Fiber Network Structure Research Articles

Enabling High‐Efficiency and Stable Binary Organic Solar Cells by Solid Additive‐Assisted Morphology Modulation

AbstractThe solid additive strategy represents a simple yet effective approach to achieving high‐efficiency organic solar cells (OSCs) by enhancing the morphology of the active layer. In this study, a highly volatile solid additive, 2,4,6‐trichloro‐1,3,5‐triazine (TCT), is employed to modulate the morphology. Unlike other solid additives previously reported, TCT exhibits remarkable intermolecular interactions with both polymer donor and acceptor, offering two distinct advantages. Firstly, TCT notably enhances the crystallinity and molecular order of the blend film, subtly optimizing the fiber network structure within, thereby facilitating carrier transport and significantly improving the mobility of the blend film. Secondly, TCT stabilizes the bi‐continuous fibrous morphology of the polymer donor and acceptor, mitigating the morphological evolution of the active layer and enhancing device stability. Consequently, the D18:L8‐BO:TCT device exhibits a higher power conversion efficiency of 19.50% compared to the D18:L8‐BO device (18.13%). Furthermore, after 960 h of storage, the OSC device treated with TCT retains 90% of its initial PCE, significantly outperforming the D18:L8‐BO device (73%). This study presents a promising avenue for achieving high‐performance OSCs through manipulating the active layer morphology with solid additives.

Highly Filled Waste Polyester Fiber/Low-Density Polyethylene Composites with a Better Fiber Length Retention Fabricated by a Two-Rotor Continuous Mixer

A key challenge in the utilization of waste polyester fibers (PET fibers) is the development of fiber-reinforced composites with high filler content and the improvement of fiber length retention. Herein, the effects of a two-rotor continuous mixer and a twin-screw extruder on the structure and properties of waste polyester fiber composites were evaluated. The results revealed that the mechanical properties of the composites were improved significantly with increasing fiber content, especially when processed using the twin-rotor continuous mixer. This mixer facilitated the formation of a robust fiber network structure, leading to substantial enhancements in tensile strength, flexural strength, and heat resistance. Specifically, compared to those processed by the twin-screw extruder, with 60 wt% fibers content, the tensile and flexural strengths of specimens processed by the twin-rotor continuous mixer increase by 21% and 13%, respectively. The average fiber length in specimens processed by the twin-rotor continuous mixer was 32% longer than that in specimens processed by the twin-screw extruder, attributable to the lower shear frequency and the higher tensile ratio of the former. This blending technique emerges as an effective strategy, contributing significantly to promoting the development and practical application of waste textile fiber-reinforced polymer composites.

Constructing Multiscale Fibrous Morphology to Achieve 20% Efficiency Organic Solar Cells by Mixing High and Low Molecular Weight D18.

This study underscores the significance of precisely manipulating the morphology of the active layer in organic solar cells (OSCs). By blending polymer donors of D18 with varying molecular weights, a multiscale interpenetrating fiber network structure within the active layer is successfully created. The introduction of 10% low molecular weight D18 (LW-D18) into high molecular weight D18 (HW-D18) produces MIX-D18, which exhibits an extended exciton diffusion distance and orderly molecular stacking. Devices utilizing MIX-D18 demonstrate superior electron and hole transport, improves exciton dissociation, enhances charge collection efficiency, and reduces trap-assisted recombination compared to the other two materials. Through the use of the nonfullerene acceptor L8-BO, a remarkable power conversion efficiency (PCE) of 20.0% is achieved. This methodology, which integrates the favorable attributes of high and low molecular weight polymers, opens a new avenue for enhancing the performance of OSCs.

Biomimetically spider web-like hydrogels for high-efficiency solar evaporators

With the increasing population, the shortage of freshwater resources has become a problem faced by human beings. Although many hydrogel solar evaporators achieved high evaporation rates by increasing the intermediate water content to reduce the enthalpy of water evaporation, it is still challenging to explore effective photothermal materials to construct efficient hydrogel solar evaporators. Here, inspired by the spider web structure, interconnected porous hydrogels were proposed by cross-linking heterojunctions and polymers. For the first time, MXene heterojunction is applied to solar evaporators. The introduction of SnS2 greatly improves the light absorption of MXene, at the same time, benefiting from the multi-scale macro/micro fiber network structure, MXene-SnS2 hydrogel (MSH) has a good “lock-in” performance, which makes the heat locally distributed near the evaporable water. As a result, the MSH evaporator has a low enthalpy of evaporation, with an evaporation rate of 3.3606 kg m−2 h−1 in 3.5 wt% salt water, and can maintain 1.9 kg m−2 h−1 even in 10.5 % brine. The evaporators present superior purification performance for seawater, could maintain high and stable evaporation performance for 72 h. This design principle and excellent performance provide a potential method and design concept for seawater desalination.

