Morphology and mechanical properties of natural rubber latex films modified by exfoliated Na‐montmorillonite/polyethyleneimine‐g‐poly (methyl methacrylate) nanocomposites

Na‐montmorillonite/polyethyleneimine‐g‐poly(methyl methacrylate) (Na‐MMT/PEI‐g‐PMMA) nanocomposite latexes were prepared by soap‐free emulsion polymerization in the aqueous suspension of Na‐MMT. The exfoliated morphology of the nanocomposites was confirmed by XRD and TEM. With the aim of improving morphology and mechanical properties of natural rubber latex (NRL) films, the synthesized Na‐MMT/PEI‐g‐PMMA nanocomposites were mixed with NRL by latex compounding technology. The results of SEM and AFM analysis showed that the surface of NRL/Na‐MMT/PEI‐g‐PMMA film was smoother and denser than that of pristine NRL film while Na‐MMT was dispersed uniformly on the fracture surface of the modified films, which suggested the good compatibility between NRL and Na‐MMT/PEI‐g‐PMMA. The tensile strength of NRL/Na‐MMT/PEI‐g‐PMMA films was increased greatly by 85% with 10 phr Na‐MMT/PEI‐g‐PMMA when Na‐MMT content was 3 wt % and the elongation at break also increased from 930% to 1073% at the same time. © 2016 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2016 , 133, 43961.     

An ambipolar polymer additive for enhanced open circuit voltage in a bulk heterojunction solar cells

Open circuit voltage (V_OC) of organic bulk heterojunction solar cell is extended by the addition of a 20 wt % of F8TBT, an ambipolar polymer in the active layer matrixes (P3HT:PCBM) and then spin casted (1000 rpm/30 s) in the optimized devices on the PEDOT:PSS layer of the ITO glass. A substantial increase in the open circuit voltage from approximately 0.61–0.88 V (44.26%) has been observed with slight increase in efficiency up to 1.91% in the fabricated devices. However, further increment of F8TBT content to 40 wt % reduces the photovoltaic efficiency and affects the J_SC values remarkably, possibly due the excess amount of resistance developed. The enhancement of V_OC is attributed to the ambipolar nature of F8TBT polymer which facilitates the generated electron and hole transfer at the respective electrodes, enhanced π–π* conjugation in polymer matrix, a superior nanoscale separation, and better molecular conformation at the film interface, thus giving an ample opportunities to explore the impact of blending of materials rather than depositing a thin buffer layer by expensive vapor phase technologies. The details of electrical and microstructure characterization of the film were analyzed by AFM, SEM, UV–Vis, J–V characteristics, and EQE techniques. © 2015 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2016 , 133, 43042.     

Solvent and relative humidity effect on highly ordered polystyrene honeycomb patterns analyzed by Voronoi tesselation

Highly ordered honeycomb‐patterned polystyrene surfaces are efficiently prepared by static breath figure method. The structured arrays can be obtained by casting a dilute solution polymer on glass substrates under various conditions. Tetrahydrofuran and chloroform are used as solvent to form cavities of several micrometers. The analysis of the surfaces indicates nonlinear relation between concentration and pore size in this system. Voronoi tessellations of the polystyrene surfaces at different relative humidity (RH) are achieved, and each conformational entropy determined. Optimum parameters of concentration and RH are obtained for both solvents. Analysis of hole size distribution and conformational entropy demonstrates the high order of the films obtained. This is a promising method for the fabrication of homogeneous and highly porous films from polystyrene. © 2016 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2016 , 133, 44004.     

