The effect of pores in hollow carbon nanofibers (HCNFs) on their electrochemical performance is investigated because the carbon shell itself acts as a reservoir for accommodating Li-ions through intercalation and simultaneously becomes a transport medium through which Li-ions migrate into the core materials in HCNFs. Porous HCNFs (pHCNFs) are prepared by the coaxial electrospinning of a sacrificial core solution and an emulsified shell solution containing sacrificial islands for pore generation. After a thermal treatment, a systematic study is carried out to relate the resulting pore size in pHCNFs to the sacrificial islands in the emulsified shell. As the pores are introduced in pHCNFs, their initial capacity and reversible capacity rate are proved to increase significantly to 1003 mAhg(-1) and 61.8%, respectively, compared to those (653 mAhg(-1) and 53.9%) of nonporous HCNFs. The increased pore size and expanded graphene layers are believed to facilitate lithium insertion/extraction behavior.

This paper reports on a simple and effective method for improving the electrochemical performance of silicon nanoparticle-core/carbon-shell (Si-core/C-shell) nanofibers. Instead of increasing the encapsulation amount of Si nanoparticles, additional conductive paths between the Si nanoparticles were formed by incorporating a small percentage of multi-walled carbon nanotubes (MWNTs) (e.g., 5 wt% with respect to Si) into the Si nanoparticle core. The electrical conductivity of a single Si-core/C-shell nanofiber was measured by a four-point probe using four nano-manipulators, which showed a more than five times increase according to MWNT addition. A galvanostatic charge-discharge test demonstrated that a small amount of MWNTs greatly improved the electrochemical performance of the Si-core/C-shell nanofibers (e.g., a 25.1% increase in the Li-ion storage capability) due to the enhanced participation of Si through the additional conductive paths formed between the Si nanoparticles.

A new nozzle system for the efficient production of multi-layered nanofibers through electrospinning is reported. Developed a decade ago, the commonly used coaxial nozzle system consisting of two concentric cylindrical needles has remained unchanged, despite recent advances in multi-layered, multi-functional nanofibers. Here, we demonstrate a core-cut nozzle system, in which the exit pipe of the core nozzle is removed such that the core fluid can form an envelope inside the shell solution. This configuration effectively improves the coaxial electrospinning behavior of two fluids and significantly reduces the jet instability, which was proved by finite element simulation. The proposed electrospinning nozzle system was then used to fabricate bi- and tri-layered carbon nanofibers.

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The performance of carbon nanotube (CNT)-based devices strongly depends on the adhesion of CNTs to the substrate on which they were directly grown. We report on the bond strength of CNTs grown on a carbon fiber (T700SC Toray), measured via in situ pulling of individual CNTs inside a transmission electron microscope. The bond strength of an individual CNT, obtained from the measured pulling force and CNT cross-section, was very high (∼200 MPa), 8-10 times higher than that of an adhesion model assuming only van der Waals interactions (25 MPa), presumably due to carbon-carbon interactions between the CNT (its bottom atoms) and the carbon substrate.