High-performance lithium metal batteries benefit from the construction of composite polymer electrolytes(CPEs)which are synthesized by incorporating inorganic fillers into polymer matrices[1].However,the random distri...High-performance lithium metal batteries benefit from the construction of composite polymer electrolytes(CPEs)which are synthesized by incorporating inorganic fillers into polymer matrices[1].However,the random distribution of added fillers within the polymer matrix can lead to tortuous ion pathways and longer transmission distances(Fig.1).As a result,the ion transport capability of CPEs may decrease,while interface contact may deteriorate.Therefore,the organized arrangement of fillers emerges as a crucial consideration in constructing electrolyte membranes.One highly effective approach is the adoption of a vertically aligned filler configuration,where ceramic fillers are constructed to be perpendicular to the electrolyte membrane.If so,the filler/electrolyte interface impedance can be significantly reduced,while continuous ion transport channels along the specified direction are formed,thus significantly enhancing the ion conduction(Fig.1(a))[1].展开更多
As a powerful synthetic tool,ruthenium-catalyzed ring-opening metathesis polymerization(ROMP)has been widely utilized to prepare diverse heteroatom-containing polymers.In this contribution,we report the synthesis of t...As a powerful synthetic tool,ruthenium-catalyzed ring-opening metathesis polymerization(ROMP)has been widely utilized to prepare diverse heteroatom-containing polymers.In this contribution,we report the synthesis of the novel imine-based polymer through the copolymerization of cyclooctene with cyclic imine comonomer via ROMP.Because of the efficient hydrolysis reactions of the imine group,the generated copolymer can be easily degraded under mild condition.Moreover,the generated degradable product was the telechelic polymer bearing amine group,which was highly challenged for its direct synthesis.And this telechelic polymer could also be used for the further synthesis of new polymer through post-transformation.The introduction of imine unit in this work provides a new example of the degradable polymer synthesis.展开更多
Aims and Scope,Chinese Journal of Polymer Science(CJPS)is a monthly journal published in Englishand sponsored by the Chinese Chemical Society and the Institute of Chemistry,,Chinese Academy of Sciences.CJPS isedited b...Aims and Scope,Chinese Journal of Polymer Science(CJPS)is a monthly journal published in Englishand sponsored by the Chinese Chemical Society and the Institute of Chemistry,,Chinese Academy of Sciences.CJPS isedited by a distinguished Editorial Board headed by Professor Qi-Feng Zhouand supported by an International Advisory Board in which many famous active polymerscientists alloverthe world are included.The journal was first published in 1983 under the title Polymer Communications and has the current name since 1985.展开更多
Chain-growth radical polymerization of vinyl monomers is essential for producing a wide range of materials with properties tailored to specific applications.However,the inherent resistance of the polymer's C―C ba...Chain-growth radical polymerization of vinyl monomers is essential for producing a wide range of materials with properties tailored to specific applications.However,the inherent resistance of the polymer's C―C backbone to degradation raises significant concerns regarding long-term environmental persistence,which also limits their potential in biomedical applications.To address these challenges,researchers have developed strategies to either degrade preexisting vinyl polymers or incorporate cleavable units into the backbone to modify them with enhanced degradability.This review explores the various approaches aimed at achieving backbone degradability in chain-growth radical polymerization of vinyl monomers,while also highlighting future research directions for the development of application-driven degradable vinyl polymers.展开更多
Incorporation of acetal groups in the backbone is a potent strategy to create polymers that are cleavable or degradable under acidic conditions.We report here an in-depth study on the ring-closing-opening copolymeriza...Incorporation of acetal groups in the backbone is a potent strategy to create polymers that are cleavable or degradable under acidic conditions.We report here an in-depth study on the ring-closing-opening copolymerization of o-phthalaldehyde(OPA)and epoxide using Lewis pair type two-component organocatalysts for producing acetal-functionalized polyether and polyurethane.Notably,triethylborane as the Lewis acid,in comparison with tri(n-butyl)borane,more effectively enhances the polymerization activity by mitigating borane-induced reduction of the aldehyde group into extra initiating(borinic ester)species.Density functional theory(DFT)calculations present comparable energy barriers of OPA-epoxide cross-propagation and epoxide self-propagation,which is consistent with the experimental finding that an alternating-rich copolymer comprising mostly OPA-epoxide units but also epoxide-epoxide linkages is produced.In particular,when epoxide is added in a large excess,the product becomes a polyether containing acetal functionalities in the central part of the backbone and thus being convertible into polyurethane with refined acid degradability.展开更多
Functional hyperbranched polymers,as an important class of materials,are widely applied in diverse areas.Therefore,the development of simple and efficient reactions to prepare hyperbranched polymers is of great signif...Functional hyperbranched polymers,as an important class of materials,are widely applied in diverse areas.Therefore,the development of simple and efficient reactions to prepare hyperbranched polymers is of great significance.In this work,trialdehydes,diamines,and trimethylsilyl cyanide could easily undergo multicomponent polymerization under mild conditions,producing hyperbranched poly(α-aminonitrile)s with high molecular weights(M_(w) up to 4.87×10^(4))in good yields(up to 85%).The hyperbranched poly(α-aminonitrile)s have good solubility in commonly used organic solvents,high thermal stability as well as morphological stability.Furthermore,due to the numerous aldehyde groups in their branched chains,these hb-poly(α-aminonitrile)s can undergo one-pot,two-step,four-component post-polymerization with high efficiency.This work not only confirms the efficiency of our established catalyst-free multicomponent polymerization of aldehydes,amines and trimethylsilyl cyanide,but also provides a versatile and powerful platform for the preparation of functional hyperbranched polymeric materials.展开更多
