Investigation and Prediction of Nano-Silver Line Quality upon Various Process Parameters in Inkjet Printing Process Based on an Experimental Method.

As an emerging additive manufacturing technology, inkjet printing has been increasingly applied in microelectronics field. However, due to the impacting and rebounding behaviors of conductive ink droplets impinging onto flat substrates, it is challenging to fabricate conductive lines with desired quality, such as suitable line width and line thickness, and matching resistance when it is used for interconnecting multifarious electronic components if there is not a proper configuration of operating parameters. To address this research gap, this article aims to investigate the effect of process parameters on the quality of conductive lines, including the platform temperature, printing speed, number of layers, and delay time (droplet interarrival time), are selected to conduct a full factorial experiment. First, the approximate parameter ranges for ensuring the continuity of conductive lines are determined. Second, this study analyzes the interactive effect among process parameters on line quality. Third, an artificial neural network (ANN) is constructed to predict the quality of printed lines. Results show that the line width does not increase with an increased number of layers, while the line thickness shows an increasing trend. The low resistance and high aspect ratio of printed line are achieved by printing 5 layers with the platform temperature of 70°C, the delay time of 12.2 ms, and the printing speed of 1139.39 mm/min. Moreover, the ANN model can be used to predict line width and line thickness with excellent performance, except for the resistance due to the irregular line edge. This study provides a useful guide for the selection of appropriate printing parameters to realize a diverse range of quality properties for 3D printed conductive lines in integrated circuits.

An investigation of methods to enhance adhesion of conductive layer and dielectric substrate for additive manufacturing of electronics.

Additive manufacturing of conductive layers on a dielectric substrate has garnered significant interest due to its promise to produce printed electronics efficiently and its capability to print on curved substrates. A considerable challenge encountered is the conductive layer's potential peeling due to inadequate adhesion with the dielectric substrate, which compromises the durability and functionality of the electronics. This study strives to facilitate the binding force through dielectric substrate surface modification using concentrated sulfuric acid and ultraviolet (UV) laser treatment. First, polyetheretherketone (PEEK) and nanoparticle silver ink were employed as the studied material. Second, the surface treatment of PEEK substrates was conducted across six levels of sulfuric acid exposure time and eight levels of UV laser scanning velocity. Then, responses such as surface morphology, roughness, elemental composition, chemical bonding characteristics, water contact angle, and surface free energy (SFE) were assessed to understand the effects of these treatments. Finally, the nanoparticle silver ink layer was deposited on the PEEK surface, and the adhesion force measured using a pull-off adhesion tester. Results unveiled a binding force of 0.37 MPa on unmodified surface, which escalated to 1.99 MPa with sulfuric acid treatment and 2.21 MPa with UV laser treatment. Additionally, cross-approach treatment investigations revealed that application sequence significantly impacts results, increasing binding force to 2.77 MPa. The analysis further delves into the influence mechanism of the surface modification on the binding force, elucidating that UV laser and sulfuric acid surface treatment methods hold substantial promise for enhancing the binding force between heterogeneous materials in the additive manufacturing of electronics.

Angiotensin II Type 2 Receptor Inhibits M1 Polarization and Apoptosis of Alveolar Macrophage and Protects Against Mechanical Ventilation-Induced Lung Injury.

