Heterostructure Engineering for Aluminum-Ion Batteries: Mechanism, Challenge, and Perspective.

Benefiting from high volumetric capacity, environmental friendliness, and high safety, aluminum-ion batteries (AIBs) are considered to be promising battery system among emerging electrochemical energy storage technologies. As an important component of AIBs, the cathode material is crucial to decide the energy density and cycle life of AIBs. However, single-component cathode materials are unable to achieve a balance between cycling stability and rate performance. In recent years, research on heterostructure cathode materials has gained significant attention in AIBs. By harnessing the synergistic effects of heterostructure, the shortcomings of individual materials can be overcome, contributing to improved conductivity and structural stability. This review offers a detailed insight into the Al-storage mechanism of heterostructure cathodes, and provides an overview of the current research progresses on heterostructure cathode materials for AIBs. Starting from the relationship between the microstructure and electrochemical performance of heterostructure materials, the different structure design strategies are elaborated. Besides, the challenges faced by heterostructure are summarized, and their potential impact on the future of the energy storage industry is anticipated. This review provides the guidelines for the future research of heterostructure as cathode materials for AIBs.

Encapsulation of Bamboosa vulgaris culms derived activated biochar into hierarchical permeable, phosphate rich and functionalized alginate aerogel composites and its contribution in U(VI) adsorption.

In this study, a facile methodology was designed to encapsulate Bamboosa vulgaris culms derived activated biochar (BVC) in a variable mass ratio, into a three-dimensional hierarchical porous and permeable and amino-thiocarbamated alginate (TSC) to prepare hybrid biosorbents (BVC-MSA). These ultralight and lyophilized phosphate rich macroporous sorbents were rationally characterized through FTIR, XRD, BET, SEM-EDS, elemental mapping, XPS techniques and employed for efficient UO22+ adsorption from aqueous solutions. The phytic acid (PA) was found to be a suitable hydrophilic and phosphorylating agent for the TSC matrix through hydrogen-bonded crosslinking when employed in a correct mass ratio (1:3). The SEM-EDS and XPS analyses confirmed the UO22+ sorption onto BVC-MSA-3 (the most suitable composite with a BVC/TSC mass ratio of 30.0 % w/w) and provided evidence of heteroatom involvement in developing the physico-chemical interactions. The BCV-MSA-3 exhibited the best response as a sorbent during kinetics/sorption process, therefore, it was selected to study the equilibrium sorption studies. The BCV-MSA-3 removal efficiency increased from 12.1 to 94.2 % using 0.2 to 1.8 g/L sorbent dose at pH (4.5). The mentioned sorbent displayed a significant maximum sorption capacity qm (309.55 mg/g at 35 °C) calculated through the best-fitted Langmuir and Temkin models (R2 ≈ 0.99). The sorption kinetics followed the pseudo-second-order (PSORE) model and exhibited fast sorption rate teq (180 min). Thermodynamic parameters clarified that the sorption process is feasible ΔGo (-25.3 to -27.6 kJ/mol kJ/mol), endothermic ΔHo (27.17 kJ/mol), and proceeds with a positive entropy (0.176 kJ/mol.K). The study shows that BCV-MSA-3 could be an alternative and auspicious sorbent for uranium removal from aqueous solution.

Electrolyte Design Strategies for Aqueous Sodium-Ion Batteries: Progress and Prospects.

Sodium-ion batteries (SIBs) have emerged as one of today's most attractive battery technologies due to the scarcity of lithium resources. Aqueous sodium-ion batteries (ASIBs) have been extensively researched for their security, cost-effectiveness, and eco-friendly properties. However, aqueous electrolytes are extremely limited in practical applications because of the narrow electrochemical stability window (ESW) with extremely poor low-temperature performance. The first part of this review is an in-depth discussion of the reasons for the inferior performance of aqueous electrolytes. Next, research progress in extending the electrochemical stabilization window and improving low-temperature performance using various methods such as "water-in-salt", eutectic, and additive-modified electrolytes is highlighted. Considering the shortcomings of existing solid electrolyte interphase (SEI) theory, recent research progress on the solvation behavior of electrolytes is summarized based on the solvation theory, which elucidates the correlation between the solvation structure and the electrochemical performance, and three methods to upgrade the electrochemical performance by modulating the solvation behavior are introduced in detail. Finally, common design ideas for high-temperature resistant aqueous electrolytes that are hoped to help future aqueous batteries with wide temperature ranges are summarized.

