The deposition behaviour of an individual nanofibre on planar and patterned silicon substrates is studied using near-field electrospinning (NFES). A high-speed camera was utilized to investigate the formation and motion process of a liquid jet. Thanks to the shorter distance from the spinneret to the collector, bending instability and splitting of the charged jet in electrospinning were overcome. In NFES, a straight-line jet between the spinneret and the collector can be utilized to direct-write an orderly nanofibre. Perturbation stemming from residual charges on the collector caused the oscillation of the charged jet, and the deposition of the non-woven nanofibre on the planar substrate. With increasing collector speed, the impact of residual charges was weakened by the strong drag force from the collector and a straight-line nanofibre could be obtained. In addition, the nanofibre can be direct-written in a special pattern by controlling the motion track of the collector. Therefore, it can be concluded that a micro-strip pattern was a good guidance for nanofibre deposition, and the nanofibre deposition track followed well along the top surface of the micro-strip pattern. The position-controlled deposition of a single nanofibre provides a new aspect for applications of electrospinning.

Effective transformation from paraelectric to a high fraction of ferroelectric phase is crucial to produce piezoelectric materials with a high piezoelectric constant for broad applications. In polyvinylidene fluoride (PVDF) thin films, both mechanical stretching and electric poling processes have been found to be critical in the α → β phase transformation. However, in PVDF fibers fabricated by the electrospinning process, the roles of mechanical stretching and electric poling have not been well explored. Here, the properties of PVDF fibers from electrospinning and forcespinning, a mechanical spinning process without electric poling, have been characterized and analyzed by FTIR and XRD spectroscopic techniques. The results show that pure mechanical stretching in the forcespun fibers can result in a high fraction of the all-trans β-phase, at 95%. Electrospun fibers from the same material system, on the other hand, can also reach a high fraction of β-phase, at approximately 99%. These results preliminarily demonstrate that mechanical stretching is the main reason for β-phase induction in PVDF fibers. Further experiments performed in this work show that higher wt% of PVDF, lower polymer solution supply rate, and more uniformly mixed solvent systems facilitate achieving a higher level of ferroelectric β-phase in electrospun PVDF fibers.

Different surfactants are introduced to study the diameter and morphology transformation characteristics of electrospun nanofiber. Surfactants increase the net charge density and instability motion of charged jet. The instability motion provides a good way to stretch the charged jets into finer ones, by which the beaded structures are also prevented. Ultrafine nanofiber with average diameter less than 65 nm can be fabricated. The nanofiber diameter decreases with the increase of surfactant concentration in polymer solution. The nanofibers with anionic surfactant sodium dodecyl sulfate (SDS) have the smallest diameter. The cationic surfactant hexadecyl trimethyl ammonium bromide (HTAB) plays the best role to prevent the formation of beaded structures in nanofibers, and helps to increase the uniformity of electrospun nanofiber. The effects of surfactants on the nanofiber diameter and morphology have been studied, which would promote the industrial application of ultrafine polymeric nanofibers.