Although solid-state polymer electrolytes(SPEs)are expected to solve the safety hazards and limited energy density in the energy storage systems,they still encounter an inferior electrode/electrolyte interface when pr...Although solid-state polymer electrolytes(SPEs)are expected to solve the safety hazards and limited energy density in the energy storage systems,they still encounter an inferior electrode/electrolyte interface when prepared in an ex situ manner.Recently,in situ polymerization of SPEs favor high interfacial infiltrability,improved interface contact,and reduced interface resistance,owing to the formation of a"superconformal"interface between electrode and electrolyte.Especially,in situ strategies employing ring-opening polymerization(ROP)are emerging as dazzling stars,further enabling moderate polymerization conditions,controllable molecular structure,and reduced interfacial side reaction.As the main monomers that can be in situ polymerized via the ROP strategy,cyclic ethers have been used to construct the CE-SPEs with many merits,including good battery electrochemical performances and a simple assembly process.Here,as a systematic summarization of the existing reports,this review focuses on the polymerization mechanism of ROP,the design principles of CE-SPEs electrolytes,and the recent application of in situ CE-SPEs.In particular,this review thoroughly discusses the selection of different cyclic monomers,initiators and various modification approaches in in situ fabricating CE-SPEs.Ending with offering future challenges and perspectives,this review envisions shedding light on the profound understanding and scientific guidance for further development of high-performance in situ CE-SPEs.展开更多
Solid polymer electrolytes(SPEs)have garnered considerable interest in the field of lithium metal batteries(LMBs)owing to their exceptional mechanical strength,excellent designability,and heightened safety characteris...Solid polymer electrolytes(SPEs)have garnered considerable interest in the field of lithium metal batteries(LMBs)owing to their exceptional mechanical strength,excellent designability,and heightened safety characteristics.However,their inherently low ion transport efficiency poses a major challenge for their application in LMBs.To address this issue,covalent organic framework(COF)with their ordered ion transport channels,chemical stability,large specific surface area,and designable multifunctional sites has shown promising potential to enhance lithium-ion conduction.Here,we prepared an anionic COF,Tp Pa-COOLi,which can catalyze the ring-opening copolymerization of cyclic lactone monomers for the in situ fabrication of SPEs.The design leverages the high specific surface area of COF to facilitate the absorption of polymerization precursor and catalyze the polymerization within the pores,forming additional COF-polymer junctions that enhance ion transport pathways.The partial exfoliation of COF achieved through these junctions improved its dispersion within the polymer matrix,preserving ion transport channels and facilitating ion transport across COF grain boundaries.By controlling variables to alter the crystallinity of Tp Pa-COOLi and the presence of-COOLi substituents,Tp Pa-COOLi with partial long-range order and-COOLi substituents exhibited superior electrochemical performance.This research demonstrates the potential in constructing high-performance SPEs for LMBs.展开更多
The recent commercialization of gene products has sparked significant interest in gene therapy,necessitating efficient and precise gene delivery via various vectors.Currently,viral vectors and lipid-based nanocarriers...The recent commercialization of gene products has sparked significant interest in gene therapy,necessitating efficient and precise gene delivery via various vectors.Currently,viral vectors and lipid-based nanocarriers are the predominant choices and have been extensively investigated and reviewed.Beyond these vectors,polymeric nanocarriers also hold the promise in therapeutic gene delivery owing to their versatile functionalities,such as improving the stability,cellar uptake and endosomal escape of nucleic acid drugs,along with precise delivery to targeted tissues.This review presents a brief overview of the status quo of the emerging polymeric nanocarriers for therapeutic gene delivery,focusing on key cationic polymers,nanocarrier types,and preparation methods.It also highlights targeted diseases,strategies to improve delivery efficiency,and potential future directions in this research area.The review is hoped to inspire the development,optimization,and clinical translation of highly efficient polymeric nanocarriers for therapeutic gene delivery.展开更多
To achieve the target of carbon neutrality,it is crucial to develop an efficient and green synthesis methodology with good atomic economy to achieve sufficient utilization of energy and sustainable development.Photoin...To achieve the target of carbon neutrality,it is crucial to develop an efficient and green synthesis methodology with good atomic economy to achieve sufficient utilization of energy and sustainable development.Photoinduced electron transfer reversible addition-fragmentation chain-transfer(PET-RAFT)polymerization is a precise methodology for constructing polymers with well-defined structures.However,conventional semiconductor-mediated PET-RAFT polymerization still has considerable limitations in terms of efficiency as well as the polymerization environment.Herein,sulfur-doped carbonized polymer dots(CPDs)were hydrothermally synthesized for catalysis of aqueous PET-RAFT polymerization at unprecedented efficiency with a highest propagation rate of 5.05 h-1.The resulting polymers have well-controlled molecular weight and narrow molecular weight dispersion(Ð<1.10).Based on the optoelectronic characterizations,we obtained insights into the photoinduced electron transfer process and proposed the mechanism for CPD-mediated PET-RAFT polymerization.In addition,as-synthesized CPDs for PET-RAFT polymerization were also demonstrated to be suitable for a wide range of light sources(blue/green/solar irradiation),numerous monomers,low catalyst loading(low as 0.01 mg mL^(-1)),and multiple polar solvent environments,all of which allowed to achieve efficiencies much higher than those of existing semiconductor-mediated methods.Finally,the CPDs were confirmed to be non-cytotoxic and catalyzed PET-RAFT polymerization successfully in cell culture media,indicating broad prospects in biomedical fields.展开更多
