a tetragonal tungsten bronze (TTB) structure, to investigate the impact of volatile point defects. Different types of defects were designed by changing the K2O content, and energy storage properties were investigated. Based on leakage current measurements, impedance spectra, and DFT calculation results, it could be concluded that K–O defects with a shallow energy level cause conduction loss, thereby influencing polarization and ESP. Consequently, a high recoverable energy storage density (Wrec) of 5.02 J cm−3 and an energy efficiency of 85.6% were simultaneously achieved for the composition with the lowest defect content. This work reveals a mechanism in which volatile defects dominate conduction behavior and relevant ESP, stresses the significance of suppressing alkaline Schottky defects, and provides a feasible solution to developing lightweight dielectric energy storage materials. [ABSTRACT FROM AUTHOR]

Subjected to mechanical stimuli, a piezo-induced built-in electric field is favorable for promoting the catalytic performance of piezo-photocatalysts via effectively separating the excitons. However, the exact correlation between the electronic structure and catalytic properties of piezo-photocatalysts is still ambiguous. Conjugated microporous polymers (CMPs) with delocalized π-conjugation bonds are a unique class of photocatalytic materials, which exhibit intramolecular transport channels for electron transfer and could be further enhanced by a built-in electric field during photocatalysis. Herein, novel piezo-photocatalytic electrospun hybrid fiber films were prepared, which endow piezoelectric poly(vinylidene fluoride-co-trifluoroethylene) (PVDF–TrFE) with the high photocatalytic activity of a pyridine-based CMP (PCMP). The compatibility of these two components was enhanced via silane modification of the PCMP (m-PCMP). Hybrids of m-PCMP 50 wt%/PVDF–TrFE showed an excellent photo-degradation efficiency (97%) towards rhodamine B (RhB) with a high pseudo-first-order kinetic constant (k) of 0.0289 min−1 which is comparable to that of the neat m-PCMP (0.0304 min−1) and nearly 15 times higher compared to that of pure PVDF–TrFE (0.0019 min−1). The excellent catalytic performance was attributed to the synergetic effect, where the addition of the m-PCMP enhanced the piezo-response of PVDF–TrFE, and the piezo-potential of PVDF–TrFE regulated the energy band of m-PCMP, favoring the redox reactions to generate reactive oxygen species (ROS) for degrading RhB. The present study proposes a new paradigm for highly active piezo-photocatalysts in terms of tuning the electronic structure and interpreting the structure-to-property correlation. [ABSTRACT FROM AUTHOR]

The magneto-optical and dielectric behavior of M-type hexaferrites as permanent magnets in the THz band is essential for potential applications like microwave absorbers and antennas, while are rarely reported in recent years. In this work, single-phase SrFe 12- x Nb x O 19 hexaferrite ceramics were prepared by the conventional solid-state sintering method. Temperature dependence of dielectric parameters was investigated here to determine the relationship between dielectric response and magnetic phase transition. The saturated magnetization increases by nearly 12%, while the coercive field decreases by 30% in the x = 0.03 composition compared to that of the x = 0.00 sample. Besides, the Nb substitution improves the magneto-optical behavior in the THz band by comparing the Faraday rotation parameter from 0.75 ( x = 0.00) to 1.30 ( x = 0.03). The changes in the magnetic properties are explained by a composition-driven increase of the net magnetic moment and enhanced ferromagnetic exchange coupling. The substitution of the donor dopant Nb on the Fe site is a feasible way to obtain multifunctional M-type hexaferrites as preferred candidates for permanent magnets, sensors, and other electronic devices.