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Electrochemical conversion of nitrate to ammonia is widely considered a "two birds with one stone" approach to alleviate the nitrate pollution in water and simultaneously to generate the valuable green NH 3 fuels. However, it remains challenging due to the lack of efficient electrocatalysts for practical utilization. Herein, we investigate the synergistic effect between asymmetric Cu-O v -W sites (O v represents oxygen vacancy) and adjacent Mo clusters in tuning the local electronic environment around active sites of catalysts for substantially enhanced nitrate reduction. The dynamic balance between the adsorption and desorption of O in NO 3 - caused by asymmetric O v and the promoted protonation process due to Mo clusters are responsible for boosting the entire process. Such synergistic effect modulates the local electronic environment for binding the reaction intermediates and dramatically facilitates the intermediate formation in rate-determining steps (*NO→*NOH and *NOH→*N), leading to the high NH 3 Faradaic efficiency and yield rate of 94.60% and 5.84 mg h−1 mg cat. −1 at − 0.7 V vs. RHE, respectively. [Display omitted] • Plasma method was applied to control the concentration of oxygen vacancies. • Oxygen vacancies act as active sites for the adsorption and activation of NO 3-. • Asymmetric vacancies balance the adsorption and desorption of O in NO 3- , facilitating the formation of *N intermediate. • Mo clusters accelerate the protonation process, leading to a relatively lower energy in the rate-determining step (*NO→*NOH). • The synergistic effect of asymmetric Cu-Ov-W and adjacent Mo clusters modulates the local electronic environment. [ABSTRACT FROM AUTHOR]

The operation stability of halide perovskite devices is the critical issue that impedes their commercialization. The main reasons are that the ambient H2O molecules can easily deteriorate the perovskites, while the metal electrodes react in different degrees with the perovskites. Herein, one kind of new electrode, the metalloids, is reported, which are much more stable than the conventional noble metals as electrical contacts for halide perovskites. The degradation mechanism of halide perovskites with noble metal electrodes is carefully studied and compared with the metalloid electrodes. It is found that the iodide ions can easily halogenate Cu and Ag in halide perovskites. Although Au is almost not halogenated, it can also decompose the perovskite film. On the contrary, after long‐term storage, the metalloid electrodes remain intact on the perovskite film without any degradation. In addition, the long‐time operation stability of the perovskite devices with metalloid electrodes is much higher than that of noble metals. First‐principles calculations confirm the exceptional stability of the metalloid electrodes.This work explores the ultra‐stable electrodes for halide perovskites, paving the way to the large‐scale deployment of perovskite‐based electronic devices. [ABSTRACT FROM AUTHOR]

Background: The oral spirochete bacterium Treponema denticola is associated with both the incidence and severity of periodontal disease. Although the biological or phenotypic properties of a significant number of T. denticola isolates have been reported in the literature, their genetic diversity or phylogeny has never been systematically investigated. Here, we describe a multilocus sequence analysis (MLSA) of 20 of the most highly studied reference strains and clinical isolates of T. denticola; which were originally isolated from subgingival plaque samples taken from subjects from China, Japan, the Netherlands, Canada and the USA. Results: The sequences of the 16S ribosomal RNA gene, and 7 conserved protein-encoding genes (flaA, recA, pyrH, ppnK, dnaN, era and radC) were successfully determined for each strain. Sequence data was analyzed using a variety of bioinformatic and phylogenetic software tools. We found no evidence of positive selection or DNA recombination within the protein-encoding genes, where levels of intraspecific sequence polymorphism varied from 18.8% (flaA) to 8.9% (dnaN). Phylogenetic analysis of the concatenated protein-encoding gene sequence data (ca. 6,513 nucleotides for each strain) using Bayesian and maximum likelihood approaches indicated that the T. denticola strains were monophyletic, and formed 6 well-defined clades. All analyzed T. denticola strains appeared to have a genetic origin distinct from that of 'Treponema vincentii' or Treponema pallidum. No specific geographical relationships could be established; but several strains isolated from different continents appear to be closely related at the genetic level. Conclusions: Our analyses indicate that previous biological and biophysical investigations have predominantly focused on a subset of T. denticola strains with a relatively narrow range of genetic diversity. Our methodology and results establish a genetic framework for the discrimination and phylogenetic analysis of T. denticola isolates, which will greatly assist future biological and epidemiological investigations involving this putative 'periodontopathogen'. [ABSTRACT FROM AUTHOR]

The gallop of artificial intelligence ignites urgent demand on information processing systems with ultralow power consumption, reliable multi-parameter control and high operation efficiency. Here, the poly(vinylidene fluoride-trifluoroethylene) (P(VDF-TrFE)) wrapped InGaAs nanowire (NW) artificial synapses capable to operate with record-low subfemtojoule power consumption are presented. The essential synaptic behaviors are mimicked and modulated effectively by adjusting the thickness of top P(VDF-TrFE) films. Moreover, the long-term depression is realized by applying visible light (450 nm) because of the negative photoconductivity of InGaAs nanowires. Combined with optimal P(VDF-TrFE) films, the synaptic devices have the more linear long-term potentiation/depression characteristics and the faster supervised learning process simulated by hardware neural networks. The Pavlovian conditioning is also performed by combining electrical and infrared stimuli. Evidently, these ultralow-operating-power synapses are demonstrated with the brain-like behaviors, effective function modulation, and more importantly, the synergistic photoelectric modulation, which illustrates the promising potentials for neuromorphic computing systems. The ferroelectric P(VDF-TrFE) top-wrapped InGaAs nanowire artificial synapses exhibit the ultralow power consumption and synergistic photoelectric modulation. The unique negative photoconductivity in visible range realizes the more linear long-term depression characteristics. Moreover, by combining the response in infrared range with electric stimuli, the classical Pavlovian conditioning is mimicked successfully, which shows great potentials in neuromorphic computing systems. [Display omitted] The ferroelectric P(VDF-TrFE) top-wrapped InGaAs nanowire artificial synapses with the ultralow power consumption and synergistic photoelectric modulation. • A recorded low sub-femtojoule (0.84 fJ) per synaptic event is realized in P(VDF-TrFE) wrapped 1D Ⅲ-Ⅴ InGaAs NWs synapses. • The negative photoconductivity is introduced to realize the more linear long-term depression characteristics. • The classical Pavlovian conditioning is mimicked by synergistic photoelectric modulation. [ABSTRACT FROM AUTHOR]

