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Dense carbon nanofiber self-supporting electrode fabricated by orientation/compaction strategy for high volumetric lithium storage capacity

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Progress in Natural science:Materials International 2025年第1期35卷 229-237页

作者： Haihui Liu Chaoqun Chen Qiang Xu Yan Song Xiangwu Zhang Chang Ma Tianjin Municipal Key Lab of Advanced Fiber and Energy Storage Technology Tiangong University CAS Key Laboratory of Carbon Materials Institute of Coal Chemistry Chinese Academy of Sciences Fiber and Polymer Science Program Department of Textile Engineering Chemistry and Science Wilson College of Textiles North Carolina State University

Low bulk density greatly restricts the large-scale application of electrospun carbon-based fiber membrane as electrode in energy storage devices. To solve the above challenges, herein an orientation-compaction densification strategy is proposed to enhance the bulk density and volumetric capacity of PAN-based carbon nanofiber membranes as self-supporting electrode used in lithium-ion batteries（LIBs）. Specifically, highly-oriented fibers are achieved by high-speed roller collecting during electrospinning, and compaction densification is conducted by hot-pressing treatment. The effects of collecting speed and hot-pressing pressure on the morphology, conductivity,bulk density, tensile strength, and flexibility of the obtained carbon nanofiber membrane are *** to conventional fiber membranes, of which fibers are disorderly stacked, the oriented fiber membrane is much easier to achieve dense stacking by compaction. The obtained dense carbon nanofiber membrane demonstrates a bulk density of 0.566 g cm-3, and shows a significantly-enhanced volumetric capacity(318.3 mA h cm-3), high-rate performance(86.6 mA h cm-3at 5 A g-1), and satisfactory cycling stability when used as selfsupporting electrode of LIBs.

关键词： Bulk density Densification Electrospinning Orientation-compaction Volumetric capacity

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One-step fabrication of ultrathin porous Janus membrane within seconds for waterproof and breathable electronic skin

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science Bulletin 2025年第5期70卷 712-721页

作者： Yufeng Ni Bing Li Chengzhen Chu Shaofan Wang Yujie Jia Shichun Cao Rasoul Esmaeely Neisiany Chuanglong He Shuo Chen Zhengwei You State Key Laboratory of Advanced Fiber Materials Institute of Functional MaterialsCollege of Materials Science and EngineeringResearch Base of Textile Materials for Flexible Electronics and Biomedical Applications(China Textile Engineering Society)Shanghai Engineering Research Center of Nano-Biomaterials and Regenerative MedicineShanghai Key Laboratory of Lightweight CompositeDonghua UniversityShanghai 201620China College of Biological Science and Medical Engineering Donghua UniversityShanghai 201620China Department of Materials and Polymer Engineering Faculty of EngineeringHakim Sabzevari UniversitySabzevar***Iran Biotechnology Centre Silesian University of TechnologyGliwice44-100Poland

It remains a challenge for a simple and scalable method to fabricate ultrathin porous Janus membranes for stretchable on-skin ***,we propose a one-step droplet spreading phase separation strategy to prepare an ultrathin and easily collected Janus thermoplastic polyurethane(TPU)membrane within *** metal-ion solvation structure mitigated migration kinetics to delay TPU solution demixing,promoting the further penetration of the coagulating ***,the developed membranes,with an average preparation rate of 25.2 cm^(2)s^(−1),had a thickness of 5μm,and the water vapor transmission rate was determined to be 663 g m^(−2) d^(−1).The small pore layer having an average pore size of 1.7μm effectively blocked external liquid *** porous Janus TPU membrane coated by liquid metal served as a building block to develop a new generation of monolithic stretchable electronics with simultaneous high permeability and waterproofness.

关键词： porous polyurethane kinetics

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Graphene-functionalized textile composites for wearable Joule heating applications

Advanced Nanocomposites

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Advanced Nanocomposites 2025年 2卷 108-123页

作者： Omar Faruk Abbas Ahmed Ashfaqul Hoque Khadem Lu Jia Luyi Sun Department of Materials Science and Engineering Binghamton University State University of New York at Binghamton NY 13902 USA Polymer Program Institute of Materials Science and Department of Chemical & Biomolecular Engineering University of Connecticut Storrs CT 06269 USA Department Mechanical Engineering College of Engineering Computing and Applied Science Clemson University Clemson SC 29634 USA College of Textile Engineering Taiyuan University of Technology Jinzhong Shanxi 030600 China

