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The author of this paper and coauthors in 2022 studied a family of self-affine tiles in R d with noncollinear digit sets, and gave a sufficient and necessary condition for such tiles to be tame balls. We in this paper mainly present a simpler proof of such equivalent condition. We replace quadric surfaces by some zigzag planes, and redefine the quasi-invariant plane which plays a key role in the construction of the desired homeomorphism. This adjustment greatly simplifies the proof. [ABSTRACT FROM AUTHOR]

In response to the increasing utilization of communication technology, there is a growing need for electromagnetic interference (EMI) shielding materials to adapt to diverse application scenarios. In this study, the self‐destructible EMI shielding films (SEFs) that possess the unique capability to reduce conductivity and shielding efficiency through temperature elevation are introduced. The SEFs effectively fulfill the requirement of triggering EMI shielding failure under specific conditions, which can be achieved by simply spraying a mixture of thermally expandable microspheres (TEMs), conductive fillers, and resin substrates. The segregated structures resulting from the incorporation of TEMs confer exceptional electrical conductivity and superior EMI shielding performance at low conductive filler content. When the ambient temperature surpasses the glass transition temperature of the TEM shell, the thermally expandable characteristics cause a disruption in the conductive path of the SEFs, leading to a significant decline in shielding effectiveness. Additionally, the SEFs exhibit outstanding Joule heating effects (90 °C) at low voltage (1.5 V) within a brief time frame (10 s). Importantly, when employed as Joule heaters, the SEFs possess an intrinsic safety mechanism that automatically ceases operation in the event of circuit overload, thus minimizing any potential risks. [ABSTRACT FROM AUTHOR]

Developing polymer‐based piezoelectric materials with multistimulus responsiveness is highly desirable for advancing multi‐source energy harvesting in wearable electronics. Inspired by the multifunctionality of muscle fibers, a nanostructure interface engineering strategy to create piezoelectric polymeric nanoheterostructures (PNHs) with remarkable responsiveness to both mechanical and nonmechanical contactless stimuli is introduced. Through precise interfacing of polymer nanofibers with nanoparticles via multiscale‐regulated interface electrostatic and chemical interactions, the study achieves a controlled assembly of stabilized and hierarchically organized nanoheterostructures featuring unique interface‐confined configurations. These configurations induce in situ stabilized dipole orientation and significant geometric stress nano‐confinement at interfaces, crucial for amplifying electricity generation. Compared to conventional polymer nanocomposites, engineered PNHs exhibit dramatically enhanced piezoelectricity, boasting a higher sensitivity of 1065 mV kPa−1 and piezoelectric coefficient of 76.2 pC N−1. Furthermore, PNHs demonstrate superior thermo‐actuated electricity generation under temperature fluctuations through cooperative spontaneous polarizations of constituent nanostructures, yielding a higher pyroelectric coefficient of 3.13 µC m2K−1. Additionally, the design enables photothermally‐activated switchable electricity generation and light‐energy harvesting, achieving a photo‐electric conversion efficiency tenfold higher than nanocomposites. This effective and versatile approach inspires the development of multi‐responsive nanogenerators for multi‐energy harvesting and self‐powered multistimulus‐sensing applications. [ABSTRACT FROM AUTHOR]

Enhancing the piezoelectricity of polymers while maintaining all components organic is still challenging but significantly important for developing flexible wearable energy harvesters and self‐powered devices. Here, a novel and versatile strategy is introduced to construct mixed‐dimensional all‐organic polymer heterostructures (MPHs) for enhanced piezoelectricity. By combining all‐polymer 1D nanofibers (NFs) with 2D crystals through epitaxial crystallization‐driven assembly (ECA), MPHs are engineered to capitalize on the synergistic effects of both dimensional nanostructures. The intrinsic piezoelectric activity of 1D NFs is amplified by the growth of 2D crystals, enhancing force‐sensitivity and overall piezoelectricity. The mixed‐dimensional assembly not only enables controlled in‐situ growth of MPHs, but also simultaneously induces preferential formation of electroactive phases through solvent‐induced phase transition. By modulating the epitaxial growth of 2D crystals on 1D NFs, effective tuning of MPH growth amount and morphology is achieved, resulting in significant improvements in deformability, dipole polarization, and durability. MPHs exhibit remarkable piezoelectric improvements, achieving higher output under lower‐level forces with a record‐high sensitivity of ≈670 mV kPa−1. Their superior responsivity enables the development of self‐powered wireless wearable motion‐monitoring systems for real‐time physiological movement detection and analysis. This work inspires the development of all‐organic piezoelectric devices for innovative flexible energy‐harvesting and sensing applications. [ABSTRACT FROM AUTHOR]

Highlights: The SiO2 nanofiber membranes and MXene@c-MWCNT6:4 as one unit layer (SMC1) were bonded together with 5 wt% PVA solution. When the structural unit is increased to three layers, the resulting SMC3 has an average electromagnetic interference SET of 55.4 dB and a low thermal conductivity of 0.062 W m−1 K−1. SMCx exhibit stable electromagnetic interference shielding and excellent thermal insulation even in extreme heat and cold environment. A lightweight flexible thermally stable composite is fabricated by combining silica nanofiber membranes (SNM) with MXene@c-MWCNT hybrid film. The flexible SNM with outstanding thermal insulation are prepared from tetraethyl orthosilicate hydrolysis and condensation by electrospinning and high-temperature calcination; the MXene@c-MWCNTx:y films are prepared by vacuum filtration technology. In particular, the SNM and MXene@c-MWCNT6:4 as one unit layer (SMC1) are bonded together with 5 wt% polyvinyl alcohol (PVA) solution, which exhibits low thermal conductivity (0.066 W m−1 K−1) and good electromagnetic interference (EMI) shielding performance (average EMI SET, 37.8 dB). With the increase in functional unit layer, the overall thermal insulation performance of the whole composite film (SMCx) remains stable, and EMI shielding performance is greatly improved, especially for SMC3 with three unit layers, the average EMI SET is as high as 55.4 dB. In addition, the organic combination of rigid SNM and tough MXene@c-MWCNT6:4 makes SMCx exhibit good mechanical tensile strength. Importantly, SMCx exhibit stable EMI shielding and excellent thermal insulation even in extreme heat and cold environment. Therefore, this work provides a novel design idea and important reference value for EMI shielding and thermal insulation components used in extreme environmental protection equipment in the future. [ABSTRACT FROM AUTHOR]