Evaluating high-resolution aviation emissions using real-time flight data.

Amidst robust global economic growth and advancing globalization, the aviation market is poised for significant expansion. Consequently, the environmental impact of aviation emissions is growing in significance. However, due to limitations in real flight data and aviation emissions index models, further clarification of the emission characteristics throughout entire flights is necessary. To better assess the emission characteristics of entire flights, this study employs real Quick Access Recorder (QAR) data and a high-precision aviation emissions index model, yielding four-dimensional emission data (time, longitude, latitude, altitude) from flights. The analysis compares QAR data with emissions from scheduled flight data (SFD) and Broadcast Automatic Correlation Monitoring (ADS-B) projections, explores seasonal variations in aviation emissions, and assesses the impact of sustainable aviation fuels (SAFs) on emissions reductions. For both number and mass of nvPM emissions, as well as nitrogen oxide emissions, the rankings are: ADS-B-E > SFD-E > QAR-E; for CO, SFD-E > ADS-B-E > QAR-E, particularly during the climb-cruise-descent (CCD) cycle. There are significant differences in the emission of aviation pollutants in airport area and high-altitude area in different seasons. Employing four types of Sustainable Aviation Fuels (SAFs) significantly reduces both the mass and the number of nvPM emissions. Therefore, it is recommended to utilize more QAR data to refine the assessment of the environmental impact of aviation emissions.

Honeycomb-like macroporous crosslinked chitosan assisted EDTA-intercalated Ca-Mg-Al layered hydrotalcite composite foams for efficient U(VI) biosorption.

The biosorption is considered to be highly efficient for the separation of radionuclide from radioactive wastewater. Herein, the crosslinked chitosan assisted EDTA intercalated Ca-Mg-Al layered double hydroxides composite foam (CS-EDTA-LDH) was synthesized by combining EDTA intercalation and freeze-drying methods. The macroporous and ultralight properties of CS-EDTA-LDH facilitates its rapid adsorption and facile recovery, and the inorganic/organic incorporation can avoid pore collapse and provide numerous adsorption sites, while the EDTA intercalation can enhance the complex capture of U(VI). The CS-EDTA-LDH presents various functional groups (carboxyl, hydroxyl and amino groups) for U(VI) adsorption, and the adsorption capacity for U(VI) reached 272.3 mg/g at pH 5.0 and 298 K. The adsorption kinetics of U(VI) conformed to PSO equation, whereas the isotherms conformed to the Freundlich model, indicating heterogeneous adsorption with diffusion process as a rate-controlling step. The thermodynamic parameters indicate that U(VI) adsorption by CS-EDTA-LDH is endothermic and spontaneous in nature. The adsorption mechanism is related to the synergic complexation by multi-functional groups, ion exchange, and possible isomeric substitution. Overall, CS-EDTA-LDH could be a promising biosorbent for the cleanup of radioactive pollution due to its high performance for U(VI) adsorption and facile recovery.

Specially Structured AgCuTi Foil Enables High-Strength and Defect-Free Brazing of Sapphire and Ti6Al4V Alloys: The Microstructure and Fracture Characteristics.