Chitosan-derived N-doped porous carbon with fiber network structure for advanced lithium‑sulfur batteries

The flexible design and construction of advanced carbon-based sulfur hosts contribute to the rapid redox and reaction kinetics of lithium polysulfides (LiPSs) in lithium‑sulfur batteries (LSBs), laying the foundation for the next generation of high-energy density energy storage devices. Herein, chitosan (CS)-derived porous N-doped carbon with fiber network structure was prepared by a simple freeze-drying method combined with sintering process. The effect of inorganic salt additives on the morphology of CS-derived carbon was investigated by SEM. The types and contents of N-doping were investigated through XPS analysis. The influence of morphology and N content on the performance of LSBs has been explored in detail through cycling and CV testing. In addition, the true active sites in the CS-derived carbon were determined by XPS and first principles calculations. As an active species, pyrrolic N exhibits superior adsorption energy and the most suitable degradation energy barrier for LiPSs. As the optimal electrode, the performance of LSBs under different electrolyte to sulfur (E/S) conditions was further investigated to explore the potential application of CS-KOH electrodes in high-energy density batteries. The results unveil that the influence of E/S on Li2S deposition is quite significant, with a limit of 5 μL mg−1. This work provides a new strategy for the preparation of high-performance advanced carbon-based materials with fiber network structures from polysaccharide biomass, and also promotes the application of CS in energy storage.

Synthesis composit electrospun based gum-resin/polycaprolactone fibers for biomedical application

Electrospun fibers for tissue engineering have recently seen significant advancements. In this study, we created composite fibers by combining Pistacia atlantica Gum-Resin and Poly(ε-caprolactone) (PCL) polymer using the electrospinning method. We examined the morphology, biodegradability, thermal stability, and hydrophilicity of the prepared scaffolds using Fourier transform infrared spectroscopy (FT-IR), scanning electron microscopy (SEM), thermogravimetric (TG) differential scanning calorimetry (DSC), and water contact angle measurements. The results indicated complete integration between the materials and successful synthesis of fibers through the electrospinning method. SEM images demonstrated bead-free fibers with different blending ratios of Gum-Resin and PCL. Fibers with a diameter of 100–200 nm and 1–7 μm were obtained with a 9:1 blending ratio of PCL to Gum-Resin. Additionally, PCL/Gum-Resin fibers with an 8:2 blending ratio exhibited an interwoven and porous fiber network structure with a 1–7 μm fiber diameter. The water contact angle measurements revealed the hydrophilic surface of the fibers, with a WCA of 61.2°. Thermogravimetric (TG) and differential scanning calorimetric (DSC) analysis showed a melting peak at approximately 57°. Cell culture results indicated good cytocompatibility of the fibers. The scaffold sample exhibited inhibitory activity against S. aureus (22 ± 0.26 mm) and E. coli (16.8 ± 0.15 mm) bacteria. These findings suggest that the fabricated fibers could serve as an effective scaffold for wound healing.

Basalt Fibers versus Plant Fibers: The Effect of Fiber-Reinforced Red Clay on Shear Strength and Thermophysical Properties under Freeze–Thaw Conditions