Conductive hydrogels are gaining significant attention as promising candidates for the fabrication materials for flexible electronics. Nevertheless, improving the tensile properties, hysteresis, durability, adhesion, and electrochemical properties of these hydrogels remains challenging. This work reports the development of a novel semi‐interpenetrating network poly(ionic liquid) hydrogel named PATV, via the in situ polymerization of acrylamide, N‐[Tris(hydroxymethyl)methyl] acrylamide, and 1‐vinyl‐3‐butylimidazolium tetrafluoroborate. The density functional theory calculations reveal that the poly(ionic liquid) in the hydrogel network acts as physical cross–linking points to construct hydrogen‐bond networks. Furthermore, the hydrogen‐bond networks dissipate energy efficiently and quickly, and thus stress concentration and hysteresis are avoided. The prepared hydrogel has a low hysteresis (9%), high tensile properties (900%), fast response (180 ms), high sensitivity (gauge factor = 10.4, pressure sensitivity = 0.14 kPa−1), and wide sensing range (tensile range: 1–600%, compression range: 0.1–20 kPa). A multifunctional sensor designed based on the designed hydrogel enables real‐time, rapid, and stable response‐ability for the detection of human movement, facial expression recognition, pronunciation, pulse, handwriting, and Morse code encryption. Furthermore, the assembled triboelectric nanogenerator displays an excellent energy harvesting capability, thus highlighting its potential application in self‐powered flexible wearable electronic devices. [ABSTRACT FROM AUTHOR]

The addition of CaCO3 powder in calcium aluminate cement (CAC) is reported to accelerate the hydration of CAC and generate mono‐carbonate C4AC̅H11, which is conducive to shortening the curing time of CAC‐bonded castables at ambient temperatures. Although the hydration of CAC is relatively fast, there is still residual un‐hydrated CAC in castables after curing. The residual CAC would continue to hydrate to produce C3AH6 and AH3 during the subsequent drying procedures in the absence of CaCO3. But it is worth pondering which type of hydrate would be generated in the presence of CaCO3 during the drying at around 110°C. In this study, the effect of micro‐sized CaCO3 addition on the hydrate formation of CAC‐bonded castables during drying at 110°C was investigated. The results indicate that the C4AC̅H11 formed at the curing temperature of 30°C is not decomposed or converted during drying. The CaCO3 remained after curing does not participate in the hydration of residual CAC during drying at 110°C, and thus the residual CAC continues to hydrate to generate C3AH6 rather than C4AC̅H11. [ABSTRACT FROM AUTHOR]

Thermosetting polyimide (PI) foams (PIFs) are usually synthesized through chemical foaming; however, this approach is environmentally toxic, and it is difficult to regulate the cell structure, remold the foam, and increase the foam compressive strength. The development of microcellular PIFs with ultrahigh compressive strength and high volume expansion ratio remains a challenge. Herein, thermoplastic PI with a branched structure and flexible ether bonds was synthesized through solution polymerization, and microcellular thermoplastic PIFs (TPIFs) with ultrahigh strength were fabricated via supercritical-carbon-dioxide foaming using 2,4,6-triamino pyrimidine (TAP) as a chain-extender monomer. Subsequently, a lattice model of a closed tetrakaidecahedral cell was used to clarify the relation between the foam compressive strength and polymer cell structure. Experimental results indicate that the optimal thermal imidization temperature is 230 °C and that the resulting branched structure considerably improves viscoelasticity, flame retardancy, and foaming performance. A TAP content of 0.75 g results in branched-structure TPIFs with a mean cell size of 16.8 μm. Notably, at high temperatures and pressures, the compressive strength of TPIFs with 0.75 g TAP is more than nine times of that of TPIFs without TAP. Increasing the TAP content beyond 0.75 g results in a crosslinked structure. Backward differentiation shows that TPIF compression is constant at 0.14–0.18 in the [0,0,1] lattice direction. The proposed physical foaming method is environment-friendly and can sustainably produce TPIFs with a high volume expansion ratio, an adjustable microcellular structure, and outstanding mechanical properties. [Display omitted] • Branched thermoplastic polyimide (TPI) synthesized via solution polymerization. • TPI offers superb flame resistance and recyclability for fireproofing. • Microcellular TPI foams are fabricated by supercritical CO 2 foaming. • TPI foams exhibit uniform structure and strong compressive strength. • Lattice model clarifiies the relationship between compressive strength and polymer cell structure. [ABSTRACT FROM AUTHOR]

Highlights In this paper, a hybrid approach was employed by integrating a high‐modulus, high‐tensile‐strength carbon fiber fabric (CFF) with a low‐density, high‐toughness silk nonwoven fabric (SNWF) to fabricate CFF‐SNWF reinforced epoxy (CFF‐SNWF/EP) hybrid composites. Through the surface freeze‐induced self‐assembly process, the multiscale hybrid modified layers were successfully constructed on the surfaces of both CFF and SNWF. This novel approach effectively enhanced the interfacial strength of the hybrid fibers (HFs). Comparing the performance of the modified composites with unmodified CFF reinforced epoxy (CFF/EP), significant improvements in both tensile strength and interlaminar shear strength were observed. Specifically, the tensile strength and interlaminar shear strength of the modified composites reached 626.7 and 39.16 MPa, a rise scope of 17.1% and 14.8%, respectively. In addition, the hybrid fibers reinforced polymers (HFRPs) exhibited a superior electromagnetic interference (EMI) shielding capabilities. For insistence, the modified CFF/EP with a thickness of 2.0 mm showed an impressive EMI shielding effectiveness value of 50 dB. These findings underscore the promising application potential of CFF‐SNWF/EP hybrid composites, particularly in the field of consumer electronics. The surface of hybrid fiber was modified by PDA‐GO‐OCNTs‐WPU. Multi‐scale structure contributes a lot in composite performance. Hybrid effect before and after interfacial modification is performed. The hybrid interface modification and hybrid structure were analyzed. [ABSTRACT FROM AUTHOR]

Electromagnetic interference (EMI) shielding fabrics are crucial in addressing the increasingly serious electromagnetic pollution. To meet wearable requirements, stretchability and thermal comfortability are often desired, but which still are challenging. Herein, a stretchable EMI shielding fabric is fabricated via electrospinning coupled with biaxial pre‐stretching spraying, in which a block stacking wrinkled silver nanowire (AgNW)/Ti3C2Tx MXene network is coated on one side of electrospun thermoplastic polyurethane (TPU)/polydimethylsiloxane (PDMS) fabric. As expected, the wrinkled structure protects conductive network from fracture during stretching process, so as to realize the strain‐invariant electrical conductivity. Thus, the fabric exhibits a stretchable EMI shielding performance of over 40 dB when subjected to 10–50% uniaxial strains or 21–125% biaxial strains. More importantly, the white TPU/PDMS side and the black AgNW/MXene side enable the fabric passive radiative cooling and heating, respectively. The cooling side exhibits high mid‐infrared emissivity (97.5%) and solar reflectance (90%), thus reducing the skin temperature by ≈4.9 °C. The heating side with high solar absorptivity (86.6%) and photothermal effect increased the skin temperature by ≈5 °C. Therefore, the fabirc with stretchable EMI shielding and Janus‐type dual‐mode personal passive thermal management is promising in future wearable products. [ABSTRACT FROM AUTHOR]

