Kinetic Evaluation on Lithium Polysulfide in Weakly Solvating Electrolyte toward Practical Lithium-Sulfur Batteries.

Lithium-sulfur (Li-S) batteries are highly considered as next-generation energy storage techniques. Weakly solvating electrolyte with low lithium polysulfide (LiPS) solvating power promises Li anode protection and improved cycling stability. However, the cathodic LiPS kinetics is inevitably deteriorated, resulting in severe cathodic polarization and limited energy density.

Inductive Effect on Single-Atom Sites.

Single-atom catalysts exhibit promising electrocatalytic activity, a trait that can be further enhanced through the introduction of heteroatom doping within the carbon skeleton. Nonetheless, the intricate relationship between the doping positions and activity remains incompletely elucidated. This contribution sheds light on an inductive effect of single-atom sites, showcasing that the activity of the oxygen reduction reaction (ORR) can be augmented by reducing the spatial gap between the doped heteroatom and the single-atom sites.

Molecular Recognition Regulates Coordination Structure of Single-Atom Sites.

Coordination engineering for single-atom sites has drawn increasing attention, yet its chemical synthesis remains a tough issue, especially for tailorable coordination structures. Herein, a molecular recognition strategy is proposed to fabricate single-atom sites with regulable local coordination structures. Specifically, a heteroatom-containing ligand serves as the guest molecule to induce coordination interaction with the metal-containing host, precisely settling the heteroatoms into the local structure of single-atom sites.

Transgenerational plasticity in morphological characteristics and biomass of the invasive plant Xanthium strumarium.

Transgenerational plasticity (TGP) allows a plant to acclimate to external variable environments and is a potential mechanism that explains the range expansion and invasion success of some exotic plants. Most studies explored the traits of TGP associated with the success of exotic plant invasions by comparison studies among exotic, native, invasive, and noninvasive species. However, studies on the TGP of invasive plants in different resource environments are scarce, and the biological mechanisms involved are not well understood.

Nitrogen deposition further increases Ambrosia trifida root exudate invasiveness under global warming.

Invasive plants can change the soil ecological environment in the invasion area to adapt to their growth and reproduction through root exudates. Root exudates are the most direct manifestation of plant responses to external environmental changes, but there is a lack of studies on root exudates of invasive plants in the context of inevitable global warming and nitrogen deposition. In this research, we used widely targeted metabolomics to investigate Ambrosia trifida root exudates during seedling and maturity under warming and nitrogen deposition to reveal the possible mechanisms of A.

Regulating Lithium Salt to Inhibit Surface Gelation on an Electrocatalyst for High-Energy-Density Lithium-Sulfur Batteries.

Lithium-sulfur (Li-S) batteries have great potential as high-energy-density energy storage devices. Electrocatalysts are widely adopted to accelerate the cathodic sulfur redox kinetics. The interactions among the electrocatalysts, solvents, and lithium salts significantly determine the actual performance of working Li-S batteries.

Working Zinc-Air Batteries at 80 °C.

Aqueous zinc-air batteries possess inherent safety and are especially commendable facing high-temperature working conditions. However, their working feasibility at high temperatures has seldom been investigated. Herein, the working feasibility of high-temperature zinc-air batteries is systemically investigated.

A clicking confinement strategy to fabricate transition metal single-atom sites for bifunctional oxygen electrocatalysis.

Rechargeable zinc-air batteries call for high-performance bifunctional oxygen electrocatalysts. Transition metal single-atom catalysts constitute a promising candidate considering their maximum atom efficiency and high intrinsic activity. However, the fabrication of atomically dispersed transition metal sites is highly challenging, creating a need for for new design strategies and synthesis methods.

Preconstructing Asymmetric Interface in Air Cathodes for High-Performance Rechargeable Zn-Air Batteries.

