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Aqueous Zn/V2O5 batteries are featured for high safety, low cost, and environmental compatibility. However, complex electrode components in real batteries impede the fundamental understanding of phase transition processes and intercalation chemistry. Here, model batteries based on V2O5 film electrodes which show similar electrochemical behaviors as the real ones are built. Advanced surface science characterizations of the film electrodes allow to identify intercalation trajectories of Zn2+, H2O, and H+ during V2O5 phase transition processes. Protons serve as the vanguard of intercalated species, facilitating the subsequent intercalation of Zn2+ and H2O. The increase of capacity in the activation process is mainly due to the transition from V2O5 to more active V2O5·nH2O structure caused by the partial irreversible deintercalation of H2O rather than the increase of active sites induced by the grain refinement of electrode materials. Eventually, accumulation of Zn species within the oxide electrode results in the formation of inactive (Zn3(OH)2V2O7·2H2O) structure. The established intercalation chemistry helps to design high‐performance electrode materials. [ABSTRACT FROM AUTHOR]

Dysregulation of the transforming growth factor‐β (TGF‐β) signaling pathway regulates cancer stem cells (CSCs) and drug sensitivity, whereas it remains largely unknown how feedback regulatory mechanisms are hijacked to fuel drug‐resistant CSCs. Through a genome‐wide CRISPR activation screen utilizing stem‐like drug‐resistant properties as a readout, the TGF‐β receptor‐associated binding protein 1 (TGFBRAP1) is identified as a TGF‐β‐inducible positive feedback regulator that governs sensitivity to tyrosine kinase inhibitors (TKIs) and promotes liver cancer stemness. By interacting with and stabilizing the TGF‐β receptor type 1 (TGFBR1), TGFBRAP1 plays an important role in potentiating TGF‐β signaling. Mechanistically, TGFBRAP1 competes with E3 ubiquitin ligases Smurf1/2 for binding to TGFΒR1, leading to impaired receptor poly‐ubiquitination and proteasomal degradation. Moreover, hyperactive TGF‐β signaling in turn up‐regulates TGFBRAP1 expression in drug‐resistant CSC‐like cells, thereby constituting a previously uncharacterized feedback mechanism to amplify TGF‐β signaling. As such, TGFBRAP1 expression is correlated with TGFΒR1 levels and TGF‐β signaling activity in hepatocellular carcinoma (HCC) tissues, as well as overall survival and disease recurrence in multiple HCC cohorts. Therapeutically, blocking TGFBRAP1‐mediated stabilization of TGFBR1 by selective inhibitors alleviates Regorafenib resistance via reducing CSCs. Collectively, targeting feedback machinery of TGF‐β signaling pathway may be an actionable approach to mitigate drug resistance and liver cancer stemness. [ABSTRACT FROM AUTHOR]

Alkaline zinc‐ferricyanide flow batteries are efficiency and economical as energy storage solutions. However, they suffer from low energy density and short calendar life. The strongly alkaline conditions (3 mol L−1 OH−) reduce the solubility of ferri/ferro‐cyanide (normally only 0.4 mol L−1 at 25 °C) and induce the formation of zinc dendrites at the anode. Here, we report a new zinc‐ferricyanide flow battery based on a mild alkalescent (pH 12) electrolyte. Using a chelating agent to rearrange ferri/ferro‐cyanide ion‐solvent interactions and improve salt dissociation, we increased the solubility of ferri/ferro‐cyanide to 1.7 mol L−1 and prevented zinc dendrites. Our battery has an energy density of ~74 Wh L−1catholyte at 60 °C and remains stable for 1800 cycles (1800 hours) at 0 °C and for >1400 cycles (2300 hours) at 25 °C. An alkalescent zinc‐ferricyanide cell stack built using this alkalescent electrolyte stably delivers 608 W of power for ~40 days. [ABSTRACT FROM AUTHOR]

Aryl diazonium intermediates have emerged as highly versatile intermediates in modern organic synthesis and chemical biology, demonstrating remarkable reactivity under mild reaction conditions. Their significance has extended to DNA‐encoded libraries (DELs), where they serve as valuable alternatives to traditional aryl halide‐based cross‐coupling reactions. Aryl diazonium intermediates as N2‐annulation synthons can efficiently transform into benzotriazinone core on DNA besides C−C coupling. This concept paper illuminates recent advances in this field, emphasizing their applications and potential across various facets of DELs, off‐DNA chemistry, DELs selection, and DNA‐based probes. It is anticipated that these developments will propel the broader utilization of DNA‐conjugated aryl diazonium salt intermediates in DELs, protein labeling, hit discovery, and other interdisciplinary fields. [ABSTRACT FROM AUTHOR]

Soluble organic molecules with diverse and highly tunable structures are receiving more and more attention as redox‐active materials for aqueous organic flow batteries (AOFBs). However, the undesirable parasitic reactions of redox‐active molecules restrict their practical application. Herein, a general molecular stabilization strategy is proposed by introducing amino groups on 3,7‐positions of polycyclic azine derivatives (phenothiazine and phenoxazine compounds) to effectively enhance the redox activity and electrochemical stability of molecules. The theoretical calculation and a series of electrochemical analyses revealed that the 3,7‐substituted amino groups serving as the redox active sites can stabilize the intermediate radicals by delocalizing the electron density in the acidic solution, preventing nucleophilic/electrophilic attack. As a result, the designed 3,7‐bis‐((2‐hydroxyethyl)(methyl)amino)phenothiazin‐5‐ium bromide not only achieved the remarkable electrochemical cycling performance in the flow cell with an ultra‐low‐capacity fade rate of 0.00029% per cycle for 18000 cycles (62 days) and but also delivered a stable high capacity of 47 Ah L−1 (with capacity fade 0.0056% per cycle, 0.077% per day) under ambient condition. Such finding undoubtedly provides a guidance to design stable redox‐active molecules for AOFBs. [ABSTRACT FROM AUTHOR]

