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Controllably Growing Topologies in One-shot RAFT polymerization via Macro-latent Monomer Strategy

Chinese Journal of polymer Science 2021年第1期39卷 60-69,I0006页

作者： Liu-Qiao Zhang Yang Gao Zhi-Hao Huang Wei Zhang Nian-Chen Zhou Zheng-Biao Zhang Xiu-Lin Zhu State and Local Joint Engineering Laboratory for Novel Functional Polymeric Materials Jiangsu Key Laboratory of Advanced Functional Polymer Design and ApplicationCollege of ChemistryChemical Engineering and Materials ScienceSoochow UniversitySuzhou 215123China Global Institute of Software Technology Suzhou 215163China

The controlled and efficient synthesis of polymers with tailored topologies is challenging but important for exploring structure/property research. Herein, we proposed a concept of macro-latent monomer to achieve the controlled growth of polymer *** macro-latent monomer was installed by a dynamic furan/maleimide covalent bond at the chain terminal. One-shot reversible additionfragmentation chain transfer(RAFT) polymerization of styrene and the macro-latent monomer created controlled growth of polymer *** temperature such as 40 ℃ could not activate the macro-latent monomer and thus the polymerization created the homo-polystyrene. By contrast, high temperature of ~110 ℃ activated the macro-latent monomer, and a maleimide-terminated macro-monomer was released via the retro-Diels Alder reaction. This macro-monomer immediately joined the cross polymerization with styrene and thus produced the side chains. By delicately manipulating the polymerization temperature, the predetermined placement of the macro-latent monomer-derived polymeric sidechains created controllably growing topologies, including star-, π-shaped, and density-variable grafting copolymers. This work paved a new way for creating on-demand topologies and would greatly enrich the topology synthesis.

关键词： Latent monomer Diels-Alder reaction Maleimide Styrene Topologies

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Construction of all-organic low dielectric polyimide hybrids via synergistic effect between covalent organic framework and cross-linking structure

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Nano Materials Science 2023年第4期5卷 429-438页

作者： Wanjing Zhao Zhaoyang Wei Chonghao Lu Yizhang Tong Jingshu Huang Xianwu Cao Dean Shi Robert KYLi Wei Wu Key Laboratory of Polymer Processing Engineering of Ministry of Education Guangdong Provincial Key Laboratory of Technique and Equipment for Macromolecular Advanced ManufacturingSchool of Mechanical and Automotive EngineeringSouth China University of TechnologyGuangzhou510640China Hubei Collaborative Innovation Center for Advanced Organic Chemical Materials Ministry of Education Key Laboratory for the Green Preparation and Application of Functional MaterialsHubei Key Laboratory of Polymer MaterialsFaculty of Materials Science and EngineeringHubei UniversityWuhan430062China Department of Materials Science and Engineering City University of Hong KongTat Chee AvenueKowloonHong Kong Special Administrative Region of China Jihua Laboratory Foshan528200China

Polyimide(PI)is a promising electronic packaging material,but it remains challenging to obtain an all-organic PI hybrid film with decreased dielectric constant and loss without modifying the ***,a series of allorganic PI hybrid films were successfully prepared by introducing the covalent organic framework(COF),which could induce the formation of the cross-linking structure in the PI *** to the synergistic effects of the COF fillers and the cross-linking structure,the PI/COF hybrid film containing 2 wt%COF exhibited the lowest dielectric constant of 2.72 and the lowest dielectric loss(tanδ)of 0.0077 at 1 *** is attributed to the intrinsic low dielectric constant of COF and a large number of mesopores within the ***,the cross-linking network of PI prevents the molecular chains from stacking and improves the fraction of free volume(FFV).The molecular dynamics simulation results are well consistent with the dielectric properties ***,the PI/COF hybrid film with 5 wt%COF showed a significant enhancement in breakdown strength,which increased to 412.8 kV/mm as compared with pure *** addition,the PI/COF hybrid film achieve to reduce the dielectric constant and thermal expansion coefficient(CTE).It also exhibited excellent thermal,hydrophobicity,and mechanical *** all-organic PI/COF hybrid films have great commercial potential as next-generation electronic packaging materials.

