Polyaniline (PANI) nanofibers (NFs) were synthesized via two chemical oxidative polymerization approaches: a rapid mixing process and a conventional stirred tank method. PANI is a promising electrode material for supercapacitors due to its conductivity, stability, and pseudocapacitive redox behavior. The rapid mixing route proved especially effective, as fast polymerization promoted homogeneous nucleation and yielded thin, uniform, and interconnected NFs, whereas conventional stirring produced thicker, irregular fibers through heterogeneous nucleation. Structural characterization (FTIR, UV-Vis, XRD, XPS, TGA) confirmed that both samples retained the typical emeraldine form of PANI, but morphological analyses (SEM, BET) revealed that only the rapid process preserved nanofiber uniformity and porosity. This morphological control proved decisive for electrochemical behavior: symmetric supercapacitor devices fabricated from rapidly synthesized NFs delivered higher specific capacitances (378.8 F g−1 at 1 A g−1), improved rate capability, and superior cycling stability (90.33% retention after 3000 cycles) compared to devices based on conventionally prepared NFs. These findings demonstrate that rapid polymerization offers a simple and scalable route to morphology-engineered PANI electrodes with enhanced performance.
Rahman et al. (Fri,) studied this question.