This review paper provides a comprehensive introduction to various numerical methods for the phase-field model used to simulate the phase separation dynamics of diblock copolymer melts.Diblock copolymer systems form c...This review paper provides a comprehensive introduction to various numerical methods for the phase-field model used to simulate the phase separation dynamics of diblock copolymer melts.Diblock copolymer systems form complex structures at the nanometer scale and play a significant role in various applications.The phase-field model,in particular,is essential for describing the formation and evolution of these structures and is widely used as a tool to effectively predict the movement of phase boundaries and the distribution of phases over time.In this paper,we discuss the principles and implementations of various numerical methodologies for this model and analyze the strengths,limitations,stability,accuracy,and computational efficiency of each method.Traditional approaches such as Fourier spectral methods,finite difference methods and alternating direction explicit methods are reviewed,as well as recent advancements such as the invariant energy quadratization method and the scalar auxiliary variable scheme are also presented.In addition,we introduce examples of the phase-field model,which are fingerprint image restoration and 3D printing.These examples demonstrate the extensive applicability of the reviewed methods and models.展开更多
Molecular dynamics simulations were performed to investigate the sliding dynamics of a small charged ring chain along rigid cyclic diblock polyelectrolyte in catenane immersed in salt solution.We found that both the m...Molecular dynamics simulations were performed to investigate the sliding dynamics of a small charged ring chain along rigid cyclic diblock polyelectrolyte in catenane immersed in salt solution.We found that both the mean-square displacement g_(3)(t)and diffusion coefficient D of ring are influenced by the salt type,electrostatic interaction strength A and salt concentration cs.D first decreases and then increases as A increases when Ais not large.At large A,D decreases with an increase in A owing to the polyelectrolyte charge reversal caused by the aggregation of ions near it.Meanwhile,g_(3)(t)exhibited intermediate oscillating behavior at moderate A in monovalent cation salt solution.The sliding dynamics of ring can be attributed to the free energy landscape for diffusion.According to the potential of mean force(PMF)of ring chain,we found that our simulation results agreed well with the theoretical results of Lifson-Jackson formula.This study can provide a practical model for the diffusion of charged particles in different dielectric and periodic media,and provides a new perspective for regulating the sliding dynamics of mechanically interlocked molecules in electrolyte solutions.展开更多
Mean-square bond length, root-mean-square end-to-end distance and gyration radius in diblock copolymer films have been studied by dissipative particle dynamics simulations. Results show evident linear trends of any pr...Mean-square bond length, root-mean-square end-to-end distance and gyration radius in diblock copolymer films have been studied by dissipative particle dynamics simulations. Results show evident linear trends of any property separately with the thickness of film, the interaction between particles of different types, the repulsion between particle and boundary, except for the dependence of the variations of mean-square bond length on the thickness of film, which exhibits as a wave trend. What＇s more, the varying trends of mean-square bond length and root-mean-square end-to-end distance can correspond to each other. The density distribution of either component in diblock copolymer film can be controlled and adjusted effectively through its interaction with boundary.展开更多
Polystyrene-styrene/butadiene diblock copolymers were synthesized via reversible addition-fragmentation chain transfer （RAFT） miniemulsion polymerization.During the polymerization process,the molecular weight distri...Polystyrene-styrene/butadiene diblock copolymers were synthesized via reversible addition-fragmentation chain transfer （RAFT） miniemulsion polymerization.During the polymerization process,the molecular weight distribution was narrow and the numerical molecular weight of the copolymers increased with increasing conversion of monomers,which was close to the theoretical.FT-IR and ^1H NMR results indicated that the microstructure of the polymer was mainly 1,4-trans-butadiene with small amount of 1,2-units,and composition in the copolymers was obtained.展开更多
The synthesis of rod-coil diblock copolymers was achieved for the first time by TEMPO-mediated 'living' free radical polymerization of styrene and 2,5-bis [(4-methoxyphenyl)oxycarbonyl] styrene(MPCS). The blo...The synthesis of rod-coil diblock copolymers was achieved for the first time by TEMPO-mediated 'living' free radical polymerization of styrene and 2,5-bis [(4-methoxyphenyl)oxycarbonyl] styrene(MPCS). The block architecture of the two diblock copolymers thus prepared, MPCS-b-St(5400/2400) and MPCS-b-St(10800/8700), was confirmed by GPC, DSC studies and the formation of multimolecular micelles. (Author abstract) 10 Refs.展开更多