Dion–Jacobson‐type 2D halide perovskites (DJPs) present an ideal alternative to their 3D counterparts due to their superior stability and exceptional optoelectronic properties. Despite the numerous DJPs proposed in recent years, the impact of different spacer cations on DJPs remains unclear. This understanding is crucial for researchers to select suitable materials and is an urgent requirement for the development of higher‐performance DJPs‐based devices. In this study, the influence of the chain‐like spacer cations with varying branch chains and chain lengths is thoroughly examined using both theoretical and experimental methods. The findings reveal that spacer cations with high polarity components along the main chain direction enhance the stability and photoelectric properties of DJPs. Additionally, it is found that the chain length of the spacer cation plays a critical role. Chain lengths that are too long or too short can detrimentally affect the photoelectric performance and stability of DJPs. These insights will guide researchers in selecting suitable spacer cations and in innovating new types of DJPs. [ABSTRACT FROM AUTHOR]

2D Ruddlesden─Popper (RP) halide perovskites are attracting increasing research interest due to their enhanced stability compared to 3D perovskites. However, the quantum confinement effect of bulk organic spacers hinders the separation and transport of photo‐generated carriers. Here, a multiple aromatic ring spacer, 3‐benzothiophene methylammonium (BTMA), is developed for a new 2D RP perovskite. The BTMA spacer is demonstrated, with a significant dipole moment, can impair the influence of the quantum confinement effect, and the presence of S atoms or thiophene is favorable for enhancing the interaction between organic spacers and inorganic sheets, improving the stability of perovskites. The perovskite photodetector with BTMA as spacers displays higher device performance than the control sample with 1‐naphthalene methylammonium (NMA) as spacers. Importantly, the outstanding stability of BTMA‐based perovskite films and devices is also confirmed under moisture, heat, and illumination conditions. Combining the asymmetric coplanar nanogap electrode architecture, the photodetectors' enhanced responsivity, detectivity, and external quantum efficiency of 314 A W−1, 3.4 × 1013 Jones, and 865%, respectively, are demonstrated. Importantly, the nanogap photodetectors display promising self‐power characteristics, which makes them attractive for numerous energy‐efficient applications. The work highlights a new route toward developing high‐performance 2D RP perovskite‐based photodetectors with excellent long‐term stability. [ABSTRACT FROM AUTHOR]

Abstract Ferroelectrics as emerging and attractive catalysts have shown tremendous potential for applications including wastewater treatment, hydrogen production, nitrogen fixation, and organic synthesis, etc. In this study, we demonstrate that molecular ferroelectric crystal TMCM-CdCl3 (TMCM = trimethylchloromethylammonium) with multiaxial ferroelectricity and superior piezoelectricity has an effective catalytic activity on the direct construction of the pharmacologically important substituted quinoline derivatives via one-pot [3 + 2 + 1] annulation of anilines and terminal alkynes by using N,N-dimethylformamide (DMF) as the carbon source. The recrystallized TMCM-CdCl3 crystals from DMF remain well ferroelectricity and piezoelectricity. Upon ultrasonic condition, periodic changes in polarization contribute to the release of free charges from the surface of the ferroelectric domains in nano size, which then quickly interacts with the substrates in the solution to trigger the pivotal redox process. Our work advances the molecular ferroelectric crystal as a catalytic route to organic synthesis, not only providing valuable direction for molecular ferroelectrics but also further enriching the executable range of ferroelectric catalysis.

Abstract Molecular ferroelectrics are attracting great interest due to their light weight, mechanical flexibility, low cost, ease of processing and environmental friendliness. These advantages make molecular ferroelectrics viable alternatives or supplements to inorganic ceramics and polymer ferroelectrics. It is expected that molecular ferroelectrics with good performance can be fabricated, which in turns calls for effective chemical design strategies in crystal engineering. To achieve so, we propose a hydrogen bond modification method by introducing the hydroxyl group, and successfully boost the phase transition temperature (T c) by at least 336 K. As a result, the molecular ferroelectric 1-hydroxy-3-adamantanammonium tetrafluoroborate [(HaaOH)BF4] can maintain ferroelectricity until 528 K, a T c value much larger than that of BTO (390 K). Meanwhile, micro-domain patterns, in stable state for 2 years, can be directly written on the film of (HaaOH)BF4. In this respect, hydrogen bond modification is a feasible and effective strategy for designing molecular ferroelectrics with high T c and stable ferroelectric domains. Such an organic molecule with varied modification sites and the precise crystal engineering can provide an efficient route to enrich high-T c ferroelectrics with various physical properties.

