A W/Al Co-doped NaMnO Cathode Material for Enhanced Sodium-Ion Storage.

The NaMnO cathode has attracted enormous interest owing to its low cost, low toxicity, and stable structure, but its practical application is still hindered by the limited sodium storage sites. Element doping is widely used to improve its capacity. However, cation and anion substitution could barely reach a satisfactory compromise between the structural stability and reversible capacity.

Targeting ribosome biogenesis as a novel therapeutic approach to overcome EMT-related chemoresistance in breast cancer.

Epithelial-to-mesenchymal transition (EMT) contributes significantly to chemotherapy resistance and remains a critical challenge in treating advanced breast cancer. The complexity of EMT, involving redundant pro-EMT signaling pathways and its paradox reversal process, mesenchymal-to-epithelial transition (MET), has hindered the development of effective treatments. In this study, we utilized a Tri-PyMT EMT lineage-tracing model in mice and single-cell RNA sequencing (scRNA-seq) to comprehensively analyze the EMT status of tumor cells.

Deciphering the Degradation Mechanisms and Realize High-Voltage Stability of AV(PO) (A = Li, Na) in Aqueous Dual-Ion Batteries.

Polyanionic AV(PO) (A = Li, Na) with open channels have been extensively utilized as cathode materials for aqueous zinc-metal batteries (AZMBs), whereas suffering from severe capacity fading and rapid operation voltage decay during cycling. when used as In this work, it is disclosed that the rapid degradation is induced by an irreversible phase change from electrochemical active LiV(PO) to nonactive monoclinic LiZnPO, as well as active NaV(PO) to nonactive rhombic Zn(PO)(HO). Subsequently, a rational dual-cation (Al-Fe) doping strategy is proposed to suppress these detrimental transformations.

Understanding the Role of Mn Substitution for Boosting High-Voltage NaFeMn(PO)PO Cathode in Sodium-Ion Batteries.

NaFe(PO)PO is regarded as the most promising polyanionic cathode for sodium-ion batteries (SIBs) due to its superior structural stability, cost-effectiveness, and environmental benignity. However, the low operating voltage inevitably weakens its competitiveness in energy density. Previous works have tried to enhance its operating voltage by Mn doping, which draws on the design idea of LiFeMnPO cathode for lithium-ion batteries, but with little success.

Reconstructing Helmholtz Plane Enables Robust F-Rich Interface for Long-Life and High-Safe Sodium-Ion Batteries.

Hard carbon (HC) is the most commonly used anode material in sodium-ion batteries. However, the solid-electrolyte-interface (SEI) layer formed in carbonate ester-based electrolytes has an imperceptible dissolution tendency and a sluggish Na diffusion kinetics, resulting in an unsatisfactory performance of HC anode. Given that electrode/electrolyte interface property is highly dependent on the configuration of Helmholtz plane, we filtrated proper solvents by PFBE (PF anion binding energy) and CAE (carbon absorption energy) and disclosed the function of chosen TFEP to reconstruct the Helmholtz plane and regulate the SEI film on HC anode.

Designing Advanced Electrolytes for High-Safety and Long-Lifetime Sodium-Ion Batteries via Anion-Cation Interaction Modulation.

Safety hazards caused by flammable electrolytes have been major obstacles to the practical application of sodium-ion batteries (SIBs). The adoption of nonflammable all-phosphate electrolytes can effectively improve the safety of SIBs; however, traditional low-concentration phosphate electrolytes are not compatible with carbon-based anodes. Herein, we report an anion-cation interaction modulation strategy to design low-concentration phosphate electrolytes with superior physicochemical properties.

MUSTANG: Multi-sample spatial transcriptomics data analysis with cross-sample transcriptional similarity guidance.

Spatially resolved transcriptomics has revolutionized genome-scale transcriptomic profiling by providing high-resolution characterization of transcriptional patterns. Here, we present our spatial transcriptomics analysis framework, MUSTANG (MUlti-sample Spatial Transcriptomics data ANalysis with cross-sample transcriptional similarity Guidance), which is capable of performing multi-sample spatial transcriptomics spot cellular deconvolution by allowing both cross-sample expression-based similarity information sharing as well as spatial correlation in gene expression patterns within samples. Experiments on a semi-synthetic spatial transcriptomics dataset and three real-world spatial transcriptomics datasets demonstrate the effectiveness of MUSTANG in revealing biological insights inherent in the cellular characterization of tissue samples under study.