Freeze–thaw cycling has a significant impact on the energy utilization and stability of roadbed fill. Given the good performance of basalt fiber (BF) and plant fiber (PF), a series of indoor tests are conducted on fiber-reinforced red clay (RC) specimens to analyze the shear strength, thermophysical, and microstructural changes and damage mechanisms of the RC under the freeze–thaw cycle–BF coupling, meanwhile, comparing the improvement effect of PF. The results indicate that the RC cohesion (c) first increases and then decreases with the increasing fiber content under BF improvement, reaching the maximum value at the content of 2%, and the change in the internal friction angle (φ) is relatively small. As the number of freeze–thaw cycles increases, cohesion (c) first decreases and then gradually stabilizes. The thermal conductivity increases with increasing moisture content, and the thermal effusivity increases and then decreases with increasing moisture content and fiber content. The heat storage capacity reaches the optimum level at a moisture content of 22.5% and a fiber content of 1%. Microanalysis reveals that at 2% fiber content, a fiber network structure is initially formed, and the gripping effect is optimal. The shear strength of PF-improved soil is higher than that of BF at a fiber content of 4–6%, and the thermal conductivity is better than that of BF. At the same fiber content, the heat storage and insulation capacity of BF-improved soil is significantly higher than that of PF.

Preparation and characterization of high load‐bearing needled composite preform based on novel ordered short fiber network needling method

AbstractNeedled preform and its composite using felt and base cloth stacked needled have small fiber volume fraction and relatively weak mechanical properties, which are difficult to meet the service requirements of structural and functional integrated components of high‐speed aircraft. Responding to this issue, this paper proposed a new method for preparing high load‐bearing needled composite preform based on ordered short fiber network needling. The high load‐bearing needled preforms were prepared by designing different structural parameters of ordered short fiber network and forming process parameters, and then preform structure was characterized and mechanical properties were tested. The results showed that using ordered short fiber network as carrier of the short fibers, the formed needled fiber bundles were longer and denser, volume content of needled fiber bundles and mechanical properties of needled preform were greatly improved, and needled fiber bundles volume content of ordered short fiber network reinforced needled preform was 1.5 times and 46.3 times that of half‐cut cloth and felt respectively. Compared with traditional felt needled preform and half‐cut cloth needled preform, the interlaminar peeling strength of the ordered short fiber network reinforced needled preform increased by up to 246.4% and 49.2%, respectively. The tensile strength of ordered short fiber network reinforced needled preform was 12.9% higher than that of half‐cut cloth in X‐axis direction. In addition, the effects of ordered short fiber network structure, short fiber length, areal density and needling density on the needled preform structure and properties were also revealed.Highlights High load‐bearing needled composite preform was prepared based on novel ordered short fiber network needling method. The needled fiber bundles formed by using ordered short fiber network were longer and denser, and their volume content was 46.3 times that of felt needled preform. The interlaminar peeling strength of the ordered short fiber network reinforced needled preform increased by up to 246.4%. The tensile strength of ordered short fiber network reinforced needled preform was 12.9% greater than half‐cut cloth in the X‐axis direction.

A robust and biodegradable hydroxyapatite/poly(lactide-co-ε-caprolactone) electrospun membrane for dura repair.

Typically occurring after trauma or neurosurgery treatments, dura mater defect and the ensuing cerebrospinal fluid (CSF) leakage could lead to a number of serious complications and even patient's death. Although numerous natural and synthetic dura mater substitutes have been reported, none of them have been able to fulfill the essential properties, such as anti-adhesion, leakage blockage, and pro-dura rebuilding. In this study, we devised and prepared a series of robust and biodegradable hydroxyapatite/poly(lactide-co-ε-caprolactone) (nHA/PLCL) membranes for dura repair via an electrospinning technique. In particular, PLLA/PCL (80/20) was selected for electrospinning due to its mechanical properties that most closely resembled natural dural tissue. Studies by SEM, XRD, water contact angle and in vitro degradation showed that the introduction of nHA would destroy PLCL's crystalline structure, which would further affect the mechanical properties of the nHA/PLCL membranes. When the amount of nHA added increased, so did the wettability and in vitro degradation rate, which accelerated the release of nHA. In addition, the high biocompatibility of nHA/PLCL membranes was demonstrated by in vitro cytotoxicity data. The in vivo rabbit dura repair model results showed that nHA/PLCL membranes provided a strong physical barrier to stop tissue adhesion at dura defects. Meanwhile, the nHA/PLCL and commercial group's CSF had a significantly lower number of inflammatory cells than the control groups, validating the nHA/PLCL's ability to effectively lower the risk of intracranial infection. Findings from H&E and Masson-trichrome staining verified that the nHA/PLCL electrospun membrane was more favorable for fostering dural defect repair and skull regeneration. Moreover, the relative molecular weight of PLCL declined dramatically after 3 months of implantation, according to the results of the in vivo degradation test, but it retained the fiber network structure and promoted tissue growth, demonstrating the good stability of the nHA/PLCL membranes. Collectively, the nHA/PLCL electrospun membrane presents itself as a viable option for dura repair.