With the continuous development of electronic devices and the information industry towards miniaturization,integration,and high-power consumption,the using of electronic devices will inevitably generate and accumulate...With the continuous development of electronic devices and the information industry towards miniaturization,integration,and high-power consumption,the using of electronic devices will inevitably generate and accumulate heat,which will cause local high temperatures and will seriously reduce their performance,reliability,and lifetime.Therefore,having efficient heat-conducting functional materials is crucial to the normal and stable operation of electrical equipment and microelectronic products.In view of the excellent comprehensive performance of polymer-based thermally conductive materials(including intrinsic polymers and filler-filled polymer-based composites),it has shown great advantages in thermal management applications.In this review,the research status of preparing polymer-based thermally conductive composites and effective strategies to improve their thermal conductivity(TC)are reviewed.Compared with the higher cost and technical support with adjusting the molecular chain structure and cross-linking mode to improve the intrinsic TC of the polymer,introducing suitable fillers into the polymer to build a thermally conductive network or oriented structure can simply and efficiently improve the overall TC.Typical applications of polymer-based composites were discussed with detailed examples in the field of electronic packaging.Challenges and possible solutions to solve the issues are discussed together with the perspectives.This study provides guidance for the future development of polymer-based thermally conductive composites.展开更多
In this work,by combining the specific selectivity of molecularly imprinted polymer(MIP)with a simple and sensitive electrochemiluminescence(ECL)detection method,a molecularly imprinted ECL sensor for kanamycin(KA)was...In this work,by combining the specific selectivity of molecularly imprinted polymer(MIP)with a simple and sensitive electrochemiluminescence(ECL)detection method,a molecularly imprinted ECL sensor for kanamycin(KA)was developed.The MIP film was synthesized on the surface of gold electrode via electrochemical polymerization,using pyrrole(PY)as the functional monomer and KA as the template molecule.The commonly used luminescent reagent Ru(bpy)32+was employed as the ECL probe,and its co-reagent tripropylamine(TPA)was added to enhance the detection sensitivity of the sensor.Quantitative analysis of KA was performed by evaluating the difference in ECL responses between MIP film electrodes after KA removal and KA rebinding.The sensor exhibited high selectivity,good reproducibility,and stability toward KA,with a linear range of 5.00×10^(-8) to 1.00×10^(-5) mol·L^(-1) and a limit of detection of 1.67×10^(-8) mol·L^(-1)(S/N=3).This work would provide a new idea for the development of simple and sensitive molecularly imprinted ECL sensors.展开更多
Building and construction sector, including infrastructures, are facing many challenges which are scarcity of raw materials, CO2 emissions, lower construction efficiency, and deterioration under corrosive environment ...Building and construction sector, including infrastructures, are facing many challenges which are scarcity of raw materials, CO2 emissions, lower construction efficiency, and deterioration under corrosive environment that cost the world economy $2.5 trillion and this translates to 3.4% of world gross domestic product. This paper presents several examples that show how the use of the nonmetallic materials improved sustainability and life cycles in the built environment by removing the corrosion issue from its root and using durable NM polymers in construction. The paper details recently patented Aramco technology for the use of nonmetallic paving panels that could be used as an alternative to concrete and asphalt paving. Other case studies presented cover use of GFRP Poles for traffic signs and signal poles to replace traditional steel poles. Details of developments for specialist structural application in bridges, in architectural applications, polymers in soils, fibers in pavement manholes and bendable concrete are presented.展开更多
Submission Papers appearing in the Journal comprise Editorials,Rapid Communications,Perspectives,Tutorials,Feature Articles,Reviews,Research Articles,which should contain original information,theoretical or experiment...Submission Papers appearing in the Journal comprise Editorials,Rapid Communications,Perspectives,Tutorials,Feature Articles,Reviews,Research Articles,which should contain original information,theoretical or experimental,on any topics in the field of polymer science and polymer material science.Papers already published or scheduled to be published elsewhere should not be submitted and certainly will not be accepted.展开更多
Natural biomolecular structures possess an inherent ability to encode chiral conformations,thus the generation and regulation of chiroptical activity is crucial.While artificial polymers hold special significance in u...Natural biomolecular structures possess an inherent ability to encode chiral conformations,thus the generation and regulation of chiroptical activity is crucial.While artificial polymers hold special significance in understanding life's origins,the fundamental connections between the racemic architecture and functional characteristics still need to be fully investigated.Herein,this study reports the generation and regulation of the global chirality and helical sense in racemic polymer systems,focusing on the synergistic effects of liquid crystallinity(LC)and solvophobic interaction.By systematically varying the length of alkyl spacers and the degree of polymerization(DP)of the core-forming azobenzene(Azo)blocks,the chiral communications,morphological transitions and chiroptical properties of the racemic nanoaggregates can be precisely controlled.Furthermore,the proposed“first come,first serve”(FF)and the“late-comer lives above”(LA)effect are broadly applicable and are expected to be applied to various types of racemic polymer systems.This work provides valuable insights into the design of self-assembled systems with tunable global chirality and morphology,thereby advancing the understanding of the origins of homochirality in nature.展开更多