Polylactic acid (PLA) aerogels with spider network structure, bead-like connected microsphere structure, and cluster petal structure were fabricated by precisely controlling the phase separation behavior (nucleation growth and spinodal separation) of the ternary solution system. The PLA aerogel with ideal spider network structure achieved an extremely high porosity of 96% and a high specific surface area of 114 m2/g, which rendered it with excellent triboelectric energy generation performance. [Display omitted] 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. [ABSTRACT FROM AUTHOR]

The prognosis for traumatic brain injury (TBI) depends largely on prompt hemostasis and effective pharmacologic interventions. Natural all‐small‐molecule self‐gelling powder, integrating the advantages of self‐assembled small‐molecule hydrogels and powders, is expected to provide timely and effective prehospital management of TBI. However, the synthesis and application of natural all‐small‐molecule self‐gelling powder is still uncharted territory. In this study, an all‐small‐molecule co‐assembled MGF‐H3BO3‐RUT (MBR) self‐gelling powder is fabricated through the co‐assembly of mangiferin (MGF) and rutin (RUT) in H3BO3/NaOH aqueous solution. Both compounds can bind with boric acid, leading to co‐assembling into hydrogels through hydrogen‐bonding interactions and π–π stacking. MBR self‐gelling powder is then obtained by drying the as‐prepared hydrogels, thus integrating hemostasis and pharmacodynamics into one. Remarkably, it displays robust regeneration capabilities, while retaining excellent self‐healing properties and injectability after drying‐hydration cycles. Moreover, MBR self‐gelling powder not only achieves rapid effective hemostasis but also attenuates conspicuously cerebral edema and inflammatory response after TBI by in situ spraying, exhibiting notable neuroprotective effects without discernible toxic side effects. This study provides a novel assembly strategy and application form for self‐assembled gel materials originating from natural small molecules, offering promising avenues for the treatment of TBI in the acute phase. [ABSTRACT FROM AUTHOR]

Recently, passive radiative cooling (PRC) that realizes thermal management without consuming any energy has attracted increasing attention. However, few studies focus on low‐cost and robust PRC film fabricated by a facile and environmentally friendly method. In this study, via coextrusion blow film molding and water leaching, sandwiched PRC film (SPRCF) is efficiently prepared, and its skin and core layer are respectively high‐density polyethylene (HDPE) film and oriented ZnO@HDPE microfiber layer. Of note, such a sandwiched structure enables SPRCF to possess remarkable mechanical properties, abrasion, and weather resistance. Moreover, with the introduction of ZnO, SPRCF shows lower sunlight transmittance (≈3.8%) but higher mid‐infrared transmittance (≈88.8%), endowing it with remarkable PRC performance (the maximum cooling power of daytime and nighttime are respectively 73.8 and 96.7 W m−2). Furthermore, the decent self‐cleaning performance of SPRCF‐45 endows it with maintenance‐free features outdoors. This work proposes a facile and environmentally friendly method for preparing low‐cost and robust SPRCF, opening a new pathway to develop PRC film following the concept of polymer “structuring” processing. [ABSTRACT FROM AUTHOR]

The use of antibacterial biodegradable polymers is of great importance nowadays in medical applications. In this manuscript, poly(butylenes adipate-co-terephthalate)/poly(lactic acid) blend-based antibacterial bionanocomposites were prepared by melt-processing. We use organically modified montmorillonite (MMT) and graphene nanoplatelets (GNP) as antibacterial property enhancers which are both processing platelike structure, while ciprofloxacin hydrochloride (CFX·HCl) was chosen as a biocide. Either MMT or GNP increases the antibacterial properties during the whole study and tunes the release of CFX·HCl from the bionanocomposites. This was proven by agar diffusion tests and antimicrobial release measurements. The morphology of the bionanocomposites was conducted by using scanning and transmission electron microscopies, and evidence of exfoliation was observed. Contact angle and water uptake of the bionanocomposites were studied showing hydrophilic performance and more percentage water uptake. The final effect on mechanical and blood compatibility was also investigated. The results reveal excellent possibility of using MMT- and GNP-modified PLA/PBAT polymer blends to tune antibacterial properties for specific biomedical applications. [ABSTRACT FROM AUTHOR]

Polyimide foams (PIFs), renowned as some of the best materials for excellent performance in harsh temperature environments, have been developed to meet the increasing demands of high-tech industries. A state-of-the-art review of advanced PIFs research was conducted, covering the general research profiles and trends, institutions and scholars, major journals, research categories, and application fields through a bibliometric analysis of publications.Research on polyimide-based foam has increased approximately 30-fold over the past 40 years. One hundred forty-two research institutions from 20 countries have conducted research related to PIFs. Literature co-citation analysis reveals that the knowledge base of the PIFs research field primarily focuses on chemical synthesis foaming. This spotlight on engineering applications systematically describes the synthesis mechanisms, various typical fabrication methods, and the microstructure of PIFs. The advantages and disadvantages of this methods have been compared. Representative functions and corresponding mechanism models, which include thermal, mechanical, sensing, electromagnetic, flame retardant, oil-water separation, and other fields, have been outlined. This review offers insights into the technological development prospects and opportunities. Finally, the arduous tasks and challenges of PIFs research are summarized, providing valuable guidance for researchers interested in this field. [Display omitted] • A state-of-the-art review of PIFs research through bibliometric analysis • The synthesis mechanism, fabrication methods, and the microstructure of PIFs were systematically described. • Representative functions and the corresponding mechanism models were concluded • Provided information on the technological development prospects and opportunities • The arduous tasks and challenges of PIFs were summarized [ABSTRACT FROM AUTHOR]

