Investigation demonstrates improved microstructure and performance in photovoltaic devices with zinc complexation.
Solution-based deposition of high-quality inorganic compound semiconductors onto a variety of substrates is a key challenge toward integrating photovoltaic technologies into a wide range of infrastructures. Cu2ZnSn(S,Se)4 (CZTSSe) is one of the most promising solar absorbers processable by solution-based methods, however there is a substantial knowledge gap linking the chemistry of cation complexes and chalcogen precursors, e.g. thiourea (TU), to the microstructure and opto-electronic properties of the thin-films. In this study, we focus our attention on the complexation of zinc chloride (ZnCl2) and zinc acetate (ZnAc2) in dimethylformamide (DMF)-based CZTS precursor inks and how this ultimately affects the performance of CZTSSe thin-film devices on F/SnO2 (FTO) substrates. Acetate coordination not only improves the overall CZTSSe composition and structural uniformity but also lowers the zinc salt decomposition temperature, from 519 to 284 °C, which significantly affects the rate of grain growth during selenization and final microstructure. ZnAc2-based CZTSSe films show densely packed grain growth due to the fast rate of selenium incorporation during annealing, while ZnCl2-based CZTSSe displays slower rates due to the high decomposition temperature of ZnCl2. Upon the incorporation of 25 nm Mo at the CZTSSe/FTO interface, a champion power conversion efficiency of 6.02% was achieved with ZnAc2 precursor salt, over two times greater than the equivalent device architecture prepared with ZnCl2, at 2.62%. This investigation illustrates the significant role of the molecular complexes in tuning the grain growth kinetics and final microstructure and therefore improving device performance on semitransparent substrates.
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Sheppard et al. (2025) studied this question.
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