Effect of [6,6]‐phenyl‐C61‐butyric acid methyl ester on the morphology of poly(3‐hexylthiophene) film

The change of morphology of poly(3‐hexylthiophene) (P3HT) film as a result of blending with [6,6]‐phenyl‐C₆₁‐butyric acid methyl ester (PCBM) was studied using a freeze‐dry method. A porous structure was observed as the P3HT/PCBM solution was freeze‐dried. The pore size decreased as the proportion of PCBM increased in the P3HT/PCBM blended film. Additionally, the freeze‐dried P3HT/PCBM film was more resistant to the formation of PCBM crystals than that prepared by a spin‐coating method during the thermal annealing process. Homogeneous distribution of PCBM in the freeze‐dried P3HT/PCBM film was the main reason for the reduction of large PCBM crystal formation. Copyright © 2011 Society of Chemical Industry     

Using water‐soluble nickel acetate as hole collection layer for stable polymer solar cells

We report polymer solar cells (PSCs) based on poly(3‐hexylthiophene (P3HT) and [6,6]‐phenyl‐C₆₁‐butyric acid methyl ester (PCBM) using water‐soluble nickel acetate (Ni(CH₃COO)₂, NiAc) instead of acidic poly(3,4‐ethylenedioxythiophene) : poly(styrenesulfonate) (PEDOT : PSS) as hole collection layer (HCL) between the indium tin oxide (ITO) electrode and photoactive layer. The NiAc layer can effectively decrease R_s and increase R_p and shows effective hole collection property. Under the illumination of AM1.5G, 100 mW/cm², the short‐circuit current density (J_sc) of the NiAc based device (ITO/NiAc/P3HT : PCBM/Ca/Al) reach 11.36 mA/cm², which is increased by 11% in comparison with that (10.19 mA/cm²) of PEDOT : PSS based device (ITO/PEDOT : PSS/P3HT : PCBM/Ca/Al). The power conversion efficiency of the NiAc based devices reach 3.76%, which is comparable to that (3.77%) of the device with PEDOT : PSS HCL under the same experimental conditions. Moreover, NiAc based PSCs show superior long‐term stability than PEDOT : PSS based PSCs. Our work gives a new option for HCL selection in designing more stable PSCs. © 2012 Wiley Periodicals, Inc. J. Appl. Polym. Sci., 2013     

Morphology,structure, and photovoltaic properties of poly(3‐hexylthiophene) and [6,6]‐phenyl‐C61‐butyric acid methyl ester‐based ternary blends doping with polystyrene of different tacticities

The influence of the polystyrene of different tacticities on the morphology, phase structure, and photovoltaic properties of poly(3‐hexylthiophene) (P3HT) and [6,6]‐phenyl‐C61‐butyric acid methyl ester (PCBM) blend has been extensively investigated. The atactic polystyrene (aPS) immiscible with P3HT tended to form the phase‐separated and columnar structure at low aPS weight ratio. Besides, the aPS could migrate to the surface of the films with PCBM phase distributing in the interfaces between P3HT and aPS domains at high aPS weight ratio of 75 wt %. The syndiotactic polystyrene (sPS) immiscible with P3HT could induce the crystallization of P3HT at low weight ratio of 3 wt %. The device based on aPS/P3HT/PCBM ternary blend showed of power conversion efficiency (PCE) of 1.2% even at aPS weight ratio of 50 wt %. However, the device based on sPS/P3HT/PCBM exhibited a sharp decrease in PCE value from 2.3% to 0.6% at sPS weight ratio of 3 wt %, due to the change in film morphology. The performance of the solar cell is believed to be determined by the morphology and phase structure of the ternary blends as revealed by the atomic force microscopy and UV‐vis spectra analysis. © 2015 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2015 , 132, 41823.     