Angiotensin II (Ang II) is associated with macrophage polarization and apoptosis, but the role of the angiotensin type 2 receptor (AT2R) in these processes remains controversial. However, the effect of AT2Rs on alveolar macrophages and mechanical ventilation-induced lung injury has not been determined. Mechanical ventilation-induced lung injury in Sprague‒Dawley (SD) rats and LPS-stimulated rat alveolar macrophages (NR8383) were used to determine the effects of AT2Rs, selective AT2R agonists and selective AT1Rs or AT2R antagonists. Macrophage polarization, apoptosis, and related signaling pathways were assessed via western blotting, QPCR and flow cytometry. AT2R expression was decreased in LPS-stimulated rat alveolar macrophages (NR8383). Administration of the AT2R agonist CGP-42112 was associated with an increase in AT2R expression and M2 polarization, but no effect was observed upon administration of the AT2R antagonist PD123319 or the AT1R antagonist valsartan. In mechanical ventilation-induced lung injury in Sprague‒Dawley (SD) rats, the administration of the AT2R agonist C21 was associated with attenuation of the pathological damage score, lung wet/dry weight, cell count and protein content in BALF. C21 can significantly reduce proinflammatory factor TNF-α, IL-1ß levels, increase anti-inflammatory factor IL-4, IL-10 levels in BALF, compared with the model group (p < 0.01). Similarly, compared with those at the same time points, the M1/M2 ratios in alveolar macrophages and apoptosis in peritoneal macrophages at 4 h, 6 h and 8 h in the mechanical ventilation models were lower after C21 administration. These findings indicated that the expression of AT2Rs in alveolar macrophages mediates M1 macrophage polarization and apoptosis and that AT2Rs play a protective role in mediating mechanical ventilation-induced lung injury.

Competition mode and soil nutrient status shape the role of soil microbes in the diversity-invasibility relationship.

Understanding the relationship between plant diversity and invasibility is essential in invasion ecology. Species-rich communities are hypothesized to be more resistant to invasions than species-poor communities. However, while soil microorganisms play a crucial role in regulating this diversity-invasibility relationship, the effects of plant competition mode and soil nutrient status on their role remain unclear. To address this, we conducted a two-stage greenhouse experiment. Soils were first conditioned by growing nine native species separately in them for 1 year, then mixed in various configurations with soils conditioned using one, three, or six species, respectively. Next, we inoculated the mixed soil into sterilized substrate soil and planted the alien species Rhus typhina and native species Ailanthus altissima as test plants. We set up two competition modes (intraspecific and interspecific) and two nutrient levels (fertilization using slow-release fertilizer and nonfertilization). Under intraspecific competition, regardless of fertilization, the biomass of the alien species was higher in soil conditioned by six native species. By contrast, under interspecific competition, the biomass increased without fertilization but remained stable with fertilization in soil conditioned by six native species. Analysis of soil microbes suggests that pathogens and symbiotic fungi in diverse plant communities influenced R. typhina growth, which varied with competition mode and nutrient status. Our findings suggest that the soil microbiome is pivotal in mediating the diversity-invasibility relationship, and this influence varies according to competition mode and nutrient status.

Macroporous, Highly Hygroscopic, and Leakage-Free Composites for Efficient Atmospheric Water Harvesting.

Hygroscopic composites based on hygroscopic salts and hydrogels are promising for atmospheric water harvesting (AWH), but their relatively low water production and possible salt leakage hinder real applications. Here, we report highly hygroscopic and leakage-free composites from loading LiCl into emulsion-templated sodium alginate and poly(vinyl alcohol) hydrogels with macroporous structures and interpenetrating polymer networks. The resulting composites exhibited an enhanced moisture uptake (up to 3.4 g g-1) and leakage-free behavior even at an extremely high relative humidity (RH) of 90%. Moreover, the composites showed accelerated adsorption, with high adsorption (0.803 g g-1 water at 25 °C and 90% RH within 1 h) and desorption due to the emulsion-templated, highly interconnected macropores. The hygroscopic composites obtained 1.12 g g-1 water per adsorption-desorption collection cycle and showed high reusability, without obvious deterioration in adsorption, desorption, and collection after 10 cycles. With the presence of carbon nanotubes, solar-driven AWH could be realized, without the requirement of additional energy. The highly hygroscopic and leakage-free composites with enhanced and accelerated adsorption and desorption are excellent candidates for efficient AWH.

UV radiation and temperature increase alter the PSII function and defense mechanisms in a bloom-forming cyanobacterium Microcystis aeruginosa.

