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A facile approach is reported to process rod-coil block copolymers (BCPs) into highly ordered nanostructures in a rapid, low-energy process. By introducing a selective plasticizer into the rod-coil BCPs during annealing, both the annealing temperature and time to achieve thermodynamic equilibrium and highly ordered structures can be decreased. This process improvement is attributed to enhanced chain mobility, reduced rod-rod interaction, and decreased rod-coil interaction from the additive. The novel method is based on kinetically facilitating thermodynamic equilibrium. The process requires no modification of polymer structure, indicating that a wide variety of desired polymer functionalities can be designed into BCPs for specific applications.

A series of isoindigo-based low-band-gap copolymers (PnTI) containing an extended thiophene unit in the donor segment of the polymer were synthesized. The results show that the extended thiophene unit with centrosymmetric conformation simultaneously broadens the polymer absorption and enhances the crystallinity and, thus, hole mobility. Consequently, with additional improved solubility, the polymer P6TI exhibits the highest PCE of 7.25% (and a high Jsc of 16.24 mA cm−2) among isoindigo-based low-band-gap copolymers. This work demonstrates that by simply adjusting the donor segment and with relatively simple synthetic schemes, a material for high-performance and scalable PSCs will become available.

Controlling the nonlamellar and bicontinuous nanostructures through changing volume fraction is a well-developed technique for coil–coil block copolymer, but it is not always effective for rod–coil block copolymer due to strong rod–rod interaction. Versatile self-assembly morphology of rod–coil copolymer can be achieved by simultaneously adjusting the rod–rod interaction, rod–coil interaction, and conformational asymmetry. This approach has been investigated by using poly(3-alkylthiophene)-b-poly(methyl methacrylate) as a model. By altering the alkyl side chain of polythiophene from linear hexyl to longer dodecyl and to branch 2-ethylhexyl, both rod–coil and rod–rod interaction are decreased with increasing spatial occupation of alkyl side chain which have been quantitatively determined for this type of rod–coil copolymer. With tunable conformational asymmetry, competition between rod–rod and rod–coil interactions, and crystallization-driven force, the presence of versatile morphology, i.e., lamellar and ...

A series of all-conjugated diblock copolythiophenes of poly(3-hexylthiophene)-b-poly(3-thiophene hexylacetate) (P3HT-b-P3THA) were synthesized via modified sequential Grignard metathesis polymerization. The living P3HT was formed first, then reacting with the monomer of P3THA. By using 2-bromo-3-hexyloxycarbonylmethylene-5-iodothiophene instead of dibromo monomer in metal exchange reaction and by controlling the polymerization temperature relatively low at 16–20 °C, the reaction between carboxylate group and Grignard reagent can be minimized and the polymerization can be controlled; low PDI ( 95%), and well-controlled block ratios of block copolymer were obtained. The introduction of carboxylate group in the side chain of one of the monomers, and controlling the side-chain length difference by only three atoms between two monomers, there are profound effects on the optical and electrochemical properties and morphologies of the block copolymers. The electron-withdrawing carboxy...

A series of poly(diethylhexyloxy-p-phenylenevinylene-b-methyl methacrylate) (DEH-PPV-b-PMMA) polymers with narrow polydispersity (PDI < 1.1) were synthesized using Siegrist polycondensation and anionic polymerizations followed by “click” chemistry. Alkyne-terminated DEH-PPV and azido-terminated PMMA were synthesized first, and then the two functionalized polymers underwent 1,3-cycloaddition reaction to obtain copolymers. Both the conversion of the end-functionalization of the homopolymers and the yield of the “click” reaction were higher than 98% as determined by 1H nuclear magnetic resonance (1H NMR) and gel permeation chromatography (GPC). Transmission electron microscopy (TEM) and small-angle X-ray scattering (SAXS) studies reveal the details of copolymer morphology. The DEH-PPV-b-PMMA system presented here has higher block segregation strength than many previously studied rod−coil block copolymers yet still shows experimentally accessible phase transitions with respect to temperature. As a result, thi...

Well-defined poly(methyl methacrylate) (Mn ¼ 3630 g mol � 1 , PDI ¼ 1.06) with a primary benzylic bromide prepared using anionic polymerization was suc- cessfully transformed into diverse end-functionalities (x- carboxyl, x-hydroxy, x-methyl-vinyl, x-trimethylsilane, and x-glycidyl-ether) via ''click'' reaction. The bromine end-terminated poly(methyl methacrylate) was first sub- stituted by an azide function and sequentially was reacted with various functional alkynes (propiolic acid, propargyl alcohol, 2-methyl-1-buten-3-yne, propargyl tri- methylsilane, and propargyl glycidylether). In all the cases, 1 H-NMR, 13 C NMR, FT-IR, and GPC measure- ments show qualitative and quantitative transformation of the chain-end poly(methyl methacrylate) into the desired functionalities with high conversion (above 99%). V C 2008 Wiley Periodicals, Inc. J Appl Polym Sci 111: 1571-1580, 2009

High refractive index transparent nanocomposites have been developed by in situ polymerization of a precursor that contains functional monomers and surface modified anatase TiO2 nanoparticles for optoelectronic applications. The monomers are in the liquid form, so environmentally friendly solventless precursors can be prepared. The precursor can be processed into various shapes or thick films (>50 microns) of the nanocomposite. The relationships of the chemical structure of the organic matrix, nanoparticle content and dispersity with the refractive index, transparency, mechanical and thermal properties are systematically investigated. The refractive index, and mechanical and thermal properties of the nanocomposite are increased with increasing TiO2 content and aromatic structure in the organic matrix due to their rigid characteristics. The transparency of the nanocomposite is increased with increasing TiO2 content and dispersity. At the same loading of nanoparticles, the higher dispersity and the better transparency are due to the less extent of Rayleigh scattering. At 18 vol% (60 wt%) of TiO2, the acetic acid modified TiO2/poly(4-vinyl benzyl alcohol) nanocomposite has a refractive index of 1.73 and excellent transparency (>85% from 500 nm to 800 nm). The refractive index of the nanocomposite can be further increased to 1.77 by replacing aliphatic acetic acid modified TiO2 with aromatic phenyl acetic acid modified TiO2. The results of this work provide new knowledge and a new pathway to design a polymer based high refractive index material.