Aqueous zinc-ion batteries(AZIBs)are recognized for their commercial viability due to their low cost,high safety,and substantial theoretical capacity.However,the challenges posed by dendrite growth and side reactions ...Aqueous zinc-ion batteries(AZIBs)are recognized for their commercial viability due to their low cost,high safety,and substantial theoretical capacity.However,the challenges posed by dendrite growth and side reactions of zinc ions hinder the widespread adoption of AZIBs.In this work,a new porous phenolphthalein-based polymer(PPH-CN)is synthesized through the polymerization of phenolphthalein and 2,6-difluorobenzonitrile and served as a protective layer of zinc anode.The PPH-CN layer not only effectively separates the zinc anode from aqueous electrolyte to suppress side reactions,but also provides abundant zincophilic sites to facilitate the deposition of zinc ions.As a result,the Zn@PPH-CN symmetric batteries achieve a notably stable cycle lifespan of 1820 h at a current density of 1 mA cm^(-2),which is thirteen times longer than that of bare Zn.Under the protection of PPH-CN,the zinc anode exhibits a high average Coulombic efficiency(CE)of 99.7%after 3550 cycles in the Zn@PPH-CN//Cu asymmetric battery.The capacity retention rate of Zn@PPH-CN//NH_(4)V_(4)O_(10)full batteries reaches 89.6%after 1000 cycles at 1 Ag^(-1).Furthermore,density functional theory(DFT)simulations identified the Zn^(2+)storage sites of PPH-CN,thereby demonstrating the viability of PPH-CN as interface coatings of zinc anode.This work offers valuable insights into the development of high-performance aqueous battery.展开更多
Driven by the dual imperatives of global plastic pollution control and carbon neutrality,research on depolymerizable polymers has become a cutting-edge focus in polymer science.With the continuous emergence of innovat...Driven by the dual imperatives of global plastic pollution control and carbon neutrality,research on depolymerizable polymers has become a cutting-edge focus in polymer science.With the continuous emergence of innovative materials,strengthened policy support,and maturing industrial chains,these polymers are demonstrating transformative potential in critical sectors,such as environmental protection,healthcare,and industrial manufacturing,promising for reshaping the future landscape of the plastics industry.展开更多
Advancing the integration of artificial intelligence and polymer science requires high-quality,open-source,and large-scale datasets.However,existing polymer databases often suffer from data sparsity,lack of polymer-pr...Advancing the integration of artificial intelligence and polymer science requires high-quality,open-source,and large-scale datasets.However,existing polymer databases often suffer from data sparsity,lack of polymer-property labels,and limited accessibility,hindering system-atic modeling across property prediction tasks.Here,we present OpenPoly,a curated experimental polymer database derived from extensive lit-erature mining and manual validation,comprising 3985 unique polymer-property data points spanning 26 key properties.We further develop a multi-task benchmarking framework that evaluates property prediction using four encoding methods and eight representative models.Our re-sults highlight that the optimized degree-of-polymerization encoding coupled with Morgan fingerprints achieves an optimal trade-off between computational cost and accuracy.In data-scarce condition,XGBoost outperforms deep learning models on key properties such as dielectric con-stant,glass transition temperature,melting point,and mechanical strength,achieving R2 scores of 0.65-0.87.To further showcase the practical utility of the database,we propose potential polymers for two energy-relevant applications:high temperature polymer dielectrics and fuel cell membranes.By offering a consistent and accessible benchmark and database,OpenPoly paves the way for more accurate polymer-property modeling and fosters data-driven advances in polymer genome engineering.展开更多
Compared to subtractive manufacturing and casting,3D printing(additive manufacturing)offers advantages,such as the rapid production of complex structures,reduced material waste,and environmental friendliness.Direct in...Compared to subtractive manufacturing and casting,3D printing(additive manufacturing)offers advantages,such as the rapid production of complex structures,reduced material waste,and environmental friendliness.Direct ink writing(DIW)is one of the most popular 3D printing techniques owing to its ability to print multiple materials simultaneously and its high compatibility with printing inks.However,DIW presents significant challenges,particularly in the printing of high-performance polymers.The main challenges are as follows:1.The rigid structures and reaction kinetics of high-performance polymers make developing new inks difficult.2.The limited types of available high-performance polymers underscore the need for new DIW-suitable materials.3.Layer-by-layer stacking weakens interlayer bonding,affecting the mechanical properties of the printed product.4.The accuracy and speed of DIW printing are insufficient for large-scale manufacturing.After introducing the topic,the requirements for DIW printing inks are first reviewed,emphasizing the importance of thixotropic agents.Then,research progress regarding DIW printing of high-performance polymers is comprehensively reviewed according to the requirements of different polymer inks.Additionally,the applications of these materials across various fields are summarized.Finally,the challenges in DIW printing of high-performance polymers,along with corresponding solutions and future development prospects,are discussed in detail.展开更多
Three-dimensional(3 D)printing has revolutionized the design and production of customized scaffolds,but the minimally invasive implantation of 3 D-printed structures into the human body remains challenging.This has pr...Three-dimensional(3 D)printing has revolutionized the design and production of customized scaffolds,but the minimally invasive implantation of 3 D-printed structures into the human body remains challenging.This has prompted the exploration of innovative materials and technical solutions.Shape-memory polymers,as advanced intelligent materials,exhibit considerable potential in minimally invasive surgical applications.Herein,we developed a novel thermosetting shape-memory polymer,poly(L-lactic acid)-trimethylene carbonate-glycolic acid(PLLA-TMC-GA),for the fabrication of bioengineered scaffolds with body temperature-activated shape-memory functionality.We comprehensively evaluated the mechanical properties,thermal stability,shape-memory capabilities,biocompatibility,biodegradability,and 3 D printing performance of PLLA-TMC-GA terpolymers with various compositions.The results indicate that PLLA-TMC-GA exhibits exceptional shape-memory performance,adjustable material properties,favorable biocompatibility,and the potential for controlled biodegradation and reabsorption.The use of PLLA-TMC-GA as a biodegradable shape-memory polymer allows the reduction of implant volume,simplifies implantation,and enables on-demand activation at body temperature.These characteristics present new opportunities for the advancement of minimally invasive surgical techniques.展开更多
基金supported by the National Natural Science Foundation of China(No.51972293)Hangzhou Key Research Program Project(2023SZD0099)LingYan Project(2024C01090).