The aim was to determine the response of a bloom-forming Microcystis aeruginosa to climatic changes. Cultures of M. aeruginosa FACHB 905 were grown at two temperatures (25°C, 30°C) and exposed to high photosynthetically active radiation (PAR: 400-700 nm) alone or combined with UVR (PAR + UVR: 295-700 nm) for specified times. It was found that increased temperature enhanced M. aeruginosa sensitivity to both PAR and PAR + UVR as shown by reduced PSII quantum yields (Fv/Fm) in comparison with that at growth temperature (25°C), the presence of UVR significantly exacerbated the photoinhibition. M. aeruginosa cells grown at high temperature exhibited lower PSII repair rate (Krec) and sustained nonphotochemical quenching (NPQs) induction during the radiation exposure, particularly for PAR + UVR. Although high temperature alone or worked with UVR induced higher SOD and CAT activity and promoted the removal rate of PsbA, it seemed not enough to prevent the damage effect from them showing by the increased value of photoinactivation rate constant (Kpi). In addition, the energetic cost of microcystin synthesis at high temperature probably led to reduced materials and energy available for PsbA turnover, thus may partly account for the lower Krec and the declination of photosynthetic activity in cells following PAR and PAR + UVR exposure. Our findings suggest that increased temperature modulates the sensitivity of M. aeruginosa to UVR by affecting the PSII repair and defense capacity, thus influencing competitiveness and abundance in the future water environment.

Hydrophilic-Oleophobic, Macroporous Polymers Enabled by In-Situ Polymerization and Foaming for Removing Water from Oils.

Porous polymers with hydrophilicity and oleophobicity are promising for removing water from various oil-water mixtures (including emulsions), but the preparation of such polymers is usually complicated and time-consuming. Herein, a novel stragey, in situ polymerization and foaming, has been developed to fabricate hydrophilic-oleophobic porous polymers in a facile manner within seconds. The porous polymers from pentaerythritol tetra(3-mercaptopropionate) and poly(ethylene glycol) diacrylate showed hydrophilicity and underwater oleophobicity, enabling the removal of water from oil-water mixtures and surfactant-stabilized, water-in-oil (w/o) emulsions, with a high efficiency of 99.9% and excellent reusability, without obvious deterioation after 10 cycles. With incorporatin of 1H,1H,2H,2H-perfluorooctyl methacrylate, the resulting porous polymers showed hydrophilicity and oleophobicty in air, providing an additional function of antioil-fouling ability both in dry state and in the process of oil-water separation. Moreover, both the two types of the porous polymers showed robust compression, without fracture and changes in wetting property after cycles of compression at 70% strain and high fatigue-resistant elasticity, without obvious plastic deformation after 1000 compression-release cycles. The facile and rapid preparation, hydrophiclity-oleophobicity, and robustness in compression and elasticity enabled the porous polymers to be good candidates for removing water from various oil-water mixtures.

Warming modulates the photosynthetic performance of Thalassiosira pseudonana in response to UV radiation.

Diatoms form a major component of phytoplankton. These eukaryotic organisms are responsible for approximately 40% of primary productivity in the oceans and contribute significantly to the food web. Here, the influences of ultraviolet radiation (UVR) and ocean warming on diatom photosynthesis were investigated in Thalassiosira pseudonana. The organism was grown at two temperatures, namely, 18°C, the present surface water temperature in summer, and 24°C, an estimate of surface temperature in the year 2,100, under conditions of high photosynthetically active radiation (P, 400-700 nm) alone or in combination with UVR (P + UVR, 295-700 nm). It was found that the maximum photochemical yield of PSII (Fv/Fm) in T. pseudonana was significantly decreased by the radiation exposure with UVR at low temperature, while the rise of temperature alleviated the inhibition induced by UVR. The analysis of PSII subunits turnover showed that high temperature alone or worked synergistically with UVR provoking fast removal of PsbA protein (KPsbA), and also could maintain high PsbD pool in T. pseudonana cells. With the facilitation of PSII repair process, less non-photochemical quenching (NPQ) occurred at high temperature when cells were exposed to P or P + UVR. In addition, irrespective of radiation treatments, high temperature stimulated the induction of SOD activity, which partly contributed to the higher PSII repair rate constant (Krec) as compared to KPsbA. Our findings suggest that the rise in temperature could benefit the photosynthetic performance of T. pseudonana via modulation of its PSII repair cycle and protective capacity, affecting its abundance in phytoplankton in the future warming ocean.