Developing novel absorbent materials targeting high-efficiency, low-energy-consumption, and environmental-friendly oil spill cleanup is still a global issue. Porous absorbents endowed with self-heating function are an attractive option because of that they are able to in-situ heat crude oil and dramatically reduce oil viscosity for efficient remediation. Herein, we facilely prepared an eco-friendly multifunctional bacterial cellulose/MXene aerogel (P-SBC/MXene aerogel) for rapid oil recovery. Thanks to excellent full solar spectrum absorption (average absorbance = 96.6 %), efficient photo-thermal conversion, and superior electrical conductivity (electrical resistance = 36 Ω), P-SBC/MXene aerogel exhibited outstanding photothermal and electrothermal capabilities. Its surface temperature could quickly reach 93 °C under 1.0 kW/m2 solar irradiation and 124 °C under 3.0 V voltage respectively, enabling effective heat transfer toward spilled oil. The produced heat significantly decreased crude oil viscosity, allowing P-SBC/MXene aerogel to rapidly absorb oil. By combining solar heating and Joule heating, P-SBC/MXene aerogel connected to a pump-assisted absorption device was capable of achieving all-weather crude oil removal from seawater (crude oil flux = 630 kg m−2 h−1). More notably, P-SBC/MXene aerogel showed splendid outdoor crude oil separation performance. Based on remarkable crude oil/seawater separation ability, the versatile aerogel provides a promising way to deal with large-area oil spills. [Display omitted] [ABSTRACT FROM AUTHOR]

Manipulating the cellular microstructure is an important means to alter the mechanical properties and expand the application of polymer foams. Herein, a vacuum-counter pressure-assisted supercritical CO 2 foaming (V-CP foaming) process was developed to fabricate polypropylene (PP) foams with closed re-entrant cell structures. The re-entrant cellular structure was realized by the combined effect of the cell over expansion during the vacuum treatment stage right after the depressurization, and the rapid cell contraction under the counter pressure of the refilled air. The morphology of the re-entrant structure could be tuned by adjusting the key processing parameters. By using butanol and scCO 2 as the co-blowing agent, the over expansion and rapid contraction of cells were greatly amplified due to the plasticizing, vaporization, and liquidation of the butanol in the V-CP process. The fabricated PP re-entrant foams that have a negative Poisson's ratio possess prominent compressive properties and impact energy absorption performance. [Display omitted] • Vacuum-counter pressure-assisted scCO 2 foaming process was developed to fabricate PP foams with re-entrant cell structures. • By using butanol and scCO 2 as the blowing agent, the over expansion and rapid contraction of cells were greatly amplified. • PP re-entrant foam has a significant increase in energy absorption compared with PP conventional foam. [ABSTRACT FROM AUTHOR]

• It is a timely and comprehensive review on the quick progress of Zn anode interface. • A detailed analysis of the challenges hindering stable zinc anode interface are introduced. • Strategies to tailor Zn metal anode interface are presented. • Highly stable Zn anode interface is promising for commercial applications. In recent years, zinc metal batteries (ZMBs) have become an important alternative to lithium-ion batteries due to their high energy density, high safety, and low cost. However, the development of ZMBs still encounters several challenges such as dendrite growth, hydrogen evolution, corrosion, and passivation. These issues likely contribute to the instability of the zinc anode/electrolyte interface, hindering practical applications of zinc batteries. Recently, extensive research on the zinc anode/electrolyte interface has been conducted globally; therefore, a comprehensive review is warranted. Initially, this paper discusses the fundamentals of the zinc anode interface and the related issues arising from its intrinsic instability. Subsequently, it systematically summarizes various effective strategies for regulating the interface including zinc anode surface modification, electrolyte regulation, zinc anode structure design, and separator optimization. Finally, it concludes with a prospect on addressing challenges and providing perspectives for optimizing the zinc anode interface in order to achieve high-performance ZMBs. [ABSTRACT FROM AUTHOR]

• A conductive fiber with synergistic conductive network is prepared for strain sensor. • The synergistic effect is beneficial for tunable and balanced sensing performances. • The sensor shows great potential for human motion monitoring and tactile sensing. • The fiber displays good photothermal performances even under 150% strain. With the rapid development of portable electronic products, smart wearable devices show great application potential in personalized motion monitoring, health monitoring and even in human-machine interaction. In particular, high-performance flexible fiber-shaped strain sensors are receiving more and more attention because they can be well integrated with clothes or human skin for real-time human activities monitoring. However, achieving improved sensitivity, wide detection range, diverse applications and easy operation of them remains a challenge. Here, we adopt a simple wet-spinning technique to prepare a porous fiber-shaped carbon nanotubes (CNTs)/silver nanoparticles (AgNPs)/thermoplastic polyurethane (TPU) fiber (CATF) for high-performance strain sensor, of which the synergistic conductive network of CNTs and AgNPs enables a wide detection range (∼248 %), high sensitivity (GF > 4295), fast response/recovery time (120 ms/140 ms) and excellent stability. Interestingly, strain sensing range and sensitivity of the sensor can be tuned by changing the AgNPs loading to make it suitable for different application scenarios. All the merits of the sensor make it capable for diverse human movements monitoring, pronunciation recognition, and gesture recognition. More importantly, our prepared CATF strain sensor can be easily weaved into wearable smart textiles, showing great potential for tactile sensing to realize multi-touch and pressure tracking. Finally, the CATF also displays efficient photothermal conversion capability even under different tensile strains up to 150 %, showing great potential in human body thermal management to improve the wearing comfort of wearable electronic fabric. [ABSTRACT FROM AUTHOR]

[Display omitted] • Higher quenching temperature and longer quenching period facilitate SC crystal formation. • The addition of deionized water to the solvent effectively enhances the formation of SC crystals. • The introduction of carbon nanotubes (CNTs) as a nucleating agent significantly impacts SC crystals formation. The formation of stereo-complex crystals (SC) in porous poly (lactic acid) (PLA) material is intricately linked with improving its comprehensive properties. In this work, the effects of process conditions, solvent composition and additional nucleating agent on SC crystals during the fabrication of porous PLA through thermally-induced phase separation method were studied. Crystallization behavior of SC crystals during the pore-forming process is systematically investigated, revealing that higher quenching temperature and longer quenching period facilitate the formation of SC crystals. Additionally, the addition of deionized water to the solvent effectively enhances SC crystals formation by reducing solution viscosity and prolonging the phase separation time. The highest crystallinity of SC crystals (X SC) can be achieved, reaching 30.6%, when the water content is controlled at 1.6%. Furthermore, the introduction of carbon nanotubes (CNTs) as a nucleating agent exhibits a pronounced effect on the formation of SC crystals. When incorporating a 3 wt% content of CNTs, X SC reaches its peak value at 37.7%. This work is helpful to provide reference for improving mechanical properties and heat resistance of porous PLA, thereby expanding its potential outdoor applications. [ABSTRACT FROM AUTHOR]

