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Co-axial electrospinning is an efficient technique to develop core-shell or hollow nanofibrous structures. In this study electrospun carbon nanofibers with three different morphologies, i.e. solid nanofibers with porous structure (P-ECNF), hollow nanofibers with solid wall (H-ECNF), and hollow nanofibers with porous wall (HP-ECNF) were developed through bicomponent electrospinning and co-axial electrospinning of polyacrylonitrile (PAN) and poly (methyl methacrylate) (PMMA) by varying proportion of the sacrificial PMMA. Through comparative electrochemical analyses, it is revealed that the primary factors for electrochemical performance, i.e. specific capacitance, of the electrospun carbon nanofibrous materials are mesopore volume and total pore volume. The hollow structure as well as ordered carbon structure and intact fiber structure also benefits electrolyte transfer and subsequent electrochemical performance but is secondary. Overall the porous carbon nanofibrous electrode material from electrospinning PAN/PMMA (50/50) solution (P-ECNF-50-50) outperformed those hollow and hollow-porous counterparts from co-axial electrospinning and demonstrated the largest specific capacitance due to the largest mesopore volume as well as the largest total pore volume. This electrode material also showed excellent cycling stability (without any loss of specific capacitance) after 3,000 cycles of charging and discharging. It even showed some increase of specific capacitance with cycling test due to its relatively large amount of micropores.
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Electrospinning of tyrosine‐based oligopeptides: Self‐assembly or forced assembly?
Abstract Short oligomeric peptides typically do not exhibit the entanglements required for the formation of nanofibers via electrospinning. In this study, the synthesis of nanofibers composed of tyrosine‐based dipeptides via electrospinning, has been demonstrated. The morphology, mechanical stiffness, biocompatibility, and stability under physiological conditions of such biodegradable nanofibers were characterized. The electrospun peptide nanofibers have diameters less than 100 nm and high mechanical stiffness. Raman and infrared signatures of the peptide nanofibers indicate that the electrostatic forces and solvents used in the electrospinning process lead to secondary structures different from self‐assembled nanostructures composed of similar peptides. Crosslinking of the dipeptide nanofibers using 1,6‐diisohexanecyanate (HMDI) improved the physiological stability, and initial biocompatibility testing with human and rat neural cell lines indicate no cytotoxicity. Such electrospun peptides open up a realm of biomaterials design with specific biochemical compositions for potential biomedical applications such as tissue repair, drug delivery, and coatings for implants.
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- Award ID(s):
- 1726239
- PAR ID:
- 10456400
- Publisher / Repository:
- Wiley Blackwell (John Wiley & Sons)
- Date Published:
- Journal Name:
- Journal of Biomedical Materials Research Part A
- Volume:
- 108
- Issue:
- 4
- ISSN:
- 1549-3296
- Page Range / eLocation ID:
- p. 829-838
- Format(s):
- Medium: X
- Sponsoring Org:
- National Science Foundation
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