Balancing transformation and dissolution-crystallization for pure phase CH3NH3PbI3 growth and its effect on photovoltaic performance in planar-structure perovskite solar cells

被引:15
作者
Sun, Kai [1 ]
Hu, Ziyang [1 ]
Shen, Baihui [1 ]
Lu, Chunyan [1 ]
Yang, Cheng [1 ]
Gao, Can [1 ]
Zhang, Jing [1 ]
Zhu, Yuejin [1 ]
机构
[1] Ningbo Univ, Dept Microelect Sci & Engn, Ningbo Collaborat Innovat Ctr Nonlinear Hazard Sy, Ningbo 315211, Zhejiang, Peoples R China
基金
美国国家科学基金会;
关键词
Dissolution-crystallization; Ostwald ripening growth; Perovskite; Solar cells; Solution engineering; SEQUENTIAL DEPOSITION; HOLE EXTRACTION; CRYSTAL-GROWTH; MORPHOLOGY; EFFICIENCY; LAYERS; FILMS; SIZE;
D O I
10.1016/j.solmat.2018.05.062
中图分类号
TE [石油、天然气工业]; TK [能源与动力工程];
学科分类号
0807 ; 0820 ;
摘要
In situ transformation and dissolution-crystallization mechanisms play a competing role in determining the characteristics of perovskite films that greatly affect the device performance of perovskite solar cells in the sequential two-step process. Herein, we develop a facile solution engineering to balance the transformation from PbI2 to CH3NH3PbI3 and dissolution-crystallization of CH3NH3PbI3 crystal growth, producing pure phase CH3NH3PbI3 crystals for high-efficient planar-structure solar cells. Low concentration of CH3NH3I in a mixed solvent of isopropanol/cyclohexane with low polarity is applied to suppress dissolution-crystallization (Ostwald ripening growth) of perovskite, while increases the transformation time from PbI2 to CH3NH3PbI3. Combination of porous PbI2 and temperature-assistance effectively promote the transformation from PbI2 to CH3NH3PbI3 and reduce the time of Ostwald ripening growth of perovskite. This solution engineering reconciles the complete PbI2 transformation and dissolution-crystallization of CH3NH3PbI3, resulting in a pure phase perovskite without any residual PbI2 in a short time. This strategy exemplified here can serve in the design and development of more sophisticated perovskites based on planar-structure applications without mesoporous TiO2 scaffold.
引用
收藏
页码:464 / 470
页数:7
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