Effect of the regioregularity of poly(3‐hexylthiophene) on the performances of organic photovoltaic devices

BACKGROUND: The highest efficiencies of bulk‐heterojunction solar cells from poly(3‐hexylthiophene) (P3HT) and [6,6]‐phenyl C₆₁‐butyric acid methyl ester (PCBM) reported so far are close to 6%. Phenomena occurring during the photovoltaic process, such as the creation, diffusion and separation of excitons, as well as charge carrier transport, are governed by the active layer morphology. The latter phenomenon, which depends on the self‐organization of P3HT, can be influenced by its degree of regioregularity. The aim of this work is to clarify the relationship between the regioregularity of P3HT, the composition of P3HT/PCBM blends and the performances of photovoltaic devices. RESULTS: Two types of P3HTs with different degrees of regioregularity have been synthesized and used as active layers with PCBM in photovoltaic cells. The higher performances in photovoltaic devices are obtained for high‐regioregular P3HT and can be explained considering the self‐organizing properties of high‐regioregular P3HT, leading to higher sunlight absorption and higher hole mobilities. In addition, this report demonstrates the importance of the ratio of P3HT versus PCBM in correlation with the regioregularity of P3HT on the optical properties, charge transport and characteristics of photovoltaic cells. CONCLUSION: We have investigated the dependence of the photovoltaic properties of P3HT/PCBM blend‐based photovoltaic devices on the degree of regioregularity of P3HT. We find that the best performance is exhibited by devices based on highly regioregular P3HT. Also, the best performances are not obtained for the same P3HT:PCBM weight ratios for high‐regioregular P3HT (1:0.8) and low‐regioregular P3HT (1:3). Copyright © 2007 Society of Chemical Industry     

Solvent vapor‐induced self assembly and its influence on optoelectronic conversion of poly(3‐hexylthiophene): Methanofullerene bulk heterojunction photovoltaic cells

Nanoscale‐phase separation of electron donor/acceptor blends is crucial for efficient charge generation and collection in polymer bulk heterojunction photovoltaic cells. We investigated solvent vapor annealing effect of poly(3‐hexylthiophene) (P3HT)/methanofullerene (PCBM) blend on its morphology and optoelectronic properties. The organic solvents of choice for the treatment have a major effect on the morphology of P3HT/PCBM blend and the device performance. Ultraviolet‐visible absorption spectroscopy shows that specific solvent vapor annealing can induce P3HT self‐assembling to form well‐ordered structure; and hence, the absorption in the red region and the hole transport are enhanced. The solvent that has a poor solubility to PCBM would cause large PCBM clusters and result in a rough blend film. By combining an appropriate solvent vapor treatment and post‐thermal annealing of the devices, the power conversion efficiency is enhanced. © 2008 Wiley Periodicals, Inc. J Appl Polym Sci, 2009     

Study of the processing pathway for cosolvent addition in active layer preparation of inverted organic solar cell

Investigation on processing pathway for co‐solvent addition in active layer preparation of an inverted organic solar cell indicated that the composite films cast out of simple marginal solvent (like cyclohexanone) addition in poly(3‐hexyl thiophene)‐[6,6]‐phenyl C₆₁‐butyric acid methyl ester (P3HT‐PCBM) solution were not effectively crystallized. A comparison of one step direct marginal solvent addition to the P3HT‐PCBM solution with the modified two step process consisting of primary P3HT crystallization in first step by marginal solvent addition to a solution of only P3HT in good solvent (like ortho‐dichloro benzene) followed by mixing of PCBM solution revealed improvement in P3HT crystallization in the latter method. Grazing incidence X‐ray diffraction measurements supported favorable vertical concentration gradient in the P3HT‐PCBM composite film. This modification of active layer morphology with the two step individually mixed cyclohexanone addition into the active layer spin coating solution results in an improved power conversion efficiency of 3.39%, an improvement of more than 10% compared to the conventional one step blended co‐solvent addition method. POLYM. ENG. SCI., 55:1758–1766, 2015. © 2014 Society of Plastics Engineers     

