甲脒
三碘化物
材料科学
钙钛矿(结构)
量子点
能量转换效率
光伏系统
离子键合
纳米技术
太阳能电池
光电子学
化学工程
化学
离子
色素敏化染料
物理化学
电解质
电极
有机化学
工程类
生物
生态学
作者
Jingjing Xue,Jin‐Wook Lee,Zhenghong Dai,Rui Wang,Selbi Nuryyeva,Michael E. Liao,Sheng‐Yung Chang,Lei Meng,Dong Meng,Pengyu Sun,Oliver Lin,Mark S. Goorsky,Yang Yang
出处
期刊:Joule
[Elsevier BV]
日期:2018-08-09
卷期号:2 (9): 1866-1878
被引量:238
标识
DOI:10.1016/j.joule.2018.07.018
摘要
In contrast to conventional colloidal quantum dots (CQDs), management of insulating ligands on perovskite CQDs is challenging because their ionic bonds are highly vulnerable to polar solvents. Consequently, there have been only a few examples of perovskite CQD solar cells incorporating relatively robust inorganic perovskite of which optoelectronic properties are not ideal for photovoltaic devices. Here, we report efficient and stable CQD solar cells based on formamidinium lead triiodide (FAPbI3) CQDs realized by rational surface regulation. Tailoring polarity of antisolvents for the post-synthetic process enabled effective removal of the insulating ligands on FAPbI3 CQDs while preserving perovskite cores. Owing to the enhanced inter-dot electrical coupling, a power-conversion efficiency of 8.38% was demonstrated. Furthermore, the FAPbI3 CQDs-based devices showed superior stability over those of bulk FAPbI3 devices. Thermodynamic and crystallographic analyses revealed that enhanced contribution of the surface energy and lattice contraction contribute to their superior stability.
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