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Electrolyte cations have been demonstrated to effectively enhance the rate and selectivity of the electrochemical CO2 reduction reaction (CO2RR), yet their implementation in electrolyte‐free membrane electrode assembly (MEA) electrolyzer presents significant challenges. Herein, an anchored cation strategy that immobilizes Cs+ on carbon vacancies was designed and innovatively implemented in MEA electrolyzer, enabling highly efficient CO2 electroreduction over commercial silver catalyst. Our approach achieves a CO partial current density of approximately 500 mA cm−2 in the MEA electrolyzer, three‐fold enhancement compared to pure Ag. In situ Raman and theoretical analyses, combined with machine learning potentials, reveal anchored Cs induces an electric field that significantly promotes the adsorption of *CO2− intermediates through performing muti‐point energy calculations on each structure. Furthermore, reduced adsorption of *OH intermediates effectively hampers competing hydrogen evolution reaction, as clarified by disk electrode experiments and density functional theory studies. Additionally, coupling our system with commercial polysilicon solar cells yields a notable solar‐to‐CO energy conversion efficiency of 8.3 %. This study opens a new avenue for developing effective cation‐promoting strategy in MEA reactors for efficient CO2RR. [ABSTRACT FROM AUTHOR]

Acute kidney injury (AKI) presents as a condition marked by a sudden and rapid decrease in kidney function over a short timeframe, resulting from diverse causes. As a transcription factor, PR domain‐containing 16 (PRDM16), has recently been implicated in brown fat biogenesis and heart diseases. Our recent works indicated that PRDM16 could suppress the occurrence of renal interstitial fibrosis in diabetic kidney disorder. Nonetheless, the effect and regulatory mechanism of PRDM16 in AKI remain elusive. Our study demonstrated that PRDM16 inhibited apoptosis induced by ischemic/reperfusion (I/R) in BUMPT (Boston University mouse kidney proximal tubular) cells and HK‐2(Human Kidney‐2) cells. Mechanistically, PRDM16 not only bound to the promoter region of S100 Calcium Binding Protein A6 (S100A6)and upregulated its expression but also interacted with its amino acids 945–949, 957–960, and 981–984 to suppress the p38MAPK and JNK axes via inhibition of PKC‐η activity and mitochondrial reactive oxygen species (ROS) production. Furthermore, cisplatin‐ and I/R‐stimulated AKI progression were ameliorated in PRDM16 proximal‐tubule‐specific knockin mice, whereas exacerbated in PRDM16 knockout proximal‐tubule‐specific mice). Moreover, we observed that formononetin ameliorated I/R‐ and cisplatin‐triggered AKI progression in mice. Taken together, these findings reveal a novel self‐protective mechanism in AKI, whereby PRDM16 regulates the S100A6/PKC‐η/ROS/p38MAPK and JNK pathways to inhibit AKI progression. [ABSTRACT FROM AUTHOR]

Although various kinds of cocatalyst are developed and decorated on the bismuth vanadate (BiVO4) photoanode, its photoelectrochemical (PEC) water splitting performance is limited owing to severe charge recombination and sluggish oxygen evolution reaction (OER). Herein, a high‐entropy hydroxide electrocatalyst (FeCoNiMoCrOOH) is constructed as a co‐catalyst deposited on BiVO4 with a good PEC activity and stability in potassium borate buffer, addressing substantial charge recombination and poor surface oxygen evolution reaction of the material. FeCoNiMoCrOOH synthesized by a simple electrodeposition stacking strategy, delivers an overpotential of 172 mV at 10 mA cm−2 with a stability of 600 h under alkaline conditions, representing one of the best performances on high‐entropy‐based catalysts. The FeCoNiMoCrOOH/BiVO4 photoanode shows a photocurrent density of 5.23 mA cm−2 at 1.23 VRHE with 100 h durability in potassium borate buffer. Experimental investigations and theoretical calculations demonstrate that the synergistic effect of Mo and Cr in FeCoNi catalyst effectively decreases the dissolution Fe, Co, and Ni after long‐term operation, increases the charge transfer kinetics, and promotes OER and PEC performances, therefore enhancing the photocorrosion resistance of BiVO4. This work provides a new avenue to design high entropy‐based electrocatalysts boosting solar water splitting activity and stability. [ABSTRACT FROM AUTHOR]

The significance of exploring optimal electrode materials cannot be overstated, particularly in mitigating the critical issues posed by sluggish redox kinetics, significant volume variations, and severe structural collapse resulting from the insertion and extraction of sodium ions. These efforts are crucial for enhancing the longevity and rapid charging capabilities of sodium‐ion batteries (SIBs). Herein, a defect engineering strategy for the in situ encapsulation of single‐phase ternary iron phosphoselenide into porous carbon by robust chemical bonds with the formation of rod‐like multicavity nanohybrids (FePSe3@C) is presented. The incorporation of Se atom not only modulates the electronic structure of the central metal Fe atom and enhances the intrinsic electrical conductivity, but also generates numerous additional reaction sites and accelerates the reaction kinetics of FePSe3@C, as corroborated by theoretical calculations and kinetic analysis. Notably, the FePSe3@C demonstrates an outstanding rate capability of 321.7 mAh g−1 even at 20 A g−1 and long cycling stability over 1000 cycles. The sodium‐ion full cell, pairing the FePSe3@C anode with the Na3V2(PO4)3@C cathode, exhibits a remarkable energy density of 202 Wh kg−1, demonstrating its practical applicability. This work provides a controllable defect and morphology engineering strategy to construct advanced materials with fast charge transfer for high‐power/energy SIBs. [ABSTRACT FROM AUTHOR]

