结晶度
钙钛矿(结构)
能量转换效率
材料科学
Crystal(编程语言)
成核
光电流
氯苯
结晶
化学工程
卤化物
异质结
纳米技术
化学
光电子学
无机化学
复合材料
有机化学
催化作用
程序设计语言
工程类
计算机科学
作者
Zengqi Huang,Xiaopeng Duan,Yong Zhang,Xiaotian Hu,Licheng Tan,Yiwang Chen
标识
DOI:10.1016/j.solmat.2016.06.011
摘要
Pure chlorobenzene (CBZ) and 2-propanol (IPA) or mixed-solvent assisted spin-coating have been applied to one-step fabricate CH3NH3PbI3 and CH3NH3PbI3−xClx perovskite films, respectively. However, with the treatment of pure- or mixed solvent, there are obvious differences in the formation of CH3NH3PbI3 and CH3NH3PbI3−xClx perovskite films with full coverage and large crystal grain size, as well as the role in the photovoltaic performance. Furthermore, the nucleation and growth dynamics of perovskite crystals have been taken into consideration with the activation energy of transporting crystallizing segments across the crystal interface and the formation free energy of a critical-sized nucleus. Planar heterojunction (PHJ) perovskite solar cells (PSCs) based on CH3NH3PbI3 by mixed-solvent treatment exhibit a poor power conversion efficiency (PCE) owing to the formation little amount of perovskite crystals with low crystallinity. While pure CBZ treatment renders the corresponding device get efficiency of 8.1%, which is due to the formation of uniform CH3NH3PbI3 thin film with higher surface coverage and crystallinity. Inversely, PSCs based on CH3NH3PbI3−xClx with mixed-solvent shows the highest PCE of 9.2%, short-circuit current density (Jsc) of 16.06 mA/cm2 and fill factor (FF) of 63.6% with high device reproducibility and low photocurrent hysteresis, because of possessing higher light absorption ascribed from bigger crystal size and better surface morphology with no pin-holes. These results will provide significant guidance for CH3NH3PbI3 and CH3NH3PbI3−xClx perovskite device performance optimization and large-scale application by pure- and mixed-solvent treatment.
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