Rechargeable zinc-air batteries afford great potential toward next-generation sustainable energy storage. Nevertheless, the oxygen redox reactions at the air cathode are highly sluggish in kinetics to induce poor energy efficiency and limited cycling lifespan. Air cathodes with asymmetric configurations significantly promote the electrocatalytic efficiency of the loaded electrocatalysts, whereas rational synthetic methodology to effectively fabricate asymmetric air cathodes remains insufficient.

Surface Gelation on Disulfide Electrocatalysts in Lithium-Sulfur Batteries.

Lithium-sulfur (Li-S) batteries are deemed as future energy storage devices due to ultrahigh theoretical energy density. Cathodic polysulfide electrocatalysts have been widely investigated to promote sluggish sulfur redox kinetics. Probing the surface structure of electrocatalysts is vital to understanding the mechanism of polysulfide electrocatalysis.

Semi-Immobilized Molecular Electrocatalysts for High-Performance Lithium-Sulfur Batteries.

Lithium-sulfur (Li-S) batteries constitute promising next-generation energy storage devices due to the ultrahigh theoretical energy density of 2600 Wh kg. However, the multiphase sulfur redox reactions with sophisticated homogeneous and heterogeneous electrochemical processes are sluggish in kinetics, thus requiring targeted and high-efficient electrocatalysts. Herein, a semi-immobilized molecular electrocatalyst is designed to tailor the characters of the sulfur redox reactions in working Li-S batteries.

An Adjacent Atomic Platinum Site Enables Single-Atom Iron with High Oxygen Reduction Reaction Performance.

The modulation effect has been widely investigated to tune the electronic state of single-atomic M-N-C catalysts to enhance the activity of oxygen reduction reaction (ORR). However, the in-depth study of modulation effect is rarely reported for the isolated dual-atomic metal sites. Now, the catalytic activities of Fe-N moiety can be enhanced by the adjacent Pt-N moiety through the modulation effect, in which the Pt-N acts as the modulator to tune the 3d electronic orbitals of Fe-N active site and optimize ORR activity.

Recent advances of noble-metal-free bifunctional oxygen reduction and evolution electrocatalysts.

Oxygen reduction and evolution reactions constitute the core process of many vital energy storage or conversion techniques. However, the kinetic sluggishness of the oxygen redox reactions and heavy reliance on noble-metal-based electrocatalysts strongly limit the energy efficiency of the related devices. Developing high-performance noble-metal-free bifunctional ORR and OER electrocatalysts has gained worldwide attention, where much important progress has been made during the last decade.

Can Aqueous Zinc-Air Batteries Work at Sub-Zero Temperatures?

Efficient energy storage at low temperatures starves for competent battery techniques. Herein, inherent advantages of zinc-air batteries on low-temperature electrochemical energy storage are discovered. The electrode reactions are resistive against low temperatures to render feasible working zinc-air batteries under sub-zero temperatures.

A ΔE = 0.63 V Bifunctional Oxygen Electrocatalyst Enables High-Rate and Long-Cycling Zinc-Air Batteries.

Rechargeable zinc-air batteries constitute promising next-generation energy storage devices due to their intrinsic safety, low cost, and feasibility to realize high cycling current density and long cycling lifespan. Nevertheless, their cathodic reactions involving oxygen reduction and oxygen evolution are highly sluggish in kinetics, requiring high-performance noble-metal-free bifunctional electrocatalysts that exceed the current noble-metal-based benchmarks. Herein, a noble-metal-free bifunctional electrocatalyst is fabricated, which demonstrates ultrahigh bifunctional activity and renders excellent performance in rechargeable zinc-air batteries.

Application of the sigma metrics to evaluate the analytical performance of cystatin C and design a quality control strategy.

Background: Sigma metrics are commonly used to evaluate laboratory management. In this study, we aimed to evaluate the analytical performance of cystatin C using sigma metrics and to develop an individualized quality control scheme for cystatin C concentrations.

Methods: Bias was calculated based on the samples used for the external quality assessment.

Intrinsic Electrocatalytic Activity Regulation of M-N-C Single-Atom Catalysts for the Oxygen Reduction Reaction.

