钝化
材料科学
钙钛矿(结构)
磺胺嘧啶
能量转换效率
分子
图层(电子)
光电子学
化学工程
离子
氢原子
Atom(片上系统)
化学物理
量子隧道
氢键
活化能
热稳定性
戒指(化学)
光化学
氢
纳米线
载流子寿命
纳米技术
表面能
接口(物质)
作者
Xinyi Wu,Wenjing Peng,Yi Yang,Mei Lyu,Jun Zhu
标识
DOI:10.1021/acsami.5c21487
摘要
Self-assembled molecules (SAMs) are widely used as hole-selective layers (HSLs) in inverted perovskite solar cells (PSCs). However, its uneven film formation and limited passivation ability for buried interface defects hinder further improvements in device performance. This work introduces sulfadiazine (SD), which contains multifunctional groups, as the interface layer between [2-(3,6-dimethoxy-9H-carbazol-9-yl)ethyl]phosphonic acid (MeO-2PACz) and perovskite layers. The SD molecules enhance carrier transport through π–π interactions with the MeO-2PACz. And also, SD also achieves improved energy level alignment, facilitating the transfer of holes at the interface. The N atom on the pyrimidine ring and the O atom in the sulfonamide group of SD can coordinate and bind with Pb 2+ ions. Additionally, the N atom in the –NH 2 group can form hydrogen bonds (N–H···N) with the FA + ions in the perovskite. The multisite passivation effect significantly reduces nonradiative recombination losses in the device. As a result, devices utilizing SD to modify buried interfaces have achieved a power conversion efficiency (PCE) of 23.27%. Furthermore, the target devices demonstrate excellent thermal stability. This study indicates that using SD as an interface layer is an effective strategy for enhancing the efficiency and stability of PSCs.
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