Stereocomplex crystallization in asymmetric diblock copolymers was studied using dynamic Monte Carlo simulations,and the key factor dominating the formation of stereocomplex crystallites(SCs)was uncovered.The asymmetr...Stereocomplex crystallization in asymmetric diblock copolymers was studied using dynamic Monte Carlo simulations,and the key factor dominating the formation of stereocomplex crystallites(SCs)was uncovered.The asymmetric diblock copolymers with higher degree of asymmetry exhibit larger difference between volume fractions of beads of different blocks,and local miscibility between different kinds of beads is lower,leading to lower SC content.To minimize the interference from volume fraction of beads,the SC formation in blends of asymmetric diblock copolymers was also studied.For the cases where the volume fractions of beads of different blocks are the same,similar local miscibility between beads of different blocks and similar SC content was observed.These findings indicate that the volume fraction of beads of different blocks is a key factor controlling the SC formation in the asymmetric diblock copolymers.The SC content can be regulated by adjusting the difference between the contents of beads of different blocks in asymmetric diblock copolymers.展开更多
The self-assembly of symmetric diblock copolymers confined in the channels of variously shaped cross sections （regu- lar triangles, squares, and ellipses） is investigated using a simulated annealing technique. In th...The self-assembly of symmetric diblock copolymers confined in the channels of variously shaped cross sections （regu- lar triangles, squares, and ellipses） is investigated using a simulated annealing technique. In the bulk, the studied symmetric diblock copolymers form a lamellar structure with period LL. The geometry and surface property of the confining channels have a large effect on the self-assembled structures and the orientation of the lamellar structures. Stacked perpendicular lamellae with period LL are observed for neutral surfaces regardless of the channel shape and size, but each lamella is in the shape of the corresponding channel＇s cross section. In the case of triangle-shaped cross sections, stacked parallel lamel- lae are the majority morphologies for weakly selective surfaces, while morphologies including a triangular-prism-shaped B-cylinder and multiple tridentate lamellae are obtained for strongly selective surfaces. In the cases of square-shaped and ellipse-shaped cross sections, concentric lamellae are the signature morphology for strongly selective surfaces, whereas for weakly selective surfaces, stacked parallel lamellae, and several types of folding lamellae are obtained in the case of square-shaped cross sections, and stacked parallel lamellae are the majority morphologies in the case of ellipse-shaped cross sections when the length of the minor axis is commensurate with the bulk lamellar period. The mean-square end- to-end distance, the average contact number between different species and the surface concentration of the A-monomers are computed to elucidate the mechanisms of the formation of the different morphologies. It is found that the resulting morphology is a consequence of competition among the chain stretching, interfacial energy, and surface energy. Our results suggest that the self-assembled morphology and the orientation of lamellae can be manipulated by the shape, the size, and the surface property of the confining channels.展开更多
The phase behaviors in a binary mixture of diblock copolymers confined between two parallel walls are investigated by using a cell dynamics simulation of the time-dependent Ginzburg-Landau theory.The morphological dep...The phase behaviors in a binary mixture of diblock copolymers confined between two parallel walls are investigated by using a cell dynamics simulation of the time-dependent Ginzburg-Landau theory.The morphological dependence of the wall-block interaction and the distance between walls（confinement degree） has been systematically studied,and the effect of repulsive interactions between different monomers is also discussed.It is interesting that multiple novel morphological transitions are observed by changing these factors,and various multilayered sandwich structures are formed in the mixture.Furthermore,the parametric dependence and physical reasons for the microdomain growth and orientational order transitions are discussed.From the simulation,we find that much richer morphologies can form in a binary mixture of diblock copolymers than those in a pure diblock copolymer.Our results provide an insight into the phase behaviors under parallel wall confinement and may provide guidance for experimentalists.This model system can also give a simple way to realize orientational order transition in soft materials through confinement.展开更多
The phase behaviours of diblock copolymers under cylindrical confinement are studied in two-dimensional space by using the self-consistent field theory. Several phase parameters are adjusted to investigate the cylindr...The phase behaviours of diblock copolymers under cylindrical confinement are studied in two-dimensional space by using the self-consistent field theory. Several phase parameters are adjusted to investigate the cylindrical-confinement-induced phase behaviours of diblock copolymers. A series of lamella-cylinder mixture phases, such as the mixture of broken-lamellae and cylinders and the mixture of square-lamellae and cylinders, are observed by varying the phase parameters, in which the behaviours of these mixture phases are discussed in the corresponding phase diagrams. Furthermore, the free energies of these mixture phases are investigated to illustrate their evolution processes. Our results are compared with the available observations from the experiments and simulations respectively, and they are in good agreement and provide an insight into the phase behaviours under cylindrical confinement.展开更多
Four new rod-coil diblock molecules, which had well-defined para-phenylene oligomers (PPP, from biphenyl to quinquephenyl) as rigid segments and poly(ethylene oxide) (PEO, M-w ca. 750) as flexible segments, were synth...Four new rod-coil diblock molecules, which had well-defined para-phenylene oligomers (PPP, from biphenyl to quinquephenyl) as rigid segments and poly(ethylene oxide) (PEO, M-w ca. 750) as flexible segments, were synthesized. The chemical structure and the number of repeating unit in PEO coil and PPP rod were characterized by H-1-NMR and MALDI-TOF mass spectrometry. The diblock oligomers showed good solubility in common organic solvents and aggregated in water as characterized by a blue shift in UV-vis absorption spectra, a red shift in emission spectra, quenching of the fluorescence and formation of the microfibrilla and fractal-like structures. The formation of different supramolecular structures meant that this effort might lead to commercial important highly organized functional materials.展开更多