Benefitting from the wearability, ductility and portability, flexible and stretchable strain sensors display a more extensive field of applications than traditional sensors in terms of medical diagnosis, smart home, environmental monitoring and so on. However, the critical sensing performances, such as sensitivity, sensing range, stability and detection limit of flexible strain sensors still need to be improved. Microstructural optimization has been considered as an efficient strategy for tuning the performances. In this work, a carbon nanotubes (CNTs)/carbon black (CB)/thermoplastic polyurethane (TPU) fibrous film (CCTF) is prepared through electrospinning, spraying and ultrasonic anchoring technique. Synergetic conductive layers by combining CNTs/CB and CB are constructed on both sides of CCTF. In virtue of the optimization of microstructures and the synergetic conductive network, the obtained CCTF possesses an ultrawide response range (up to 500 % strain), high sensitivity (gauge factor, GF up to 1516), short response/recovery time (80/80 ms), low detection limit (0.05 % strain), favorable sensing stability and long-term durability. CCTF with excellent strain sensing performances is assembled as a strain sensor, which accounts for full range human biological signal acquisition, including joint movements, muscle tension, and facial micro-expressions. This paper provides a certain reference significance for the preparation and fabrication of next-generation flexible strain sensors with high performances. A flexible strain sensor based on carbon nanotubes (CNTs)/carbon black (CB)/thermoplastic polyurethane (TPU) film (CCTF) is fabricated through electrospinning, spraying and ultrasonic anchoring technologies. CCTF possesses excellent sensing performance due to the optimization of the microstructure, achieving a wide sensing range (up to 500 % strain), high sensitivity (GF up to 1516), low detection limit (0.05 % strain), and short response/recovery time (80/80 ms). [Display omitted] • A fibrous strain sensor with synergetic conductive networks of CNTs/CB and CB is fabricated. • The sensor possesses both a wide sensing range (500 % strain) and high sensitivity (GF up to 1516). • Low detection limit (0.05 % strain) and short response/recovery time have also been achieved. • The sensor is demonstrated to precise full range human biological signal acquisition. [ABSTRACT FROM AUTHOR]

Metal-organic frameworks (MOF)-polymer hybrid hydrogel solves the processable forming of MOF powder and energy consumption of uranium extraction. However, the hybrid hydrogel by conventional synthesis methods inevitably lead to MOF agglomeration, poor filler-polymer interfacial compatibility and slowly adsorption. Herein, we designed that ZIF-67 was implanted into the carboxymethyl cellulose/polyacrylamide (CMC/PAM) by network-repairing strategy. The carboxyl and amino groups on the surface of CMC/PAM drive the uniform growth of ZIF-67 inside the CMC/PAM, which form an array of oriented and penetrating microchannels through coordination bonds. Our strategy eliminate the ZIF-67 agglomeration, increase the interfacial compatibility between MOF and polymer. The method also improve the free and fast diffusion of uranium in CMC/PAM/ZIF-67 hydrogel. According to the experimental, these enhancements synergistically enabled the CMC/PAM/ZIF-67 have a maximum adsorption capacity of 952 mg g−1. The adsorption process of CMC/PAM/ZIF-67 fits well with pseudo-second-order model and Langmuir isotherm. Meanwhile, the CMC/PAM/ZIF-67 maintain a high removal rate (87.3 %) and chemical stability even during ten adsorption-desorption cycles. It is worth noting that the adsorption amount of CMC/PAM/ZIF-67 in real seawater is 9.95 mg g−1 after 20 days, which is an ideal candidate adsorbent for uranium extraction from seawater. • The CMC/PAM/ZIF-67 aerogel is successfully designed via network-repairing strategy. • The CMC/PAM/ZIF-67 aerogel has a maximum adsorption capacity of 952 mg g−1 at pH = 5. • The adsorption capacity of CMC/PAM/ZIF-67 aerogel in real seawater is 9.95 mg g−1 after 20 days. [ABSTRACT FROM AUTHOR]

Metal-organic frameworks (MOF)-polymer hybrid hydrogel solves the processable forming of MOF powder and energy consumption of uranium extraction. However, the hybrid hydrogel by conventional synthesis methods inevitably lead to MOF agglomeration, poor filler-polymer interfacial compatibility and slowly adsorption. Herein, we designed that ZIF-67 was implanted into the carboxymethyl cellulose/polyacrylamide (CMC/PAM) by network-repairing strategy. The carboxyl and amino groups on the surface of CMC/PAM drive the uniform growth of ZIF-67 inside the CMC/PAM, which form an array of oriented and penetrating microchannels through coordination bonds. Our strategy eliminate the ZIF-67 agglomeration, increase the interfacial compatibility between MOF and polymer. The method also improve the free and fast diffusion of uranium in CMC/PAM/ZIF-67 hydrogel. According to the experimental, these enhancements synergistically enabled the CMC/PAM/ZIF-67 have a maximum adsorption capacity of 952 mg g−1. The adsorption process of CMC/PAM/ZIF-67 fits well with pseudo-second-order model and Langmuir isotherm. Meanwhile, the CMC/PAM/ZIF-67 maintain a high removal rate (87.3 %) and chemical stability even during ten adsorption-desorption cycles. It is worth noting that the adsorption amount of CMC/PAM/ZIF-67 in real seawater is 9.95 mg g−1 after 20 days, which is an ideal candidate adsorbent for uranium extraction from seawater. • The CMC/PAM/ZIF-67 aerogel is successfully designed via network-repairing strategy. • The CMC/PAM/ZIF-67 aerogel has a maximum adsorption capacity of 952 mg g−1 at pH = 5. • The adsorption capacity of CMC/PAM/ZIF-67 aerogel in real seawater is 9.95 mg g−1 after 20 days. [ABSTRACT FROM AUTHOR]

Nowadays, passive radiative cooling (PRC) has being attracted intensive attention because it can realize cooling effect without consuming any energy. Unfortunately, fabricating polymer film with radiative cooling effect by a facile, continuous and environmentally friendly method is still a large challenge. In this study, high density polyethylene (HDPE)/polyvinyl oxide (PEO) film were first fabricated by melt extrusion casting method, and polyethylene film composed of directional microfibrils (PFCDM) were finally obtained after selective dissolution of PEO phase in deionized water at 70 °C. The as-prepared PFCDM shows higher average solar reflectivity of 85.17% in the visible range and stronger average mid-infrared emissivity of 82.04% within the atmospheric window. It shows a sub-ambient cooling of 23.28 °C during the day and 3.1 °C at night, suggesting that it has a remarkable PRC performance. Moreover, the as-prepared PFCDM has outstanding wearability and self-cleaning property, showing promising potential of personal thermal management. This study proposes a facile but environmentally friendly method for fabricating PFCDM, paving a new way to develop wearable PRC film following the concept of thermoplastic polymers "functionalized" processing. [Display omitted] • PFCDM was efficiently prepared via melt extrusion casting and water leaching. • PFCDM shows remarkable passive radiative cooling performance. • PFCDM has higher day and night cooling power. • PFCDM has outstanding wearability and self-cleaning property. [ABSTRACT FROM AUTHOR]