关键词： Polyimide Covalent organic framework All-organic Cross-linking structure Dielectric property Hybrid film

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具有超高碱性稳定性和尺寸稳定性的聚芳烃N-甲基奎宁基阴离子交换膜

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Science China Materials 2024年第3期67卷 965-973页

作者：文菊贺显颖张干兵曾梦莹钱宇黎明 Collaborative Innovation Center for Advanced Organic Chemical Materials Co-constructed by the Province and Ministry Ministry-of-Education Key Laboratory for the Synthesis and Application of Organic Functional MoleculesHubei Key Laboratory of Polymer MaterialsCollege of Chemistry and Chemical EngineeringHubei UniversityWuhan 430062China

阴离子交换膜水电解槽的阴离子交换膜成本低、无需铂族贵金属催化剂,有望取代高成本的质子交换膜水电解槽.然而,阴离子交换膜的尺寸稳定性差以及在高温、高浓度碱液中的稳定性差,阻碍了阴离子交换膜水电解槽的发展.最近,我们合成了一种... 详细信息

阴离子交换膜水电解槽的阴离子交换膜成本低、无需铂族贵金属催化剂,有望取代高成本的质子交换膜水电解槽.然而,阴离子交换膜的尺寸稳定性差以及在高温、高浓度碱液中的稳定性差,阻碍了阴离子交换膜水电解槽的发展.最近,我们合成了一种具有优异碱性稳定性的聚(三苯基-N-甲基奎宁基)阴离子交换膜,为了进一步提高这种阴离子交换膜的机械强度和尺寸稳定性,在本工作中,我们添加了三氟苯乙酮来制备聚(三苯基-三氟苯乙酮-N-甲基奎宁基)阴离子交换膜.这种共聚阴离子交换膜具有超高的碱性稳定性(在80℃,10 mol L^(-1)的NaOH溶液中浸泡1600小时后OH^(-)电导率和机械强度不发生衰减),优异的尺寸稳定性(30–80℃温度下,纯水中溶胀率不超过7%;10 mol L^(-1)的NaOH溶液中溶胀率不超过2%),高氢氧根电导率(80°C时达134.5 mS cm^(-1))和高机械强度(抗拉伸强度达43.2 MPa).这种阴离子交换膜和镍合金泡沫电极组装的简易水电解槽在80°C下,2.0 V和5 mol L^(-1)的KOH水电解质中具有1780 mA cm^(-2)的优异电流密度,并且具有高耐久性.

关键词： anion exchange membrane N-methylquinuclidinium alkaline stability dimensional stability water electrolyser

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Advancements in graphene-based composites: A review of the emerging applications in healthcare

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Smart Materials in Medicine 2025年第1期6卷 120-138页

作者： Batool, Farwa Muhammad, Saz Muazzam, Rabia Waqas, Muhammad Ullah, Zia Roy, Shubham Zhang, Yinghe Wang, Ke Guo, Bing Department of Chemistry Lahore Garrison University DHA Phase VI Lahore Pakistan School of System Design and Intelligent Manufacturing Southern University of Science and Technology Shenzhen518055 China School of Science Shenzhen Key Laboratory of Flexible Printed Electronics Technology Shenzhen Key Laboratory of Advanced Functional Carbon Materials Research and Comprehensive Application Harbin Institute of Technology Shenzhen518055 China Government Queen Mary Graduate College Lahore Pakistan