Systematic comparison between computer simulation results and those predicted by Scheutjens-Fleer (SF) self-consistent-field theory is presented for the adsorption of diblock copolymers from a non-selective solvent on...Systematic comparison between computer simulation results and those predicted by Scheutjens-Fleer (SF) self-consistent-field theory is presented for the adsorption of diblock copolymers from a non-selective solvent on attractive surface. It is shown that although SF is a mean-field theory, it can qualitatively describe the adsorption phenomena of diblock copolymers. However, systematic discrepancy between the theory and simulation still exists. The approximations inherited in the mean-field theory such as random mixing inside a layer and the allowance of direct back folding may be responsible to those deviations.展开更多
The liquid-liquid phase separation(LLPS)widely exists in biology,synthetic chemistry,crystallization kinetics and other fields,and it is very important to realize the related functions.The research on the competition ...The liquid-liquid phase separation(LLPS)widely exists in biology,synthetic chemistry,crystallization kinetics and other fields,and it is very important to realize the related functions.The research on the competition between LLPS and micellization/vesiculation has made considerable progress.However,the way to effectively control the formation paths from homogeneous state to aggregates has not been completely solved,which is vital to determine its structure and properties and even its future functions.Here we describe the phenomenon of LLPS and its effect on the dynamic process of self-assembly of amphiphilic diblock copolymers(BCPs).Starting from the establishment of phase diagram,we explore the existence conditions of LLPS state,the internal morphology and external size of large droplets,and its significant implications to the dynamic path of vesicle formation.Vesicles formed via LLPS have larger sized outer dimensions and inner cavities,and contain more solvents during certain stages.The detailed research of LLPS and its self-assembly simulation has contributed to completing its theoretical basis and practical applications in the future in various fields.展开更多
The diblock copolymers intercalated layered silicate was prepared via a melt dispersion technique. Then the effect of intercalated hybrid as filler on acrylonitrile- butadiene-styrene resin was characterized by X-ray ...The diblock copolymers intercalated layered silicate was prepared via a melt dispersion technique. Then the effect of intercalated hybrid as filler on acrylonitrile- butadiene-styrene resin was characterized by X-ray diffraction, transmission electron microscopy, stress-strain measurements in elongation.展开更多
A rod-rod diblock copolymer (diBCP), poly(3-hexylthiophene)-block-poly(furfuryl isocyanate)(P3HT-b-PFIC), was synthesized through the anionic polymerization with an oxyanionic macroinitiator of P3HT. The properties of...A rod-rod diblock copolymer (diBCP), poly(3-hexylthiophene)-block-poly(furfuryl isocyanate)(P3HT-b-PFIC), was synthesized through the anionic polymerization with an oxyanionic macroinitiator of P3HT. The properties of the diBCP (molecular weight, dispersity, composition, thermal stability, UV-visible absorption, and thin film morphology) were determined by various analytical methods. P3HT-b-PFIC was blended with C60 in a toluene solution to prepare a thin film of binary electron donor/acceptor system. Such blending enabled partial conjugation of the two components by the Diels-Alder reaction between furan and C60 at 60℃ for 3 h;the mixture was then spin-cast as a thin film, and annealed at 250℃ for 24 h. Tapping-mode atomic force microscopy (AFM) revealed that P3HT and C60 domains had nanoscale interfaces without a large phase segregation. This result indicated that the microphase separation of C60-functionalized P3HT-b-PFIC preserved even at high temperature provided free C60 molecules with channels to diffuse on the sides of P3HT domain, thus preventing the macroscopic crystallization of free C60 through the interfacial stabilization.展开更多
Transformation of living ring-opening metathesis polymerization into coordination polymerization by converting the titanacyclobutane group attached to a polynorbornene chain into titanocene alkoxide has been used for ...Transformation of living ring-opening metathesis polymerization into coordination polymerization by converting the titanacyclobutane group attached to a polynorbornene chain into titanocene alkoxide has been used for the synthesis of polynorbornene-poly(ethylene-co-propylene) block copolymer. Preliminary characterizations of the copolymerization products by solvent extraction and C-13 NMR spectrum are reported.展开更多
