Magnetization and electric transport properties of single-crystal MgB2 nanowires.

High quality single-crystal magnesium diboride (MgB(2)) nanowires with lengths exceeding 10 µm were successfully synthesized by hybrid physical chemical vapor deposition. The magnetization and electrical transport properties of single-crystal MgB(2) nanowires (NWs) were measured. The superconducting transition temperature of the NWs was 37 K, as confirmed by magnetization measurements. The disordered behavior of the nanowires was observed by four-terminal current-voltage characteristic measurements of an individual NW from T = 10 to 300 K. The temperature-dependent resistivity curves for seven NWs collapsed into a universal curve described by the variable range hopping model, showing intrinsic nonmetallic transport properties. This implies that the granular superconducting defect states are critical to the superconductivity of the individual MgB(2) NWs.

Magnetization reversal and anisotropy with chains of superparamagnetic Ni nanoparticles.

Chains of superparamagnetic (SPM) Ni nanoparticles of 20 and 33 nm in diameter are synthesized by a facile, template-free, wet chemical method in magnetic field. The blocking temperature for the sample of 20 nm appears at T(B) approximately 255 K, above which the sample exhibits SPM behaviors by a M(H) measurement. At T < T(B), the temperature dependent coercivity, Hc(T), is beyond the description by the simple two-well model proposed by Neel and Brown in the early day. In contrast, for the Ni nanochains of diameter larger than the coherence length, Lcoh approximately 25 nm, the magnetization reversal properties are well described by this model. The magnetization reversal behavior of the SPM Ni nanochains with the diameter much smaller than the coherence length is one of the interesting points to study. Possible transition from the localized magnetization reversal mode in the high temperature end to the coherently rotational mode at low temperature is discussed.

Porosity Tunable Poly(Lactic Acid)-Based Composite Gel Polymer Electrolyte with High Electrolyte Uptake for Quasi-Solid-State Supercapacitors.

The growing popularity of quasi-solid-state supercapacitors inevitably leads to the unrestricted consumption of commonly used petroleum-derived polymer electrolytes, causing excessive carbon emissions and resulting in global warming. Also, the porosity and liquid electrolyte uptake of existing polymer membranes are insufficient for well-performed supercapacitors under high current and long cycles. To address these issues, poly(lactic acid) (PLA), a widely applied polymers in biodegradable plastics is employed to fabricate a renewable biocomposite membrane with tunable pores with the help of non-solvent phase inversion method, and a small amount of poly (vinylidene fluoride-co-hexafluoropropylene) (PVDF-HFP) is introduced as a modifier to interconnect with PLA skeleton for stabilizing the porous structure and optimizing the aperture of the membrane. Owing to easy film-forming and tunable non-solvent ratio, the porous membrane possesses high porosity (ca. 71%), liquid electrolyte uptake (366%), and preferable flexibility endowing the GPE with satisfactory electrochemical stability in coin and flexible supercapacitors after long cycles. This work effectively relieves the environmental stress resulted from undegradable polymers and reveals the promising potential and prospects of the environmentally friendly membrane in the application of wearable devices.

Low-temperature fabrication of Au-Co cluster mixed nanohybrids with high magnetic moment of Co.

In recent years, the synergistic effects of Au-based hybrids have generated enormous scientific interest. The hybrids of Au and Co are expected to exhibit attractive properties. In this paper, we report the successful fabrication of the nanohybrids between bulk-immiscible Au and Co with chain-like structures via a mild solution method. Elemental mapping, XRD and EXAFS data reveal that the as-prepared AuCo nanohybrids might be of cluster mixed configuration. A sequential redox and imperfection-promoted aggregation/diffusion process is proposed to elucidate the formation mechanism of the nanohybrids. The as-prepared products exhibit a temperature-independent saturation magnetization with the magnetic moment of Co as high as ~2.95 µ(B) for each Co atom at 300 K, much higher than the bulk value (~1.7 µ(B) for each Co atom) and approaching the theoretical value of an atomic Co (~3.0 µ(B) for each Co atom).

Surface magnetic states of Ni nanochains modified by using different organic surfactants.

Three powder samples of Ni nanochains formed of polycrystalline Ni nanoparticles with an estimated diameter of about 30 nm have been synthesized by a wet chemical method using different organic surfactants. These samples, having magnetically/structurally core-shell structures, all with a ferromagnetic Ni core, are Ni@Ni(3)C nanochains, Ni@Ni(SG) nanochains with a spin glass (SG) surface layer, and Ni@Ni(NM) nanochains with a nonmagnetic (NM) surface layer. The average thickness of the shell for these three samples is determined as about 2 nm. Magnetic properties tailored by the different surface magnetism are studied. In particular, suppression in the saturation magnetization, usually observed with magnetic nanoparticles, is revealed to arise from the surface magnetic states with the present samples.

Well-aligned Nickel Nanochains Synthesized by a Template-free Route.

Highly uniform and well-aligned one-dimensional Ni nanochains with controllable diameters, including 33, 78, and 120 nm, have been synthesized by applying an external magnetic field without any surface modifying agent. The formation can be explained by the interactions of magnetic dipoles in the presence of applied magnetic field. Magnetic measurements demonstrate that the shape anisotropy dominates the magnetic anisotropy. The demagnetization factor, ∆N, is in the range of 0.23-0.36.