High Stability Research Articles

Research on influence of wear ring clearance on energy loss of reactor coolant pump

Reactor coolant pump (RCP), the only rotating equipment in the nuclear island, directly determines the safety of the nuclear power system, has been likened to the “heart” of a nuclear power plant. The RCP needs to have very high reliability and stability. Its independent design and construction have always been the focus and difficulty of promoting the independent construction of nuclear power. To study the effect of the wear ring clearance on the energy loss characteristics of the RCP, the numerical simulation of the internal flow field of computation models with different wear ring clearance dimensions were conducted. The results indicate: As the wear ring clearance increases, the trend of performance reduction becomes more significant, especially under the large flow conditions; The increase of the wear ring clearance results in an increase of the pressure loss in the impeller and diffuser, and the variation in pressure distribution in different flow passages under different wear ring clearance dimensions is influenced by the position of the blade; The distribution of turbulent dissipation entropy production rate corresponds significantly to the distribution of direct dissipation entropy production rate, and the dissipation entropy production being more significantly affected by the wear ring clearance dimension closer to the shroud; The change of wear ring clearance dimension has limited impact on the wall shear stress entropy production of the impeller blade, while its effect on the diffuser blade is more pronounced; With the increase of the wear ring clearance, the scale of vortices near the impeller front shroud significantly increases, and the entropy production on the surface of vortex core at the impeller inlet gradually increases. This study is of great significance to ensure the secure and stable operation of the RCP, and provides an important reference for the hydraulic optimization design of the RCP.

Incorporation of electronically and ionically conductive additives in high-loading sulfur cathodes in lean-electrolyte lithium–sulfur cells

Low-cost, high-energy-density lithium–sulfur electrochemical batteries have emerged as a promising solution for next-generation energy-storage technologies. To facilitate the practical application of such batteries, it is necessary to address the remaining scientific and engineering challenges, especially those associated with the high-loading sulfur cathode in a lean-electrolyte cell. In this study, we investigate the electrochemical and overall performance of lithium–sulfur cells with a high-loading sulfur cathode. Notably, this cathode is fabricated using a novel hot-pressing method and incorporates electronically and ionically conductive additives, specifically lithium lanthanum titanate (LLTO) and carbon black, respectively. Material analysis reveals the uniform distribution of additives in the cathodes, with the ionically conductive LLTO effectively adsorbing and converting polysulfides and carbon black enhancing the cathode conductivity. Electrochemical analysis of the lean-electrolyte cells shows that the incorporation of LLTO improves cell performance, with enhanced discharge capacity of 715–836 mAh g−1 at C/5–C/10 rates and notable capacity retention after 100 cycles, compared with cathodes without additives or with carbon black. Further investigations demonstrate the superior performance of the cell incorporating LLTO in a LiNO3-free electrolyte, attributable to the promotion of ion transport and polysulfide adsorption by LLTO, resulting in high discharge capacities (846 mAh g−1 at C/10), efficiency (93–99 %), and stability. Overall, this study compares the effects of electronically and ionically conductive additives on cell performance and highlights the effectiveness of the ionically conductive LLTO. The incorporation of such additives offers innovative solutions to the key challenges for the development of high-performance energy-storage devices.

Zinc-based organophyllosilicate nanosheets as novel carbonic anhydrase-like nanozyme for efficient CO2 fixation

The unparalleled catalytic activity of carbonic anhydrases (CAs) towards CO2 hydrolysis can potentially contribute to carbon capture, utilization, and storage technology aimed at global decarbonization; however, the high cost and low stability of CAs significantly limit their practical applications. Recently, the development of robust and effective nanozymes with CA-mimicking activity has been proposed as a promising solution to this challenge. Herein, a novel zinc-based organophyllosilicate (ZnAC) nanozyme with CA-like catalytic activity was synthesized by a facile one-pot sol–gel method for the first time, leading to a Zn-O coordination structure that mimicked the catalytic center fragments of natural CAs, with surface amino groups acting as the affinity sites and proton shuttles. The synergistic effect of the two components on the open surface of the layered structure resulted in excellent CA-like activity with a Michaelis–Menten constant (Km) of 4.071 mM, maximum velocity (Vmax) of 0.220 mM/s, and turnover number (kcat) of 11.213 /s at 25 °C and pH=7.5, which were superior to those of most previously reported CA-like nanozymes. The catalytic performance of ZnAC significantly improved with increasing pH and temperature; furthermore, ZnAC exhibited excellent stability, maintaining high catalytic activity after the exposure to extreme temperatures or pH values, eight reaction cycles, and 30 d of storage. Additionally, ZnAC significantly increased the rate of CO2 hydration and the extent of CO2 mineralization and precipitation. This work proposes a new strategy for designing and constructing efficient CA-like nanozymes, providing valuable insights into the structure–activity relationship and new perspectives for the implementation of CO2 fixation.

