材料科学
钙钛矿(结构)
结晶
电子迁移率
X射线光电子能谱
晶界
能量转换效率
微晶
离子迁移光谱法
载流子寿命
化学工程
光电子学
离子
结晶学
化学
硅
复合材料
有机化学
工程类
微观结构
冶金
作者
Xiaoli Gong,Haimin Li,Xingchong Liu,Dewei Zhao,Hanyu Wang,Yafei Ni,Yue Lei,Yanling Tang,Shuqian Liu
标识
DOI:10.1002/smtd.202200260
摘要
Perovskite solar cells (PSCs) have made significant progress in power conversion efficiency (PCE) by optimizing deposition method, composition, interface, etc. Although the two-step method demonstrates the advantage of being easy to operate, too much residual PbI2 not only forms defect centers, but affects the perovskite crystallization by arising more grain boundaries (GBs) due to the easy-to-crystallize nature of PbI2 . And GBs in polycrystalline perovskite usually provide main channel for ion migration, leading to accumulation of charges at the interface to form a barrier, thus reducing carrier mobility and resulting in degradation of perovskite devices. Here, an organic molecule N-(4-acetylphenyl)maleimide (N-APMI) is used to modify interface between perovskite and hole transport layer. X-ray photoelectron spectroscopy, scanning electron microscope, and nuclear magnetic resonance results show that ketone group (CO) in N-APMI forms a strong coordination with Pb2+ , which effectively reduces the residual amount of PbI2 nanoparticles on the perovskite surface, giving rise to improved crystallization of perovskite. Temperature-dependent current response demonstrates that ion migration is effectively suppressed, and hole mobility validly increases from 10.74 to 19.48 cm2 V-1 s-1 , leading to a champion fill factor (FF) of 82.5% (PCE 21.96%), and the maximum PCE of the device improves from 20.09% to 23.03%.
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