Flexible transparent electromagnetic interference (EMI) shielding films in visual windows are crucial for the innovation of optoelectronic devices, but the challenge of balancing light transmittance and EMI shielding effectiveness (SE) still exists. Herein, this work described a flexible transparent MXene@SWNTs/PC film with a hierarchical conductive layer that was fabricated via an alternating rotation spraying method. The multi-scale hierarchical structure configured with 1D SWNTs and 2D MXene endow the obtained film with good comprehensive properties, i. e, low sheet resistance of 32.8 Ω/sq at 56.1% light transmittance, thus causing a satisfactory EMI SE of 20.8 dB. Moreover, the transparent shielding films exhibit remarkable flexibility, which can maintain steady EMI SE after 1000 continuous bending cycles. More importantly, the low sheet resistance and high light absorption capacity of hybrid conductive layer facilitate the transparent shielding film with low-voltage-driven electric heating effect and outstanding photothermal conversion ability, respectively, ensuring the normal operation under extreme cold condition. The combination of good light transmittance, satisfactory EMI shielding performance, and multi-source thermal response enables MXene@SWNTs/PC film to have great potential as a transparent shielding film in emerging optoelectronic devices. A multifunctional MXene@SWNTs/PC film with hierarchical structure prepared via an alternating rotation spraying process, integrating capabilities of light transmittance, EMI shielding, and multi-source thermal response together. [Display omitted] [ABSTRACT FROM AUTHOR]

Using solar energy for freshwater generation presents an effective and economical solution to address water shortages. Here, we introduced a structural strategy involving the incorporation of fixed-shape inverted pyramid-shaped grooves onto the evaporator surface. This innovation approach integrated delignified wood and MXene-based photothermal material to establish an interfacial solar steam generator (ISSG) dedicated to freshwater production. The carefully designed surface structure empowered the ISSG with remarkable heat localization capabilities, resulting in an exceptional steam generation capacity and resistance against salt deposition. The as-prepared sample, labeled MIDW-5, achieved an impressive evaporation rate of 1.927 kg m−2 h−1. Furthermore, the simulation results by COMSOL are in agreement with the experimental results. Therefore, the incorporation of MXene into delignified wood, complemented by the imprinted structure, yields a high-performance evaporator with substantial potential for low-cost freshwater production. • A MXene@wood evaporator with inverted pyramid-shaped grooves was constructed. • The evaporator has excellent thermal localization efficiency. • The evaporator shows splendid high light absorption and evaporate rate. • The evaporator is easy to prepare and environmentally friendly. • The evaporator performs outstanding desalting performance. [ABSTRACT FROM AUTHOR]

[Display omitted] • An aligned TPU electrospun mat with wave-like structure is selected as the substrate. • The microcrack structure is constructed by pre-stretching technology. • The strain sensor can achieve sign language interpretation and multi-angle recognition. • The visual sensing function expands the application area of the CNTs/AgNWs/TPU sensor. Recently, flexible strain sensors have attracted great attention on account of the application potential in medical treatment, flexible prosthetics and human–machine interaction. Nevertheless, traditional uniaxial strain sensors cannot detect movement in different directions, limiting the applications in sensing technologies. In addition, it is still a significant challenge to simultaneously acquire visualized and high-performance strain sensors. Here, a highly flexible sensor with visual sensing function was fabricated by spraying silver nanowires (AgNWs)/carbon nanotubes (CNTs) ink on the aligned thermoplastic polyurethane (TPU) electrospun mat. The sensing performances of AgNWs/CNTs aligned TPU fluorescent mats (ACUM-F) are individually explored in vertical and parallel directions. Herein, the ACUM-F in vertical can exhibit high sensitivity (gauge factor (GF) up to 244.3), wide working range (0.1 ∼ 380 % strain), fast response/recovery time (80 ms/80 ms), good sensing durability and reproducibility (1000 stretching/releasing test cycles). Furthermore, ACUM-F is assembled as strain sensors to monitor various human body movements, which can achieve sign language interpretation through finger gesture monitoring, demonstrating its great potential in human–machine interaction. The direction-aware application of novel multidirectional sensors with visual sensing functions may bring inspiration for a new era of flexible electronics development. [ABSTRACT FROM AUTHOR]

Poly(lactic acid) (PLA) inherently shows the distinct brittleness at room temperature, which is a major drawback limiting its practical applications. Great efforts have been done to improve the toughness by adding high content of flexible polymers or low content of nanoparticles, which is often at the expense of tensile strength. In this work, supertoughened PLA blend with high elongation at break (247.7%) containing low content of poly(ethylene oxide) (PEO) (8%) was directly fabricated by melt extrusion method. Interestingly, its tensile strength and modulus are only slightly decreased (<25%). The reasons for the balanced mechanical property can be understood as follows: I) The increasing mobility of amorphous chains of PLA due to the plasticizing effect of PEO. II) The strengthening effect of mesophase can hinder tensile strength to be severely sacrificed. III) The rod-like PEO phase can initiate more crazes and further prevents them from developing into cracks, allowing effective energy dissipation. This study proposes a facile but efficient strategy to fabricate PLA blends containing low content of PEO with balanced mechanical property, which would provide a clue for toughening other brittle thermoplastics. [Display omitted] • PLA blend with balanced mechanical property is directly prepared by melt extrusion. • A low content of PEO can realize the supertoughness of PLA. • The tensile strength and modulus are only slightly decreased. • Mesophase and rod-like phase morphology are keys to supertoughness. [ABSTRACT FROM AUTHOR]

