A Non-parametric Gradient-Based Shape Optimization Approach for Solving Inverse Problems in Directed Self-Assemblyof Block Copolymers

We consider the inverse problem of finding guiding pattern shapes that result in desired self-assembly morphologies of block copolymer melts.Specifically,we model polymer selfassembly using the self-consistent field theory and derive,in a non-parametric setting,the sensitivity of the dissimilarity between the desired and the actual morphologies to arbitrary perturbations in the guiding pattern shape.The sensitivity is then used for the optimization of the confining pattern shapes such that the dissimilarity between the desired and the actual morphologies is minimized.The efficiency and robustness of the proposed gradient-based algorithm are demonstrated in a number of examples related to templating vertical interconnect accesses(VIA).

Synthesis and Properties of a New Kind of High Performance Composite Resin Matrix-Poly (Aryl Ether Ketones)/Poly (Ether Sulfone) Block Copolymers

A new kind of high performance composite resin matrix PEEK/PES, PEEKK/PES block copolymers have been prepared from the corresponding oligomers via a nucleophilic aromatic substitution reaction. The different properties of the copolymers are investigated by differential scanning calorimetry (d. s. c), thermogravimetric analysis (t. g. a) and dynamic mechanical analysis (d. m. a). The results show that the relationship between Tg and the compositions of the copolymers approximately follows the formula 1/Tg=W1/Tg1 +W2/Tg2 for PEEKK/PES block copolymers, and Tg=Tg1W1 +Tg2W2 for PEEK/PES block copolymers. The PES content and the segment length of the copolymers have a significant influence on their melting point. The thermal properties and dynamic mechanical behaviour of the copolymers are also studied. The introduction of PES segment into the molecular main chain increases the glass transition temperature of poly aryl ether ketones and decreases their melting temperature, that is to say it decreases their melting processing temperature. The block copolymers keep the high temperature stability and solvent resistance of poly aryl ether ketones. They are expected to be a new kind of high performance composite resin matrix.

Synthesis of poly[methyl(3,3,3-trifluoropropyl)siloxane]-b-poly(ethylene oxide) block copolymers

A series of new amphiphilic poly[methyl（3,3,3-trifluoropropyl）siloxane]-b-poly（ethylene oxide） （PMTFPS-b-PEO） diblock copolymers with different ratios of hydrophobic segment to hydrophilic segment were prepared by coupling reactions of end-functlonal PMTFPS and PEO homopolymers. Copolymers were shown to be well defined and narrow molecular weight distribution （MWD） （1.07-1.3） by characterizations such as gel permeation chromatography （GPC） and ^1H-nudear magnetic resonance （^1H-NMR）.

Synthesis and characterization of H-type amphiphilic liquid crystalline block copolymers by ATRP

H-type amphiphilic liquid crystalline block copolymers containing azobenzene were synthesized by atom transfer radical polymerization （ATRP）. Macroinitiators prepared by the esterification between poly（ethylene oxide） （PEG） and 2,2-dichloroacetyl chloride were utilized to initiate the polymerization of 6-[4-（4-ethoxyphenylazo）phenoxy]hexyl rnethacrylate （M6C）. The resulting macroinitiators and block copolymers were characterized by ^1H NMR, gel permeation chromatography （GPC）. Polarizing optical microscopy （POM） and differential scanning calorimetry （DSC） preliminarily revealed the liquid crystalline property of these block copolymers. This series of liquid crystalline block copolymers are promising in some areas, such as optical data storage, optical switch, and molecular devices.

Y-shaped block copolymers of poly(ethylene glycol) and poly(N-isopropylacrylamide) synthesized by ATRP

Novel Y-shaped block copolymers of poly（ethylene glycol） and poly（N-isopropylacrylamide）, PEG-b-（PNIPAM）2, were successfully synthesized through atom transfer radical polymerization （ATRP）. A difunctional macroinitiator was prepared by esterification of 2,2-dichloroacetyl chloride with poly（ethylene glycol） monomethyl ether （PEG）. The copolymers were obtained via the ATRP ofN-isopropylacrylamide （NIPAM） at 30℃ with CuCl/Me6TREN as a catalyst system and DMF/H2O （v/v = 3：1） mixture as solvent. The resulting copolymers were characterized by gel permeation chromatography （GPC） and ^1H NMR. These block copolymers show controllable molecular weights and narrow molecular weight distributions （PDI 〈 1.15）. Their phase transition temperatures and the corresponding enthalpy changes in aqueous solution were measured by differential scanning calorimetry （DSC）. As a result, the phase transition temperature of PEG45-b-（PNIPAM55）2 is higher than that of PNIPAM, however, the corresponding enthalpy change is much lower, indicating the significant influence of the macromolecular composition and architecture on the phase transition.

