Encapsulation Structure Research Articles

CapD deletion in the Elizabethkingia miricola capsular locus leads to capsule production deficiency and reduced virulence.

Elizabethkingia miricola is a multidrug-resistant pathogen that can cause life-threatening infections in immunocompromised humans and outbreaks in amphibians. However, the specific virulence factors of this microorganism have not been described. In this study, we identified the polysaccharide biosynthesis protein-encoding gene capD, which is located in the conserved region of the Wzy-dependent capsule synthesis gene cluster in the E. miricola strain FL160902, and investigated its role in the pathogenesis of E. miricola. Our results revealed that the capD deletion strain (ΔcapD) lost its typical encapsulated structure, with a 45% reduction in cell wall thickness. CapD affects wza expression in the capsule polysaccharide synthesis pathway. Furthermore, the survival rates were significantly reduced in ΔcapD in response to complement-mediated killing, desiccation stress, and macrophage phagocytosis, whereas biofilm formation, surface hydrophobicity, and adherence to both endothelial and epithelial cells were increased. Additionally, the deletion of capD sharply attenuated the virulence of E. miricola in a frog infection model. Complementation of the capD gene restored the biological properties and virulence to wild-type levels. Overall, these findings suggest that CapD contributes to polysaccharide synthesis and plays a crucial role in the pathogenesis of E. miricola.

A General Approach for Metal Nanoparticle Encapsulation Within Porous Oxides.

Encapsulation of metal nanoparticles within oxide materials has been shown as an effective strategy to improve activity, selectivity, and stability in several catalytic applications. Several approaches have been proposed to encapsulate nanoparticles, such as forming core-shell structures, growing ordered structures (zeolites or metal-organic frameworks) on nanoparticles, or directly depositing support materials on nanoparticles. Here, a general nanocasting method is demonstrated that can produce diverse encapsulated metal@oxide structures with different compositions (Pt, Pd, Rh) and multiple types of oxides (Al2O3, Al2O3-CeO2, ZrO2, ZnZrOx, In2O3, Mn2O3, TiO2) while controlling the size and dispersion of nanoparticles and the porous structure of the oxide. Metal@polymer structures are first prepared, and then the oxide precursor is infiltrated into such structures and the resulting material is calcined to form the metal@oxide structures. Most Pt@oxides catalysts show similar catalytic activity, demonstrating the availability of surface Pt sites in the encapsulated structures. However, the Pt@Mn2O3 sample showed much higher CO oxidation activity, while also being stable under aging conditions. This work demonstrated a robust nanocasting method to synthesize metal@oxide structures, which can be utilized in catalysis to finely tune metal-oxide interfaces.

A self‐packaged multilayer all‐metal integrated suspended slotline dual‐band filter

AbstractThis paper introduces a novel implementation technology for realizing dual‐band bandpass filtering responses using high‐ slotline resonators with self‐packaged multilayer configuration. The concept of a 3D slotline is introduced, which utilizes the innovative metal‐integrated suspended line (MISL) technology. This technology utilizes an all‐metal structure, effectively eliminating dielectric loss. Furthermore, the implementation of an encapsulated structure significantly reduces radiation loss in the slotlines. Thus, the factors are greatly improved. Based on MISL, a dual‐band bandpass filter with wideband responses and multiple transmission zeros was designed, fabricated, and tested based on 3D cascaded‐mode half‐wavelength resonators. The test results demonstrated a high level of consistency with the simulation results, confirming the high‐ characteristics of the proposed 3D slotlines.

Sterilization mechanism of CuCeOx on fungus: Oxidative damage and energy metabolism disequilibrium

Pathogens in bioaerosols and aquatic environment cause epidemic outbreak frequently. Relative to bacteria and virus, fungi has not received attention enough. The development of sterilization materials and mechanism on fungi are limited. In this study, we proposed a non-noble metal sterilization material CuCeOx in order to investigate its sterilization mechanism on target fungal Hanseniaspora uvarum collected from the air. The active components of CuCeOx were uniformly distributed and induced the production of R·. The reactive oxygen species (ROS) changed from R· to RO· upon contact with fungal cells. Transcriptomics identified 1665 Differentially Expressed Genes (DEGs), including 1540 up-regulated and 125 down-regulated genes. The cell wall and external encapsulation structure were firstly damaged when the fungus contacted with CuCeOx, and the related DEGs were significantly down-regulated. CuCeOx could exert great impact on the energy metabolism of the cell, especially on the process of oxidative phosphorylation, which contained 59 up-regulated and 2 down-regulated genes. The cell is not sufficient to cope with the adverse environment caused by oxidative stress and metal ion homeostatic imbalance, which then modulates the intrinsic apoptotic pathway triggering apoptosis.