In both the manufacturing and chemical industries, benzoquinone is a crucial chemical product. A perfect and economical method for making benzoquinone is the electrochemical oxidation of phenol, thanks to the traditional thermal catalytic oxidation of phenol process requires high cost, serious pollution and harsh reaction conditions. Here, a unique heterostructure electrocatalyst on nickel foam (NF) consisting of nickel sulfide and nickel oxide (Ni9S8‐Ni15O16/NF) was produced, and this catalyst exhibited a low overpotential (1.35 V vs. RHE) and prominent selectivity (99 %) for electrochemical phenol oxidation reaction (EOP). Ni9S8‐Ni15O16/NF is beneficial for lowering the reaction energy barrier and boosting reactivity in the EOP process according to density functional theory (DFT) calculations. Additionally, an alkali/acid hybrid flow cell was successfully established by connecting Ni9S8‐Ni15O16/NF and commercial RuIr/Ti in series to catalyze phenol oxidation in an alkaline medium and hydrogen evolution in an acid medium, respectively. A cell voltage of only 0.60 V was applied to produce a current density of 10 mA cm−2. Meanwhile, the system continued to operate at 0.90 V for 12 days, showing remarkable long‐term stability. The unique configuration of the acid‐base hybrid flow cell electrolyzer provides valuable guidance for the efficient and environmentally friendly electrooxidation of phenol to benzoquinone. [ABSTRACT FROM AUTHOR]

The electrochemical desalination technique is recognized as a promising solution to alleviate freshwater shortages, challenges yet persists in achieving optimal energy efficiency and cost‐effectiveness. Herein, a hybrid acid/alkali zinc air desalination battery (hAA‐ZADB) capable of concurrent desalination and high‐power density is reported. To improve cathodic efficiency and cost‐effectiveness, an electrocatalyst with dual atomic Fe–Mn sites on porous dodecahedral carbon (Mn‐Fe/p‐DC) is fabricated through a simple direct pyrolysis strategy for oxygen reduction reaction (ORR). The Mn–Fe/p‐DC‐900 electrocatalyst demonstrates exceptional electrocatalytic activity (E1/2 = 0.8 V in 0.5 m H2SO4) for ORR. This innovative hybrid acid/alkali cell design, coupled with advanced electrocatalysts, empowers the hAA‐ZADB system to achieve outstanding performance benchmarks with a high open circuit voltage of 2.22 V, an impressive power density of 375 mW cm−2, and notably elevated energy output of 106.9 kJ mol−1 even at a current density of 100 mA cm−2 during desalination. Distinguishing this work is its additional functionality, evident in a rapid salt removal rate of 3.64 mg cm−2 min−1 during desalination, achieving an impressive 88.67% removal of 0.6 M NaCl. This study highlights the promising potential of employing metallic air batteries for a self‐powered desalination technique applicable to specific scenarios. [ABSTRACT FROM AUTHOR]

Rechargeable Zn–air batteries (ZABs) are considered highly competitive technologies for meeting the energy demands of the next generation, whether for energy storage or portable power. However, their practical application is hindered by critical challenges such as low voltage, CO2 poisoning at the cathode, low power density, and poor charging efficiency Herein, a rechargeable hybrid alkali/acid Zn–air battery (h‐RZAB) that effectively separates the discharge process in an acidic environment from the charging process in an alkaline environment, utilizing oxygen reduction reaction (ORR) and glycerol oxidation reaction (GOR) respectively is reported. Compared to previously reported ZABs, this proof‐of‐concept device demonstrates impressive performance, exhibiting a high power density of 562.7 mW cm−2 and a high operating voltage during discharging. Moreover, the battery requires a significantly reduced charging voltage due to the concurrent utilization of biomass‐derived glycerol, resulting in practical and cost‐effective advantages. The decoupled system offers great flexibility for intermittently generated renewable power sources and presents cost advantages over traditional ZABs. As a result, this technology holds significant promise in opening avenues for the future development of renewable energy‐compatible electrochemical devices. [ABSTRACT FROM AUTHOR]

The pathogenesis of Diabetic kidney disease(DKD) involves pathological changes in both tubulo‐interstitium and the glomerulus. Surprisingly, tubulo‐interstitial fibrosis (TIF), does not develop significantly until the late stage of DKD. Here, it is demonstrated that PR domain‐containing 16 (PRDM16) is a key to the low level of TIF in DKD. In the experiments, PRDM16 is upregulated in high glucose‐treated renal tubular cells, DKD mouse kidneys, and renal biopsy of human DKD patients via activation of NF‐κB signal pathway. High glucose‐induced expression of fibrotic proteins in renal tubular cells is suppressed by PRDM16. Mechanistically, PRDM16 bound to the promotor region of Transient receptor potential ankyrin 1 (TRPA1) to transactivate its expression and then suppressed MAPK (P38, ERK1/2) activation and downstream expression of TGF‐β1. Knockout of PRDM16 from kidney proximal tubules in mice blocked TRPA1 expression and enhanced MAPK activation, TGF‐β1 production, TIF development, and DKD progression, whereas knock‐in of PRDM16 has opposite effects. In addition, overexpression of PRDM16 or its induction by formononetin ameliorated renal dysfunction and fibrosis in db/db diabetic mice. Finally, the above finding are detected in renal biopsies of DKD patients. Together, these results unveil PRDM16/TRPA1 as the mechanism responsible for the low level of TIF in the early stage of DKD by suppressing and TGF‐β1 expression. [ABSTRACT FROM AUTHOR]