文摘High-performance lithium metal batteries benefit from the construction of composite polymer electrolytes(CPEs)which are synthesized by incorporating inorganic fillers into polymer matrices[1].However,the random distribution of added fillers within the polymer matrix can lead to tortuous ion pathways and longer transmission distances(Fig.1).As a result,the ion transport capability of CPEs may decrease,while interface contact may deteriorate.Therefore,the organized arrangement of fillers emerges as a crucial consideration in constructing electrolyte membranes.One highly effective approach is the adoption of a vertically aligned filler configuration,where ceramic fillers are constructed to be perpendicular to the electrolyte membrane.If so,the filler/electrolyte interface impedance can be significantly reduced,while continuous ion transport channels along the specified direction are formed,thus significantly enhancing the ion conduction(Fig.1(a))[1].
基金financially supported by National Key R&D Program of China(No.2021YFA1501700)CAS Project for Young Scientists in Basic Research(No.YSBR-094)+1 种基金Natural Science Foundation of Anhui Province(Nos.2308085Y35 and 2023AH030002)Hefei Natural Science Foundation(No.202304)。
文摘As a powerful synthetic tool,ruthenium-catalyzed ring-opening metathesis polymerization(ROMP)has been widely utilized to prepare diverse heteroatom-containing polymers.In this contribution,we report the synthesis of the novel imine-based polymer through the copolymerization of cyclooctene with cyclic imine comonomer via ROMP.Because of the efficient hydrolysis reactions of the imine group,the generated copolymer can be easily degraded under mild condition.Moreover,the generated degradable product was the telechelic polymer bearing amine group,which was highly challenged for its direct synthesis.And this telechelic polymer could also be used for the further synthesis of new polymer through post-transformation.The introduction of imine unit in this work provides a new example of the degradable polymer synthesis.
文摘Aims and Scope,Chinese Journal of Polymer Science(CJPS)is a monthly journal published in Englishand sponsored by the Chinese Chemical Society and the Institute of Chemistry,,Chinese Academy of Sciences.CJPS isedited by a distinguished Editorial Board headed by Professor Qi-Feng Zhouand supported by an International Advisory Board in which many famous active polymerscientists alloverthe world are included.The journal was first published in 1983 under the title Polymer Communications and has the current name since 1985.
基金funding from the National Natural Science Foundation of China(No.22401037)funding from JST CREST(No.JPMJCR23L1)。
文摘Chain-growth radical polymerization of vinyl monomers is essential for producing a wide range of materials with properties tailored to specific applications.However,the inherent resistance of the polymer's C―C backbone to degradation raises significant concerns regarding long-term environmental persistence,which also limits their potential in biomedical applications.To address these challenges,researchers have developed strategies to either degrade preexisting vinyl polymers or incorporate cleavable units into the backbone to modify them with enhanced degradability.This review explores the various approaches aimed at achieving backbone degradability in chain-growth radical polymerization of vinyl monomers,while also highlighting future research directions for the development of application-driven degradable vinyl polymers.
基金financially supported by the National Key R&D Program of China(No.2022YFC2805103)the National Natural Science Foundation of China(Nos.52022031 and 52263001)the Foundation from Qinghai Science and Technology Department(No.2022-ZJ-944Q)。
文摘Incorporation of acetal groups in the backbone is a potent strategy to create polymers that are cleavable or degradable under acidic conditions.We report here an in-depth study on the ring-closing-opening copolymerization of o-phthalaldehyde(OPA)and epoxide using Lewis pair type two-component organocatalysts for producing acetal-functionalized polyether and polyurethane.Notably,triethylborane as the Lewis acid,in comparison with tri(n-butyl)borane,more effectively enhances the polymerization activity by mitigating borane-induced reduction of the aldehyde group into extra initiating(borinic ester)species.Density functional theory(DFT)calculations present comparable energy barriers of OPA-epoxide cross-propagation and epoxide self-propagation,which is consistent with the experimental finding that an alternating-rich copolymer comprising mostly OPA-epoxide units but also epoxide-epoxide linkages is produced.In particular,when epoxide is added in a large excess,the product becomes a polyether containing acetal functionalities in the central part of the backbone and thus being convertible into polyurethane with refined acid degradability.
基金financially supported by the Scientific Research Start-up Fund Project of Anhui Polytechnic University for Introducing Talents(No.2022YQQ081)Natural Science Research Project of Anhui Educational Committee(No.2024AH050133)the National Natural Science Foundation of China(No.22001078).
文摘Functional hyperbranched polymers,as an important class of materials,are widely applied in diverse areas.Therefore,the development of simple and efficient reactions to prepare hyperbranched polymers is of great significance.In this work,trialdehydes,diamines,and trimethylsilyl cyanide could easily undergo multicomponent polymerization under mild conditions,producing hyperbranched poly(α-aminonitrile)s with high molecular weights(M_(w) up to 4.87×10^(4))in good yields(up to 85%).The hyperbranched poly(α-aminonitrile)s have good solubility in commonly used organic solvents,high thermal stability as well as morphological stability.Furthermore,due to the numerous aldehyde groups in their branched chains,these hb-poly(α-aminonitrile)s can undergo one-pot,two-step,four-component post-polymerization with high efficiency.This work not only confirms the efficiency of our established catalyst-free multicomponent polymerization of aldehydes,amines and trimethylsilyl cyanide,but also provides a versatile and powerful platform for the preparation of functional hyperbranched polymeric materials.
