Table 3.
Composition and Design |
Morphology | Fabrication of Nonwovens | Electrical and Mechanical Properties | Biocompatibility | Applications | Ref. |
---|---|---|---|---|---|---|
CA matrix with PANI nanoparticles (0.1 wt% or 0.5 wt%) dispersed | Membranes’ thickness: 100 µm |
Electrospinning: Needle inner diameter: 0.21 mm; Applied voltage: 20 kV; Distance to collector: 20 cm; Solution flow rate: 2.0 mL/h; Solution concentration: 20 wt/v% in DMAc/acetone 2:1 v/v |
Ionic conductivity: 8.7·10−4 S·cm−1 in pure CA, 10.6·10−4 S·cm−1, and 19.2·10−4 S·cm−1 in 0.1 wt% and 0.5 wt% CA/PANI samples, respectively | Fibroblast cell line (NIH/3T3) attachments and spreading over the electrospun membranes were observed | A dry PANI/CA bio-composite actuator showing electrically driven bending deformations | [27] |
CA matrix with fullerenol (0.1 wt% or 0.5 wt%) dispersed |
Nanofibers’ diameter range: 400–800 nm; Membranes’ thickness: 100 µm |
Electrospinning: Solution (20 wt/v%) of cellulose acetate in DMAc/acetone (2:1 v/v) with 0.1 or 0.5 wt% fullerenols; Needle inner diameter: 0.21 mm; Applied voltage: 25 kV; Distance to collector: 15 cm; Solution flow rate: 2.0 mL/h |
Ionic conductivity: 8.2·10−4 S·cm−1 in CA, 11.5·10−4 S·cm−1, and 18.1·10−4 S·cm−1 in 0.1 wt% and 0.5 wt% CA/fullerenol samples; Tensile strength of CA fibers: 1.6 MPa; Tensile strength of CA fibers with 0.5 wt% fullerenol: 2.75 MPa |
All electrospun nanofibers did not show any inhibition of Escherichia coli K-12 bacteria on agar plates, indicating a good biocompatibility of the membranes | Biocompatible actuators |
[97] |
PVA/PANI nanofibers deposited on interdigitated electrodes | Fiber diameter between 100 and 200 nm; density of nanofibers: 106 nanofibers per square centimeter |
Electrospinning: Applied voltage: 20 kV; Distance to collector: 13 cm; Solution flow rate: 0.5 mL/h; Solution concentration: 4% or 5% (v/v) in water; Speed of collector: 400 rpm |
Electrical conductivity: 4% solution: 10−5 S·m−1; 5% solution: 3·10−6 S·m−1 |
No data | Gas sensor for ammonia detection | [90] |
Composite meshes of PANI and well-blended PLCL/SF with NGF incorporated |
Fiber diameter between 683 ± 138 and 411 ± 98 nm; average thicknesses of meshes were between 0.032 and 0.037 mm |
Electrospinning of PLCL/SF/PANI nanofibers: Needle inner diameter: 0.51 mm; Applied voltage: 12 kV; Distance to collector: 5–6 cm; Solution flow rate: 1.0 mL/h; Solution concentration: 4% (v/v) in water; Speed of collector: 4000 rpm NGF-loaded PLCL/SF/PANI core–shell fibers were fabricated by coaxial electrospinning |
Electrical conductivity: 30.5 ± 3.1 mS cm−1; Tensile strength from 5.7 ± 0.9 MPa to 13.7 ± 1.5 MPa depends on composition |
Effective support of rat pheochromocytoma 12 (PC12) neurite outgrowth, increased percentage of neurite-bearing cells and the median neurite length; enhanced proliferation and decrease in the toxicity effect of PANI in Schwann cells |
Electrical stimulation and nerve growth factor (NGF) on neuron growth | [91] |
Blends of PANI and PLCL | Fiber diameter between 100 and 800 nm | Electrospinning of PANI/PLCL: Solution concentration (v/v %): 15:85 in HFP (0.515 g/mL); Needle inner diameter: 0.337 mm; Applied voltage: 18–20 kV; Distance to collector: 20 cm; Solution flow rate: 20 µL/min; Speed of collector: 2600 rpm |
Electrical conductivity: about 0.00641 S·cm−1 |
Based on viability tests, morphological changes, and expression of differentiation proteins in PC12 cells, PANI/PLCL fibers enhanced the NGF-induced neurite outgrowth of PC12 cells | Development of electrically conductive, engineered nerve grafts | [92] |