Sodium borohydride (NaBH4) has earned recognition as a promising hydrogen carrier, attributed to its exceptional hydrogen storage capacity, boasting a high theoretical storage capacity of 10.8 wt %. Nonetheless, the utilization of traditional pyrolysis and hydrolysis methods still presents a formidable challenge in achieving controlled hydrogen generation especially under ambient conditions. In this work, we report an innovative electrochemical strategy for production H2 by coupling NaBH4 electrooxidation reaction (BOR) at anode in alkaline media with hydrogen evolution reaction (HER) at cathode in acidic media. To implement this, we have developed a bifunctional electrocatalyst denoted as Pd‐Mo2C@CNTs, wherein Pd nanoparticles are grown in situ on Mo2C embedded within N‐doped carbon nanotubes. This electrocatalyst demonstrates exceptional performance in catalyzing both alkaline BOR and acidic HER. We have developed a hybrid acid/alkali cell, utilizing Pd/Mo2C@CNTs as the anode and cathode electrocatalysts. This configuration showcases remarkable capabilities for self‐sustained, precise, and uninterrupted indirect release of H2 stored in NaBH4, even at high current densities of 100 mA cm−2 with a Faraday efficiency approaching 100 %. Additionally, this electrochemical device exhibits significant promise as a fuel cell, with the ability to deliver a maximum power density of 20 mW cm−2. [ABSTRACT FROM AUTHOR]

Transition metal single atoms anchored on nitrogen‐doped carbon (M‐N‐C) matrix with M‐N‐C active sites have shown to be promising catalysts for both hydrogen evolution reaction (HER) and oxygen reduction reaction (ORR). Herein, a hybrid catalyst with low‐level loading of atomic Pt and Co species encapsulated in nitrogen‐doped graphene (Pt@CoN4‐G) is developed. The Pt@CoN4‐G shows low overpotential for HER in wide‐pH electrolyte and manifests improved mass activity with almost eight times greater than that of Pt/C at an overpotential of 50 mV. The Pt@CoN4‐G also exhibits a top‐level ORR activity (half‐wave potential, E1/2 = 0.893 V) and robust stability (>200 h) in alkaline medium. Using theoretical calculations and comprehensive characterizations , the strong metal–support interactions between Pt species and CoN4‐G support and synergistical cooperation of multiple active sites are clarified. A flow alkali‐Al/acid hybrid fuel cell using Pt@CoN4‐G as cathode catalyst delivers a large power density of 222 mW cm−2 with excellent stability to achieve simultaneously hydrogen evolution and electricity generation. In addition, Pt@CoN4‐G endows a flow Zn‐air battery with high power density (316 mW cm−2), good stability under large current density (>100 h at 100 mA cm−2), and long cycle life (over 600 h at 5 mA cm−2). [ABSTRACT FROM AUTHOR]

The development of high‐performance sodium ion batteries (SIBs) is heavily relied on the exploration of the appropriate electrode material for Na+ storage, which ought to feature merits of high capacity, easy‐to‐handle synthesis, high conductivity, expedite mass transportation, and stable structure upon charging–discharging cycle. Herein, a universal source‐template method is reported to synthesize a variety of transition metal (e.g., V, Sb, W, Zn, Fe, Co, Ni, and Cu) selenides implanting on N doped 3D carbon nanoarchitecture hybrids (MmSen@3D‐CN) with powerful SeC bonding rivet. Benefiting from the superior architecture and potent SeC bonding between Cu2−xSe and N‐doped 3D carbon (3D‐CN), the Cu2−xSe@3D‐CN nanohybrids, as anode of SIBs, show high capacity, high‐rate capability, and long‐cycle durability, which can deliver a reversible capacity of as high as 386 mAh g−1, retain 219 mAh g−1 even at 10 A g−1, and run durably over thousands of charging–discharging cycles. The Cu2−xSe@3D‐CN as anode is also evaluated by developing a full SIB by coupling with the Na3V2(PO4)3 cathode, which can deliver high energy density and show excellent stability, shedding light on its potential in practical application. [ABSTRACT FROM AUTHOR]

Electrosynthesis of H2O2 has great potential for directly converting O2 into disinfectant, yet it is still a big challenge to develop effective electrocatalysts for medical‐level H2O2 production. Herein, we report the design and fabrication of electrocatalysts with biomimetic active centers, consisting of single atomic iron asymmetrically coordinated with both nitrogen and sulfur, dispersed on hierarchically porous carbon (FeSA‐NS/C). The newly‐developed FeSA‐NS/C catalyst exhibited a high catalytic activity and selectivity for oxygen reduction to produce H2O2 at a high current of 100 mA cm−2 with a record high H2O2 selectivity of 90 %. An accumulated H2O2 concentration of 5.8 wt.% is obtained for the electrocatalysis process, which is sufficient for medical disinfection. Combined theoretical calculations and experimental characterizations verified the rationally‐designed catalytic active center with the atomic Fe site stabilized by three‐coordinated nitrogen atoms and one‐sulfur atom (Fe‐N3S‐C). It was further found that the replacement of one N atom with S atom in the classical Fe‐N4‐C active center could induce an asymmetric charge distribution over N atoms surrounding the Fe reactive center to accelerate proton spillover for a rapid formation of the OOH* intermediate, thus speeding up the whole reaction kinetics of oxygen reduction for H2O2 electrosynthesis. [ABSTRACT FROM AUTHOR]

Aqueous zinc‐based batteries with high energy density are highly sought after to satisfy the increasing demands on the electrochemical energy device thanks to the advantages of high safety, low cost, and fast kinetics. In this work, a high‐performance hybrid Zn–S battery (h‐ZnSB) is reported by coupling an alkali Zn anode with an acidic sulfur electrode. To this end, atomic Zn–N4 dispersed on nitrogen‐doped hollow porous carbon (Zn–NHPC) is developed as the host of sulfur that enhances efficiency due to the higher affinity of Zn–N4 to CuS than N‐doped graphene, which can reduce the vulcanization reaction barrier that is too high on N‐doped graphene. The hybrid Zn–S battery shows desired electrochemical properties, including a high open‐circuit voltage of 1.81 V, high specific capacities of 2250 mAh g−1 at 1 A g−1 and 1500 mAh g−1 at 10 A g−1, as well as a high energy density of 2372 Wh kg−1 at 10 A g−1 based on the total mass of S/C composites. The present work may provide a promising route for the development of high‐energy and high‐safety aqueous batteries. [ABSTRACT FROM AUTHOR]