Surfactant-assisted hydrothermal synthesis of FeVO4 nanoparticles for supercapacitor applications.

Due to their high capacitance, stability, and conductivity, binary transition metal oxides, such as iron vanadate, have the potential to be ideal electrode materials for supercapacitors. The effect of surfactants such as Polyethylene glycol (PEG), cetyltrimethylammonium bromide (CTAB), and thioglycolic acid (TGA) on the formation and properties (structural, morphological, optical and vibrational) of iron vanadate nanoparticles has been investigated using various analytical techniques. The results show that the surfactants significantly influence the morphology of the prepared FeVO4 nanoparticles. The nanoparticles prepared using TGA show a nano-mat like structure with the smallest particle size, and they were subjected to Cyclic Voltammetry analysis, showing a specific capacitance of 48 Fg−1 and demonstrating potential to be used for supercapacitors.

Addition of Coffee Waste-Derived Plasticizer Improves Processability and Barrier Properties of Poly(3-hydroxybutyrate-co-3-hydroxyvalerate)-Natural Rubber Bioplastic

This study aimed to develop a value-added bio-based polymer product for food packaging. Poly(3-hydroxybutyrate-co-3-hydroxyvalerate) (PHBV) is a promising bioplastic with limitations in processability and brittleness, which our group previously addressed by incorporating high-molecular-weight natural rubber (NR) compatibilized with peroxide and coagent. Yet, processability in an industrial setting proved difficult. Coffee oil epoxide (COE), a waste-derived plasticizer, was incorporated into the PHBV/NR/peroxide/coagent matrix via extrusion, and properties of resulting sheets were evaluated. COE incorporation significantly decreased the oxygen and water permeability of the PHBV/NR sheets. Maximum degradation temperature Tpeak (°C) increased by ~4.6 °C, and degree of crystallinity decreased by ~15.5% relative to pristine PHBV, indicating good thermal stability. Melting (Tm) and glass transition temperatures (Tg) of the PHBV/NR blend remained unchanged with COE incorporation. X-ray diffraction (XRD) revealed ~10.36% decrease in crystal size for the plasticized blend. Energy-dispersive X-ray analysis (EDAX) and scanning electron microscopy (SEM) confirmed good dispersion with no phase separation. The water uptake capacity of the plasticized blend was reduced by 61.02%, while surface contact angle measurements showed improved water resistance. The plasticized PHBV sheet shows promise for environmentally friendly packaging films due to its high thermal stability, effective barrier properties, and industrial scalability.

Near space detection technology combining van der Waals heterojunction photodetectors with long-range infrared target detection algorithms

To test the target detection accuracy of infrared detectors in practical applications, this study proposes a near space detection (NSD) technology that integrates van der Waals heterojunction photodetectors with long-range infrared target detection algorithms (ITDAs). A van der Waals heterojunction infrared photodetector (MoS2/CdTe) is prepared by combining molybdenum disulfide thin film and cadmium telluride substrate, and depositing gold electrodes on both substrates. A fusion algorithm of spatiotemporal target detection network and local contrast method is proposed for long-distance detection of weak infrared targets, and a near-space infrared detection system is designed. The data showed that the MoS2/CdTe heterojunction photodetector had a detection range of 200–1700 nm and a response of 36.7 mA/W, demonstrating excellent optoelectronic performance. The false alarm rates of the long-distance ITDA were 0.006% and 0.009%, respectively, which are significantly better than the target detection algorithm based on local contrast. In the testing of the near-space infrared detection system, the errors in the shortwave and longwave field of view tests were 2.5% and 5.2%, respectively, and the resolution test errors were 3.6% and 3.7%. The infrared detection system meets the performance standards, has high detection ability and stability, and provides a more effective solution for NSD.