The target of the present investigation is synthesis and characterization of an amphiphilic diblock copolymer with antibacterial property. Ring opening polymerization （ROP） of ε-caprolactone （CL） and tetrahydrofu...The target of the present investigation is synthesis and characterization of an amphiphilic diblock copolymer with antibacterial property. Ring opening polymerization （ROP） of ε-caprolactone （CL） and tetrahydrofuran （THF） was carried out under inert atmosphere by using L-cysteine as a bridging agent in the presence of stannous octoate （SO） as a catalyst. The nano silver end capped diblock copolymer was synthesized by in situ method. Thus obtained nano silver end capped L-cysteine bridged diblock copolymer was characterized by various analytical methods like Fourier transform infrared （FTIR） spectroscopy, nuclear magnetic resonance （NMR） spectroscopy, circular dichroism （CD）, fluorescence spectroscopy, gel permeation chromatography （GPC）, X-ray photoelectron spectroscopy （XPS）, thermogravimetric analysis （TGA）, differential scanning calorimetry （DSC）, field emission scanning electron microscopy （FESEM）, high resolution transmission electron microscopy （HRTEM） and zeta potential. The antimicrobial property of the nano silver end capped diblock copolymer against e-coli was tested.展开更多
By mechanism-transformation (anionic --> cationic) poly(styrene-6-2-ethyl-2-oxazoline) diblock copolymer, PS-b-PEOx, was synthesized in two steps. The first step is the polymerization of styrene block capped with e...By mechanism-transformation (anionic --> cationic) poly(styrene-6-2-ethyl-2-oxazoline) diblock copolymer, PS-b-PEOx, was synthesized in two steps. The first step is the polymerization of styrene block capped with ethylene oxide and its tosylation; the second step is the cationic ring-opening polymerization of 2-ethyl-2-oxazoline. The products were thoroughly characterized by various methods, such as H-1-NMR, IR, DMA, TEM and SAXS. The results show that the copolymer obtained possesses high molecular weight and narrow molecular weight distribution.展开更多
The surface-induced effect on the morphologies of lamella-forming diblock copolymers in nanorod arrays is studied by using the self-consistent field theory. In the simulation study, a rich variety of novel morphologie...The surface-induced effect on the morphologies of lamella-forming diblock copolymers in nanorod arrays is studied by using the self-consistent field theory. In the simulation study, a rich variety of novel morphologies are observed by variations in the strength of the surface field for the diblock copolymers. Different surface-field-induced effects are examined for the diblock copolymers in the arrays with distinct preferential surfaces. It is observed that the majority-block preferential surfaces have more obvious induced effects than those of minority-block preferential surfaces. The strong surface fields exhibit different behaviours from those observed in the weak surface fields, by which the morphologies possess cylindrical symmetries. Results from this research deepen the knowledge of surface-induced effects in a confinement system, which may aid the fabrication of polymer-based na^omaterials.展开更多
The phase behaviors of symmetric diblock copolymer thin films confined between two hard, parallel and diversified patterned surfaces are investigated by three-dimensional dissipative particle dynamics (DPD) simulation...The phase behaviors of symmetric diblock copolymer thin films confined between two hard, parallel and diversified patterned surfaces are investigated by three-dimensional dissipative particle dynamics (DPD) simulations. The induction of diversified patterned surfaces on phase separation of symmetric diblock copolymer films in snapshots, density profiles and concentration diagrams of the simulated systems are presented. The phase separations can be controlled by the patterned surfaces. In the meantime, the mean-square end-to-end distance of the confined polymer chains < R(2)> is also discussed. Surface-induced phase separation for diblock copolymers can help us to create novel and controlled nanostructured materials.展开更多
The real time and in situ investigation of the crystallization process and structure transitions of asymmetric crystalline-crystalline diblock copolymers from the melt was performed with synchrotron simultaneous SAXS/...The real time and in situ investigation of the crystallization process and structure transitions of asymmetric crystalline-crystalline diblock copolymers from the melt was performed with synchrotron simultaneous SAXS/WAXS. The asymmetric poly（ethylene oxide）-b-poly（ε-caprolactone） diblock copolymers were chosen for the present study. It was shown that the short blocks crystallized later than the long blocks and final lamellar structure was formed in all of the asymmetric diblock copolymers. The final lamellar structure was confirmed by AFM observation. The SAXS data were analyzed with different methods for the early stage of the crystallization. The Guinier plots indicated that there were no isolated domains formed before the formation of lamellae in the asymmetric diblock copolymers during the crystallization process. Debye- Bueche plots implied the formation of correlated domains during crystallization.展开更多
文摘This review paper provides a comprehensive introduction to various numerical methods for the phase-field model used to simulate the phase separation dynamics of diblock copolymer melts.Diblock copolymer systems form complex structures at the nanometer scale and play a significant role in various applications.The phase-field model,in particular,is essential for describing the formation and evolution of these structures and is widely used as a tool to effectively predict the movement of phase boundaries and the distribution of phases over time.In this paper,we discuss the principles and implementations of various numerical methodologies for this model and analyze the strengths,limitations,stability,accuracy,and computational efficiency of each method.Traditional approaches such as Fourier spectral methods,finite difference methods and alternating direction explicit methods are reviewed,as well as recent advancements such as the invariant energy quadratization method and the scalar auxiliary variable scheme are also presented.In addition,we introduce examples of the phase-field model,which are fingerprint image restoration and 3D printing.These examples demonstrate the extensive applicability of the reviewed methods and models.
