上海科技大学知识管理系统

Dion-Jacobson (DJ)-type quasi-two-dimensional perovskites exhibit improved stabilities than their 3D counterparts but meanwhile limited charge transport properties. Knowledge to manipulate the crystal orientation and crystallinity is the primary issue for DJ perovskite with high power conversion efficiencies (PCEs). Herein, the nucleation of DJ perovskite films is divided into three stages and the formation of PbI2-N,N-dimethylformamide (DMF)-based solvated phase (PDS) is highlighted as the initial stage. For the first time, it is demonstrated that regulating the amount of PDS precipitation in stage I by MACl additive is the key to ensure the downward growth of DJ perovskites with out-of-plane orientation and high crystallinity in stage III, which is valid for DJ perovskites with different bukly organic cations includingp-phenylenediamine (PPD),p-xylylenediamine (PXD), and propane-1,3-diammonium (PDA). For (PXD)(MA)(2)Pb3I10-based perovskite solar cells, the PDS engineering lead to a dramtically improved PCE from 1.2% to 15.6%. Moreover, based on temperature-dependent ionic conductivity measurement, it is confirmed that the ion migration in DJ perovskite films is efficiently suppressed, despite the possible coexisting 3D perovskite phase. The unencapsulated PXD-based DJ perovskite devices retain over 90% efficiencies after 700 h of continuous illumination or 1500 h of storage in glove box.