Self-Organized One-Dimensional TiO

We review the use of self-assembled, vertically oriented one-dimensional (1D) titania nanowire and nanotube geometries in several third-generation excitonic solar cell designs including those based upon bulk heterojunction, ordered heterojunction, Förster resonance energy transfer (FRET), and liquid-junction dye-sensitized solar cells (DSSCs)

Direct observation of the fracture behavior of the polyether ketone ketone (PEKK) spherulites

This article reports the direct observation of the fracture of individual poly‐ether‐ketone‐ketone (PEKK) spherulites. A single layer of PEKK spherulites was obtained by bonding a PEKK film in‐between two sandblasted Ti alloy plates using an autoclave. The crack of an individual PEKK spherulite was achieved by opening the Ti/PEKK/Ti sandwich using a double cantilever beam test. The fracture morphology of the PEKK spherulite was characterized using scanning electron microscopy and atomic force microscopy. It was found that under tensile stress the crack of the individual spherulite propagates along the middle plane and crosses the nucleation core. This is due to the symmetric radial structure of the spherulite. Moreover, it was found that the fracture surface morphology at the core of the spherulite is strongly influenced by the local crystalline structure, which is anisotropic and determined by the initial nucleation growth direction. As a result, the area fraction experiencing plastic deformation during the fracture of PEKK spherulites at different orientations may vary by an order of 10. Our results show the important role of the initial nucleation growth direction on the mechanical properties of the polymer crystals and may provide a new approach to the design of high‐performance polymer materials with tailored crystalline structures

3D Yolk–Shell Structured Si/void/rGO Free-Standing Electrode for Lithium-Ion Battery

In this study, we have successfully prepared a free-standing Si/void/rGO yolk–shell structured electrode via the electrostatic self-assembly using protonated chitosan. When graphene oxide (GO) is dispersed in water, its carboxyl and hydroxyl groups on the surface are ionized, resulting in the high electronegativity of GO. Meanwhile, chitosan monomer contains -NH2 and -OH groups, forming highly electropositive protonated chitosan in acidic medium. During the electrostatic interaction between GO and chitosan, which results in a rapid coagulation phenomenon, Si/SiO2 nanoparticles dispersed in GO can be uniformly encapsulated between GO sheets. The free-standing Si/void/rGO film can be obtained by freeze-drying, high-pressure compression, thermal reduction and HF etching technology. Our investigation shows that after 200 charge/discharge cycles at the current density of 200 mA·g−1, the specific discharge capacity of the free-standing electrode remains at 1129.2 mAh·g−1. When the current density is increased to 4000 mA·g−1, the electrode still has a specific capacity of 469.2 mAh·g−1, showing good rate performance. This free-standing electrode with a yolk–shell structure shows potential applications in the field of flexible lithium-ion batteries

Microstructure and Morphology Control of Potassium Magnesium Titanates and Sodium Iron Titanates by Molten Salt Synthesis

Titanates materials have attracted considerable interest due to their unusual functional and structural properties for many applications such as high-performance composites, devices, etc. Thus, the development of a large-scale synthesis method for preparing high-quality titanates at a low cost is desired. In this study, a series of quaternary titanates including K0.8Mg0.4Ti1.6O4, Na0.9Mg0.45Ti1.55O4, Na0.75Fe0.75Ti0.25O2, NaFeTiO4, and K2.3Fe2.3Ti5.7O16 are synthesized by a simple molten salt method using inexpensive salts of KCl and NaCl. The starting materials, intermediate products, final products, and their transformations were studied by using TG-DSC, XRD, SEM, and EDS. The results show that the grain size, morphology, and chemical composition of the synthesized quaternary titanates can be controlled simply by varying the experimental conditions. The molar ratio of mixed molten salts is critical to the morphology of products. When KCl:NaCl = 3:1, the morphology of K0.8Mg0.4Ti1.6O4 changes from platelet to board and then bar-like by increasing the molar ratio of molten salt (KCl–NaCl) to raw materials from 0.7 to 2.5. NaFeTiO4 needles and Na0.75Fe0.75Ti0.25O2 platelets are obtained when the molar ratio of molten salt (NaCl) to raw materials is 4. Pure phase of Na0.9Mg0.45Ti1.55O4 and K2.3Fe2.3Ti5.7O16 are also observed. The formation and growth mechanisms of both potassium magnesium titanates and sodium iron titanates are discussed based on the characterization results

High-Strength GO/PA66 Nanocomposite Fibers via In Situ Precipitation and Polymerization

The uniform dispersion of graphene oxide (GO) and strong interfacial bonding are the key factors in achieving the high mechanical strength of GO/polymer composites. It is still challenging to prepare GO/PA66 composites with uniform GO dispersion by the in situ polymerization method. In this paper, we prepare GO/PA66 salt nanocomposite by in situ precipitating PA66 salt with GO in ethanol. The GO/PA66 nanocomposite fibers are then fabricated using the as-prepared GO/PA66 salt by in situ polymerizing and melt spinning. By tuning the GO content, the tensile strength and Young’s modulus of the GO/PA66 fibers are increased from 265 ± 18 to 710 ± 14 MPa (containing 0.3 wt% GO) and from 1.1 ± 0.08 to 3.8 ± 0.19 GPa (containing 0.5 wt% GO), respectively. The remarkable improvements are attributed to the uniform dispersion of GO in the GO/PA66 salt nanocomposite via ionic bonding and hydrogen bonding in the in situ precipitation process, and the covalent interfacial bonding between the GO and PA66 during the in situ polymerization process. This work sheds light on the easy fabrication of high-performance PA66-based nanocomposites