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621.
Tan Y Steinmiller EM Choi KS 《Langmuir : the ACS journal of surfaces and colloids》2005,21(21):9618-9624
Zinc oxide films with ordered lamellar structures can be electrochemically produced by interfacial surfactant templating. This method utilizes amphiphile assemblies at the solid-liquid interface (i.e., the surface of a working electrode) as a template to electrodeposit inorganic nanostructures. To gain the ability to precisely tailor inorganic lamellar structures, the effect of various chemical and electrochemical parameters on the repeat distances, homogeneity, orientation, and quality of the interfacial amphiphilic bilayers were investigated. Surfactants with anionic headgroups (e.g., 1-hexadecanesulfonate sodium salt, dodecylbenzenesulfonate sodium salt, dioctyl sulfosuccinate sodium salt, mono-dodecyl phosphate, and sodium dodecyl sulfate) are critical because they incorporate Zn(2+) ions into their bilayer assemblies as counterions and guide the lamellar growth of ZnO films. Unlike surfactant structures in solution, the interfacial surfactant assemblies are insensitive to the surfactant concentration in solution. The use of organic cosolvents (e.g., ethylene glycol, dimethyl sulfoxide) can increase the homogeneity of bilayer assemblies when multiple repeat distances are possible in a pure aqueous medium. In addition, organic cosolvents can make the interfacial structure responsive to the change in bulk surfactant concentrations. The presence of quaternary alkylammonium salts (e.g., cetyltrimethylammonium bromide) as cationic cosurfactants improves the ordering of anionic bilayers significantly. Consequently, it also affects the orientation of lamellar structures relative to the substrate as well as the surface texture of the films. The quality of lamellar structures incorporated in ZnO films is also dependent on the deposition potentials that determine deposition rates. A higher degree of ordering is achieved when a slower deposition rate (I < 0.15 mA/cm(2)) is used. The results described here will provide a useful foundation to design and optimize synthetic conditions for the electrochemical construction of broader types of inorganic nanostructures. 相似文献
622.
Ellen L. Heeley Darren J. Hughes Eleanor M. Crabb James Bowen Oier Bikondoa Beatriz Mayoral Tony McNally 《Journal of Polymer Science.Polymer Physics》2017,55(2):132-137
Here, the confirmation of an oriented nanohybrid shish‐kebab (NHSK) crystalline structure in a series of composites of poly(ethylene terephthalate) (PET) and multiwall carbon nanotubes (MWCNTs) is reported. The combined use of small‐ and wide‐angle X‐ray scattering (SAXS/WAXS) and thermal analysis has been used to investigate the morphology development in PET‐MWCNT nanocomposites under hot isothermal crystallization conditions. The MWCNTs act as both heterogeneous nucleating agents and surfaces (oriented shish structures) for the epitaxial growth of PET crystallites (kebabs) giving an oriented crystalline morphology. In contrast, the PET homopolymer does not show any residual oriented crystalline morphology during isothermal crystallization but gave a sporadic nucleation of a classic unoriented lamellar structure with slower crystallization kinetics. The results provide a valuable insight into the role of MWCNTs as nanoparticulate fillers in the morphology development and subsequent modification of physical properties in engineering polymers. © 2016 Wiley Periodicals, Inc. J. Polym. Sci., Part B: Polym. Phys. 2017 , 55, 132–137 相似文献
623.
Sourav Chakraborty Eric Schreiber Karla R. Sanchez-Lievanos Mehrin Tariq William W. Brennessel Kathryn E. Knowles Ellen M. Matson 《Chemical science》2021,12(38):12744
We report the synthesis and characterisation of a series of siloxide-functionalised polyoxovanadate–alkoxide (POV–alkoxide) clusters, [V6O6(OSiMe3)(OMe)12]n (n = 1−, 2−), that serve as molecular models for proton and hydrogen-atom uptake in vanadium dioxide, respectively. Installation of a siloxide moiety on the surface of the Lindqvist core was accomplished via addition of trimethylsilyl trifluoromethylsulfonate to the fully-oxygenated cluster [V6O7(OMe)12]2−. Characterisation of [V6O6(OSiMe3)(OMe)12]1− by X-ray photoelectron spectroscopy reveals that the incorporation of the siloxide group does not result in charge separation within the hexavanadate assembly, an observation that contrasts directly with the behavior of clusters bearing substitutional dopants. The reduced assembly, [V6O6(OSiMe3)(OMe)12]2−, provides an isoelectronic model for H-doped VO2, with a vanadium(iii) ion embedded within the cluster core. Notably, structural analysis of [V6O6(OSiMe3)(OMe)12]2− reveals bond perturbations at the siloxide-functionalised vanadium centre that resemble those invoked upon H-atom uptake in VO2 through ab initio calculations. Our results offer atomically precise insight into the local structural and electronic consequences of the installation of hydrogen-atom-like dopants in VO2, and challenge current perspectives of the operative mechanism of electron–proton co-doping in these materials.We report the synthesis and characterisation of a series of siloxide-functionalised polyoxovanadate–alkoxide clusters, [V6O6(OSiMe3)(OMe)12]n (n = 1−, 2−), that serve as molecular models for proton and hydrogen-atom uptake in vanadium dioxide. 相似文献
624.
In this contribution, the numerical modeling of electro-viscoelastic material is considered. The electro-mechanical problem formulated in terms of a symmetrized stress tensor is extended to a viscoelastic material model. For the incorporation of the viscosity model, the logarithmic strain space setting is utilized which mimics the small strain setting. Therefore a rheological model for viscosity from the geometrically linear theory can be used. Numerical examples for a typical uniaxial tensile test show the capability of the method to demonstrate typical relaxation and creep behavior. (© 2010 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim) 相似文献