Modulation of Colloidal Assembly Behavior Enables Printable Low-Dimensional Perovskite Photovoltaics.

Abstract

The multiple quantum wells (QWs) distribution in low-dimensional perovskite films hinders charge transport due to the fundamental difficulty of controlling crystal growth from precursor solutions, yielding poorly homogeneous low-dimensional perovskite solar cells (PSCs), especially in upscaling fabrication. Here, efficient low-dimensional PSCs are realized by modulating the colloidal assembly behavior in the precursor solution to induce intermediate structures. In combination with in situ liquid time-of-flight secondary ion mass spectrometry, the assembly behavior of organic cations involved lead iodide-dominated colloidal soft framework is visualized by investigating the precursor species differences under hydrogen bonding interactions. Subsequently, solid-state reactions emerge and the formamidine (FA)-based perovskite films exhibit significantly suppressed multiple QWs distribution. Encouragingly, the FA device (n = 9, by meniscus-assisted coating) achieves a power conversion efficiency (PCE) of 20.28% for a size of 0.04 cm2 and a PCE of 15.35% for a mini-module of 16.94 cm2 with superior stability.