Dual-shell protection enables highly efficient and stable all-inorganic perovskite composites for light-emitting-diodes

Lead-halide perovskite nanocrystals (NCs) present superior photoelectric properties, but the poor stability seriously hinders their practical application. The encapsulation of perovskite NCs inside mesoporous silica (m-SiO2) matrix is considered as one of the most feasible pathways to improve the stability of NCs. However, the challenges of loose encapsulation structure, aggregation of particles, high energy consumption during the preparation of CsPbX3@m-SiO2 composites have not yet been overcome, which throw a shadow over the large-scale commercial applications. Here, we present a dual-shell encapsulation strategy that enables the formation of highly emissive CsPbBr3@m-SiO2@SiO2 composites, achieving an exceptional photoluminescence quantum yield (PLQY) of 97.37 %. The reaction parameters for the preparation of composites are meticulous investigated. The CsPbBr3 NCs can be well formed inside the pores of m-SiO2 as the m-SiO2 is introduced into the precursor solution. The secondary SiO2 shells can effectively seal the open pores of m-SiO2. As a result, the as-prepared CsPbBr3@m-SiO2@SiO2 composites present excellent stability, in which the composites can maintain 93.16 % of initial intensity after storage for 84 days. Besides, a series of CsPbX3@m-SiO2@SiO2 composites with tunable emission wavelength in the range of 428.6–630.6 nm are prepared through facile designing the halide ratios of precursor solution, which present a wide color gamut (148.48 % of the National Television Standards Committee). In addition, a white light-emitting diode (LED) is fabricated by combining CsPbBr3@m-SiO2@SiO2 composites and K2SiF6:Mn4+ phosphors with a 455 nm LED chip, which exhibits good photoelectric performances. This facile low-temperature dual-shell encapsulation strategy reported here provides a new pathway for preparing high-performance perovskite composites, facilitating their practical photoelectric application.

Ultrafine Fe-Mn bimetallic nanoparticles anchored in nitrogen-doped carbon nanofiber electro-Fenton membrane with strong metal-support interactions for sustainable water decontamination in wide pH ranges

Designing a membrane electrode with high activity and anti-scaling ability in a wide pH range is crucial to the development of flow-through electro-Fenton system. Herein, we reported a novel porous membrane composed of ultrafine FeMn bimetallic nanoparticles anchored in nitrogen-doped carbon nanofibers (FeMn/N-CNF) obtained through a facile electrospinning-carbonization process. The strong metal-support interaction (SMSI) phenomena including carbon encapsulation structure and electron transfer from metal to N-CNF, beneficial to the intrinsic activities, were successfully induced by the enhanced interfacial metal-nitrogen bonding in FeMn/N-CNF. Microstructural characterizations and leaching test revealed that the SMSI encapsulation structure could promote the formation of ultrafine FeMn nanoparticles in N-CNF during the high-temperature carbonization process and prevent leaching of active Fe/Mn metals into solution across a wide pH range. The constructed gravity-driven flow-through electro-Fenton system based on a FeMn/N-CNF cathode membrane exhibited superior performance to generate H2O2 (36.23 mmol L−1 h−1) and subsequent activate H2O2 decomposition to hydroxyl radicals (0.1024 min−1), achieving remarkable degradation efficiencies of 96.8%, 92.3%, and 90.3% within 60 min for Rhodamine B, Tetracycline, and Methyl Orange, respectively. Furthermore, the FeMn/N-CNF membrane filter demonstrated good pH adaptability, excellent cycle stability and anti-scaling ability during the degradation process. This work offers a viable avenue to enhance degradation performance and environmental robustness for practical water decontamination via achieving SMSI effect in carbon-supported electro-Fenton membranes.

