The traditional inflexible electromagnetic interference(EMI)shielding materials have poor adaptability to wearable and portable flexible electronic devices due to their shortcomings such as brittleness and difficulty ...The traditional inflexible electromagnetic interference(EMI)shielding materials have poor adaptability to wearable and portable flexible electronic devices due to their shortcomings such as brittleness and difficulty in machinability.As an optimized alternative,the conductive polymer composites(CPCs)constructed by integrating MXene and polymer have become one of the most promising EMI shielding materials.To cope with the more harsh application conditions,the processing-structure-property relationship of MXene/polymer EMI shielding composites urgently needs to be clarified.In this review,the EMI shielding mechanism and theory of CPCs are first outlined.Then,the recent advances in processing strategies for MXene/polymer EMI shielding composites with different structures are comprehensively summarized,including layered structure,segregated structure,and porous structure.Next,the multifunctionality of MXene/polymer EMI shielding composites in hydrophobicity,flame retardancy,thermal conductivity,infrared thermal camouflage,electrothermal conversion,photothermal conversion,and sensing function,is systematically introduced.Finally,the prospects and challenges for the future development and application of multifunctional MXene/polymer EMI shielding composites are discussed.This review aims to put forward effective guidance for fabricating intelligent,adaptable,and integrated MXene/polymer EMI shielding composites,thus promoting the upgrading of advanced MXene-based CPCs.展开更多
The chemical structure of polyamide 6(PA6)dictates that only 50%of hydrogen bonds participate in crystallization during the crystallization process,resulting in the properties of its products being significantly depen...The chemical structure of polyamide 6(PA6)dictates that only 50%of hydrogen bonds participate in crystallization during the crystallization process,resulting in the properties of its products being significantly dependent on the molding process.Therefore,the design and development of nucleating agents suitable for PA6 holds great practical significance for high-performance PA6 materials.Amide-based nucleating agents can effectively improve the crystallization rate by increasing intermolecular hydrogen bond density.Further introduction of hydroxyl groups can enhance the hydrogen bonding interactions between the nucleating agent and PA6.In this study,a hydroxyl-containing amidebased nucleating agent,BHT,was designed and synthesized using a tyramine-based biomass as the raw material.These results demonstrated that BHT exhibited good structural compatibility with PA6.After adding 1 wt%BHT,the crystallization temperature of PA6 increased from 170.9℃to 193.3℃,the crystallinity increased 16.6%,the heat distortion temperature and Vicat softening temperature rose to 89.5 and 187.8℃,respectively,the haze decreased to 46%,achieving the synergistic optimization of mechanical,thermal,and optical properties.The in situ time-resolved FTIR results indicated that the addition of BHT increased the enthalpy of hydrogen bond formation during the nucleation stage,facilitated the segmental conformation adjustment of PA6,and enhanced the molar concentration of trans-conformations,ultimately leading to an improvement in the crystallization rate.展开更多
The miniaturization and high-power density of electronic devices presents new challenges in thermal management.The precise control of microstructure arrangement,particularly in boron nitride nanosheets(BNNS),is essent...The miniaturization and high-power density of electronic devices presents new challenges in thermal management.The precise control of microstructure arrangement,particularly in boron nitride nanosheets(BNNS),is essential for achieving efficient heat dissipation in highly thermally conductive composites within electrically insulating package.In this work,manganese ferrite was hydrothermally synthesized on BNNS,creating a layered structure in a magnetically responsive nanohybrid material named BNNS@M.This material was then integrated into a waterborne polyurethane(WPU)solution and shaped under a magnetic field to produce thermally conductive film.By altering the magnetic field direction,the mi-crostructure orientation of BNNS@M was controlled,resulting in anisotropic thermally conductive com-posite films with horizontal and vertical orientations.Specifically,under a vertical magnetic field,the film 30-Ve-BNNS@WPU,containing 30 wt.%BNNS@M,achieved a through-plane thermal conductivity of 8.5 W m^(−1)K^(−1)and an in-plane thermal conductivity of 1.8 W m^(−1)K^(−1),showcasing significant anisotropic thermal conductivity.Meanwhile,these films demonstrated excellent thermal stability,mechanical per-formance,and flame retardancy.Furthermore,employing Foygel’s theory elucidated the impact of filler arrangement on thermal conductivity mechanisms and the actual application of 5 G device chips and LED lamps emphasizing the potential of these thermally conductive films in thermal management appli-cations.This investigation contributes valuable design concepts and foundations for the development of anisotropic thermally conductive composites suitable for electron thermal management.展开更多
Mini light-emitting diodes(Mini-LEDs)show great application potential in high-end displays owing to their superior pixel density,brightness,responsiveness,and efficiency.However,current packaging materials for Mini-LE...Mini light-emitting diodes(Mini-LEDs)show great application potential in high-end displays owing to their superior pixel density,brightness,responsiveness,and efficiency.However,current packaging materials for Mini-LEDs are predominantly thermally cured,which is energy-and time-consuming and can adversely affect electronic components.In this study,a novel UV-curable silicone resin containing phenyl,disulfide,and acryloyl groups(SPASR)is developed from commercially available siloxanes.The resin exhibits a refractive index(n_(d))higher than 1.5,and it can be cured within 30 s under UV irradiation.After curing,it exhibits an optical transparency exceeding 92%,a lap adhesion strength of up to1.84 MPa,and good thermostability(T_(5%)>265℃).Notably,the volume shrinkage is less than 4.83%,attributed to the release of photopolymerization stress via UV-induced disulfide metathesis during UV curing.Mini-LEDs encapsulated with this resin show luminescence properties comparable to those of conventional thermally-cured sealants,and show excellent sealability wihtout visible penetration after being immersed in red ink for 12 h.Consequently,these excellent properties make the SPASR resin an ideal candidate for microelectronic encapsulation,offering a more reliable and efficient solution for the electronics industry.展开更多