基金supported by the National Natural Science Foundation of China(Nos.22173080,22403062,and22363005)the Jiangxi Provincial Natural Science Foundation(No.20202BABL203015)。
文摘Molecular dynamics simulations were performed to investigate the sliding dynamics of a small charged ring chain along rigid cyclic diblock polyelectrolyte in catenane immersed in salt solution.We found that both the mean-square displacement g_(3)(t)and diffusion coefficient D of ring are influenced by the salt type,electrostatic interaction strength A and salt concentration cs.D first decreases and then increases as A increases when Ais not large.At large A,D decreases with an increase in A owing to the polyelectrolyte charge reversal caused by the aggregation of ions near it.Meanwhile,g_(3)(t)exhibited intermediate oscillating behavior at moderate A in monovalent cation salt solution.The sliding dynamics of ring can be attributed to the free energy landscape for diffusion.According to the potential of mean force(PMF)of ring chain,we found that our simulation results agreed well with the theoretical results of Lifson-Jackson formula.This study can provide a practical model for the diffusion of charged particles in different dielectric and periodic media,and provides a new perspective for regulating the sliding dynamics of mechanically interlocked molecules in electrolyte solutions.
文摘Mean-square bond length, root-mean-square end-to-end distance and gyration radius in diblock copolymer films have been studied by dissipative particle dynamics simulations. Results show evident linear trends of any property separately with the thickness of film, the interaction between particles of different types, the repulsion between particle and boundary, except for the dependence of the variations of mean-square bond length on the thickness of film, which exhibits as a wave trend. What＇s more, the varying trends of mean-square bond length and root-mean-square end-to-end distance can correspond to each other. The density distribution of either component in diblock copolymer film can be controlled and adjusted effectively through its interaction with boundary.
基金supported by Major Program of National Natural Science Foundation of China(No. 20836007)National Natural Science Foundation of China(No.20806067).
文摘Polystyrene-styrene/butadiene diblock copolymers were synthesized via reversible addition-fragmentation chain transfer （RAFT） miniemulsion polymerization.During the polymerization process,the molecular weight distribution was narrow and the numerical molecular weight of the copolymers increased with increasing conversion of monomers,which was close to the theoretical.FT-IR and ^1H NMR results indicated that the microstructure of the polymer was mainly 1,4-trans-butadiene with small amount of 1,2-units,and composition in the copolymers was obtained.
基金This project was supported by the Foundation of Peking University for Young Scientist and the National Natural Science Foundation of China.
文摘The synthesis of rod-coil diblock copolymers was achieved for the first time by TEMPO-mediated 'living' free radical polymerization of styrene and 2,5-bis [(4-methoxyphenyl)oxycarbonyl] styrene(MPCS). The block architecture of the two diblock copolymers thus prepared, MPCS-b-St(5400/2400) and MPCS-b-St(10800/8700), was confirmed by GPC, DSC studies and the formation of multimolecular micelles. (Author abstract) 10 Refs.
基金supported by the National Natural Science Foundation of China(No.21404050)the Research Foundation of Jiangsu University(No.14JDG059)+2 种基金Hao also thanks the supports from Postdoctoral Science Foundation of China(No.2019M651478)Natural Science Foundation of Jiangsu Province(No.BK20190866)Natural Science Foundation of the Higher Education Institutions of Jiangsu Provinee(No.18KJB150009).
文摘Stereocomplex crystallization in asymmetric diblock copolymers was studied using dynamic Monte Carlo simulations,and the key factor dominating the formation of stereocomplex crystallites(SCs)was uncovered.The asymmetric diblock copolymers with higher degree of asymmetry exhibit larger difference between volume fractions of beads of different blocks,and local miscibility between different kinds of beads is lower,leading to lower SC content.To minimize the interference from volume fraction of beads,the SC formation in blends of asymmetric diblock copolymers was also studied.For the cases where the volume fractions of beads of different blocks are the same,similar local miscibility between beads of different blocks and similar SC content was observed.These findings indicate that the volume fraction of beads of different blocks is a key factor controlling the SC formation in the asymmetric diblock copolymers.The SC content can be regulated by adjusting the difference between the contents of beads of different blocks in asymmetric diblock copolymers.