基金supported by the National Natural Science Foundation of China(22022813)the Zhejiang Provincial Natural Science Foundation of China(LQ24B030002)the China Postdoctoral Science Foundation(2022M722729,2023T160571).
文摘Although solid-state polymer electrolytes(SPEs)are expected to solve the safety hazards and limited energy density in the energy storage systems,they still encounter an inferior electrode/electrolyte interface when prepared in an ex situ manner.Recently,in situ polymerization of SPEs favor high interfacial infiltrability,improved interface contact,and reduced interface resistance,owing to the formation of a"superconformal"interface between electrode and electrolyte.Especially,in situ strategies employing ring-opening polymerization(ROP)are emerging as dazzling stars,further enabling moderate polymerization conditions,controllable molecular structure,and reduced interfacial side reaction.As the main monomers that can be in situ polymerized via the ROP strategy,cyclic ethers have been used to construct the CE-SPEs with many merits,including good battery electrochemical performances and a simple assembly process.Here,as a systematic summarization of the existing reports,this review focuses on the polymerization mechanism of ROP,the design principles of CE-SPEs electrolytes,and the recent application of in situ CE-SPEs.In particular,this review thoroughly discusses the selection of different cyclic monomers,initiators and various modification approaches in in situ fabricating CE-SPEs.Ending with offering future challenges and perspectives,this review envisions shedding light on the profound understanding and scientific guidance for further development of high-performance in situ CE-SPEs.
基金the National Natural Science Foundation of China(grant nos.52020105012 and 523B2025)the Innovation and Talent Recruitment Base of New Energy Chemistry and Device(B21003)the Analysis and Testing Center of HUST for the assistance in analysis and testing。
文摘Solid polymer electrolytes(SPEs)have garnered considerable interest in the field of lithium metal batteries(LMBs)owing to their exceptional mechanical strength,excellent designability,and heightened safety characteristics.However,their inherently low ion transport efficiency poses a major challenge for their application in LMBs.To address this issue,covalent organic framework(COF)with their ordered ion transport channels,chemical stability,large specific surface area,and designable multifunctional sites has shown promising potential to enhance lithium-ion conduction.Here,we prepared an anionic COF,Tp Pa-COOLi,which can catalyze the ring-opening copolymerization of cyclic lactone monomers for the in situ fabrication of SPEs.The design leverages the high specific surface area of COF to facilitate the absorption of polymerization precursor and catalyze the polymerization within the pores,forming additional COF-polymer junctions that enhance ion transport pathways.The partial exfoliation of COF achieved through these junctions improved its dispersion within the polymer matrix,preserving ion transport channels and facilitating ion transport across COF grain boundaries.By controlling variables to alter the crystallinity of Tp Pa-COOLi and the presence of-COOLi substituents,Tp Pa-COOLi with partial long-range order and-COOLi substituents exhibited superior electrochemical performance.This research demonstrates the potential in constructing high-performance SPEs for LMBs.
基金supported by National Natural Science Foundation of China(82104082)Natural Science Foundation of Qinghai Province(2024-ZJ-911).
文摘The recent commercialization of gene products has sparked significant interest in gene therapy,necessitating efficient and precise gene delivery via various vectors.Currently,viral vectors and lipid-based nanocarriers are the predominant choices and have been extensively investigated and reviewed.Beyond these vectors,polymeric nanocarriers also hold the promise in therapeutic gene delivery owing to their versatile functionalities,such as improving the stability,cellar uptake and endosomal escape of nucleic acid drugs,along with precise delivery to targeted tissues.This review presents a brief overview of the status quo of the emerging polymeric nanocarriers for therapeutic gene delivery,focusing on key cationic polymers,nanocarrier types,and preparation methods.It also highlights targeted diseases,strategies to improve delivery efficiency,and potential future directions in this research area.The review is hoped to inspire the development,optimization,and clinical translation of highly efficient polymeric nanocarriers for therapeutic gene delivery.
基金supported by the National Natural Science Foundation of China(NSFC)under Grant No.22035001 and No.52233005.
文摘To achieve the target of carbon neutrality,it is crucial to develop an efficient and green synthesis methodology with good atomic economy to achieve sufficient utilization of energy and sustainable development.Photoinduced electron transfer reversible addition-fragmentation chain-transfer(PET-RAFT)polymerization is a precise methodology for constructing polymers with well-defined structures.However,conventional semiconductor-mediated PET-RAFT polymerization still has considerable limitations in terms of efficiency as well as the polymerization environment.Herein,sulfur-doped carbonized polymer dots(CPDs)were hydrothermally synthesized for catalysis of aqueous PET-RAFT polymerization at unprecedented efficiency with a highest propagation rate of 5.05 h-1.The resulting polymers have well-controlled molecular weight and narrow molecular weight dispersion(Ð<1.10).Based on the optoelectronic characterizations,we obtained insights into the photoinduced electron transfer process and proposed the mechanism for CPD-mediated PET-RAFT polymerization.In addition,as-synthesized CPDs for PET-RAFT polymerization were also demonstrated to be suitable for a wide range of light sources(blue/green/solar irradiation),numerous monomers,low catalyst loading(low as 0.01 mg mL^(-1)),and multiple polar solvent environments,all of which allowed to achieve efficiencies much higher than those of existing semiconductor-mediated methods.Finally,the CPDs were confirmed to be non-cytotoxic and catalyzed PET-RAFT polymerization successfully in cell culture media,indicating broad prospects in biomedical fields.