In this article,graphene oxide(GO)and benzotriazole-loaded mesoporous silica nanoparticles(BTA/MSNs)are combined on micro scale through the in situ polymerization of polydopamine(PDA),preparing a selfhealing bi-functi...In this article,graphene oxide(GO)and benzotriazole-loaded mesoporous silica nanoparticles(BTA/MSNs)are combined on micro scale through the in situ polymerization of polydopamine(PDA),preparing a selfhealing bi-functional GO(fGO)used as nano-fillers for anti-corrosion enhancement of waterborne epoxy(WEP)coatings.Scanning electronic microscopy(SEM)images show that the BTA/MSNs are uniformly distributed on the surface of high aspect ratio GO nanosheets to endow GO nanocontainer characteristics.UV-vis profiles demonstrate that fGO has p H-controlled release function.Modulus at lowest frequency is generally used for comparing the corrosion resistance of organic coatings.Modulus at lowest frequency(1.42×10^(5)Ωcm^(2))after 30 days immersion in 3.5 wt.%Na Cl solution revealed 2 orders of magnitude higher that of blank WEP(1.17×10^(7)Ωcm^(2)).With artificial cracks on its coatings,fGO/WEP had no obvious rust compared with blank WEP after 240 h of immersion.We anticipate that self-healing and physical barrier bi-functional nanocontainers improve the traditional anticorrosion coating efficiency with better,longer-lasting performance for shipping,oil drilling or bridge maintenance.展开更多
The effect of Ti3C2 MXene nanosheets on the intumescent flame retardant(IFR)poly(lactic acid)(PLA)composites was investigated among a series of PLA/IFR/MXene,which were prepared by melt blending 0-2.0 wt%MXene,10.0 wt...The effect of Ti3C2 MXene nanosheets on the intumescent flame retardant(IFR)poly(lactic acid)(PLA)composites was investigated among a series of PLA/IFR/MXene,which were prepared by melt blending 0-2.0 wt%MXene,10.0 wt%-12.0 wt%IFR and PLA together.The results of limiting oxygen index(LOI)and vertical burning(UL-94)discover that the combination of 0.5 wt%MXene and 11.5 wt%IFR synergistically improves the fire safety of PLA to reach UL-94 V-0 rating with LOI value of 33.0%.The PLA/IFR/MXene composites perform an obvious reduction in peak of heat release rate(HRR)in cone calorimeter tests(CCTs).Furthermore,the carbon residues after CCTs were characterized by scanning electron microscope(SEM),laser Raman spectroscopy(LRS),X-ray diffraction(XRD)and X-ray photoelectron spectroscopy(XPS).It is demonstrated that both the titanium composition of the MXene structure and the characteristics of the two-dimensional material enhance the PLA/IFR/MXene composite materials’ability to produce a dense barrier layer to resist burnout during thermal degradation.展开更多
The risk of leakage and low thermal conductivity severely hinder the wide application of phase change materials(PCMs).In this work,the high-density polyethylene/carbon nanotubes(HDPE/CNTs)porous scaffolds were success...The risk of leakage and low thermal conductivity severely hinder the wide application of phase change materials(PCMs).In this work,the high-density polyethylene/carbon nanotubes(HDPE/CNTs)porous scaffolds were successfully fabricated via a sacrificial template method followed by the general melt blending and water solvent etching.Subsequently,a series of paraffin wax HDPE/CNTs/PW composite PCMs were obtained combined with the simple vacuum impregnation method.The obtained HDPE/CNTs porous scaffolds can effectively avoid the leakage of PW,meanwhile,the thermal conductivity and electrical conductivity of HDPE/CNTs/PW-3:7 are increased by 2.94 times and 13 orders of magnitude compared with the HDPE/PW-3:7 respectively,also,it exhibits high phase change enthalpy(153.95 J/g for melting enthalpy and 152.82 J/g for crystallization enthalpy).From the above perspectives,the HDPE/CNTs/PW-3:7 has promising potential value in the application of light-to-thermal conversion,electro-to-thermal conversion and thermal energy storage.展开更多
The development of miniaturized,flexible,and portable electronic devices has led to an increasing demand for multifunctional flexible films that can provide temperature regulation,electromagnetic interference(EMI)shie...The development of miniaturized,flexible,and portable electronic devices has led to an increasing demand for multifunctional flexible films that can provide temperature regulation,electromagnetic interference(EMI)shielding,and thermal management.In this study,a novel hierarchical multifunctional flexible composite film is presented.The first step involves the synthesis of phase change microcapsule(PCMC)latex through in-situ polymerization.Next,PCMC and waterborne polyurethane(WPU)latex were mixed and dried using a binary colloidal approach to produce a flexible composite phase change film(WPU/PCMC)with complete anti-leakage and satisfying melting enthalpy(147.86 J g^(-1)).To enhance the EMI performance and mechanical strength,a thin layer of antioxidant MXene@poly tannin acid(PTA)was directly sprayed onto the surface of WPU/PCMC,resulting in the WPU/PCMC/MXene@PTA film(WPM).Consequently,the WPM displays exceptional thermal management performance for multiple drives and outstanding EMI performance(56.86 dB),making it an ideal candidate for future multifunctional products.展开更多
Phase change materials(PCMs)offer a promising solution to address the challenges posed by intermittency and fluctuations in solar thermal utilization.However,for organic solid-liquid PCMs,issues such as leakage,low th...Phase change materials(PCMs)offer a promising solution to address the challenges posed by intermittency and fluctuations in solar thermal utilization.However,for organic solid-liquid PCMs,issues such as leakage,low thermal conductivity,lack of efficient solar-thermal media,and flamma-bility have constrained their broad applications.Herein,we present an innova-tive class of versatile composite phase change materials(CPCMs)developed through a facile and environmentally friendly synthesis approach,leveraging the inherent anisotropy and unidirectional porosity of wood aerogel(nanowood)to support polyethylene glycol(PEG).The wood modification process involves the incorporation of phytic acid(PA)and MXene hybrid structure through an evaporation-induced assembly method,which could impart non-leaking PEG filling while concurrently facilitating thermal conduction,light absorption,and flame-retardant.Consequently,the as-prepared wood-based CPCMs showcase enhanced thermal conductivity(0.82 W m^(-1)K^(-1),about 4.6 times than PEG)as well as high latent heat of 135.5 kJ kg^(-1)(91.5%encapsula-tion)with thermal durability and stability throughout at least 200 heating and cooling cycles,featuring dramatic solar-thermal conversion efficiency up to 98.58%.In addition,with the synergistic effect of phytic acid and MXene,the flame-retardant performance of the CPCMs has been significantly enhanced,showing a self-extinguishing behavior.Moreover,the excellent electromagnetic shielding of 44.45 dB was endowed to the CPCMs,relieving contemporary health hazards associated with electromagnetic waves.Overall,we capitalize on the exquisite wood cell structure with unidirectional transport inherent in the development of multifunctional CPCMs,showcasing the operational principle through a proof-of-concept prototype system.展开更多
