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International Journal of Bioprinting                      High-performance electrospun PVDF/AgNP/Mxene fiber






























            Scheme 1. Experiment process for fabricating PVDF/AgNP/MXene composite fibers through NFES: (A) Electrospinning the solution, (B) Testing the
            conductivity, (C) NFES, (D) Packing the sensor, (E) Measuring the output voltage, (F) Harvesting energy, and (G) Turning on an LED.

            The porous structures and high specific surface areas of   (Ti AlC ) using minimally intensive layer delamination
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            electrospun PVDF composite fibrous films engender them   (MILD) etching. Commercial lithium fluoride (LiF)
            as ideal substrates for producing low-cost films [87,88] .  powder (2 g) was dissolved in concentrated hydrochloride
               In this study, we prepared new types of PVDF/   (HCl; 9 M, 30 mL) and deionized (DI) water (10 mL),
            AgNP/MXene  composite nanofibers (Scheme  1A–C),   and continuously magnetically stirred (300 rpm) at room
            characterized them using various techniques (Fourier   temperature for 10 mins. Ti AlC  powder was added slowly
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            transform infrared [FTIR] spectroscopy, X-ray diffraction   and carefully, and the mixture was continuously stirred
            [XRD], scanning electron microscopy [SEM], and     (300 rpm) at 35°C for 36 h. The resultant suspension was
            piezoelectric measurements), and employed them in self-  centrifuged (5 min per cycle) with DI water (3500 rpm),
            powered wearable devices (Scheme 1D  and E). These   and then decanted until the pH of the supernatant neared
            composite fiber materials displayed extremely high   6. At the end of the process, the products were washed
            conductivity as well as good mechanical and piezoelectric   with ethanol and dried overnight under vacuum at 60°C to
            capabilities. The integration of AgNP/MXene composites   obtain a stable liquid-free delaminated MXene in powdered
            into the PVDF matrix developed the electroactive   form. The overall process is illustrated in Figure 1A.
            β-phase and improved the piezoelectric properties of   2.2. AgNP/Mxene hybrid composites
            PVDF. These are potentially advantageous for future self-  MXene  was  dispersed  in  DMSO.  The  mixture  was
            powered flexible and wearable optoelectronic devices. We   sonicated for at least 30 min to break up any agglomerates
            encapsulated interdigitated electrodes (IDEs), comprising   and was then magnetically stirred at 250 rpm for 30 min
            copper  (Cu), PVDF/AgNP/MXene piezoelectric  fibers,   on a heater. AgNO  (content kept at 10 wt% relative to the
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            and flexible poly(ethylene terephthalate) (PET) substrates,   weight of MXene) was introduced into the suspension.
            into poly(dimethyl siloxane) (PDMS). These piezoelectric   After sonication for another 30 min, the solution appeared
            devices were packaged in PDMS to enhance their durability   black, and the mixture was stirred magnetically for 30 min.
            (Scheme 1F). We achieved a high-voltage output from the
            PVDF/AgNP/MXene piezoelectric fibers with the desired   2.3. Conductivity measurements
            morphology, thus enabling them to turn on an LED   In order to measure the conductivity, a clean CON30
            (Scheme 1G).                                       conductivity meter was used.

            2. Materials and methods                           2.4. Morphological characterization
                                                               The surface morphology of the synthesized Ti C
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            2.1. Synthesis of MXene                            MXene was examined under ultrahigh resolution using
            MXene (Ti C ) was synthesized by eliminating an    transmission electron microscopy (TEM); its selected area
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            intermediary element (Al atoms) from the MAX phase   electron diffraction (SAED) patterns were also obtained.
            V                                              339                      https://doi.org/10.18063/ijb.v9i1.647
            Volume 9 Issue 1 (2023)olume 9 Issue 1 (2023)
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