Abstract The treatment of hepatocellular carcinoma (HCC) is particularly challenging due to the inherent tumoral heterogeneity and easy resistance towards chemotherapy and immunotherapy. Arsenic trioxide (ATO) has emerged as a cytotoxic agent effective for treating solid tumors, including advanced HCC. However, its effectiveness in HCC treatment remains limited, and the underlying mechanisms are still uncertain. Therefore, this study aimed to characterize the effects and mechanisms of ATO in HCC. By evaluating the susceptibilities of human and murine HCC cell lines to ATO treatment, we discovered that HCC cells exhibited a range of sensitivity to ATO treatment, highlighting their inherent heterogeneity. A gene signature comprising 265 genes was identified to distinguish ATO-sensitive from ATO-insensitive cells. According to this signature, HCC patients have also been classified and exhibited differential features of ATO response. Our results showed that ATO treatment induced reactive oxygen species (ROS) accumulation and the activation of multiple cell death modalities, including necroptosis and ferroptosis, in ATO-sensitive HCC cells. Meanwhile, elevated tumoral immunogenicity was also observed in ATO-sensitive HCC cells. Similar effects were not observed in ATO-insensitive cells. We reported that ATO treatment induced mitochondrial injury and mtDNA release into the cytoplasm in ATO-sensitive HCC tumors. This subsequently activated the cGAS-STING-IFN axis, facilitating CD8+ T cell infiltration and activation. However, we found that the IFN pathway also induced tumoral PD-L1 expression, potentially antagonizing ATO-mediated immune attack. Additional anti-PD1 therapy promoted the anti-tumor response of ATO in ATO-sensitive HCC tumors. In summary, our data indicate that heterogeneous ATO responses exist in HCC tumors, and ATO treatment significantly induces immunogenic cell death (ICD) and activates the tumor-derived mtDNA-STING-IFN axis. These findings may offer a new perspective on the clinical treatment of HCC and warrant further study.

Background: The classification of benign and malignant microcalcification clusters (MCs) is an important task for computer-aided diagnosis (CAD) of digital breast tomosynthesis (DBT) images. Influenced by imaging method, DBT has the characteristic of anisotropic resolution, in which the resolution of intra-slice and inter-slice is quite different. In addition, the sharpness of MCs in different slices of DBT is quite different, among which the clearest slice is called focus slice. These characteristics limit the performance of CAD algorithms based on standard 3D convolution neural network (CNN).Methods: To make full use of the characteristics of the DBT, we proposed a new ensemble CNN, which consists of the 2D ResNet34 and the anisotropic 3D ResNet to extract the 2D focus slice features and 3D contextual features of MCs, respectively. Moreover, the anisotropic 3D convolution is used to build 3D ResNet to avoid the influence of DBT anisotropy.Results: The proposed method was evaluated on 495 MCs in DBT images of 275 patients, which are collected from our collaborative hospital. The area under the curve (AUC) of receiver operating characteristic (ROC) and accuracy of classifying benign and malignant MCs using decision-level ensemble strategy were 0.8837 and 82.00%, which were significantly higher than the experimental results of 2D ResNet34 (AUC: 0.8264, ACC: 76.00%) and anisotropic 3D ResNet (AUC: 0.8455, ACC: 76.00%). Compared with the results of 3D features classification in the radiomics, the AUC of the deep learning method with decision-level ensemble strategy was improved by 0.0435, and the F1 score was improved from 79.37 to 85.71%. More importantly, the sensitivity increased from 78.13 to 84.38%, and the specificity increased from 66.67 to 77.78%, which effectively reduced the false positives of diagnosis CONCLUSION: The results fully prove that the ensemble CNN can effectively integrate 2D features and 3D features, improve the classification performance of benign and malignant MCs in DBT, and reduce the false positives. [ABSTRACT FROM AUTHOR]

Van der Waals (vdW) heterostructures have gained significant attention in photodetectors due to their seamless integration with materials possessing diverse functionalities. In this study, the fabrication of a Te nanomesh/black‐Si vdW heterostructure is presented, and investigated its photoresponse properties. The heterostructure exhibits a pronounced rectification behavior, characterized by a rectification ratio of 2.2 × 104. Notably, the heterostructure device demonstrates commendable photoresponse properties, including a high responsivity of 350 mA W−1, an extensive linear dynamic range of 45.5 dB, a high specific detectivity of 9.6 × 1011 Jones, and a wide spectral response ranging from 400 to 1550 nm. Furthermore, the heterostructure exhibits rapid response, with a rise time and a decay time of 70 and 140 µs, respectively. These exceptional photoresponse properties can be attributed to the robust internal built‐in electrical field at the hetero‐interface and the augmented light absorption in black‐Si. The outstanding photoresponse properties of the heterostructure make it a promising candidate for multiwavelength single‐pixel imaging, enabling the collection of mask patterns under varying wavelengths of light radiation. This work provides a novel approach for fabricating mixed‐dimensional vdW heterostructures, offering promising prospects for advancements in optoelectronics. [ABSTRACT FROM AUTHOR]

Ferroelectricity, which has diverse important applications such as memory elements, capacitors, and sensors, was first discovered in a molecular compound, Rochelle salt, in 1920 by Valasek. Owing to their superiorities of lightweight, biocompatibility, structural tunability, mechanical flexibility, etc., the past decade has witnessed the renaissance of molecular ferroelectrics as promising complementary materials to commercial inorganic ferroelectrics. Thus, on the 100th anniversary of ferroelectricity, it is an opportune time to look into the future, specifically into how to push the boundaries of material design in molecular ferroelectric systems and finally overcome the hurdles to their commercialization. Herein, we present a comprehensive and accessible review of the appealing development of molecular ferroelectrics over the past 10 years, with an emphasis on their structural diversity, chemical design, exceptional properties, and potential applications. We believe that it will inspire intense, combined research efforts to enrich the family of high-performance molecular ferroelectrics and attract widespread interest from physicists and chemists to better understand the structure–function relationships governing improved applied functional device engineering. [ABSTRACT FROM AUTHOR]