Ppb-Level Ammonia Sensor for Exhaled Breath Diagnosis Based on UV-DOAS Combined with Spectral Reconstruction Fitting Neural Network.

Ammonia (NH3) in exhaled breath (EB) has been a biomarker for kidney function, and accurate measurement of NH3 is essential for early screening of kidney disease. In this work, we report an optical sensor that combines ultraviolet differential optical absorption spectroscopy (UV-DOAS) and spectral reconstruction fitting neural network (SRFNN) for detecting NH3 in EB. UV-DOAS is introduced to eliminate interference from slow change absorption in the EB spectrum while spectral reconstruction fitting is proposed for the first time to map the original spectra onto the sine function spectra by the principle of least absolute deviations. The sine function spectra are then fitted by the least-squares method to eliminate noise signals and the interference of exhaled nitric oxide. Finally, the neural network is built to enable the detection of NH3 in EB at parts per billion (ppb) level. The laboratory results show that the detection range is 9.50-12425.82 ppb, the mean absolute percentage error (MAPE) is 0.83%, and the detection accuracy is 0.42%. Experimental results prove that the sensor can detect breath NH3 and identify EB in simulated patients and healthy people. Our sensor will serve as a new and effective system for detecting breath NH3 with high accuracy and stability in the medical field.

Two-dimensional fused π-conjugated multi-activity covalent organic framework as high-performance cathode for lithium-ion batteries

Electrochemically active covalent organic frameworks (COFs) with robust skeletons and permanent porosity are attracting wide interest as promising electrode materials for Li-ion batteries (LIBs). However, current COF-based electrodes suffer from poor capacity and rate performance due to limited redox-active sites and low conductivity. To address these challenges, combining the advantages of high stability of the macromolecular skeleton and high-density redox-active CO and CN groups, a novel two-dimensional (2D) fused π-conjugated COF (denoted as HAPT-COF) with ultrahigh theoretical capacity is fabricated. In particular, the post-hydrothermal reaction between HAPT-COF and graphene oxide (GO) affords intercalated COF-based nanocomposites (HAPT-COF@rGO), featuring with improved utilization of redox-active sites, electronic conductivity, and structure stability. The CO and CN groups on the walls contribute to reversible 18 Li-ions storage for each HAPT-COF repeating unit across three stages. Owing to these advantages, the HAPT-COF@rGO exhibited an excellent reversible capacity (558 mAh g−1 at 0.1 C), cycling stability (92% capacity retention after 1000 cycles at 10 C), and superior rate performance (318 mAh g−1 at 10 C), ranking the best among reported polymer cathodes in LIBs.

Intranuclear Irradiation Inhibits Solid Tumor Growth by Upregulating Caspase8 and Activating Apoptosis.

Radioimmunotherapy (RIT) is a novel and promising cancer treatment method, with ongoing research focusing on RIT antibody selection, radionuclides, treatment options, and benefited patient groups. As we dive into the mechanisms of tumor biology, a deeper exploration of how RIT affects tumor tissue is needed to provide new ways to improve clinical treatment outcome and patient prognosis. We labeled the anti-PD-L1 monoclonal antibody atezolizumab with iodine-131 (131I), separated and purified the labeled mAb with Sephadex G-25 medium gel filtration resin, and tested product stability. We detected the in vivo activity of 131I-PD-L1 mAb by analyzing its in vivo biodistribution and performing SPECT imaging and then set different treatment groups to study the effect of 131I-atezolizumab on the survival of tumor-bearing mice. Western blot, real-time quantitative PCR, and immunohistochemistry were used to detect the expression level of Caspase8 and Nlrp3 in tumor. TUNEL fluorescence staining was used to detect the apoptosis in the tumor. The radiopharmaceutical molecular probe 131I-atezolizumab showed high stability and in vivo biological activity. The treatment regimen adopted had a positive effect on the survival of tumor-bearing mice. 131I internal irradiation upregulated Caspase8 in tumor and ultimately inhibited solid tumor growth by activating apoptosis pathways. We also found a significant increase in the expression of NLRP3, which plays an important role in the pyroptosis pathway, in tumor. In summary, our data demonstrated that radiopharmaceuticals combined with immunotherapy affected tumor tissue by modulating relevant biological pathways, thereby achieving better antitumor effects compared with single therapy and providing new insights for promoting better patient prognosis and combination treatment strategies.