Rational design of hybrid carbon host with high electrical conductivity and strong adsorption toward soluble lithium polysulfides is the main challenge for achieving high-performance lithium-sulfur batteries(LSBs).Her...Rational design of hybrid carbon host with high electrical conductivity and strong adsorption toward soluble lithium polysulfides is the main challenge for achieving high-performance lithium-sulfur batteries(LSBs).Herein,novel binder-free Ni@N-doped carbon nanospheres(N-CNSs)films as sulfur host are firstly synthesized via a facile combined hydrothermal-atomic layer deposition method.The cross-linked multilayer N-CNSs films can effectively enhance the electrical conductivity of electrode and provide physical blocking“dams”toward the soluble long-chain polysulfides.Moreover,the doped N heteroatoms and superficial NiO layer on Ni layer can work synergistically to suppress the shuttle of lithium polysulfides by effective chemical interaction/adsorption.In virtue of the unique composite architecture and reinforced dual physical and chemical adsorption to the soluble polysulfides,the obtained Ni@N-CNSs/S electrode is demonstrated with enhanced rate performance(816 mAh g?1 at 2 C)and excellent long cycling life(87%after 200 cycles at 0.1 C),much better than N-CNSs/S electrode and other carbon/S counterparts.Our proposed design strategy offers a promising prospect for construction of advanced sulfur cathodes for applications in LSBs and other energy storage systems.展开更多
Black phosphorus(BP),as one of the most promising fillers for flame retarding polymer,has been seriously limited in practical application,due to the agglomeration and poor structural stability challenges.Here,the BP w...Black phosphorus(BP),as one of the most promising fillers for flame retarding polymer,has been seriously limited in practical application,due to the agglomeration and poor structural stability challenges.Here,the BP was modified by MXene and polydopamine(PDA)via ultrasonication and dopamine modification strategy to improve the structural stability and dispersibility in the matrix.Then,the obtained(BP-MXene@PDA)nanohybrid was employed to promote the mechanical performance,thermal stability,and flame retardancy of thermoplastic polyurethane elastomer(TPU).The resultant TPU composite containing 2 wt.%of BP1-MXene2@PDA showed a 19.2%improvement in the tensile strength and a 13.8%increase in the elongation at break compared to those of the pure TPU.The thermogravimetric analysis suggested that BP-MXene@PDA clearly enhances the thermal stability of TPU composites.Furthermore,the introduction of the BP-MXene@PDA nanohybrids could considerably improve the flame retardancy of TPU composite,i.e.,64.2%and 27.3%decrease in peak heat release rate and total heat release,respectively.The flame-retardant mechanisms of TPU/BP-MXene@PDA in the gas phase and condensed phase were investigated systematically.This work provides a novel strategy to simultaneously enhance the fire safety and mechanical properties of TPU,thus expanding its industrial applications.展开更多
The crystalline and amorphous regions were alternately arranged in the hard elastic polypropylene(PP)films with row-nucleated lamellae.In this work,their structure evolution during stretching and recovery at room temp...The crystalline and amorphous regions were alternately arranged in the hard elastic polypropylene(PP)films with row-nucleated lamellae.In this work,their structure evolution during stretching and recovery at room temperature was followed and the elastic recovery mechanism was discussed by twice cyclic tensile experiment.During the first stretching to 100%,the lamellae crystals are parallel separated and the intercrystallite crazing is formed at the first yield point.Many nano-cavities within the intercrystallite crazing appear when the strain reaches 20%.The strain-hardening process accompanies with the lamellae long period increasing and the intercrystallite crazing enlargement.After the secondary yield point,the lamellae cluster is further separated and more nano-cavities appear.The first and second recovery processes are complete overlap.During recovery,firstly,the energy elasticity provided by nano-cavities surface tension drives the shrinkage of material,and then the entropy elasticity related to amorphous chain relaxation plays a leading role when the strain is smaller than the secondary yield point.The elastic recovery process of hard elastic material is the co-contribution of energy elasticity and entropy elasticity.This work gives a clearer recognition about the source of hard elastic property and the role of amorphous region in material's deformation.展开更多
Microencapsulation of phase change materials(MPCM)is an effective way to achieve solar energy management.However,the crystallization of phase change materials(PCMs)in microcapsules will produce supercooling,which will...Microencapsulation of phase change materials(MPCM)is an effective way to achieve solar energy management.However,the crystallization of phase change materials(PCMs)in microcapsules will produce supercooling,which will affect the energy storage efficiency of MPCM.The incorporation of TiO_(2)nanoparticles into MPCM can alleviate supercooling.In this work,octadecyltrimethoxysilane(ODTMS)was used to modify the solid nucleating agent TiO_(2)(m-TiO_(2))to improve its compatibility with n-Octadecane.Then,MPCM based on m-TiO_(2)nucleating agent,melamine-formaldehyde resin(MF)shell material,and n-Octadecane core material was prepared.Differential scanning calorimetry(DSC)results demonstrate that the supercooling degree(ΔT)of MPCM(MPCM-02)decreases to 0℃with a tiny level of 0.25 wt%m-TiO_(2),while the MPCM with unmodified TiO_(2)is 6.1℃and the MPCM without nucleating agent is 4.1℃.Besides,the phase change enthalpy(ΔHm)and encapsulation efficiency(E)of MPCM-02 remain at 183.7 J/g and 95.3%,respectively.Finally,phase change composite materials with photothermal conversion capabilities were constructed by MXenes,MPCM,and polyurethane acrylate(PUA).When 1 wt%MXenes and 30 wt%MPCM were incorporated into PUA matrix,the thermal conductivity and surface temperature after 1200s of infrared light irradiation were 48.8%and 8.2℃higher than pure PUA matrix.These results demonstrate the good solar energy storage capabilities of the MPCM,which possesses promising application potential in the field of solar energy thermal management and human thermal regulation.展开更多
Core-shell colloidal particles with a polymer layer have broad applications in different areas.Herein,we developed a two-step method combining aqueous surface-initiated photoinduced polymerization-induced self-assembl...Core-shell colloidal particles with a polymer layer have broad applications in different areas.Herein,we developed a two-step method combining aqueous surface-initiated photoinduced polymerization-induced self-assembly and photoinduced seeded reversible addition-fragmentation chain transfer(RAFT)polymerization to prepare a diverse set of core-shell colloidal particles with a well-defined polymer layer.Chemical compositions,structures,and thicknesses of polymer layers could be conveniently regulated by using different types of monomers and feed[monomer]/[chain transfer agent]ratios during seeded RAFT polymerization.展开更多
