A comparative study of pure, SiC, and C doped MgB2 wires has revealed that the SiC doping allowed C substitution and MgB2 formation to take place simultaneously at low temperatures. C substitution enhances H_{c2}, while the defects, small grain size, and nanoinclusions induced by C incorporation and low-temperature processing are responsible for the improvement in J_{c}. The irreversibility field (H_{irr}) for the SiC doped sample reached the benchmarking value of 10 T at 20 K, exceeding that of NbTi at 4.2 K. This dual reaction model also enables us to predict desirable dopants for enhancing the performance properties of MgB2.

The effect of doping MgB2 with carbon nanotubes on transition temperature, lattice parameters, critical current density and flux pinning was studied for MgB2−xCx with x=0, 0.05, 0.1, 0.2, and 0.3. The carbon substitution for B was found to enhance Jc in magnetic fields but depress Tc. The depression of Tc, which is caused by the carbon substitution for B, increases with an increasing doping level, sintering temperature, and duration. By controlling the extent of the substitution and addition of carbon nanotubes we can achieve the optimal improvement on critical current density and flux pinning in magnetic fields while maintaining the minimum reduction in Tc. Under these conditions, Jc was enhanced by two orders of magnitude at 8 T and 5 K and 7 T and 10 K. Jc was more than 10 000 A/cm2 at 20 K and 4 T and 5 K and 8.5 T, respectively.

The effects on transition critical temperature, lattice parameters, critical current density, and flux pinning of doping MgB2 with carbon nanoparticles, were studied for bulk, wire and tape under a wide range of processing conditions. Under the optimum conditions, magnetic Jc was enhanced by two orders of magnitude at 5 K for a field of 8 T, and by a factor of 33 at 20 K for a field of 5 T for bulk samples, whereas enhancement by a factor of 5.7 was observed in the transport Ic at 12 T and 4.2 K for a wire sample. Samples sintered at high temperature (900 and 1000 °C) exhibited excellent Jc, approximately 10 000 A cm−2 in fields up to 8 T at 5 K. This result indicates that flux pinning was enhanced by the carbon substitution for B with increasing sintering temperature. Highly dispersed nanoparticles are believed to enhance the flux pinning directly, in addition to the introduction of pinning centres by carbon substitution. Nano-C is proposed to be one of the most promising dopants besides SiC and CNT for the enhancement of flux pinning for MgB2 in high fields.

Lithium-sulfur batteries have been plagued for a long time by low Coulombic effi ciency, fast capacity loss, and poor high rate performance. Here, the synthesis of 3D hyperbranched hollow carbon nanorod encapsulated sulfur nanocomposites as cathode materials for lithium-sulfur batteries is reported. The sulfur nanocomposite cathodes deliver a high specifi c capacity of 1378 mAh g −1 at a 0.1C current rate and exhibit stable cycling performance. The as-prepared sulfur nanocomposites also achieve excellent high rate capacities and cyclability, such as 990 mAh g −1 at 1C, 861 mAh g −1 at 5C, and 663 mAh g −1 at 10C, extending to more than 500 cycles. The superior electrochemical performance are ascribed to the unique 3D hyperbranched hollow carbon nanorod architectures and high length/radius aspect ratio of the carbon nanorods, which can effectively prevent the dissolution of polysulfi des, decrease self-discharge, and confi ne the volume expansion on cycling. High capacity, excellent high-rate performance, and long cycle life render the as-developed sulfur/carbon nanorod nanocomposites a promising cathode material for lithium-sulfur batteries.

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