Thermal comfort is essential for maintaining physiological well-being, with textile materials traditionally serving as the primary medium for regulating heat exchange between the body and its environment. However, conventional textiles often fall short of maintaining optimal thermal balance. So, there is an increasing demand for advanced thermoregulation systems that can effectively reduce heat loss and enhance warmth, ensuring consistent comfort. Recent research has highlighted the promise of advanced functional materials, especially graphene and its composites, for modifying textiles to improve thermal properties. This article comprehensively reviews recent advancements in graphene-functionalized textile composites, focusing on their applications in wearable Joule heaters designed for personalized thermal comfort or thermal therapy. Various graphene-functionalized textile composites are reviewed from the perspectives of material properties, processing strategies and device fabrication methods. Key challenges and future opportunities are summarized for graphene-functionalized textile-based Joule heaters as innovative solutions in wearable thermal regulation.

关键词： Graphene textile Composite Wearable electronics Joule heater

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一步秒级制备超薄多孔Janus膜及其在防水透气电子皮肤的应用（英文）

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science Bulletin 2025年第5期 712-721页

作者：倪宇峰李兵储成臻王少凡贾宇杰曹诗春 Rasoul Esmaeely Neisiany 何创龙陈硕游正伟 State Key Laboratory of Advanced Fiber Materials Institute of Functional Materials College of Materials Science and Engineering Research Base of Textile Materials for Flexible Electronics and Biomedical Applications (China Textile Engineering Society) Shanghai Engineering Research Center of Nano-Biomaterials and Regenerative Medicine Shanghai Key Laboratory of Lightweight Composite Donghua University College of Biological Science and Medical Engineering Donghua University Department of Materials and Polymer Engineering Faculty of Engineering Hakim Sabzevari University Biotechnology Centre Silesian University of Technology

It remains a challenge for a simple and scalable method to fabricate ultrathin porous Janus membranes for stretchable on-skin ***,we propose a one-step droplet spreading phase separation strategy to prepare an ultrathin and easily collected Janus thermoplastic polyurethane （TPU） membrane within *** metal-ion solvation structure mitigated migration kinetics to delay TPU solution demixing,promoting the further penetration of the coagulating ***,the developed membranes,with an average preparation rate of 25.2 cm2s-1,had a thickness of 5μm,and the water vapor transmission rate was determined to be 663 *** small pore layer having an average pore size of 1.7μm effectively blocked external liquid *** porous Janus TPU membrane coated by liquid metal served as a building block to develop a new generation of monolithic stretchable electronics with simultaneous high permeability and waterproofness.

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The Soft-Confined Method for Creating Molecular Models of Amorphous polymer Surfaces (vol 116, pg 1570, 2012)

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JOURNAL OF PHYSICAL CHEMISTRY B 2012年第8期116卷 2633-2633页

作者： Liu, Hongyi Li, Yan Krause, Wendy E. Rojas, Orlando J. Pasquinelli, Melissa A. †Fiber and Polymer Science Program and the Department of Textile Engineering Chemistry and Science North Carolina State University Raleigh NC 27695 United States

The goal of this work was to use molecular dynamics (MD) simulations to build amorphous surface layers of polypropylene (PP) and cellulose and to inspect their physical and interfacial properties. A new method to produce molecular models for these surfaces was developed, which involved the use of a “soft” confining layer comprised of a xenon crystal. This method compacts the polymers into a density distribution and a degree of molecular surface roughness that corresponds well to experimental values. In addition, calculated properties such as density, cohesive energy density, coefficient of thermal expansion, and the surface energy agree with experimental values and thus validate the use of soft confining layers. The method can be applied to polymers with a linear backbone such as PP as well as those whose backbones contain rings, such as cellulose. The developed PP and cellulose surfaces were characterized by their interactions with water. It was found that a water nanodroplet spreads on the amorphous cellulose surfaces, but there was no significant change in the dimension of the droplet on the PP surface; the resulting MD water contact angles on PP and amorphous cellulose surfaces were determined to be 106 and 33°, respectively. [ABSTRACT FROM AUTHOR]

关键词： MOLECULAR models AMORPHOUS substances SURFACES (Technology) INTERFACES (Physical sciences) MOLECULAR dynamics -- Simulation methods COMPACTING SURFACE energy

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High specific capacity lithium-ion batteries based on ZnO/MnO hybrid porous carbon nanofiber anode

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Journal of Power Sources 2025年 648卷

