Abstract:In this study, inspired by cucumber tendrils, nanofibers with helical morphology are fabricated in co-electrospinning systems with different spinneret configurations. Poly(m-phenylene isophthalamide) (Nomex) and thermoplastic polyurethane are chosen as the two components in co-electrospinning. Using simulation and experimental methods, the electric field distribution and the morphology of nanofibers from the three co-electrospinning systems are analyzed. The helical nanofibers generated from the off-centered s… Show more
“…During jet thinning, the highly reactive sol rapidly condenses and solidifies into a rigid xerogel. This rigid core bonds to the shell at the interface and constrains the further thinning of the ductile polymer shell, causing the fiber surface to shrink against the stretching direction. , Such longitudinal compression leads to cracks on the fiber shell, which distribute asymmetrically about the fiber axis and rotate along the change of the curving direction (Figure S13 in the Supporting Information). To validate these assumptions, we conducted coelectrospinning of TiP sol and PVP solution at a reduced polymer solution feeding rate of 0.5 mL/h.…”
Section: Resultsmentioning
confidence: 99%
“…Helical structures in nature, such as tendrils, awns, and the xylem vessels of vascular plants, are formed due to asymmetric contraction of the cells and the chirality of the molecules. Electrospun fibers have potential in creating periodically curved structures because the electrified jets carrying multiple bending instabilities undergo mechanical buckling upon landing on the collector surface. , However, helical fibers only form at the beginning of the electrospinning process, i.e., appearing at the first several layers of the deposited fiber, so prior work relied on generating helical fibers by blending different polymers and using non-centrosymmetric nozzles. − Herein, we report the creation of ceramic springs based on the sol/polymer coelectrospinning method. Figure a shows a typical TiO 2 spring, where the geometrical parameters are the fiber diameter (2 r ), spring diameter (2 D ), and pitch ( P ).…”
Electrospinning has been applied to produce ceramic fibers using sol gel-based spinning solutions consisting of ceramic precursors, a solvent, and a polymer to control the viscosity of the solution. However, the addition of polymers to the spinning solution makes the process more complex, increases the processing time, and results in porous mechanically weak ceramic fibers. Herein, we develop a coelectrospinning technique, where a nonspinnable sol (<10 mPa s) consisting of only the ceramic precursor(s) and solvent(s) is encapsulated inside a polymeric shell, forming core−shell precursor fibers that are further calcined into ceramic fibers with reduced porosity, decreased surface defects, uniform crystal packing, and controlled diameters. We demonstrate the versatility of this method by applying it to a series of nonspinnable sols and creating high-quality ceramic fibers containing TiO 2 , ZrO 2 , SiO 2 , and Al 2 O 3 . The polycrystalline TiO 2 fibers possess excellent flexibility and a high Young's modulus reaching 54.3 MPa, solving the extreme brittleness problem of the previously reported TiO 2 fibers. The single-component ZrO 2 fibers exhibit a Young's modulus and toughness of 130.5 MPa and 11.9 KJ/m 3 , respectively, significantly superior to the counterparts prepared by conventional sol−gel electrospinning. We also report the creation of ceramic fibers in micro-and nanospring morphologies and examine the formation mechanisms using thermomechanical simulations. The fiber assemblies constructed by the helical fibers exhibit a density-normalized toughness of 3.5−5 times that of the straight fibers due to improved fracture strain. This work expands the selection of the electrospinning solution and enables the development of ceramic fibers with more attractive properties.
“…During jet thinning, the highly reactive sol rapidly condenses and solidifies into a rigid xerogel. This rigid core bonds to the shell at the interface and constrains the further thinning of the ductile polymer shell, causing the fiber surface to shrink against the stretching direction. , Such longitudinal compression leads to cracks on the fiber shell, which distribute asymmetrically about the fiber axis and rotate along the change of the curving direction (Figure S13 in the Supporting Information). To validate these assumptions, we conducted coelectrospinning of TiP sol and PVP solution at a reduced polymer solution feeding rate of 0.5 mL/h.…”
Section: Resultsmentioning
confidence: 99%
“…Helical structures in nature, such as tendrils, awns, and the xylem vessels of vascular plants, are formed due to asymmetric contraction of the cells and the chirality of the molecules. Electrospun fibers have potential in creating periodically curved structures because the electrified jets carrying multiple bending instabilities undergo mechanical buckling upon landing on the collector surface. , However, helical fibers only form at the beginning of the electrospinning process, i.e., appearing at the first several layers of the deposited fiber, so prior work relied on generating helical fibers by blending different polymers and using non-centrosymmetric nozzles. − Herein, we report the creation of ceramic springs based on the sol/polymer coelectrospinning method. Figure a shows a typical TiO 2 spring, where the geometrical parameters are the fiber diameter (2 r ), spring diameter (2 D ), and pitch ( P ).…”
Electrospinning has been applied to produce ceramic fibers using sol gel-based spinning solutions consisting of ceramic precursors, a solvent, and a polymer to control the viscosity of the solution. However, the addition of polymers to the spinning solution makes the process more complex, increases the processing time, and results in porous mechanically weak ceramic fibers. Herein, we develop a coelectrospinning technique, where a nonspinnable sol (<10 mPa s) consisting of only the ceramic precursor(s) and solvent(s) is encapsulated inside a polymeric shell, forming core−shell precursor fibers that are further calcined into ceramic fibers with reduced porosity, decreased surface defects, uniform crystal packing, and controlled diameters. We demonstrate the versatility of this method by applying it to a series of nonspinnable sols and creating high-quality ceramic fibers containing TiO 2 , ZrO 2 , SiO 2 , and Al 2 O 3 . The polycrystalline TiO 2 fibers possess excellent flexibility and a high Young's modulus reaching 54.3 MPa, solving the extreme brittleness problem of the previously reported TiO 2 fibers. The single-component ZrO 2 fibers exhibit a Young's modulus and toughness of 130.5 MPa and 11.9 KJ/m 3 , respectively, significantly superior to the counterparts prepared by conventional sol−gel electrospinning. We also report the creation of ceramic fibers in micro-and nanospring morphologies and examine the formation mechanisms using thermomechanical simulations. The fiber assemblies constructed by the helical fibers exhibit a density-normalized toughness of 3.5−5 times that of the straight fibers due to improved fracture strain. This work expands the selection of the electrospinning solution and enables the development of ceramic fibers with more attractive properties.
scite is a Brooklyn-based organization that helps researchers better discover and understand research articles through Smart Citations–citations that display the context of the citation and describe whether the article provides supporting or contrasting evidence. scite is used by students and researchers from around the world and is funded in part by the National Science Foundation and the National Institute on Drug Abuse of the National Institutes of Health.