First-principles study of aromatic amino acid encapsulation in single-walled BN and AlN nanotubes

Aromatic molecules exhibit strong non-covalent interactions with nanotubes, influencing their encapsulation properties. This study uses DFT calculations to explore the encapsulation of aromatic amino acids within zigzag (ZZ), chiral (R/S), and armchair (AC) single-walled aluminum nitride nanotubes (AlNNTs) and boron nitride nanotubes (BNNTs). The results reveal that zigzag AlNNTs exhibit the highest encapsulation affinity compared to other chiralities, while chiral BNNTs show enhanced encapsulation. Encapsulation energy decreases with increasing nanotube radius, indicating reduced affinity. Overall, the studied BNNTs demonstrate stronger encapsulation energy compared to AlNNTs. The bandgap energy of the encapsulated structures varies significantly with nanotube diameter and chirality. The physisorption process plays a major role in encapsulation, affecting the geometric and electronic properties of the nanotubes and enhancing the stability and efficacy of the encapsulated amino acids. These findings highlight the potential of these nanostructures for advanced applications, including targeted drug delivery and molecular sensing.

Facile recycling of porous Si waste for stable Si/C anodes

As the rapid development of photovoltaic industry, vast of polycrystalline Si has been produced for photovoltaic products. Meanwhile, large amount of Si waste is generated from mechanical slicing process and retired electronic products. Reasonable recycling the Si waste can save resources and reduce environmental pollution. Herein, porous Si is prepared from Si waste by magnesium thermal reduction and then embedded in industry lignin alkali-based carbon matrix (LAC) via co-precipitation and sintering process to obtain Si/C composite anode for lithium-ion batteries. Owing to the encapsulation structure, the carbon matrix can alleviate the volumetric expansion of Si and improve electronic conductivity of composite, the obtained Si@LAC anode exhibits high charge capacity of 1017.5 mAh g−1 at 0.1 A g−1 and high capacity retention of 94.9 % at 0.5 A g−1 after 200 cycles. Furthermore, the Si@LAC composite displays superior rate performance with high capacity of 596.7 mAh g−1 at 2 A g−1 which is 61.5 % of the value at 0.2 A g−1. Such a high performance Si/C anode from facile preparation demonstrates a viable route to utilization of photovoltaic Si waste and industrial lignin.

Life cycle assessment of decommissioned silicon photovoltaic module recycling using different technological configurations in China

The intricate encapsulation structure and material composition of photovoltaic modules necessitate full materials recycling involving multiple stages and different technological configurations, thereby increasing environmental burden of recycling process. Consequently, environmental impact assessments are imperative. However, previous studies primarily focused on a single technology or compared different technologies within a specific recycling stage, overlooking various technological configurations and thus engendering incomprehensive assessment. Hence, we employ a comparative life-cycle assessment to evaluate the environmental performance of six recycling alternatives with different technological configurations for silicon photovoltaic waste in China, which encompasses five recycling stages and glass/silicon remanufacturing processes. Results shows thermal delamination reduces the normalized environmental impact by 8.73% and 4.62% compared with mechanical and chemical delamination, respectively; electrolysis for metals extraction carries 35.72%–36.35% higher environmental benefits than precipitation. Additionally, introducing silicon/glass remanufacturing provides an additional 6.27%–11.55% environmental benefits. Therefore, integrating disassembly, thermal delamination, leaching & etching, electrolysis, and remanufacturing exhibits the best environmental performance, with −4796 kg CO2-eq/tonne carbon emission and −46400 MJ/tonne energy demand. Environmental hotspots analysis identifies key contributors to environmental impact and benefits. Further sensitivity analysis highlights the importance of enhancing silver and copper recovery efficiency. Finally, targeted strategies are proposed for green recycling routes of photovoltaic waste.

