High density polyethylene (HDPE) with moderate content of crosslink network (CPE) was successfully prepared through chemical method. Specimens for structural characterization have been molded by conventional injection molding (CIM) and pressure vibration injection molding (PVIM). Influence of crosslink network on hierarchical morphology distribution and mechanical properties was systematically studied. Polarized light microscopy (PLM) revealed that both CIM and PVIM PE samples have a typical “skin-core” structure and the thickness of shear layer of CIM PE and PVIM CPE samples obviously increase. Scanning electron microscopy (SEM) showed that shish-kebab structures are clearly observed in shear layer of CIM CPE sample, indicating that the crosslink network can surely improve the formation of shish-kebab structures. Moreover, we suppose that shish-kebab structures emerged in shear and core layer of PVIM CPE sample. Wideangle X-ray diffraction (WAXD) and small-angle X-ray scattering (SAXS) confirmed that more orientation and shish-kebab structures form even in core layer of PVIM CPE sample, which demonstrated that the hierarchical morphology was apparently altered by periodical shear and crosslink network. Finally, the mechanical properties revealed that this oriented structure increase the tensile strength from 31 MPa of CIM PE sample to 46 MPa of PVIM CPE sample. However, the tensile behavior tended to change from ductile fracture to brittle fracture. 相似文献
Formation of shish-kebab crystals using a bimodal polyethylene system containing high molecular weight(HMW)component with different ethyl branch contents was investigated.In situ small-angle X-ray scattering(SAXS)and wide-angle X-ray diffraction(WAXD)techniques were used to monitor the formation and evolution of shish-kebab structure sheared at low temperature in simple shear mode and low rate.Only the bimodal PE with no branch formed shish-kebab crystals at the shear temperature of 129℃,and the shish length increased with the crystallization time,while bimodal PE with branch has no observable shish under the same conditions.The degree of crystallization for bimodal PE with no branch increased with time up to above 7％,while those with ethyl branch increased continually up to above 23％.Furthermore,bimodal PE's Hermans orientation factor with no branch increased to 0.60,while those with ethyl branch only increased to a value below 0.15.This study indicated that the shish-kebab crystal formed at the low temperature of 129℃is due to the stretch of entangled chains under shear for the bimodal PE with no branch.Only partly oriented lamellar crystals were formed for the bimodal PE with ethyl branch.All the results at the shear temperatures higher,closed to,and lower than the melting point,the modulation of shish crystals formation owing to different mechanisms of the coil-stretch transition and the stretched network by changing shear temperature was achieved in the bimodal PE samples. 相似文献
Nanostructured polymer‐based solar cells (PSCs) have emerged as a promising low‐cost alternative to conventional inorganic photovoltaic devices and are now a subject of intensive research both in academia and industry. For PSCs to become practical efficient devices, several issues should still be addressed, including further understanding of their operation and stability, which in turn are largely determined by the morphological organisation in the photoactive layer. The latter is typically a few hundred nanometres thick film and is a blend composed of two materials: the bulk heterojunction consisting of the electron donor and the electron acceptor. The main requirements for the morphology of efficient photoactive layers are nanoscale phase segregation for a high donor/acceptor interface area and hence efficient exciton dissociation, short and continuous percolation pathways of both components leading through the layer thickness to the corresponding electrodes for efficient charge transport and collection, and high crystallinity of both donor and acceptor materials for high charge mobility. In this paper, we review recent progress of our understanding on how the efficiency of a bulk heterojunction PSC largely depends on the local nanoscale volume organisation of the photoactive layer.
On the premise of strongly crystalline materials involved, it is a challenge to control the phase separation of bulk-heterojunction donor/acceptor active layer to fabricate high-performance polymer solar cells (PSCs). Herein, we develop a molecular design strategy of the third component to synthesize three guest materials (namely BTPT, BTP-Th, and BTP-2Th) to address this issue. We investigate and reveal the effect of crystallinity and miscibility of the third component in controlling the phase separation of Y6-derivatives-based blend film. As a result, a remarkable power-conversion efficiency of 18.53 % is obtained in the ternary PSC based on PTQ10 : m-BTP-PhC6 with BTP-Th as the third component, which is a significant improvement with regard to the efficiency of 17.22 % for the control binary device. Our study offers a molecular design strategy to develop a third component for building ternary PSCs in terms of crystallinity and miscibility regulation. 相似文献
The morphological features of carbon nanotube (CNT) polymer composites and their influence on the effective modulus are evaluated. The considered features include bundle formation from the helical sub‐bundles made of individual CNTs. The formation of bundles is considered as a result of agglomeration of individual nanotubes above and below onset of percolation and is related to electrical conductivity. The proposed geometrical model yields a bundle diameter that agrees closely with that of the experimentally measured by voltage‐contrast method and scanning electron microscopy analysis of polyimide nanocomposites. The proposed micromechanical analytical model includes the helical structure of a bundle and provides close agreement of the effective Young's modulus of nanocomposite over a wide range of CNT content. It is shown that considering the helical structure of CNT bundles and its effect on bundle modulus is vital for predicting the effective modulus of CNT‐polymer nanocomposite.