基金Project supported by the National Natural Science Foundation of China(Grant Nos.11204215,51302187,20990234,20925414,21204040,and 91227121)the Natural Science Foundation of Tianjin City,China(Grant Nos.12JCYBJC32500 and 14JCZDJC32100)+1 种基金the Program for Changjiang Scholars and Innovative Research Team in University(PCSIRT)(Grant No.IRT1257)the 111 Project.A.C.Shi gratefully acknowledges the supports from the Natural Sciences and Engineering Research Council(NSERC)of Canada
文摘The self-assembly of symmetric diblock copolymers confined in the channels of variously shaped cross sections （regu- lar triangles, squares, and ellipses） is investigated using a simulated annealing technique. In the bulk, the studied symmetric diblock copolymers form a lamellar structure with period LL. The geometry and surface property of the confining channels have a large effect on the self-assembled structures and the orientation of the lamellar structures. Stacked perpendicular lamellae with period LL are observed for neutral surfaces regardless of the channel shape and size, but each lamella is in the shape of the corresponding channel＇s cross section. In the case of triangle-shaped cross sections, stacked parallel lamel- lae are the majority morphologies for weakly selective surfaces, while morphologies including a triangular-prism-shaped B-cylinder and multiple tridentate lamellae are obtained for strongly selective surfaces. In the cases of square-shaped and ellipse-shaped cross sections, concentric lamellae are the signature morphology for strongly selective surfaces, whereas for weakly selective surfaces, stacked parallel lamellae, and several types of folding lamellae are obtained in the case of square-shaped cross sections, and stacked parallel lamellae are the majority morphologies in the case of ellipse-shaped cross sections when the length of the minor axis is commensurate with the bulk lamellar period. The mean-square end- to-end distance, the average contact number between different species and the surface concentration of the A-monomers are computed to elucidate the mechanisms of the formation of the different morphologies. It is found that the resulting morphology is a consequence of competition among the chain stretching, interfacial energy, and surface energy. Our results suggest that the self-assembled morphology and the orientation of lamellae can be manipulated by the shape, the size, and the surface property of the confining channels.
基金Project supported by the National Natural Science Foundation of China (Grant No. 20673070)the Natural Science Foundation of Shanxi Province (Grant No. 2007011055)+1 种基金the Natural Science Foundation for Young Scientists of Shanxi Province (Grant No. 2011021008-1)the Soft Science Program of Shanxi Province (Grant No. 2011041015-01)
文摘The phase behaviors in a binary mixture of diblock copolymers confined between two parallel walls are investigated by using a cell dynamics simulation of the time-dependent Ginzburg-Landau theory.The morphological dependence of the wall-block interaction and the distance between walls（confinement degree） has been systematically studied,and the effect of repulsive interactions between different monomers is also discussed.It is interesting that multiple novel morphological transitions are observed by changing these factors,and various multilayered sandwich structures are formed in the mixture.Furthermore,the parametric dependence and physical reasons for the microdomain growth and orientational order transitions are discussed.From the simulation,we find that much richer morphologies can form in a binary mixture of diblock copolymers than those in a pure diblock copolymer.Our results provide an insight into the phase behaviors under parallel wall confinement and may provide guidance for experimentalists.This model system can also give a simple way to realize orientational order transition in soft materials through confinement.
基金supported by the National Natural Science Foundation of China (Grant Nos. 20574052 and 20774066)the Program for New Century Excellent Talents in University, China (Grant No. NCET-05-0538)the Natural Science Foundation of Zhejiang Province, China (Grant Nos. R404047, Y4090174, and Y405553)
文摘The phase behaviours of diblock copolymers under cylindrical confinement are studied in two-dimensional space by using the self-consistent field theory. Several phase parameters are adjusted to investigate the cylindrical-confinement-induced phase behaviours of diblock copolymers. A series of lamella-cylinder mixture phases, such as the mixture of broken-lamellae and cylinders and the mixture of square-lamellae and cylinders, are observed by varying the phase parameters, in which the behaviours of these mixture phases are discussed in the corresponding phase diagrams. Furthermore, the free energies of these mixture phases are investigated to illustrate their evolution processes. Our results are compared with the available observations from the experiments and simulations respectively, and they are in good agreement and provide an insight into the phase behaviours under cylindrical confinement.