Scaling Effects in Perovskite Ferroelectrics: Fundamental Limits and Process‐Structure‐Property Relations

Ferroelectric materials are well‐suited for a variety of applications because they can offer a combination of high performance and scaled integration. Examples of note include piezoelectrics to transform between electrical and mechanical energies, capacitors used to store charge, electro‐optic devices, and nonvolatile memory storage. Accordingly, they are widely used as sensors, actuators, energy storage, and memory components, ultrasonic devices, and in consumer electronics products. Because these functional properties arise from a noncentrosymmetric crystal structure with spontaneous strain and a permanent electric dipole, the properties depend upon physical and electrical boundary conditions, and consequently, physical dimension. The change in properties with decreasing physical dimension is commonly referred to as a size effect. In thin films, size effects are widely observed, whereas in bulk ceramics, changes in properties from the values of large‐grained specimens is most notable in samples with grain sizes below several micrometers. It is important to note that ferroelectricity typically persists to length scales of about 10 nm, but below this point is often absent. Despite the stability of ferroelectricity for dimensions greater than ~10 nm, the dielectric and piezoelectric coefficients of scaled ferroelectrics are suppressed relative to their bulk counterparts, in some cases by changes up to 80%. The loss of extrinsic contributions (domain and phase boundary motion) to the electromechanical response accounts for much of this suppression. In this article, the current understanding of the underlying mechanisms for this behavior in perovskite ferroelectrics is reviewed. We focus on the intrinsic limits of ferroelectric response, the roles of electrical and mechanical boundary conditions, grain size and thickness effects, and extraneous effects related to processing. In many cases, multiple mechanisms combine to produce the observed scaling effects.     

Facile growth of 1‐D nanowire‐based WO3 thin films with enhanced photoelectrochemical performance

A flame reactor embedded with a constant tungsten wire feeding system to prepare one‐dimensional (1‐D) nanostructured tungsten oxide thin film for photoelectrochemical (PEC) water splitting was developed. Photoactive vertically‐aligned nanowire‐based WO₃ thin films could be obtained with a controlled thickness via a flame vapor deposition process followed by air‐annealing. The PEC performances of WO₃ photoelectrodes for different thin film thicknesses were examined. The optimum thickness of WO₃ thin film was found to be about 7.2 μm for PEC water splitting based on incident photon‐to‐current efficiency plots and I–V curves. The WO₃ prepared with optimum thickness showed better PEC performance than those of recently reported nanostructured WO₃ photoanodes. © 2015 American Institute of Chemical Engineers AIChE J, 62: 421–428, 2016     

All Solution‐Based Fabrication of Copper Oxide Thin Film/Cobalt‐Doped Zinc Oxide Nanowire Heterojunctions

Versatile and intriguing solution‐based processes are utilized to synthesize nanostructured materials for device applications to reduce material production and device fabrication costs. This study presents results on the fabrication and characterization of copper oxide (CuO) coated cobalt‐doped zinc oxide nanowires (Co‐doped ZnO NWs)‐based heterojunction diodes prepared by a two‐step synthesis route through combined hydrothermal growth and sol–gel spin coating. Highly dense, well‐ordered, undoped, and Co‐doped ZnO NWs were successfully grown by hydrothermal method. Complementary CuO thin films were synthesized by sol–gel method and subsequently coated onto both undoped and Co‐doped ZnO NWs through spin‐coating technique. Enhanced diode properties with a rectification ratio of 10³ at ±2 V and an ideality factor of n = 2.4 (in dark) were obtained for Co‐doped ZnO NWs‐based heterojunction diodes. The obtained results demonstrated that the investigated heterojunction diode structure fabricated by facile and cost‐effective solution‐based processes can be a promising candidate for the next generation optoelectronic devices.     

Large Piezoelectricity and Ferroelectricity in Mn‐Doped (Bi0.5Na0.5)TiO3‐BaTiO3 Thin Film Prepared by Pulsed Laser Deposition

Mn‐doped (Bi_0.5Na_0.5)_0.94Ba_0.06TiO₃ (MnBNBT) thin films were prepared on SrRuO₃ (SRO)‐coated (001) SrTiO₃ (STO) single crystal substrates by pulsed laser deposition under different processing conditions. Structural characterization (i.e., XRD and TEM) confirms the epitaxial growth of STO/SRO/MnBNBT heterostructures. Through the judicious control of deposition temperature, the defect level within the films can be finely tuned. The MnBNBT thin film deposited at the optimized temperature exhibits superior ferroelectric and piezoelectric responses with remanent polarization P_r of 33.0 μC/cm² and piezoelectric coefficient d₃₃ of 120.0 ± 20 pm/V.     