Production and characterization of bacterial cellulose by Rhizobium sp. isolated from bean root

Bacterial cellulose (BC) is a natural polymer renowned for its unique physicochemical and mechanical attributes, including notable water-holding capacity, crystallinity, and a pristine fiber network structure. While BC has broad applications spanning agriculture, industry, and medicine, its industrial utilization is hindered by production costs and yield limitations. In this study, Rhizobium sp. was isolated from bean roots and systematically assessed for BC synthesis under optimal conditions, with a comparative analysis against BC produced by Komagataeibacter hansenii. The study revealed that Rhizobium sp. exhibited optimal BC synthesis when supplied with a 1.5% glucose carbon source and a 0.15% yeast extract nitrogen source. Under static conditions at 30 °C and pH 6.5, the most favorable conditions for growth and BC production (2.5 g/L) were identified. Modifications were introduced using nisin to enhance BC properties, and the resulting BC-nisin composites were comprehensively characterized through various techniques, including FE-SEM, FTIR, porosity, swelling, filtration, and antibacterial activity assessments. The results demonstrated that BC produced by Rhizobium sp. displayed properties comparable to K. hansenii-produced BC. Furthermore, the BC-nisin composites exhibited remarkable inhibitory activity against Escherichia coli and Pseudomonas aeruginosa. This study contributes valuable insights into BC’s production, modification, and characterization utilizing Rhizobium sp., highlighting the exceptional properties that render it efficacious across diverse applications.

Carbonized cellulose microspheres loaded with Pd NPs as catalyst in p-nitrophenol reduction and Suzuki-Miyaura coupling reaction

Catalytic reduction of p-nitrophenol is usually carried out using transition metal nanoparticles such as gold, palladium, silver, and copper, especially palladium nanoparticles (Pd NPs), which are characterized by fast reaction rate, high turnover frequency, good selectivity, and high yield. However, the aggregation and precipitation of the metals lead to the decomposition of the catalyst, which results in a significant reduction of the catalytic activity. Therefore, the preparation of homogeneous stabilized palladium nanoparticles catalysts has been widely studied. Stabilized palladium nanoparticles mainly use synthetic polymers. Cellulose microspheres, as a natural polymer material with low-cost and porous fiber network structure, are excellent carriers for stabilizing metal nanoparticles. Cellulose microspheres impregnated with palladium metal nanoparticles were carbonized to have a larger specific surface area and highly dispersed palladium nanoparticles, which exhibited excellent catalytic activity in the catalytic reduction of p-nitrophenol. In this work, the cellulose carbon-based microspheres palladium (Pd@CCM) catalysts were designed and characterized by SEM, TEM, EDS, XRD, FTIR, XPS, TGA, BET, and so on. Furthermore, the catalytic performance of Pd@CCM catalysts was investigated via p-nitrophenol reduction, which showed high catalytic activity. This catalyst also exhibited excellent catalytic performance in the Suzuki-Miyaura coupling reaction. Linking aromatic monomer and benzene through Suzuki-Miyaura coupling was presented as an effective route to obtaining biaryls, and the synthesis method is low-cost and simple. In addition, Pd@CCM showed desirable recyclability while maintaining its catalytic activity even after five recycles. This work is highly suggestive of the design and application of the heterogeneous catalyst.

The Multiscale Structural Properties and In‐Vitro Digestibility of High Amylose Corn Starch During Autoclaving‐Cooling Treatment

AbstractThis work investigates the relationship between multiscale structural properties in high amylose corn starch (HACS) and its in‐vitro digestibility by analyzing the effects of autoclaving‐cooling treatment (ACT). Differential scanning calorimetry (DSC) shows that HACS displays a higher gelatinization temperature, wider endothermic gelatinization range, and higher enthalpy. Autoclaved corn starch exhibits enhanced thermal stability than the raw corn starch. X‐ray diffraction (XRD) shows that ACT does not change the crystalline type but increases the relative crystallinity (RC). Fourier transform infrared spectroscopy (FTIR) indicates that HACS exhibits a higher degree of order (DO) and double helixes (DHs) than normal corn starch (NCS), which are reduced by ACT. Scanning electron microscopy (SEM) reveals that HACS displays denser structures and smaller particle morphologies than NCS. After ACT, the granular of autoclaved corn starch shows a rough fiber network structure. Digestibility analysis reveals a positive correlation between the amylose content and resistant starch (RS) level in raw starch, while ACT promotes significant RS formation. This suggests that amylose promotes ordered structure formation, while autoclaving increased digestive resistance.

