Thermal conduction-induced crystallization and achieving high efficiency in HTM-free carbon-based CsPbI2Br solar cells by regulating the dipole moment of aliphatic amine acetate additives

Abstract

Despite the advancements in film fabrication techniques for emerging perovskite solar cells, achieving a high-quality film by solution processing, while maintaining considerable performance remains a significant challenge. To tackle the issue of inferior CsPbI₂Br perovskite films deposited via solution-based methods, a novel thermal conduction heating approach was devised and implemented, significantly enhancing film uniformity. Crucially, aliphatic amine acetates (3A) were introduced into the precursor solution to regulate the crystallization process and therefore to mitigate defects. Systematic investigation into the impact of 3A molecules featuring varying alkyl chain lengths on defect passivation revealed that the molecular dipole moment of these additives contributed to both defect mitigation and grain size refinement. Notably, the integration of alkyl chains significantly bolstered the hydrophobic properties of the perovskite film. Consequently, an impressive efficiency of 13.50% for HTM-free carbon-based CsPbI₂Br perovskite solar cells was achieved, and the device exhibited robust stability retaining 92.4% of its initial efficiency at room temperature after being stored in dry air for 5400 h. This research offers profound insights into defect passivation mechanisms and perovskite crystallization dynamics, paving the way for further advancements in the field of perovskite solar cell technology.