Zinc (Zn) has arisen as a significant suppressor of vacancy formation in halide perovskites, establishing its pivotal role in defect engineering for these materials. Herein, the Zn‐catalyzed vapor‐liquid‐solid (VLS) route is reported to render black‐phase CsPbI3 nanowires (NWs) operationally stable at room temperature. Based on first‐principle calculations, the doped Zn2+ can not only lead to the partial crystal lattice distortion but also reduce the formation energy (absolute value) from the black phase to the yellow phase, improving the stability of the desired black‐phase CsPbI3 NWs. A series of contrast tests further confirm the stabilization effect of the Zn‐doped strategy. Besides, the polarization‐sensitive characteristics of black‐phase CsPbI3 NWs are revealed. This work highlights the importance of phase stabilization engineering for CsPbI3 NWs and their potential applications in anisotropic optoelectronics. [ABSTRACT FROM AUTHOR]

Abstract Over the past years, the application potential of ferroelectric nanomaterials with unique physical properties for modern electronics is highlighted to a large extent. However, it is relatively challenging to fabricate inorganic ferroelectric nanomaterials, which is a process depending on a vacuum atmosphere at high temperatures. As significant complements to inorganic ferroelectric nanomaterials, the nanomaterials of molecular ferroelectrics are rarely reported. Here a low‐cost room‐temperature antisolvent method is used to synthesize free‐standing 2D organic–inorganic hybrid perovskite (OIHP) ferroelectric nanosheets (NSs), that is, (CHA)2PbBr4 NSs (CHA = cyclohexylammonium), with an average lateral size of 357.59 nm and a thickness ranging from 10 to 70 nm. This method shows high repeatability and produces NSs with excellent crystallinity. Moreover, ferroelectric domains in single NSs can be clearly visualized and manipulated using piezoresponse force microscopy (PFM). The domain switching and PFM‐switching spectroscopy indicate the robust in‐plane ferroelectricity of the NSs. This work not only introduces a feasible, low‐cost, and scalable method for preparing molecular ferroelectric NSs but also promotes the research on molecular ferroelectric nanomaterials.

Nicotine exposure from smoking constitutes a significant global public health concern. Furthermore, smoking represents a pivotal risk factor for head and neck squamous cell carcinoma (HNSCC). However, the influence of nicotine on HNSCC remains relatively underexplored. Our aim was to unravel the molecular mechanisms that underlie the effect of nicotine on the metastatic cascade of HNSCC. In this study, we discovered a significant association between smoking and HNSCC metastasis and prognosis. Nicotine significantly enhanced HNSCC cell proliferation, migration, invasion, and epithelial-mesenchymal transition (EMT) in vitro. Analysis of TCGA-HNSCC and FDEENT-HNSCC cohorts revealed reduced miR-375–3p levels in HNSCC tumor tissues, particularly among current smokers. Additionally, miR-375–3p level was strongly correlated with both lymph node metastasis and tumor stage. By downregulating miR-375–3p, nicotine promotes HNSCC cell metastasis in vitro and hematogenous metastatic capacity in vivo. Utilizing transcriptomic sequencing, molecular docking, dual-luciferase reporter assay, and fluorescence in situ hybridization (FISH), we demonstrated that miR-375–3p specifically binds to 3′ untranslated region (3’UTR) of NTRK2 mRNA. Thus, this study uncovers a novel nicotine-induced mechanism involving miR-375–3p-mediated NTRK2 targeting, which promotes HNSCC metastasis. These findings have implications for improving the prognosis of patients with HNSCC, especially in smokers.

ObjectiveTo establish the diagnostic accuracy of RASSF1A (Ras association domain family 1 isoform) methylation using bronchial aspirates as an auxiliary method for diagnosing lung cancer through a systematic review and meta-analysis.MethodsStudies published prior to October 30, 2022, were retrieved from the Embase, PubMed, Web of Science, and Wan Fang databases using the keywords "lung cancer", "RASSF1A", "methylation", and "bronchial aspirates". A fixed or random effect model was used to calculate the combined sensitivity, specificity, positive likelihood ratios (LR), negative LR, diagnostic odds ratio (DOR), along with the respective 95% confidence intervals (CIs) and the area under the curve (AUC) with Q index. The threshold effect was defined by using the Spearman correlation coefficient, and the Deeks funnel plot was generated to evaluate publication bias.ResultsAmong the 12 trials that met the inclusion criteria, a total of 2388 participants were involved. The pooled results for the diagnosis of lung cancer were as follows, when compared to the pathological diagnosis: sensitivity of 0.47 (95% CI: 0.45-0.50), specificity of 0.96 (95% CI: 0.95-0.97), positive LR of 12.18 (95% CI: 8.96-16.55), negative LR of 0.56 (95% CI: 0.52-0.61), DOR of 24.05 (95% CI: 17.29-33.47), and AUC of 0.78 (Q index = 0.72), respectively. The sensitivity of the RASSF1A methylation assay was relatively low in a detailed subgroup analysis, fluctuating between 0.39 and 0.90, indicating a limitation in its diagnostic value for lung cancer. The RASSF1A methylation assay, on the other hand, demonstrated excellent specificity, suggesting a high exclusion value. Of note, the diagnostic sensitivity, specificity, DOR, and AUC for small cell lung cancer were 0.90 (0.84-0.94), 0.95 (0.94-0.97), 249.5 (103.94-598.8), and 0.98, respectively, showing that RASSF1A methylation was a promising biomarker for diagnosing small cell lung cancer with both high diagnostic and exclusion value. Furthermore, RASSF1A methylation using bronchial washings and bronchial aspirates showed a high AUC of 0.998 and 0.93, respectively, indicating excellent diagnostic performance.ConclusionsThe methylation of RASSF1A in bronchial aspirates demonstrated a high level of diagnostic accuracy and has the potential to be a valuable supplementary diagnostic method, especially for identifying small cell lung cancer.