Polymerization-induced self-assembly(PISA)has become one of the most versatile approaches for scalable preparation of linear block copolymer nanoparticles with various morphologies.However,the controlled introduction ...Polymerization-induced self-assembly(PISA)has become one of the most versatile approaches for scalable preparation of linear block copolymer nanoparticles with various morphologies.However,the controlled introduction of branching into the core-forming block and the effect on the morphologies of block copolymer nanoparticles under PISA conditions have rarely been explored.Herein,a series of multifunctional macromolecular chain transfer agents(macro-CTAs)were first synthesized by a two-step green light-activated photoiniferter polymerization using two types of chain transfer monomers(CTMs).These macro-CTAs were then used to mediate reversible addition-fragmentation chain transfer(RAFT)dispersion polymerization of styrene(St)to prepare block copolymers with different core-forming block structures and the assemblies.The effect of the core-forming block structure on the morphology of block copolymer nanoparticles was investigated in detail.Transmission electron microscopy(TEM)analysis indicated that the brush-like core-forming block structure facilitated the formation of higher-order morphologies,while the branched core-forming block structure favored the formation of lower-order morphologies.Moreover,it was found that using macroCTAs with a shorter length also promoted the formation of higher-order morphologies.Finally,structures of block copolymers and the assemblies were further controlled by changing the structure of macro-CTA or using a binary mixture of two different macro-CTAs.We expect that this work not only sheds light on the synthesis of block copolymer nanoparticles but also provide important mechanistic insights into PISA of nonlinear block copolymers.展开更多
Herein,a simple and effective outer-surface interactions assisted supramolecular hierarchical assembly has been first exploited to uniformly distribute tungstosilicic acid(TSA)inside the porous structure of cucurbit[1...Herein,a simple and effective outer-surface interactions assisted supramolecular hierarchical assembly has been first exploited to uniformly distribute tungstosilicic acid(TSA)inside the porous structure of cucurbit[10]uril-based single-layer 2D supramolecular-organic-frameworks(Q[10]-SOFs)in water.Importantly,the 2D Q[10]-SOFs can further serve as light harvesting antenna,achieving fast energy transfer to the embedded redox-active TSA upon photoexcitation,resulting in efficient visible light-driven selective oxidation of benzyl alcohols into the corresponding aldehydes in high yield at room temperature.Further studies revealed that the integrated of 2D Q[10]-SOFs and TSA played a key role in the catalytic process,due to the presence of a novel stepwise electron transfer route in the single-layer hybrid 2D structures.展开更多
The rapid development of industrialization necessitates advancements in nanomaterials.Black phospho-rus(BP)nanosheets have garnered extensive attention due to their highly anisotropic optoelectronic properties,high ca...The rapid development of industrialization necessitates advancements in nanomaterials.Black phospho-rus(BP)nanosheets have garnered extensive attention due to their highly anisotropic optoelectronic properties,high carrier mobility,and excellent mechanical properties.These unique attributes make BP nanosheets advantageous in various research fields.Combining BP nanosheets with polymers results in functional coatings and films with flame retardancy,antibacterial properties,wear resistance,and cor-rosion resistance.In this review,we first introduce various preparation methods for BP nanosheets.We discuss the degradation mechanisms of BP nanosheets and the passivation techniques employed to en-hance their environmental stability.Subsequently,we provide a detailed and comprehensive review of the applications of BP nanosheets in polymer coatings and films.Finally,we outline the development challenges and future research opportunities for BP-based polymer coatings and films.This article aims to summarize existing research and provide objective insights,serving as a constructive reference for the advancement of modern multifunctional polymer coatings and films.展开更多
Polymerization-induced self-assembly(PISA)is an emerging method for the preparation of block copolymer nano-objects at high concentrations.However,most PISA formulations have oxygen inhibition problems and inert atmos...Polymerization-induced self-assembly(PISA)is an emerging method for the preparation of block copolymer nano-objects at high concentrations.However,most PISA formulations have oxygen inhibition problems and inert atmospheres(e.g.argon,nitrogen)are usually required.Moreover,the large-scale preparation of block copolymer nano-objects at room temperature is challenging.Herein,we report an enzyme-assisted photoinitiated polymerization-induced self-assembly(photo-PISA)in continuous flow reactors with oxygen toleranee.The addition of glucose oxidase(GOx)and glucose into the reaction mixture can consume oxygen efficiently and constantly,allow the flow photo-PISA to be performed under open-air conditions.Polymerization kinetics indicated that only a small amount of GOx(0.5 μmol/L)was needed to achieve the oxygen tolerance.Block copolymer nano-objects with different morphologies can be prepared by varying reaction conditions including the degree of polymerization(DP)of core-forming block,monomer concentration,reaction temperature,and solvent composition.We expect this study will provide a facile platform for the large-scale production of block copolymer nano-objects with different morphologies at room temperature.展开更多
The development of fast rechargeable lithium ion batteries(LIBs)is highly dependent on the innovation of advanced high-power electrode materials.In this work,for the first time,we report a sacrificial NiO arrays templ...The development of fast rechargeable lithium ion batteries(LIBs)is highly dependent on the innovation of advanced high-power electrode materials.In this work,for the first time,we report a sacrificial NiO arrays template method for controllable synthesis of self-supported hierarchical porous Li_(4)Ti_(5)O_(12)/C(LTO/C)nanoflakes arrays,for use as fast rechargeable anodes for LIBs.The ultrathin(2-3 nm)carbon layer was uniformly coated on the LTO forming arrays architecture.The hierarchical porous LTO/C nanoflakes consisted of primary cross-linked nanoparticles of 50-100 nm and showed large porosity.Because of the enhanced electrical conductivity and accelerated ion transfer channels,the well-designed binderfree porous LTO/C nanoflakes arrays exhibited notable high-rate lithium ion storage performance with smaller polarization,better electrochemical reactivity,higher specific capacity(157 mAh g^(-1) at the current density of 20C)and improved long-term cycling life(96.2% after 6000 cycles at 20C),superior to the unmodified porous LTO arrays counterpart(126 mAh g^(-1) at 20C and 88.0%after 6000 cycles at 20C).Our work provides a new template for the construction of high-performance high-rate electrodes for electrochemical energy storage.展开更多
Stimulus-responsive vesicles have broad applications in a variety of areas. Herein, oxidation-responsive framboidal triblock copolymer vesicles are prepared by photoinitiated RAFT seeded emulsion polymerization of a t...Stimulus-responsive vesicles have broad applications in a variety of areas. Herein, oxidation-responsive framboidal triblock copolymer vesicles are prepared by photoinitiated RAFT seeded emulsion polymerization of a thioether-functionalized monomer using diblock copolymer vesicles as seeds. The obtained framboidal vesicles can transform into worms or spheres in the presence of reactive oxygen species,which can be further used for controlled release of cargos(e.g., silica nanoparticles).展开更多
基金financially supported by the National Natural Science Foundation of China(No.52436003)the Science and Technology Program of Guangzhou(No.2024A04J3710).