Sodium based dual‐ion battery (SDIB) has been regarded as one of the promising batteries technologies thanks to its high working voltage and natural abundance of sodium source, its practical application yet faces critical issues of low capacity and sluggish kinetics of intercalation‐type graphite anode. Here, a tubular nanohybrid composed of building blocks of carbon‐film wrapped WS2 nanosheets on carbon nanotube (WS2/C@CNTs) was reported. The expanded (002) interlayer and dual‐carbon confined structure endowed WS2 nanosheets with fast charge transportation and excellent structural stability, and thus WS2/C@CNTs showed highly attractive electrochemical properties for Na+ storage with high reversible capacity, fast kinetic, and robust durability. The full sodium‐based dual ion batteries by coupling WS2/C@CNTs anode with graphite cathode full cell presented a high reversible capacity (210 mAh g−1 at 0.1 A g−1), and excellent rate performance with a high capacity of 137 mAh g−1 at 5.0 A g−1. [ABSTRACT FROM AUTHOR]

The development of precious‐metal alternative electrocatalysts for oxygen reduction reaction (ORR) is highly desired for a variety of fuel cells, and single atom catalysts (SACs) have been envisaged to be the promising choice. However, there remains challenges in the synthesis of high metal loading SACs (>5 wt.%), thus limiting their electrocatalytic performance. Herein, a facile self‐sacrificing template strategy is developed for fabricating Co single atoms along with Co atomic clusters co‐anchored on porous‐rich nitrogen‐doped graphene (Co SAs/AC@NG), which is implemented by the pyrolysis of dicyandiamide with the formation of layered g‐C3N4 as sacrificed templates, providing rich anchoring sites to achieve high Co loading up to 14.0 wt.% in Co SAs/AC@NG. Experiments combined with density functional theory calculations reveal that the co‐existence of Co single atoms and clusters with underlying nitrogen doped carbon in the optimized Co40SAs/AC@NG synergistically contributes to the enhanced electrocatalysis for ORR, which outperforms the state‐of‐the‐art Pt/C catalysts with presenting a high half‐wave potential (E1/2 = 0.890 V) and robust long‐term stability. Moreover, the Co40SAs/AC@NG presents excellent performance in Zn–air battery with a high‐peak power density (221 mW cm−2) and strong cycling stability, demonstrating great potential for energy storage applications. [ABSTRACT FROM AUTHOR]

The metal‐plastic combination is widely used in frontier fields such as energy storage technology and aerospace. This study proposes two metal surface treatment processes for metal‐plastic composite injection molding. The first only involves the chemical treatment, whose interfacial bonding strength reaches 10.24 MPa. In the second, the plasma treatment is added to the chemical treatment process to increase the interface bonding strength to 17.58 MPa. The characterization result shows that the plastic is injected into the undercut microstructures to form a physical bolting force due to the countless microstructures after the metal surface treatment. Through the step‐by‐step study of the surface treatment process, it is found that hydrochloric acid solution causes a large‐scale microstructure to appear on the metal surface, and the undercut nanostructure is obtained through the plasma treatment. This multilevel microporous undercut structure of micro‐nano bonding is beneficial to the formation of physical bolting force at the interface, thereby achieving high bonding strength of the interface. At the same time, we also confirmed the relationship between the injection process, annealing parameters, and interfacial bonding strength. When the plastic was injected into the multilevel microporous undercut structure at an injection pressure of 110 MPa and annealed at 110°C for 4 h after molding, the maximum interface bonding strength of 17.58 MPa would be obtained. This process provides a new solution for engineering applications in metal‐plastic bonding. [ABSTRACT FROM AUTHOR]

Transition metal dichalcogenides with high theoretical capacity usually suffer from poor intrinsic electronic conductivity and drastic volumetric change upon cycling, degrading their attractiveness for electrochemical high‐power and long‐term applications. Herein, a high‐efficiency and extensible synthetic strategy for in situ encapsulating nanostructured SnSe0.5S0.5 into N‐doped graphene (SnSe0.5S0.5 @ NG) by robust interfacial CSeSn bonds with formation of 3D porous network nanohybrids, is reported. Systematic electrochemical studies indicate that interface and structure engineering on SnSe0.5S0.5, including defects implantation, chemical bonding interaction, and nanospace confinement design, endow it with robust structural stability, ultrafast Na+ storage kinetics, and highly reversible redox reaction. In addition, the introduction of foreign Se ligand not only facilitates the transport of electrons/ions by enhancing the conductivity and decreasing the diffusion energy barrier but also generates more reactivity sites, as demonstrated by density functional theory calculations. By virtue of these superiorities, the SnSe0.5S0.5 @ NG exhibits superior sodium storage performance with high‐rate capability and long durability over 2000 cycles at 2 A g−1. Impressively, the full battery, when coupling SnSe0.5S0.5 @ NG anode with Na3V2(PO4)3/C cathode, can deliver high energy density of 213 Wh kg−1. This work provides an effective structural engineering strategy to design advanced electrode material with potential application for sodium‐ion batteries. [ABSTRACT FROM AUTHOR]

