Two-dimensional Perovskitoids Enhance Stability in Perovskite Solar Cells.
Cheng LiuYi YangHao ChenIoannis SpanopoulosAbdulaziz S R BatiIsaiah W GilleyJianhua ChenAidan MaxwellBadri VishalRobert P ReynoldsTaylor E WigginsZaiwei WangChuying HuangJared FletcherYuan LiuLin X ChenStefaan De WolfBin ChenDing ZhengTobin J MarksAntonio FacchettiEdward H SargentMercouri G KanatzidisPublished in: Nature (2024)
Two-dimensional (2D)/three-dimensional (3D) perovskite heterostructures have played a key role in advancing the performance of perovskite solar cells (PSCs) 1,2 . However, the migration of cations between 2D and 3D layers results in the disruption of octahedral networks that leads to degradation in performance over time 3,4 . We hypothesized that perovskitoids, with robust organic-inorganic networks enabled by edge- and face-sharing, could impede ion migration. We explored a set of perovskitoids of varying dimensionality, and found that cation migration within perovskitoid/perovskite heterostructures was suppressed compared to the 2D/3D perovskite case. Increasing the dimensionality of perovskitoids improves charge transport when they are interfaced with 3D perovskite surfaces - this the result of enhanced octahedral connectivity and out-of-plane orientation. The 2D perovskitoid (A6BfP) 8 Pb 7 I 22 (A6BfP: N-aminohexyl-benz[f]-phthalimide) provides efficient passivation of perovskite surfaces and enables uniform large-area perovskite films. Devices based on perovskitoid/perovskite heterostructures achieve a certified quasi-steady-state power conversion efficiency of 24.6% for centimeter-area PSCs. We removed the fragile hole transport layers and showed stable operation of the underlying perovskitoid/perovskite heterostructure at 85°C for 1,250 hours for encapsulated large-area devices in an air ambient.