作者： Yang, Xiaochuan Wen, Shunfang Ji, Shuyu Zhang, Yu Zhang, Guangyu Li, Guang Dai, Jiamu Zhang, Wei Nie, Du College of Textile and Clothing National & Local Joint Engineering Research Center of Technical Fiber Composites for Safety and Protection Nantong University No.9 Seyuan Road Chongchuan District Nantong226019 China State Key Laboratory for Modification of Chemical Fibers and Polymer Materials College of Materials Science and Engineering Donghua University Shanghai 201620 China College of Materials Xiamen University 422 Siming Nan Road Xiamen361005 China

The development of anodes with high specific capacity and excellent cycle stability remains challenging, as the active material tends to undergo powdering and structural collapse during prolonged lithium/delithiation processes. In this study, we report a Zn7Mn7@PCNFs electrode designed based on the synergistic effects of multi-metal oxide-carbon composites. Porous nano carbon fibers forms a three-dimensional porous network, enabling rapid electron transfer via its large specific surface area. The integration of ZnO/MnO not only mitigates voltage attenuation during charge-discharge cycles but also enhances electrochemical performance. As a result, the material exhibits significantly improved specific capacity and cycle stability. Specifically, at a current density of 5 A g−1, the composite electrode exhibits a specific capacity of 425 mAh·g−1 and an initial coulombic efficiency of 65.7 %. Even after 2000 cycles at a current density of 1 A g−1, the electrode maintains a specific capacity of approximately 315 mAh·g−1, attributed to the high specific capacitance contributed by ZnO and MnO. This study offers innovative design strategies for utilizing multi-element co-doped carbon-metal hybrid materials in lithium-ion batteries. © 2025 Elsevier B.V.

关键词： Lithium-ion batteries

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Simultaneous Improvement of Mechanical Strength, Toughness, and Self-healability of Elastomers Enabled by F─H-Bond-Based Nanoconfinement

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Angewandte Chemie - International Edition 2025年 e202505848页

作者： Jia, Yujie Chu, Chengzhen Wu, Zekai Ni, Yufeng Cao, Shichun Liao, Tao Shi, Ce Men, Yongfeng Sun, Junfen You, Zhengwei State Key Laboratory of Advanced Fiber Materials Institute of Functional Materials College of Materials Science and Engineering Research Base of Textile Materials for Flexible Electronics and Biomedical Applications (China Textile Engineering Society) Shanghai Engineering Research Center of Nano-Biomaterials and Regenerative Medicine Donghua University 2999 North Renmin Road Shanghai 201620 China State Key Laboratory of Polymer Science and Technology Changchun Institute of Applied Chemistry Chinese Academy of Sciences Renmin Street 5625 Changchun 130022 China

There are often trade-offs among high mechanical strength, high toughness, and efficient self-healing. Herein, we present a biomimetic strategy utilizing F─H bonds for nanoconfinement to achieve the simultaneous enhancement of these conflicting properties. The mechanical strength, toughness, and self-healing efficiency of a fluorinated crosslinked poly(urethane-urea) (CPUU-FA) elastomer are improved 1.3-, 1.5-, and 1.2-fold, respectively, compared with those of its nonfluorinated counterpart. Notably, the CPUU-FA has the highest recorded puncture energy (887 mJ) among polymeric elastomers and the highest fracture energy (117 kJ m⁻²) among reported thermoset elastomers. Moreover, it exhibits excellent self-healing efficiency (99%), remarkable reprocessability, and a low surface energy (56 MJ m⁻²). The application of self-healing elastomers in the fabrication of soft electronics is further demonstrated. The molecular design strategy is anticipated to inspire new developments in high-performance materials for cutting-edge applications. © 2025 Wiley-VCH GmbH.

关键词： Elastomers F─H bonds Poly(urethane-urea) Self-healing

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Polyacrylonitrile Nanofber‑Reinforced Flexible Single‑Ion Conducting polymer Electrolyte for High‑Performance,Room‑Temperature All‑Solid‑State Li‑Metal Batteries

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Advanced fiber Materials 2022年第3期4卷 532-546页

作者： Hui Cheng Chaoyi Yan Raphael Orenstein Mahmut Dirican Shuzhen Wei Nakarin Subjalearndee Xiangwu Zhang Fiber and Polymer Science Program Department of Textile EngineeringChemistry and ScienceWilson College of TextilesNorth Carolina State UniversityRaleighNC 27695USA