Graphene and related materials are emerging revolutionary materials due to fascinating stimuli-responsive physiochemical properties having widespread applications in developing advanced nano-systems for detection, diagnostics, and therapeutics in biomedical fields. Various materials like metal nanoparticles, polymers, dyes, drugs, and proteins could be combined yielding graphene-based composite materials (GBCMs) to synergistically fulfill different biomedical requirements. The 2D conjugated structure, easy surface functionalization via covalent or van der Waal interactions, and combination with different components for versatile functionalities altogether contribute to the development of GBCM for healthcare applications. This review specifically focuses on GBCMs and discusses specific material properties relevant to their material applications in healthcare. Furthermore, the synthesis, toxicity, and biocompatibility of these GBCMs, and their interactions with biological materials are thoroughly discussed. Importantly, the recent cutting-edge applications in the field of healthcare, including its role in the development of antibacterial, anti-viral, and photothermal therapies, wound healing, drug delivery, neurodegenerative disease therapy, and biosensing based on GBCMs are well-updated. Additionally, the applications of GBCMs in point-of-care devices, wearable electronics, and tissue engineering are well summarized. We hope this review opens up more possibilities to design more innovative healthcare materials derived from graphene. © 2025 The Authors

关键词： Biocompatibility

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Maleimide Chemistry:Enabling the Precision polymer Synthesis

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Chinese Journal of Chemistry 2021年第12期39卷 3177-3187页

作者： Glauber Mejia Yongquan Wang Zhihao Huang Qiunan Shi Zhengbiao Zhang Joint Engineering Laboratory for Novel Functional Polymeric Materials Jiangsu Key Laboratory of Advanced Functional Polymer Design and ApplicationCollege of ChemistryChemical Engineering and Materials ScienceSoochow UniversitySuzhouJiangsu 215123China State Key Laboratory of Radiation Medicine and Protection Soochow UniversitySuzhouJiangsu 215123China

Herein is presented a compilation of the main characteristics of maleimide chemistry in developing the precisely controlled polymers,including the design of sequence-controlled polymers,topological polymers,and polymeric single-chain *** synthetic methods,relied on the versatilities of the maleimide moieties as a latent monomer which leads to an efficient alternative in various innovative applications,especially in self-healing material,self-reporting materials for real-time monitoring,and also in data storage and anticounterfeiting *** core of the content in this review is focused on the up-to-data advances and publications on the major of maleimide chemistry in our research group.

关键词： Maleimide chemistry Precision polymer synthesis polymers Topochemistry Dendrimers

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Host-Guest Strategy Enabling Nonhalogenated Solvent Processing for High-Performance All-polymer Hosted Solar Cells

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Chinese Journal of Chemistry 2023年第9期41卷 1066-1074页

作者： Yuting Huang Haiyang Chen Qunping Fan Ziyuan Chen Junyuan Ding Heyi Yang Zhe Sun Rui Zhang Weijie Chen Changduk Yang Feng Gao Yaowen Li Laboratory of Advanced Optoelectronic Materials Suzhou Key Laboratory of Novel Semiconductor-optoelectronics Materials and DevicesCollege of ChemistryChemical Engineering and Materials ScienceSoochow UniversitySuzhouJiangsu 215123China Jiangsu Key Laboratory of Advanced Negative Carbon Technologies Soochow UniversitySuzhouJiangsu 215123China State and Local Joint Engineering Laboratory for Novel Functional Polymeric Materials Jiangsu Key Laboratory of Advanced Functional Polymer Design and ApplicationCollege of ChemistryChemical Engineering and Materials ScienceSoochow UniversitySuzhouJiangsu 215123China State Key Laboratory for Mechanical Behavior of Materials Xi'an Jiaotong UniversityXi'anShaanxi 710049China Department of Energy Engineering School of Energy and Chemical EngineeringPerovtronics Research CenterLow Dimensional Carbon Materials CenterUlsan National Institute of Science and Technology(UNIST)UlsanRepublic of Korea Department of Physics Chemistry and Biology(IFM)Linkoping UniversityLinkopingSweden

The power conversion efficiencies(PCEs)of all-polymer solar cells(all-PSCs),usually processed from low-boiling-point and toxic sol-vents,have reached high values of 18%.However,poor miscibility and uncontrollable crystallinity in polymer blends lead to a nota-ble drop in the PCEs when using green solvents,limiting the practical development of ***,a third component(guest)BTO was employed to optimize the miscibility and enhance the crystallinity of PM6/PY2Se-F host film processed from green solvent toluene(TL),which can effectively suppress the excessive aggregation of PY2Se-F and facilitate a nano-scale interpenetrating net-work morphology for exciton dissociation and charge *** a result,TL-processed all-polymer hosted solar cells(all-PHSCs)exhibited an impressive PCE of 17.01%.Moreover,the strong molecular interaction between the host and guest molecules also en-hances the thermal stability of the *** host-guest strategy provides a unique approach to developing high-efficiency and stable all-PHSCs processed from green solvents,paving the way for the industrial development of all-PHSCs.