SYNTHESIS AND CHARACTERIZATION OF HYDROPHOBIC-HYDROPHILIC MULTIBLOCK COPOLYMERS FOR BIOMEDICAL APPLICATIONS

The synthesis and characterization of amphiphilic copolymers of poly（dimethyl siloxane）(PDMS),poly（ethylene oxide）(PEO), and heparin（Hep） were investigated. These multiblock copolymers wereidentified using;H-NMR, FTIR, end group analysis, and sulfur elemental analysis. The multiblockcopolymers were characterized by using DSC and X-ray diffractometry. The glass transition temperature,crystalline melting characteristics, annealing effect, and cold crystallization of the block copolymers weredetermined by DSC. The crystallinity of the block copolymers was also determined by X-ray diffractionmethod.

NUCLEATION AND CRYSTALLIZATION OF H-SHAPED(PS)_2PEG(PS)_2 BLOCK COPOLYMERS

A series of H-shaped （PS）2PEG（PS）2 block copolymers with different PS chain lengths were prepared. The influence of different confinements active on the crystallization and self-nucleation （SN） behavior of the PEG blocks was investigated by differential scanning calorimetry （DSC）. When the content of the crystalline block was high, a classical SN behavior was obtained. The block copolymer with PEG content of 49% （by weight） showed a classical SN behavior with a narrow self-nucleation domain and had bimodal crystallization exotherms. When the PEG dispersed as separated microdomains in the block copolymer, the self-nucleation domain disappeared and only annealing was observed.

Synthesis and characterization of poly(phthalazinone ether nitrile) (PPEN)-polydimethylsiloxane (PDMS) block copolymers

Block copolymers with different backbone compositions have been prepared by the condensation of dimethylamino terminated poly（dimethylsiloxane） （PDMS） and hydroquinone terminated poly（phthalazinone ether nitrile） （PPEN） in the presence of chlorobenzcne/N-methyl pyrrolidone （NMP） as solvents. The products were characterized by FTIR, ^1H NMR and gel permeation chromatography. Differential scanning calorimetry analysis indicated that the block copolymers showed separated microphase.

Synthesis of Well-Defined Dendritic-Linear Diblock and Triblock Copolymers by Controlled Free Radical Polymerization

The design and synthesis of novel dendritic-linear block copolymers were described. The copolymers were synthesized by atom transfer radical polymerization (ATRP) using dendritic polyarylether 2-bromoisobutyrate macroinitiator. ATRP carried out in bulk with CuBr/bipy catalyst at 120癈, yielded well-defined block copolymers with polydispersities less than 1.36.

Directed self-assembly of block copolymers for sub-10 nm fabrication

Directed self-assembly(DSA)emerges as one of the most promising new patterning techniques for single digit miniaturization and next generation lithography.DSA achieves high-resolution patterning by molecular assembly that circumvents the diffraction limit of conventional photolithography.Recently,the International Roadmap for Devices and Systems listed DSA as one of the advanced lithography techniques for the fabrication of 3-5 nm technology node devices.DSA can be combined with other lithography techniques,such as extreme ultra violet(EUV)and 193 nm immersion(193i),to further enhance the patterning resolution and the device density.So far,DSA has demonstrated its superior ability for the fabrication of nanoscale devices,such as fin field effect transistor and bit pattern media,offering a variety of configurations for high-density integration and low-cost manufacturing.Over 1 T in-2 device density can be achieved either by direct templating or coupled with nanoimprinting to improve the throughput.The development of high x block copolymer further enhances the patterning resolution of DSA.In addition to its superiority in high-resolution patterning,the implementation ofDSA on a 300 mm pivot line fully demonstrates its potential for large-scale,high-throughput,and cost-effective manufacturing in industrial environment.

Understanding the Impact of Fluorine Substitution on the Photovoltaic Performance of Block Copolymers

Fluorine substitution was applied to the donor and acceptor segments of block copolymers to understand the impact of molecular structure on photovoltaic block copolymers and explore efficient materials for single-component organic solar cells(SCOSCs).Along this line,three fluorinated block copolymers,namely PBDB-T-b-PTYF6,PM6-b-PTY6,and PM6-bPTYF6,derived from PBDB-T-b-PTY6 were designed and synthesized.The UV-Vis absorption,energy level,and thin-film morphology of these block copolymers were systematically characterized.All fluorinated block copolymers show narrow bandgap and improved crystallinity.An enhanced open-circuit voltage was observed in the SCOSC based on PM6-b-PTY6.However,SCOSCs based on all fluorinated block copolymers exhibited low short-circuit current due to energy level mismatch and therefore had low power conversion efficiency at around 4%.By contrast,the SCOSCs based on control block copolymer PBDB-T-b-PTY6 exhibited the highest power conversion efficiency approaching 10%,with a high short-circuit current of 18.57 mA/cm~2.Our study was the first to perform fluorination on photovoltaic block copolymers and provides insight into precisely controlling the polymer structure and understanding the structure-property relationship in SCOSCs based on block copolymers.

