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Highly elastic and degradable vitrimeric elastomers using polycondensation

Chinese Chemical Letters 2024年第3期35卷 434-438页

作者： Yue Liu Yongshuang Huang Chao Li Guifu Si Min Chen Institutes of Physical Science and Information Technology Key Laboratory of Structure and Functional Regulation of Hybrid Materials of Ministry of EducationAnhui UniversityHefei 230601China CAS Key Laboratory of Soft Matter Chemistry Department of Polymer Science and EngineeringUniversity of Science and Technology of ChinaHefei 230026China

Introducing covalently crosslinked network to polymer matrix can merge the advantages in reprocessing and durability of *** this contribution,a series of high-performance vitrimeric elastomers were achieved via *** topological structures of polymers were tuned by varying the feeding ratios of bisacetoacetate,hex–substituted bisacetoacetate,bisamine and tris(2-aminoethyl)*** these structural manipulations,the vitrimeric elastomers presented great elastic recovery properties(strain recovery value up to 80%)benefiting from the introduction of long chain ***,the elastomers exhibited excellent reprocessing property,water vapor/oxygen barrier and adhesive ***,the elastomers could be degraded into monomer under acid conditions which enabled the elastomer synthesis again in closed loop recycling *** ease of the polycondensation in this work to prepare highly elastic and recyclable vitrimeric elastomers demonstrated exciting opportunities for the synthesis of sustainable polymers.

关键词： Polycondensation Vitrimeric elastomers Highly elastic Degradable polymers

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An interfacial robust and entire self-healing ionogel-elastomer hybrid for elastic electronics enables discretionary assembly and reconfiguration

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science China Chemistry 2024年第4期67卷 1316-1323页

作者： Lei Yang Lijie Sun Hongfei Huang Rasoul Esmaeely Neisiany Zhengwei You State Key Laboratory for Modification of Chemical Fibers and Polymer Materials Institute of Functional MaterialsCollege of Materials Science and EngineeringDonghua UniversityResearch Base of Textile Materials for Flexible Electronics and Biomedical Applications(China Textile Engineering Society)Shanghai Engineering Research Center of Nano-Biomaterials and Regenerative MedicineShanghai 201620China Department of Polymer Engineering Hakim Sabzevari UniversitySabzevar ***Iran Biotechnology Centre Silesian University of TechnologyGliwice 44-100Poland

Inspired by the multi-layer architecture of mammal skins,interfacial robust,stretchable,and entirely healable gel-elastomer hybrids hold great potential in diverse fields including biomedical devices,wearable electrical devices,and soft ***,existing gel-elastomer hybrids have numerous limitations including low interfacial bonding toughness,complex and time-consuming preparation process,unhealable,and ***,we propose a simple and general chemical strategy through the interfacial dynamic bonding between gel and elastomer to simultaneously address the abovementioned *** covalent bonds readily and repeatably covalent bonding ionogel and elastomer(interfacial toughness:390 J m^(-2)),endowed the hybrids with entire self-healing features like skin and enabled discretionary assembly and ***,this strategy resolved the troublesome contradiction between interfacial stability and *** advantage of the aforementioned features,we readily constructed a multi-module,self-healing,self-powered,and realtime monitoring of personal status integrated elastic electronics,which could simply reconfigure the output signal of elastic electronics into an input signal of the devices-braille keyboard.

关键词： ionogel elastomer interface bonding self-healing dynamic covalent bond

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CO_(2)-Sourced Poly(chloropropylene carbonate) with High Flame-Retardant Performance

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Chinese Journal of polymer science 2025年第1期43卷 110-119,I0010页

作者： Yue Gong Xiao-Feng Zhu Guan-Wen Yang Meng Ma Xu Wang Jie Xu Xin Shu Guang-Peng Wu MOE Key Laboratory of Macromolecular Synthesis and Functionalization Key Laboratory of Adsorption and Separation Materials&Technologies of Zhejiang ProvinceDepartment of Polymer Science and EngineeringZhejiang UniversityHangzhou 310058China Zhejiang Key Laboratory of Plastic Modification and Processing Technology College of Materials Science and EngineeringZhejiang University of Technology Hangzhou 310014China Shanxi Coal Chemical Industry Technology Research Institute Co Ltd.Xi'an 710100China

