The unprecedentedly fast rise in power conversion efficiencies (PCEs) of perovskite solar cells (PSCs) over the last decade [1] now surpassing 25%-triggered enormous scientific and industrial interest in solution-processed, large-area perovskite photovoltaics. [2] However, PCEs of PSCs and perovskite modules processed with scalable coating techniques lag behind solution-processed small-area PSCs. [3] The record certified PCE of a large, solution-processed perovskite module (802 cm 2 ) of 17.9% was achieved by Panasonic. [4] Some of the losses on upscaling to modules originate from the monolithic interconnection schemes, including the sheet resistances of the transparent conductive oxides (TCOs), the series resistances of the TCO-Electrode interconnections, and the inactive areas due to the scribing lines. [5] A decrease in PCE of around 1.5% abs is typical for laser patterning of the three scribe lines (p1, p2, p3), nearly independent on the module's aperture area. [6] However, just as in other researched thin-film photovoltaic (PV) technologies, [7] the dominant losses of PCE on large-area perovskite modules are caused by morphological defects in the absorber layer such as microcracks, material impurities, or, most commonly, shunt paths. Even one defect in the perovskite thin film can shunt a whole subcell or decrease its performance substantially by introducing nonradiative recombination. [6] These upscaling losses statistically increase with the modules' aperture area because the probability of defects scales with the area, limiting the achievable PCE of the whole module. [8] The challenge of depositing homogeneous high-quality perovskite thin films on large areas arises from the complexity of the involved kinetic and thermodynamic processes. [9] In this work, we will focus on scalable perovskite processing from solution (although thermal coevaporation of the precursor materials [10] is a very promising fabrication route, as well). The reason for this focus is simply that the experimental techniques presented here are not yet adapted to operation in vacuum.The formation of perovskite thin films from solution is commonly described via the following four stages: [3] I) coatingdeposition of a wet film of precursor solution; II) drying-