结晶
钙钛矿(结构)
氯化铅
碘化物
氯化物
异质结
材料科学
化学工程
Crystal(编程语言)
晶体生长
沉积(地质)
无机化学
化学
结晶学
光电子学
计算机科学
地质学
冶金
工程类
古生物学
沉积物
程序设计语言
作者
Andreas Binek,Irene Grill,Niklas Huber,Kristina Peters,Alexander G. Hufnagel,Matthias Handloser,Pablo Docampo,Achim Hartschuh,Thomas Bein
标识
DOI:10.1002/asia.201501379
摘要
State-of-the-art solar cells based on methylammonium lead iodide (MAPbI3 ) now reach efficiencies over 20 %. This fast improvement was possible with intensive research in perovskite processing. In particular, chloride-based precursors are known to have a positive influence on the crystallization of the perovskite. Here, we used a combination of in-situ X-ray diffraction and charge-transport measurements to understand the influence of chloride during perovskite crystallization in planar heterojunction solar cells. We show that MAPbCl3 crystallizes directly after the deposition of the starting solution and acts as a template for the formation of MAPbI3 . Additionally, we show that the charge-carrier mobility doubles by extending the time for the template formation. Our results give a deeper understanding of the influence of chloride in the synthesis of MAPbI3 and illustrate the importance of carefully controlling crystallization for reproducible, high-efficiency solar cells.
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