材料科学
钙钛矿(结构)
结晶
光伏系统
能量转换效率
化学工程
相(物质)
热稳定性
晶体生长
纳米技术
动力学
化学物理
光电子学
结晶学
化学
物理
有机化学
工程类
生物
量子力学
生态学
作者
Youkui Xu,Meng Wang,Yutian Lei,Zhipeng Ci,Zhiwen Jin
标识
DOI:10.1002/aenm.202002558
摘要
Abstract 2D perovskites demonstrate higher moisture stability, oxygen content, thermal stability, and a significantly lower ion migration/phase transition occurrence in comparison to 3D perovskite. These advantages imply huge potential for 2D perovskite in commercial applications in the photovoltaic field. However, the horizontal arrangement of the organic layer severely hinders the transport of carriers, and thus, the power conversion efficiency of 2D perovskite solar cells (PSCs) is significantly lower than that of 3D. Controlling the crystallization orientation to achieve rapid carrier transport can effectively avoid or reduce such adverse effects. Hence, an in‐depth understanding of the formation mechanism and crystallization kinetics of 2D perovskite films is crucial to the development of high‐performing 2D PSCs. This review explores the studies conducted on crystallization kinetics, which is the key issue for 2D perovskite, and discusses their effects on the performance of various types of 2D PSCs to date. The crystal/natural quantum well structures and origin of the stability for 2D perovskite are also summarized. Finally, the remaining challenges in terms of development bottlenecks for 2D PSCs are discussed, alongside the proposal of possible solutions.
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