To get strong and anti-freezing hydrogel with multiple contact and non-contact sensing performance, a facial method is proposed in this work using multiple physical bonding crosslinking and glycerol (GL) immersing strategy. The obtained hydrogels show a tensile stress at break of 5.4 MPa, an elongation at break of 1420 %, and a compression strength of 12.2 MPa at 80 % strain. Additionally, benefiting from the GL immersing the hydrogel shows superior anti-freezing (no ice formation at −60 °C) and water retention ability (water loss less than 17 % after storing at 50 °C for 7 h). Furthermore, the volume resistance of hydrogels exhibits excellent responses against humidity, temperature, strain, and stress. The variation of the resistance against temperature can be well described by the Arrhenius equation with an activation energy of 501.3 meV, verifying a band-gap dominated diffusion hopping conductive mechanism of the hydrogel. The sufficient humidity and temperature responses make the hydrogel applicable as a non-contact sensor, and the wide temperature strain sensing (−40 to 50 °C) and stress sensing capability ensures that the hydrogel can be used as a contact sensor, ensuring that the hydrogel can be used as perfect flexible sensor for monitoring human motion and physiological signals. [Display omitted] • Strong and anti-freezing hydrogel with multiple sensing performance is obtained. • The hydrogel is prepared using multiple physical bonding crosslinking and glycerol immersing strategy. • The resistance variation against temperature is described by the Arrhenius equation with an activation energy of 501.3 meV. [ABSTRACT FROM AUTHOR]

Addressing water pollution issues is directly related to green sustainable development. In this work, a heterostructure polyurethane-based (PU) sponge was prepared by a facile "dip-adhere" strategy to achieve simultaneous and efficient removal of oils and dyes from water. This innovatively designed sponge comprises two functional layers. The hydrophobic/lipophilic octadecylamine-molybdenum disulfide coated PU sponge (ODA-MoS 2 @PU) layer exhibits excellent sorption capacity, ranging from 37.35 to 63.52 times its own weight, for eight organic solvents (DMSO, isopropanol, n-hexane, petroleum ether, n-butanol, glycol, acetone, xylene) and five oils (soybean oil, olive oil, gasoline, diesel, and lubrication). Furthermore, it exhibits robust stability in extreme environments and maintains a high separation efficiency (99 % after 50 separations). The photocatalytic/superhydrophilic polydopamine-molybdenum disulfide coated PU sponge (PDA-MoS 2 @PU) layer demonstrates great photocatalytic degradation efficiency for dyes (96.80 % for methylene blue and 97.39 % for methyl orange). Consequently, the heterostructure PU sponge holds application potential in environment remediation. [Display omitted] • A dual-functional heterostructure sponge was prepared. • Continuous oil-water separation was realized with the oil-gathering device. • The simultaneous treatment of removing oils and dyes was achieved. [ABSTRACT FROM AUTHOR]

For smart devices, there is a growing demand for multi-functional soft actuators, nevertheless, well-developed actuators always respond to single stimulus, and it is still challenging to achieve the application diversity standards. Herein, a bidirectional multi-stimuli responsive soft actuator based on Ti 3 C 2 T X MXene-cellulose nanowhiskers (CNWs)-polyvinyl alcohol (PVA)/polydimethylsiloxane (PDMS) multilayer membranes is proposed (MXCP-P). By grafting CNWs onto MXene nanosheets, a freestanding composite film with gradient layered structure was prepared. Due to the hygroscopicity among MXene nanosheets, increased interlayer space is in favor of adsorption/desorption of water molecules, causing invertible shape change and humidity-driven deformation with a rapid response. Based on high photothermal conversion capacity of MXene and large difference of coefficient of thermal expansion between PDMS and MXene, the MXCP-P achieves an ultra-large amplitude and fast response driven by natural light. A Venus flytrap soft robot is constructed with good actuation behaviors. The MXCP-P film was employed as actuators in the opera of The Male Phoenix Pursui from Han Dynasty and in shadow puppetry "Monkey King Subdus the White-Bone Demon" of China, both exhibiting excellent performances towards humidity and light stimuli synchronously. This paper inspires a new strategy for multi-stimuli responsive soft bionic robots and intelligent traditional shadow play. MXCP-P based multi-stimuli responsive flexible actuator was fabricated, showing improved mechanical properties and bidirectional bending characteristics. In addition to its application in traditional fly traps and rolling robots, the MXCP-P actuator is also employed to develop traditional Chinese opera culture, such as "The Male Phoenix Pursui" and "Shadow puppetry". [Display omitted] [ABSTRACT FROM AUTHOR]

[Display omitted] • Self-adhesive, self-healing and multimodal sensing organohydrogel was prepared. • Environmental stability of organohydrogel is enhanced by glycerol and PA. • The organohydrogel shows wide humidity response and temperature detection range. • The organohydrogel displays reliable strain sensing ability in a wide strain range. Conductive hydrogel (CH) has drawn widespread interest in flexible electronics, human–computer interaction, and electronic skins (e-skins). However, it is challenging to integrate satisfactory self-adhesion, self-healing, environmental stability, and multi-stimulus response into a single CH system. Herein, a conductive nanocomposite organohydrogel with the above characteristics is well-designed and developed via incorporating carboxylic cellulose nanofibers-carrying carboxylic carbon nanotubes (C-CNTs) and phytic acid (PA) into polyacrylamide network through free-radical polymerization plus glycerol solvent displacement strategy, aiming for a high-performance multimodal sensing platform. Here, the coupling of C-CNTs and ionization of PA contributes a favorable conductivity, and the coexistence of glycerol and PA is beneficial for the formation of amounts of hydrogen bonds that endow the organohydrogel with outstanding stretchability, self-healing, and favorable adhesion in a wide temperature range of −30 to 60 °C. Besides, the resultant organohydrogel can effectively detect multiple external stimuli, manifesting high strain sensitivity over a broad strain range (0–1566 %), good humidity detectability at 0–85 % RH, and reliable thermosensation capability over a wide temperature window (−30 to 60 °C). Significantly, the application of the organohydrogel as e-skins are conducted to detect full-range human activity movements even in the extreme environments, identify hand gestures, and recognize the spatial distribution of humidity in noncontact sensing. All these indicate the preponderance of our organohydrogel in the fields of flexible smart electronics. [ABSTRACT FROM AUTHOR]