文摘The traditional inflexible electromagnetic interference(EMI)shielding materials have poor adaptability to wearable and portable flexible electronic devices due to their shortcomings such as brittleness and difficulty in machinability.As an optimized alternative,the conductive polymer composites(CPCs)constructed by integrating MXene and polymer have become one of the most promising EMI shielding materials.To cope with the more harsh application conditions,the processing-structure-property relationship of MXene/polymer EMI shielding composites urgently needs to be clarified.In this review,the EMI shielding mechanism and theory of CPCs are first outlined.Then,the recent advances in processing strategies for MXene/polymer EMI shielding composites with different structures are comprehensively summarized,including layered structure,segregated structure,and porous structure.Next,the multifunctionality of MXene/polymer EMI shielding composites in hydrophobicity,flame retardancy,thermal conductivity,infrared thermal camouflage,electrothermal conversion,photothermal conversion,and sensing function,is systematically introduced.Finally,the prospects and challenges for the future development and application of multifunctional MXene/polymer EMI shielding composites are discussed.This review aims to put forward effective guidance for fabricating intelligent,adaptable,and integrated MXene/polymer EMI shielding composites,thus promoting the upgrading of advanced MXene-based CPCs.
文摘The chemical structure of polyamide 6(PA6)dictates that only 50%of hydrogen bonds participate in crystallization during the crystallization process,resulting in the properties of its products being significantly dependent on the molding process.Therefore,the design and development of nucleating agents suitable for PA6 holds great practical significance for high-performance PA6 materials.Amide-based nucleating agents can effectively improve the crystallization rate by increasing intermolecular hydrogen bond density.Further introduction of hydroxyl groups can enhance the hydrogen bonding interactions between the nucleating agent and PA6.In this study,a hydroxyl-containing amidebased nucleating agent,BHT,was designed and synthesized using a tyramine-based biomass as the raw material.These results demonstrated that BHT exhibited good structural compatibility with PA6.After adding 1 wt%BHT,the crystallization temperature of PA6 increased from 170.9℃to 193.3℃,the crystallinity increased 16.6%,the heat distortion temperature and Vicat softening temperature rose to 89.5 and 187.8℃,respectively,the haze decreased to 46%,achieving the synergistic optimization of mechanical,thermal,and optical properties.The in situ time-resolved FTIR results indicated that the addition of BHT increased the enthalpy of hydrogen bond formation during the nucleation stage,facilitated the segmental conformation adjustment of PA6,and enhanced the molar concentration of trans-conformations,ultimately leading to an improvement in the crystallization rate.
基金supported by the National Natural Science Foundation of China(No.22268025)the Guangdong Basic and Applied Basic Research Foundation(No.2023A1515011985)the Applied Basic Research Program of Yunnan Province(Nos.202201AT070115,202201BE070001–031).
文摘The miniaturization and high-power density of electronic devices presents new challenges in thermal management.The precise control of microstructure arrangement,particularly in boron nitride nanosheets(BNNS),is essential for achieving efficient heat dissipation in highly thermally conductive composites within electrically insulating package.In this work,manganese ferrite was hydrothermally synthesized on BNNS,creating a layered structure in a magnetically responsive nanohybrid material named BNNS@M.This material was then integrated into a waterborne polyurethane(WPU)solution and shaped under a magnetic field to produce thermally conductive film.By altering the magnetic field direction,the mi-crostructure orientation of BNNS@M was controlled,resulting in anisotropic thermally conductive com-posite films with horizontal and vertical orientations.Specifically,under a vertical magnetic field,the film 30-Ve-BNNS@WPU,containing 30 wt.%BNNS@M,achieved a through-plane thermal conductivity of 8.5 W m^(−1)K^(−1)and an in-plane thermal conductivity of 1.8 W m^(−1)K^(−1),showcasing significant anisotropic thermal conductivity.Meanwhile,these films demonstrated excellent thermal stability,mechanical per-formance,and flame retardancy.Furthermore,employing Foygel’s theory elucidated the impact of filler arrangement on thermal conductivity mechanisms and the actual application of 5 G device chips and LED lamps emphasizing the potential of these thermally conductive films in thermal management appli-cations.This investigation contributes valuable design concepts and foundations for the development of anisotropic thermally conductive composites suitable for electron thermal management.
基金financially supported by the National Natural Science Foundation of China(No.52273104)。
文摘Mini light-emitting diodes(Mini-LEDs)show great application potential in high-end displays owing to their superior pixel density,brightness,responsiveness,and efficiency.However,current packaging materials for Mini-LEDs are predominantly thermally cured,which is energy-and time-consuming and can adversely affect electronic components.In this study,a novel UV-curable silicone resin containing phenyl,disulfide,and acryloyl groups(SPASR)is developed from commercially available siloxanes.The resin exhibits a refractive index(n_(d))higher than 1.5,and it can be cured within 30 s under UV irradiation.After curing,it exhibits an optical transparency exceeding 92%,a lap adhesion strength of up to1.84 MPa,and good thermostability(T_(5%)>265℃).Notably,the volume shrinkage is less than 4.83%,attributed to the release of photopolymerization stress via UV-induced disulfide metathesis during UV curing.Mini-LEDs encapsulated with this resin show luminescence properties comparable to those of conventional thermally-cured sealants,and show excellent sealability wihtout visible penetration after being immersed in red ink for 12 h.Consequently,these excellent properties make the SPASR resin an ideal candidate for microelectronic encapsulation,offering a more reliable and efficient solution for the electronics industry.
基金supported by the National Natural Science Foundation of China(Grant No.51908031)the China Scholarship Council for a graduate fellowship(201906150013)+2 种基金the support from Guangdong Special Support Program(Grant No.2017TX04N371)ERC Enercapsule project(647969)Royal Society project IECR2202163。
文摘In this article,graphene oxide(GO)and benzotriazole-loaded mesoporous silica nanoparticles(BTA/MSNs)are combined on micro scale through the in situ polymerization of polydopamine(PDA),preparing a selfhealing bi-functional GO(fGO)used as nano-fillers for anti-corrosion enhancement of waterborne epoxy(WEP)coatings.Scanning electronic microscopy(SEM)images show that the BTA/MSNs are uniformly distributed on the surface of high aspect ratio GO nanosheets to endow GO nanocontainer characteristics.UV-vis profiles demonstrate that fGO has p H-controlled release function.Modulus at lowest frequency is generally used for comparing the corrosion resistance of organic coatings.Modulus at lowest frequency(1.42×10^(5)Ωcm^(2))after 30 days immersion in 3.5 wt.%Na Cl solution revealed 2 orders of magnitude higher that of blank WEP(1.17×10^(7)Ωcm^(2)).With artificial cracks on its coatings,fGO/WEP had no obvious rust compared with blank WEP after 240 h of immersion.We anticipate that self-healing and physical barrier bi-functional nanocontainers improve the traditional anticorrosion coating efficiency with better,longer-lasting performance for shipping,oil drilling or bridge maintenance.