Metal-organic-framework derived Zn-V-based oxide with charge storage mechanism as high-performance anode material to enhance lithium and sodium storage.

Transition metal oxides have been extensively studied due to their large theoretical capacities, but their practical application has been hampered by low electrical conductivity and dramatic volume fluctuation during cycling. In this work, we synthesized Zn3V2O8 material using Zn-V-MOF (metal-organic framework) as a sacrificial template to improve the electrochemical characteristics of lithium-ion batteries (LIBs) and sodium-ion batteries (SIBs). Unique dodecahedral structure, larger specific surface area and higher ability to mitigate volume changes, improve the electrochemical reaction active site while accelerating ion transport. Zn3V2O8 with 2-methylimidazole as a ligand demonstrated a discharge capacity of 1225.9 mAh/g in LIBs and 761.6 mAh/g in SIBs after 300 cycles at 0.2 C. Density functional theory (DFT) calculation illustrates the smaller diffusion barrier energy and higher specific capacity in LIBs that is ascribed to the fact that Li has a smaller size and hence its diffusion is easier. This study may lead to a path for the manufacturing of high-performance LIBs and SIBs.

Metal-organic frameworks-derived MCo2O4 (M = Zn, Ni, Cu) two-dimensional nanosheets as anodes materials to boost lithium storage.

Transition metal oxides (TMOs) have received significant consideration. Because of their enormous theoretical capacity, cheap, and less toxicity. Notably, cobalt-based materials hold promises as negative electrode materials for batteries, but they suffer from less electrical conductivity and significant volume changes during operation. In order to address these challenges, sacrificial templating techniques at the nanoscale offer a potential solution for improving the electrochemical stability and rate performance of these materials. More specifically, these tactics have proven popular for designing Li-ion storages. To ascertain the impact of multiple metal ions on the electrochemical capacity, metal organic frameworks (MOFs) derived MCo2O4-MOF (M = Zn, Ni, Cu) were developed. Among these, ZnCo2O4 showed the best electrochemical performance (927.2 mAh g-1 at 0.1 A g-1 after 250 cycles). Furthermore, calculations based on density functional theory (DFT) revealed that ZnCo2O4 had the lowest Li+ adsorption energy, with a minimum value of -1.61 eV. Moreover, this research aims to design controllable nanostructures in order to enhance the design of transition bimetallic oxide composites for energy storage applications.

Recent Advances in Electrospun Membranes for Radiative Cooling.

Radiative cooling is an approach that maximizes the thermal emission through the atmospheric window in order to dissipate heat, while minimizing the absorption of incoming atmospheric radiation, to realize a net cooling effect without consuming energy. Electrospun membranes are made of ultra-thin fibers with high porosity and surface area, which makes them suitable for radiative cooling applications. Many studies have investigated the use of electrospun membranes for radiative cooling, but a comprehensive review that summarizes the research progress in this area is still lacking. In this review, we first summarize the basic principles of radiative cooling and its significance in achieving sustainable cooling. We then introduce the concept of radiative cooling of electrospun membranes and discuss the selection criteria for materials. Furthermore, we examine recent advancements in the structural design of electrospun membranes for improved cooling performance, including optimization of geometric parameters, incorporation of highly reflective nanoparticles, and designing multilayer structure. Additionally, we discuss dual-mode temperature regulation, which aims to adapt to a wider range of temperature conditions. Finally, we provide perspectives for the development of electrospun membranes for efficient radiative cooling. This review will provide a valuable resource for researchers working in the field of radiative cooling, as well as for engineers and designers interested in commercializing and developing new applications for these materials.

High Conductivity, Semiconducting, and Metallic PEDOT:PSS Electrode for All-Plastic Solar Cells.