A novel AgCuTi brazing foil with a unique microstructure was developed, which could achieve strong vacuum brazing of Ti6Al4V (TC4) and sapphire. The brazing foil was composed of Ag solid solution (Ag(s,s)), Cu solid solution (Cu(s,s)), and layered Ti-rich phases, and had a low liquidus temperature of 790 °C and a narrow melting range of 16 °C, facilitating the defect-free joining of TC4 and sapphire. The sapphire/TC4 joint fabricated by using this novel AgCuTi brazing foil exhibited an outstanding average shear strength of up to 132.2 MPa, which was the highest value ever reported. The sapphire/TC4 joint had a characteristic structure, featuring a brazing seam reinforced by TiCu particles and a thin Ti3(Cu,Al)3O reaction layer of about 1.3 µm. The fracture mechanism of the sapphire/TC4 joint was revealed. The crack originated at the brazing seam with TiCu particles, then propagated through the Ti3(Cu,Al)3O reaction layer, detached the reaction layer from the sapphire, and finally penetrated into the sapphire. This study offers valuable insights into the design of active brazing alloys and reliable metal-ceramic bonding.

Accelerating Toluene Oxidation over Boron-Titanium-Oxygen Interface: Steric Hindrance of the Methyl Group Induced by the Plane-Adsorption Configuration.

Elimination of dilute gaseous toluene is one of the critical concerns within the field of indoor air remediation. The typical degradation route on titanium-based catalysts, "toluene-benzaldehyde-carbon dioxide", necessitates the oxidation of the methyl group as a prerequisite for photocatalytic toluene oxidation. However, the inherent planar adsorption configuration of toluene molecules, dominated by the benzene rings, leads to significant steric hindrance for the methyl group. This steric hindrance prevents the methyl group from contacting the active species on the catalyst surface, thereby limiting the removal of toluene under indoor conditions. To date, no effective strategy to control the steric hindrance of the methyl group has been identified. Herein, we showed a B-Ti-O interface that exhibits significantly enhanced toluene removal efficiency under indoor conditions. In-depth investigations revealed that, compared to typical Ti-based photocatalysts, the steric hindrance between the methyl group and the catalyst surface decreased from 3.42 to 3.03 Å on the designed interface. This reduction originates from the matching of orbital energy levels between Ti 3dz2 and C 2pz of the benzene ring. The decreased steric hindrance improved the efficiency of toluene being attacked by surface active species, allowing for rapid conversion into benzaldehyde and benzoic acid species for subsequent reactions. Our work provides novel insights into the steric hindrance effect in the elimination of aromatic volatile organic compounds.

Theoretical model of dynamics and stability of nanobubbles on heterogeneous surfaces.

Surface nanobubbles have revealed a new mechanism of gas-liquid-solid interaction at the nanoscale; however, the nanobubble evolution on real substrates is still veiled, because the experimental observation of contact line motions at the nanoscale is too difficult. HYPOTHESIS: This study proposes a theoretical model to describe the dynamics and stability of nanobubbles on heterogeneous substrates. It simultaneously considers the diffusive equilibrium of the liquid-gas interface and the mechanical equilibrium at the contact line, and introduces a surface energy function to express the substrate's heterogeneity. VALIDATION: The present model unifies the nanoscale stability and the microscale instability of surface bubbles. The theoretical predictions are highly consistent to the nanobubble morphology on heterogeneous surfaces observed in experiments. As the nanobubbles grow, a lower Laplace pressure leads to weaker gas adsorption, and the mechanical equilibrium can eventually revert to the classical Young-Laplace equation above microscale. FINDINGS: The analysis results indicate that both the decrease in substrate surface energy and the increase in gas oversaturation are more conducive to the nucleation and growth of surface nanobubbles, leading to larger stable sizes. The larger surface energy barriers result in the stronger pinning, which is beneficial for achieving stability of the pinned bubbles. The present model is able to reproduce the continual behaviors of the three-phase contact line during the nanobubble evolution, e.g., "pinning, depinning, slipping and jumping" induced by the nanoscale defects.

Investigating the synergetic effect of tungsten oxide doping into the 1,3-dicarbonyl moiety grafted chitosan and phytic acid impregnated sodium alginate for efficient U(VI) adsorption.