基金support from the National Natural Science Foundation of China(Grant Nos.21908031 and 51903092)the China Postdoctoral Science Foundation funded project(Grant No.2019M652884)support from Guangdong Special Support Program(Grant No.2017TX04N371)。
文摘The effect of Ti3C2 MXene nanosheets on the intumescent flame retardant(IFR)poly(lactic acid)(PLA)composites was investigated among a series of PLA/IFR/MXene,which were prepared by melt blending 0-2.0 wt%MXene,10.0 wt%-12.0 wt%IFR and PLA together.The results of limiting oxygen index(LOI)and vertical burning(UL-94)discover that the combination of 0.5 wt%MXene and 11.5 wt%IFR synergistically improves the fire safety of PLA to reach UL-94 V-0 rating with LOI value of 33.0%.The PLA/IFR/MXene composites perform an obvious reduction in peak of heat release rate(HRR)in cone calorimeter tests(CCTs).Furthermore,the carbon residues after CCTs were characterized by scanning electron microscope(SEM),laser Raman spectroscopy(LRS),X-ray diffraction(XRD)and X-ray photoelectron spectroscopy(XPS).It is demonstrated that both the titanium composition of the MXene structure and the characteristics of the two-dimensional material enhance the PLA/IFR/MXene composite materials’ability to produce a dense barrier layer to resist burnout during thermal degradation.
基金supported by the National Natural Science Foundation of China(Grant No.51903092)support from Guangdong Special Support Program(Grant No.2017TX04N371)。
文摘The risk of leakage and low thermal conductivity severely hinder the wide application of phase change materials(PCMs).In this work,the high-density polyethylene/carbon nanotubes(HDPE/CNTs)porous scaffolds were successfully fabricated via a sacrificial template method followed by the general melt blending and water solvent etching.Subsequently,a series of paraffin wax HDPE/CNTs/PW composite PCMs were obtained combined with the simple vacuum impregnation method.The obtained HDPE/CNTs porous scaffolds can effectively avoid the leakage of PW,meanwhile,the thermal conductivity and electrical conductivity of HDPE/CNTs/PW-3:7 are increased by 2.94 times and 13 orders of magnitude compared with the HDPE/PW-3:7 respectively,also,it exhibits high phase change enthalpy(153.95 J/g for melting enthalpy and 152.82 J/g for crystallization enthalpy).From the above perspectives,the HDPE/CNTs/PW-3:7 has promising potential value in the application of light-to-thermal conversion,electro-to-thermal conversion and thermal energy storage.
基金the Guangdong Basic and Applied Basic Research Foundation(No.2023A1515011985)the National Natural Science Foundation of China(No.U20A20299)the Scientific and Technological Innovation Strategy Program of Guangdong Province:Guangdong-Hong Kong-Macao Technology Cooperation Funding Scheme(No.2022A0505030026).
文摘The development of miniaturized,flexible,and portable electronic devices has led to an increasing demand for multifunctional flexible films that can provide temperature regulation,electromagnetic interference(EMI)shielding,and thermal management.In this study,a novel hierarchical multifunctional flexible composite film is presented.The first step involves the synthesis of phase change microcapsule(PCMC)latex through in-situ polymerization.Next,PCMC and waterborne polyurethane(WPU)latex were mixed and dried using a binary colloidal approach to produce a flexible composite phase change film(WPU/PCMC)with complete anti-leakage and satisfying melting enthalpy(147.86 J g^(-1)).To enhance the EMI performance and mechanical strength,a thin layer of antioxidant MXene@poly tannin acid(PTA)was directly sprayed onto the surface of WPU/PCMC,resulting in the WPU/PCMC/MXene@PTA film(WPM).Consequently,the WPM displays exceptional thermal management performance for multiple drives and outstanding EMI performance(56.86 dB),making it an ideal candidate for future multifunctional products.
基金funding from the National Natural Science Foundation of China(No.22268025)China Postdoctoral Science Foundation(NO.2022MD713757)+2 种基金Yunnan Provincial Postdoctoral Science Foundation(NO.34Y2022)Yunnan Province Joint Special Project for Enterprise Fundamental Research and Applied Basic Research(No.202101BC070001-016)Guangdong Basic and Applied Basic Research Foundation(No.2023A1515011985).
文摘Phase change materials(PCMs)offer a promising solution to address the challenges posed by intermittency and fluctuations in solar thermal utilization.However,for organic solid-liquid PCMs,issues such as leakage,low thermal conductivity,lack of efficient solar-thermal media,and flamma-bility have constrained their broad applications.Herein,we present an innova-tive class of versatile composite phase change materials(CPCMs)developed through a facile and environmentally friendly synthesis approach,leveraging the inherent anisotropy and unidirectional porosity of wood aerogel(nanowood)to support polyethylene glycol(PEG).The wood modification process involves the incorporation of phytic acid(PA)and MXene hybrid structure through an evaporation-induced assembly method,which could impart non-leaking PEG filling while concurrently facilitating thermal conduction,light absorption,and flame-retardant.Consequently,the as-prepared wood-based CPCMs showcase enhanced thermal conductivity(0.82 W m^(-1)K^(-1),about 4.6 times than PEG)as well as high latent heat of 135.5 kJ kg^(-1)(91.5%encapsula-tion)with thermal durability and stability throughout at least 200 heating and cooling cycles,featuring dramatic solar-thermal conversion efficiency up to 98.58%.In addition,with the synergistic effect of phytic acid and MXene,the flame-retardant performance of the CPCMs has been significantly enhanced,showing a self-extinguishing behavior.Moreover,the excellent electromagnetic shielding of 44.45 dB was endowed to the CPCMs,relieving contemporary health hazards associated with electromagnetic waves.Overall,we capitalize on the exquisite wood cell structure with unidirectional transport inherent in the development of multifunctional CPCMs,showcasing the operational principle through a proof-of-concept prototype system.
基金supported by National Natural Science Foundation of China(Nos.51772272 and 51728204)Fundamental Research Funds for the Central Universities(No.2018QNA4011)+3 种基金Science and Technology Program of Guangdong Province of China(No.2016A010104020)Pearl River S&T Nova Program of Guangzhou(No.201610010116)Qianjiang Talents Plan D(QJD1602029)Startup Foundation for Hundred-Talent Program of Zhejiang University.