Abstract With outstanding advantages of chemical synthesis, structural diversity, and mechanical flexibility, molecular ferroelectrics have attracted increasing attention, demonstrating themselves as promising candidates for next‐generation wearable electronics and flexible devices in the film form. However, it remains a challenge to grow high‐quality thin films of molecular ferroelectrics. To address the above issue, a volume‐confined method is utilized to achieve ultrasmooth single‐crystal molecular ferroelectric thin films at the sub‐centimeter scale, with the thickness controlled in the range of 100–1000 nm. More importantly, the preparation method is applicable to most molecular ferroelectrics and has no dependency on substrates, showing excellent reproducibility and universality. To demonstrate the application potential, two‐dimensional (2D) transitional metal dichalcogenide semiconductor/molecular ferroelectric heterostructures are prepared and investigated by optical spectroscopic method, proving the possibility of integrating molecular ferroelectrics with 2D layered materials. These results may unlock the potential for preparing and developing high‐performance devices based on molecular ferroelectric thin films.

Electrochemically converting waste nitrate (NO3−) into ammonia (NH3) is a green route for both wastewater treatment and high‐value‐added ammonia generation. However, the NO3−‐to‐NH3 reaction involves multistep electron transfer and complex intermediates, making it a grand challenge to drive efficient NO3− electroreduction with high NH3 selectivity. Herein, an in‐operando electrochemically synthesized Cu2O/NiO heterostructure electrocatalyst is proven for efficient NH3 electrosynthesis. In situ Raman spectroscopy reveals that the obtained Cu2O/NiO, induced by the electrochemistry‐driven phase conversion, is the real active phase. This electronically coupled phase can modulate the interfacial charge distribution, dramatically lower the overpotential in the rate‐determining step and thus requiring lower energy input to proceed with the NH3 electrosynthesis. The orbital hybridization calculations further identify that Cu2O is beneficial for NO3− adsorption, and NiO could promote the desorption of NH3, forming an excellent tandem electrocatalyst. Such a tandem system leads to NH3 Faradaic efficiency of 95.6%, a super‐high NH3 selectivity of 88.5% at −0.2 V versus RHE, surpassing most of the NH3 electrosynthesis catalysts at an ultralow reaction voltage. [ABSTRACT FROM AUTHOR]

PdSe2, a semiconductor with a narrow band gap, shows tremendous promise for high‐performance broadband photodetectors. In this study, highly sensitive, broadband, and flexible PdSe2 thin film photodetectors on polyimide (PI) substrates that can detect light from the UV (365 nm) to infrared (2200 nm) regions are reported. The devices with thick (21 nm) PdSe2 films show decent performance with a decent responsivity of 37.6 mA W−1 at 1550 nm and a fast response time. For the thick PdSe2 film, the bolometric effect dominates the positive photoresponse across all wavelength regions, whereas for the thin PdSe2 film (4.5–13 nm), which shows both positive and negative photoresponses, it dominates in the infrared region. The negative photoresponse of thin PdSe2 in the UV to the VIS region is attributed to the charge transfer‐related adsorption‐desorption of gas molecules. Detailed investigations revealed that the temperature coefficient of resistance (TCR) value is closely correlated to film thickness, with the thinnest film exhibiting the highest absolute TCR value of up to 4.3% °C−1. The value is much larger than that of metals, most 2D materials, amorphous Si, and even commercial VOx. These findings suggest that PdSe2 films have a promising future in broadband photodetectors. [ABSTRACT FROM AUTHOR]

Abstract Abundant chemical diversity and structural tunability make organic–inorganic hybrid perovskites (OIHPs) a rich ore for ferroelectrics. However, compared with their inorganic counterparts such as BaTiO3, their ferroelectric key properties, including large spontaneous polarization (P s), low coercive field (E c), and strong second harmonic generation (SHG) response, have long been great challenges, which hinder their commercial applications. Here, a quasi-one-dimensional OIHP DMAGeI3 (DMA = Dimethylamine) is reported, with notable ferroelectric attributes at room temperature: a large P s of 24.14 μC/cm2 (on a par with BaTiO3), a low E c below 2.2 kV/cm, and the strongest SHG intensity in OIHP family (about 12 times of KH2PO4 (KDP)). Revealed by the first-principles calculations, its large P s originates from the synergistic effects of the stereochemically active 4s 2 lone pair of Ge2+ and the ordering of organic cations, and its low kinetic energy barrier of small DMA cations results in a low E c. Our work brings the comprehensive ferroelectric performances of OIHPs to a comparable level with commercial inorganic ferroelectric perovskites.

Breast cancer (BC) is the most commonly diagnosed cancer and second leading cause of cancer-related death in women worldwide. Ferroptosis, an iron-dependent newly discovered mode of cell death, can be induced by lenaltinib and plays an important role in the biological behaviors of BC. Therefore, the prognostic value of ferroptosis-related genes (FRGs) in BC warrants further investigation. FRG expression profiles and clinical data were downloaded from The Cancer Genome Atlas (TCGA) database and Gene Expression Omnibus (GEO). Immune-related pathways were found in the functional analysis. Significant differences in enrichment scores for immune cells were observed. Some patients from TCGA-BRCA were included as the training cohort. A six-gene prediction signature was constructed with the least absolute shrinkage and selection operator Cox regression. This model was validated in the rest of the TCGA-BRCA and GEO cohort. The expressions of the six FRGs were verified with real-time quantitative polymerase chain reaction and immunohistochemistry in the Human Protein Atlas. Relapse or metastasis was more likely in the high-risk group. Risk score was an independent predictor of disease-free survival. Collectively, the ferroptosis-related risk model established in this study may serve as an effective tool to predict the prognosis in BC. [ABSTRACT FROM AUTHOR]