Control interfacial charge transfer behavior by creating surface defects on structure unit of heterojunction to drive carrier separation for enhancing photocatalytic CO2 reduction

Controlling interfacial charge transfer behavior of heterojunction is an arduous issue to efficiently drive separation of photogenerated carriers for improving the photocatalytic activity. Herein, the interface charge transfer behavior is effectively controlled by fabricating an unparalleled VO-NiWO4/PCN heterojunction that is prepared by encapsulating NiWO4 nanoparticles rich in surface oxygen vacancies (VO-NiWO4) in the mesoporous polymeric carbon nitride (PCN) nanosheets. Experimental and theoretical investigations show that, differing with the traditional p-n junction, the direction of built-in electric field between p-type NiWO4 and n-type PCN is reversed interestingly. The strongly codirectional built-in electric field is also produced between the surface defect region and inside of VO-NiWO4 besides in the space charge region, the dual drive effect of which forcefully propels interface charge transfer through triggering Z-Scheme mechanism, thus significantly improving the separation efficiency of photogenerated carriers. Moreover, the unique mesoporous encapsulation structure of VO-NiWO4/PCN heterostructure can not only afford the confinement effect to improve the reaction kinetics and specificity in the CO2 reduction to CO, but also significantly reduce mass transfer resistance of molecular diffusion towards the reaction sites. Therefore, the VO-NiWO4/PCN heterostructure demonstrates the preeminent activity, stability and reusability for photocatalytic CO2 reduction to CO reaction. The average evolution rate of CO over the optimal 10 %-VO-NiWO4/PCN composite reaches around 2.5 and 1.8 times higher than that of individual PCN and VO-NiWO4, respectively. This work contributes a fresh design approach of interface structure in the heterojunction to control charge transfer behaviors and thus improve the photocatalytic performance.

Preparation of β-Cyclodextrin(CD)/Flavour CD Powder and Its Application on Flavour Improvement of Regular Coffee.

To improve the overall sensory evaluation of regular coffee, a mixture of β-CD/flavour CD powder was prepared by a freeze-drying method. Cyclodextrin inclusion complexes consist of eight compounds that are naturally present in coffee, specifically: 2,5-dimethylpyrazine, benzaldehyde, citral, linalool, limonene, phenethyl acetate, furfural, and ethyl acetate. These eight compounds naturally occur in coffee, making them safer than using other compounds. Moreover, these eight compounds are the primary active ingredients in coffee, significantly influencing its flavour profile. Therefore, choosing to complex these eight compounds with cyclodextrins can effectively enhance the taste of the coffee. XRD, FT-IR, and SDE-GC-FID were presented to study the formation of inclusion CD powder, the storage stability, chemical composition changes, and safety. Results show that by the cyclodextrin method of freeze-drying, the CD powder showed a stable encapsulated structure and increased stability of flavour compounds. Based on the coffee aroma analysis results, prepared CD powder can enhance the coffee's aroma score by 3.0-4.0 points and increase the flavour score by 2.1-3.5 points, and it can achieve preservation for a minimum of 181 days at 25 °C. Furthermore, under the requirements of the China national standard for additives, the mixture of β-CD/flavour CD powder was used for the cup testing with four regular coffees to obtain improved coffees. With the full score is 10, improved coffees could score extra 3.0-4.0 points on aroma and 2.1-3.5 on flavour compared to regular coffee. In addition, the CD powder also improves the quality of the coffee in terms of aftertaste, body, and sweetness. Overall, β-CD/flavour CD powders provide several advantages over the currently popular coffee bean processing methods, including improved reproducibility, enhanced controllability, and increased flexibility, while prioritizing safety. And it should be explored further with appropriate compounds given its potential for coffee aroma modulation.