文摘Rational design of hybrid carbon host with high electrical conductivity and strong adsorption toward soluble lithium polysulfides is the main challenge for achieving high-performance lithium-sulfur batteries(LSBs).Herein,novel binder-free Ni@N-doped carbon nanospheres(N-CNSs)films as sulfur host are firstly synthesized via a facile combined hydrothermal-atomic layer deposition method.The cross-linked multilayer N-CNSs films can effectively enhance the electrical conductivity of electrode and provide physical blocking“dams”toward the soluble long-chain polysulfides.Moreover,the doped N heteroatoms and superficial NiO layer on Ni layer can work synergistically to suppress the shuttle of lithium polysulfides by effective chemical interaction/adsorption.In virtue of the unique composite architecture and reinforced dual physical and chemical adsorption to the soluble polysulfides,the obtained Ni@N-CNSs/S electrode is demonstrated with enhanced rate performance(816 mAh g?1 at 2 C)and excellent long cycling life(87%after 200 cycles at 0.1 C),much better than N-CNSs/S electrode and other carbon/S counterparts.Our proposed design strategy offers a promising prospect for construction of advanced sulfur cathodes for applications in LSBs and other energy storage systems.
基金supported by the National Natural Science Foundation of China(No.21908031)Scientific Research Funds of Yunnan Education Department(No.2021Y111)。
文摘Black phosphorus(BP),as one of the most promising fillers for flame retarding polymer,has been seriously limited in practical application,due to the agglomeration and poor structural stability challenges.Here,the BP was modified by MXene and polydopamine(PDA)via ultrasonication and dopamine modification strategy to improve the structural stability and dispersibility in the matrix.Then,the obtained(BP-MXene@PDA)nanohybrid was employed to promote the mechanical performance,thermal stability,and flame retardancy of thermoplastic polyurethane elastomer(TPU).The resultant TPU composite containing 2 wt.%of BP1-MXene2@PDA showed a 19.2%improvement in the tensile strength and a 13.8%increase in the elongation at break compared to those of the pure TPU.The thermogravimetric analysis suggested that BP-MXene@PDA clearly enhances the thermal stability of TPU composites.Furthermore,the introduction of the BP-MXene@PDA nanohybrids could considerably improve the flame retardancy of TPU composite,i.e.,64.2%and 27.3%decrease in peak heat release rate and total heat release,respectively.The flame-retardant mechanisms of TPU/BP-MXene@PDA in the gas phase and condensed phase were investigated systematically.This work provides a novel strategy to simultaneously enhance the fire safety and mechanical properties of TPU,thus expanding its industrial applications.
基金supported by the National Natural Science Foundation of China(Nos.51773044 and 51603047)Research and Development Plan for Key Areas in Guangdong Province(No.2019B090914002)+1 种基金Guangdong Province Science and Technology Plan Project(No.2016A010103030)the PhD Start-up Fund of Natural Science Foundation of Guangdong Province,China(No.2016A030310344).
文摘The crystalline and amorphous regions were alternately arranged in the hard elastic polypropylene(PP)films with row-nucleated lamellae.In this work,their structure evolution during stretching and recovery at room temperature was followed and the elastic recovery mechanism was discussed by twice cyclic tensile experiment.During the first stretching to 100%,the lamellae crystals are parallel separated and the intercrystallite crazing is formed at the first yield point.Many nano-cavities within the intercrystallite crazing appear when the strain reaches 20%.The strain-hardening process accompanies with the lamellae long period increasing and the intercrystallite crazing enlargement.After the secondary yield point,the lamellae cluster is further separated and more nano-cavities appear.The first and second recovery processes are complete overlap.During recovery,firstly,the energy elasticity provided by nano-cavities surface tension drives the shrinkage of material,and then the entropy elasticity related to amorphous chain relaxation plays a leading role when the strain is smaller than the secondary yield point.The elastic recovery process of hard elastic material is the co-contribution of energy elasticity and entropy elasticity.This work gives a clearer recognition about the source of hard elastic property and the role of amorphous region in material's deformation.
基金supported by the National Natural Science Foundation of China(No.U20A20299)the Guangdong Basic and Applied Basic Research Foundation(No.2023A1515011985)the support from the Scientific and Technological Innovation Strategy Program of Guangdong Province:Guangdong-Hong Kong-Macao Technology Cooperation Funding Scheme(No.2022A0505030026).
文摘Microencapsulation of phase change materials(MPCM)is an effective way to achieve solar energy management.However,the crystallization of phase change materials(PCMs)in microcapsules will produce supercooling,which will affect the energy storage efficiency of MPCM.The incorporation of TiO_(2)nanoparticles into MPCM can alleviate supercooling.In this work,octadecyltrimethoxysilane(ODTMS)was used to modify the solid nucleating agent TiO_(2)(m-TiO_(2))to improve its compatibility with n-Octadecane.Then,MPCM based on m-TiO_(2)nucleating agent,melamine-formaldehyde resin(MF)shell material,and n-Octadecane core material was prepared.Differential scanning calorimetry(DSC)results demonstrate that the supercooling degree(ΔT)of MPCM(MPCM-02)decreases to 0℃with a tiny level of 0.25 wt%m-TiO_(2),while the MPCM with unmodified TiO_(2)is 6.1℃and the MPCM without nucleating agent is 4.1℃.Besides,the phase change enthalpy(ΔHm)and encapsulation efficiency(E)of MPCM-02 remain at 183.7 J/g and 95.3%,respectively.Finally,phase change composite materials with photothermal conversion capabilities were constructed by MXenes,MPCM,and polyurethane acrylate(PUA).When 1 wt%MXenes and 30 wt%MPCM were incorporated into PUA matrix,the thermal conductivity and surface temperature after 1200s of infrared light irradiation were 48.8%and 8.2℃higher than pure PUA matrix.These results demonstrate the good solar energy storage capabilities of the MPCM,which possesses promising application potential in the field of solar energy thermal management and human thermal regulation.
基金support from the Science and Technology Program of Guangzhou(No.2024A04J2821)the National Natural Science Foundation of China(Nos.52222301,22171055)the Guangdong Natural Science Foundation for Distinguished Young Scholar(No.2022B1515020078)。
文摘Core-shell colloidal particles with a polymer layer have broad applications in different areas.Herein,we developed a two-step method combining aqueous surface-initiated photoinduced polymerization-induced self-assembly and photoinduced seeded reversible addition-fragmentation chain transfer(RAFT)polymerization to prepare a diverse set of core-shell colloidal particles with a well-defined polymer layer.Chemical compositions,structures,and thicknesses of polymer layers could be conveniently regulated by using different types of monomers and feed[monomer]/[chain transfer agent]ratios during seeded RAFT polymerization.
