钝化
钙钛矿(结构)
材料科学
光伏
离子键合
分子
氢键
盐(化学)
载流子寿命
化学物理
光电子学
化学工程
光伏系统
离子
图层(电子)
纳米技术
物理化学
有机化学
化学
硅
生态学
工程类
生物
作者
Deyu Gao,Ru Li,Xihan Chen,Cong Chen,Chenglin Wang,Boxue Zhang,Mengjia Li,Xueni Shang,Xuemeng Yu,Shaokuan Gong,Thierry Pauporté,Hua Yang,Liming Ding,Jianxin Tang,Jiangzhao Chen
标识
DOI:10.1002/adma.202301028
摘要
Interfacial nonradiative recombination loss is a huge barrier to advance the photovoltaic performance. Here, one effective interfacial defect and carrier dynamics management strategy by synergistic modulation of functional groups and spatial conformation of ammonium salt molecules is proposed. The surface treatment with 3-ammonium propionic acid iodide (3-APAI) does not form 2D perovskite passivation layer while the propylammonium ions and 5-aminopentanoic acid hydroiodide post-treatment lead to the formation of 2D perovskite passivation layers. Due to appropriate alkyl chain length, theoretical and experimental results manifest that COOH and NH3+ groups in 3-APAI molecules can form coordination bonding with undercoordinated Pb2+ and ionic bonding and hydrogen bonding with octahedron PbI64- , respectively, which makes both groups be simultaneously firmly anchored on the surface of perovskite films. This will strengthen defect passivation effect and improve interfacial carrier transport and transfer. The synergistic effect of functional groups and spatial conformation confers 3-APAI better defect passivation effect than 2D perovskite layers. The 3-APAI-modified device based on vacuum flash technology achieves an alluring peak efficiency of 24.72% (certified 23.68%), which is among highly efficient devices fabricated without antisolvents. Furthermore, the encapsulated 3-APAI-modified device degrades by less than 4% after 1400 h of continuous one sun illumination.
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