Silicon anodes with a high capacity of 4200 mAh g−1 and a low potential of 0.3 V (vs Li+/Li) enable lithium‐ion batteries with improved energy density. However, the thickened 3D solid‐electrolyte interphase (SEI) formation on Si particles in the liquid electrolytes consumes the electrolyte/active Si and blocks the Li+/e− transport, resulting in fast capacity fading. Herein, a high‐concentration polymer electrolyte (HCPE) is designed to build 2D SEI on the Si anode surface instead of the particles, which accommodates the volume change and maintains the continuous Li+/e− transport pathways as well. The retarding effect of NO3− lowers the polymerization rate of 1,3‐dioxolane (DOL), enabling 6 m LiFSI dissolution. The high concentration of LiFSI takes part in constructing the solvation structure and pulls the DOL away, reducing the decomposition of DOL and poly‐DOL (PDOL) and inducing the generation of a LiF‐ and Li3N‐rich SEI with high mechanical strength and fast Li+ transport capability. As a result, the cell using HCPE delivers a high capacity of 1765 mAh g−1 at 2C and maintains a high capacity of 2000 mAh g−1 after 100 cycles at 0.2C, which is superior to that of a liquid electrolyte (617 mAh g−1) and a low‐concentration polymer electrolyte (45 mAh g−1). [ABSTRACT FROM AUTHOR]

Bromine‐based flow batteries (Br‐FBs) are highly competitive for stationary energy storage due to their high energy density and cost‐effectiveness. However, adding bromine complexing agents (BCAs) to electrolytes slows down Br2/Br− reaction kinetics, causing higher polarization and lower power density of Br‐FBs. Herein, in situ vertically aligned MoS2 nanosheet arrays on traditional carbon felt substrates as electrodes to construct high power–density BCA‐free Br‐FBs are proposed. MoS2 arrays exhibit strong adsorption capacity to bromine, which helps the electrodes capture and retain bromine species. Even without BCAs, the battery self‐discharge caused by bromine diffusion is also inhibited. Moreover, the rate‐determining step of Br2/Br− reactions is boosted and the vertically aligned array structure provides sufficient sites, motivating Br2/Br− reaction kinetics and decreasing the battery polarization. The capacity retention rate of the BCA‐free Br‐FB based on MoS2 arrays‐based electrodes reaches 46.34% after the 24‐h standing test at 80 mA cm−2, meeting the requirements of practical applications. Most importantly, this BCA‐free Br‐FB exhibits a high Coulombic efficiency of 97.00% and an ultralong cycle life of 1000 cycles at a high current density of 200 mA cm−2. This work provides an available approach to developing advanced electrode materials for high power–density and long‐lifespan Br‐FBs. [ABSTRACT FROM AUTHOR]

Effective treatment for metastasis, a leading cause of cancer‐associated death, is still lacking. To seed on a distal organ, disseminated cancer cells (DCCs) must adapt to the local tissue microenvironment. However, it remains elusive how DCCs respond the pro‐metastatic niche signals. Here, systemic motif‐enrichment identified myocyte enhancer factor 2D (MEF2D) as a critical sensor of niche signals to regulate DCCs adhesion and colonization, leading to intrahepatic metastasis and recurrence of liver cancer. In this context, MEF2D transactivates Itgb1 (coding β1‐integrin) and Itgb4 (coding β4‐integrin) to execute temporally unique functions, where ITGB1 recognizes extracellular matrix for early seeding, and ITGB4 acts as a novel sensor of neutrophil extracellular traps‐DNA (NETs‐DNA) for subsequent chemotaxis and colonization. In turn, an integrin‐FAK circuit promotes a phosphorylation‐dependent USP14‐orchastrated deubiquitination switch to stabilize MEF2D via circumventing degradation by the E3‐ubiquitin‐ligase MDM2. Clinically, the USP14(pS432)‐MEF2D‐ITGB1/4 feedback loop is often hyper‐active and indicative of inferior outcomes in human malignancies, while its blockade abrogated intrahepatic metastasis of DCCs. Together, DCCs exploit a deubiquitination‐dependent switch on MEF2D to integrate niche signals in the liver mesenchyme, thereby amplifying the pro‐metastatic integrin‐FAK signaling. Disruption of this feedback loop is clinically applicable with fast‐track potential to block microenvironmental cues driving metastasis. [ABSTRACT FROM AUTHOR]

The development of water‐soluble redox‐active molecules with high potentials is one of the effective ways to enhance the energy density of aqueous organic flow batteries (AOFBs). Herein, a series of promising N‐substituted benzidine analogues as water‐soluble catholyte candidates with controllable redox potentials (0.78–1.01 V vs. standard hydrogen electrode (SHE)) were obtained by the molecular engineering of aqueous irreversible benzidines. Theoretical calculations reveal that the redox potentials of these benzidine derivatives in acidic solution are determined by their electronic structure and alkalinity. Among these benzidine derivatives, N,N,N′,N′‐tetraethylbenzidine(TEB) shows both high redox potential (0.82 V vs. SHE) and good solubility (1.1 M). Pairing with H4[Si(W3O10)4] anolyte, the cell displayed discharge capacity retention of 99.4 % per cycle and a high coulombic efficiency (CE) of ~100 % over 1200 cycles. The stable discharge capacity of 41.8 Ah L−1 was achieved at the 1.0 M TEB catholyte with a CE of 97.2 % and energy efficiency (EE) of 91.2 %, demonstrating that N‐substituted benzidines could be promising for AOFBs. [ABSTRACT FROM AUTHOR]

Silicon (Si) is regarded as a promising anode material for high‐energy‐density lithium‐ion batteries due to its high specific capacity (4200 mAh g−1) and low potential (0.3 V vs Li+/Li). However, the large volume change (over 300%) of Si during the lithiation/delithiation process leads to severe pulverization, electrode structure destruction, and finally capacity fading, which slows down its step to practical application. Herein, a poly(vinylamine) (PVAm) binder containing amino (NH2) and amide (NHCHO) is proposed to improve the stability of Si anodes from particle to electrode structure. The N‐containing functional groups show strong interaction with the Si particles and form a uniform and thin layer on the surface, which would decompose and form an N‐rich inorganic solid electrolyte interphase (SEI) layer during discharging. The high mechanical stability N‐rich SEI helps relieve the pulverization of Si particles through stress dissipation, maintains electrode structural stability, and reduces the loss of active materials. Thus, the Si anode with PVAm binder exhibits high capacity of ≈2000 mAh g−1 after 200 cycles, which is much higher than that of using Poly(vinylidene fluoride) (PVDF) binder (66 mAh g−1) and Poly(vinyl alcohol) PVA binder (820 mAh g−1). This facile and practical strategy provides a new perspective for the application of Si anodes in advanced batteries. [ABSTRACT FROM AUTHOR]