In this work, chemical modification of the chitosan with ethyl acetoacetate was performed through a base-catalyzed reaction in which epichlorohydrin facilitated the insertion as well as nucleophilic substitution reaction to graft the 1,3-dioxo moiety across the linear chains of the base biopolymer to establish specificity and selectivity for U(VI) removal. The modified chitosan (EAA-CS) was intercalated into phosphate rich alginate matrix (PASA). Later on, the WO3-doped composites with different WO3 to PASA mass ratio were prepared and characterized using FTIR, XPS, SEM-EDS, XRD, and elemental mapping analysis. WO3 significantly contributed to chemically stable inorganic-organic composites with improved porous texture. Among the prepared composites, MCPS-3 microspherical beads, having mass ratio of 30.0 % w/w, exhibited excellent sorption capacity for U(VI) at an optimal pH 4.5. The successful U(VI) sorption was validated by the existence of two U4f peaks at 392.25 and 381.36 eV due to U4f5/2 and U4f7/2 sub-peaks with an intensity ratio of 3:4, respectively. Batch mode sorption kinetics followed pseudo-second-order rate equation (R2 ≈ 0.99, qe,th ≈ 116.88 mg/g, k2 = 0.86 × 10-4 g/mg.min-1) and equilibrium sorption data aligns with Langmuir (R2 = 0.99, qm = 343.85 mg/g at 310 K and pH = 4.5, KL = 2.00 × 10-2 L/mg) and Temkin models (R2 ≈ 0.99). Thermodynamic parameters ΔHo (30.51 kJ/mol), ΔSo (0.19 kJ/mol.K) and ΔGo (-25.64, -26.89, and - 27.91 kJ/mol) at 298, 305, and 310 K, respectively, suggested that the uptake process is feasible, endothermic and spontaneous. Based on these findings, it is reasonable to conclude that MCPS-3 could be a better hydrogel-based biomaterial for appreciable uranium recovery.

Immediate fever during anaesthesia recovery after surgical procedure with scoliosis: A case report and literature review.

INTRODUCTION AND IMPORTANCE: Fever is a common clinical symptom in patients with postoperative scoliosis. However, there are rare reports of immediately fevers occurring following operative procedures. CASE PRESENTATION: A 15-year-old female with a 1-year history of scoliosis was admitted to the hospital after a health examination. The patient was diagnosed with idiopathic scoliosis and underwent a posterior idiopathic scoliosis procedure and correction for pedicle fixation. The clinical symptoms, including chills, fever, increased heart rate and increased blood pressure, were observed immediately following surgery during anaesthesia recovery. The patient was discharged from the hospital 12 days post-surgery. Over the 90-day follow-up, no chills, fever (≥38 °C), deep tissue infection, or surgery-related complications were reported. This remained consistent for the subsequent 3-year follow-up. CLINICAL DISCUSSION: The patient was discharged 12 days after the operation, and no chills or fever (≥38 °C) occurred during the 90-day follow-up. Furthermore, there were no instances of deep tissue infection or any other surgery-related complications throughout the subsequent 3-year follow-up duration. A literature review has performed for this subject by systematic review. We identified only three reports that specifically examined postoperative fever as an observational measure among spine surgical patients. Unfortunately, none of these reports mentioned immediate postoperative fever. CONCLUSION: Based on the available clinical data and research evidence, it is recommended to exercise caution when treating patients who experience postoperative chill and fever, as it may be caused by a combination of intraoperative hypothermia and anaesthesia inhibition. While these symptoms may be self-limiting in nature, close monitoring and appropriate management should be implemented to ensure patient safety and to identify any potential complications.

Characteristics of Gaseous Elemental Mercury in a Suburban Area of Shanghai, China.

To clarify gaseous elemental mercury (GEM) in suburban megacities in the Yangtze River Delta region, China, we observed GEM concentrations from December 2019 to November 2020 in Wujing town, a suburban area of Shanghai. The annual mean GEM concentration was 1.44 ± 0.88 ng m-3. Compared with the historical monitoring data of GEM in Shanghai over the past 10 years, the concentration of GEM showed a decreasing trend. The monthly mean concentrations of GEM showed clear seasonal variation, with higher values in the spring and winter. In spring and winter, typical Hg pollution events were observed, which could be mostly associated with increased local anthropogenic activity and temperature inversion. The results of the correlation analysis of the daily mean GEM concentrations with the AQI and backward trajectory calculations indicate that mercury pollution at monitoring sites can be affected by local, regional and interregional influences.