基金We acknowledge the Henan Young Backbone Teachers Foundation(No.2021GGJS135)。
文摘With the continuous development of electronic devices and the information industry towards miniaturization,integration,and high-power consumption,the using of electronic devices will inevitably generate and accumulate heat,which will cause local high temperatures and will seriously reduce their performance,reliability,and lifetime.Therefore,having efficient heat-conducting functional materials is crucial to the normal and stable operation of electrical equipment and microelectronic products.In view of the excellent comprehensive performance of polymer-based thermally conductive materials(including intrinsic polymers and filler-filled polymer-based composites),it has shown great advantages in thermal management applications.In this review,the research status of preparing polymer-based thermally conductive composites and effective strategies to improve their thermal conductivity(TC)are reviewed.Compared with the higher cost and technical support with adjusting the molecular chain structure and cross-linking mode to improve the intrinsic TC of the polymer,introducing suitable fillers into the polymer to build a thermally conductive network or oriented structure can simply and efficiently improve the overall TC.Typical applications of polymer-based composites were discussed with detailed examples in the field of electronic packaging.Challenges and possible solutions to solve the issues are discussed together with the perspectives.This study provides guidance for the future development of polymer-based thermally conductive composites.
文摘In this work,by combining the specific selectivity of molecularly imprinted polymer(MIP)with a simple and sensitive electrochemiluminescence(ECL)detection method,a molecularly imprinted ECL sensor for kanamycin(KA)was developed.The MIP film was synthesized on the surface of gold electrode via electrochemical polymerization,using pyrrole(PY)as the functional monomer and KA as the template molecule.The commonly used luminescent reagent Ru(bpy)32+was employed as the ECL probe,and its co-reagent tripropylamine(TPA)was added to enhance the detection sensitivity of the sensor.Quantitative analysis of KA was performed by evaluating the difference in ECL responses between MIP film electrodes after KA removal and KA rebinding.The sensor exhibited high selectivity,good reproducibility,and stability toward KA,with a linear range of 5.00×10^(-8) to 1.00×10^(-5) mol·L^(-1) and a limit of detection of 1.67×10^(-8) mol·L^(-1)(S/N=3).This work would provide a new idea for the development of simple and sensitive molecularly imprinted ECL sensors.
文摘Building and construction sector, including infrastructures, are facing many challenges which are scarcity of raw materials, CO2 emissions, lower construction efficiency, and deterioration under corrosive environment that cost the world economy $2.5 trillion and this translates to 3.4% of world gross domestic product. This paper presents several examples that show how the use of the nonmetallic materials improved sustainability and life cycles in the built environment by removing the corrosion issue from its root and using durable NM polymers in construction. The paper details recently patented Aramco technology for the use of nonmetallic paving panels that could be used as an alternative to concrete and asphalt paving. Other case studies presented cover use of GFRP Poles for traffic signs and signal poles to replace traditional steel poles. Details of developments for specialist structural application in bridges, in architectural applications, polymers in soils, fibers in pavement manholes and bendable concrete are presented.
文摘Submission Papers appearing in the Journal comprise Editorials,Rapid Communications,Perspectives,Tutorials,Feature Articles,Reviews,Research Articles,which should contain original information,theoretical or experimental,on any topics in the field of polymer science and polymer material science.Papers already published or scheduled to be published elsewhere should not be submitted and certainly will not be accepted.
基金support from the National Natural Science Foundation of China(22301208,92356305)Natural Science Foundation of Anhui Province(2308085J15)+2 种基金Natural Science Foundation of Anhui Provincial Higher Education Institutions(2023AH010012)Natural Science Foundation of Jiangsu Province(BK20230505)Jiangsu Funding Program for Excellent Postdoctoral Talent,Key Laboratory of Polymeric Material Design and Synthesis for Biomedical Function,the Priority Academic Program Development(PAPD)of Jiangsu Higher Education Institutions,Program of Innovative Research Team of Soochow University and Postgraduate Research&Practice Innovation Program of Jiangsu Province.
文摘Natural biomolecular structures possess an inherent ability to encode chiral conformations,thus the generation and regulation of chiroptical activity is crucial.While artificial polymers hold special significance in understanding life's origins,the fundamental connections between the racemic architecture and functional characteristics still need to be fully investigated.Herein,this study reports the generation and regulation of the global chirality and helical sense in racemic polymer systems,focusing on the synergistic effects of liquid crystallinity(LC)and solvophobic interaction.By systematically varying the length of alkyl spacers and the degree of polymerization(DP)of the core-forming azobenzene(Azo)blocks,the chiral communications,morphological transitions and chiroptical properties of the racemic nanoaggregates can be precisely controlled.Furthermore,the proposed“first come,first serve”(FF)and the“late-comer lives above”(LA)effect are broadly applicable and are expected to be applied to various types of racemic polymer systems.This work provides valuable insights into the design of self-assembled systems with tunable global chirality and morphology,thereby advancing the understanding of the origins of homochirality in nature.
