A donor-acceptor zwitterion as a self-assembled hole-selective layer for highly efficient tin-based perovskite solar cells.

The development of tin-based perovskite solar cells (TPSCs) has lagged far behind that of their lead-based counterparts. Although high-efficiency TPSCs have been reported in recent years, they are all based on poly(3,4-ethylenedioxythiophene):poly(styrenesulfonate) (PEDOT:PSS) as the hole-selective layer (HSL), whose strong acidity and hygroscopicity are undoubtedly highly detrimental to the long-term stability of the devices. Here, a donor-acceptor-type zwitterionic molecule (PyPs) was designed by employing a triphenylamine donor and a benzo[c][1,2,5]thiadiazole acceptor as the molecular backbone, functionalized with a pyridinium sulfonate terminal group. The ionic sulfonate group in PyPs not only exhibits stronger coordination with indium tin oxide (ITO), enabling uniform surface coverage and improved energy-level alignment, but also assists the growth and defect passivation of a tin perovskite. As a result, high-quality Sn-based perovskite films can be obtained along with accelerated interfacial charge extraction and suppressed non-radiative recombination losses. Encouragingly, PyPs-based devices deliver a champion power conversion efficiency (PCE) of 12.18%, representing the highest efficiency reported to date for TPSCs based on alternative HSLs to PEDOT:PSS. Moreover, unencapsulated PyPs-based devices retain 90% of their initial PCE after 1800 h of storage. This work highlights the potential of rational molecular design in the exploration of alternative HSLs for efficient and stable TPSCs.