Sodium‐tellurium (Na‐Te) battery, thanks to high theoretical capacity and abundant sodium source, has been envisaged as one promising battery technology, its practical application yet faces daunting challenges regarding how to mitigate the critical issues of uncontrollable dendrites growth at Na anode and polytellurides shuttling effect at Te cathode. We here report an elaborative design for fabrication of microsphere skeleton nanohybrids with three‐dimensional (3D) hierarchical porous carbon loading CeO2 quantum dots (CeO2‐QDs/HPC), which feature highly favorable properties of sodiophilic and catalysis for hosting sodium and tellurium, respectively. The systematic investigations coupling with first‐principle calculations demonstrate the CeO2‐QDs/HPC not only offers favorable structure and abundant electrocatalytic sites for facilitating interconversion between Te and NaxTe as a cathode host, but also can function as dendrite inhibitor anode host for reversible sodium electro‐plating/deposition. Such Na‐Te battery exhibits admiring electrochemical performance with an impressive specific capacity of 392 mAh g−1, a long cycling stability over 1000 cycles, as well as remarkably high energy density of 192 Wh kg−1 based on the total mass of anode and cathode. Such proof‐of‐concept bifunctional host design for active electrode materials can render a new insight and direction to the development of high‐performance Na‐Te batteries. [ABSTRACT FROM AUTHOR]

A simple and economic atmospheric plasma spraying method for thermal barrier coatings (TBCs) preparation on the mold cavity was developed to improve the injection parts properties. 7 wt% yttria stabilized zirconia was used as spray material with polyamide 11 (PA 11) as pore‐forming agents to improve the coating properties. The effect of PA 11 powder contents on the microstructure, thermal conductivity, bonding strength and hardness of TBCs were studied. The results show that the thermal conductivity of TBCs decreased with the addition of PA 11, and the bonding strength reached maximum of 21.38 MPa with 10% PA 11 addition. Further studies confirm that TBCs were able to maintain a high and stable temperature in the mold cavity due to its low thermal conductivity, validated by the elimination of the welding line. With TBCs, the average tensile strength and elongation at yield of the injection parts increased by 25.6% and 128%, respectively. [ABSTRACT FROM AUTHOR]

Background: Endobronchial microwave ablation via flexible catheter offers the potential for local therapy for inoperable peripheral lung cancer. The study aimed to evaluate the feasibility and safety of navigation bronchoscopy‐guided water‐cooled microwave ablation catheter for nonsurgical peripheral lung cancer. Methods: This was a prospective single arm pilot study. Patients with early stage or multiple primary peripheral lung cancer who were nonsurgical candidates for surgery were enrolled in the study. Bronchoscopic microwave ablation was performed via a flexible water‐cooled microwave ablation antenna under the guidance of navigation bronchoscopy. Radial probe endobronchial ultrasound combined with fluoroscopy was used to confirm the position. Treatment outcomes were evaluated based on follow‐up chest CT and positron emission tomography scans. Primary endpoints were technical success and safety. Secondary endpoints were complete ablation rate, 2‐year local control rate, and progression‐free survival. Results: Thirteen patients were enrolled in the study from April 2018 to July 2019. A total of 19 sessions of microwave ablation were performed on 14 tumors under the guidance of navigation bronchoscopy. The technical success was 100%. Treatment‐related complications occurred in two patients. The complete ablation rate was 78.6% (11/14). The 2‐year local control rate was 71.4%. Median progression‐free survival was 33 months for all patients. Conclusions: In this pilot study, bronchoscopic microwave ablation appears to be feasible with acceptable occurrence of complication in the treatment of peripheral lung cancer under the guidance of navigation bronchoscopy. [ABSTRACT FROM AUTHOR]

In this study, polyethylene (PP)/polyethylene terephthalate (PET)/multiwalled carbon nanotube (MWCNT) nanocomposites with nanofibrillary structure were processed by hot drawing‐assisted extrusion technology, and nonfoaming and microfoaming samples were processed by injection molding machine. Scanning electron microscope micrographs showed that when PET content was 2.5 wt%, PET fibers had a larger aspect ratio, which brought an outstanding promotion on microfoaming of PP matrix, and further details were provided by DSC and rheology analysis. When foaming sample loaded with 2.5 wt% PET and 3 wt% MWCNT, the best shielding effectiveness achieved 29.91 dB·cm3·g−1 in the test frequency range about 8.2–12.4 GHz. The results proved that the introduction of PET fibers optimized the microfoaming effect, and the uniform cell structure promoted the MWCNT dispersion and internal reflection of electromagnetic wave. Therefore, the shielding property is absorption‐dominated type and meets the requirements of lightweight and ultraefficient shielding demand of industry. [ABSTRACT FROM AUTHOR]

Recent trends in energy and environmental protection have led to many studies of high‐performance microcellular foams. Polymer blends provide an effective way to improve foamability, microstructure, and performance versus single component thermoplastics. However, challenges remain for morphological control of polymer blends because the reinforcing effect depends upon the morphology of the dispersed phase. In this work, we present a feasible method for attaining microfibrils with high aspect ratios based on the in situ fibrillation of immiscible polymers to improve the morphology and distribution of the blend phase and improve the microcellular structure and mechanical properties of composite foams. Composite foams of polypropylene (PP)/thermoplastic polyester elastomer (TPEE)/polytetrafluoroethylene (PTFE) were fabricated, which were the polymer matrix, blend phase, and in situ fibrillation phase, respectively. The presence of PTFE and its effect on crystallization, rheology behavior, cellular structure, and mechanical properties were investigated. The results showed that PTFE microfibrils can promote melt strength, crystallization, and rheology properties. Thus, the multi‐composite foams achieve improved microcellular structure and mechanical properties, and improvements in these properties indicate the positive effects of an in situ fibrillation phase on the polymer blend foams. [ABSTRACT FROM AUTHOR]

WS2 nanosheets hold great promise for a variety of applications yet faces a grand challenge in terms of large‐scale synthesis. We report a reliable, scalable, and high‐yield (>93 %) synthetic strategy to fabricate WS2 nanosheets, which exhibit highly desirable electrocatalytic properties toward both the alkaline sulfion (S2−) oxidation reaction (SOR) and the acidic hydrogen evolution reaction (HER). The findings prompted us to develop a hybrid alkali‐acid electrochemical cell with the WS2 nanosheets as bifunctional electrode catalysts of alkaline anodic SOR and acidic cathodic HER. The proof‐of‐concept device holds promise for self‐power or low‐electricity electrolytic H2 generation and environmentally friendly recycling of sulfion with enhanced electron utilization efficiency. [ABSTRACT FROM AUTHOR]