基金financially supported by the National Natural Science Foundation of China(Nos.22475035 and 22071021)
文摘Aqueous zinc-ion batteries(AZIBs)are recognized for their commercial viability due to their low cost,high safety,and substantial theoretical capacity.However,the challenges posed by dendrite growth and side reactions of zinc ions hinder the widespread adoption of AZIBs.In this work,a new porous phenolphthalein-based polymer(PPH-CN)is synthesized through the polymerization of phenolphthalein and 2,6-difluorobenzonitrile and served as a protective layer of zinc anode.The PPH-CN layer not only effectively separates the zinc anode from aqueous electrolyte to suppress side reactions,but also provides abundant zincophilic sites to facilitate the deposition of zinc ions.As a result,the Zn@PPH-CN symmetric batteries achieve a notably stable cycle lifespan of 1820 h at a current density of 1 mA cm^(-2),which is thirteen times longer than that of bare Zn.Under the protection of PPH-CN,the zinc anode exhibits a high average Coulombic efficiency(CE)of 99.7%after 3550 cycles in the Zn@PPH-CN//Cu asymmetric battery.The capacity retention rate of Zn@PPH-CN//NH_(4)V_(4)O_(10)full batteries reaches 89.6%after 1000 cycles at 1 Ag^(-1).Furthermore,density functional theory(DFT)simulations identified the Zn^(2+)storage sites of PPH-CN,thereby demonstrating the viability of PPH-CN as interface coatings of zinc anode.This work offers valuable insights into the development of high-performance aqueous battery.
文摘Driven by the dual imperatives of global plastic pollution control and carbon neutrality,research on depolymerizable polymers has become a cutting-edge focus in polymer science.With the continuous emergence of innovative materials,strengthened policy support,and maturing industrial chains,these polymers are demonstrating transformative potential in critical sectors,such as environmental protection,healthcare,and industrial manufacturing,promising for reshaping the future landscape of the plastics industry.
基金financially supported by the National Natural Science Foundation of China (Nos. 92372126,52373203)the Excellent Young Scientists Fund Program
文摘Advancing the integration of artificial intelligence and polymer science requires high-quality,open-source,and large-scale datasets.However,existing polymer databases often suffer from data sparsity,lack of polymer-property labels,and limited accessibility,hindering system-atic modeling across property prediction tasks.Here,we present OpenPoly,a curated experimental polymer database derived from extensive lit-erature mining and manual validation,comprising 3985 unique polymer-property data points spanning 26 key properties.We further develop a multi-task benchmarking framework that evaluates property prediction using four encoding methods and eight representative models.Our re-sults highlight that the optimized degree-of-polymerization encoding coupled with Morgan fingerprints achieves an optimal trade-off between computational cost and accuracy.In data-scarce condition,XGBoost outperforms deep learning models on key properties such as dielectric con-stant,glass transition temperature,melting point,and mechanical strength,achieving R2 scores of 0.65-0.87.To further showcase the practical utility of the database,we propose potential polymers for two energy-relevant applications:high temperature polymer dielectrics and fuel cell membranes.By offering a consistent and accessible benchmark and database,OpenPoly paves the way for more accurate polymer-property modeling and fosters data-driven advances in polymer genome engineering.
基金supported by National Key Research and Development Program of China(Grant No.2022YFB3809000)Major Science and Technology Project of Gansu Province(Grant No.23ZDGA011)+1 种基金National Natural Science Foundation of China(Grant No.22275199,52105224)the Strategic Priority Research Program of the Chinese Academy of Sciences(Grant No.XDB04701022021).
文摘Compared to subtractive manufacturing and casting,3D printing(additive manufacturing)offers advantages,such as the rapid production of complex structures,reduced material waste,and environmental friendliness.Direct ink writing(DIW)is one of the most popular 3D printing techniques owing to its ability to print multiple materials simultaneously and its high compatibility with printing inks.However,DIW presents significant challenges,particularly in the printing of high-performance polymers.The main challenges are as follows:1.The rigid structures and reaction kinetics of high-performance polymers make developing new inks difficult.2.The limited types of available high-performance polymers underscore the need for new DIW-suitable materials.3.Layer-by-layer stacking weakens interlayer bonding,affecting the mechanical properties of the printed product.4.The accuracy and speed of DIW printing are insufficient for large-scale manufacturing.After introducing the topic,the requirements for DIW printing inks are first reviewed,emphasizing the importance of thixotropic agents.Then,research progress regarding DIW printing of high-performance polymers is comprehensively reviewed according to the requirements of different polymer inks.Additionally,the applications of these materials across various fields are summarized.Finally,the challenges in DIW printing of high-performance polymers,along with corresponding solutions and future development prospects,are discussed in detail.
基金supported by the National Natural Science Foundation of China(Nos.82402822,82360427,82372425,82072443,and 32200559)the Priority Union Foundation of Yunnan Provincial Science and Technology Department and Kunming Medical University(No.202301AY070001-164)+1 种基金the Natural Science Foundation of Sichuan Province(No.23NSFSC5880)the Central Government of Sichuan Province Guiding the Special Project of Local Science and Technology Development(No.2024ZYD0155).
文摘Three-dimensional(3 D)printing has revolutionized the design and production of customized scaffolds,but the minimally invasive implantation of 3 D-printed structures into the human body remains challenging.This has prompted the exploration of innovative materials and technical solutions.Shape-memory polymers,as advanced intelligent materials,exhibit considerable potential in minimally invasive surgical applications.Herein,we developed a novel thermosetting shape-memory polymer,poly(L-lactic acid)-trimethylene carbonate-glycolic acid(PLLA-TMC-GA),for the fabrication of bioengineered scaffolds with body temperature-activated shape-memory functionality.We comprehensively evaluated the mechanical properties,thermal stability,shape-memory capabilities,biocompatibility,biodegradability,and 3 D printing performance of PLLA-TMC-GA terpolymers with various compositions.The results indicate that PLLA-TMC-GA exhibits exceptional shape-memory performance,adjustable material properties,favorable biocompatibility,and the potential for controlled biodegradation and reabsorption.The use of PLLA-TMC-GA as a biodegradable shape-memory polymer allows the reduction of implant volume,simplifies implantation,and enables on-demand activation at body temperature.These characteristics present new opportunities for the advancement of minimally invasive surgical techniques.