Instant duodenal decompression after endoscopic retrograde cholangiopancreatography can effectively reduce the incidence of post-ERCP pancreatitis and hyperamylasemia.

Background: Post-ERCP pancreatitis (PEP) is significantly influenced by the reflux of duodenal fluid. While gastrointestinal decompression represents a fundamental approach in acute pancreatitis management, the effectiveness of immediate duodenal decompression following ERCP to prevent PEP remains uncertain. This study aimed to investigate the impact of immediate duodenal decompression after ERCP on reducing the incidence of hyperamylasemia and PEP. Methods: This retrospective study encompassed patients with native papilla who underwent therapeutic ERCP for choledocholithiasis at the Department of Gastroenterology, Chun'an Branch of Zhejiang Provincial People's Hospital (Zhejiang, China) between January 2020 and June 2023. Based on the immediate placement of a duodenal decompression tube post-ERCP, patients were categorized into two groups: the duodenal decompression group and the conventional procedure group. Primary outcomes included the incidence of PEP and hyperamylasemia. Results: A total of 195 patients were enrolled (94 in the duodenal decompression group and 101 in the conventional procedure group). Baseline clinical and procedural characteristics exhibited no significant differences between the two groups. PEP occurred in 2 patients (2.1%) in the duodenal decompression group, in contrast to 11 patients (10.9%) in the conventional procedure group (Risk difference [RD] 8.8%; 95% confidence interval [CI] 1.7%-16.5%, P = 0.014). Hyperamylasemia was observed in 8 patients (8.5%) in the duodenal decompression group, compared to 20 patients (19.8%) in the conventional procedure group (RD 11.3%; 95% CI 1.4%-21.0%; P = 0.025). Patients with PEP in both groups showed improvement after receiving active treatment. No severe cases of PEP occurred in either group, and no serious adverse events related to duodenal catheter decompression were reported. Conclusion: Immediate duodenal decompression following ERCP demonstrates an effective reduction in the incidence of hyperamylasemia and PEP.

Achieving enhanced multifunctional performance for structural composite supercapacitors by reinforcing interfaces with polymer coating.

Carbon fiber structural composite supercapacitors possess the multifunctionality of storing electrochemical energy and withstanding mechanical loads simultaneously, attracting increased attention in electric vehicles, drones, and aircraft sectors. A polymer-based coating was meticulously constructed at the electrode/electrolyte interface to enhance adhesion and stability between active materials and the carbon fiber fabric collector under diverse conditions, especially mechanical stress. Mechanical testing and corresponding physical characterization substantiated the superior performance of the polymer coating. With the protective polymer coating, the optimized structural composite Zn-ion supercapacitor (SZSC), consisting of carbon fiber@active carbon-P (CF@AC-P) cathode, ionogel electrolyte, and Zn anode, displayed a maximum energy density of 164.6 mWh kg-1, at power density of 563.3 mW kg-1. Moreover, the optimized SZSC demonstrated stable operation over more than 8000 cycles at 0.3 mA cm-2 without capacity degradation. The optimized SZSC exhibited a tensile strength of 399.7 MPa and Young's modulus of 11.5 GPa. Furthermore, employing vacuum infusion techniques, the fabricated three-dimensional (3D) wing skin model shell and tube shell curved-surface structural composite Zn-ion supercapacitor component composites showcased exceptional electrochemical performance. These achievements further validate the practicality of 3D multifunctional composites. Consequently, this research presented a practical and straightforward interface engineering approach to develop multifunctional structural devices with remarkable electrochemical and mechanical properties.