Zinc‐based flow batteries are promising for distributed energy storage due to their low‐cost and high‐energy density advantages. One of the most critical issues for their practical application is the reliability that results from the heterogeneous zinc deposition and dead zinc from falling off the electrode. Herein, nitrogen‐doped carbon nanotubes (N‐CNTs)‐based composite membrane through a facilely partially embedded method is reported to enable a dendrite‐free alkaline zinc‐based flow battery. The results indicate that the electrically conductive N‐CNTs functional layer can enhance the transport dynamics of charge carriers and homogenize electric field distribution in membrane–electrode interface, which induces the initial nucleation of metallic zinc from the carbon felt electrode to N‐CNTs functional layer and further achieve a uniform and dense plating of metallic zinc in alkaline media. Thus, the engineered membrane enables a stable alkaline zinc–iron flow battery performance for more than 350 h at a current density of 80 mA cm−2. Moreover, an energy efficiency of over 80% can be afforded at a current density of 200 mA cm−2. The scientific finding of this study provides a new strategy on composite membranes design and their capability to adjust the plating of metallic zinc in alkaline media. [ABSTRACT FROM AUTHOR]

Ion conductive membranes with rapid and selective ion transport are in high demand for high‐power energy storage devices. Surface periodic Turing microstructures are scientifically compelling for their high specific surface area which can promote ion transport of membranes. Here, high‐conductivity thin Turing membranes prepared by Co2+ coordination with polybenzimidazole (OPBI) are designed and their efficient ion transport in the alkaline zinc‐iron flow battery (AZIFB) is demonstrated. In this design, the Turing structure increases the effective contact area with the electrolyte, and the 7.9 µm thickness shortens the transmembrane pathway for ions. Molecular dynamics simulations further show that Co2+‐coordination enlarges the inner‐chain volume of membranes and forms continuous water channels for rapid ion transport. The boosting effect of membranes with high ion conductivity is proven by the peak power density and energy efficiency of the AZIFB, which shows an ultrahigh peak power density of 1147 mW cm−2 and demonstrates an energy efficiency of 80% even at a high current density of 200 mA cm−2. [ABSTRACT FROM AUTHOR]

As a green route for large‐scale energy storage, aqueous organic redox flow batteries (AORFBs) are attracting extensive attention. However, most of the reported AORFBs were operated in an inert atmosphere. Herein, we clarify this issue by using the reported AORFB (i.e. 3, 3′‐(9,10‐anthraquinone‐diyl)bis(3‐methylbutanoicacid) (DPivOHAQ)||Ferrocyanide) as an example. We demonstrate that the dissolved O2 can oxidize the discharged DPivOHAQ in anolyte, leading to capacity‐imbalance between anolyte and catholyte. Therefore, this cell shows continuous capacity fading when operated in an air atmosphere. We propose a simple strategy for this challenge, in which the oxygen evolution reaction (OER) in catholyte is employed to balance oxygen reduction reaction (ORR) in anolyte. When using the Ni(OH)2‐modifed carbon felt (CF) as a current collector for catholyte, this cell shows an excellent stability in air atmosphere because the Ni(OH)2‐induced OER capacity in catholyte exactly balances the ORR capacity in anolyte. Such O2‐balance strategy facilitates AORFBs' practical application. [ABSTRACT FROM AUTHOR]

Poly(ether sulfone) (PES) is a kind of polymer materials with excellent electrical insulation and acid/alkali stability. PES can be operated at high temperature continuously for a long time and still maintain excellent property stability in the environments with rapidly changed temperature, namely, great thermostability. Moreover, PES has low molding shrinkage, good dimensional stability and excellent film‐forming characteristics. Compared with inorganic membranes, PES‐based membranes have lower cost, which have received more attention and wide recognition in the field of clean energy technologies in recent years, such as flow batteries, fuel cells, water treatment, and gas separation. Therefore, this review summarizes the research status and prospect of the utilization of PES‐based membranes in clean energy fields, in order to further promote their development and application. [ABSTRACT FROM AUTHOR]

Mn2+/Mn3+ redox pair has been considered as a promising cathode for high energy density batteries, due to its attractive features of high redox potential, solubility and outstanding kinetics. However, the disproportionation side reaction of Mn3+, which results in accumulation of "dead" MnO2 limits its reversibility and further energy density. Herein, a novel catholyte based on mixture of Mn2+ and Br− was proposed for flow batteries with high energy density and long cycle life. In the design, the "dead" MnO2 can be fully discharged via Br− by a chemical‐electrochemical reaction. Coupled with Cd/Cd2+ as anode, the assembled Bromine‐Manganese flow battery (BMFB) demonstrates a high energy efficiency of 76 % at 80 mA cm−2 with energy density of 360 Wh L−1. The battery assembled with silicotungstic acid as anode could continuously run for over 2000 cycles at 80 mA cm−2. With high power density, energy density and durability, the BMFB shows great potential for large‐scale energy storage. [ABSTRACT FROM AUTHOR]

Mn2+/Mn3+ redox pair has been considered as a promising cathode for high energy density batteries, due to its attractive features of high redox potential, solubility and outstanding kinetics. However, the disproportionation side reaction of Mn3+, which results in accumulation of "dead" MnO2 limits its reversibility and further energy density. Herein, a novel catholyte based on mixture of Mn2+ and Br− was proposed for flow batteries with high energy density and long cycle life. In the design, the "dead" MnO2 can be fully discharged via Br− by a chemical‐electrochemical reaction. Coupled with Cd/Cd2+ as anode, the assembled Bromine‐Manganese flow battery (BMFB) demonstrates a high energy efficiency of 76 % at 80 mA cm−2 with energy density of 360 Wh L−1. The battery assembled with silicotungstic acid as anode could continuously run for over 2000 cycles at 80 mA cm−2. With high power density, energy density and durability, the BMFB shows great potential for large‐scale energy storage. [ABSTRACT FROM AUTHOR]