PEDOT nanofibers obtained on the electrospun PVP |
Fiber diameter of 350 ± 60 nm | (1) Electrospinning of PVP: Needle inner diameter: 0.58 mm; Applied voltage: 27 ± 1 kV; Distance to collector: 15 cm; Solution flow rate: 1.0 mL/h; Solution concentration: 1.0 and 1.5 wt% in iron(III) p-TS 40 wt% in butanol (2) In situ vapor-phase polymerization of EDOT (3) Removal of PVP |
Electrical conductivity: 60 ± 10 S·cm−1 |
No data | Electronic devices requiring flexibility and/or significant surface area, such as sensors or energy storage systems | [94] |
The PVA/PANI hybrid mat consisted of PANI nanostructures grown on the surface of individual nanofibers; in the wet state, mats were rolled up conveniently into a multilayered cylindrical structure |
Diameter of PVA nanofibers: 450 nm; individual PVA/PANI fibers: 1.2 µm diameter of PANI nanostructures: <70 nm |
(1) Electrospinning of PVA: Applied voltage: 10 kV; Distance to collector: 12 cm; Solution flow rate: 10 μL/min; Solution concentration: 7.5 wt% PVA in water (2) In situ chemical polymerization of aniline on PVA mats |
Electrical conductivity: 2.35 S·cm−1 |
No data | For fabricating high-performance electrochemical actuators | [95] |
PANI/gelatin fibers | Fiber diameter decreased from 803 ± 121 nm for pure gelatin fibers to 61 ± 13 nm for 60:40 PANI–gelatin blend fibers. | Electrospinning of PANI/Gelatin: Volume ratios of PANI:gelatin were 0:100, 15:85, 30:70, 45:55, and 60:40. The following concentrations (w/v) of the solutions in HFP were 8.00, 6.85, 5.69, 4.54, and 3.38%, respectively. Applied voltage: 10 kV; Distance to collector: 10 cm |
Sample with 45:55 ratio of PANI to gelatin; Tensile strength: 10.49 ± 0.96 MPa; Elongation at break: 0.09 ± 0.03%; Tensile modulus: 1384 ± 105 MPa; Conductivity (S·cm−1): 0.005, 0.01, 0.015, 0.017, and 0.021 for volume ratios of PANI to gelatin of 0:100, 15:85, 30:70, 45:55, and 60:40, respectively |
PANI–gelatin blend fibers supported H9c2 rat cardiac myoblast cell attachment and proliferation to a similar degree as the control tissue culture-treated plastic (TCP) and smooth glass substrates | “Intelligent” biomaterials for cardiac and neuronal tissue engineering | [98] |
SF scaffolds coated with PPy | PPy-SF mesh: 80–90 µm thickness | (1) Electrospinning of SF: Needle inner diameter: 0.45 mm; Applied voltage: +6 kV was applied to the capillary tube and −5 kV to the collector; Distance to collector: 10 cm; Solution flow rate: 6.0 mL/h; Solution concentration: 17 wt/v% in HFIP; (2) Polymerization of pyrrole on the SF meshes |
Young’s modulus range: 266.7 ± 17.3 MPa for the SF meshes and 310.5 ± 37.6 MPa for the PPy-SF meshes; Voltametric responses ranging between 10 and 0.5 mV·s–1 |
Uncoated and PPy-coated materials support the adherence and proliferation of adult human mesenchymal stem cells (ahMSCs) or human fibroblasts (hFbs) | Biocompatible actuators |
[100] |
Nanofibrous PU/PPy | Thickness of the PU, PU/PPy-ClO4, PU/PPy-pTS, and PU/PPy-TFSI nanofibers: 10 ± 1, 24 ± 2, 23 ± 2, and 43 ± 3 µm, respectively; Diameter of PU/PPy nanofibers: 719 ± 74 nm, 571 ± 73 nm, and 556 ± 77 nm, respectively, for ClO4, pTS, and TFSI dopants. |
(1) Electrospinning of PU: Needle inner diameter: 0.718 mm; Applied voltage: 14 kV; Distance to collector: 25 cm; Solution flow rate: 0.3 mL/h; Speed of the collector: 5 rps; Solution concentration: 7 wt/v% in DMF (2) Polymerization of pyrrole on the PU meshes |