Preparation and characterization of methanofullerenes for polymer–fullerene bulk heterojunction solar cells

A series of alkyl 4-benzoylbutyrate p-tosylhydrazones were synthesized and reacted with C₆₀ in the presence of sodium methoxide. Interestingly, n-butyl 4-benzoylbutyrate p-tosylhydrazone causes a high yield of the undesired compound-[6,6]-phenyl C₆₁-butyric acid methyl ester (PCBM). Photovoltaic cells with these derivatives as electron acceptors were fabricated. The surface morphology of poly(3-hexylthiophene)(P3HT)/C₆₀ derivatives was characterized by atomic force microscopy. The nano-scale phase separation was observed in P3HT/PCBM film through a slow-growth process. This phenomenon is indistinguishable in P3HT/PCBiB ([6,6]-phenyl C₆₁-butyric acid iso-butyl ester) film because of the higher solubility of PCBiB in P3HT. The power conversion efficiency of the device that was made of P3HT/PCBiB blend is 2.8%, which is lower than that of P3HT/PCBM-based device (4.0%).     

Effect of co‐solvents on the photovoltaic performance of an inverted organic solar cell

We investigated the effect of varying polymer crystallinity, morphology, and optical property, produced by adding four different co‐solvents in to the poly(3‐hexylthiophene) (P3HT): [6,6]‐phenyl C₆₁‐butyric acid methyl ester (PCBM) active layer blend solution, on the functioning of an inverted polymeric solar device. Photovoltaic devices primed with cyclohexanone co‐solvent showed the best performance with power conversion efficiency (PCE) reaching a value of 3.01 ± 0.04%. Improvement in efficiency is related to an increase in photocurrent which is due to a combined result of ordered P3HT crystallite growth, as well as of the precise size and phase separation of domains. POLYM. ENG. SCI., 55:1382–1388, 2015. © 2015 Society of Plastics Engineers     

Controlling the morphology of poly(3‐hexylthiophene)/methanofullerene film through a dynamic‐cooling and freeze‐drying process

A dynamic‐cooling and freeze‐drying (DCFD) process has been applied to the fabrication of polymer solar cells. The dynamic‐cooling process allows poly(3‐hexylthiophene) molecules to aggregate in solution into a more organized structure during the cooling process; the freeze‐drying process prevents severe agglomeration of [6,6]‐phenyl‐C₆₁‐butyric acid methyl ester (PCBM) during the solvent removing process. Application of these two processes to the preparation of the poly(3‐hexylthiophene)/methanofullerene photoactive layer results in an enhanced poly(3‐hexylthiophene) aggregation and smaller PCBM agglomerates. Devices fabricated using the DCFD process generate 14% more in current density than those prepared by the spin‐coating process under AM1.5G illumination. © 2015 Society of Chemical Industry     

Butterfly nanostructures via regioregularly grafted multi‐walled carbon nanotubes and poly(3‐hexylthiophene) to improve photovoltaic characteristics

Butterfly nanostructures were designed using multi‐walled carbon nanotubes (CNTs) grafted with regioregular poly(3‐hexylthiophene) (RR‐P3HT) chains (CNT‐graft‐P3HT). The secondary crystallization of RR‐P3HT free chains onto CNT‐graft‐P3HT reflected the donor–acceptor supramolecules with a butterfly configuration, in which the CNT acted as the body of the butterfly and seeded crystallization of P3HT free chains resulted in the wings having a width of 37–38 nm. Butterfly supramolecules demonstrated high melting point (241.2 °C), fusion enthalpy (31.5 J g^?1) and crystallinity (85.13%). High photoluminescence quenching and thus donating–accepting property were also detected for the butterfly nanohybrids with a bandgap energy of 1.94 eV. Incorporation of butterfly nanostructures in the active layer of photovoltaic devices (P3HT:butterfly) conspicuously affected the system characteristics including short circuit current density (J_sc; 10.84 mA cm^?2), fill factor (FF; 56%) and power conversion efficiency (PCE; 3.94%). The inclusion of phenyl‐C71‐butyric acid methyl ester molecules as second acceptor in thin‐film active layers further increased the efficacy of systems, i.e. J_sc of 12.23 mA cm^?2, FF of 63%, open circuit voltage of 0.66 V and PCE of 5.08%, without considering external treatments and additives. © 2018 Society of Chemical Industry     