Design of efficient and robust electrocatalysts for hydrogen evolution reaction (HER) under all pH conditions has attracted significant attention. In particular, it is still a considerable challenge since the HER kinetics of Pt in alkaline solutions is about two to three orders of magnitude lower than that in acidic conditions. Herein, a heterogeneous yolk–shell nanostructure with Rh nanoparticles embedded in S, N co‐doped carbon nanospheres prepared by a facile self‐template method is reported. The optimized electrocatalyst can achieve an extremely small overpotential of 13.5 mV at 10 mA cm‐2, low Tafel slope of 25.5 mV dec‐1, high turnover frequency of 0.143 s‐1 (at −75 mV vs. reversible hydrogen electrode), and long‐term durability for 10 h, which is the record‐high alkaline HER activity among the ever‐reported noble metal based catalysts. These striking performances are ascribed to the optimized electronic structure and unique heterogeneous yolk–shell nanostructure. More importantly, it is also demonstrated that the obtained electrocatalyst exhibits superior activities in all pH range, which is better than commercial Pt/C and Rh/C catalysts. This work proves that Rh‐based nanomaterials are promising superior electrocatalysts in a wide pH range and nanostructure design is a powerful tool to increase the mass/electron transfer during reaction. [ABSTRACT FROM AUTHOR]

[Display omitted] Although a large number of intercalation cathode materials for aqueous Zn batteries have been reported, limited intercalation capacity precludes achieving a higher energy density. Here we develop a high-performance aqueous Zn battery based on BiSb alloy (Bi 0.5 Sb 0.5) using a high-concentrated strong-basic polyelectrolyte. We demonstrate that a conversion-dissolution/deposition electrochemical mechanism (BiSb ↔ Bi + SbO 2 − ↔ Bi + SbO 3 − ↔ Bi 2 O 3) through in situ X-ray diffraction (XRD), Raman, and ex-situ X-ray photoelectron spectrometry (XPS) characterizations with the help of density functional theory calculations. The BiSb cathode delivers large capacity of 512 mAh g−1 at 0.3 Ag−1 and superior rate capability of 90 mAh g−1 even at 20 Ag−1, and long-term cyclability with capacity retentions of 184 mAh g−1 after 600 cycles at 0.5 Ag−1 and 130 mAh g−1 after 1300 cycles at 1 Ag−1. Remarkably, even at temperatures as low as −10 and −20 °C, capacities of 210 and 197 mAh g−1 are reserved at 1 Ag−1, respectively. Moreover, the prepared pouch Zn//BiSb battery delivers a high energy density of 303 Wh kg−1 BiSb at 0.3 Ag−1. When coupled with a high concentration polyelectrolyte, the Zn/BiSb battery exhibits an excellent performance over a wide temperature range (−40 to 40 °C). Our research reveals the metal cathode is promising for Zn batteries to achieve a high performance with the unique mechanism and alloys can be an effective approach to stabilize metal electrodes for cycling. [ABSTRACT FROM AUTHOR]

Ferroelectrics are attractive due to their great application potential in information storage, optoelectronics, spintronics and sensing. As an important characteristic affecting semiconducting applications, the energy band structure is important for the development of light-emitting devices. Although it is a tremendous challenge to tune the bandgap in inorganic ferroelectric materials due to the strict requirement of structural symmetry for the fragile ferroelectricity, hybrid organic–inorganic perovskite (HOIP) ferroelectrics, which have a flexible structure, provide a new method to optimize the ferroelectric performance and bandgap. Based on the overview of methods for designing ferroelectrics, this Perspective systematically provides in-depth insight into the relationships between the structure–property and bandgap of HOIP ferroelectrics. In addition, we discussed the challenges and directions of HOIP ferroelectrics in semiconducting applications for the future.

Royal jelly (RJ) is known as a functional food for its diverse health-beneficial properties and complicated chemical compositions. Trans-10-hydroxy-2-decenoic acid (10-HDA) is the exclusive lipid component in RJ. In the present study, the in vitro anti-inflammatory effect of 10-HDA in LTA (Lipoteichoic acid from Staphylococcus aureus) induced RAW 264.7 macrophages are evaluated. The results showed that 10-HDA had potent, dose-dependent inhibitory effects on the release of major inflammatory mediators and NO. Several key inflammatory genes, including IL-1β, IL-6, MCP-1 and COX-2 have also been suppressed by 10-HDA. Furthermore, the effects of 10-HDA on LTA-induced pulmonary damage were also examined in mice. It was found that the administration of 10-HDA (100 mg/kg) can provide protective effects by attenuating lung histopathological changes and modulating the secretion of LTA-stimulated inflammatory cytokines in mice, such as IL-10, MCP-1 and TNF-α. Conclusively, the results reveal the potent anti-inflammatory properties of 10-HDA and provide biological information for the future application.

Molecular recognition is an important biological process where guest and host molecules interact through non-covalent bonding. Yeet al. show that this can be sensed by the dielectric and ferroelectric signals of the final complexes in a series of metal-coordination compounds with different diol molecules.

Ferroelectric phase transitions are normally accompanied by structural changes in the materials. Here, Li et al. synthesize homochiral molecular crystals and utilize their ferroelectric transitions to achieve optical switches with different refractive indices for left- and right-handed polarizations.

Royal jelly (RJ), a hive product with versatile pharmacological activities, has been used as a traditional functional food to prevent or treat inflammatory diseases. However, little is known about the anti-inflammatory effect of RJ in microglial cells. The aim of this study is to assess the anti-inflammatory effects of RJ in lipopolysaccharide- (LPS-) induced murine immortalized BV-2 cells and to explore the underlying molecular mechanisms. Our results showed that in LPS-stimulated BV-2 cells, RJ significantly inhibited iNOS and COX-2 expression at mRNA and protein levels. The mRNA expression of IL-6, IL-1β, and TNF-α was also downregulated by RJ in a concentration-dependent manner. Additionally, RJ protected BV-2 cells against oxidative stress by upregulating heme oxygenase-1 (HO-1) expression and by reducing reactive oxygen species (ROS) and nitric oxide (NO) production. Mechanistically, we found that RJ could alleviate inflammatory response in microglia by suppressing the phosphorylation of IκBα, p38, and JNK and by inhibiting the nucleus translocation of NF-κB p65. These findings suggest that RJ might be a promising functional food to delay inflammatory progress by influencing the microglia function.