The electrical conductivity of PU/PPy nanofibers produced using ClO4, pTS, and TFSI dopants was measured to be 158, 277, and 315 S·cm−1. In LiTFSI electrolyte solution, the PU/PPy nanofibrous artificial muscle achieved a bending displacement of 720° in a potential cycle between −0.8 and +0.8 V. |
No data | Nanofibrous artificial muscles | [102] |
PU/PPy-pTS nanofibers |
Diameter of PU nanofibers: 221 ± 30 nm; Coated nanofibers: 566 ± 67 nm |
(1) Electrospinning of PU: Applied voltage: 10, 12, and 14 kV; Distance to collector: 15, 20, and 25 cm; Solution flow rate: 0.3 mL/h; Solution concentration: 7, 8, and 9 wt/v% in DMF (2) Polymerization of pyrrole and sodium p-TS on the PU meshes |
Conductivity of 276.34 S·cm−1; Reversible angular displacement capability about of 141° |
No data | Artificial muscles | [103] |
PANI/Au microtubes | The inner diameters of PANI/Au microtubes in the range of 1.2–1.5 µm | (1) Electrospinning of PMMA: Applied voltage: 20 kV; Distance to collector: 17 cm; Solution flow rate: 0.5 mL/h; Solution concentration: 10 wt/v% in DMF; Collector rotation speed: 2000 rpm (2) Coating fibers with Au (3) Electrochemical PANI deposition process (4) Removal of PMMA by immersing in DCM |
By switching the voltage between −0.2 and 1 V, PANI-coated microtubes could reversibly bend | No data | Artificial muscles | [108] |
PU/PANI hybrid nanofibrous bundle |
Diameter of individual hybrid nanofibers in the bundles: about 900 nm; Average diameter of PU/PANI hybrid nanofibrous bundle: about 90 µm; Average diameter of PU nanofiber: about 400 nm; Thickness of PANI coating: about 250 nm |
(1) Electrospinning of PU: Needle inner diameter: 0.337 mm; Applied voltage: +7 kV in the capillary tube and −5 kV in the collector; Distance to collector: 13 cm; Solution flow rate: 4.0 µL/min; Solution concentration: 10 wt% in chloroform (2) In situ chemical polymerization of aniline |
Conductivity of 0.5 S·cm−1 | No data | Nanofibrous artificial muscles | [109] |
PVDF with 0.05 wt% and 0.1 wt% BCNW |
Thickness of the PVDF membrane: 215 µm; PVDF-BCNW composites: 176 µm and 151 µm, respectively, for 0.05 and 0.1% |
Electrospinning of PVDF: Needle inner diameter 0.838 mm; Applied voltage: 12 kV; Distance to collector: 24 cm; Solution flow rate: 1.5 mL/h; Solution concentration: 25 wt% in DMF and acetone (1:1, v/v) |
PVDF/BCNW (0.1 wt%) actuator had a fast response and large tip displacement. Young’s modulus and yield strength around 3.5 GPa and around 9.5 MPa, respectively. |
No data | Actuators anticipated in the fields of biomimetic robotics, medical devices, various actuators, and sensors |
[110] |
Free-standing Nylon-6/6 PPy-coated microribbons |
Widths of the gold-coated electrospun microribbons: 1–1.5 µm; Thickness of the PPy layer: ~80 nm |
(1) Electrospinning of Nylon-6/6: Needle inner diameter 0.838 mm; Applied voltage: 25 kV; Distance to collector: 15, 20 cm; Solution flow rate: 0.05–0.10 mL/h; Solution concentration: 22 wt% in formic acid (2) Coating of fibers with Au (3) Electrochemical PPy deposition process |
The fabricated actuator responded by curling and straightening when the external stimulus current, pH, and temperature was applied | No data | Soft actuators sensing different external stimuli, bifunctional electrochemical devices | [111,112] |
Au/Nylon-PDMS - Au covered Nylon-6/6 micrometric fibers attached to a thin PDMS film |
Average diameter of the fibers: 2.08 ± 0.1 µm; Total thickness of the device: 250 ± 2.5 µm |
