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As promising photovoltaic materials, halide perovskites display large structural modifiability specific to their organic‐inorganic hybrid lattices, thus providing key to unlock many enhanced and novel physical properties. In particular, hybrid perovskites exhibit extraordinary functional responses to mechanical stimulation due to their soft lattices. However, a general pattern describing the evolution of perovskite properties under pressure is missing, rendering such research without theoretical guidance and further the optimization of optoelectronic performance. Here, a framework delineating the pressure‐dependent evolutions of lattice structure, bandgap, and photoluminescence (PL) across four distinct regions in all perovskites assuming 3D and 2D structures is unveiled, accrediting long‐range disorderness to be the common origin of bandgap blueshift, PL annihilation, and structural amorphization. Using such developed model as an instructional guideline, an optical bandgap and luminescent evolutions in quasi‐2D tin(II) iodide perovskites are revealed, where (C4H9NH3)2(CH3NH3)Sn2I7 (C4H9NH3+: butylammonium; CH3NH3+: methylammonium) is found to be the softest perovskite (bulk modulus ≈4.8 GPa) known so far. By meticulously choosing appropriate peak pressure ≈4 GPa, (C4H9NH3)2(CH3NH3)Sn2I7 shows irreversible defect healing (carrier lifetime prolongation from 7 to 22 ns) and permanent PL enhancement upon decompression to ambient condition, signifying practicality of the pressure‐driven behaviors unveiled in this work. [ABSTRACT FROM AUTHOR]

In the pursuit of low‐dose flat‐panel X‐ray detection and imaging, controlling dark current is pivotal. Modulating the bandgap and resistivity of photosensitive materials is one of the methods to reduce dark current. The study introduces a novel approach by first demonstrating a non‐perovskite orthorhombic phase δ‐CsPbI2Br thick film, fabricated using an innovative elastic molecular‐assisted coating strategy. This technique results in a material with an optimized bandgap of 2.30 eV and a significantly elevated resistivity of 2.42 × 10¹⁰ Ω cm. Consequently, this leads to an ultralow dark current of 1.34 nA cm⁻2. Leveraging this advancement, the developed X‐ray detectors showcase a groundbreaking low detection limit of 53 nGyair s⁻¹, surpassing the performance of their cubic‐phase counterparts. Remarkably, the material exhibits excellent phase stability, maintaining its properties for up to 80 days. By integrating with a thin‐film transistor array, a flat‐panel X‐ray detector that delivers high‐quality 8‐bit imaging across a 64 × 64 matrix is successfully engineered. This work not only presents a transformative approach to substantially reduce dark current in low‐dose X‐ray detection but also sets a new benchmark in the field by combining enhanced imaging capability with robust long‐term stability. [ABSTRACT FROM AUTHOR]

Polymers undergoing controlled degradation are of significant current interest. Among the classes of degradable polymers, self-immolative polymers (SIPs) are attracting increasing attention due to their ability to completely depolymerize from end to end following the cleavage of their endcap or backbone. Their amplified responses to stimuli, along with their ability to readily tune the stimulus to which they respond by changing only their endcap, are useful features for a variety of applications. This review covers the major classes of SIPs, including poly(benzyl carbamate)s, poly(benzyl ether)s, polyphthalaldehydes, polyglyoxylates, polydisulfides, polythioesters, and their related derivatives along with their endcaps. Distinctive features of their syntheses and depolymerizations are discussed. Applications of SIPs including imaging and sensing, therapeutics, gels, micro- and nanopatterning, transient or recyclable materials, and adhesives are described. We conclude with some challenges and future perspectives for the field. [ABSTRACT FROM AUTHOR]

Acting as a growth regulator, Indole-3-acetic acid (IAA) is an important phytohormone that can be produced by several Bacillus species. However, few studies have been published on the comprehensive evaluation of the strains for practical applications and the effects of selenium species on their IAA-producing ability. The present study showed the selenite reduction strain Bacillus altitudinis LH18, which is capable of producing selenium nanoparticles (SeNPs) at a high yield in a cost-effective manner. Bio-SeNPs were systematically characterized by using DLS, zeta potential, SEM, and FTIR. The results showed that these bio-SeNPs were small in particle size, homogeneously dispersed, and highly stable. Significantly, the IAA-producing ability of strain was differently affected under different selenium species. The addition of SeNPs and sodium selenite resulted in IAA contents of 221.7 µg/mL and 91.01 µg/mL, respectively, which were 3.23 and 1.33 times higher than that of the control. This study is the first to examine the influence of various selenium species on the IAA-producing capacity of Bacillus spp., providing a theoretical foundation for the enhancement of the IAA-production potential of microorganisms. [ABSTRACT FROM AUTHOR]

