16 research outputs found

    Huge enhancement of electronmechanical responses in compositionally modulated PZT

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    Monte Carlo simulations based on a first-principles-derived Hamiltonian are conducted to study the properties of PZT alloys compositionally modulated along the [100] pseudocubic direction near the morphotropic phase boundary (MPB). It is shown that compositional modulation causes the polarization to continuously rotate away from the modulation direction, resulting in the unusual triclinic and C-type monoclinic ground states and huge enhancement of electromechanical responses (the peak of piezoelectric coefficient is as high as 30000 pC/N). The orientation dependence of dipole-dipole interaction in modulated structure is revealed as the microscopic mechanism to be responsible for these anomalies.Comment: 5 pages, 4 figure

    A new three-dimensional (3D) multilayer organic material : synthesis, swelling, exfoliation, and application

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    A novel fully rigid, rod-shaped oligo(p-benzamide) (OPBA-6) molecule was designed and synthesized, which can be recrystallized into a three-dimensional (3D) multilayer material via an antiparallel molecular packing model. Intermolecular hydrogen bonding and π–π interaction are brought to ensure a strong intralayer interaction, while decoration of layer surface with sulfonic groups promotes water to enter interlayer space and facilitates the swelling and exfoliation of sample. With a simple dispersion in water, the obtained multilayer material can be easily swollen by water without destruction of in-plane morphology and subsequently delaminated into 2D nanosheets with thickness of about 5.38 nm. This achievement may be the first attempt to exfoliate layered organic materials and thus provide a new strategy to prepare 2D organic nanosheets without using any substrates or templates as required by conventional and widely used self-assembly routes. Based on exfoliated nanosheets, poly(vinyl alcohol) nanocomposites were prepared using a simple water solution processing method. A 64% increase in tensile stress and a 63% improvement in Young’s modulus were achieved by addition of 7 wt % OPBA-6 loading

    Ferroelectricity in Pb

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    Mixing Assisted Direct Formation of Isotactic Poly(1-butene) Form I′ Crystals from Blend Melt of Isotactic Poly(1-butene)/Polypropylene

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    The influence of mixing of iPB-1/iPP blend on the polymorphism of iPB-1 under processing-relevant conditions is studied with emphasis on the competition between the thermodynamically stable form I′ crystal and the kinetically favored form II. <i>In situ</i> optical microscopy measurements reveal that the upper critical solution temperature (UCST) of iPB-1/iPP blend locates in the range of 180–200 °C. Unexpectedly, by quenching mixed iPB-1/iPP melt down to temperatures below UCST and melting point, form I/I′ can be produced directly which is further identified as form I′ by temperature-dependent WAXS and DSC. The formation of form I′ is promoted by increasing the annealing time above UCST, while is suppresses by raising the quenching temperature. In addition, the crystallization of iPP also displays a similar trend as iPB-1 does. The correlated crystallization of each constituent with dependence on the initial mixing degree suggests that the crystallization behavior of the binary blends is determined by the interplay between simultaneous processes concomitant with the liquid–solid transition. The experimental results reveal the possibility to modify the crystallization pathway of iPB-1 in iPB-1/iPP blend through the mixing degree which is initially controlled by annealing but is subject to evolve during the subsequent thermal treatment. Possible mechanisms are discussed including the roles of phase separation and concentration fluctuation in crystallization

    Modulating the Arrangement of Charged Nanotubes by Ionic Strength in Salty Water

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    Despite the important role and potential application of charged cylindrical polyelectrolytes, biomacromolecules, and self-assembles, salt-modulated organization of those 1D charged nanostructures remains a topic relatively unexplored with an obscure underlying mechanism. In this Letter, the aggregation of oriented nanotubes self-assembled by ionic aromatic oligoamide in aqueous solution of NaCl over a wide concentration range is probed via small-angle X-ray scattering and a transmission electron microscope. The arrangement of nanotubes undergoes order–disorder transition sequences from an ordered rectangular phase to hexagonal packing and then to a lamellar gel. The observed transitions are understood by ionic effects on the electrostatic interaction between charged nanotubes and osmotic pressure due to ion partitioning. Above the physiological condition, electrostatic interactions are largely screened by the salts, while osmotic effects start to regulate the aggregation behavior and concomitantly deform the nanotubes. The study demonstrates rich phase behaviors of ordered, charged 1D nanostructures by tuning the ionic strength and underlying key physical principles

