Controllable fabrication of formamidinium (FA)‐based perovskite solar cells (PSCs) with both high efficiency and long‐term stability is the key to their further commercialization. However, the diversity of PbI 2 complexes and perovskite compositions usually leads to light sensitive PbI 2 residues and phase impurities in the film, which can accelerate the device degradation. Here, the crystallization kinetics of FA‐based perovskite films are studied and a bridging‐solvent strategy is proposed to modulate the reaction kinetics between PbI 2 and ammonium salts by prohibiting the formation of undesired intermediates. N‐methylpyrrolidone (NMP) solvent is introduced into the PbI 2 precursor solution to obtain stable and homogeneous PbI 2 ‐NMP complex films. The strong interaction between NMP and formamidinium iodide (FAI) molecules promotes the conversion from PbI 2 ‐NMP into (001)‐oriented quasi‐single‐crystal perovskite films with negligible impurities, long carrier lifetime of 1.5 µs and a large grain size of 3 µm. The optimized PSCs exhibit a high power conversion efficiency of 24.1%, as well as superior shelf stability which maintains 95% initial efficiency after storage in air for 1200 h (T 95 = 1200 h), and operating stability with T 96 = 300 h under continuous working at the maximum power point. This work offers a simple and reproducible method for fabricating phase‐pure and uniaxially oriented perovskite films.
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