Plastic electrodes are desirable for the rapid development of flexible organic electronics. In this article, a plastic electrode has been prepared by employing traditional conducting polymer poly(3,4-ethylenedioxythiophene):poly(styrene sulfonate) (PEDOT:PSS) and plastic substrate polyethersulfone (PES). The completed electrode (Denote as HC-PEDOT:PSS) treated by 80% concentrated sulfuric acid (H2SO4) possesses a high electrical conductivity of over 2673 S/cm and a high transmittance of over 90% at 550 nm. The high conductivity is attributed to the regular arrangement of PEDOT molecules, which has been proved by the X-ray diffraction characterization. Temperature-dependent conductivity measurement reveals that the HC-PEDOT:PSS possesses both semiconducting and metallic properties. The binding force and effects between the PEDOT and PEI are investigated in detail. All plastic solar cells with a classical device structure of PES/HC-PEDOT:PSS/PEI/P3HT:ICBA/EG-PEDOT:PSS show a PCE of 4.05%. The ITO-free device with a structure of Glass/HC-PEDOT:PSS/Al4083/PM6:Y6/PDINO/Ag delivers an open-circuit voltage (VOC) of 0.81 V, short-circuit current (JSC ) of 23.5 mA/cm2, fill factor (FF) of 0.67 and a moderate power conversion efficiency (PCE) of 12.8%. The above results demonstrate the HC-PEDOT:PSS electrode is a promising candidate for all-plastic solar cells and ITO-free organic solar cells.

Bibliometric analysis of single-cell sequencing researches on immune cells and their application of DNA damage repair in cancer immunotherapy.

Introduction: In recent decades, single-cell sequencing technology has developed rapidly and used widely in various fields of life sciences, especially for the detection of immune cells. A bibliometric analysis of single-cell sequencing research work on immune cells published during the 2011-2021 period should provide new insight on the use of single-cell sequencing. Methods: We screened 1,460 publications on single-cell sequencing on immune cells according to the publication date, article type, language, and country. Reults: The United States published the first and largest number of articles, while China's research started relatively late, but ranked second in the number of publications. T cells were the most commonly studied immune cells by single-cell sequencing, followed by mononuclear macrophages. Cancer biology was the most common field of immune cell research by single-cell sequencing. Single-cell sequencing studies using γδ T cells were mainly in the fields of cancer biology and cell development, and focused over time from cell surface receptor to cell function. Through in-depth analysis of the articles on single-cell sequencing of T cells in the oncology field, our analysis found that immunotherapy and tumor microenvironment were the most popular research directions in recent years. Discussion: The combination of DNA damage repair and immunotherapy seems to provide a new strategy for cancer therapy.

Cellulose-based, flexible polyurethane polyHIPEs with quasi-closed-cell structures and high stability for thermal insulation.

Cellulose-based, closed-cell porous materials templated from emulsions are promising for thermal insulation, but their low stability imposed by physical interaction hinders the materials from real applications. Herein, we report the fabrication of cellulose-based, flexible polyurethane polyHIPEs with quasi-closed-cell structures, high stability and flexibility for thermal insulation. The polyHIPEs were prepared from cellulose-stabilized Pickering high internal phase emulsions through interfacial crosslinking using isocyanate. The resulting polyurethane polyHIPEs showed controllable external shapes, quasi-closed-cell structures, high flexibility, low density, and robust compression (without fracture even after compression to 30 % original height). The crosslinking enabled the polyHIPEs to show hydrophobicity, good stability (without breakage and dissolution observed after immersing in NaOH solution at pH 12, HCl solution at pH 1 and hot water at 100 °C, for 24 h) and decreased moisture uptake (below 1 %). The low density and quasi-closed-cell structures endowed the polyHIPEs with high thermal insulation, with thermal conductivity as low as 33.1 mW/(m K). These features make the cellulose-based, closed-cell polyHIPEs as an excellent candidate for thermal insulting.

Highly Stable Supercapacitors Enabled by a New Conducting Polymer Complex PEDOT:CF3 SO2(x) PSS(1-x).