Linkage Engineering in Covalent Organic Frameworks for Metal-Free Electrocatalytic CH Production from CO.

Electrocatalytic carbon dioxide reduction reaction (CORR) to produce ethylene (CH) is conducive to sustainable development of energy and environment. At present, most electrocatalysts for CH production are limited to the heavy metal copper, meanwhile, achieving metal-free catalysis remains a challenge. Noted piperazine with sp N hybridization is beneficial to CO capture, but CORR performance and mechanism have been lacking.

Sulfur-Defect-Induced TiS as a High-Capacity and Long-Life Anode Material for Zinc-Ion Batteries.

Aqueous zinc-ion batteries (ZIBs) are competitive among the elective candidates for electrochemical energy storage systems, but the intrinsic drawbacks of zinc metal anodes such as dendrites and corrosion severely hinder their large-scale application. Developing alternative anode materials capable of high reversibility and stability for storing Zn ions is a feasible approach to circumvent the challenge. Herein, a sulfur-defect-induced TiS (D-TiS) as a promising intercalation anode material for ZIBs is designed.

MoS Cluster-Based Cathodes for Rechargeable Magnesium Batteries: Reversible Magnesium Association/Dissociation at the Bridging Disulfur along with Sulfur-Sulfur Bond Break/Formation.

Multivalent cation batteries are attracting increasing attention in energy-storage applications, but reversible storage of highly polarizing multivalent cations is a major difficulty for the electrode materials. In the present study, charge-delocalizing MoS cluster-based materials (crystalline (NH)MoS and amorphous MoS) are designed and investigated as cathodes for rechargeable magnesium batteries. Both of the cathodes show high magnesium storage capacities (296 and 302 mAh g at 100 mA g) and superior rate performances (76 and 80 mAh g at 15 A g).

Aromatic Ketones as Mild Presodiating Reagents toward Cathodes for High-Performance Sodium-Ion Batteries.

Chemical presodiation (CP) is an effective strategy to enhance energy density of sodium ion batteries. However, the sodiation reagents reported so far are basically polycyclic aromatic hydrocarbons (PAHs) wth low reductive potential (~0.1 V vs.

LiNO -Based Electrolytes via Electron-Donation Modulation for Sustainable Nonaqueous Lithium Rechargeable Batteries.

LiPF as a dominant lithium salt of electrolyte is widely used in commercial rechargeable lithium-ion batteries due to its well-balanced properties, including high solubility in organic solvents, good electrochemical stability, and high ionic conductivity. However, it suffers from several undesirable properties, such as high moisture sensitivity, thermal instability, and high cost. To address these issues, herein, we propose an electron-donation modulation (EDM) rule for the development of low-cost, sustainable, and electrochemically compatible LiNO -based electrolytes.

Enabling Ultralow-Temperature (-70 °C) Lithium-Ion Batteries: Advanced Electrolytes Utilizing Weak-Solvation and Low-Viscosity Nitrile Cosolvent.

Low-temperature performance of lithium-ion batteries (LIBs) has always posed a significant challenge, limiting their wide application in cold environments. In this work, the high-performance LIBs working under ultralow-temperature conditions, which is achieved by employing the weak-solvation and low-viscosity isobutyronitrile as a cosolvent to tame the affinity between solvents and lithium ions, is reported. The as-prepared electrolytes exhibit a sufficiently high conductivity (1.

Correlating the Solvating Power of Solvents with the Strength of Ion-Dipole Interaction in Electrolytes of Lithium-ion Batteries.

The solvation structure of Li plays a significant role in determining the physicochemical properties of electrolytes. However, to date, there is still no clear definition of the solvating power of different electrolyte solvents, and even the solvents that preferentially participate in the solvation structure remain controversial. In this study, we comprehensively discuss the solvating power and solvation process of Li ions using both experimental characterizations and theoretical calculations.

Thermodynamics and kinetics of Mg/Li and Mg/Na co-intercalation into layered titanium disulfide.

Hybrid Mg/A (A = Li, K, or Na) batteries are promising energy-storage devices combining the merits of a metallic Mg anode and A intercalation cathodes. Mg/Li co-intercalations into the cathodes have been reported, and it is believed that Li-intercalation would reduce the activation energy of the Mg-intercalation and improve the kinetics. Herein, a new understanding of the Mg/Li and Mg/Na co-intercalations is revealed for layered TiS from the point of view of the thermodynamics and kinetics.