Sorption/release of diclofenac sodium in/from free‐standing poly(acrylic acid)/poly(ethyleneimine) multilayer films

Polyelectrolyte multilayer films deposited onto various substrates have been used extensively as drug delivery systems. However, little attention has been paid to the release of drugs from free‐standing polymeric films. Herein, we report the construction of thermal crosslinked free‐standing poly(acrylic acid) (PAA)/branched poly(ethyleneimine) (PEI) multilayer films composed of 25 double layers [(PAA/PEI)₂₅] and their use in sorption/release of diclofenac sodium (DS). The (PAA/PEI)₂₅ multilayer films were characterized by scanning electron microscopy, potentiometric titrations and Fourier transform infrared spectroscopy, while the sorption/release of DS was monitored by UV – Vis spectroscopy. The DS sorption equilibrium data were fitted with five isotherm models (Langmuir, Freundlich, Sips, Dubinin–Radushkevich, and Temkin). The maximum equilibrium sorption capacity, q_m, given by the Langmuir model was 32.42 mg DS/g. The Korsmeyer–Peppas semiempirical equation showed that the release of DS from the free‐standing (PAA/PEI)₂₅ films proceeded by pseudo‐Fickian diffusion, irrespective of the releasing media. © 2016 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2016 , 133, 43752.     

Poly(butylene succinate‐co‐butylene adipate)/polyethylene oxide blends for controlled release materials: A morphological study

Varying the formulation and processing conditions of polymer blends allows the design of materials with a large range of morphologies. Active materials embedding active compounds in a devoted phase are promising applications of such blends, offering possible various transport properties. In this study, 13 poly(butylene succinate‐co‐butylene adipate) (PBSA)/polyethylene oxide (PEO) blends were extruded in a slit die. Their morphologies were characterized by water extraction (selective PEO dissolution), FTIR spectroscopy, and differential scanning calorimetry. Transport properties were assessed by water vapor permeation and fluorescein release as model migrant. Indeed, the desorption in water of fluorescein (previously entrapped in PEO) was monitored to preliminary investigate the release properties of these materials: two morphologies were obtained (i) pseudo multilayer films made of PEO‐rich layer/PBSA‐rich layer/PEO‐rich layer and (ii) PEO nodules dispersed in the PBSA‐rich matrix for the highest PBSA contents. The first systems were erodible ones with an uncontrolled fast delivery by PEO dissolution whereas the second ones showed a controlled release by permeation through the PBSA matrix from PEO nodules. © 2015 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2016 , 133, 42874.     

Dispersion and microwave processing of nano-sized ITO powder for the fabrication of transparent conductive oxides

Aqueous dispersions of tin-doped indium oxide (ITO) nanopowder were prepared and the effect of the addition of PEG 400, Tween 80 and β-alanine as dispersants was investigated using zeta potential and particle size distribution measurements. Both PEG 400 and β-alanine were found to produce stable dispersions that were used to deposit ITO thin films on glass substrates by dip and spin coating methods. The ITO thin films were heat-treated using both conventional and microwave heat treatment in order to improve the inter-particle connections and hence the resistivity and transparency of the films. All the films exhibited an average transmittance of >80% over the visible spectrum after being subjected to the heat treatment process. ITO films prepared with no dispersant showed very high resistivity values for both heating methods, however addition of 2 wt% PEG 400 to the dispersion yielded a reduction in the resistivity values to 1.4×10⁻¹ Ω cm and 3.8×10⁻² Ω cm for conventionally and microwave treated films, respectively. The surface morphological studies confirmed that addition of dispersants improved the film uniformity and inter-particle connections of the ITO films considerably.