A High-Voltage Cathode Material with Ultralong Cycle Performance for Sodium-Ion Batteries.

Vanadium-based polyanionic materials are promising electrode materials for sodium-ion batteries (SIBs) due to their outstanding advantages such as high voltage, acceptable specific capacity, excellent structural reversibility, good thermal stability, etc. Polyanionic compounds, moreover, can exhibit excellent multiplicity performance as well as good cycling stability after well-designed carbon covering and bulk-phase doping and thus have attracted the attention of multiple researchers in recent years. In this paper, after the modification of carbon capping and bulk-phase nitrogen doping, compared to pristine Na3 V2 (PO4 )3 , the well optimized Na3 V(PO3 )3 N/C possesses improved electromagnetic induction strength and structural stability, therefore exhibits exceptional cycling capability of 96.11% after 500 cycles at 2 C (1 C = 80 mA g-1 ) with an elevated voltage platform of 4 V (vs Na+ /Na). Meanwhile, the designed Na3 V(PO3 )3 N/C possesses an exceptionally low volume change of ≈0.12% during cycling, demonstrating its quasi-zero strain property, ensuring an impressive capacity retention of 70.26% after 10,000 cycles at 2 C. This work provides a facial and cost-effective synthesis method to obtain stable vanadium-based phosphate materials and highlights the enhanced electrochemical properties through the strategy of carbon rapping and bulk-phase nitrogen doping.

Ion-imprinted macroporous polyethyleneimine incorporated chitosan/layered hydrotalcite foams for the selective biosorption of U(VI) ions.

In order to prevent uranium pollution and recovery uranium resources, it was necessary to find a highly efficient adsorbent for radioactive wastewater treatment. Herein, U(VI) imprinted polyethyleneimine (PEI) incorporated chitosan/layered hydrotalcite composite foam (IPCL) was synthesized by combining ion-imprinting and freeze-drying techniques. IPCL has a high amino/imino content and an ultralight macroporous structure, making it capable of efficiently adsorbing U(VI) and easy to separate; Especially after ion-imprinting, vacancies matching the size of uranyl ions were formed, significantly improving U(VI) selectivity. The adsorption isotherms and adsorption kinetics were in accordance with the Freundlich model and PSO model respectively, indicating that heterogeneous adsorption of U(VI) by the adsorbents. The adsorption capacity of IPCL-2 for U(VI) reached 278.8. mg/g (under the conditions of optimal pH 5.0, temperature of 298 K, contact time of 2 h, and adsorbent dosage of 0.2 g/L), which is almost double of that for the non-imprinted foam (PCL-2, 138.2 mg/g), indicating that IPCL-2 can intelligently recognize U(VI). The heterogeneous adsorption mechanism of U(VI) by IPCL-2 involves complexation, ion-exchange and isomorphic substitution. The adsorption of U(VI) by IPCL-2 is spontaneous and endothermic. IPCL-2 has excellent adsorption performance for U(VI), and is a promising adsorbent for radioactive pollution control.

Review and perspectives on TS-1 catalyzed propylene epoxidation.

Titanium silicate zeolite (TS-1) is widely used in the research on selective oxidations of organic substrates by H2O2. Compared with the chlorohydrin process and the hydroperoxidation process, the TS-1 catalyzed hydroperoxide epoxidation of propylene oxide (HPPO) has advantages in terms of by-products and environmental friendliness. This article reviews the latest progress in propylene epoxidation catalyzed by TS-1, including the HPPO process and gas phase epoxidation. The preparation and modification of TS-1 for green and sustainable production are summarized, including the use of low-cost feedstocks, the development of synthetic routes, strategies to enhance mass transfer in TS-1 crystal and the enhancement of catalytic performance after modification. In particular, this article summarizes the catalytic mechanisms and advanced characterization techniques for propylene epoxidation in recent years. Finally, the present situation, development prospect and challenge of propylene epoxidation catalyzed by TS-1 were prospected.

Lysosome targeting fluorescent probe for NAAA imaging and its applications in the drug development for anti-inflammatory.

