Two-dimensional Ruddlesden-Popper (2DRP) phase perovskites have excellent long-term environmental and structure stability. However, the efficiency of 2DRP perovskite solar cells (PSCs) still lags seriously behind 3D counterparts due to the large exciton binding energy between the large-volume organic spacer and the inorganic plate compared to their 3D analogs. Here, a thin layer of self-assembled monolayer material (2-(3,6-dibromo-9H-carbazol-9-yl)ethyl)phosphonic acid (2PACz-Br) is employed between poly (3,4-ethylene dioxythiophene): poly(styrene sulfonate) (PEDOT: PSS) and β-guanidinopropanoic acid (β-GUA)-based perovskite film (β-GUA)2(FA)4Pb5I16 for efficient and stable 2DRP-based PSCs. The 2PACz-Br-based 2DRP perovskite films show superior crystallinity and quality compared with the control perovskite films. The defect density in 2PACz-Br-based perovskite films is reduced, and the non-radiative recombination is further suppressed. The experimental results show that introducing 2PACz-Br can effectively promote the matched energy levels between the perovskite thin film and the charge-carrier transport layer. Benefiting from the conducive collection and transmission of charge carriers, (β-GUA)2(FA)4Pb5I16 (n = 5)-based PSCs can realize an outstanding power conversion efficiency of 19.13 %, much higher than that of devices without 2PACz-Br modification (17.70 %). Moreover, 2PACz-Br-based 2DRP PSCs show better stability than the control devices. Our work paves the way to efficient and stable 2DRP-based PSCs by inserting a multifunctional self-assembled monolayer.
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