A Regenerative Coking‐resistant CO2 Hydrogenation Reactor using a Protonic Ceramic Electrolysis Cell with Thin and Robust Fuel Electrode

AbstractA CO2 hydrogenation reactor based on protonic ceramic electrolysis cells (PCECs) is one of the most promising options for the efficient and clean conversion of CO2. However, insufficient performance and durability have hindered the practical application of such CO2 hydrogenation reactors. Here, fabricates a large‐area (≈10 cm2) tubular air electrode supported PCEC (AES‐PCEC) and develop a fuel electrode regeneration strategy for efficient and durable CO2 hydrogenation. The AES‐PCEC demonstrates a CO yield of 2.88 mL min−1 at 650 °C while maintaining excellent durability for over 1100 h. The high stability of the AES‐PCEC can be attributed to the robust and thin fuel electrode structure as well as the water‐mediated carbon removal regeneration mechanism. Density functional theory calculations have confirmed the regeneration mechanism facilitated by the excellent water hydration and dissociation capability of the BaCe0.4Zr0.4Y0.1Yb0.1O3‐σ. This work offers a feasible strategy to design high‐performance and durable PCEC‐based CO2 hydrogenation reactors.

Accelerated de-chelation of EDTA-metal complexes: A novel and versatile approach for wastewater and solid waste remediation

Industrial waste, including wastewater and solid waste, often contains toxic heavy metals that necessitate extraction and separation prior to safe disposal or reusing them. Sewage sludge incineration ash (SSIA), a non-incinerable waste, holds significant amounts of heavy metals such as iron, zinc, copper, nickel, chromium, and lead. Recovery and reuse of heavy metals from SSIA and further application of treated SSIA sludge remain challenging. Ethylenediaminetetraacetic acid (EDTA) is widely used for heavy metals chelation in different applications. While its chelation with heavy metals is rapid and easy to achieve, the de-chelation of the metal complexes is otherwise slow (∼3 days) and challenging due to their high stability constants. In this study, we investigate the recovery of heavy metals from SSIA through chelation using EDTA, and develop, for the first time, a method to rapidly de-chelate the EDTA-metal complexes through the facile chilling process (1 – 3 h) that accelerates the separation of EDTA and metal ions. A sequential precipitation of high-purity heavy metals from the EDTA-metal complexes was demonstrated with and without de-chelation. This novel and versatile method allows the separation of many valuable compounds from the treated SSIA, including regenerated EDTA, potassium hexafluorosilicate, iron phosphate, iron(III) hydroxide, iron silicate, titanium phosphate, calcium phosphate, copper(I) thiocyanate, nickel bis(dimethylglyoximate), lead(II) sulfate, and zinc sulfide. This approach opens doors for more sustainable waste management and the recovery of valuable resources from industrial waste.