Advances in nanocarrier-mediated delivery of chrysin: Enhancing solubility, bioavailability, and anticancer efficacy

Chrysin, a natural phytochemical compound found in various plant sources, possesses diverse pharmacological benefits, including anticancer, antioxidant, antidiabetic, neuroprotective, cardioprotective, hepatoprotective, immunoregulatory, and anti-inflammatory properties. Despite its well-documented biological activities, chrysin's low water solubility and bioavailability hinder its clinical development. This review explores the application of nanocarriers as a strategic approach to overcome these challenges and enhance the delivery of chrysin. Nanocarriers, including polymer-based nanoparticles (NPs), lipid-based NPs, and inorganic nanocarriers, have shown promise in improving the solubility, bioavailability, and tumor-targeted delivery of chrysin. The paper discusses chrysin's anticancer effects on different types of human cancers, elucidating its impact on crucial signaling pathways involved in tumorigenesis. The review categorizes and analyzes various nanocarriers, providing insights into their structural properties and drug release profiles. Among the nanocarriers, polymer-based NPs, especially those utilizing PLGA, emerge as promising strategies for chrysin encapsulation, demonstrating improvements in drug release, stability, and bioavailability. Lipid-based NPs and inorganic nanocarriers also exhibit potential in enhancing chrysin delivery. The comprehensive insights provided contribute to a deeper understanding of chrysin's pharmacological properties and its potential clinical applications, offering valuable perspectives for future research and translation into clinical settings. The review underscores the importance of selecting suitable structures for chrysin encapsulation to enhance its physicochemical properties and anticancer effects, paving the way for innovative nanomedicine approaches in cancer therapy.

Flexible phase change film based on lignin-derived porous carbon/Eicosane for wearable thermal management and microwave absorption

A flexible phase-change film with thermal management and microwave absorption capabilities was developed for use in wearable devices. The film was created using a solution casting method based on a porous carbon-loaded eicosane (LP33/EI) material. LP33 served as the porous encapsulation medium, while Eicosane (EI) acted as the phase change component. The flexible substrate was a blend of polyvinyl alcohol (PVA) and bacterial cellulose nanocellulose (BC). The ultrathin film had a thickness of 0.262 mm, and LP33/EI-4 exhibited exceptional mechanical strength of 188 MPa. Testing revealed that the phase transition process had melting and crystallization enthalpies of 134.71 J/g and 126.11 J/g, respectively. The encapsulation structure effectively prevented any leakage during the phase transition process. Under simulated solar irradiation of 200 mW/cm2, LP33/EI-4 achieved a photothermal conversion efficiency (η) of 89.46 %. Additionally, the porous LP33 structure and high dielectric loss contributed to remarkable microwave absorption capabilities of −42 dB in the X-band and − 52 dB in the Ku-band. Overall, LP33/EI films demonstrated exceptional performance in thermal management, energy storage, and microwave absorption, making them an ideal choice for a variety of applications in wearable devices.

Integration of Heterogeneous Interfaces and Multi‐Dimensional Encapsulation Structure in Fe2N@CNTs Enabling Highly Efficient Thermal Management and Microwave Absorption

AbstractThe opposing effects of interface effect on phonon heat conduction and microwave absorption hinder the integration of thermal conduction with microwave absorption. Reconciling this contradiction by rationally optimizing the material structure remains a challenge. Herein, Fe2N@CNTs with heterogeneous interfaces and multi‐dimensional encapsulated structures are fabricated through in situ chemical vapor deposition (CVD) to realize excellent thermal conductivity and microwave absorption. When the mass fraction of active material is 40 wt.%, the thermal conductivity (λ//) of Fe2N@CNTs composite films is 6.69 W m−1 K−1. The minimum reflection loss (RLmin) is up to −54.55 dB at a thickness of 3.43 mm, and the effective absorption bandwidth (EAB) is 5.52 GHz at 1.82 mm. The well‐designed Fe2N@CNTs is an ideal model for gaining insight into electron transportation and phonon multi‐dimensional heat transport. Heterogeneous interface improves the dielectric loss and facilitates microwave and phonon absorption and conversion. The multi‐dimensional encapsulation structure increases the electron transport path and phonon heat transport paths making axial and radial co‐transfer possible. The multi‐dimensional encapsulation structure demonstrates extremely high microwave absorption and thermal management capabilities, which open up new possibilities for multifunctional applications in host materials with internal hollows.

Catalytic Oxidation of Toluene over Pt/CeO2 Catalysts: A Double-Edged Sword Effect of Strong Metal-Support Interaction.

