Interfacial interaction is one of the most critical issues in carbon nanotube/polymer composites. In this paper the role of nonionic surfactant is investigated. With the surfactant as the processing aid, the addition of only 1 wt % carbon nanotubes in the composite increases the glass transition temperature from 63 °C to 88 °C. The elastic modulus is also increased by more than 30%. In contrast, the addition of carbon nanotubes without the surfactant only has moderate effects on the glass transition temperature and on the mechanical properties. This work points to the pathways to improve dispersion and to modify interfacial bonding in carbon nanotube/polymer composites.

Large‐scale electrical energy storage has become more important than ever for reducing fossil energy consumption in transportation and for the widespread deployment of intermittent renewable energy in electric grid. However, significant challenges exist for its applications. Here, the status and challenges are reviewed from the perspective of materials science and materials chemistry in electrochemical energy storage technologies, such as Li‐ion batteries, sodium (sulfur and metal halide) batteries, Pb‐acid battery, redox flow batteries, and supercapacitors. Perspectives and approaches are introduced for emerging battery designs and new chemistry combinations to reduce the cost of energy storage devices.

Simple synthesis methods for mesoporous fibers and powders by rapid evaporation of hydrolyzed silicon alkoxide−surfactant solutions are described. Mesoporous fibers are prepared by dry spinning, and mesoporous powders by spray drying of alkoxide−surfactant solutions. Precursor solutions, containing fully hydrolyzed tetraethoxysilane, cetyltrimethylammonium chloride surfactant, and, in the case of the fibers, a fiber-forming polymer, in an acidic alcohol/water mixture, are drawn into continuous filaments or atomized into droplets in a heated air stream. During solvent drying, silica and surfactant self-assemble to form the hexagonally ordered mesophase structure, and all of the nonvolatile components (silica, polymer, and surfactant) are incorporated into the mesophase. The pore diameter and surface area of calcined fibers were 20 Å and 1100 m2/g, respectively. For the powders, pore sizes of 25 Å and surface areas as high as 1770 m2/g were measured. Spray-dried powders consisting of hollow spherical particles with mesoporous shells were also produced with this approach.

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