The alternating copolymer of CO_(2) with epoxide is a green plastic that can efficiently transform CO_(2) into valuable chemicals. Despite the significant advances made, the restricted practical application of CO_(2)-sourced polycarbonates due to their lack of functionality has hindered field development. We successfully demonstrated the flame retardancy of poly(chloropropylene carbonate) (PCPC), a perfectly alternating copolymer of epichlorohydrin (ECH) and CO_(2). This was prepared at a 200-gram scale using a high-efficacy tetranuclear organoborane catalyst. PCPC’s excellent flame-retardant performance has been proven by both the vertical combustion test (UL94 V-0) and the limiting oxygen index (LOI) value (29.1%). The underlaid flame-retardant mechanism of PCPC was clearly elucidated. As a result, we confirmed that the generated cyclic carbonates and concurrently released flame-retardant chlorine radicals, hydrogen chloride, and CO_(2) during combustion render PCPC an excellent flame retardant. Furthermore, we investigated the practicability of PCPC as a halogen-rich polymeric flame retardant by blending it with commercial bisphenol A polycarbonate (BPA-PC). PCPC upgraded the flame retardancy rating of BPA polycarbonate from V-2 to V-0 even with a mere 1 wt% addition. It is our hope that this result will prove useful in future developments of advanced CO_(2)-sourced polymeric materials.

关键词： Carbon dioxide Ring-Opening polymerization Organocatalysis Sustainable materials Flame-retardant polymer

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Magnesium implants with alternating magnetic field-enhanced hydrogen release and proton depletion for anti-infection treatment and tissue repair

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Bioactive materials 2024年第8期38卷 374-383页

作者： Nailin Yang Xiaoyuan Yang Shuning Cheng Xiang Gao Shumin Sun Xuan Huang Jun Ge Zhihui Han Cheng Huang Yuanjie Wang Chong Cheng Liang Cheng Macao Institute of Materials Science and Engineering Macao University of Science and TechnologyTaipa999078Macao SARChina Institute of Functional Nano&Soft Materials(FUNSOM) Jiangsu Key Laboratory for Carbon-Based Functional Materials and DevicesSoochow UniversitySuzhou215123China Department of Orthopedics The Second Affiliated Hospital of Soochow UniversitySuzhou215004China Department of Orthopedics The First Affiliated Hospital of Soochow UniversitySuzhou215006China College of Polymer Science and Engineering State Key Laboratory of Polymer Materials EngineeringSichuan UniversityChengdu610065China

Implant-related osteomyelitis is a formidable hurdle in the clinical setting and is characterized by inflammation,infection,and consequential bone ***,effective reactive oxygen species(ROS)scavenging,bacterial killing,and subsequent bone tissue repair are urgently needed for the treatment of difficult-to-heal ***,we utilized the eddy-thermal effect of magnesium(Mg)implants under an alternating magnetic field(AMF)for the controlled release of H_(2)gas and ions(OH^(-)and Mg^(2+))for the treatment of osteomyelitis.H_(2)released by Mg rods under AMFs effectively scavenged cytotoxic ROS,exhibiting anti-inflammatory effects and consequently disrupting the environment of bacterial *** addition,the OH-hindered the energy metabolism of bacteria by effectively neutralizing protons within the ***,H_(2)impaired the permeability of bacterial membranes and expedited the damage induced by OH-.This synergistic AMF-induced H_(2)and proton depletion treatment approach not only killed both gram-negative and gram-positive bacteria but also effectively treated bacterial infections(abscesses and osteomyelitis).Moreover,Mg^(2+)released from the Mg rods enhanced and accelerated the process of bone ***,our work cleverly exploited the eddy-thermal effect and chemical activity of Mg implants under AMFs,aiming to eliminate the inflammatory environment and combat bacterial infections by the simultaneous release of H_(2),OH^(-),and Mg^(2+),thereby facilitating tissue *** therapeutic strategy achieved multiple benefits in one,thus presenting a promising avenue for clinical application.

关键词： Magnesium implants Bacterial infection Alternating magnetic field Gas therapy Proton consumption Anti-inflammatory

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Boost Up the Mechanical and Electrical Property of CNT Fibers by Governing Lyotropic Liquid Crystalline Mesophases with Aramid polymers for Robust Lightweight Wiring Applications

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Advanced Fiber materials 2023年第2期5卷 514-526页