One–step synthesis of silver nanoparticles by lignocellulose nanofibrils to obtain antimicrobial hydrogels with accelerated wound healing

Lignin–containing cellulose nanofibrils (LCNF) have attracted extensive attention in the field of antibacterial due to the properties both of lignin and nanofibrils. The evenly distributed nano–lignin in LCNF can reduce Ag+, and the fiber network structure of nanofibrils may prevent the sedimentation of silver nanoparticles (AgNPs), which makes LCNF promising candidates for one–step preparation and deposition of AgNPs. Herein, carboxylated lignocellulose nanofibrils (CLCNF) with high stability were used to initiate the redox reaction. AgNPs (∼10.45 nm) were successfully prepared and homogeneously anchored onto CLCNF (Ag–L NPs–CLCNF). After compositing with polyvinyl alcohol (PVA) and tetracycline hydrochloride (TH), Ag–L NPs–CLCNF constructed a reversible redox quinone/catechol chemistry, imparting hydrogels with long–lasting reproducible adhesion and antimicrobial activity. Moreover, the incorporation of Ag–L NPs–CLCNF significantly improved the tensile strength (30.87 kPa), compressive strength (368.11 kPa) and thermal stability of the hydrogels, and that the Ag–L NPs–CLCNF hydrogel were self–healing. Importantly, the hydrogel containing Ag–L NPs–CLCNF can realize the controlled delivery of TH, giving it excellent antibacterial activity with accompanied good biocompatibility and significantly promoting full–thickness skin wound healing. This work offers a novel idea for preparing antibacterial hydrogels from lignocellulosic nanofibrils and the hydrogels have great application prospects in wound dressing.

Tin-antimony/carbon composite porous fibers: electrospinning synthesis and application in sodium-ion batteries

In this work, tin-antimony/carbon composites porous fibers were successfully synthesized by an electrospinning method combined with two-step heat treatment processes, in which SnCl2 and SbCl3 were used as tin and antimony sources, and polyacrylonitrile (PAN) and polymethyl methacrylate (PMMA) were used as binders and pore-forming agents. The as-synthesized tin-antimony/carbon composites were systematically characterized by x-ray Diffraction (XRD), Transmission Electron Microscope (TEM), Scanning Electron Microscope (SEM), Energy-Dispersive Spectrometer (EDS), x-ray Photoelectron Spectroscopy (XPS), and Thermogravimetric Analysis-Differential Scanning Calorimetry (TG-DSC). The results indicate that the composite material consists of one-dimensional nitrogen-doped carbon porous fibers as the main matrix, with a three-dimensional network structure in which Sn, SnO2, and SnSb particles are encapsulated. Furthermore, the tin-antimony/carbon composites porous fibers were utilized as self-supported negative electrode for sodium-ion batteries. The results showed that the SNbM-2 sample electrode calcined at 800 °C demonstrated the best cycling stability and rate capability among all the sample electrodes, with a discharge capacity of 319.5 mAh·g−1 maintained after 100 cycles at a current density of 0.1 A·g−1. The excellent electrochemical performance of the SNbM-2 sample electrode is benefited from its unique porous structure and the carbon fiber network structure encapsulating Sn, SnO2, and SnSb particles, which could effectively shorten the Na+ ion transport distance and mitigate electrode volume expansion.