Single-atom catalysts (SACs) with highly active sites atomically dispersed on substrates exhibit unique advantages regarding maximum atomic efficiency, abundant chemical structures, and extraordinary catalytic performances for multiple important reactions. In particular, M-N-C SACs (M=transition metal atom) demonstrate optimal electrocatalytic activity for the oxygen reduction reaction (ORR) and have attracted extensive attention recently. Despite substantial efforts in fabricating various M-N-C SACs, the principles for regulating the intrinsic electrocatalytic activity of their active sites have not been sufficiently studied.

Asymmetric Air Cathode Design for Enhanced Interfacial Electrocatalytic Reactions in High-Performance Zinc-Air Batteries.

The rechargeable zinc-air battery (ZAB) is a promising energy storage technology owing to its high energy density and safe aqueous electrolyte, but there is a significant performance bottleneck. Generally, cathode reactions only occur at multiphase interfaces, where the electrocatalytic active sites can participate in redox reactions effectively. In the conventional air cathode, the 2D multiphase interface on the surface of the gas diffusion layer (GDL) inevitably results in an insufficient amount of active sites and poor interfacial contact, leading to sluggish reaction kinetics.

A Composite Bifunctional Oxygen Electrocatalyst for High-Performance Rechargeable Zinc-Air Batteries.

Rechargeable zinc-air batteries are considered as next-generation energy storage devices because of their ultrahigh theoretical energy density of 1086 Wh kg (including oxygen) and inherent safety originating from the use of aqueous electrolyte. However, the cathode processes regarding oxygen reduction and evolution are sluggish in terms of kinetics, which severely limit the practical battery performances. Developing high-performance bifunctional oxygen electrocatalysts is of great significance, yet to achieve better bifunctional electrocatalytic reactivity beyond the state-of-the-art noble-metal-based electrocatalysts remains a great challenge.

Electrolyte Regulation towards Stable Lithium-Metal Anodes in Lithium-Sulfur Batteries with Sulfurized Polyacrylonitrile Cathodes.

Lithium-sulfur (Li-S) batteries are highly regarded as the next-generation energy-storage devices because of their ultrahigh theoretical energy density of 2600 Wh kg . Sulfurized polyacrylonitrile (SPAN) is considered a promising sulfur cathode to substitute carbon/sulfur (C/S) composites to afford higher Coulombic efficiency, improved cycling stability, and potential high-energy-density Li-SPAN batteries. However, the instability of the Li-metal anode threatens the performances of Li-SPAN batteries bringing limited lifespan and safety hazards.

Favorable Lithium Nucleation on Lithiophilic Framework Porphyrin for Dendrite-Free Lithium Metal Anodes.

Lithium metal constitutes promising anode materials but suffers from dendrite growth. Lithiophilic host materials are highly considered for achieving uniform lithium deposition. Precise construction of lithiophilic sites with desired structure and homogeneous distribution significantly promotes the lithiophilicity of lithium hosts but remains a great challenge.

Electrosynthesis of Hydrogen Peroxide Synergistically Catalyzed by Atomic Co-N -C Sites and Oxygen Functional Groups in Noble-Metal-Free Electrocatalysts.

Hydrogen peroxide (H O ) is a green oxidizer widely involved in a vast number of chemical reactions. Electrochemical reduction of oxygen to H O constitutes an environmentally friendly synthetic route. However, the oxygen reduction reaction (ORR) is kinetically sluggish and undesired water serves as the main product on most electrocatalysts.

Association between serum lipoprotein-associated phospholipase A2, ischemic modified albumin and acute coronary syndrome: a cross-sectional study.

Lipoprotein-associated phospholipase A2 (Lp-PLA2) is a newly emerging biomarker with strong pro-inflammatory effects, and is an independent risk predictor of atherosclerotic plaque rupture and thrombosis. In addition, ischemic modified albumin (IMA) is another important marker for the evaluation of myocardial ischemia, and has been approved by the U.S.