基金This work has been supported by the National Natural Science Foundation of China (Grants 29874003 and 29992590-4), the Research Fund for Doctoral Program of Higher Education (Grant 99000136) and the Teaching and Research Award Fund for Outstanding Young
文摘Four new rod-coil diblock molecules, which had well-defined para-phenylene oligomers (PPP, from biphenyl to quinquephenyl) as rigid segments and poly(ethylene oxide) (PEO, M-w ca. 750) as flexible segments, were synthesized. The chemical structure and the number of repeating unit in PEO coil and PPP rod were characterized by H-1-NMR and MALDI-TOF mass spectrometry. The diblock oligomers showed good solubility in common organic solvents and aggregated in water as characterized by a blue shift in UV-vis absorption spectra, a red shift in emission spectra, quenching of the fluorescence and formation of the microfibrilla and fractal-like structures. The formation of different supramolecular structures meant that this effort might lead to commercial important highly organized functional materials.
基金Supported by the National Natural Science Foundation of China(No. 20025618)the Doctoral Research Foundation by Ministry of Education of China (No.1999025103) and the Dawn Project of Education Committee of Shanghai.
文摘Systematic comparison between computer simulation results and those predicted by Scheutjens-Fleer (SF) self-consistent-field theory is presented for the adsorption of diblock copolymers from a non-selective solvent on attractive surface. It is shown that although SF is a mean-field theory, it can qualitatively describe the adsorption phenomena of diblock copolymers. However, systematic discrepancy between the theory and simulation still exists. The approximations inherited in the mean-field theory such as random mixing inside a layer and the allowance of direct back folding may be responsible to those deviations.
基金This work was financially supported by the National Natural Science Foundation of China(Nos.21973041,21674047,21474051 and 21734005)the Program for Changjiang Scholars and Innovative Research Team in University(PCSIRT)the Fundamental Research Funds for the Central Universities.
文摘The liquid-liquid phase separation(LLPS)widely exists in biology,synthetic chemistry,crystallization kinetics and other fields,and it is very important to realize the related functions.The research on the competition between LLPS and micellization/vesiculation has made considerable progress.However,the way to effectively control the formation paths from homogeneous state to aggregates has not been completely solved,which is vital to determine its structure and properties and even its future functions.Here we describe the phenomenon of LLPS and its effect on the dynamic process of self-assembly of amphiphilic diblock copolymers(BCPs).Starting from the establishment of phase diagram,we explore the existence conditions of LLPS state,the internal morphology and external size of large droplets,and its significant implications to the dynamic path of vesicle formation.Vesicles formed via LLPS have larger sized outer dimensions and inner cavities,and contain more solvents during certain stages.The detailed research of LLPS and its self-assembly simulation has contributed to completing its theoretical basis and practical applications in the future in various fields.
基金Chinese Education Ministry Foundation for Nankai University and Tianjin University Joint Academy
文摘The diblock copolymers intercalated layered silicate was prepared via a melt dispersion technique. Then the effect of intercalated hybrid as filler on acrylonitrile- butadiene-styrene resin was characterized by X-ray diffraction, transmission electron microscopy, stress-strain measurements in elongation.
基金financially supported by the Basic Science Research Program through the National Research Foundation of Korea (NRF)funded by the Ministry of Science, ICT and Future Planning (Nos. NRF-2015R1A2A1A01002493 and NRF-2018R1A2B6003616)supported by “Nobel Research Project” grant for Grubbs Center for Polymers and Catalysis funded by the GIST in 2019
文摘A rod-rod diblock copolymer (diBCP), poly(3-hexylthiophene)-block-poly(furfuryl isocyanate)(P3HT-b-PFIC), was synthesized through the anionic polymerization with an oxyanionic macroinitiator of P3HT. The properties of the diBCP (molecular weight, dispersity, composition, thermal stability, UV-visible absorption, and thin film morphology) were determined by various analytical methods. P3HT-b-PFIC was blended with C60 in a toluene solution to prepare a thin film of binary electron donor/acceptor system. Such blending enabled partial conjugation of the two components by the Diels-Alder reaction between furan and C60 at 60℃ for 3 h;the mixture was then spin-cast as a thin film, and annealed at 250℃ for 24 h. Tapping-mode atomic force microscopy (AFM) revealed that P3HT and C60 domains had nanoscale interfaces without a large phase segregation. This result indicated that the microphase separation of C60-functionalized P3HT-b-PFIC preserved even at high temperature provided free C60 molecules with channels to diffuse on the sides of P3HT domain, thus preventing the macroscopic crystallization of free C60 through the interfacial stabilization.
文摘Transformation of living ring-opening metathesis polymerization into coordination polymerization by converting the titanacyclobutane group attached to a polynorbornene chain into titanocene alkoxide has been used for the synthesis of polynorbornene-poly(ethylene-co-propylene) block copolymer. Preliminary characterizations of the copolymerization products by solvent extraction and C-13 NMR spectrum are reported.