基金financially supported by the National Natural Science Foundation of China(Nos.22171055 and 52222301)the Guangdong Natural Science Foundation for Distinguished Young Scholar(No.2022B1515020078)the Science and Technology Program of Guangzhou(No.2024A04J2821)。
文摘Polymerization-induced self-assembly(PISA)has become one of the most versatile approaches for scalable preparation of linear block copolymer nanoparticles with various morphologies.However,the controlled introduction of branching into the core-forming block and the effect on the morphologies of block copolymer nanoparticles under PISA conditions have rarely been explored.Herein,a series of multifunctional macromolecular chain transfer agents(macro-CTAs)were first synthesized by a two-step green light-activated photoiniferter polymerization using two types of chain transfer monomers(CTMs).These macro-CTAs were then used to mediate reversible addition-fragmentation chain transfer(RAFT)dispersion polymerization of styrene(St)to prepare block copolymers with different core-forming block structures and the assemblies.The effect of the core-forming block structure on the morphology of block copolymer nanoparticles was investigated in detail.Transmission electron microscopy(TEM)analysis indicated that the brush-like core-forming block structure facilitated the formation of higher-order morphologies,while the branched core-forming block structure favored the formation of lower-order morphologies.Moreover,it was found that using macroCTAs with a shorter length also promoted the formation of higher-order morphologies.Finally,structures of block copolymers and the assemblies were further controlled by changing the structure of macro-CTA or using a binary mixture of two different macro-CTAs.We expect that this work not only sheds light on the synthesis of block copolymer nanoparticles but also provide important mechanistic insights into PISA of nonlinear block copolymers.
基金supported by the National Natural Science Foundation of China(No.22271090)。
文摘Herein,a simple and effective outer-surface interactions assisted supramolecular hierarchical assembly has been first exploited to uniformly distribute tungstosilicic acid(TSA)inside the porous structure of cucurbit[10]uril-based single-layer 2D supramolecular-organic-frameworks(Q[10]-SOFs)in water.Importantly,the 2D Q[10]-SOFs can further serve as light harvesting antenna,achieving fast energy transfer to the embedded redox-active TSA upon photoexcitation,resulting in efficient visible light-driven selective oxidation of benzyl alcohols into the corresponding aldehydes in high yield at room temperature.Further studies revealed that the integrated of 2D Q[10]-SOFs and TSA played a key role in the catalytic process,due to the presence of a novel stepwise electron transfer route in the single-layer hybrid 2D structures.
基金supported by the Science and Tech-nology Program of Guangzhou(No.2024A04J3710)the Na-tional Natural Science Foundation of China(No.22268025).
文摘The rapid development of industrialization necessitates advancements in nanomaterials.Black phospho-rus(BP)nanosheets have garnered extensive attention due to their highly anisotropic optoelectronic properties,high carrier mobility,and excellent mechanical properties.These unique attributes make BP nanosheets advantageous in various research fields.Combining BP nanosheets with polymers results in functional coatings and films with flame retardancy,antibacterial properties,wear resistance,and cor-rosion resistance.In this review,we first introduce various preparation methods for BP nanosheets.We discuss the degradation mechanisms of BP nanosheets and the passivation techniques employed to en-hance their environmental stability.Subsequently,we provide a detailed and comprehensive review of the applications of BP nanosheets in polymer coatings and films.Finally,we outline the development challenges and future research opportunities for BP-based polymer coatings and films.This article aims to summarize existing research and provide objective insights,serving as a constructive reference for the advancement of modern multifunctional polymer coatings and films.
基金This work was financially supported by the National Natural Science Foundation of China(Nos.21971047 and 21504017)Innovation Project of Education Department in Guangdong(No.2018KTSCX053)+1 种基金Y.C.acknowledges the support from Guangdong Special Support Program(No.2017TX04N371)J.T.acknowledges the support from Pearl River Young Scholar of Guangdong.
文摘Polymerization-induced self-assembly(PISA)is an emerging method for the preparation of block copolymer nano-objects at high concentrations.However,most PISA formulations have oxygen inhibition problems and inert atmospheres(e.g.argon,nitrogen)are usually required.Moreover,the large-scale preparation of block copolymer nano-objects at room temperature is challenging.Herein,we report an enzyme-assisted photoinitiated polymerization-induced self-assembly(photo-PISA)in continuous flow reactors with oxygen toleranee.The addition of glucose oxidase(GOx)and glucose into the reaction mixture can consume oxygen efficiently and constantly,allow the flow photo-PISA to be performed under open-air conditions.Polymerization kinetics indicated that only a small amount of GOx(0.5 μmol/L)was needed to achieve the oxygen tolerance.Block copolymer nano-objects with different morphologies can be prepared by varying reaction conditions including the degree of polymerization(DP)of core-forming block,monomer concentration,reaction temperature,and solvent composition.We expect this study will provide a facile platform for the large-scale production of block copolymer nano-objects with different morphologies at room temperature.
基金supported by the National Natural Science Foundation of China(Grant No.51772272)Natural Science Funds for Distinguished Young Scholar of Zhejiang Province(Grant No.LR20E020001)+1 种基金Startup Foundation for Hundred-Talent Program of Zhejiang UniversityPearl River S&T Nova Program of Guangzhou(Grant No.201710010143)。
文摘The development of fast rechargeable lithium ion batteries(LIBs)is highly dependent on the innovation of advanced high-power electrode materials.In this work,for the first time,we report a sacrificial NiO arrays template method for controllable synthesis of self-supported hierarchical porous Li_(4)Ti_(5)O_(12)/C(LTO/C)nanoflakes arrays,for use as fast rechargeable anodes for LIBs.The ultrathin(2-3 nm)carbon layer was uniformly coated on the LTO forming arrays architecture.The hierarchical porous LTO/C nanoflakes consisted of primary cross-linked nanoparticles of 50-100 nm and showed large porosity.Because of the enhanced electrical conductivity and accelerated ion transfer channels,the well-designed binderfree porous LTO/C nanoflakes arrays exhibited notable high-rate lithium ion storage performance with smaller polarization,better electrochemical reactivity,higher specific capacity(157 mAh g^(-1) at the current density of 20C)and improved long-term cycling life(96.2% after 6000 cycles at 20C),superior to the unmodified porous LTO arrays counterpart(126 mAh g^(-1) at 20C and 88.0%after 6000 cycles at 20C).Our work provides a new template for the construction of high-performance high-rate electrodes for electrochemical energy storage.
基金support from the Science and Technology Program of Guangzhou(No.202102020631)the National Natural Science Foundation of China(Nos.22171055 and 21971047)+1 种基金Innovation Project of Education Department in Guangdong(No.2018KTSCX053)support from Guangdong Special Support Program(No.2017TX04N371)。
文摘Stimulus-responsive vesicles have broad applications in a variety of areas. Herein, oxidation-responsive framboidal triblock copolymer vesicles are prepared by photoinitiated RAFT seeded emulsion polymerization of a thioether-functionalized monomer using diblock copolymer vesicles as seeds. The obtained framboidal vesicles can transform into worms or spheres in the presence of reactive oxygen species,which can be further used for controlled release of cargos(e.g., silica nanoparticles).