Aqueous lithium‐ion batteries are normally limited at low temperatures, because of the consequent low conductivity of electrolytes and the sluggish kinetics of electrode materials. Herein, a high‐performance ultra‐low temperature aqueous lithium ion‐bromine battery (ALBB) realized by a tailored functionalized electrolyte (TFE) consisting of lithium bromide and tetrapropylammonium bromide (TPABr) is reported, which can maintain liquid state with high conductivity (1.89 mS cm‐1) at −60 °C. In addition, with the help of excellent bromine‐fixation of TPABr, the high reversible capacity can be provided by the fast redox reaction of Br2/Br‐ couple in the cathode from room temperature (RT) to −60 °C. Moreover, 1,4,5,8‐naphthalenetetracarboxylic dianhydride‐derived polyimide anode can deliver excellent low‐temperature capacity retention as well as enhanced rate capability and reversibility at RT in TFE. As a result, the designed TFE can endow ALBB with high energy densities (98, 64, and 32 Wh kgdry‐1 at RT, −40, and −60 °C, respectively), outstanding power densities (24.6 and 1.2 kW kgdry‐1 at RT and −40 °C, respectively), and superior capacity retentions (94% and 98% after running 1000 cycles at RT and −40 °C, respectively). This work demonstrates a novel strategy to widen the temperature range of aqueous batteries. [ABSTRACT FROM AUTHOR]

Improving power density is considered as one of the most effective methods to decrease the cost of vanadium flow batteries (VFBs). To reduce the polarization loss of VFBs, a hollow porous carbon sphere, whose inner and outer surfaces can both provide active sites catalyzing the redox reactions of vanadium redox couples, is designed and prepared by using nickel metal–organic framework (Ni‐MOF) as a template with the assistance of polyvinylpyrrolidone (PVP). This catalyst with its high specific surface area can be simply in situ loaded on the graphite felt forming a composite electrode. The composite electrode exhibits outstanding electrocatalytic activity, as the vanadium ions can participate in the reaction on both inner and outer surfaces of the hollow spheres. As a result, a VFB single cell assembled with this electrode can achieve a high energy efficiency of 82.7% at a current density of 200 mA cm−2 and a peak power density of 958 mW cm−2, which is much higher than those of pristine graphite felts. This work provides a new idea for the development of highly active electrocatalysts for VFBs and further improves the power density of a VFB. [ABSTRACT FROM AUTHOR]

A membrane with low vanadium ion permeability and excellent electrochemical stability is crucial for a vanadium flow battery (VFB). Herein, a highly stable anion exchange membrane based on a bi‐guanidinium crosslinking quaternized poly(arylene ether sulfone) (PSF) is reported. The positively charged guanidinium groups can not only form continuous and smooth ion transport channels but also prevent the mutual penetration of vanadium electrolyte at positive and negative sides, respectively, based on the Donnan exclusion effect. Moreover, the crosslinking structure endows the membrane high mechanical strength to meet the requirements of the harsh environment of VFBs. As a result, the anion exchange membrane fabricated by the poly(arylene ether sulfone) crosslinked with bi‐guanidinium (BG‐PSF) shows an impressive VFB performance with a coulombic efficiency of 99.8% and an energy efficiency of above 85.8% at a current density of 80 mA cm−2, which is much higher than that of Nafion115. Furthermore, this battery can continuously work for over 200 cycles at a current density of 80 mA cm−2, indicating good stability of the membrane. Therefore, the rationally designed BG‐PSFs are promising for VFB applications. [ABSTRACT FROM AUTHOR]

Due to decoupled energy and power, the aqueous organic redox flow battery (AORFB) represents a promising energy storage technology that stores energy in redox‐active organic compounds dissolved in aqueous electrolytes. The organic compounds are composed of earth‐abundant elements and are therefore potentially cost‐effective. Their structures are diverse and highly tunable, rendering it possible to regulate the redox potential, water solubility, and cycling lifespan. Therefore, the adoption of redox‐active organics greatly expands the space for enabling exceeding performance merits compared to their inorganic counterparts. Herein, this work reviews the molecular design and engineering scheme of organic electrolytes, focusing exclusively on pH‐neutral AORFB that uses non‐corrosive and nonflammable pH‐neutral aqueous electrolytes with inexpensive inorganic salts as supporting electrolytes and features high safety, low corrosivity, low cost, and environmental benignity. Some comments on the present challenges and prospects of this ascendant domain are also presented. [ABSTRACT FROM AUTHOR]

Uncontrollable lithium dendrite growth and severe Li/electrolyte side reactions under high operating current densities seriously hinder the development of high‐performance Li metal batteries (LMBs). To address the aforementioned critical issues, spherical Li nuclei are designed via an "all‐in‐one" nitrocellulose (NC)/LiFSI electrolyte to achieve high‐energy/power‐density and long‐cycle LMBs. First, the synergistic effect of LiFSI induced LiF‐rich interface and the nitro group in the NC scaffold promote uniform Li nucleation, resulting in spherical nuclei morphology instead of dendritic even under high current densities. Moreover, NC exhibits strong adsorption energy on the electrode surface, which facilitates the formation of an organic protection layer to suppress side reactions, which enables highly reversible Li cycling, even in a lean‐electrolyte environment. With the assistance of the unique interphase, the Li|Li symmetric cells using NC/LiFSI electrolyte can stably run at a high current density of 10 mA cm‐2. Moreover, the assembled Li|LiFePO4 pouch cell achieves excellent cycling stability of 210 cycles with 100% capacity retention. This finding provides a new strategy relying on electrolyte engineering to achieve high‐energy/power‐density and long‐cycling‐life LMBs. [ABSTRACT FROM AUTHOR]