Synthesis and characterization of three‐arm star‐shaped conjugated poly(3‐hexylthiophene)s: impact of the core structure on optical properties

Star‐shaped molecules consisting of regioregular poly(3‐hexylthiophene) (P3HT) chains as the arms, attached to either a propeller‐like triphenylamine or a planar triphenylbenzene core, have been synthesized via Suzuki coupling. The structures of the three‐arm star‐shaped poly(3‐hexylthiophene) (s‐P3HT) materials obtained were studied using Fourier transform infrared, ¹H and ¹³C NMR, XRD, gel permeation chromatography and DSC. The s‐P3HT polymers were soluble in common organic solvents and exhibited number‐average molecular weights of 6000–7200 g mol^?1. Their optical properties in solutions and in solid state films were investigated using the UV?visible absorption and photoluminescence techniques, and were compared with those of linear P3HT. © 2015 Society of Chemical Industry     

Electroactive polythiophene/polystyrene bottlebrushes as morphology compatibilizers in photovoltaic systems

Poly(3‐thiophene ethanol) (P3ThEt)‐graft‐polystyrene (PSt) bottlebrushes were synthesized and applied in active layers of poly(3‐hexylthiophene) (P3HT):phenyl‐C71‐butyric acid methyl ester (PC71BM) solar cells as morphology compatibilizers. In the presence of 15 wt% of P3ThEt‐graft‐PSt bottlebrush compatibilizers, the P3HT crystallite dimensions (D₍₁₀₀₎ = 45.67 nm and D₍₀₂₀₎ = 30.12 nm) and R_mean (38.96 nm) of PCBM clusters were the largest and the layer spacings were all the smallest (d₍₁₀₀₎ = 1.054 nm, d₍₀₂₀₎ = 0.301 nm and d_(PCBM) = 0.406 nm). These dimensional properties led to better hole (1.9 × 10^?3 cm² V^?1 s^?1) and electron (1.2 × 10^?2 cm² V^?1 s^?1) mobilities. The content of bottlebrushes was optimized at 15 wt%, and thereby the best photovoltaic results including the maximum cell efficiency of 5.37% were obtained for this turning point (12.75 mA cm^?2, 61%, 0.69 V). On exceeding the optimum weight percentage, all photovoltaic parameters decreased markedly and reached even less than that of pristine devices (1.92% versus 2.24%). After an optimum weight percentage of compatibilizers, further enhancement in bottlebrush content in active layers saturated and finally oversaturated the system and, consequently, the cell parameters significantly decreased. Accumulation of bottlebrushes in interfaces and donor/acceptor phases ruined the system function even with large and packed P3HT crystallites and PC71BM clusters. © 2019 Society of Chemical Industry     

Chemical vapor deposition of poly(3‐alkylthiophene) nanoparticles on fabric: Chemical and electrochemical characterization

Chemical vapor deposition of poly(3‐methylthiophene) and poly (3‐hexylthiophene) as conductive polymers on the surface of polyester fabrics was successfully obtained. Fourier transform infrared spectroscopy confirmed the formation of polymers on surface of fabrics (the fingerprint of polythiophenes, υ 600–1500 cm^?1). The uniformity of deposition and nanoparticles (average size of 60 nm) were proved with scanning electron microscopy. Electrochemical impedance spectroscopy showed that P3HT‐coated samples offer higher conductivity in compared to P3MT‐coated samples. The impedance modulus of P3HT‐coated samples was lowered nine times to that of row materials and reached to c8000 Ω. The samples have also shown electrochromic properties under electrical current, changing its color from yellowish green at 0 V to dark green at +12 V for poly (3‐hexylthiophene) samples and from brown at 0 V to red at +12 V for poly(3‐methylthiophene)‐coated fabrics (V = 0 V, λ = 450 nm; V = 12 V, λ = 650 nm). © 2014 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2014 , 131, 40673.     