Strong metal-support interaction (SMSI), which has drawn widespread attention in heterogeneous catalysis, is thought to significantly affect the catalytic performance for volatile organic chemical (VOC) abatement. In the present study, strong interactions between platinum and ceria are constructed by modulating the oxygen vacancy concentration of CeO2 through a NaBH4 reduction method. For a catalyst with higher content of oxygen vacancy, more electrons would transfer from ceria to Pt, which is attributed to the stronger effect of SMSI. The obtained electron-richer Pt sites exhibit higher ability for toluene activation, contributing to better performance for toluene oxidation. On the other hand, the stronger metal-support interaction would facilitate CeOx species migrating to the Pt nanoparticle surface and forming an encapsulated structure. Smaller Pt dispersion leads to fewer sites for toluene adsorption and activation, which is to the disadvantage of the reaction. Therefore, taking the negative and positive effects together, the Pt/CeO2-0.5 catalyst has the highest catalytic performance for toluene abatement. Our study provides new insights into strong metal-support interaction on toluene oxidation and contributes to designing noble metal catalysts for VOC abatement.

Microwave-assisted synthesis of dual-functional NiSe2@NC nanocomposites for advanced power-type and energy-type storage devices

The battery-supercapacitor hybrid energy storage system, composed of energy-type and power-type storage devices, is essential to improve energy storage systems' comprehensive performance and economy significantly. The current research uses a convenient and economical microwave-assisted heating method to describe the preparation of NiSe2@NC nanocomposites with a core-shell carbon encapsulation structure. When used as an electrode material for power-type storage devices (Supercapacitors, SCs), the optimized NiSe2@NC-1-3 can achieve 555.7 F g−1 at 0.5 A g−1. The assembled asymmetric NiSe2@NC//AC has a wide operating voltage of 1.6 V and maintains 92.73 % durability after 10,000 cycles. For energy-type storage devices (Sodium-ion battery, SIBs) from the NiSe2@NC-1-3 electrode material exhibits a capacity of 384.4 mAh g−1 at 0.1 A g−1, a good rate capability (298.8 mAh g−1 at 5.0 A g−1), and excellent cycling life (311.7 mAh g−1 at 1.0 A g−1 for 1200 cycles). Considering the exceptional electrochemical performance of the NiSe2@NC nanocomposite in both power-type and energy-type storage devices, the rational design of this work will provide a new sight for the construction of a battery-supercapacitor hybrid energy storage system which will accelerate the rapid development of the world's energy storage.

Thermal Stability of Encapsulated Carbon-Based Multiporous-Layered-Electrode Perovskite Solar Cells Extended to Over 5000 h at 85 °C.

The key to the practical application of organometal-halide crystals perovskite solar cells (PSCs) is to achieve thermal stability through robust encapsulation. This paper presents a method to significantly extend the thermal stability lifetime of perovskite solar cells to over 5000 h at 85 °C by demonstrating an optimal combination of encapsulation methods and perovskite composition for carbon-based multiporous-layered-electrode (MPLE)-PSCs. We fabricated four types of MPLE-PSCs using two encapsulation structures (over- and side-sealing with thermoplastic resin films) and two perovskite compositions ((5-AVA)x(methylammonium (MA))1-xPbI3 and (formamidinium (FA))0.9Cs0.1PbI3), and analyzed the 85 °C thermal stability followed by the ISOS-D-2 protocol. Without encapsulation, FA0.9Cs0.1PbI3 exhibited higher thermal stability than (5-AVA)x(MA)1-xPbI3. However, encapsulation reversed the phenomenon (that of (5-AVA)x(MA)1-xPbI3 became stronger). The combination of the (5-AVA)x(MA)1-xPbI3 perovskite absorber and over-sealing encapsulation effectively suppressed the thermal degradation, resulting in a PCE value of 91.2% of the initial value after 5072 h. On the other hand, another combination (side-sealing on (5-AVA)x(MA)1-xPbI3 and over- and side-sealing on FA0.9Cs0.1PbI3) resulted in decreased stability. The FACs-based perovskite was decomposed from these degradation mechanisms by the condensation reaction between FA and carbon. For side-sealing, the space between the cell and the encapsulant was estimated to contain approximately 1,260,000 times more H2O than in over-sealing, which catalyzed the degradation of the perovskite crystals. Our results demonstrate that MA-based PSCs, which are generally considered to be thermally sensitive, can significantly extend their thermal stability after proper encapsulation. Therefore, we emphasize that finding the appropriate combination of encapsulation technique and perovskite composition is quite important to achieve further device stability.