作者： Ki‑Hyun Ryu Jeong‑Gil Kim Dongju Lee Seo Gyun Kim Bon‑Cheol Ku Jun Yeon Hwang Kwang‑Un Jeong Nam Dong Kim Dae‑Yoon Kim Functional Composite Materials Research Center Korea Institute of Science and TechnologyWanju 55324Republic of Korea Carbon Composite Materials Research Center Korea Institute of Science and TechnologyWanju 55324Republic of Korea Department of Polymer‑Nano Science and Technology Department of Nano Convergence EngineeringJeonbuk National UniversityJeonju 54896Republic of Korea Department of Chemical and Biomolecular Engineering Korea Advanced Institute of Science and TechnologyDaejeon 34141Republic of Korea

Monofilament type of polyaromatic amide(PA)and carbon nanotube(CNT)composite fibers is presented.A concept of a lyotropic liquid crystal(LLC)constructed via a spontaneous self-assembly is introduced to mitigate the extremely low com-patibility between PA and *** approaches provide an effective co-processing route of PA and CNT simultaneously to fabricate the uniform,continuous,and reliable composite fibers through a ***,the addition of a small amount PA into the dope solution of CNT governs the LLC mesophase not only in a spinneret stage but also in a coagulant ***,the developed PA/CNT composite fibers have the high uniaxial orientational order and the close interfacial packing compared to the pure CNT *** PA/CNT composite fibers achieve the outstanding tensile strength,electrical conductivity,and electrochemical response,while maintaining a *** also exhibit the chemical,mechanical,and thermal *** of these advantages can make flexible,sewable,and washable PA/CNT composite fibers ideal nanocomposite materials for use in next-generation information and energy transporting system by replacing conventional metal electrical conductors.

关键词： Carbon nanotube Aramid polymer Liquid crystal Composite fiber Electrical wire

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Effect of curing temperature of phthalonitrile resin on the properties of resultant hierarchical porous carbon

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Chinese Journal of Chemical engineering 2025年第3期79卷 45-52页

作者： Xing Yun Kewen Zhang Zhaojun Chu Beitao Liu Yan Kou Xigao Jian Zhihuan Weng State Key Laboratory of Fine Chemicals Frontiers Science Center for Smart Materials Oriented Chemical EngineeringLiaoning Technology Innovation Center of High Performance Resin MaterialsDepartment of Polymer Science&EngineeringDalian University of TechnologyDalian 116024China Thermochemistry Laboratory Liaoning Province Key Laboratory of Thermochemistry for Energy and MaterialsDalian National Laboratory for Clean EnergyDalian Institute of Chemical PhysicsChinese Academy of SciencesDalian 116023China

Heteroatom-doped porous carbon materials have been widely studied due to their high specific surface area and high heteroatom content,but it is difficult to achieve high specific surface area and high heteroatom content at the same ***,a simple method is introduced to prepare N/O co-doped hierarchical porous carbon materials(DNZKs).Phthalonitrile resins(DNZs)were prepared by using 1,3-bis(3,4-dicyanophenoxy)benzene as raw material and ZnCl_(2)/urea as composite curing agent,and then using KOH as activator to successfully prepare DNZKs with high specific surface area,developed pores and high N/O *** porous carbon material(DNZK@400)obtained at a curing temperature of 400℃ has the highest N content(4.97%(mass)),a large specific surface area(2026 m^(2)·g^(-1)),a high micropore proportion(0.9),a high O content(7.53%(mass)),and the best specific capacitance(up to 567 F·g^(-1) at 0.1 A·g^(-1)),which can be attribute to the high temperature resistance of the nitrogencontaining aromatic heterocyclic structure in *** the mass ratio of resin and KOH is 1:1,the specific capacitance of the sample tested by the acid three-electrode system is obtained,and it is found that the material has high cycling stability(119%specific capacitance retention after 100,000 cycle tests).This work proposes a simple and easy-to-operate method for the preparation of multifunctional porous carbon.

关键词： Supercapacitor Phthalonitrile resin N/O co-doped Porous carbon High cycling stability

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Constructing an efficient deep-blue TADF emitter by host-guest interactions towards solution-processed OLEDs with narrowband emission

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science China Chemistry 2023年第3期66卷 826-836页

作者： Yanchao Xie Lei Hua Zhi Wang Yuerong Liu Shian Ying Yuchao Liu Zhongjie Ren Shouke Yan Department Key Laboratory of Rubber-Plastics Ministry of Education/Shandong Provincial Key Laboratory of Rubber-PlasticsSchool of Polymer Science and EngineeringQingdao University of Science&TechnologyQingdao 266042China State Key Laboratory of Chemical Resource Engineering College of Materials Science and EngineeringBeijing University of Chemical TechnologyBeijing 100029China