(1) Electrospinning of Nylon-6/6: Needle inner diameter 0.838 mm; Applied voltage: 20 kV ± 2 kV; Distance to collector: 15 cm; Solution flow rate: 0.2 mL/h; Solution concentration: 30 wt% in formic acid (2) Coating fibers with Au (3) Assembly of metalized fiber network to the PDMS sheet |
Displacement of 0.8 cm when applying 2.2 V (500-cycle test performed) | No data | Artificial muscle | [113] |
Glucose–gelatin nanofiber scaffolds chemically coated with PPy | PPy covered individual fibers separately, resulting in uniformly coated fibers with a similar diameter of 1.58 ± 0.1 µm in aqueous electrolyte and 1.43 ± 0.12 µm in PC electrolyte | (1) Electrospinning of glucose/gelatin (in 1:10 wt% ratio, dissolved in 10 M acetic acid): Applied voltage: 17.5 kV; Distance to collector: 14.5 cm; Solution flow rate: 5–7 µL/min; (2) Crosslinking the nonwovens at 175 °C (3) Electrochemical PPy deposition process |
PPy coated the CFS fibers showing electrochemomechanical activity in both aqueous and organic (PC) electrolyte solutions; In water: conductivity: 0.45 ± 0.034 S·cm−1; reversible strain and stress of 1.2% and 3.15 kPa, respectively. |
No data | Wearable devices, such as e-skin or in soft robotics devices | [114] |
Poly(ether-ester-urethane) (PU): poly [4,4′-methylenebis(phenyl isocyanate)-alt-1,4-butanediol/di(propylene glycol)/polycaprolactone] | Mean diameter: 0.88 ± 0.36 µm; Volume fraction: 0.47 ± 0.08; Bundles were homogeneous (diameters of random bundles 468 ± 33 µm and aligned ones 419 ± 37 µm without the presence of beads) |
Electrospinning of PU: Four needles with inner diameter of 0.51 mm; Applied voltage: 23 kV; Distance to collector: 18 cm; Solution flow rate: 0.3 mL/h; Solution concentration: 25 w/v in THF:DMF (70:30, v/v) collector, with a speed of 1500 mm min–1 |
A failure force of the random mats: FF = 0.83 ± 0.08 N (εF = 232 ± 17%); Of bundles: FF = 0.50 ± 0.08 N (εF = 182 ± 18%) |
No data | Muscle tissue engineering and soft actuators | [115] |
RM 257 as a liquid crystal mesogen and HDT as a chain extender doped with PDA | The diameters of microfibers ranged from 10 to 100 µm | (1) Electrospinning of ink (RM257, HDT, HHMP): Four needles with inner diameters of 1.194 mm; Applied voltage: 6 kV; Solution flow rate: 0.02 mL/min; Solution concentration: 20 wt% in TCM During the electrospinning process, the LCE microfibers were exposed to UV light (365 nm wavelength) to trigger the crosslinking reaction (2) Preparation of PDA-coated LCE microfibers through a simple dip-coating process |
Longitudinal contraction under the exposure of NIR light of PDA-LCE; Actuation strain: >50%; actuation stress: 0.3 MPa; response speed: 300%/s; and work density: 20 kJ/m3 The temperature actuation strains were 55, 33, and 30% at 120 °C when the applied stresses were 0.02, 0.08, and 0.16 MPa, respectively |
No data | LCE microfiber actuator for artificial muscles, microrobots, or microfluidic pumps. | [116] |
Abbreviations: CA: cellulose acetate; PANI: polyaniline; PVA: poly(vinyl alcohol); NGF: nerve growth factor; PLCL: poly[(L-lactide)-co-(ε-caprolactone)]; SF: silk fibroin; PEDOT: poly(3,4-ethylenodioxythiophene); PVP: polyvinylpyrrolidone; EDOT: 3,4-ethylenedioxythiophene; PPy: polypyrrole; p-TS: p-toluenesulfonate; PU: polyurethane; PMMA: poly(methyl methacrylate); BCNW: bacterial cellulose nanowhiskers; PDMS: polydimethylsiloxane, HDT: hexane dithiol; HHMP: (2-hydroxyethoxy)-2-methylpropiophenone; DPA: polydopami.