We present a coral‐like FeP composite with FeP nanoparticles anchored and dispersed on a nitrogen‐doped 3D carbon framework (FeP@NC). Due to the highly continuous N‐doped carbon framework and a spring‐buffering graphitized carbon layer around the FeP nanoparticle, a sodium‐ion battery with the FeP@NC composite exhibits an ultra‐stable cycling performance at 10 A g−1 with a capacity retention of 82.0 % in 10 000 cycles. Also, particle refinement leads to a capacity increase during cycling. The FeP nanoparticles go through a refining–recombination process during the first cycle and present a global refining trend after dozens of cycles, which results in a gradually increase in graphitization degree and interface magnetization, and further provides more active sites for Na+ storage and contributes to a rising capacity with cycling. The capacity ascending phenomenon can also extend to lithium‐ion batteries. [ABSTRACT FROM AUTHOR]

Aim Background Methods Results Conclusion Implications for nursing and policy This study aimed to explore 1) factors that influenced the evidence‐based practice competencies and behaviors of clinical nurses and 2) the interaction between the organizational evidence‐based practice culture, head nurses' implementation leadership, and nurses' evidence‐based practice competencies and behaviors.The significance of organizational evidence‐based practice culture and head nurses' implementation leadership in enhancing nurses' evidence‐based practice competencies and behavior is widely recognized in healthcare settings. However, there is limited knowledge of how these factors influence nurses' evidence‐based practice competencies and behavior.A cross‐sectional survey was conducted at 10 hospitals in China. Data were collected via online questionnaires from October to December 2020, utilizing social characteristic questionnaires, the Evidence‐Based Practice Questionnaire, the Organizational Culture and Readiness Scale for System‐wide Implementation of Evidence‐Based Practice, and the Implementation Leadership Scale. All data were imported into the IBM Statistical Program for the Social Sciences (SPSS) 27.0 and PROCESS version 4.1 macro on SPSS for statistical analysis. The design and reporting of our study adhered to the Strengthening the Reporting of Observational Studies in Epidemiology (STROBE) Checklist.We received 1047 (99.15%) valid questionnaires. The multiple linear regression analysis showed that significant factors were organizational evidence‐based practice culture, implementation leadership, and years of experience in nursing. After controlling for the impact of the covariate (years of experience in nursing), it was found that organizational evidence‐based practice culture partially mediated the relationship between head nurses' implementation leadership and nurses' evidence‐based practice competencies and behaviors. Additionally, head nurses' implementation leadership partially mediated the relationship between organizational evidence‐based practice culture and nurses' evidence‐based practice competencies and behaviors.Organizational evidence‐based practice culture, head nurses' implementation leadership, and years of experience in nursing significantly predict nurses' evidence‐based practice competencies and behaviors. Organizational evidence‐based practice culture and head nurses' implementation leadership mutually mediated their influence on nurses' implementation of evidence‐based practice.Head nurses should proactively seek opportunities to enhance their implementation leadership, such as participating in training programs (e.g., mentoring and coaching programs) and attending conferences, workshops, or seminars on implementation leadership. Policymakers should also consider providing more policy support for implementing leadership development and cultivating a positive evidence‐based practice culture. [ABSTRACT FROM AUTHOR]

Rechargeable aqueous zinc‐based flow batteries (ZFBs) are promising candidates for large scale energy storage devices. However, the challenges from zinc dendrites and limited areal capacity considerably impede their wide application. Here, an in situ vertical growth of layered double hydroxide membrane (LDH‐G) is constructed to enable long‐life ZFBs. Owing to the high hydroxide ion conductivity and ion selectivity nature of LDH nanosheets, specifically, the precise control of directional ion transport in vertical arrangement LDHs, a superior battery performance can be realized. Moreover, the defect‐free LDHs layer serves as a buffer layer to enable a uniform Zn deposition, which effectively enhances the areal capacity of the battery. As a result, the designed membrane endows an alkaline zinc‐iron flow battery with excellent rate performance and cycling stability, maintaining an energy efficiency of 80% at 260 mA cm−2 for 800 cycles, which is the highest performance ever reported. Most importantly, the LDHs layer enables the battery for 1200 h long‐cycle stability with a uniform Zn deposition and high areal capacity of 240 mAh cm−2. This work realizes an in situ growth of 3D LDHs arrays on the polymer substrate, which provides a strategy toward high areal capacity and dendrite‐free Zn deposition for ZFBs. [ABSTRACT FROM AUTHOR]

Zinc‐bromine flow batteries (ZBFBs) are regarded as one of the most promising technologies for energy storage owing to high energy density and low cost. However, the sluggish reaction kinetics of Br2/Br− couples and zinc dendrite issue lead to low power density and poor cycle stability. Herein, a multifunctional carbon felt‐based electrode (NTCF) with N‐rich defects is fabricated for ZBFBs. The defects with abundant N‐containing groups on carbon fibers of NTCF provide high catalytic activity on Br2/Br− reactions. Simultaneously, the lower energy barrier of N‐rich defects to adsorb zinc atoms, and more deposition sites on NTCF induce more uniform zinc deposition. Thus, a ZBFB using NTCF as both the anode and cathode can stably operate at an unprecedentedly high current density of 180 mA cm−2 with a coulombic efficiency of 97.25%. Moreover, a long cycle life of over 140 cycles with a coulombic efficiency of 98.93% for a Zn symmetric flow battery at 80 mA cm−2 is achieved under a high areal capacity of 40 mAh cm−2. This current density and areal capacity are by far the highest values ever reported for Zn symmetry flow batteries. Therefore, this work provides an available approach to improve the power density and cycle life of ZBFBs. [ABSTRACT FROM AUTHOR]