关键词： All-polymer solar cells Host-guest systems Crystal engineering Nonhalogenated green solvent Stability Morphology Miscibility Ternary blend solar cells

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Polydopamine modified CuS@HKUST for rapid sterilization through enhanced photothermal property and photocatalytic ability

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Rare Metals 2022年第2期41卷 663-672页

作者： Dong-Lin Han Peng-Li Yu Xiang-Mei Liu Ying-De Xu Shui-Lin Wu College of Materials Science and Engineering Jilin Institute of Chemical TechnologyJilin 132022China School of Materials Science and Engineering the Key Laboratory of Advanced Ceramics and Machining Technology by the Ministry of Education of ChinaTianjin UniversityTianjin 300072China Ministry-of-Education Key Laboratory for the Green Preparation and Application of Functional Materials Hubei Key Laboratory of Polymer MaterialsSchool of Materials Science and EngineeringHubei UniversityWuhan 430062China

Because of the impressive evolution of the drugresistant bacteria,the development of efficient,antibioticfree agent is in great ***,an efficient antibacterial agent,CuS@HKUST-polydopamine(PDA),was exquisitely designed,where the Cu-based metal-organic framework(MOF)—HKUST nanoparticles served as the porous frame,and the CuS was synthesized within the structure of the MOF through the process of in situ sulfuration,followed with polydopamine(PDA)covering the *** structure of the HKUST preventing the aggregation of the CuS nanoparticles,which improved their photothermal and photocatalytic *** covering with PDA,the nanoparticles’abilities to produce heat and free radicals were further *** was because that the PDA itself could transform light into heat,which not only benefited the photothermal property,but also improved the photocatalytic property of the nanoparticles by accelerating the charge ***,the PDA could also transfer the photo-induced electrons fast and thus prevented the recombination of the photo-generated electron–hole pairs,which resulted in the enhanced ability to produce free *** a result,under light irradiation,the antibacterial efficiency of the CuS@HKUST-PDA against Staphylococcus aureus(***)and Escherichia coli(***)could reach 99.77%and 99.57%.Hence,the synthesized CuS@HKUST-PDA can be promising for anti-infection and sterilization application without using antibiotics.

关键词： Antibacterial CuS Polydopamine(PDA) Photothermal Photocatalytic Metal-organic framework(MOF)

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Tri-Monomer Polyamide Acid Nanofiber Separator for Safe and High Performance Lithium-Ion Batteries

SSRN

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SSRN 2024年

作者： Lv, Shuo Zhang, Mingzu He, Jinlin Ni, Peihong College of Chemistry Chemical Engineering and Materials Science State and Local Joint Engineering Laboratory for Novel Functional Polymeric Materials Jiangsu Key Laboratory of Advanced Functional Polymer Design and Application Soochow University Suzhou215123 China