Single-ion conducting polymer electrolytes(SIPEs)can be formed by anchoring charge delocalized anions on the side chains of a crosslinked polymer matrix,thereby eliminating the severe concentration polarization efect in conventional dual-ion polymer *** of a plasticizer into the polymer matrix confers advantages of both liquid and solid ***,plasticized SIPEs usually face a trade-of between conductivity and mechanical *** insufcient strength,potentially there is short-circuiting failure during *** address this challenge,a simple and mechanicallyrobust SIPE was developed by crosslinking monomer lithium(4-styrenesulfonyl)(trifuoromethylsulfonyl)imide(LiSTFSI)and crosslinker poly(ethylene glycol)diacrylate(PEGDA),with plasticizer propylene carbonate(PC),on electrospun polyacrylonitrile nanofbers(PAN-NFs).The well-fabricated polymer matrix provided fast and efective Li^(+) conductive pathways with a remarkable ionic conductivity of 8.09×10^(-4) S cm^(−1) and a superior lithium-ion transference number close to unity(t_(Li+)=0.92).The introduction of PAN-NFs not only improved the mechanical strength and fexibility but also endowed the plasticized SIPE with a wide electrochemical stability window(4.9 V ***^(+)/Li)and better cycling *** longterm lithium cycling stability and dynamic interfacial compatibility were demonstrated by lithium symmetric cell *** importantly,the assembled all-solid-state Li metal batteries showed stable cycling performance and remarkable rate capability both in low and high current ***,this straightforward and mechanically reinforced SIPE exhibits great potential in the development of advanced all-solid-state Li-metal batteries.

关键词： Single-ion conducting polymer electrolyte Electrospun nanofbers Mechanical properties All-solid-state batteries Rate capability

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EXTRUSION, fiber FORMATION, AND CHARACTERIZATION OF THERMOTROPIC COPOLYESTERS

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JOURNAL OF polymer science PART B-polymer PHYSICS 1988年第1期26卷 179-200页

作者： CUCULO, JA CHEN, GY Fiber and Polymer Science Program Department of Textile Chemistry North Carolina State University Raleigh North Carolina 27695

The flow behavior and the effect of the spinning conditions on the fiber properties and structure of poly(ethylene terephthalate) modified with 60 mol% p -hydroxybenzoic acid (PET/60PHB) were investigated. PET and its copolyesters with 28 and 80 mol% PHB were used as control samples. The melt of PET/60PHB at temperatures above 265°C exhibited extremely low viscosity and low flow activation energy. High birefringence, indicating the presence of a mesophase, was observed between 265 and 300°C on a hot-stage polarizing light microscope. The maximum tensile strength and initial modulus, 438 MPa and 37 GPa, respectively, were obtained at 275°C for a 0.69 IV polymer. The fiber strength and modulus were significantly lowered when extrusion was conducted at temperatures below 265°C. The fiber properties could also be improved when a high extrusion rate and/or a high draw down ratio was used. Scanning electron microscopy revealed that the fibers spun at temperatures above 265°C had a well-developed, highly oriented fibrillar structure. The fibers spun at lower temperatures, however, were poorly oriented and nonfibrillar in character. The high orientation and superior mechanical performance achieved at high temperatures were attributed to the presence of the nematic mesophase in the polymer melt.

关键词： POLYESTERS

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EFFECTS OF PRESSURE ON THE COMPRESSIBILITY AND CRYSTALLIZATION OF fiber-FORMING polymerS

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JOURNAL OF polymer science PART B-polymer PHYSICS 1983年第7期21卷 1091-1101页

作者： WEI, KY CUCULO, JA IHM, DW Fiber and Polymer Science Program Department of Textile Chemistry North Carolina State University Raleigh North Carolina 27650

The effects of pressure on the compressibility and crystallization of three fiber-forming polymers, poly(tetramethylene terephthalate), nylon 66, and Qiana® nylon, have been studied. The Instron capillary rheometer was adapted as a high-pressure dilatometer for all the high-pressure experiments. The compressibility results reaffirmed that polymers are highly compressible, and their compressibilities are nonlinear at temperatures above the glass transition temperatures. polymer melts show higher compressibility than do polymers in the solid state. The kinetics of crystallization of these polymer melts under high pressures were studied. Analysis of the data revealed low Avrami exponents at high pressures. It seems that the kinetics of crystallization of these polymers from the melt under high pressure are different from those at normal pressure. Crystallization temperatures of these polymers were also measured. The crystallization temperatures are considerably higher at higher pressures.

关键词： polymers

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