The precise, controllable, and safe application of pesticides can effectively reduce pesticide consumption and minimize chemical pollution at the source. Here, a light‐responsive controlled‐release system with flexible control, precise release, easy recovery, and suitability for future pesticide application in aquatic environments is proposed. The system precisely controls the release of pesticides through a light‐responsive composite nanochannel membrane (CTC@SNM/PET) with reactive coumarin derivatives (CTC) as gating molecules. The prepared nanochannel membrane has an ultrathin thickness of 67.5 nm and well‐ordered vertical nanochannels with a uniform size of 1.9 nm, providing a prerequisite for precise molecular gating and high permeability for mass transport. CTC monomers can realize cycloaddition/cyclocracking and nanochannel closing/opening to control the release of pesticides by controlling 365/254 nm ultraviolet light irradiation. As a proof of concept, the light‐responsive controlled‐release system based on CTC@MSF/PET against Saprolegnia parasitica achieves an inhibition rate of more than 95% and reduces pesticide residues by 56.5% compared to the control group. The proposed membrane system has great application potential to easily enable remote, quantitative, timed, and positioned pesticide application, thereby reducing pesticide residues and providing a prospective approach to reducing environmental and human risks. [ABSTRACT FROM AUTHOR]

Secondary trastuzumab resistance represents an evolutionary adaptation of HER2‐positive breast cancer during anti‐HER2 treatment. Most current studies have tended to prioritize HER2 and its associated signaling pathways, often overlooking broader but seemingly less relevant cellular processes, along with their associated genetic and epigenetic mechanisms. Here, transcriptome data is not only characterized but also examined epigenomic and 3D genome architecture information in both trastuzumab‐sensitive and secondary‐resistant breast cancer cells. The findings reveal that the global metabolic reprogramming associated with trastuzumab resistance may stem from genome‐wide alterations in both histone modifications and chromatin structure. Specifically, the transcriptional activities of key genes involved in lipid metabolism appear to be regulated by variant promoter H3K27me3 and H3K4me3 modifications, as well as promoter‐enhancer interactions. These discoveries offer valuable insights into how cancer cells adapt to anti‐tumor drugs and have the potential to impact future diagnostic and treatment strategies. [ABSTRACT FROM AUTHOR]

Simple Summary: tRF-27 has been identified as upregulated in both naïve trastuzumab-resistant HER2-positive breast cancer cells and patient samples, positioning it as a potential biomarker. However, the underlying mechanisms of this upregulation remain unclear. This study proposes that the abnormal transcription of specific tRNA-Cys-GCA isodecoders in naïve trastuzumab-resistant cells might contribute to the accumulation of tRF-27. Additionally, the reduction in H3K27me3 modifications at these tRNA genes, attributed to imbalances in histone modification enzymes, appears to influence tRNA transcription alterations. Building upon these findings, our research demonstrates that the application of a demethylase inhibitor may offer a potential strategy to overcome trastuzumab resistance. tRNA-derived fragments (tRFs) play crucial roles in cancer progression. Among them, tRF-27 has been identified as a key factor in promoting naïve trastuzumab resistance in HER2-positive breast cancer. However, the origin of tRF-27 remains uncertain. In this study, we propose that the upregulated expression of specific cysteine tRNAs may lead to the increased accumulation of tRF-27 in trastuzumab-resistant JIMT1 cells. Mechanistically, the reduced inhibitory H3K27me3 modification at the promoter regions of tRF-27-related tRNA genes in JIMT1 cells, potentially resulting from decreased EZH2 and increased KDM6A activity, may be a critical factor stimulating the transcriptional activity of these tRNA genes. Our research offers fresh insights into the mechanisms underlying elevated tRF-27 levels in trastuzumab-resistant breast cancer cells and suggests potential strategies to mitigate trastuzumab resistance in clinical treatments. [ABSTRACT FROM AUTHOR]

Perovskite/silicon tandem solar cells (TSCs) have aroused much attentions in recent years. One of keys for achieving highly efficient and stable TSCs is to guarantee effective charge transfer, especially on the rough textured silicon substrate due to the poor adhesion between interlayers. Here, a 2‐fluoroisonicotinic acid (2‐FNA) additive that possesses fluorine (‐F), carboxylic acid (‐COOH), and pyridine nitrogen as functional groups in the perovskite precursor to assist the crystallization process is utilized. It shows that 2‐FNA can efficiently reduce the defects and suppress non‐radiative recombination of perovskite layers by bonding with the uncoordinated Pb2+ ions, formamidinium (FA+), and halide vacancies, leading to notably prolonged carrier lifetime. Most importantly, this found that 2‐FNA aids in the formation of better interfacial contact between the perovskite and C60 layer on top, thus enhancing the interfacial electron extraction therein, eventually leading to an increased power conversion efficiency (PCE) of 28.61% on champion perovskite/silicon TSCs from 27.08% on control counterparts. This work provides a practical route to further advance the PV performance and applicability of perovskite/silicon TSCs. [ABSTRACT FROM AUTHOR]