Isoindigo based conducting polymers have attracted extensive interest for polymer solar cell application since isoindigo is a green material and renewable from plants. We have synthesized four soluble low band gap isoindigo based polymers (PCI) with cyclopentadithiophene (CPDT) as the donor unit and isoindigo (I) as the acceptor unit, decorated with two kinds of alkyl side chains, octyl (8) and 2-ethylhexyl (e), via the Stille cross-coupling reaction denoted as PC8I8, PC8Ie, PCeI8 and PCeIe. By changing the side chain of copolymers from linear (PC8I8) to branched (PCeIe), the λmax of absorption is blue shifted from 1.37 to 1.48 eV and the HOMO level is lowered from −5.24 to −5.45 eV. The changes are due to the twist coplanarity of the polymer backbone. The density functional theory calculation revealed that the dihedral angle of copolymers has been increased from 14° to 20°. The properties of PC8Ie and PCeI8 lie between those of PC8I8 and PCeIe. The type of the side chain plays a major role in determining the photovoltaic performance of copolymers. The branched side chain improves the solubility of the polymer and increases the effective phase separation between the copolymer and PCBM. This results in favorable nanomorphology of the active layer. Thus, PCeIe with branched side chains on both donor and acceptor units exhibits the best photovoltaic properties with a Voc of 0.80 eV, Jsc of 11.6 mA cm−2 and fill factor of 43.0% and power conversion efficiency of 4.0%. The power conversion efficiency of this type of polymer could be further improved by optimizing the fabrication conditions and interlayer modification. This study offers a useful guideline for the molecular design of high efficiency isoindigo-based polymer solar cells.

In this communication, the morphology of well-defined P3DDT-b-PMMA with a 65.2% PMMA coil volume fraction is revealed as a hexagonally packed cylinder structure by X-ray scattering experiments after thermal annealing. Upon heating, an order-to-order transition (OOT) between cylindrical and gyroidal structures is observed at temperatures above 170 °C. The evolution of the cylinder to the gyroid occurs while the crystalline structure of the P3DDT block disappears, suggesting the conformation of the P3DDT-b-PMMA at high temperatures is similar to coil–coil block copolymers. The phenomena reported here can provide a different viewpoint of the self-assembly behaviors of poly(3-alkylthiophene)-containing rod–coil block copolymers. The novel rare gyroid structure of this rod–coil copolymer is useful to fabricate long sought of bicontinuous structure for highly efficient polymer solar cells.

A new class of ABC π-conjugated rod–coil–coil triblock copolymers of poly(diethylhexyloxy-p-phenylene vinylene)-b-poly (2-vinyl pyridine)-b-polystyrene (PPV-PVP-PS) was synthesized and its self-assembly behavior was explored. Three different triblock copolymers of PPV-PVP-PS1, PPV-PVP-PS2, and PPV-PVP-PS3, each with PPV, PS, and PVP, respectively, as the major species in the copolymers, were used to study the effects of copolymer composition and rod–rod interaction between PPV blocks on their morphology. Transmission electron microscopy (TEM), polarizing optical microscopy (POM), and simultaneously measured small-angle (SAXS) and wide-angle (WAXS) X-ray scattering experiments as a function of different annealing conditions revealed the details of the copolymer morphology, molecular packing, and their phase transitions. Despite their large differences in the rod volume fraction, fPPV, from 0.43 to 0.18, all three triblock copolymers adopted a self-assembled lamellar structure, in sharp constrast with the observation of many non-lamellar structures typically exhibited by ABC coil–coil–coil triblock copolymers with similar segregation strength. For PPV-PVP-PS1 with its major species PPV rod coupled with a single-phase symmetric PVP-PS diblock precursor, PPV-PVP-PS1 self-organized to form a triple-lamellar phase with each domain corresponding to the three respective blocks. Investigation of the molecular packing of PPV rods within their domain through the analysis of the 1D electron density profile suggests the PPV rods adopted a smectic C monolayer organization below its order–disorder transition temperature (TODT). For PPV-PVP-PS2 with its PS-rich asymmetric PVP-PS diblock precursor that displayed a disordered micelle structure, PPV-PVP-PS2 with fPPV of only 0.19 still exhibited a triple-lamellar phase with PPV forming a broken lamellar layer, thus preventing the excessive chain stretching of the coil blocks on the otherwise long-range ordered PPV lamellar phase. A similar broken triple-lamellar phase can also be observed for the PVP-rich PPV-PVP-PS3 with a low fPPV of only 0.18. Simultaneous SAXS and WAXS measurements show that all three triblock copolymers undergo the ordered lamella-to-disorder transition and the smectic/isotropic transition at the same temperature, indicating that the rod–rod interaction between PPV rods plays a critical role in forming and stabilizing these lamellar structures. The observation of the phase transformations is in good agreement with a recent mean-field prediction of a rod–coil–coil triblock copolymer system.