The separators play a crucial role in ensuring the safety of lithium batteries and greatly affect the electrochemical performance of the battery. However, the weak thermal stability and non-polar surface of commercial polyolefin separators severely restrict the development of the high-performance lithium batteries. In this work, we initially proposed polyamide acid (PAA) nanofiber separator with three monomers through a two-step synthesis method, which was prepared by electrospinning. By controlling different processing temperatures, PAA separators containing different amount of carboxyl groups were obtained. PAA separator had better wettability and thermal stability than PE separator. Meanwhile, the electrospinning method brings ultra-high porosity (490%) to the membrane, resulting a much higher electrolyte absorption and retention rate of PAA (initially 3214%, 240% at 50 min) compared to PE separator. In particular, carboxyl groups serve as functional groups to provide an electronegative atmosphere, promoting the transport of lithium ion between the anode and cathode, and playing an important role in improving ionic conductivity. Consequently, batteries with PAA-SOH-50 separator showed the best rate charging/discharging performance, maintaining 87.72% and 73.6% of its initial capacity at 2 C. Moreover, cells with PAA separator exhibited much higher initial discharge capacity (164.3 mAh g-1) than that with PE separator (126.8 mAh g-1). After 100 cycles at 0.5 C, the PAA nanofiber separator achieved an ultralow attenuation rate of only 0.04% per cycle, which was less than half of the commercial PE separator (0.10% per cycle). This work provides a new vision for the development of separator materials, revealing the great influence of functional groups, such as carboxyl groups, on the performance of separators, which provides a strong basis for the further research of high-performance separators. © 2024, The Authors. All rights reserved.

关键词： Lithium-ion batteries

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Photoluminescent chiral carbon dots derived from glutamine

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Chinese Chemical Letters 2021年第12期32卷 3916-3920页

作者： Wenyan Ma Bolun Wang Yonggang Yang Jiyang Li State Key Laboratory of Inorganic Synthesis and Preparative Chemistry College of ChemistryJilin UniversityChangchun 130012China Jiangsu Key Laboratory of Advanced Functional Polymer Design and Application Department of Polymer Science and Engineering College of ChemistryChemical Engineering and Materials ScienceSoochow UniversitySuzhou 215123China

The integration of luminescence and chirality in carbon dots(CDs) encourages candidates to explore novel functions and applications of CDs, however, the preparation of chiral CDs is very limited. Herein, we report a hydrothermal method to fabricate chiral CDs by utilizing amino acid enantiomers as the precursors. LGln-CDs or DGln-CDs with uniform size of 3–4 nm show excitation-dependent blue fluorescence in solutions. Circular dichroism measurement confirms the opposite optical rotation of chiral CDs in the region from 200 nm to 300 nm, and the signals can be regulated by concentrations of CDs solution. Timedependent density functional calculation reveals that polypeptides may exist on the surface of CDs due to the polycondensation of L/DGln at high temperature, and the optical activity of CDs originates from the stacking of neighboring carbonyl groups. The facile synthetic methodology proposed will provide potential opportunities for the preparation and application of chiral and chiroptical CDs-based materials.

关键词： Chirality Carbon dots Photoluminescence Circular dichroism Sensors

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Recent advances in carbonized non-noble metal–organic frameworks for electrochemical catalyst of oxygen reduction reaction

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Rare Metals 2021年第10期40卷 2657-2689页

作者： Chan Li Dao-Hui Zhao Hua-Li Long Ming Li Hubei Collaborative Innovation Center for Advanced Organic Chemical Materials Ministry-of-Education Key Laboratory for the Synthesis and Application of Organic Functional MoleculesHubei Key Laboratory of Polymer MaterialsCollege of Chemistry and Chemical EngineeringHubei UniversityWuhan 430062China

The non-noble metal oxygen reduction reaction(ORR) catalysts prepared by carbonization of metal–organic framework(MOF) have attracted more and more attentions in the fields of fuel cells and metal-air batteries due to their unique intrinsic advantages such as high catalytic activity, low price, simple synthesis and good adaptability. Different from the study of traditional high active noble metal catalysts, this review systematically summarizes recent developments on non-noble metal(Fe,Co, Cu, Ni, Mn and Mo) ORR catalysts prepared by various MOFs carbonization in different metal centers. The effects of synthesis strategies and pyrolysis conditions on the catalyst properties are discussed. Meanwhile, the key parameters of catalytic performances(including active sites, dispersed state and specific surface area) are discussed and the prospect is presented. It is expected that this review will provide effective guidance for future studies on carbonized non-noble MOFs for ORR electrochemical catalyst.

关键词： Non-noble metal MOF Pyrolysis Catalyst ORR

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