Cardamine violifolia, a species belonging to the Brassicaceae family, is a novel vegetable crop that is rich in glucosinolates. However, the specific glucosinolate profiles in this species remain unknown. In the present study, four parts of C. violifolia were collected including central leaves (CLs), outer leaves (OLs), petiole (P), and root (R). The highest level of total glucosinolate was observed in the R. A total of 19 glucosinolates were found in C. violifolia. The predominant glucosinolate compounds were 3-methylbutyl glucosinolate, 6-methylsulfinylhexyl glucosinolate, Indol-3-ylmethyl glucosinolate, 4-methoxyglucobrassicin, and neoglucobrassicin. A transcriptome analysis showed that 16 genes, including BCAT1, BCAT3-6, CYP79A2, CYP79B2-3, CYP83A1, CYP83B1, and SOT17-18, and nine metabolites, such as valine, tryptophan, and 1-methylpropyl glucosinolate, were enriched in the glucosinolate biosynthesis pathway. These genes may be involved in the regulation of glucosinolate accumulation among the four parts. A weighted gene co-expression analysis showed that five genes were predicted to regulate glucosinolate accumulation, including ABC transporter G family member 19, 3-ketoacyl-CoA synthase 19, and pyruvate decarboxylase 1. This study deepens our understanding of the nutrient quality of C. violifolia and provides insights into the regulatory mechanism of glucosinolate accumulation in C. violifolia. [ABSTRACT FROM AUTHOR]

Osteoarthritis (OA) is a progressive disease, involving the progressive breakdown of cartilage, as well as changes to the synovium and bone. There are currently no disease-modifying treatments available clinically. An increasing understanding of the disease pathophysiology is leading to new potential therapeutics, but improved approaches are needed to deliver these drugs, particularly to cartilage tissue, which is avascular and contains a dense matrix of collagens and negatively charged aggrecan proteoglycans. Cationic delivery vehicles have been shown to effectively penetrate cartilage, but these studies have thus far largely focused on proteins or nanoparticles, and the effects of macromolecular architectures have not yet been explored. Described here is the synthesis of a small library of polycations composed of N-(2-hydroxypropyl)methacrylamide (HPMA) and N-(3-aminopropyl)methacrylamide (APMA) with linear, 4-arm, or 8-arm structures and varying degrees of polymerization (DP) by reversible addition fragmentation chain-transfer (RAFT) polymerization. Uptake and retention of the polycations in bovine articular cartilage was assessed. While all polycations penetrated cartilage, uptake and retention generally increased with DP before decreasing for the highest DP. In addition, uptake and retention were higher for the linear polycations compared to the 4-arm and 8-arm polycations. In general, the polycations were well tolerated by bovine chondrocytes, but the highest DP polycations imparted greater cytotoxicity. Overall, this study reveals that linear polymer architectures may be more favorable for binding to the cartilage matrix and that the DP can be tuned to maximize uptake while minimizing cytotoxicity. [ABSTRACT FROM AUTHOR]

Highlights: The fundamental properties of electric dipoles and their specific roles in perovskite solar cells are discussed. Research progress of interfacial dipoles in perovskite solar cells is summarized. Challenges of deterministic characterization of electric dipoles and future perspectives are highlighted. Design and modification of interfaces have been the main strategies in developing perovskite solar cells (PSCs). Among the interfacial treatments, dipole molecules have emerged as a practical approach to improve the efficiency and stability of PSCs due to their unique and versatile abilities to control the interfacial properties. Despite extensive applications in conventional semiconductors, working principles and design of interfacial dipoles in the performance/stability enhancement of PSCs are lacking an insightful elucidation. In this review, we first discuss the fundamental properties of electric dipoles and the specific roles of interfacial dipoles in PSCs. Then we systematically summarize the recent progress of dipole materials in several key interfaces to achieve efficient and stable PSCs. In addition to such discussions, we also dive into reliable analytical techniques to support the characterization of interfacial dipoles in PSCs. Finally, we highlight future directions and potential avenues for research in the development of dipolar materials through tailored molecular designs. Our review sheds light on the importance of continued efforts in this exciting emerging field, which holds great potential for the development of high-performance and stable PSCs as commercially demanded. [ABSTRACT FROM AUTHOR]