Small but mighty: Empowering sodium/potassium‐ion battery performance with S‐doped SnO2 quantum dots embedded in N, S codoped carbon fiber network

AbstractSnO2 has been extensively investigated as an anode material for sodium‐ion batteries (SIBs) and potassium‐ion batteries (PIBs) due to its high Na/K storage capacity, high abundance, and low toxicity. However, the sluggish reaction kinetics, low electronic conductivity, and large volume changes during charge and discharge hinder the practical applications of SnO2‐based electrodes for SIBs and PIBs. Engineering rational structures with fast charge/ion transfer and robust stability is important to overcoming these challenges. Herein, S‐doped SnO2 (S–SnO2) quantum dots (QDs) (≈3 nm) encapsulated in an N, S codoped carbon fiber networks (S–SnO2–CFN) are rationally fabricated using a sequential freeze‐drying, calcination, and S‐doping strategy. Experimental analysis and density functional theory calculations reveal that the integration of S–SnO2 QDs with N, S codoped carbon fiber network remarkably decreases the adsorption energies of Na/K atoms in the interlayer of SnO2–CFN, and the S doping can increase the conductivity of SnO2, thereby enhancing the ion transfer kinetics. The synergistic interaction between S–SnO2 QDs and N, S codoped carbon fiber network results in a composite with fast Na+/K+ storage and extraordinary long‐term cyclability. Specifically, the S–SnO2–CFN delivers high rate capacities of 141.0 mAh g−1 at 20 A g−1 in SIBs and 102.8 mAh g−1 at 10 A g−1 in PIBs. Impressively, it delivers ultra‐stable sodium storage up to 10,000 cycles at 5 A g−1 and potassium storage up to 5000 cycles at 2 A g−1. This study provides insights into constructing metal oxide‐based carbon fiber network structures for high‐performance electrochemical energy storage and conversion devices.

Regulating microstructures of aerogels by controlling phase separation mechanism for improving specific surface area and energy harvesting

Aerogels with 3D porous structures have been attracting increasing attention among functional materials due to their advantages of being lightweight and high specific surface area. Precise control of the porous structure of aerogel is essential to improve its performance. In this work, polylactic acid (PLA) aerogels with distinctly different microstructures were fabricated by precisely controlling the phase separation behavior of the ternary solution system. Rheological and theoretical analyses have revealed that the interactions between polymer molecules, solvents and non-solvents play a crucial role in determining the nucleation and growth of poor olymer and rich polymer phases. By adjusting the non-solvent type and the solution composition, aerogels with spider network structure, bead-like connected microsphere structure, and cluster petal structure were obtained. Ideal spinodal phase separation conditions were obtained to produce aerogels with a homogeneous fiber network structure. The optimum PLA aerogel achieved an extremely porosity of 96 % and a high specific surface area of 114 m2/g, which rendered it with excellent triboelectric generation performance. Thus, this work provides fundamental insights into the precise regulation of the phase separation behavior and the structure of the aerogel, which can help boost the performance and expand the applications of PLA aerogels.

Predicting moisture penetration dynamics in paper with machine learning approach

In this work, we predicted the gradient of the deformational moisture dynamics in a sized commercial paper by observing the curl deformation in response to the one-sided water application. The deformational moisture is a part of the applied liquid which ends up in the fibers causing swelling and subsequent mechanical response of the entire fiber network structure. The adapted approach combines traditional experimental procedures, advanced machine learning techniques and continuum modeling to provide insights into the complex phenomenon relevant to ink-jet digital printing in which the sized and coated paper is often used, meaning that not all the applied moisture will reach the fibers. Key material properties including elasticity, plastic parameters, viscoelasticity, creep, moisture dependent behavior, along with hygroexpansion coefficients are identified through extensive testing, providing vital data for subsequent simulation using a continuum model. Two machine learning models, a Feedforward Neural Network (FNN) and a Recurrent Neural Network (RNN), are probed in this study. Both models are trained using exclusively numerically generated moisture profile histories, showcasing the value of such data in contexts where experimental data acquisition is challenging. These two models are subsequently utilized to predict moisture profile history based on curl experimental measurements, with the RNN demonstrating superior accuracy due to its ability to account for temporal dependencies. The predicted moisture profiles are used as inputs for the continuum model to simulate the associated curl response comparing it to the experiment representing “never seen” data. The result of comparison shows highly predictive capability of the RNN. This study melds traditional experimental methods and innovative machine learning techniques, providing a robust technique for predicting moisture gradient dynamics that can be used for both optimizing the ink solution and paper structure to achieve desirable printing quality with lowest curl propensities during printing.

Underactuated Humanoid Peeling Approach for Pickled Mustard Tuber Based on Metamorphic Constraints.