The application of microcellular parts in the field of high appearance quality is limited due to its appearance defects. In order to improve the appearance quality of microcellular parts, low heat transfer coefficient mold coating with PTFE and zirconia was employed in this study. The appearance quality of microcellular was evaluated by the surface roughness of microcellular parts. The numerical and experimental results show that delayed heat transfer between the melt and the mold can be achieved through both mold coatings, which improve the melt fluidity and reduce the shear force of the mold on the melt effectively. It is demonstrated that the PTFE has a better effect of delay heat transfer under thinner coating. The polished zirconia coating shows more conducive to the melt wall slip due to its stable molecular structure and smooth surface, resulting in microcellular parts with better appearance quality. [ABSTRACT FROM AUTHOR]

Background: Transbronchial lung biopsy (TBLB) is usually performed to obtain a definitive diagnosis for peripheral pulmonary lesions (PPLs). Ultrathin bronchoscopy combined with virtual bronchoscopic navigation (VBN) and radial endobronchial ultrasound (R‐EBUS) are generally considered appropriate diagnostic methods for PPLs; however, they have not yet been explored in combination with fluoroscopy. Therefore, the present prospective randomized controlled trial determined the role of fluoroscopy in ultrathin bronchoscopy combined with VBN and R‐EBUS for the diagnosis of PPLs. Methods: Patients with potentially malignant PPLs were enrolled in the study and randomized into fluoroscopy or nonfluoroscopy groups. In both groups, a 3.0‐mm outer and 1.7‐mm internal diameter ultrathin bronchoscope was used for transbronchial lung biopsy combined with R‐EBUS and VBN. In addition, the fluoroscopy group (FG) underwent fluoroscopy, while the nonfluoroscopy group (NFG) did not. Results: A total of 126 patients were enrolled and randomized in the study. Among them, 120 patients (60 in the NFG and 60 in the FG) were analyzed. The mean lesion sizes were 26.3 ± 11.4 mm and 29.0 ± 11.3 mm in the NFG and FG, respectively. The diagnostic yield was 73.3% (44/60) in the NFG and 81.7% (49/60) in the FG without statistically significant difference (p = 0.38). No obvious complications occurred in either group. Conclusions: Ultrathin bronchoscope combined with VBN and R‐EBUS without fluoroscopy is a feasible and safe diagnostic method for PPLs. [ABSTRACT FROM AUTHOR]

Electrocatalytic nitrogen reduction reaction (NRR) plays a vital role for next‐generation electrochemical energy conversion technologies. However, the NRR kinetics is still limited by the sluggish hydrogenation process on noble‐metal‐free electrocatalyst. Herein, we report the rational design and synthesis of a hybrid catalyst with atomic iron sites anchored on a N,O‐doped porous carbon (FeSA‐NO‐C) matrix of an inverse opal structure, leading to a remarkably high NH3 yield rate of 31.9 μgNH3 h−1 mg−1cat. and Faradaic efficiency of 11.8 % at −0.4 V for NRR electrocatalysis, outperformed almost all previously reported atomically dispersed metal‐nitrogen‐carbon catalysts. Theoretical calculations revealed that the observed high NRR catalytic activity for the FeSA‐NO‐C catalyst stemmed mainly from the optimized charge‐transfer between the adjacent O and Fe atoms homogenously distributed on the porous carbon support, which could not only significantly facilitate the transportation of N2 and ions but also effectively decrease the binding energy between the isolated Fe atom and *N2 intermediate and the thermodynamic Gibbs free energy of the rate‐determining step (*N2 → *NNH). [ABSTRACT FROM AUTHOR]

Two‐dimensional (2D) monometallic pnictogens (antimony or Sb, and bismuth or Bi) nanosheets demonstrate potential in a variety of fields, including quantum devices, catalysis, biomedicine and energy, because of their unique physical, chemical, electronic and optical properties. However, the development of general and high‐efficiency preparative routes toward high‐quality pnictogen nanosheets is challenging. A general method involving a molten‐salt‐assisted aluminothermic reduction process is reported for the synthesis of Sb and Bi nanosheets in high yields (>90 %). Electrocatalytic CO2 reduction was investigated on the Bi nanosheets, and high catalytic selectively to formate was demonstrated with a considerable current density at a low overpotential and an impressive stability. Bi nanosheets continuously convert CO2 into formate in a flow cell operating for one month, with a yield rate of 787.5 mmol cm−2 h−1. Theoretical results suggest that the edge sites of Bi are far more active than the terrace sites. [ABSTRACT FROM AUTHOR]

It remains great challenge to develop precious‐metal‐free electrocatalysts to implement high‐activity electrochemical conversion of O2 into value‐added hydroperoxide species (HO2−), which are vulnerable when exposed to various transition‐metal‐based catalysts. A strategy based on steric hindrance and layered nickel‐based layered double hydroxide (Ni‐LDH) induction has been developed for one‐pot inlaying high‐density ultrathin 2 D Ni‐LDH chips on in situ‐grown carbon nanosheets (Ni‐LDH C/CNSs). The resulting material exhibits high electrocatalytic selectivity with a faradaic efficiency up to 95 % for oxygen reduction into peroxide and attains a fairly high mass activity of approximately 22.2 A g−1, outperforming most metal‐based catalysts reported previously. Systematic studies demonstrate that the greatly increased defect concentration at Ni edge sites of Ni‐LDH chips results in more active sites, which contributes a favorable thermodynamically neutral adsorption of OOH* and adsorbed H2O2 molecules relatively weakly. Additionally, the modified CNSs effectively suppress H2O2 decomposition and avoid O−O bond cleavage to produce H2O by steric effects. The synergistic effect of CNSs and Ni‐LDH chips therefore leads to high activity and high selectivity in a two‐electron pathway. A proof‐of‐concept zinc–air fuel cell is proposed and set up to demonstrate the feasibility of green synthesis of peroxide, generating an impressive H2O2 production rate of 5239.67 mmol h−1 gcat.−1. [ABSTRACT FROM AUTHOR]

