Significant role of thorny surface morphology of polyaniline on adsorption of triiodide ions towards counter electrode in dye-sensitized solar cells

This paper investigates the adsorption behavior of polyaniline (PANI) towards triiodide ion (I-3(-)) solution in acetonitrile. Two different types of PANI, namely PANI emeraldine salt (PANI ES) and nanostructured PANI ES (NPES) were prepared by the rapid mixing and interfacial polymerization methods, respectively. FTIR and Raman spectroscopy results show that both PANI ES and NPES have similar vibrational features, indicating a similar molecular structure. NPES particles are interconnected granules with thorny durian-like surface morphology and better shape uniformity than PANI ES. The maximum adsorption capacity of NPES towards triiodide (I-3(-)) ions is higher than that of PANI ES; however, both of them obey the dual-site Langmuir-Freundlich isotherm. The calculated thermodynamic parameters reveal the spontaneous and endothermic adsorption processes for both types of PANI. The positively charged group in PANI (C-N+) provides more favorable adsorption sites for I-3(-) ions through electrostatic interactions, as confirmed by Raman spectroscopy. The photovoltaic and electrochemical performance data confirm the higher power conversion efficiency (similar to 30%) of the NPES counter electrode compared to that of PANI ES. The thorny durian-like surface morphology of NPES enhances the number of adsorption sites for I-3(-) ions, thereby facilitating better electrolyte regeneration in dye-sensitized solar cells (DSSC).

Automated summary

This study investigates the adsorption behavior of PANI towards triiodide ion in acetonitrile, finding that nanostructured PANI NPES has a higher adsorption capacity than PANI ES. Both types of PANI follow the dual-site Langmuir-Freundlich isotherm model, with NPES providing more favorable adsorption sites through electrostatic interactions. The thorny durian-like surface morphology of NPES increases the number of adsorption sites for ions, leading to enhanced electrolyte regeneration in DSSC.