AMPHIPHILIC STAR-BLOCK COPOLYMERS BY IODIDE-MEDIATED RADICAL POLYMERIZATION

Amphiphilic star-block copolymers composed of polystyrene and poly（acrylic acid） were synthesized by iodide- mediated radical polymerization. Firstly, free radical polymerization of styrene was carried out with AIBN as initiator and 1,1,1-trimethyolpropane tri（2-iodoisobutyrate） as chain transfer agent, giving iodine atom ended star-shaped polystyrene with three arm chains, R（polystyrene）3. Secondly, tert-butyl acrylate was polymerization using polystyrene obtained as macro-chain transfer agent, and star-block copolymer, R（polystyrene-b-poly（tert-butyl acrylate））3 with controlled molecular weight was obtained. Finally, amphiphilic star-block copolymer, R（polystyrene-b-poly（acrylic acid））3 was obtained by hydrolysis of R（polystyrene-b-poly（tert-butyl acrylate））3 under acidic condition.

STRUCTURE EVOLUTION OF THE CYLINDRICAL PHASE OF DIBLOCK COPOLYMERS IN FILMS

In the weak segregation limit,the structure evolution of the hexagonal cylindrical phase of diblock copolymers in films was investigated.Employing the Landau-Brazovskii mean field theory,we obtained three amplitude parameters as functions of temperature,surface field strength and film thickness.By controlling confinement size and surface field strength, lamellae and undulated lamellae appear in the cylindrical bulk phase of diblock copolymers.'Phase diagrams'of confinement-induced structures are constructed...

A COMPARATIVE STUDY OF CHAIN DYNAMICS OF DI-AND TRI-BLOCK COPOLYMERS IN SEMIDILUTE SOLUTION IN A NON-SELECTIVE SOLVENT

The chain dynamics of a pair of diblock poly(styrene-b-butadiene) (PS210-b-PB960) and triblock poly(styrene-b-butadiene-b-styrene) (PS200-b-PB1815-b-PS200) copolymers in both dilute and semidilute toluene solutions has been comparatively studied by dynamic laser light scattering. As expected, the mutual diffusion of individual chain changes into a fast cooperative diffusion of the chain segments ('blobs') between two neighboring entanglement points for both the copolymers as the solution changes from dilute to semidilute. Further increases of the concentration lead to a second slow relaxation mode. For the triblock chains, there exists an additional middle relaxation between the fast and the slow modes. The concentration (c) dependent study of the average characteristic decay time of the fast mode ((tau(f))) reveals that 1/(tau(f)) - c(-a) with 0.33 < alpha < 0.44, much smaller than 0.75 predicted or 0.72 observed for linear homopolymer chains in good solvent. It implies that the solvent quality of toluene for PB might not be as good as that for PS. Due to such a difference in solubility, it is reasonable to speculate that the PB and PS blocks are transiently segregated in semidilute solution. The relaxation of these transient PB and PS richer domains leads to the observed slow relaxation. Such a speculation is supported by the appearance of an additional slow relaxation mode in the study of polyisoprene-b-polystyrene-b-polyisoprene in semidilute solution in cyclohexane, a non-selective solvent, in which we alternated the solubility difference by a variation of the solution temperature.

