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Bication lead iodide 2D perovskite component to stabilize inorganic α-CsPbI 3 perovskite phase for high-efficiency solar cells
Author(s) -
Taiyang Zhang,
M. Ibrahim Dar,
Ge Li,
Feng Xu,
Nanjie Guo,
Michaël Grätzel,
Yixin Zhao
Publication year - 2017
Publication title -
science advances
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 5.928
H-Index - 146
ISSN - 2375-2548
DOI - 10.1126/sciadv.1700841
Subject(s) - halide , perovskite (structure) , iodide , materials science , phase (matter) , band gap , ethylenediamine , chemical engineering , tandem , inorganic chemistry , chemistry , optoelectronics , crystallography , organic chemistry , engineering , composite material
Among various all-inorganic halide perovskites exhibiting better stability than organic-inorganic halide perovskites, α-CsPbI3 with the most suitable band gap for tandem solar cell application faces an issue of phase instability under ambient conditions. We discovered that a small amount of two-dimensional (2D) EDAPbI4 perovskite containing the ethylenediamine (EDA) cation stabilizes the α-CsPbI3 to avoid the undesirable formation of the nonperovskite δ phase. Moreover, not only the 2D perovskite of EDAPbI4 facilitate the formation of α-CsPbI3 perovskite films exhibiting high phase stability at room temperature for months and at 100°C for >150 hours but also the α-CsPbI3 perovskite solar cells (PSCs) display highly reproducible efficiency of 11.8%, a record for all-inorganic lead halide PSCs. Therefore, using the bication EDA presents a novel and promising strategy to design all-inorganic lead halide PSCs with high performance and reliability.

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