钝化
钙钛矿(结构)
结晶度
材料科学
能量转换效率
化学工程
聚苯乙烯
磁滞
光电子学
纳米技术
复合材料
图层(电子)
聚合物
量子力学
物理
工程类
作者
Ritesh Kant Gupta,Rabindranath Garai,Parameswar Krishnan Iyer
标识
DOI:10.1021/acsaem.1c01973
摘要
Dual-passivation of MAPbI3-based perovskite using p-toluenesulfonic acid (PTSA) in the bulk and hydrophobic polystyrene (PS) at the surface significantly diminishes the trap-density and improves the device performances substantially. The sulfonic acid functional group of PTSA interacts with the defects in perovskite and passivates the trap-states, while PS repairs the surface defects and increases the moisture resistance of perovskites. Thus, improvement in perovskite crystallinity and formation of larger grain size occurs because of dual-passivation, thereby enhancing the power conversion efficiency (PCE) to 20.62% from 15.14% of the device without passivation. Notably, the large-area dual-passivated device also displays a PCE of ∼18.5%. The modified device (PTSA2PS2) showcases reduced hysteresis and a steady-state output of >20%. The PTSA2PS2-based devices exhibit higher photogenerated charges, lower charge recombination, reduced trap-density, and better charge transport than the control devices. The modified device retains 93% of the original PCE after 1000 h under ambient condition.
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