Preparation of porous poly(3‐hexylthiophene) by freeze‐dry method and its application to organic photovoltaics

Poly(3‐hexylthiophene)(P3HT) with a microporous network structure was prepared from a 1% p‐xylene solution by freeze‐dry method. Scanning electron microscopy (SEM) showed P3HT molecules formed swollen gel‐like structures with different extent of compactness depending on the length of the aggregation period. Absorption spectrum of this P3HT film showed a characteristic peak at 620 nm, which indicated a high degree of order between polymer chains. Photoluminescence (PL) of this highly ordered P3HT film appeared at 712 nm revealing large extent of π–π stacking between P3HT molecules in the freeze‐dry film. Both absorption and photoluminescence results indicated that the original aggregated states of P3HT molecules in gel form had been preserved throughout the freeze‐dry operation. X‐ray diffraction of the annealed samples showed a strong characteristic peak for the side chain aggregation at 2θ = 5.1°, which proved that the freeze‐dry film was with highly order structure. The interconnected and highly ordered P3HT film is used in the study of organic photovoltaics (OPV) after applying an n‐type semiconductor to the surface of the dry porous fibers. A prototype OPV device with power conversion efficiency of 1.47% was prepared by this method. © 2011 Wiley Periodicals, Inc. J Appl Polym Sci, 2011.     

Nano‐dimensional self assembly of regioregular poly (3‐hexylthiophene) in toluene: Structural,optical, and morphological properties

This article presents the optimization and systematic analysis of the growth kinetics of fiber formation of the regio‐regular poly (3‐hexylthiophene), rr‐P3HT. In addition to it a comparative study of as‐prepared fiber with fresh, quenched (at ?7°C) and commercial rr‐P3HT formed in toluene solvent. The rr‐P3HT (M_w ≈ 5340; polydispersity ≈ 1.22) is synthesized using a well known Grignard metathesis reaction and characterized by ¹HNMR and FTIR techniques. The films obtained by the ageing of rr‐P3HT solution for 20 days contain nanostructured fiber with 6–10 nm thickness. However, it acquires a nanostructured globular shape when same concentration of solution is sudden quenched at ?7°C. A saturation point for the growth of nano fiber is observed under UV–visible study and it is found that 10 days are sufficient for fiber growth. The concentration dependent free exciton band width of fiber growth is studied by Frank–Condon principle and correlated with AFM morphological studies. © 2014 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2014 , 131, 40931.     

Improved stability in P3HT:PCBM photovoltaics by incorporation of well‐designed polythiophene/graphene compositions