NaVPO4F is regarded as one of the most competitive cathodes in high performance sodium ion batteries (SIBs). Two polymorphs with the tetragonal and monoclinic NaVPO4F have been reported, while the true presentation of the fluorophosphates is still poorly understood. Herein, fluorophosphates with a molar ratio of 1:1:1:1 for Na, V, P, F are fabricated at different temperatures. The presentation of tetragonal and monoclinic NaVPO4F is strikingly confirmed. For the first time, the accurate atomic arrangement in the crystal, and the irreversible phase transition from tetragonal to monoclinic with temperature variation are unveiled by combining series of advanced in/ex situ characterizations. From both the thermodynamic and kinetic perspectives, the sodium storage behavior and the electron/Na+ conduction, contributing to notably different electrochemical performance for the two fluorophosphates, are elaborately studied based on experimental and density functional theory calculations. The comprehensive expositions indicate that the tetragonal and monoclinic NaVPO4F have the potential to be employed as high‐energy‐density and high‐power‐density cathodes, respectively. This research answers the question of the true state of the fluorophosphates and reveals some of their previously unexplored mysteries, which provides an instructive selection principle for NaVPO4F compounds for serving in well‐defined application scenarios and is expected to become an accelerator for the next generation of high‐performance SIBs. [ABSTRACT FROM AUTHOR]

Bromine‐based flow batteries (Br‐FBs) are considered one of the most promising energy storage systems due to their features of high energy density and low cost. However, they generally suffer from uncontrolled diffusion of corrosive bromine particularly at high temperatures. That is because the interaction between polybromide anions and the commonly used complexing agent (N–methyl–N–ethyl–pyrrolidinium bromide [MEP]) decreases with increasing temperatures, which causes serious self‐discharge and capacity fade. Herein, a novel bromine complexing agent, 1–ethyl–2–methyl–pyridinium bromide (BCA), is introduced in Br‐FBs to solve the above problems. It is proven that BCA can combine with polybromide anions very well even at a high temperature of 60 °C. Moreover, the BCA contributes to decreasing the electrochemical polarization of Br−/Br2 couple, which in turn improves their power density. As a result, a zinc–bromine flow battery with BCA as the complexing agent can achieve a high energy efficiency of 84% at 40 mA cm−2, even at high temperature of 60 °C and it can stably run for more than 400 cycles without obvious performance decay. This paper provides an effective complexing agent to enable a wide temperature range Br‐FB. [ABSTRACT FROM AUTHOR]

Nitrocellulose (NC) is proposed to stabilize the electrolytes for Li metal batteries. The nitro group of NC preferentially reacts with Li metal, and along with the cellulose skeleton is tightly wrapped on the surface, so that the polymer–inorganic double layer is formed on the Li surface. XPS profile analysis and corroborative cryo‐environmental TEM reveal that the flexible outer layer of the bilayer is a C‐O organic layer, while the dense inner layer is mainly composed of crystalline lithium oxide, lithium oxynitride, and lithium nitride. The Li deposition process was observed via in situ optical microscopy, which indicated that the NC‐derived bilayer facilitates the uniform deposition of Li ions and inhibits the growth of dendrites. After the introduction of NC into the electrolyte, the cycle life of the Li battery is twice than that of the Li battery without NC at 1.0 and 3.0 mA cm−2. [ABSTRACT FROM AUTHOR]

Electrode design enabling more active materials makes it possible to improve the energy density for sodium‐ion batteries (SIBs) on the device level, yet suffer from sluggish ion transport. Herein, a low‐tortuosity Na3V2(PO4)3‐based cathode is demonstrated based on a nonsolvent‐induced phase separation method. The targeted low‐tortuosity morphology can be achieved by thermodynamic and kinetic modulation. Benefiting from the structural advantages, the electrode with an ultra‐high mass loading (60 mg cm−2) and areal capacity (4.0 mAh cm−2) is successfully achieved. Even at a high rate of 10 C, the areal capacity remains 1.0 mAh cm−2. Comprehensive understanding on the effects of low‐tortuosity architecture to the spatial and temporal distribution of the multi‐physical field parameters has been elucidated by the finite element method. A homogeneous Na+ distribution, gentle and uniform local current density, and polarization inside the electrode are illustrated. Combining numerical simulations and experiments, it reveals that the low‐tortuosity architecture can contribute to an impressive ion transport capability and consequently significant improvements in electrochemical performance. This study exhibits a prospective solution for the design and optimization of the low‐tortuosity electrodes with ultra‐high mass loading, which opens a new door for developing advanced SIBs with high energy/power density. [ABSTRACT FROM AUTHOR]

Zinc oxide (ZnO) nanostructures have received widespread attention due to their unique structure and broad application possibilities, but high preparation costs and agglomeration limit their usage. In this article, low‐cost and environmentally friendly cellulose and ZnCl2 are used to synthesize ZnO nanoparticles (ZnO NPs). Subsequently, multifunctional ZnO/polyacrylonitrile hybrid nanofiber mats (ZnO/PAN@NFMs) with mechanical stability suitable for large‐scale application are prepared via solution blow‐spinning. The synthesized ZnO/PAN@NFMs exhibit higher photodegradation of organic dyes than earlier reported semiconductors and good recycling performance with an organic dye degradation above 94%–98% after five cycles, which is ascribed to fixation of the ZnO NPs in the nanofibers. In addition, the inhibition rate for Escherichia coli and Staphylococcus aureus is above 99.9% and the bacteriostatic rate against E. coli remains as high as 99% after 10 cycles. From these properties, the synthesized composite ZnO/PAN@NFMs are promising for wastewater cleaning and antibacterial fabrics. [ABSTRACT FROM AUTHOR]

Membranes with precise control of selective layer are designed and prepared by adjusting diffusion of solvents. Combining experiments and theoretical calculations, the formation mechanism of ion conductive membranes prepared by a non‐solvent induced phase separation (NIPS) method is found to be related to internal diffusion flux of solvent to the non‐solvent bath and external diffusion flux of non‐solvent to the casting solution. By regulating the internal and external diffusion rates via a two‐step NIPS method, a series of polybenzimidazole (PBI) porous membranes with independently controlled thin selective skin layers and highly porous support layers are fabricated, which achieve a simultaneous improvement in ion selectivity and proton conductivity. A vanadium flow battery assembled with a PBI membrane demonstrates an energy efficiency of 80% at a current density of 220 mA cm−2, which is the highest value among the reported PBI membranes. This provides a simple and effective way to fabricate membranes with well‐defined morphologies. [ABSTRACT FROM AUTHOR]