Designing a Refractory Binary Alloy with Low Oxygen Solubility

Refractory metals such as Ti, Zr, Hf, V, Nb, and Ta can dissolve oxygen up to 33 %, 29 %, 20 %, 17 %, 9 %, and 5.7 %, respectively, at high temperatures. The high solubility of oxygen causes brittleness in these metals. When designing a refractory high entropy alloy, efforts should be focused on reducing oxygen solubility. We find that the high solubility of oxygen is related to the thermodynamic stability of oxygen interstitials in pure refractory metals. To understand the impact of alloy composition on oxygen solubility in refractory alloys, we examine the thermodynamic stability of oxygen interstitials across various refractory binary alloys. Using first-principles Density Functional Theory (DFT), we calculate the Oxygen Interstitial Formation Energy (OIFE) of nine refractory metals and their 24 equiatomic binary alloys. The OIFE is determined by the bond strength between oxygen and the nearest neighbor (NN) metal atoms. It is a strong function of the nature of NN atoms that surround the interstitial site rather than the overall composition of the alloy. For a given alloy, the OIFE can vary based on the NN atoms around the oxygen interstitial. These observations indicate that an alloy with even a small amount of metal of high oxygen affinity (or highly negative OIFE), like Ti, can result in the high stability of oxygen in specific interstitial sites where the nearest neighbors are predominantly Ti atoms. It also explains Re as a choice of alloying elements to ductilize W instead of Ti. Although both Ti and Re alloying in W similarly improve its ductility, Ti’s tendency to stabilize oxygen interstitials makes the W-Ti alloy brittle, while Re does not stabilize oxygen interstitials.

MXene-Deposited Melamine Foam-Based Iontronic Pressure Sensors for Wearable Electronics and Smart Numpads.

Iontronic pressure sensors hold significant potential to emerge as vital components in the field of flexible and wearable electronics, addressing a variety of applications spanning wearable technology, health monitoring systems, and human-machine interactions. This study introduces a novel iontronic pressure sensor structure based on a seamlessly deposited Ti3C2Tx MXene layer onto highly porous melamine foam as parallel plate electrodes and an ionically conductive electrolyte of 1-ethyl-3-methylimidazolium bis(trifluoromethylsulfonyl)imide/thermoplastic polyurethane coupled with carbon cloth as current collecting layers for improved sensitivity and high mechanical stability of more than 7000 cycles. MXene-deposited melamine foam-based iontronic pressure sensors (MIPS) showed a high sensitivity of 5.067 kPa-1 in the range of 45-60kPa and a fast response/recovery time of 28/18ms, respectively. The high sensitivity, high mechanical stability, and fast response/recovery time of the designed sensor make them highly promising candidates for real-time body motion monitoring. Moreover, sensors are employed as a smart numpad for integration into advanced ATM security systems utilizing machine learning algorithms. This research marks a significant advance in iontronic pressure sensor technology, offering promising avenues for application in wearable electronics and security systems.

Ultrathin 2D/2D ZnIn2S4/La2Ti2O7 nanosheets with a Z-scheme heterojunction for enhanced photocatalytic hydrogen evolution.

Layered lanthanum titanate (La2Ti2O7) perovskite is a good photocatalytic material owing to its high stability, strong redox ability, and non-toxicity. However, its inherent wide bandgap limits its application in photocatalytic hydrogen evolution. Therefore, combining La2Ti2O7 with two-dimensional (2D) narrow-bandgap semiconductors to form 2D/2D layered structures is the preferred strategy to improve its photocatalytic performance. In this study, a novel 2D/2D ZnIn2S4/La2Ti2O7 Z-scheme heterojunction was prepared through a solvothermal method. The experimental results show that when the molar ratio of La2Ti2O7 to ZnIn2S4 is 1 : 4, the hydrogen evolution rate of the composite under ultraviolet-visible light reaches 6.97 mmol g-1 h-1, which is 3.5 times higher than that of the pure ZnIn2S4. The results of the morphological characterization studies of the samples and the photoelectrochemical measurements show that channels for the rapid transfer of carriers are generated by the unique 2D/2D structure of these samples, and the separation and migration efficiency of the photogenerated carriers significantly improved due to the formation of the Z-scheme heterojunction. This study provides useful insights into the modulation of wide-bandgap semiconductors and research into solar energy conversion.

Covalent Transition Metal Borosilicides: Reaction Pathways in Molten Salts for Water Oxidation Electrocatalysis.