    A New Three-Dimensional (3D) Multilayer Organic Material: Synthesis, Swelling, Exfoliation, and Application

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    A novel fully rigid, rod-shaped oligo­(<i>p</i>-benzamide) (OPBA-6) molecule was designed and synthesized, which can be recrystallized into a three-dimensional (3D) multilayer material via an antiparallel molecular packing model. Intermolecular hydrogen bonding and π–π interaction are brought to ensure a strong intralayer interaction, while decoration of layer surface with sulfonic groups promotes water to enter interlayer space and facilitates the swelling and exfoliation of sample. With a simple dispersion in water, the obtained multilayer material can be easily swollen by water without destruction of in-plane morphology and subsequently delaminated into 2D nanosheets with thickness of about 5.38 nm. This achievement may be the first attempt to exfoliate layered organic materials and thus provide a new strategy to prepare 2D organic nanosheets without using any substrates or templates as required by conventional and widely used self-assembly routes. Based on exfoliated nanosheets, poly­(vinyl alcohol) nanocomposites were prepared using a simple water solution processing method. A 64% increase in tensile stress and a 63% improvement in Young’s modulus were achieved by addition of 7 wt % OPBA-6 loading

    Unveiling Reinforcement and Toughening Mechanism of Filler Network in Natural Rubber with Synchrotron Radiation X‑ray Nano-Computed Tomography

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    Double network structure constructed with filler network of carbon black and molecular network of natural rubber possesses excellent toughness and strength. However, due to lack of proper <i>in situ</i> imaging techniques to detect the structural evolutions under loading, the reinforcement mechanism of filler network is still under debate. Here <i>in situ</i> synchrotron radiation X-ray nano-computed tomography with high spatial resolution (100 nm) is employed to study structural evolution of carbon black in a large volume of natural rubber matrix. For the first time, strain-induced deformation, destruction, and reconstruction of filler network are directly observed under cyclic loading. Combining mechanical test, the reinforcing and toughening effect of filler network is quantitatively assigned to three mechanisms, namely elastic deformation, destruction, and friction of filler network. Elastic deformation mainly occurs at low strain for energy storage, while network destruction plays the dominant role at larger strain to dissipate strain energy. Additionally, friction is another energy dissipation mainly at low strain

    Kinetic Process of Shish Formation: From Stretched Network to Stabilized Nuclei

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    On the basis of the duality of the shish-kebab superstructure, coil–stretch transition (CST) is well recognized as the molecular mechanism for shish-kebab formation in polymer melts, which, however, is challenged by recent results in flow-induced crystallization (FIC). In this work, we perform a real time investigation on FIC of polyethylene bimodal blends by combing a unique homemade extensional rheometer and synchrotron radiation small-angle X-ray scattering. The results show that the critical strain for shish formation decreases with increasing long chain concentration, which contradicts the role of CST but agrees well with stretched network model (SNM). Quantitative analyses indicate that the formation of shish is determined by the degree of network deformation rather than solely by strain or long chain concentration at a specific temperature. In addition, three types of shish with different stability are observed sequentially by increasing strain. On the basis of our results, strong support is given to the idea that shish formation is a kinetic process. When stretched to a critical deformation degree, the aligned segments couple with each other to form fibrillar-like type I shish, which further transform into type II shish embedded with sporadic lamellae and type III shish embedded with well-defined periodic lamellae sequentially by increasing flow intensity. Our results and the resulting conceptual model not only demonstrates that shish formation is derived from SNM but unveils its kinetic process from initial chain configuration to final stable nuclei
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