Cation-vacancy-rich NiFe2O4 nanoparticles embedded in Ni3Se2 nanosheets as an advanced catalyst for oxygen evolution reaction

Developing efficient and economically viable approaches to produce non-noble metal electrocatalysts with high performance is crucial for anion exchange membrane water electrolyzers. Here, we present a novel and mild two-step method to producing highly active and stability NiFe2O4/Ni3Se2 electrocatalyst by utilizing the dissolution/redeposition effect. Notably, the NiFe2O4 nanoparticles (∼10 nm) wrapped by Ni3Se2 nanosheets creating plentiful heterostructures and strong coupling forces to realize high-efficient alkaline water electrocatalysis. Therefore, the NiFe2O4/Ni3Se2 electrocatalyst delivers current densities of 1000 mA cm−2 under overpotentials of 379 mV for alkaline oxygen evolution and operates over 1200 h across a range of current densities from 50 to 1000 mA cm−2. An anion exchange membrane water electrolyzers with NiFe2O4/Ni3Se2 electrocatalyst exhibits performance (1.85 V @ 0.5 A cm−2, 2.08 @ 1.0 A cm−2) superior to that of the benchmark device at room temperature, and robust stability under industrial conditions. Experimental results and theoretical investigations demonstrate that the special encapsulation structure effectively mitigated catalyst migration and modulated the adsorption of O-containing intermediates. This work provides a rational synthesis strategy and provides useful guidelines to facilely fabricate oxygen evolution reaction electrocatalyst with high performance for an industrial water electrolyzer.

Structural Optimization of PA12/MVQ@POE-g-MAH Ternary Composite for Superior Toughness and Low-Temperature Resistance.

To enhance the low-temperature toughness and resistance of the engineering plastic polyamide PA12, this study introduces novel PA12/MVQ@POE-g-MAH ternary composites using a two-step process and dynamic curing. Analytical results indicate that incorporating MVQ@POE-g-MAH into the PA12 matrix markedly enhances its toughness and heat resistance. As the MVQ@POE-g-MAH content increases, the elongation at break of PA12 composites significantly expands from 52.83% to 204.69%, and the notch impact strength escalates from 8.69 to 74.34kJ m-2. In addition, the brittleness temperature of PA12 decreases from -59.5 to -67.0°C. Experimental findings confirm that POE-g-MAH is dispersed at the interface between MVQ and PA12, creating an encapsulated structure of MVQ@POE-g-MAH. This enhancement significantly broadens the potential applications of PA12 by improving its toughness, and resistance to both low and high temperatures, as well as impact endurance.

An Equalized Flow Velocity Strategy for Perovskite Colloidal Particles in Flexible Perovskite Solar Cells.

The non-uniform distribution of colloidal particles in perovskite precursor results in an imbalanced response to the shear force during flexible printing process. Herein, it is observed that the continuous disordered migration occurring in perovskite inks significantly contributes to the enlargement of colloidal particles size and diminishes the crystallization activity of the inks. Therefore, a molecular encapsulation architecture by glycerol monostearate to mitigate colloidal particles collisions in the precursor ink, while simultaneously homogenizing the size distribution of perovskite colloids to minimize their diffusion disparities, is devised. The utilization of colloidal particles with a molecular encapsulation structure enables the achievement of uniform deposition during the printing process, thereby effectively balancing the crystallization rate and phase transition in the film and facilitating homogeneous crystallization of perovskite films. The large-area flexible perovskite device (1.01 cm2 and 100 cm2) fabricated through printing processes, achieves an efficiency of 24.45% and 15.87%, respectively, and manifests superior environmental stability, maintaining an initial efficiency of 91% after being stored in atmospheric ambiences for 150 days (unencapsulated). This work demonstrates that the dynamic evolution process of colloidal particles in both the precursor ink and printing process represents a crucial stride toward achieving uniform crystallization of perovskite films.