The advancement of renewable energy is intricately relied on the development of diverse sustainable electrochemical devices. Persuing exceptionally efficient multifunctional electrocatalysts is imperative, as it promises to significantly streamline the electrode fabrication process, thereby enhancing the overall effectiveness of these devices. Herein, a trifunctional electrocatalysts of N‐doped carbon (NC) supported intermetallic PtZn catalyst (PtZn‐IMC@NC) are reported, which performs highly attractively toward the electrocatalysis of glycerol oxidation reactions (GOR), oxygen reduction reactions (ORR), and hydrogen evolution reactions (HER). Its effectiveness are demonstrated as electrocatalysts for both the anode and cathode in a hybrid acid/alkali direct glycerol fuel cell (AA‐DGFC) and a hybrid acid/alkali glycerol‐hydrogen electrolyzer (AA‐GHEC). The AA‐DGFC can release an impressive peak power density of 286.8 mW cm−2, while the AA‐GHEC achieves a noteworthy current density of 100 mA cm−2 at a significantly low applied voltage of 0.47 V. Such intermetallic PtZn‐based trifunctional electrocatalyst empowers them to establish a self‐powered integrated electrochemical device with the AA‐DGFC driving the AA‐GHEC. This setup exemplifies efficient valorization of glycerol into formate in both cells and hydrogen production in electrolyzer device. This study sparks innovation across diverse applications of multifunctional electrocatalysts and infuses renewed momentum into the realm of advanced energy devices. [ABSTRACT FROM AUTHOR]

Abstract: Developing cost‐effective electrocatalysts for high‐selectivity CO2 electroreduction remains challenging. We herein report a perfluorinated covalent triazine framework (CTF) electrocatalyst that displays very high selectivity in the electroreduction of CO2 to CH4 with a faradaic efficiency of 99.3 % in aqueous electrolyte. Systematic characterization and electrochemical studies, in combination with density functional theory calculations, demonstrate that the presence of both nitrogen and fluorine in the CTF provides a unique pathway that is inaccessible with the individual components for CO2 electroreduction. [ABSTRACT FROM AUTHOR]

Abstract: Sodium‐ion batteries (SIBs) have recently attracted increasing attention as the promising alternative to lithium‐ion batteries due to their multiple advantages of abundant reserves and low cost. However, the development of highly desirable anode materials suitable for SIBs is still hampered by a rather low capacity, poor rate capability, and cycling stability. Herein, a deliberate design to implement reliable and simple fabrication of an inverse opal structured nanohybrid of carbon‐confined various transition metal sulfides quantum dots (QDs) is presented. Comprehensive characterizations demonstrate that the hybrids hold a 3D architecture with uniform dispersion of QDs in a conductive carbon matrix that in turn encapsulates these quantum dots. With Co9S8 as an example, such a unique architecture, when applied as the anode of SIBs, endows the hybrids with multiple advantages including a high reversible specific capacity, extraordinary high rate capability, and excellent durability over 2000 cycles charging–discharging process. [ABSTRACT FROM AUTHOR]

Abstract: Zn−air batteries have attracted enormous research interest, driven by the promise for vehicle propulsion owing to their advantages of high‐level safety, low cost, and high specific energy density. Here, we report an asymmetric‐electrolyte Zn−air battery with acid catholyte and alkaline anolyte separated by a bipolar membrane. We demonstrate that the as‐designed Zn−air battery, thanks to the as‐formed concentration cell, can deliver a maximum power density of 380 mW cm−2 and a specific energy density of 1522 Wh kg−1 with an open‐circuit voltage of 2.25 V. The as‐proposed Zn−air battery performance is superior to the conventional Zn−air battery in terms of these pivotal performance parameters. [ABSTRACT FROM AUTHOR]

The development of high-activity electrocatalysts for water splitting that comprise only inexpensive, earth-abundant elements is critical but remains a daunting challenge. In this work, yolk-shell Ni3Fe/Ni3FeN was prepared by a spray-pyrolysis technique, which could be scaleable. The yolk-shell Ni3Fe/Ni3FeN presents excellent catalytic activity for the oxygen evolution reaction (OER) and the hydrogen evolution reaction (HER) with overpotentials of 268 and 166 mV at 10 mA cm−2, respectively, and bears a prominent electrochemical durability. Overall water splitting with an electrolyzer containing the yolk-shell Ni3Fe/Ni3FeN as the cathode and anode only requires a cell voltage of 1.62 V to reach a current density of 10 mA cm−2. The present research not only introduces a new route for the synthesis of advanced functional electrocatalysts for overall water splitting but also sheds light on their potential commercial applications. [ABSTRACT FROM AUTHOR]

A novel OER electrocatalyst, namely oxygen-incorporated amorphous cobalt sulfide porous nanocubes (A-CoS4.6O0.6 PNCs), show advantages over the benchmark RuO2 catalyst in alkaline/neutral medium. Experiments combining with calculation demonstrate that the desirable O* adsorption energy, associated with the distorted CoS4.6O0.6 octahedron structure and the oxygen doping, contribute synergistically to the outstanding electrocatalytic activity. [ABSTRACT FROM AUTHOR]