High-efficiency thermally activated delayed fluorescence(TADF) emitters and corresponding well-designed solution-processed organic light emitting diodes(OLEDs) are presently attractive due to their potential for exploiting large-area flexible displays. In this context, we innovatively integrate 2,12-di-tert-butyl-5,9-dioxa-13b-boronaphtho [3,2,1] anthracene as the acceptor with 3,6-bis(3,6-di-tert-butylcarbazol-N-yl) carbazole as the donor to construct a rigid deep-blue emitter, TB-3t BuCz, which exhibits a narrow emission with full-width-at-half-maximum(FWHM) of 46 nm. TB-3t BuCz itself dispalys no TADF characteristics both in solution or in pure film states. However, the significant TADF behavior can be observed when TB-3t BuCz is doped with 2,6-DCzPPy host due to the formation of exciplex-like species in 2,6-DCzPPy/TB-3t BuCz system. It is also found that the discernible spin-flip of triplet excitons is feasible when the S1/T1states of the formed exciplex stay slightly lower than S1 and T1states of TB-3t BuCz for the other host/TB-3t BuCz systems. Eventually, thanks to the synergetic effect of rigid structure and favorable photophysical properties of TB-3t BuCz, the solution-processed OLEDs based on 2,6-DCzPPy/TB-3t BuCz as emitting layer has achieved the significantly improved external quantum efficiency(EQE) of 14.6% with suppressed efficiency *** CIE1931 coordinate of(0.158, 0.052) is typically in deep-blue region. Note that, this EQE value is among the highest echelon of solution-processed OLEDs with deep-blue emission by utilizing boron-containing TADF emitters.

关键词： thermally activated delayed fluorescence oxygen-bridged cyclized boron host-guest interactions solution-processed OLEDs narrowband deep-blue emission

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Semitransparent organic photovoltaics enabled by transparent p-type inorganic semiconductor and near-infrared acceptor

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Journal of Energy Chemistry 2024年第9期96卷 351-358页

作者： Xue Yan Jiayu Wang Wei He Top Archie Dela Peña Can Zhu Hailin Yu Yingyue Hu Cenqi Yan Shengqiang Ren Xingyu Chen Zhe Wang Jiaying Wu Mingjie Li Jianlong Xia Lei Meng Shirong Lu Dewei Zhao Mikhail Artemyev Yongfang Li Pei Cheng College of Polymer Science and Engineering State Key Laboratory of Polymer Materials EngineeringSichuan UniversityChengdu 610065SichuanChina Department of Applied Physics The Hong Kong Polytechnic UniversityKowloonHong Kong 999077China Beijing National Laboratory for Molecular Sciences CAS Key Laboratory of Organic SolidsInstitute of ChemistryChinese Academy of SciencesBeijing 100190China College of Materials Science and Engineering&Engineering Research Center of Alternative Energy Materials&Devices Ministry of EducationSichuan UniversityChengdu 610065SichuanChina Department of Material Science and Technology Taizhou UniversityTaizhou 318000ZhejiangChina Advanced Materials Thrust Function HubThe Hong Kong University of Science and Technology(Guangzhou)Guangzhou 511400GuangdongChina State Key Laboratory of Advanced Technology for Materials Science and Processing Center of Smart Materials and DevicesWuhan University of TechnologyWuhan 430070HubeiChina Department of Civil1nd Environmental Engineering The Hong Kong University of Science and TechnologyHong Kong 999077China Research Institute for Physical Chemical Problems Belarusian State UniversityMinsk 220006Belarus

Semitransparent organic photovoltaics(STOPVs)have gained wide attention owing to their promising applications in building-integrated photovoltaics,agrivoltaics,and floating *** semiconductors with high charge carrier mobility usually have planar and conjugated structures,thereby showing strong absorption in visible *** this work,a new concept of incorporating transparent inorganic semiconductors is proposed for high-performance ***(I)thiocyanate(CuSCN)is a visible-transparent inorganic semiconductor with an ionization potential of 5.45 eV and high hole *** transparency of CuSCN benefits high average visible transmittance(AVT)of *** energy levels of CuSCN as donor match those of near-infrared small molecule acceptor BTP-eC9,and the formed heterojunction exhibits an ability of exciton *** mobility of CuSCN contributes to a more favorable charge transport channel and suppresses charge *** control STOPVs based on PM6/BTP-eC9 exhibit an AVT of 19.0%with a power conversion efficiency(PCE)of 12.7%.Partial replacement of PM6 with CuSCN leads to a 63%increase in transmittance,resulting in a higher AVT of 30.9%and a comparable PCE of 10.8%.