The properties of transition metal borides and silicides are intimately linked to the covalent character of the chemical bonds within their crystal structures. Bringing boron and silicon together within metal borosilicides can then engender different competing covalent networks and complex charge distributions. This situation results in unique structures and atomic environments, which can impact charge transport and catalytic properties. Metal borosilicides, however, hold the status of unusual exotic species, difficult to synthesize and with poor knowledge of their properties. Our strategy consists of developing a redox pathway to synthesize transition metal borosilicides in inorganic molten salts as high-temperature solvents. By studying the formation of Ni6Si2B, Co4.75Si2B, Fe5SiB2, and Mn5SiB2 with in situ X-ray diffraction, we highlight how new reaction routes, maintaining covalent structural building blocks, draw a general scheme of their formation. This pathway is driven by the covalence of the chemical bonds within the boron coordination framework. Next, we demonstrate high efficiency for water oxidation electrocatalysis, especially for Ni6Si2B. We ascribe the strongly increased resistance to corrosion, high stability, and electrocatalytic activity of the Ni6Si2B-derived material to three factors: (1) the two entangled boron and silicon covalent networks; (2) the ability to codope with boron and silicon an in situ generated catalytic layer; and (3) a rare electron enrichment of the transition metal by back-donation from boron atoms, previously unknown within this compound family. With this work, we then unveil a new chemical dimension for Earth-abundant water oxidation electrocatalysts by bringing to light a new family of materials.

The synergistic effect of Cd-doped and S-vacancies in CdxZn1-xIn2S4 2D nanosheets for high-performance triethylamine sensing

Ternary metal sulfides with suitable band gaps, high physicochemical stability, and unique two-dimensional (2D) nanostructures are expected to be the next-generation high-performance gas sensors following the MOS type. Doping engineering is utilized as an effective strategy to improve the semiconductor surface activity and enhance its gas-sensitive properties. In this paper, the energy band structure and surface chemical oxygen of ZnIn2S4 (ZIS) materials was tuned by selectively introducing substitutional Cd to replace the Zn sites in ZIS crystals. Meanwhile, the introduction of Cd-ions brings more abundant S vacancy defects, enhances the acid-base interactions at the interface, and pushes the extent of surface redox reactions. In addition, by combining the strong adsorption of ZIS to triethylamine, the CdxZn1-xIn2S4 nanosheets achieved highly improved sensing properties, including better response (63.38–100 ppm), enhanced selectivity (STEA/sother = 12.9), and accelerated response/recovery (4 s/32 s). The results confirm the feasibility of developing low-cost, high-performance 2D metal sulfide gas sensing materials through rational structural design and optimization.

Anchored Weakly‐Solvated Electrolytes for High‐Voltage and Low‐Temperature Lithium‐ion Batteries

AbstractElectrolytes endowed with high oxidation/reduction interfacial stability, fast Li‐ion desolvation process and decent ionic conductivity over wide temperature region are known critical for low temperature and fast‐charging performance of energy‐dense batteries, yet these characteristics are rarely satisfied simultaneously. Here, we report anchored weakly‐solvated electrolytes (AWSEs), that are designed by extending the chain length of polyoxymethylene ether electrolyte solvent, can achieve the above merits at moderate salt concentrations. The −O−CH2−O− segment in solvent enables the weak four‐membered ring Li+ coordination structure and the increased number of segments can anchor the solvent by Li+ without largely sacrificing the ionic dissociation ability. Therefore, the single salt/single solvent AWSEs enable solvent co‐intercalation‐free behavior towards graphite (Gr) anode and high oxidation stability towards high‐nickel cathode (LiNi0.8Co0.1Mn0.1O2‐NCM811), as well as the formation of inorganic rich electrode/electrolyte interphase on both of them due to the anion‐rich solvation shells. The capacity retention of Gr||NCM811 Ah‐class pouch cell can reach 70.85 % for 1000 cycles at room‐temperature and 75.86 % for 400 cycles at −20 °C. This work points out a promising path toward the molecular design of electrolyte solvents for high‐energy/power battery systems that are adaptive for extreme conditions.

Effects of PEGylation on Imaging Contrast of 68Ga-Labeled Bicyclic Peptide PET Probes Targeting Nectin-4.