NUCLEATION MECHANISM OF PEO BLOCK IN DOUBLE-CRYSTALLINE POLY(ETHYLENE-co-BUTENE)-b-POLY(ETHYLENE OXIDE) BLOCK COPOLYMERS

In this paper, we proposed a method to determine the nucleation effect of pre-existing crystals on crystallization of the second block in double crystalline block copolymers, which is usually covered by the suppression effect. The nucleation mechanism of poly（ethylene oxide） （PEO） block from the pre-crystallized polyethylene （PE） block in poly（ethylene-cobutene）-b-poly（ethylene glycol） （EmEOn） diblock copolymers was investigated under variable crystallization environments. The crystallization environment for the PEO block was altered by cooling at different cooling rates or successive selfnucleation （SSN） to the PE block. It was found that the presence of nucleation effect is strongly dependent on composition of the block copolymers. The crystallization temperature （Tc） of PEO block in E174EO90 increases as cooling rate applied to the PE block decreases, indicating that PE block can nucleate the crystallization of PEO block and more perfect PE crystals have stronger nucleation effect. In E182EO41 crystallization of the PEO block is confined, shown by the disappearance of selfnucleation domain, and the PE block has no nucleation effect on the crystallization of PEO block. Double crystallization peaks are observed for the PEO block in E182EO41 and the intensity of the crystallization peak at higher temperature increases as the PE crystals become more perfect. After exclusion of homogeneous nucleation mechanism, the higher temperature crystallization peak of the PEO block in E182EO41 is tentatively ascribed to surface nucleation.

Self-assembly of block copolymers grafted onto a flat substrate:Recent progress in theory and simulations

Block copolymers are a class of soft matter that self-assemble to form ordered morphologies on the scale of nanome- ters, making them ideal materials for various applications. These applications directly depend on the shape and size of the self-assembled morphologies, and hence, a high degree of control over the self-assembly is desired. Grafting block copolymer chains onto a substrate to form copolymer brushes is a versatile method to fabricate functional surfaces. Such surfaces demonstrate a response to their environment, i.e., they change their surface topography in response to different external conditions. Furthermore, such surfaces may possess nanoscale patterns, which are important for some applica- tions; however, such patterns may not form with spun-cast films under the same condition. In this review, we summarize the recent progress of the self-assembly of block copolymers grafted onto a flat substrate. We mainly concentrate on the self-assembled morphologies of end-grafted AB dibloek eopolymers, junction p0int-grafted AB diblock copolymers （i.e., Y-shaped brushes）, and end-grafted ABA triblock copolymers. Special emphasis is placed on theoretical and simulation progress.

Synthesis of Dendritic-Linear Block Copolymers by Atom Transfer Radical Polymerization

The dendritic polyarylether 2-bromoisobutyrate as the macromolecular initiator for the controlled free radical polymerization of styrene was investigated. The polymerization was carried out with CuBr/2,2 ' -bipyridine catalyst at 110 degreesC. It is found that the hybrid dendritic-linear block copolymers possess well-defined molecular weights and low polydispersities.

STRUCTURE-PROPERTY RELATIONSHIP OF THERMOPLASTIC ELASTOMERS——BLOCK COPOLYMERS

Block copolymers are marked by alternation of hard blocks and soft blocks, whereby the hard blocks are believed to form crystalline domains in non-crystalline matrix formed by aggregation of the soft blocks and a fraction of the hard blocks escaping crystallization. On the basis of this two-phase model a number of studies has been made varying the nature and length of hard and soft blocks. After reviewing some papers published in this field, it may be concluded that the system in which properties of thermoplastic elastomers are exhibited can be generally divided into three catalogues, they are polyurethane, polyether-ester, polyesteramide elastomers. Structure-property relationship of these thermoplastic elastomers are given in this paper.

RELAXATION IN DOMAINS:STRUCTURE AND SEGMENTAL DYNAMICS OF LC/I DIBLOCK COPOLYMERS

A series of block copolymers consisting of an isotropic (polystyrene) block and a side-chain liquid crystallineblock (LC) have been studied using small-angle X-ray scattering and dielectric spectroscopy. The triblock copolymer (PS-LC-PS) displays an order-to-order transition (OOT) together with the isotropic/nematic transition of the LC phase. The seriesof diblock copolymers show no clear OOT but the phase diagram differs from that of non-LC block copolymers. Thesegmental dynamics as measured with dielectric spectroscopy is dominated by the α and δ relaxation of the LC block. Bothdisplay a WLF like temperature dependence. The relaxation times are influenced by the constraints of the nanoscale domains.They are decreased for the LC confined in the domain as compared to the LC in the continuous matrix.

DETERMINATION OFTHE CRYSTALLINITY IN DIFFERENT TYPE POLY (OXYETHYLENE-STYRENE)BLOCK COPOLYMERS BY X-RAY DIFFRACTION METHOD

By means of the intensity theory of X-ray scattering and the two-phase concept of high polymer, the basic formula of the crystaUinity in block copolymers has been proposed after the corrections of atomic, temperature, absorption, Lorentz and polarization factor. Application of this method to different type poly (oxyethylene-styrene)block copolymers and the same type block copolymers with different EO contents indicates that the crystallinity in poly (oxyethylene-styrene ) block copolymers increases with the increase of the EO content and decreases in the order: PEO-PS-PEO>PEO-PS>PS-PEO-PS.