Publication date: 15th December 2025
Narrow-bandgap tin and mixed Sn–Pb halide perovskites attract growing interest for optoelectronic applications, yet their development is limited by irreproducible and poorly understood crystallization. Although additive engineering has effectively improved film formation, the fundamental origins of their distinct crystallization behavior remain unclear. Here, we uncover the unique reactivity and colloidal chemistry of Sn-based perovskite precursor solutions through a direct comparison with Pb analogues. By combining NMR and SAXS, we achieve detailed structural and dynamical insight into these solutions. Our results show that Sn-based precursor solutions exhibit inherently higher reactivity than Pb, and higher sensitivity to the environment and composition. We propose that this behavior stems from reduced electrostatic repulsion within the electric double-layer, which leads to less stable colloidal networks and a stronger tendency for particle agglomeration. [1] These insights provide a mechanistic basis that supports observations reported in recent studies [2,3] and highlight the opportunities of solvent engineering to finally overcome the longstanding limitations in Sn perovskite thin-film fabrication.