It is known that CH3NH3PbI3 is particularly promising for next-generation solar devices; therefore, molecular perovskite structures have recently received extraordinary attention from the academic community because of their potential in producing unique physical properties. However, although great efforts have been made, molecular ferroelectrics with three-dimensional (3D) perovskite structures are still rare. So far, reported perovskite-like molecular ferroelectrics are basically one- or two-dimensional, significantly deviating from the inorganic perovskite ferroelectrics. Thus, their ferroelectric properties have to be greatly improved to meet the requirements of practical applications. Here, we report a 3D molecular perovskite ferroelectric: (3-ammoniopyrrolidinium)RbBr3 [(AP)RbBr3], with a high Curie temperature (Tc = 440 K) beyond that of BaTiO3. To the best of our knowledge, such above-room-temperature ferroelectricity in the 3D molecular perovskite compound is unprecedented. Furthermore, (AP)RbBr3 has great potential for applications due to its high thermal stability, ultrafast polarization reversal (greater than 20 kHz), and fascinating multiaxial characteristic. This finding opens a new avenue to the design and controllable synthesis of molecular ferroelectric perovskites, where the metal ion, halogen ion, and organic cation can be easily tuned. [ABSTRACT FROM AUTHOR]

Human cytomegalovirus (HCMV) is a large DNA virus and a member of the betaherpesvirus family. HCMV infection is extremely common in human populations and can cause severe diseases in immunocompromised hosts. Ganciclovir is the most widely used antiviral drug for cytomegalovirus infection and works by blocking the amplification of HCMV. HCMV strains resistant to ganciclovir have been detected in recent decades and mainly result from mutations in UL97 (protein kinase) and UL54 (DNA polymerase) genes. In order to understand the prevalence of resistance of HCMV in Taiwan, we studied 40 clinical isolates to detect the mutations of UL97 and UL54 that might be related to resistance. The results showed that no mutation known to cause ganciclovir resistance was detected in any strain, but some polymorphisms (N685S, A688V, A885T, N898D in UL54; D605E in UL97) were frequently observed. Our results suggest that resistant HCMV strains are not prevalent in Taiwan.

Additive manufacturing technologies have been proved as a promising method to achieve electrocatalysts with periodic micro-size pores, while the nano-sized interspace of the material structures and their corresponding gas bubbles transfer process are not explored in detail. Herein, we employ the shear force alignment in additive manufacturing to design NiMo-based structures with anisotropic porous channels as electrocatalysts for hydrogen evolution reaction (HER) in seawater. Based on the complementary experimental and theoretical investigation, the unique anisotropic structure not only fully exposes the active sites in the electrolyte, but also facilitates the rapid electrolyte-hydrogen phase conversion during electrochemical reactions. In this case, the obtained 3D electrode exhibits superior electrocatalytic performance and excellent long-term operational stability with an extremely low overpotential of ∼150 mV at a current density of 500 mA/cm2 in 1 M KOH seawater. This work will provide a practical scenario for designing highly-efficient HER electrocatalysts. [Display omitted] • Electrocatalysts with the anisotropic structure were fabricated with 3D printing technology. • The anisotropic porous structure was beneficial for gas bubble transfer behaviors. • The catalyst exhibits an overpotential of ∼150 mV (500 mA/cm2) in 1 M KOH seawater. [ABSTRACT FROM AUTHOR]

Molecular ferroelectrics are attracting much attention as valuable complements to conventional ceramic ferroelectrics owing to their solution processability and nontoxicity. Encouragingly, the recent discovery of a multiaxial molecular ferroelectric, tetraethylammonium perchlorate, is expected to be able to solve the problem that in the technologically relevant thin-film form uniaxial molecular ferroelectrics have been found to perform considerably more poorly than in bulk. However, it can show good polarization-electric field (P-E) hysteresis loops only at very low frequency, severely hampering practical applications such as ferroelectric random access memory. Here, we present a biaxial molecular ferroelectric thin film of [Hdabco]ClO4 (dabco = 1,4-diazabicyclo[2.2.2]octane) (1), where a perfect ferroelectric hysteresis loop can be observed even at 10 kHz. It is the first example of a molecular ferroelectric thin film whose polarization can be switched at such a high frequency. Moreover, using piezoresponse force microscopy, we clearly observed the coexistence of 180° and non-180° ferroelectric domains and provided direct experimental proof that 180° ferroelectric switching and non-180° ferroelastic switching are both realized; that is, a flexible alteration of the polarization axis direction can occur in the thin film by applying an electric field. These results open a new avenue for applications of molecular ferroelectrics and will inspire further exploration of high-performance multiaxial molecular ferroelectric thin films. [ABSTRACT FROM AUTHOR]

Coupling of ferroelectricity and optical properties has become an interesting aspect of material research. The switchable spontaneous polarization in ferroelectrics provides an alternative way to manipulate the light-matter interaction. The recent observation of strong photoluminescence emission in ferroelectric hybrid organic-inorganic compounds, (pyrrolidinium)MnX3 (X = Cl or Br), is an attractive approach to high efficiency luminescence with the advantages of ferroelectricity. However, (pyrrolidinium)MnX3 only displays ferroelectricity near or below room temperature, which limits its future applications in optoelectronics and multifunctional devices. Here, we rationally designed and synthesized high-temperature luminescent ferroelectric materials. The new hybrid compound (3-pyrrolinium)MnCl3 has a very high Curie temperature, Tc = 376 K, large spontaneous electronic polarization of 6.2 μC/cm², and high fatigue resistance, as well as high emission efficiency of 28%. This finding is a further step to the practical use of ferroelectric luminescence based on organic-inorganic compounds. [ABSTRACT FROM AUTHOR]