关键词： Copper(I)thiocyanate Inorganic semiconductor Semitransparent Organic photovoltaics Charge dissociation

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Review Article Electrocatalysts in lithium-sulfur batteries

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Nano Research 2023年第4期16卷 4438-4467页

作者： Shanying Wang Ziwei Wang Fangzheng Chen Bo Peng Jie Xu Junzhe Li Yaohui Lv Qi Kang Ailin Xia Lianbo Ma Key Laboratory of Green Fabrication and Surface Technology of Advanced Metal Materials&Low-Carbon New Materials Research Center&School of Materials Science and Engineering Anhui University of TechnologyMaanshan 243002China Department of Polymer Science and Engineering Shanghai Key Laboratory of Electrical Insulation and Thermal AgeingShanghai Jiao Tong UniversityShanghai 200240China Department of Mechanical and Aerospace Engineering The Hong Kong University of Science and Technology(HKUST)Clear Water BayHong KongChina

Lithium-sulfur(Li-S)batteries with the merits of high theoretical capacity and high energy density have gained significant attention as the next-generation energy storage ***,the main pressing issues of sluggish reaction kinetics and severe shuttling of polysulfides hampered their practical *** overcome these obstacles,various strategies adopting high-efficient electrocatalysts have been explored to enable the rapid polysulfide conversions and thereby suppressing the polysulfide *** review first summarizes the recent progress on electrocatalysts involved in hosts,interlayers,and protective ***,these electrocatalysts in Li-S batteries are analyzed by listing representative works,from the viewpoints of design concepts,engineering strategies,working principles,and electrochemical ***,the remaining issues/challenges and future perspectives facing electrocatalysts are given and *** review may provide new guidance for the future construction of electrocatalysts and their further utilizations in high-performance Li-S batteries.

关键词： lithium-sulfur batteries slow reaction kinetics polysulfide shuttling electrocatalysts electrochemical energy storage

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Reuse of sodium–doped iridium oxide nanoparticles as a bio–stimulating electrode by a chemical and electrochemical recovery process

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Ceramics International 2024年第4期50卷 6220-6228页

作者： Tso, Kuang-Chih Chen, Chieh-Hsuan Chen, Po-Chun Li, Shao-Sian Chen, Jeng-Lung Ohta, Jun Wu, Pu-Wei Division of Materials Science Graduate School of Science and Technology Nara Institute of Science and Technology Nara630-0192 Japan Graduate Degree Program of Science and Technology of Accelerator Light Source National Yang Ming Chiao Tung University Hsinchu300 Taiwan Department of Materials Science and Engineering National Yang Ming Chiao Tung University Hsinchu300 Taiwan Institute of Materials Science and Engineering National Taipei University of Technology Taipei106 Taiwan National Synchrotron Radiation Research Center Hsinchu300 Taiwan

A sequential chlorination and electrochemical reduction process is demonstrated to convert Na–doped iridium oxide nanoparticles into useful IrIIICl63−(aq) serving as the precursor for the fabrication of bio–stimulating electrode. The Na–doped iridium oxide nanoparticles are treated in 35 wt% hydrochloric acid at 70 °C for 18 h to form IrIVCl62−(aq) with pH of 0.3, so the latter could be readily reduced to IrIIICl63−(aq) at a potentiostatic mode of 0.6 V (vs. SCE). The oxidation state and the nature of complexing ligands for the regenerated IrIIICl63− and IrIVCl62−, as well as commercially available IrIIICl63− are validated by X–ray Absorption Spectroscopy. UV–Vis profiles of regenerated IrIVCl62−(aq) are recorded and the absorbance at 487 nm signal is benchmarked against that of standard IrIVCl62−(aq) to obtain the effective regeneration ratio of 68.6%. X–ray diffraction patterns of Na–doped iridium oxide nanoparticles before and after the annealing treatment indicate the amorphous structure facilitates the chlorination step. The regenerated IrIIICl63− is reused to synthesize Na–doped iridium oxide thin film serving as a bio–stimulating electrode for implantable bio–electronics. The regenerated Na–doped iridium oxide thin film reveals a charge-storage capacity of 0.32 mC/cm2-nm and impressive stability that are comparable to those of fresh Na–doped iridium oxide thin film derived from commercially available IrIIICl63−. © 2023 Elsevier Ltd and Techna Group S.r.l.

关键词： Transition metal oxides

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