Summary: Plants maintain a dynamic balance between plant growth and stress tolerance to optimise their fitness and ensure survival. Here, we investigated the roles of a clade A type 2C protein phosphatase (PP2C)‐encoding gene, OsPP2C09, in regulating the trade‐off between plant growth and drought tolerance in rice (Oryza sativa L.).The OsPP2C09 protein interacted with the core components of abscisic acid (ABA) signalling and showed PP2C phosphatase activity in vitro. OsPP2C09 positively affected plant growth but acted as a negative regulator of drought tolerance through ABA signalling.Transcript and protein levels of OsPP2C09 were rapidly induced by exogenous ABA treatments, which suppressed excessive ABA signalling and plant growth arrest. OsPP2C09 transcript levels in roots were much higher than those in shoots under normal conditions. After ABA, polyethylene glycol and dehydration treatments, the accumulation rate of OsPP2C09 transcripts in roots was more rapid and greater than that in shoots. This differential expression between the roots and shoots may increase the plant's root‐to‐shoot ratio under drought‐stress conditions.This study sheds new light on the roles of OsPP2C09 in coordinating plant growth and drought tolerance. In particular, we propose that OsPP2C09‐mediated ABA desensitisation contributes to root elongation under drought‐stress conditions in rice. [ABSTRACT FROM AUTHOR]

Flow batteries (FBs) are one of the most attractive candidates for stationary energy storage and vital in realizing the wide application of renewable energies. Membranes play an important role in isolating redox couples while transporting ions to close the internal electrical circuit. Therefore, membranes with high selectivity and conductivity are highly important. Among different membranes, a composite membrane with independent design of support layer and thin selective top layer becomes one of the most promising candidates to break the trade‐off between selectivity and conductivity. In this Review, recent studies on composite membranes for FBs and the principles of membrane design in different systems are discussed and summarized. Finally, the future direction on membrane design for different FBs is presented, which will provide an extensive, comprehensive reference to design and construct high‐performance composite membranes for FBs. [ABSTRACT FROM AUTHOR]

The capability to maintain a constant system temperature is vital in nature, since it endows the system with enhanced lifetime. This trait also works for zinc‐based batteries, because their cycle‐life is limited by notorious zinc dendrite/accumulation, which are highly affected by the inhomogeneous distribution of temperature on electrode and relatively low mechanical strength of membrane. Herein, boron nitride nanosheets (BNNSs) with high mechanical strength serving as heat‐porter are introduced onto a porous substrate to enable uniform deposition of zinc and further a zinc‐based flow battery with long‐cycle life. The results indicate that BNNSs can effectively adjust the deposited zinc from needle‐like to French fries‐like morphology, thus affording the battery with a stable performance for nearly 500 cycles at 80 mA cm−2. Most importantly, an energy efficiency of above 80 % can be obtained even at 200 mA cm−2, which is by far the highest value ever reported among zinc‐based flow batteries. [ABSTRACT FROM AUTHOR]

The stability control of surrounding rock for a large or super‐large section chamber group is a difficult technical problem in deep mining conditions, and this stability control has become one of the most important factors restricting the safety of a large‐scale coal mine. Based on the in‐site geological conditions of a super‐large section chamber group that functions for a coal gangues separation system in the Longgu Coal Mine, we first researched the stress, deformation, and failure characteristics of the in‐site chamber group surrounding rocks by using the FLAC3D software. Simulation results showed that the maximum vertical stress, deformation, and failure range of the surrounding rock for a super‐large section chamber group are larger than those of an ordinary section chamber. In addition, the roof subsidence and the plastic zone radius at the intersection are obviously larger than that of other parts, which increase by approximately 50.8% and 44.4%, respectively. Therefore, the chamber group intersection should be taken as the key area for surrounding rock control. Then, the influences of two key parameters of the chamber group, spacing and angle, were researched in detail to help in the design of the chamber group. Results show that when the chamber spacing is 80 m, the interaction begins to occur. When the angle is 70°, the stress of the surrounding rock and roof subsidence reach the minimum. Thus, the optimum chamber group parameters are determined to be a spacing of 80 m and an angle of 70°. Finally, from the perspective of chamber group stability, the optimal chamber group parameters can better meet the normal use for the super‐large section chamber group. This research provides a reference for the design of a super‐large section chamber group under the same or similar conditions and provides a strategy for controlling the surrounding rock. [ABSTRACT FROM AUTHOR]

Flow batteries (FBs) have become a central topic recently, due to their promising prospect of addressing the issues of the random and intermittent nature of renewable energy sources. However, the successful industrialization of current FB systems is still limited by their relatively low energy densities and high cost. Research and development into novel aqueous FB systems with high energy density, high safety, and low cost are accordingly urgently required. Some novel aqueous FB systems have been explored in recent years to overcome issues of traditional FBs and vanadium FBs, in particular. Further modifications have also been made to improve their performance. In this review, appealing novel aqueous FB systems, such as zinc‐ and quinone‐based FB systems, are reviewed, in terms of the operating principles, advantages, drawbacks, corresponding performance, and subsequent modifications. Moreover, recent investigations and advancements, and prospective research directions for novel aqueous FB systems, are summarized. Therefore, this review will provide guidance and perspectives for developing new aqueous FB systems. Go with the flow: Appealing aqueous flow battery systems, in terms of the principles, advantages, drawbacks, corresponding performance, and subsequent modifications, are summarized here. Recent developments and prospective research directions for these flow battery systems are also summarized. [ABSTRACT FROM AUTHOR]

