A simple ultrasonic nanowelding technique has been developed to reliably bond single-wall carbon nanotubes (SWCNTs) onto metal electrodes, by pressing SWCNTs against electrodes under a vibrating force at ultrasonic frequency. The bonds formed have been demonstrated to be mechanically robust. Using this technique, a stable low-Ohmic contact between SWCNTs and metal electrodes was achieved, with resistances in the range of 8-24 k for a 1 µm long metallic SWCNT at room temperature. The performance of carbon nanotube field-effect transistors (FETs) fabricated using this ultrasonic nanowelding method has also been greatly improved. Transconductance as high as 3.6 µS among the solid-state back-gate individual nanotube FETs has been achieved.

Single-crystal ␤-SiC nanowires coated with amorphous SiO 2 were synthesized by a simple thermal evaporation technique. The photocatalytic activity of the SiC nanowires was characterized by measuring the photodegradation rate of acetaldehyde catalyzed by SiC as a function of UV irradiation time. It exhibited excellent photocatalytic activity, leading to the efficient decomposition of acetaldehyde by irradiation with UV light. The progress of the photocatalytic reaction can be monitored by the evolution of one of the products, CO 2. It has been observed that the as-synthesized SiC nanowires ͑with the SiO 2 coating͒ have higher catalytic activity than the HF-etched, oxide-free SiC nanowires.

The formation of methane hydrate in wet activated carbon was studied. The experimental results demonstrated that the formation of methane hydrate could be enhanced by immersing activated carbon in water. A maximum actual storage capacity of 212 standard volumes of gas per volume of water was achieved. The apparent storage capacity of the activated carbon + hydrate bed increased with the increasing of mass ratio of water to carbon until reaching a maximum, then decreased drastically as the bulk water phase emerged above the wet carbon bed. The highest apparent storage capacity achieved was 140 v/v. A hydrate formation mechanism in the wet activated carbon was proposed and a mathematical model was developed. It has been shown that the proposed model is adequate for describing the hydrate formation kinetics in wet activated carbon. The kinetic model and the measured kinetic data were used to determine the formation conditions of methane hydrate in wet carbon, which are in good agreement with literature values and demonstrate that hydrate formation in wet carbon requires lower temperature or higher pressure than in the free water system.

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Intrinsic spatial inhomogeneity or phase separation in cuprates, manganites, etc., related to electronic and/or magnetic properties, has attracted much attention due to its significance in fundamental physics and applications. Here we use scanning Kerr microscopy and scanning electron microscopy with polarization analysis with in situ electric fields to reveal the existence of intrinsic spatial inhomogeneity of the magnetic response to an electric field on a mesoscale with the coexistence of looplike (nonvolatile) and butterfly-like (volatile) behaviors in Co40Fe40B20/Pb(Mg1/3Nb2/3)0.7Ti0.3O3 ferromagnetic/ferroelectric (FM/FE) multiferroic heterostructures. Both the experimental results and micromagnetic simulations suggest that these two behaviors come from the 109° and the 71°/180° FE domain switching, respectively, which have a spatial distribution. This FE domain-switching-controlled magnetism is significant for understanding the nature of FM/FE coupling on the mesoscale and provides a path for designing magnetoelectric devices through domain engineering.