材料科学
钙钛矿(结构)
能量转换效率
八面体
密度泛函理论
图层(电子)
曲面(拓扑)
钝化
限制
重组
工作(物理)
纳米技术
离子
表面能
电子
光电子学
化学物理
结合能
载流子寿命
氢
电子迁移率
混合功能
曲面重建
接受者
局部密度近似
能量转换
作者
Renxuan Wang,Jiafan Zhang,Yang Cao,Nan Yan,Yanyan Li,Haoyi Zhang,Danyang Qi,Jiacheng Pi,Lu Zhang,Xingyu Gao,Yucheng Liu,Shengzhong Liu,Jiangshan Feng
标识
DOI:10.1002/adfm.202517633
摘要
Abstract Energy level misalignment‐induced interfacial non‐radiative recombination and interface defect‐induced carrier transport loss are key factors limiting the power conversion efficiency (PCE) of perovskite solar cells. To address these issues, this work introduces 3‐Piperidinecarboxamide (PDN) to reconstruct the surface of the 3D perovskite. PDN passivates both shallow and deep defects simultaneously, forming an n‐type quasi‐2D perovskite surface layer that enhances electron extraction and reduces the energy level barrier. Density functional theory (DFT) calculations reveal that the electron donor unit (R‐C‐NH) of PDN preferentially binds to undercoordinated Pb 2+ defects sites on the perovskite (PVK) surface. The hydrogen bonding formed between the R‐NH 2 group of PDN and I − ions on the [PbI 6 ] 4− octahedra enhances the above binding capability. The device adopting this strategy achieves a champion PCE of 26.10%. Furthermore, unencapsulated PSCs also exhibits excellent stability, retaining 88% of the initial PCE retained after ≈1400 h at 25 °C under 30% humidity.
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