Revealing the structural chemistry in NaFe(SO) (1.5 ≤ x ≤ 2.0) for low-cost and high-performance sodium-ion batteries.

Fe-based polyanionic sulfate materials are one of the most promising candidates for large-scale applications in sodium-ion batteries due to their low cost and excellent electrochemical performance. Although great achievements have been gained on a series of NaFe(SO) (NFSO-x, 1.5 ≤ x ≤ 2.

δ-VOPO as a high-voltage cathode material for aqueous zinc-ion batteries.

Aqueous zinc-ion batteries (AZIBs) with excellent safety, low-cost and environmental friendliness have great application potential in large-scale energy storage systems and thus have received extensive research interest. Layered oxovanadium phosphate dihydrate (VOPO·2HO) is an appealing cathode for AZIBs due to the unique layered framework and desirable discharge plateau, but bottlenecked by low operation voltage and unstable cycling. Herein, we propose delta-oxovanadium phosphate (δ-VOPO) without conventional pre-embedding of metal elements or organics into the structure and paired it into AZIBs for the first time.

Targeting Ribosome Biogenesis as a Novel Therapeutic Approach to Overcome EMT-related Chemoresistance in Breast Cancer.

Unlabelled: Epithelial-to-mesenchymal transition (EMT) contributes significantly to chemotherapy resistance and remains a critical challenge in treating advanced breast cancer. The complexity of EMT, involving redundant pro-EMT signaling pathways and its paradox reversal process, mesenchymal-to-epithelial transition (MET), has hindered the development of effective treatments. In this study, we utilized a Tri-PyMT EMT lineage-tracing model and single-cell RNA sequencing (scRNA-seq) to comprehensively analyze the EMT status of tumor cells.

Self-assembled nanoflower-like FeSe/MoSe heterojunction anode with enhanced kinetics for superior-performance Na-ion half/full batteries.

Transition metal selenides are a research hotspot in sodium-ion batteries (SIBs). However, slow kinetics and rapid capacity decay due to volume changes during cycling limit their commercial applications. Heterostructures have the ability to accelerate charge transport and are widely used in energy storage devices due to their abundant active sites and lattice interfaces.

A Molybdenum Polysulfide Generated from Ammonium Tetrathiomolybdate for High-Capacity and High-Power Rechargeable Magnesium Battery Cathodes.

Rechargeable magnesium batteries (RMBs) are a promising large-scale energy-storage technology with low cost and high reliability. However, developing high-performance cathode materials remains the most prominent obstacle because of the insufficient magnesium-storage active sites and unfavorable magnesium cation transport paths, as well as the strong interaction between the cathode material and the bivalent magnesium cation. Herein, ammonium tetrathiomolybdate is demonstrated to be a high-performance RMB cathode material.

Ion-Migration Mechanism: An Overall Understanding of Anionic Redox Activity in Metal Oxide Cathodes of Li/Na-Ion Batteries.

The anionic redox reaction (ARR) has attracted extensive attention due to its potential to enhance the reversible capacity of cathode materials in Li/Na-ion batteries (LIBs/SIBs). However, the understanding of its activation mechanism is still limited by the insufficient mastering of the underlying thermodynamics and kinetics. Herein, a series of Mg/Li/Zn-substituted Na MnO and Li MnO cathode materials are designed to investigate their ARR behaviors.

High-Voltage and Intrinsically Safe Sodium Metal Batteries Enabled by Nonflammable Fluorinated Phosphate Electrolytes.

Sodium metal is a promising anode for high-energy-density sodium rechargeable batteries (RSBs). However, the low Coulombic efficiency (CE) of the Na plating/stripping process and the problem of safety hinder their practical application. Herein, we report a facile strategy for employing the fluorinated phosphate solvents to realize highly reversible Na plating/stripping and improve the safety performance.

Will Vanadium-Based Electrode Materials Become the Future Choice for Metal-Ion Batteries?

Metal-ion batteries have emerged as promising candidates for energy storage system due to their unlimited resources and competitive price/performance ratio. Vanadium-based compounds have diverse oxidation states rendering various open-frameworks for ions storage. To date, some vanadium-based polyanionic compounds have shown great potential as high-performance electrode materials.