Abstract

The increasing global demand for renewable energy has intensified the search for high-efficiency and cost-effective solar cell technologies. Quantum dot-sensitized solar cells (QDSSCs) have emerged as promising candidates due to their tunable optoelectronic properties and enhanced light absorption. In this study, SnS quantum dots were synthesized from dithiocarbamate complexes using different ligands, namely m-toluidine (SnS1), aniline (SnS2), and p-toluidine (SnS3), to investigate the influence of precursor chemistry on material properties and device performance. Structural analysis confirmed the formation of an orthorhombic phase for all samples, while morphological studies revealed well-dispersed nanocrystals for SnS1 (5.93 nm), increased aggregation for SnS2 (8.57 nm), and partially fused domains with an intermediate size for SnS3 (6.67 nm). Optical measurements showed bandgap energies of 2.8, 2.2, and 2.7 eV for SnS1, SnS2, and SnS3, respectively, with SnS3 exhibiting reduced charge-recombination behaviour. Photovoltaic devices fabricated using these materials yielded power conversion efficiencies of 3.40, 2.03, and 7.63% for SnS1, SnS2, and SnS3, respectively, with no significant improvement observed for bifacial configurations. The superior performance of SnS3 is attributed to an optimal balance between light absorption, morphology, and charge transport properties, highlighting the critical role of precursor ligand selection in tuning quantum dot characteristics for improved QDSSC performance.

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