Nectin cell adhesion molecule 4 (Nectin-4) is overexpressed in various malignant tumors and has emerged as a promising target for tumor imaging. Bicyclic peptides, known for their conformational rigidity, metabolic stability, and membrane permeability, are ideal tracers for positron emission tomography (PET) imaging. In this study, we evaluated the feasibility of visualizing Nectin-4-positive tumors using radiolabeled bicyclic peptide derivatives and optimized the pharmacokinetics of radiotracers by introducing PEG chains of different lengths. Five PEGylated radiotracers radiolabeled with 68Ga3+ exhibited high radiochemical purity and stability. As the chain length increased, the Log D values decreased from -2.32 ± 0.13 to -2.50 ± 0.16, indicating a gradual increase in the hydrophilicity of the radiotracers. In vitro cell-binding assay results showed that the PEGylated bicyclic peptide exhibits nanomolar affinity, and blocking experiments confirmed the specific binding of the tracers to the Nectin-4 receptor. In vivo PET imaging and biodistribution studies in SW780 and 5637 xenograft mice showed that [68Ga]Ga-NOTA-PEG12-BP demonstrated optimal pharmacokinetics, characterized by rapid and good tumor uptake, faster background clearance, and improved tumor-to-tissue contrast. Finally, compared with 18F-FDG, PET imaging, in vivo blocking assays of [68Ga]Ga-NOTA-PEG12-BP and histological staining confirmed that specific tumor uptake was mediated by Nectin-4 receptors. The results indicated that [68Ga]Ga-NOTA-PEG12-BP was a promising PET radiotracer for Nectin-4 targeting, with applications for clinical translation.

A Unique Wide‐Spacing Fence‐Type Superstructure for Robust High‐Voltage O3‐Type Sodium Layered Cathode

AbstractEnhancing the energy density of layered oxide cathode materials is of great significance for realizing high‐performance sodium‐ion batteries and promoting their commercial application. Lattice oxygen redox at high voltage usually enables a high capacity and energy density. But the structural degradation, severe voltage decay, and the resultant poor cycling performance caused by irreversible oxygen release seriously restrict the practical application. Herein we introduce a novel fence‐type superstructure (2a×3a type supercell) into O3‐type layered cathode material Na0.9Li0.1Ni0.3Mn0.3Ti0.3O2 and achieve a stable cycling performance at a high voltage of 4.4 V. The fence‐type superstructure effectively inhibits the formation of the vacancy clusters resulting from out‐of‐plane Li migration and in‐plane transition metal migration at high voltage due to the wide d‐spacing, thereby significantly reducing the irreversible release of lattice oxygen and greatly stabilizing the crystal structure. The cathode exhibits a high energy density of 545 Wh kg−1, a high rate capability (112.8 mAh g−1 at 5 C) and a high cycling stability (85.8 %@200 cycles with a high initial capacity of 148.6 mAh g−1 at 1 C) accompanied by negligible voltage attenuation (98.5 %@200 cycles). This strategy provides a distinct spacing effect of superstructure to design stable high‐voltage layered cathode materials for Na‐ion batteries.

A Unique Wide-Spacing Fence-Type Superstructure for Robust High-Voltage O3-Type Sodium Layered Cathode.

Enhancing the energy density of layered oxide cathode materials is of great significance for realizing high-performance sodium-ion batteries and promoting their commercial application. Lattice oxygen redox at high voltage usually enables a high capacity and energy density. But the structural degradation, severe voltage decay, and the resultant poor cycling performance caused by irreversible oxygen release seriously restrict the practical application. Herein we introduce a novel fence-type superstructure (2a × 3a type supercell) into O3-type layered cathode material Na0.9Li0.1Ni0.3Mn0.3Ti0.3O2 and achieve a stable cycling performance at a high voltage of 4.4 V. The fence-type superstructure effectively inhibits the formation of the vacancy clusters resulting from out-of-plane Li migration and in-plane transition metal migration at high voltage due to the wide d-spacing, thereby significantly reducing the irreversible release of lattice oxygen and greatly stabilizing the crystal structure. The cathode exhibits a high energy density of 545 Wh kg-1, a high rate capability (112.8 mAh g-1 at 5C) and a high cycling stability (85.8%@200 cycles with a high initial capacity of 148.6 mAh g-1 at 1C) accompanied by negligible voltage attenuation (98.5%@200 cycles). This strategy provides a distinct spacing effect of superstructure to design stable high-voltage layered cathode materials for Na-ion batteries.