Solution-processed lead halide perovskites have established themselves as one of the most important absorber materials in solar cells with power conversion efficiencies now exceeding 22%. [1] Unfortunately, the over reliance on highly toxic Pb 2+ remains a key issue for widespread commercial applications. The significant concentration of Pb 2+ in high performing halide perovskites and its water solubility make it highly hazardous compound to the environment. [2] Another apparent issue is the inherent instability of lead-based halide perovskites in ambient atmosphere. [3] Although the stability of Pb-based halide perovskites has improved impressively in recent times along with the simultaneous development of passivation techniques, the fabrication of lead-based halide perovskites still requires stringent environmental control. [4] To address these potential issues, there is an increased interest toward leadfree halide perovskites and their analogues in photovoltaics. Replacing Pb 2+ with Sn 2+ or Ge 2+ could minimize the toxicity associated with lead-based halide perovskite; however, the increased environmental instability of these compounds poses significant challenges in solar cell development. [5] Even after incorporating 2D/3D mixtures of perovskites, the efficiency of the highest performing Sn-based system reduced to nearly 50% of its original value within 3 d under 20% humidity. [6] Considering atmospheric stability, trivalent cations such as bismuth and antimony-based ternary halides were also investigated as potential absorber materials due to their inherent atmospheric stability and low toxicity. [7] The incorporation of protonated cations such as MA or Cs with Bi-I octahedra forms Bi-based ternary halides (structural formula A 3 Bi 2 I 9 : A = Cs, MA) exhibits high absorption coefficients and facile solution processability. Nevertheless, the photovoltaic performances of Bi-based ternary halides remained poor mostly due to high optical bandgap and low electronic dimensionality. [8] Replacement of the A-site protonated cations with transition metals such as Ag or Cu is a promising strategy to improve the dimensionality. These transition metals also take part in bonding with Bi-I octahedra, resulting in complex halide bismuthates. In comparison to Bismuth-based ternary halides have recently gained a lot of attention as lead-free perovskite materials. However, photovoltaic performances of these devices remain poor, mostly due to their low-dimensional crystal structure and large bandgap. Here, a dynamic hot casting technique to fabricate silver bismuth iodide-based perovskite solar cells under an ambient atmosphere with power conversion efficiencies above 2.5% is demonstrated. Silver bismuth iodides are 3D analogs of complex ternary bismuth halides with a suitable bandgap for a single junction solar cell. As far as it is known, these results represent the highest efficiency for solution processed air-stable lead-free perovskite solar cells. The enhanced solar cell performance via this dynamic hot casting ...