Zinc deposition and dissolution is a significant process in zinc‐based batteries. During this process, the formation of zinc dendrites is pervasive, which leads to the loss of efficiency and capacity of batteries. The continually growing dendrites will finally pierce the separator and cause the batteries to short circuit. Thus, employing effective methods to inhibit the formation and growth of zinc dendrites is vital for the practical application of zinc‐based batteries. This Minireview first clarifies the formation and growth principles of zinc dendrites. Then, the research and development of methods to solve the problem of zinc dendrites are reviewed, including ways to suppress the further formation and growth of dendrites as far as possible, to minimize the adverse effects of dendrites, along with ways to produce dendrite‐free deposition processes. The mechanisms, advantages, drawbacks, and perspectives of these methods are illustrated. Thus, this overview of these methods will aid understanding of the formation process of zinc dendrites and provide an extensive, comprehensive, and professional reference to resolve the problem of zinc dendrites completely. Growth misconduct: Zinc deposition and dissolution is a significant process in zinc‐based batteries, whereby the formation of zinc dendrites can lead to the loss of efficiency and capacity of the batteries. This Minireview concerns the formation and growth principles of zinc dendrites, along with the effective methods to solve the zinc dendrite problem in zinc‐based batteries. [ABSTRACT FROM AUTHOR]

Abstract: Electrochemical reduction of CO2 (ERC) to useful chemicals is an environmentally and technologically significant process. The process is confronted with significant challenges to simultaneously enhance the catalyst activity and product selectivity. In this paper, the effects of organic additives on the ERC process were systematically investigated by using DFT to screen additives with different functional groups for enhanced activity and selectivity. In particular, the additives with −NH3+ and −SO3H groups had a remarkably positive effect on the ERC activity and hydrocarbon selectivity, which were predicted to impart a positive shift on onset potential of approximately 162 and 108 mV, respectively. Importantly, the additive can accelerate the electron transfer of the intermediate and tune the electronic structure of the catalyst surface, resulting in a clear deviation from transition‐metal scaling lines. Combining bonding energy of crucial intermediates with partial atomic charge analysis, we rationalized the negative effect of high concentration additives and confirmed the proposed electron transfer model. Furthermore, additive molecules containing functional groups with positive charges and maximizing the deviation from transition‐metal scaling lines are meaningful strategies to design and choose organic additives to enhance activity and selectivity of ERC. [ABSTRACT FROM AUTHOR]

Abstract: A zinc–iodine flow battery (ZIFB) with long cycle life, high energy, high power density, and self‐healing behavior is prepared. The long cycle life was achieved by employing a low‐cost porous polyolefin membrane and stable electrolytes. The pores in the membrane can be filled with a solution containing I3− that can react with zinc dendrite. Therefore, by consuming zinc dendrite, the battery can self‐recover from micro‐short‐circuiting resulting from overcharging. By using KI, ZnBr2, and KCl as electrolytes and a high ion‐conductivity porous membrane, a very high power density can be achieved. As a result, a ZIFB exhibits an energy efficiency (EE) of 82 % at 80 mA cm−2, which is 8 times higher than the currently reported ZIFBs. Furthermore, a stack with an output of 700 W was assembled and continuously run for more than 300 cycles. We believe this ZIFB can lead the way to development of new‐generation, high‐performance flow batteries. [ABSTRACT FROM AUTHOR]

Abstract: Most of single‐component white‐light‐emitting materials focus on organic–inorganic hybrid perovskites, metal–organic frameworks, as well as all‐inorganic semiconductors. In this work, we successfully assembled an all‐inorganic layered perovskite by mixing two halogens of distinct ionic radii, namely, Rb2CdCl2I2, which emits “warm” white light with a high color rendering index of 88. To date, Rb2CdCl2I2 is the first single‐component white‐light‐emitting material with an all‐inorganic layered perovskite structure. Furthermore, Rb2CdCl2I2 is thermally highly stable up to 575 K. A series of luminescence measurements show that the white‐light emission arises from the lattice deformation, which are closely related to the [CdCl4I2]2− octahedra with high distortion from the distinct ionic radii of Cl and I. The first‐principles calculations reveal that both the Cl and I components make significant contributions to the electronic band structures of Rb2CdCl2I2. These findings indicate that mixing halogens is an effective route to design and synthesize new single‐component white‐light‐emitting materials. [ABSTRACT FROM AUTHOR]

Abstract: Development of flexible Li–S batteries brings along the flourishing prospective for energy‐hungry wearable devices. However, it is still seriously restricted due to lack of facile methods to solve its inherent problems and flexible device‐related current collection issues. Herein, quasi‐stable electroless deposition method is firstly proposed to solve these problems by fabricating 3D tunable Ni–P networks in the C/S free‐standing electrode. The ultrathin Ni–P layers which are highly conductive and strongly adhesive with electrode substrates improve the electronic conductivity by two orders of magnitude and rise initial specific capacity from 1200 to 1600 mAh g−1. The harmful shuttle effect of polysulfide is also effectively alleviated due to the chemical adsorption and physical sieving properties of the 3D networks. The flexible pouch Li–S batteries assembled with commercially applicable structure also show high flexibility and as high as 1420 mAh g−1 output capacity at 0.1C in cycling test. This method can definitely be extended to other flexible devices such as Li‐ion batteries, Li–O2 batteries, and supercapacitors. [ABSTRACT FROM AUTHOR]

Abstract: Organic–inorganic hybrid perovskites, with the formula ABX3 (A=organic cation, B=metal cation, and X=halide; for example, CH3NH3PbI3), have diverse and intriguing physical properties, such as semiconduction, phase transitions, and optical properties. Herein, a new ABX3‐type semiconducting perovskite‐like hybrid, (hexamethyleneimine)PbBr3 (1), consisting of one‐dimensional inorganic frameworks and cyclic organic cations, is reported. Notably, the inorganic moiety of 1 adopts a perovskite‐like architecture and forms infinite columns composed of face‐sharing PbBr6 octahedra. Strikingly, the organic cation exhibits a highly flexible molecular configuration, which triggers an above‐room‐temperature phase transition, at Tc=338.8 K; this is confirmed by differential scanning calorimetry (DSC), specific heat capacity (Cp), and dielectric measurements. Further structural analysis reveals that the phase transition originates from the molecular configurational distortion of the organic cations coupled with small‐angle reorientation of the PbBr6 octahedra inside the inorganic components. Moreover, temperature‐dependent conductivity and UV/Vis absorption measurements reveal that 1 also displays semiconducting behavior below Tc. It is believed that this work will pave a potential way to design multifeatured perovskite hybrids by utilizing cyclic organic amines. [ABSTRACT FROM AUTHOR]