材料科学
钙钛矿(结构)
结晶
原位
平面的
调制(音乐)
接口(物质)
光电子学
化学工程
纳米技术
复合材料
计算机科学
哲学
物理
计算机图形学(图像)
毛细管数
毛细管作用
气象学
工程类
美学
作者
Long Cheng,Fang Wang,Dongsheng Wang,Hanqing Liu,Fanning Meng,Guiqiang Wang
标识
DOI:10.1021/acsami.5c12588
摘要
The charge recombination resulting from the numerous perovskite defects and the inferior buried interface remarkably deteriorates the performance of inorganic perovskite solar cells. Here, we introduce 4-aminobenzenesulfonic acid (ABSA) into the CsPbI 3 perovskite precursor to simultaneously reduce perovskite defects through modulating CsPbI 3 perovskite crystallization and heal the buried interface through in situ forming a ABSA dipolar interlayer. The interaction of the ABSA molecule with CsPbI 3 precursor components hinders CsPbI 3 perovskite crystallization, resulting in forming a compact and smooth CsPbI 3 perovskite film with reduced defects and enhanced crystallinity. Meanwhile, ABSA molecules are excluded from the CsPbI 3 perovskite crystal and pushed downward during the perovskite crystallization process. Consequently, ABSA molecules accumulate at the bottom surface of the CsPbI 3 perovskite and in situ form an ABSA dipolar interlayer, which effectively heals the buried interface and promotes interfacial charge transfer. As a consequence, the planar carbon-based CsPbI 3 cell with the ABSA additive demonstrates a largely improved performance with a power conversion efficiency up to 17.89%. In particular, the unencapsulated CsPbI 3 cell maintains over 90% of the original efficiency in ambient air after 480 h of storage, indicating superior long-term stability.
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