Herein, a novel conducting polymer complex PEDOT:CF3 SO2(x) PSS(1-x) [denoted as S-PEDOT:CF3 SO2(x) PSS(1-x) , where PEDOT is poly(3,4-ethylenedioxythiophene) and PSS is poly(styrene sulfonate)], is fabricated with the assistance of zinc di[bis(trifluoromenthylsulfonyl) imide][Zn(TFSI)2 ] (CFE). The introduction of CF3 SO2 - group is expected to bring better stability of PEDOT:CF3 SO2 than PEDOT:PSS due to its strong Coulomb force. Electrochemical measurement shows that a high specific capacitance of 194 F cm-3 was achieved from the novel complex S-PEDOT:CF3 SO2(x) PSS(1-x) , the highest value reported so far. An all-solid-state supercapacitor assembly with a structure of S-PEDOT:CF3 SO2(x) PSS(1-x) /H2 SO4 :polyvinyl alcohol (PVA)/S-PEDOT:CF3 SO2(x) PSS(1-x) shows a record specific capacitance of 70.9 F cm-3 and a maximum energy density of 6.02 mWh cm-3 at a power density of 397 mW cm-3 . This supercapacitor device demonstrates excellent electrochemical stability with a capacitance retention rate of 98 % after 10 000 cycles and extreme air stability of 96 % capacitance retention rate after 10 000 cycles, even if the device is exposed to air over 2880 h, much better than that of PEDOT:PSS based supercapacitors. Excellent capacitance can be achieved from PEDOT:CF3 SO2(x) PSS(1-x) electrode under electrolyte-free conditions. This work provides a novel method for high performance stable supercapacitors and may pave the way for the commercialization of PEDOT based supercapacitors.

Advanced 1D Metal-Organic Coordination Polymer for Lithium-Ion Batteries: Designing, Synthesis, and Working Mechanism.

Anthraquinone (AQ) and its derivatives have been attracting more attention as promising electrode materials for lithium storage because of their high specific capacity, structural diversity, and environmental friendliness. The dissolution and poor electrical conductivity of AQ, however, limit its practical application. Here, a novel metal-organic coordination polymer with a one-dimensional (1D) chain ([C14H6O4Cu]n denoted as Cu-DHAQ; DHAQ, 1,5-dihydroxyl anthraquinone) and its composite with graphene (Cu-DHAQ/G; G, graphene) are developed by the introduction of graphene and copper ion into DHAQ. The fabricated polymer with a 1D chain not only well inhibits the dissolution of DHAQ in organic electrolytes but also facilitates lithium-ion insertion/extraction on carbonyl groups and shortens the migration path of lithium ions. Furthermore, the addition of the conductive network of graphene provides fast transfer rates of electrons. As a result, Cu-DHAQ/G delivers a high discharge capacity, long cycle life, and excellent rate capability. The lithium storage mechanism shows lithium ion insertion/extraction on two carbonyl groups of Cu-DHAQ in the range of 1.6-2.0 V and the redox reaction of Cu+/Cu2+ between 2.8 and 3.0 V, and Cu2+ and Cu+ coexist in the Cu-DHAQ/G electrode during the charge/discharge process. This study provides meaningful guidance to develop metal-organic coordination polymer electrodes for high-performance Li-ion batteries.

Elevated CO2 modulates the physiological responses of Thalassiosira pseudonana to ultraviolet radiation.

Diatoms account for a large proportion of marine primary productivity, they tend to be the predominant species in the phytoplankton communities in the surface ocean with frequent and large light fluctuations. To understand the impacts of increased CO2 on diatoms' capacity in exploitation of variable solar radiation, we cultured a model diatom Thalassiosira pseudonana with 400 or 1000ppmv CO2 and exposed it to high photosynthetically active radiation (PAR) alone or PAR plus ultraviolet radiation (UVR) to examine its physiological performances. The results showed that the maximum photochemical efficiency (Fv/fm) was significantly reduced by high PAR and PAR + UVR in T. pseudonana, UVR-induced inhibition on PSII activity was exacerbated by high CO2. PSII activity drops coincide approximately with PsbA content in the cells exposed to high PAR or PAR + UVR, which was pronounced at high CO2. The removal of PsbD in T. pseudonana cells declined under high CO2 during UVR exposure, limiting the repair capacity of PSII. In addition, high CO2 reversed the induction of energy-dependent form of NPQ by UVR to the increase of Y(No), indicating the severe damage of the photoprotective reactions. Our findings suggest that the adverse impacts of UVR on PSII function of T. pseudonana were aggravated by the elevated CO2 through modulating its capacity in repair and protection, which thereby would influence its abundance and competitiveness in phytoplankton communities.

