RESUMO
Fiber-based supercapacitors are the potential power sources in the field of wearable electronics and energy storage textiles due to their unique advantages of electrochemical properties and mechanical flexibility, but achieving high energy density and practical energy supply still presents some challenges. In this study, we reported an approach of microfluidic assisted wet-spinning to fabricate SnO2 quantum dots encapsulated polyaniline/graphene hybrid fibers (SnO2 QDs@PGF) by incorporating uniformly polyaniline into graphene fibers and covalently bridging SnO2 quantum dots. The assembled SnO2 QDs@PGF fiber-typed flexible supercapacitors exhibit an ultralarge specific areal capacitance of 925 mF cm-2 in PVA/H2SO4, superior rate capabilities, and capacitance retention of 88% after 8000 cycles, indicating that the SnO2 QDs@PGF possess near-ideal capacitance properties, efficient ion transfer rate, and good cycling stability. In the EMITFSI/PVDF-HFP electrolyte system, SnO2 QDs@PGF realize a wide operating potential window of 2.5 V, a specific areal capacitance of 678.4 mF cm-2, and an energy density of 147.2 µWh cm-2 at 500 µW cm-2, which can be utilized to power an alarm clock, an electronic timer, and a desk lamp with a requirement of a 3 V battery. The exceptional performance of the SnO2 QDs@PGF can be attributed to the molecular-level homogeneous composite of granular polyaniline and graphene nanosheets and the interfacial C-O-Sn covalent coupling strategy employed between SnO2 QDs and PGF. These avenues not only effectively prevent the undesirable restacking of graphene nanosheets but also increase the interlayer electroactive sites, ordered ion diffusion channels, and strong interfacial charge transfer.