Due to the multiple electronic transmission channels established at the interface between NiMo cores and C 3 N 5 shells, the obtained NiMo@C 3 N 5 hybrids exhibit stable and efficient HER performance in seawater, which is superior to that of commercial Pt/C. [Display omitted] • Multiple electronic transmission channels were established between NiMo and C 3 N 5. • Induced electron redistribution effect optimized the HER reaction pathway. • The NiMo@C 3 N 5 catalyst shows excellent HER performance and stability in seawater. Designing highly efficient and stable electrocatalysts for hydrogen evolution reaction (HER), particularly in seawater, still remains a challenging task. Herein, the unique heterostructures composed of 1D NiMo cores and 2D C 3 N 5 shells (NiMo@C 3 N 5) are rationally designed and demonstrated as the robust HER catalysts in both alkaline electrolytes and natural seawater, where the carbon-based shell can effectively protect the catalyst core from seawater poisoning. Based on the experimental investigation and density functional theory calculation, multiple electronic transmission channels were found to establish at the interface between NiMo cores and C 3 N 5 shells, thus providing efficiently optimized HER pathways to achieve minimized overpotential with a reduced energy barrier of the rate-determining step. More importantly, the NiMo@C 3 N 5 hybrids exhibit stable HER performance with a high Faradaic efficiency of 94.8% in seawater, which is superior to that of commercial Pt/C. All these results can evidently highlight a feasible strategy to develop high-performance HER electrocatalysts via interface engineering. [ABSTRACT FROM AUTHOR]

Epstein-Barr virus (EBV) alters the regulation and expression of a variety of cytokines in its host cells to modulate host immune surveillance and facilitate viral persistence. Using cytokine antibody arrays, we found that, in addition to the cytokines reported previously, two chemotactic cytokines, CCL3 and CCL4, were induced in EBV-infected B cells and were expressed at high levels in all EBV-immortalized lymphoblastoid cell lines (LCLs). Furthermore, EBV latent membrane protein 1 (LMP1)-mediated Jun N-terminal protein kinase activation was responsible for upregulation of CCL3 and CCL4. Inhibition of CCL3 and CCL4 in LCLs using a short hairpin RNA approach or by neutralizing antibodies suppressed cell proliferation and caused apoptosis, indicating that autocrine CCL3 and CCL4 are required for LCL survival and growth. Importantly, significant amounts of CCL3 were detected in EBV-positive plasma from immunocompromised patients, suggesting that EBV modulates this chemokine in vivo. This study reveals the regulatory mechanism and a novel function of CCL3 and CCL4 in EBV-infected B cells. CCL3 might be useful as a therapeutic target in EBV-associated lymphoproliferative diseases and malignancies. [ABSTRACT FROM AUTHOR]

• Corrosion behaviors of nickel foam substrates during hydrothermal process are investigated. • A considerable number of nickel ions are detected in the non-nickel containing solution. • Increasing temperature leads to more nickel incorporated into the non-nickel based electrocatalysts. • Special cautions and considerations should be made when employing nickel foams as substrates. Nickle foams (NFs) have been widely used as substrates to support various electrocatalysts due to their extended framework structures, low-cost and high-conductivity. At the same time, as a kind of relatively active metals, nickel substrates are also prone to get corroded or chemically etched during hydro-/solvothermal synthesis of catalyst materials. However, as far as we know, when using NFs as the scaffold to support Ni-free electrocatalysts, most of the published works overlook or even ignore the effect of nickel corrosion on the activities of electrocatalysts directly fabricated on NFs. By using a simple comparison method, we systematically studied such effects from the aspects of material-synthesis temperature, precursors and aqueous solution involved. Our results indicate that the nickel substrates do indeed corrode with ions out-diffused into the reaction solution and incorporated into the fabricated electrocatalysts, which in turn affect their electrocatalytic performances. Special cautions and considerations should be made accordingly when employing nickel foams as substrates for electrocatalysts. [ABSTRACT FROM AUTHOR]

Composition-adjustable semiconductor nanomaterials have garnered significant attention due to their controllable bandgaps and electronic structures, providing alternative opportunities to regulate photoelectric properties and develop the corresponding multifunction optoelectronic devices. Nevertheless, the large-scale integration of semiconductor nanomaterials into practical devices remains challenging. Here, we report a synthesis strategy for the well-aligned horizontal CdS x Se 1- x ( x = 0-1) nanowall arrays, which are guided grown on an annealed M-plane sapphire using chemical vapor deposition (CVD) approaches. Microstructural characterizations demonstrate these structures as horizontally guided nanowalls with high-quality crystallinity. Microphotoluminescence (μ-PL) reveals the CdS x Se 1- x nanowalls exhibiting continuously tunable spontaneous emissions from 509 nm (pure CdS) to 713 nm (pure CdSe), further confirming that CdS x Se 1- x alloys have a continuously tunable bandgap. Notably, a photodetector based on CdS x Se 1- x nanowalls displays excellent photoelectric performance, such as high responsivity (3 × 10 2 ∼ 1 × 10 3 A/W), high external quantum efficiency (1.01 × 10 3 ∼ 2.93 × 10 3 ), and fast response speed in the millisecond magnitude. Furthermore, the CdS nanowall-based photodetectors exhibit a remarkable image-sensing capability, indicating potential applications in high-performance image sensing in the future. Bandgap continuously tunable nanowall arrays with high-quality crystallinity inject great vitality into the manufacturing of high-performance integrated optoelectronic devices.