2D Bismuth@N-Doped Carbon Sheets for Ultrahigh Rate and Stable Potassium Storage.

Metallic Bi, as an alloying-type anode material, has demonstrated tremendous potential for practical application of potassium-ion batteries. However, the giant volume expansion, severe structure pulverization, and sluggish dynamics of Bi-based materials result in unsatisfied rate performance and unstable cycling stability. Here, 2D bismuth@N-doped carbon sheets with BiOC bond and internal void space (2D Bi@NOC) are successfully fabricated via a self-template strategy to address these issues, which own ultrafast electrochemical kinetics and impressive long-term cycling stability for delivering an admirable capacity of 341.7 mAh g-1 after 1000 cycles at 10 A g-1 and impressive rate capability of 220.6 mAh g-1 at 50 A g-1 . Particularly, the in situ transmission electron microscopy observations visualize the real-time alloying/dealloying process and reveal that plastic carbon shell and void space can availably relieve dramatic volume stress and powerfully maintain structural integrity. Density functional theory calculation and ultraviolet photoelectron spectroscopy test certify that the robust BiOC bond is thermodynamically and kinetically beneficial for adsorption/diffusion of K+ . This work will light on designing advanced high-performance energy materials and provide important evidence for understanding the energy storage mechanism of alloy-based materials.

Multifunctional MXene/Aramid Nanofiber Composite Films for Efficient Electromagnetic Interference Shielding and Repeatable Early Fire Detection.

Rapid development of highly integrated electronic and telecommunication devices has led to urgent demands for electromagnetic interference (EMI) shielding materials that incorporate flame retardancy, and more desirably the early fire detection ability, due to the potential fire hazards caused by heat propagation and thermal failure of the devices during operation. Here, multifunctional flexible films having the main dual functions of high EMI shielding performance and repeatable fire detection ability are fabricated by vacuum filtration of the mixture of MXene and aramid nanofiber (ANF) suspensions. ANFs serve to reinforce MXene films via the formation of hydrogen bonding between the carbonyl groups of ANFs and the hydroxyl groups of MXene. When the ANF content is 20 wt %, the tensile strength of the film is increased from 24.6 MPa for a pure MXene film to 79.5 MPa, and such a composite film (9 µm thickness) exhibits a high EMI shielding effectiveness (SE) value of ∼40 dB and a specific SE (SSE) value of 4361.1 dB/mm. Upon fire exposure, the composite films can trigger the fire detection system within 10 s owing to the thermoelectric property of MXene. The self-extinguishing feature of ANFs ensures the structural integrity of the films during burning, thus allowing for continuous alarm signals. Moreover, the films also exhibit excellent Joule heating and photothermal conversion performances with rapid response and sufficient heating reliability.

Emulsion-based, flexible and recyclable aerogel composites for latent heat storage.

Although emulsion-based, phase change material-encapsulated monolithic composites are promising for latent heat storage, their rigidity and non-recyclability imposed by the relatively dense covalent crosslinking hinder the composites from real applications. Herein, we report the fabrication of aerogel composites with flexibility and recyclability from cellulose nanocrystal-stabilized, octadecane-encapsulated Pickering emulsions solidified using physical gelation. The resulting monolithic composites exhibited controllable external shapes, and the introduction of poly(vinyl alcohol) significantly reduced the leakage of the encapsulated octadecane. The aerogel composites showed flexibility at temperature over 30 °C, and robust compressive behavior, without fracture at 70% compressive strain. The composites possessed similar heat storage (melting) temperature and heat release (crystallization) temperature to that of bulk octadecane, high heat capacity (up to 253 J.g-1) and high reusability, without obvious deterioration in heat capacity after 100 heating-cooling cycles. Moreover, the aerogel composites exhibited recyclability, simply by dissolving the composites in hot water to form emulsions and then by freeze drying to form aerogel composites. The flexibility and recyclability, together with robust compression, controllable external shapes, high heat capacity and good reusability, make the aerogel composites to be excellent candidates for latent heat storage.