Pickled mustard tuber (PMT), also known as Brassica juncea var. tumida, is a conical tuberous vegetable with a scaly upper part and a coarse fiber skin covering the lower part. Due to its highly distorted and complex heterogeneous fiber network structure, traditional manual labor is still used for peeling and removing fibers from pickled mustard tuber, as there is currently no effective, fully automated method or equipment available. In this study, we designed an underactuated humanoid pickled mustard tuber peeling robot based on variable configuration constraints that emulate the human "insert-clamp-tear" process via probabilistic statistical design. Based on actual pickled mustard tuber morphological cluster analysis and statistical features, we constructed three different types of pickled mustard tuber peeling tool spectral profiles and analyzed the modular mechanical properties of three different tool configurations to optimize the variable configuration constraint effect and improve the robot's end effector trajectory. Finally, an ADAMS virtual prototype model of the pickled mustard tuber peeling robot was established, and simulation analysis of the "insert-clamp-tear" process was performed based on the three pickled mustard tuber statistical classification selection. The results showed that the pickled mustard tuber peeling robot had a meat loss rate of no more than 15% for each corresponding category of pickled mustard tuber, a theoretical peeling rate of up to 15 pieces per minute, and an average residual rate of only about 2% for old fibers. Based on reasonable meat loss, the efficiency of peeling was greatly improved, which laid the theoretical foundation for fully automated pickled mustard tuber peeling.

Colloidal Nanoplatelets‐Based Soft Matter Technology for Photonic Interconnected Networks: Low‐Threshold Lasing and Polygonal Self‐Coupling Microlasers

AbstractSoft matter‐based microlasers are widely regarded as excellent building blocks for realizing photonic interconnected networks in optoelectronic chips, owing to their flexibility and functional network topology. However, the potential of these devices is hindered by challenges such as poor lasing stability, high lasing threshold, and gaps in knowledge regarding cavity interconnection characteristics. In this study, the first demonstration of a high‐quality, low‐threshold nanoplatelets (NPLs)‐based polymer microfiber laser fabricated using capillary immersion techniques and its photonic interconnected networks are presented. CdSe/CdS@Cd1‐xZnxS core/buffer shell@graded‐shell NPLs with high optical gain characteristics are adopted as the gain medium. The study achieves a lasing threshold below 14.8 µJ cm−2, a single‐mode quality (Q)‐factor of ≈5500, and robust lasing stability in the fabricated NPLs‐based microfibers. Furthermore, the study pioneers the exploration of polygonal self‐coupling microlasers and the optical characteristics of their interconnected fiber network. Based on the signal generation mechanism observed in the photonic networks, an interconnected NPLs‐based fiber network structure achieving single‐mode lasing emission and laser mode modulation is successfully designed. The work contributes a novel method for realizing microlasers fabricated via soft‐matter technologies and provides a key foundation and new insights for unit design and programming for future photonic network systems.

Electrospun PTFE nanofibrous composite membranes featuring a fiber network structure for organic solvent nanofiltration (OSN)

The practical implementation of organic solvent nanofiltration (OSN) was still hindered by the drawback of substrate swelling and dissolution in organic solvents. As the substrate of nanofiltration membranes, polytetrafluoroethylene (PTFE) had gained increasing attention due to its stable chemical characteristics. However, it was difficult to construct functional nanofiltration layers on the surface of PTFE due to its hydrophobicity induced by its intrinsic low surface energy, resulting into poor adhesion between substrate and functional layer. In this study, a polydopamine (PDA)-PA/PTFE composite nanofiltration membrane with a three-layer was fabricated by utilizing the poly (tetrafluoroethylene-hexafluoropropylene) (FEP) resins as the pore structure regulator of the PTFE substrate with fiber network structure, and PDA as the surface modifier of the PTFE substrate. The resultant composite nanofiltration membrane exhibited a notable rejection rate of 96.26 % for Rose Bengal (RB), and a long-term stable ethanol permeance of 2.28 (L·m−2·h−1·bar−1). After continuous filtration for 48 h, soaking in polar organic solvents (DMF) for 20 days, and circulating experiments exhibiting excellent solvent resistance and long-term stability. These results provided a useful strategy for the application of PTFE nanofiber substrates in the OSN field.