The photovoltaic (PV) performance of perovskite solar cells (PSCs) has rapidly advanced in the recent years; yet, the stability issue remains one of the last‐mile challenges on the road to commercialization. Charge transport layers and their interfaces with perovskites stand for critical tuning knobs that determine the device stability of PSCs. This review focuses on the effects of modification of SnO2 electron transport layers (ETLs) on the interfacial physicochemical properties and stability of PSC devices. In detail, the intrinsic defects, surface hydroxyls, and nonuniform morphology of SnO2 will negatively impact its interfacial physicochemical properties, thus degrading the device stability of PSCs. To tackle these existing issues, three modification approaches, such as surface morphology control, surface physicochemical modifications, and surface composite‐structure design, are categorized. Lastly, future perspectives in further promoting the stability of PSCs from SnO2 ETLs are raised based on the currently unresolved issues from both material and device levels. [ABSTRACT FROM AUTHOR]

Perennial trees develop and coordinate endogenous response signaling pathways, including their crosstalk and convergence, to cope with various environmental stresses which occur simultaneously in most cases. These processes are involved in gene transcriptional regulations that depend on dynamic interactions between regulatory proteins and corresponding chromatin regions, but the mechanisms remain poorly understood in trees. In this study, we detected chromatin regulatory landscapes of poplar under abscisic acid, methyl jasmonate, salicylic acid and sodium chloride (NaCl) treatment, through integrating ATAC-seq and RNA-seq data. Our results showed that the degree of chromatin accessibility for a given gene is closely related to its expression level. However, unlike the gene expression that shows treatment-specific response patterns, changes in chromatin accessibility exhibit high similarities under these treatments. We further proposed and experimentally validated that a homologous gene copy of RESPONSIVE TO DESICCATION 26 mediates the crosstalk between jasmonic acid and NaCl signaling pathways by directly regulating the stress-responsive genes and that circadian clock-related transcription factors like REVEILLE8 play a central role in response of poplar to these treatments. Overall, our study provides a chromatin insight into the molecular mechanism of transcription regulatory networks in response to different environmental stresses and raises the key roles of the circadian clock of poplar to adapt to adverse environments. [ABSTRACT FROM AUTHOR]

Second-order correlation [ g 2 (τ) ] measurement has been utilized to characterize a nanolaser with high spontaneous emission coupling factor. Pulse excitation with low repetition rate is usually preferred for nanolasers due to its heat accumulation or photobleaching induced problem; however, introducing pulse-to-pulse timing jitter issue hinders the g 2 (τ) measurement from functioning. Here, a jitter-calibrated method is proposed by adding an extra reference time channel so that the g 2 (τ) can be calculated accurately. To verify the validity of this calibration method, the lasing threshold of a CdSe nanowire excited by a pulsed laser with a repetition rate of 1 kHz is studied. The descent of g 2 (0) to 1 coincides with the kink in light-in vs light-out curve, which confirms the effectiveness of this method. [ABSTRACT FROM AUTHOR]

Layered halide perovskites (LHPs) with crystallographically 2D structures have gained increasing interest for photovoltaic applications due to their superior chemical stability and intriguing anisotropic properties, which are in contrast to their conventional 3D perovskite counterparts. The most frequently studied LHPs are Ruddlesden–Popper (RP) phases, which suffer from a carrier‐transport bottleneck due to the van der Waals gap associated with their intrinsic organic interlayer structures. To address this issue, Dion–Jacobson (DJ) and alternating‐cation‐interlayer (ACI) LHPs have rapidly emerged, which exhibit unique structural and (opto)electronic characteristics that may resemble those of the 3D counterparts owing to the eliminated or reduced van der Waals gap. Improved photophysical properties have been achieved in DJ and ACI LHPs, leading towards better photovoltaic performance. Here we provide a comprehensive discussion on the merits and promises of DJ and ACI LHPs from a chemistry perspective. Then, we review recent progress on the synthesis and tailoring of DJ and ACI LHP crystals and thin films, as well as their optoelectronic properties and photovoltaic performance. Finally, we discuss possible pathways to overcome critical challenges to realize the full potential of DJ and ACI LHPs for high‐performance solar cells and beyond. [ABSTRACT FROM AUTHOR]

In recent years, significant efforts have been made to develop ultrafast laser source around 2- $\mu \text{m}$ wavelength. Meanwhile, the characterization of the ultrashort pulses within ultracompact footprints has been attracting growing interests. Here relying on the transverse second-harmonic generation in a single CdTe microwire, we successfully demonstrate an optical autocorrelator for femtosecond pulse characterization at 2- $\mu \text{m}$ wavelength. With 220-fs laser pulses (38 pJ/pulse) as input light, the measured pulse width after calibration is 236 fs, showing a good accuracy of this microwire autocorrelator. Due to the low-loss transmission window and high nonlinearity of CdTe in the mid-infrared (MIR) region, the microwire-based autocorrelator shows great potential for MIR applications ranging from on-chip optical communication to ultracompact laser spectroscopy. [ABSTRACT FROM AUTHOR]