• Layer-by-layer scraping can produce a powerful shearing effect for UHPE/GNPs gel. • Strong shearing induced dense stacking and ordered alignment of GNPs and PE chains. • The dense and ordered structure drastically enhanced in-plane TC up to 28.88 W/mK. • The solar-thermal conversion ability was also improved by the ordered structure. The simultaneous achievement of ordered alignment for fillers and polymer matrix is highly desired in polymer-based thermally conductive composites, but it is still extremely challenging. Herein, we put forward a layer-by-layer scraping (LbLS) method to simultaneously arrange ultra-high molecular weight polyethylene (UHPE) chains and graphene nanoplates (GNP) into a highly oriented structure. When UHPE/GNP gel suffering the strong shearing effect during LbLS process, the inner UHPE chains and GNP were dragged and orderly arranged along shearing direction, and these oriented structures were retained after rapidly drying by distillation. After layer-by-layer stacking, nacre-like UHPE/GNP films with tightly layered structure were obtained. By adjusting the scraping gap from 200 to 50 μm, the oriented structure can be effectively reinforced with the Herman orientation factors f increasing from 0.83 to 0.88 for GNP and 0.75 to 0.82 for UHPE chains. The highly ordered structure can form a tight and oriented thermal conduction network with low interfacial thermal resistance in plane. The LbLS composite film thus significantly enhanced the in-plane thermal conductivity up to 28.88 W/mK, compared with traditional solution casting film (9.63 W/mK). Moreover, the highly oriented structure can significantly increase the solar-thermal conversion performance (58.1 °C@100 mW/cm2) by improving its light absorption ability comparing to that of solution casting film. Besides, the mechanical strength and toughness that depend on the filler and chain alignment were effectively increased by the oriented structure. [ABSTRACT FROM AUTHOR]

[Display omitted] • Breathable electronic skin with 3D skeleton and microcrack structures is designed. • High sensitivity and wide working range are realized for the strain sensor. • The strain sensor can accurately distinguish various human movements. • The device has photo-thermo-electric and self-powered sensing applications. With the rapid development of wearable electronic, electronic skin with excellent performance for human motion detection have been widely investigated recently. In this work, a multifunctional electronic skin with three-dimensional conductive network skeleton was prepared based on synergistic conductive filler (carboxylated multi-walled carbon nanotubes (C-MWCNT) and poly(3,4-ethylenedioxythiophene):poly(styrenesulfonic acid) (PEDOT:PSS)) decorated breathable thermoplastic polyurethane (TPU) electrospinning fibrous membrane. Then, microcrack structure was constructed via pre-stretching and the strain sensitivity of the resultant C-MWCNT/PEDOT:PSS/TPU (CPT) conductive fibrous membrane could be effectively adjusted by changing the microcrack density. Due to the three-dimensional conductive network skeleton, microcrack structure and the bridging effect of C-MWCNT between the adjacent crack fragments, ethylene glycol treated CPT (mass ratio of C-MWCNT and PEDOT:PSS is 9/1) (e-CPT 9/1) strain sensor exhibited high sensitivity (6008.3), wide response range (680 %), fast response/recovery time (200 ms/200 ms), low detection limit (0.5 %), excellent durability and repeatability (6000 cycles). The excellent strain sensing performances enables it to accurately monitor motion activities and physiological signals, and can also be used as a smart sensing glove to identify different letters gesture and numeric gestures. Furthermore, owing to the photothermal conversion ability and thermoelectric effect of C-MWCNT and PEDOT:PSS, the obtained e-CPT 9/1 device also displayed efficient "light-thermal-electric" conversion ability and showed the great potential as self-powered strain sensor. [ABSTRACT FROM AUTHOR]

Polyimide foams (PIFs) are usually synthesized by solution polymerization, followed by chemical foaming to prepare thermosetting foam. In this research, lightweight microcellular thermoplastic polyimide foams (TPIFs) were fabricated via a novel two-step foaming approach using supercritical carbon dioxide (scCO 2) as a blowing agent. The poly(amic acid) (PAA) and polyester ammonium salt (PEAS) precursor solutions were synthesized with pyromellitic dianhydride (PMDA) as dianhydride reagents and polyether amine Jeffamine D230 as aliphatic diamine reagent via blending and solution polymerization, respectively. The solution polymerization process demonstrated a higher molecular weight and superior formability than the blending process. The optimum thermal imidization temperature of 200 °C was optimized via the thermal and rheological property analysis. The cell morphology and mechanical properties of the TPIFs could be turned by varying the saturation time, foaming pressure, and imidization temperature. At a thermal imidization temperature of 200 °C, the TPIFs exhibited a branched structure with a small mean cell diameter (123.78 μm), and a high compressive strength (0.4 MPa) under 10 % strain at high temperature and pressure, which was more than ten times that of the TPIFs with thermal imidization temperature of 130 °C. This research provides a feasible method for producing high volume expansion ratio TPIFs with adjustable microcellular structures and outstanding mechanical properties. [Display omitted] • Poly(amic acid) and polyester ammonium salt precursor were synthesized by blending and solution polymerization, respectively. • Adding a flexible linkage provided the torsional capacity of the chain segment, and improved its flexibility. • Microcellular TPI foams were fabricated via a novel two-step foaming approach using supercritical CO 2 as a blowing agent. • The branched molecular structure was favourable for improving cell uniformity and mechanical properties. [ABSTRACT FROM AUTHOR]

With the rapid development of multi-function touch panels, more requirements are raised for touch screens including anti-smudge, anti-fingerprint, and high wear resistance, hardness, and UV resistance. Herein, ladder-like poly(2-(3,4-epoxycyclohexyl)ethyltrimethoxy- co -1H,1H,2H,2H-perfluorodecyltriethoxysilsesquioxane)s (LPEFSQs) were synthesized by the sol-gel reaction of 2-(3,4-Epoxycyclohexyl)ethyltrimethoxysilane (ECTMS) with 1H,1H,2H,2H-Perfluorodecyltriethoxysilane (PFDTES) to reduce the surface energy of the coating. The incorporation of fluorine chains resulted in an improvement of water contact angle from 77.1° to 115.5°, and oil contact angle from 35.4° to 94.7°, respectively. The omniphobic property rendered the coating excellent anti-smudge and anti-fingerprint properties while maintaining an extraordinary visible light transparency of 90.1 %. A proper PFDTES fraction of 5 % and the curing agent of I-250 are desired for the coating to simultaneously realize excellent pencil hardness of 6H, anti-smudge, and wear resistance performance. The optimized LPEFSQ coating could withstand a steel wool abrasion for 500 cycles. In addition, the developed LPEFSQ coating maintained excellent omniphobicity when subjected to ultraviolet (UV) irradiation for 200 h demonstrating excellent UV resistance. Therefore, this work provides insights into the synthesis of multifunctional coatings integrated with high transparency, wear resistance, and hardness as well as anti-smudge, and anti-fingerprint properties for touch screens. [Display omitted] • A ladder-like polysesquioxane coating containing long fluorine chains is developed. • The coating has high transparency, omniphobic surface, and anti-fouling properties. • The UV curing agent I-250 rendered the coating superior hardness and wear resistance. • The coating has excellent mechanical robustness, anti-fingerprint, and UV resistance. [ABSTRACT FROM AUTHOR]