N-acylethanolamine acid amidase (NAAA) is a nucleophilic lysosomal cysteine hydrolase, which primarily mediates the hydrolytic inactivation of endogenous palmitoylethanolamide (PEA), which further influences the inflammatory process by regulating peroxisome proliferator-activated receptor-α (PPAR-α). Herein, a novel lysosome (Lyso)-targeting fluorescent probe (i.e., PMBD) was designed and synthesized for detecting endogenous NAAA selectively and sensitively, allowing real-time visual monitoring of endogenous NAAA in living cells. Moreover, PMBD can target Lyso with a high colocalization in Lyso Tracker. Finally, a high-throughput assay method for NAAA inhibitor screening was established using PMBD, and the NAAA-inhibitory effects of 42 anti-inflammatory Traditional Chinese medicines were evaluated. A novel potent inhibitor of NAAA, ellagic acid, was isolated from Cornus officinalis, which can suppress LPS-induced iNOS upregulation and NO production in RAW264.7 cells that display anti-inflammatory activities. PMBD, a novel Lyso-targeting fluorescent probe for visually imaging NAAA, could serve as a useful molecular tool for exploring the physiological functions of NAAA and drug development based on NAAA-related diseases.

Fe, N-Inducing Interfacial Electron Redistribution in NiCo Spinel on Biomass-Derived Carbon for Bi-functional Oxygen Conversion.

Herein, an interfacial electron redistribution is proposed to boost the activity of carbon-supported spinel NiCo2O4 catalyst toward oxygen conversion via Fe, N-doping strategy. Fe-doping into octahedron induces a redistribution of electrons between Co and Ni atoms on NiCo1.8Fe0.2O4@N-carbon. The increased electron density of Co promotes the coordination of water to Co sites and further dissociation. The generation of proton from water improves the overall activity for the oxygen reduction reaction (ORR). The increased electron density of Ni facilitates the generation of oxygen vacancies. The Ni-VO-Fe structure accelerates the deprotonation of *OOH to improve the activity toward oxygen evolution reaction (OER). N-doping modulates the electron density of carbon to form active sites for the adsorption and protonation of oxygen species. Fir wood-derived carbon endows catalyst with an integral structure to enable outstanding electrocatalytic performance. The NiCo1.8Fe0.2O4@N-carbon express high half-wave potential up to 0.86 V in ORR and low overpotential of 270 mV at 10 mA cm-2 in OER. The zinc-air batteries (ZABs) assembled with the as-prepared catalyst achieve long-term cycle stability (over 2000 cycles) with peak power density (180 mWcm-2). Fe, N-doping strategy drives the catalysis of biomass-derived carbon-based catalysts to the highest level for the oxygen conversion in ZABs.

Two-dimensional Cu Plates with Steady Fluid Fields for High-rate Nitrate Electroreduction to Ammonia and Efficient Zn-Nitrate Batteries.

Nitrate electroreduction reaction (eNO3 -RR) to ammonia (NH3) provides a promising strategy for nitrogen utilization, while achieving high selectivity and durability at an industrial scale has remained challenging. Herein, we demonstrated that the performance of eNO3 -RR could be significantly boosted by introducing two-dimensional Cu plates as electrocatalysts and eliminating the general carrier gas to construct a steady fluid field. The developed eNO3 -RR setup provided superior NH3 Faradaic efficiency (FE) of 99 %, exceptional long-term electrolysis for 120 h at 200 mA cm-2, and a record-high yield rate of 3.14 mmol cm-2 h-1. Furthermore, the proposed strategy was successfully extended to the Zn-nitrate battery system, providing a power density of 12.09 mW cm-2 and NH3 FE of 85.4 %, outperforming the state-of-the-art eNO3 -RR catalysts. Coupled with the COMSOL multiphysics simulations and in situ infrared spectroscopy, the main contributor for the high-efficiency NH3 production could be the steady fluid field to timely rejuvenate the electrocatalyst surface during the electrocatalysis.