钙钛矿(结构)
结晶度
材料科学
成核
量子点
化学工程
能量转换效率
光电子学
复合材料
化学
工程类
有机化学
作者
Weitao Yang,Jiehuan Chen,Xiaomei Lian,Jun Li,Fenfa Yao,Gang Wu,Weiming Qiu,Chuanhong Jin,Paul Heremans,Hongzheng Chen
出处
期刊:Solar RRL
[Wiley]
日期:2019-05-17
卷期号:3 (8)
被引量:53
标识
DOI:10.1002/solr.201900132
摘要
Crystallinity and trap‐state density of a perovskite film play a critical role in the performance of corresponding perovskite solar cells (PVSCs). Herein, liquid‐phase‐exfoliated black phosphorus quantum dots (BPQDs) are incorporated into the perovskite precursor solution as additives to direct the formation of the perovskite film, i.e., methylammonium lead iodide (MAPbI 3 ). It is found that the perovskite films made with BPQDs have higher crystallinity and less nonradiative detects compared with the pristine ones, leading to longer carrier lifetime and higher carrier collection efficiency. Time‐of‐flight secondary‐ion mass spectra and surface density calculation of BPQDs reveal that the improvement of the perovskite film quality may be related to the heterogeneous nucleation of the perovskite film at the BPQDs. PVSCs using MAPbI 3 films made with BPQDs achieve a maximum power conversion efficiency of 20.0% and an encouraging thermal stability of T 80 = 100 h at 100 °C. Both values are remarkably higher than the devices with pristine perovskite films. Therefore, this work demonstrates the potential of the 2D materials quantum dots‐assisted growth method for high‐performance PVSCs.
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