文摘The target of the present investigation is synthesis and characterization of an amphiphilic diblock copolymer with antibacterial property. Ring opening polymerization （ROP） of ε-caprolactone （CL） and tetrahydrofuran （THF） was carried out under inert atmosphere by using L-cysteine as a bridging agent in the presence of stannous octoate （SO） as a catalyst. The nano silver end capped diblock copolymer was synthesized by in situ method. Thus obtained nano silver end capped L-cysteine bridged diblock copolymer was characterized by various analytical methods like Fourier transform infrared （FTIR） spectroscopy, nuclear magnetic resonance （NMR） spectroscopy, circular dichroism （CD）, fluorescence spectroscopy, gel permeation chromatography （GPC）, X-ray photoelectron spectroscopy （XPS）, thermogravimetric analysis （TGA）, differential scanning calorimetry （DSC）, field emission scanning electron microscopy （FESEM）, high resolution transmission electron microscopy （HRTEM） and zeta potential. The antimicrobial property of the nano silver end capped diblock copolymer against e-coli was tested.
基金Supported by the National Natural Science Foundation of China(Grant no.59503002)and Polymer Physics Laboratory of Changchun Institute of Applied Chemistry,Chinese Academy of Sciences
文摘By mechanism-transformation (anionic --> cationic) poly(styrene-6-2-ethyl-2-oxazoline) diblock copolymer, PS-b-PEOx, was synthesized in two steps. The first step is the polymerization of styrene block capped with ethylene oxide and its tosylation; the second step is the cationic ring-opening polymerization of 2-ethyl-2-oxazoline. The products were thoroughly characterized by various methods, such as H-1-NMR, IR, DMA, TEM and SAXS. The results show that the copolymer obtained possesses high molecular weight and narrow molecular weight distribution.
基金Project supported by the National Natural Science Foundation of China (Grant Nos.20374050,20934004,21074096,50773072,and 90403022)the Outstanding Youth Fund of China (Grant No.20525416)+3 种基金the National Basic Research Program of China(Grant No.2005CB623800)Program for New Century Excellent Talents in University (Grant No.NCET-05-0538)the Natural Science Foundation of Zhejiang Province (Grant Nos.Y4090174 and Y6100033)the Science Technology Development Plan of Wenzhou City,China (Grant No.H20080041)
文摘The surface-induced effect on the morphologies of lamella-forming diblock copolymers in nanorod arrays is studied by using the self-consistent field theory. In the simulation study, a rich variety of novel morphologies are observed by variations in the strength of the surface field for the diblock copolymers. Different surface-field-induced effects are examined for the diblock copolymers in the arrays with distinct preferential surfaces. It is observed that the majority-block preferential surfaces have more obvious induced effects than those of minority-block preferential surfaces. The strong surface fields exhibit different behaviours from those observed in the weak surface fields, by which the morphologies possess cylindrical symmetries. Results from this research deepen the knowledge of surface-induced effects in a confinement system, which may aid the fabrication of polymer-based na^omaterials.
基金supported by the National Natural Science Foundation of China(Nos.20574052,20774066)the Program for New Century Excellent Talents in Universities(No.NCET-05-0538).
文摘The phase behaviors of symmetric diblock copolymer thin films confined between two hard, parallel and diversified patterned surfaces are investigated by three-dimensional dissipative particle dynamics (DPD) simulations. The induction of diversified patterned surfaces on phase separation of symmetric diblock copolymer films in snapshots, density profiles and concentration diagrams of the simulated systems are presented. The phase separations can be controlled by the patterned surfaces. In the meantime, the mean-square end-to-end distance of the confined polymer chains < R(2)> is also discussed. Surface-induced phase separation for diblock copolymers can help us to create novel and controlled nanostructured materials.
基金supported by the National Natural Science Foundation of China (Nos. 20974077, 51173130)Synchrotron experiments at Beam line A2 were supported by HASYLAB project (I-20110306, II20090111)
文摘The real time and in situ investigation of the crystallization process and structure transitions of asymmetric crystalline-crystalline diblock copolymers from the melt was performed with synchrotron simultaneous SAXS/WAXS. The asymmetric poly（ethylene oxide）-b-poly（ε-caprolactone） diblock copolymers were chosen for the present study. It was shown that the short blocks crystallized later than the long blocks and final lamellar structure was formed in all of the asymmetric diblock copolymers. The final lamellar structure was confirmed by AFM observation. The SAXS data were analyzed with different methods for the early stage of the crystallization. The Guinier plots indicated that there were no isolated domains formed before the formation of lamellae in the asymmetric diblock copolymers during the crystallization process. Debye- Bueche plots implied the formation of correlated domains during crystallization.
