Enhancing Chemical Stability and Suppressing Ion Migration in CH3NH3PbI3 Perovskite Solar Cells via Direct Backbone Attachment of Polyesters on Grain Boundaries

Organic-inorganic halide perovskites feature excellent optoelectronic properties but poor chemical stability. While passivating perovskite grain boundary (GB) by polymers shows prospects on long-term performance of perovskite solar cells (PSCs), its detailed impact on the ion migration phenomenon, which largely deteriorates the PSC stability, remains less probed. Here, we introduce a new polar polymer, polycaprolactone (PCL), to passivate GBs of methylammonium lead triiodide (MAPbI(3)) perovskite with only 1-2 polymer monolayers via direct backbone attachment. The PSCs with passivated MAPbI(3), using a classic but less stable Spiro-OMeTAD (2,2',7,7'-tetrakis [N,N-di(4-methoxyphenyl) amino] -9,9'-spirobifluorene) hole transport layer (HTL), exhibit improved power conversion efficiencies up to 20.1%, with 90% of the initial PCE being preserved after 400 h ambient storage, and 80% even after 100 h, 85 degrees C aging. The improved PSC stability indicates critical roles of PCL GB passivation in retarding moisture-induced decomposition and suppressing ion migration within the perovskite. Time-of-flight secondary ion mass spectrometry reveals that I- ions can actively migrate into the electrode, HTL, and their interface in nonpassivated PSCs, even without an externally applied electric field, while such migration is significantly mitigated in PCL-passivated PSCs. This effective GB passivation by PCL suggests an important potential of polymer additives toward the development of stable high-performance PSCs.