The development of oxygen‐dependent fuel cells is frequently hindered by the high cost of cathode materials and the sluggish kinetics of the oxygen reduction reaction (ORR). It is thus crucial to explore low‐cost and high‐activity catalysts with accelerated mass transport. Here, a high‐throughput screening method is developed by integrating an explicit solvation model with machine learning potential‐based molecular dynamics simulations, which enables the efficient evaluation of a vast array of diverse diatomic combinations and ultimately identifying Fe–Co dual‐atomic sites as the optimal ORR electrocatalysts. The superior electrocatalytic performance of the diatomic Fe/Co sites loaded on 3D‐interconnected ordered macroporous carbon (FeCo‐3DMNC) is experimentally verified, achieving high ORR activity with half‐wave potentials of 0.806 V in acidic and 0.905 V in alkaline environments. Additionally, innovative hybrid acid/alkali aluminum–air fuel cells (hA/A‐AAFCs) incorporating FeCo‐3DMNC as the cathode catalyst demonstrate a notably high open‐circuit voltage of 2.72 V and a record‐breaking power density of 827 mW cm−2, significantly outperforming conventional alkaline aluminum–air fuel cells. This work marks a significant advancement by combining cutting‐edge computational screening with rigorous experimental validation to develop promising electrocatalysts, potentially paving the way for the advanced energy storage and conversion technologies. [ABSTRACT FROM AUTHOR]

Electrocatalytic nitrate reduction to ammonia (NO3RR) in a neutral medium is a green and effective strategy for treating nitrate pollution meanwhile producing ammonia. However, the insufficient active hydrogen (H*) on the catalyst surface resulting from the sluggish Volmer step (H2O → H+ + OH−), and the competitive hydrogen evolution reaction (HER) caused by H* coupling severely restrict the enhancement of NO3RR activity. Herein, a hydration‐effect boosted H*‐rich strategy facilitating neutral ammonia electrosynthesis from nitrate reduction is proposed. The introduction of the hydration‐effect‐promoting element aluminum into the copper‐based catalyst forming CuAlO2, which adjusts the electron density distribution in the catalyst system, and the resulting hydration‐effect significantly promotes the H* generation in a neutral medium. Moreover, the rapid charge transfer at the CuO/CuAlO2 interface facilitates the reaction kinetics and the H* diffusion. More importantly, the introduction of Al weakens the overly strong adsorption of intermediates by CuO, thereby accelerating the hydrogenation process and suppressing HER. Thus, under neutral conditions, CuO/CuAlO2 reached a Faradaic efficiency and an ammonia yield as high as 97.81 ± 1.94% and 10.21 ± 0.64 mg h−1 cm−2 at −1.0 V versus RHE toward NO3RR. [ABSTRACT FROM AUTHOR]

Transition‐metal dichalcogenides have emerged as promising anodes of sodium ion batteries (SIBs). Their practical SIB application calls for an easy‐to‐handle synthetic technique capable of fabricating favorable properties with high conductivity and stable structure. Here, a solvothermal strategy is reported for bottom‐up self‐assembling of nanoflowers' building block, i.e., conductive interlayer‐expanded 2D WS2 nanosheets thanks to in situ interlayer modification by nitrogen‐doped carbon matrix, into 3D hollow microflower bud‐like hybrids (H‐WS2@NC). The 3D nano/microhierarchical hollow structures are constructed by conductive interlayer‐expanded WS2 nanosheets' building blocks, providing abundant channels facilitating mass transport/electrons transfer, robust protection layer to avoid the direct contact between WS2 nanosheets and electrolyte, sufficient inner space for accommodating volume variation, and decreased ions diffusion energy barrier for accelerating electrochemical kinetics, as revealed by density functional theory calculations. As such, the 3D H‐WS2@NC hybrids exhibit quite attractive sodium storage performance with high reversible capacity, superior rate capability, and impressively long cycling life. The 3D H‐WS2@NC is further verified as anode of sodium‐ion full cell pairing with Na3V2(PO4)3/rGO cathode, delivering a stable reversible capacity of 296 mAh g−1 at 0.5 A g−1 with high energy density of 128 Wh kg−1total at a power density of 386 W kg−1total. [ABSTRACT FROM AUTHOR]

Potassium‐ion hybrid capacitors (PIHCs) hold the advantages of high‐energy density of batteries and high‐power output of supercapacitors and thus present great promise for the next generation of electrochemical energy storage devices. One of the most crucial tasks for developing a high‐performance PIHCs is to explore a favorable anode material with capability to balance the kinetics mismatch between battery‐type anodes and capacitor‐type cathode. Herein, a reliable route for fabricating sulfur and nitrogen codoped 3D porous carbon nanosheets (S‐N‐PCNs) is reported. Systematic characterizations coupled with kinetics analysis indicate that the doped heteroatoms of sulfur and nitrogen and the amplified graphite interlayer can provide ample structural defects and redox active sites that are beneficial for improving pseudocapacitive activity, enabling fast kinetics toward efficient potassium‐ion storage. The S‐N‐PCNs are demonstrated to exhibit superior potassium storage capability with a high capacity of 107 mAh g−1 at 20 A g−1 and long cycle stability. The as‐developed PIHCs present impressive electrochemical performance with an operating voltage as high as 4.0 V, an energy density of 187 Wh kg−1, a power density of 5136 W kg−1, and a capacity retention of 86.4% after 3000 cycles. [ABSTRACT FROM AUTHOR]

Potassium-Ion Hybrid Capacitors: Fast Redox Kinetics in Bi-Heteroatom Doped 3D Porous Carbon Nanosheets for High-Performance Hybrid Potassium-Ion Battery Capacitors (Adv. Keywords: fast kinetics; porous carbon nanosheets; potassium-ion hybrid capacitors; sulfur and nitrogen codoped Fast kinetics, porous carbon nanosheets, potassium-ion hybrid capacitors, sulfur and nitrogen codoped. [Extracted from the article]