Predicting the Morphology of Perovskite Thin Films Produced by Sequential Deposition Method: A Crystal Growth Dynamics Study

被引:36
作者
Ko, Hyomin [1 ]
Sin, Dong Hun [1 ]
Kim, Min [1 ]
Cho, Kilwon [1 ]
机构
[1] Pohang Univ Sci & Technol, Dept Chem Engn, Pohang 790784, South Korea
关键词
HOLE-TRANSPORTING MATERIAL; SOLAR-CELLS; ORGANOLEAD TRIHALIDE; PHASE-CHANGE; PERFORMANCE; EFFICIENCY; PLANAR; LAYER; CRYSTALLIZATION; NUCLEATION;
D O I
10.1021/acs.chemmater.6b04507
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
We performed a kinetic analysis of the sequential deposition method (SDM) to investigate how to form perovskite (CH3NH3PbI3) phases, and the effects of processing conditions on the final perovskite morphology. The reaction was found to consist of two periods with distinct kinetics. During the first period, perovskite crystals nucleated on the lead iodide (PbI2) surface, and the reaction proceeded until the surface was completely converted to perovskites. The reaction during this period determined the surface morphology of the perovskites. We were able to extract the value of the rate of the phase transformation during the first period by applying the Johnson-Mehl-Avrami-Kolmogorov model, in which the rate r is related to the average grain size R by R proportional to r(-1/3). In this way, r was used to predict the surface morphology of the perovskite under certain processing conditions. During the second period, the remaining lead iodide under the top perovskite layer was converted. Methylammonium iodide (CH3NH3I, MAI) molecules apparently diffused into the buried PbI2 through intergrain gaps of the top perovskite layers. Added MAI molecules reacted with PbI2 but also generated single-crystal perovskite nanorods, nanoplates, and nanocubes. The current study has furthered the understanding of detailed features of the SDM, enabled a reliable prediction of the final perovskite morphology resulting from specified processing conditions, and contributed to a reproducible fabrication of high-quality perovskite films.
引用
收藏
页码:1165 / 1174
页数:10
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