Morphological and photovoltaic stabilities of poly(3‐hexylthiophene) (P3HT):phenyl‐C₆₁‐butyric acid methyl ester (PC₇₁BM) solar cells were investigated in pristine and modified states. To this end, four types of patterned/assembled nanostructures, namely reduced graphene oxide (rGO)‐g‐poly(3‐dodecylthiophene)/P3HT patched‐like pattern, rGO–polythiophene/P3HT/PC₇₁BM nanofiber, rGO‐g‐P3HT/P3HT cake‐like pattern and supra(polyaniline (PANI)‐g‐rGO/P3HT), were designed on the basis of rGO and various conjugated polymers. Intermediately covered rGO nanosheets by P3HT crystals (supra(PANI‐g‐rGO/P3HT)) performed better than sparsely (patched‐like pattern) and fully (cake‐like pattern) covered ones in P3HT:PC₇₁BM solar cell systems. Supra(PANI‐g‐rGO/P3HT) nanohybrids largely phase‐separated in active layers (root mean square = 0.88 nm) and also led to the highest performance (power conversion efficiency of 5.74%). The photovoltaic characteristics demonstrated decreasing trends during air aging for all devices, but with distinct slopes. The steepest decreasing plots were obtained for the unmodified P3HT:PC₇₁BM devices (from 1.77% to 0.28%). The two supramolecules with the most ordered structures, that is, cake‐like pattern (10.12 mA cm^?2, 51%, 0.58 V, 2.2 × 10^?6 cm² V^?1 s^?1, 4.3 × 10^?5 cm² V^?1 s^?1, 0.69 nm and 2.99%) and supra(PANI‐g‐rGO/P3HT) (12.51 mA cm^?2, 57%, 0.63 V, 1.2 × 10^?5 cm² V^?1 s^?1, 3.4 × 10^?4 cm² V^?1 s^?1, 0.82 nm and 4.49%), strongly retained morphological and photovoltaic stabilities in P3HT:PC₇₁BM devices after 1 month of air aging. According to the morphological, optical, photovoltaic and electrochemical results, the supra(PANI‐g‐rGO/P3HT) nanohybrid was the best candidate for stabilizing P3HT:PC₇₁BM solar cells. © 2020 Society of Chemical Industry     

Block copolymer alignment method for mobility anisotropy and enhancement of poly(3‐hexylthiophene) thin‐film transistors

In this article, a new alignment‐layer approach based on block copolymers (BCPs) is proposed for mobility anisotropy and enhancement of organic thin‐film transistors (OTFTs). In particular, the poly(3‐hexylthiophene) (P3HT) TFT with polystyrene‐block‐poly(methyl methacrylate) alignment layer was studied. With max dichroic ratio 1.23 in polarized absorption spectra of P3HT and corresponding device mobility anisotropy 4.63, taking place at the highest annealing temperature of 230°C, the BCP alignment approach proved to be an effective tool for orientation control of polymers such as the P3HT. However, because of negative effect of thermal annealing that causes twisting in P3HT backbones, the achieved mobility enhancement was only a meager 41%. Nevertheless, with rich varieties in the composition and complexity of BCPs, the proposed BCP alignment design represents an interesting alternative to existing alignment approaches to orientation control of P3HT and mobility anisotropy and enhancement of the resultant OTFTs. Besides, the phase‐alternate surface morphology of the BCP alignment layer was confirmed through a series of atomic force microscopy, X‐ray photoelectron microscopy, and field‐emission scanning electron microscopy. POLYM. ENG. SCI., 2012. © 2012 Society of Plastics Engineers     

Efficiency above 6% in poly(3‐hexylthiophene):phenyl‐C‐butyric acid methyl ester photovoltaics via simultaneous addition of poly(3‐hexylthiophene) based grafted graphene nanosheets and hydrophobic block copolymers

A combination of reduced graphene oxide (rGO) nanosheets grafted with regioregular poly(3‐hexylthiophene) (P3HT) (rGO‐g‐P3HT) and P3HT‐b‐polystyrene (PS) block copolymers was utilized to modify the morphology of P3HT:[6,6]‐phenyl‐C71‐butyric acid methyl ester (PC71BM) active layers in photovoltaic devices. Efficiencies greater than 6% were acquired after a mild thermal annealing. To this end, the assembling of P3HT homopolymers and P3HT‐b‐PS block copolymers onto rGO‐g‐P3HT nanosheets was investigated, showing that the copolymers were assembled from the P3HT side onto the rGO‐g‐P3HT nanosheets. Assembling of P3HT‐b‐PS block copolymers onto the rGO‐g‐P3HT nanosheets developed the net hole and electron highways for charge transport, thereby in addition to photoluminescence quenching the charge mobility (μ_h and μ_e) values increased considerably. The best charge mobilities were acquired for the P3HT₅₀₀₀₀:PC71BM:rGO‐g‐P3HT₅₀₀₀₀:P3HT₇₀₀₀‐b‐PS₁₀₀₀ system (μ_h = 1.9 × 10^?5 cm² V^–1 s^–1 and μ_e = 0.8 × 10^?4 cm² V^–1 s^–1). Thermal annealing conducted at 120 °C also further increased the hole and electron mobilities to 9.8 × 10^?4 and 2.7 × 10^?3 cm² V^–1 s^–1, respectively. The thermal annealing acted as a driving force for better assembly of the P3HT‐b‐PS copolymers onto the rGO‐g‐P3HT nanosheets. This phenomenon improved the short circuit current density, fill factor, open circuit voltage and power conversion efficiency parameters from 11.13 mA cm^?2, 0.63 V, 62% and 4.35% to 12.98 mA cm^?2, 0.69 V, 68% and 6.09%, respectively. © 2019 Society of Chemical Industry     

