Mixed-cation engineering improves power conversion efficiency in quasi-2D Sn perovskite solar cells, suggesting better crystallographic orientation and charge transport.
Low-n-member quasi-two-dimensional (quasi-2D) Sn perovskites, particularly those based on a Dion-Jacobson (DJ) phase, have attracted attention for their enhanced stability and Pb-free composition. However, their practical application is limited by poor out-of-plane crystallographic orientation and high defect densities, which hinder efficient charge transport. To address these challenges, we introduce a mixed-cation engineering strategy combining N,N-dimethyl-p-phenylenediammonium (DMPhDA²⁺) and phenylethylammonium (PEA⁺) spacers. PEA⁺ acts as an orientation-directing spacer that reduces steric hindrance in the DMPhDA-based framework, facilitating vertical growth and enhancing crystallographic alignment. This approach effectively modulates crystallization, enhances vertical orientation, and suppresses both structural defects and Sn²⁺ oxidation. As a result, the optimized low-n quasi-2D DJ/RP perovskite solar cells exhibit improved performance, achieving an outstanding power conversion efficiency (PCE) of 6.76%. This work provides a viable route to overcome orientation- and defect-related limitations in low-n Sn-based perovskites, advancing the development of stable and efficient Pb-free solar cells.
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Li et al. (2025) studied this question.
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