钙钛矿(结构)
材料科学
降级(电信)
光伏系统
钙钛矿太阳能电池
分解
相(物质)
太阳能电池
能量转换效率
化学工程
化学物理
纳米技术
光电子学
化学
生物
工程类
电信
有机化学
计算机科学
生态学
作者
Zhaoning Song,Antonio Abate,Suneth C. Watthage,Geethika K. Liyanage,Adam B. Phillips,Ullrich Steiner,Michaël Grätzel,Michael J. Heben
标识
DOI:10.1002/aenm.201600846
摘要
After rapid progress over the past five years, organic–inorganic perovskite solar cells (PSCs) currently exhibit photoconversion efficiencies comparable to the best commercially available photovoltaic technologies. However, instabilities in the materials and devices, primarily due to reactions with water, have kept PSCs from entering the marketplace. Here, laser beam induced current imaging is used to investigate the spatial and temporal evolution of the quantum efficiency of perovskite solar cells under controlled humidity conditions. Several interesting mechanistic aspects are revealed as the degradation proceeds along a four‐stage process. Three of the four stages can be reversed, while the fourth stage leads to irreversible decomposition of the photoactive perovskite material. A series of reactions in the PbI 2 ‐CH 3 NH 3 I‐H 2 O system explains the interplay between the interactions with water and the overall stability. Understanding of the degradation mechanisms of PSCs on a microscopic level gives insight into improving the long‐term stability.
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