A novel electrochemically and thermally stable polythiophene for photovoltaic application

Conjugated polymers having good electrochemical and thermal stability are highly desired in optoelectronics. We report a new polythiophene consisting of alternating 4,4′‐didodecyl‐2,2′‐bithiophene and terthiophene units (HPL1) synthesized via Stille coupling reaction. The optical band gap of HPL1 (1.92 eV) is similar to that of regioregular poly(3‐hexylthiophene) (rr‐P3HT, 1.89 eV). In comparison to rr‐P3HT, the HPL1 when subjected to the cyclic voltammetry as thin film shows much superior electrochemical stability and a lower highest occupied molecular orbital energy level (?4.87 eV for rr‐P3HT and ?4.95 eV for HPL1). The transient photoluminescence study of HPL1 and rr‐P3HT shows that both materials have two exciton decay processes, and the excitons of rr‐P3HT are quenched more quickly. The onset decomposition, T_d for rr‐P3HT (465°C) is 4°C lower than HPL1 (469°C). Preliminary photovoltaic study disclosed that the polymer solar cell based on HPL1:[6,6]‐phenyl‐C₆₁‐butyric acid methyl ester blend showed a power conversion efficiency of 0.63%, with a V_oc of 0.6 V, and a short circuit current (J_sc) of 2.79 mA cm^?2 under AM 1.5 illumination (100 mW cm^?2). The whole study provided an important example to design new electrochemically and thermally stable polymers with longer exciton life time for application in bulk heterojunction polymer solar cells. © 2012 Wiley Periodicals, Inc. J. Appl. Polym. Sci., 2013     

Thermal and mechanical properties of homogeneous ternary nanocomposites of regioregular poly(3‐hexylthiophene)‐wrapped multiwalled carbon nanotube dispersed in thermoplastic polyurethane: Dynamic‐ and thermomechanical analysis

An interesting correlation between initial loading and nature of wrapping of regioregular poly(3‐hexylthiophene) (rrP3HT) on multiwalled carbon nanotube and their combined effect on dynamic‐ and thermomechanical properties in ternary system (thermoplastic polyurethane as matrix) is highlighted. Wrapping of rrP3HT on carbon nanotube (CNT) makes the hexyl side chains thermally nonequivalent and composites more stable. Dynamic‐ and thermomechanical analysis ascertained the miscibility (single T_g = ?40°C), large mechanical reinforcement, and improved storage modulus of nanocomposites in the presence of CNT compared to its blends. Two breaks at ～ ?100 and ～ ?40°C for TPU‐P3HT composites (PHs) and TPU‐P3HT‐MWCNT composites (PHCs) in the loss modulus vs. temperature plot indicates two different types of transitions in P3HT chains. Dimensional stability by expansion probe technique measures low coefficient of thermal expansion of PHCs compared to its blends. Softening property by penetration probe technique suggests that 2.5 wt % loading of P3HT exhibits lowest degree of penetration compared to other nanocomposites. © 2012 Wiley Periodicals, Inc. J. Appl. Polym. Sci., 2013